Staff profile

Research Interests

We are principally interested in the fundamental synthetic, chemical and physical properties of luminescent compounds. They are characterised by spectroscopic (NMR, IR, UV-vis, MS, Raman), computational (DFT) and diffraction (X-ray) methods available from the excellent departmental research facilities here along with (spectro)electrochemical and photophysical measurements to explore their emission properties. Luminescent compounds of interest include ON/OFF photoswitches, phosphorescent metal complexes and thermally activated delayed fluorescence (TADF) molecules.

 

Prompt fluorescence molecules

Compounds containing carboranes (stable clusters of boron, carbon and hydrogen) have intriguing photophysical properties. Some derivatives of ortho-carborane (1,2-C₂B₁₀H₁₂) have dual emissions where one emission is due to charge transfer (CT) or excimer/aggregation formation. 

Chem. Commun., 2021, 57, 9466-9469 https://doi.org/10.1039/D1CC03248H

Chem. Sci., 2022, 13, 5205-5219 https://doi.org/10.1039/D1SC06867A

Nat. Commun., 2024, 15, 5205-5219  https://doi.org/10.1038/s41467-024-47384-4 

 

Phosphorescent complexes

Certain metal complexes are used as emitters in phosphorescent organic light-emitting diodes (PHOLEDs). Iridium complexes are shown to emit desirable blue colours and can be incorporated in PHOLEDs with high efficiencies.

Dalton Trans., 2020, 49, 2190-2208 https://doi.org/10.1039/C9DT04672K

Organometallics, 2022, 41, 2487-2493 https://doi.org/10.1021/acs.organomet.2c00292

Inorg. Chem., 2023, 62, 2793-2805  https://doi.org/10.1021/acs.inorgchem.2c03934 

Dalton Trans., 2024, 53, 17518-17524 https://doi.org/10.1039/D4DT02321H

 

Thermally activated delayed fluorescence (TADF)

TADF is a recent area of intense research as inexpensive organic compounds are exploited as suitable emitters in organic light-emitting diodes (OLEDs) due to high efficiencies made possible by harvesting energy from both singlet and triplet states like in expensive iridium complexes.

Mater. Chem. Front., 2020, 4, 3602-3615  https://doi.org/10.1039/D0QM00429D

Chem. Mater., 2021, 33, 3066–3080  https://doi.org/10.1021/acs.chemmater.0c03783

J. Org. Chem., 2021, 86, 429–445  https://doi.org/10.1021/acs.joc.0c02174

Chem. Mater., 2024, 36, 7135–7150   https://doi.org/10.1021/acs.chemmater.4c00850 

 

• Carboranes
• Luminescence
• Electrochemistry
• Computational DFT

Chapter in book

• Polyhedral Carboranes
  
  Fox, M. (2007). Polyhedral Carboranes. In D. M. P. Mingos & R. H. Crabtree (Eds.), Comprehensive Organometallic Chemistry III. (pp. 49-112). Elsevier. https://doi.org/10.1016/B0-08-045047-4/00043-1
• Towards experimental mapping of the mechanism of heteroborane isomerisation
  
  Barbera, G., Dunn, S., Fox, M., Garrioch, R., Hodson, B., Low, K., Rosair, G., Teixidor, F., Vinas, C., Welch, A. J., & Weller, A. (2000). Towards experimental mapping of the mechanism of heteroborane isomerisation. In M. G. Davidson, K. Wade, T. Marder, & A. K. Hughes (Eds.), Contemporary Boron Chemistry (pp. 329-336).
• Studies of icosahedral carboranes with iminotris(dimethylamino)phosphorane, HNP(NMe2)(3)
  
  Davidson, M., Fox, M., Gray, F., Hibbert, T., & Wade, K. (2000). Studies of icosahedral carboranes with iminotris(dimethylamino)phosphorane, HNP(NMe2)(3). In M. Davidson, A. Hughes, T. Marder, & K. Wade (Eds.), Contemporary Boron Chemistry (pp. 223-228). Royal Society of Chemistry.
• Synthesis and structural characterisation of the anion nido-[B8H11](-), and new insights into the structures of other octaborane species
  
  Condick, P., Fox, M., Greatrex, R., & Ormsby, D. (2000). Synthesis and structural characterisation of the anion nido-[B8H11](-), and new insights into the structures of other octaborane species. In M. G. Davidson, K. Wade, T. Marder, & A. K. Hughes (Eds.), Contemporary Boron Chemistry (pp. 179-186). Royal Society of Chemistry.
• Reactions of unsaturated hydrocarbons with small boranes: New insights and recent advances
  
  Greatrex, R., & Fox, M. A. (1998). Reactions of unsaturated hydrocarbons with small boranes: New insights and recent advances. In J. Casanova (Ed.), Borane, Carborane, Carbocation Continuum (pp. 289-305).
• The borane-carborane structural pattern: Some correlations and implications
  
  Greatrex, R., & Fox, M. (1998). The borane-carborane structural pattern: Some correlations and implications. In J. Casanova (Ed.), The Borane, Carborane, Carbocation Continuum (pp. 57-84).

Journal Article

• Diiridium(III) Complexes with Fluorenylpyridyl Cyclometalating and μ 2 ‐Oxamidato Bridging Ligands and their High Efficiency Phosphorescent Solution‐Processed OLEDs
  
  M’hamedi, A., Fox, M. A., Batsanov, A. S., Al‐Attar, H. A., & Bryce, M. R. (2025). Diiridium(III) Complexes with Fluorenylpyridyl Cyclometalating and μ 2 ‐Oxamidato Bridging Ligands and their High Efficiency Phosphorescent Solution‐Processed OLEDs. European Journal of Inorganic Chemistry, 28(6), Article e202400745. https://doi.org/10.1002/ejic.202400745
• Dual phosphorescent emissions from conformers of iridium complex rotors.
  
  Hsu, Y., Bhagani, C., Aguilar, J. A., Fox, M. A., Yufit, D., Davidson, R., & Beeby, A. (2024). Dual phosphorescent emissions from conformers of iridium complex rotors. Dalton Transactions, 53(43), 17518-17524. https://doi.org/10.1039/D4DT02321H
• Exciplex, Not Heavy-Atom Effect, Controls the Triplet Dynamics of a Series of Sulfur-Containing Thermally Activated Delayed Fluorescence Molecules
  
  Öner, S., Kuila, S., Stavrou, K., Danos, A., Fox, M. A., Monkman, A. P., & Bryce, M. R. (2024). Exciplex, Not Heavy-Atom Effect, Controls the Triplet Dynamics of a Series of Sulfur-Containing Thermally Activated Delayed Fluorescence Molecules. Chemistry of Materials, 36(15), 7135-7150. https://doi.org/10.1021/acs.chemmater.4c00850
• Optically induced charge-transfer in donor-acceptor-substituted p - and m - C₂ B₁₀ H₁₂ carboranes
  
  Wu, L., Holzapfel, M., Schmiedel, A., Peng, F., Moos, M., Mentzel, P., Shi, J., Neubert, T., Bertermann, R., Finze, M., Fox, M. A., Lambert, C., & Ji, L. (2024). Optically induced charge-transfer in donor-acceptor-substituted p - and m - C₂ B₁₀ H₁₂ carboranes. Nature Communications, 15(1), Article 3005. https://doi.org/10.1038/s41467-024-47384-4
• Structural Diversity in Cyclometalated Diiridium(III) Complexes with Bridging syn and anti μ2‐Oxamidato and μ2‐Dithioxamidato Ligands
  
  M’hamedi, A., Batsanov, A. S., Fox, M. A., Aguilar, J. A., & Bryce, M. R. (2023). Structural Diversity in Cyclometalated Diiridium(III) Complexes with Bridging syn and anti μ2‐Oxamidato and μ2‐Dithioxamidato Ligands. European Journal of Inorganic Chemistry, 26(34), Article e202300423. https://doi.org/10.1002/ejic.202300423
• Tuning Emission Lifetimes of Ir(C^N)2(acac) Complexes with Oligo(phenyleneethynylene) Groups
  
  Davidson, R., Hsu, Y., Fox, M. A., Aguilar, J. A., Yufit, D., & Beeby, A. (2023). Tuning Emission Lifetimes of Ir(C^N)2(acac) Complexes with Oligo(phenyleneethynylene) Groups. Inorganic Chemistry, 62(6), 2793-2805. https://doi.org/10.1021/acs.inorgchem.2c03934
• Vapor Sorption and Halogen-Bond-Induced Solid-Form Rearrangement of a Porous Pharmaceutical
  
  Andrews, J. L., Yufit, D. S., McCabe, J. F., Fox, M. A., & Steed, J. W. (2023). Vapor Sorption and Halogen-Bond-Induced Solid-Form Rearrangement of a Porous Pharmaceutical. Crystal Growth & Design, 23(4), 2628-2633. https://doi.org/10.1021/acs.cgd.2c01464
• Iridium‐Catalysed C−H Borylation of Fluoroarenes: Insights into the Balance between Steric and Electronic Control of Regioselectivity
  
  Ding, M., Reuven, J. A., Hones, A. C., Fox, M. A., & Steel, P. G. (2022). Iridium‐Catalysed C−H Borylation of Fluoroarenes: Insights into the Balance between Steric and Electronic Control of Regioselectivity. European Journal of Organic Chemistry, 2022(47). https://doi.org/10.1002/ejoc.202201005
• Divergent Approach for Tris-Heteroleptic Cyclometalated Iridium Complexes Using Triisopropylsilylethynyl-Substituted Synthons
  
  Edkins, R. M., Hsu, Y., Fox, M. A., Yufit, D., Beeby, A., & Davidson, R. J. (2022). Divergent Approach for Tris-Heteroleptic Cyclometalated Iridium Complexes Using Triisopropylsilylethynyl-Substituted Synthons. Organometallics, 41(17), 2487-2493. https://doi.org/10.1021/acs.organomet.2c00292
• Structure and hydration of polyvinylpyrrolidone-hydrogen peroxide
  
  Chambers, L. I., Yufit, D. S., Fox, M. A., Musa, O. M., & Steed, J. W. (2022). Structure and hydration of polyvinylpyrrolidone-hydrogen peroxide. Chemical Communications, 58(1), 80-83. https://doi.org/10.1039/d1cc06047c
• Thermodynamic equilibrium between locally excited and charge-transfer states through thermally activated charge transfer in 1-(pyren-2′-yl)-o-carborane
  
  Ji, L., Riese, S., Schmiedel, A., Holzapfel, M., Fest, M., Nitsch, J., Curchod, B. F., Friedrich, A., Wu, L., Al Mamari, H. H., Hammer, S., Pflaum, J., Fox, M. A., Tozer, D. J., Finze, M., Lambert, C., & Marder, T. B. (2022). Thermodynamic equilibrium between locally excited and charge-transfer states through thermally activated charge transfer in 1-(pyren-2′-yl)-o-carborane. Chemical Science, 13, 5205-5219. https://doi.org/10.1039/d1sc06867a
• Carborane photochromism: A fatigue resistant carborane switch
  
  Li, C., Aldred, M. P., Harder, R. A., Chen, Y., Yufit, D. S., Zhu, M., & Fox, M. A. (2021). Carborane photochromism: A fatigue resistant carborane switch. Chemical Communications, 57(74), 9466-9469. https://doi.org/10.1039/d1cc03248h
• Vibrational Damping Reveals Vibronic Coupling in Thermally Activated Delayed Fluorescence Materials
  
  Hempe, M., Kukhta, N. A., Danos, A., Fox, M. A., Batsanov, A. S., Monkman, A. P., & Bryce, M. R. (2021). Vibrational Damping Reveals Vibronic Coupling in Thermally Activated Delayed Fluorescence Materials. Chemistry of Materials, 33(9), 3066-3080. https://doi.org/10.1021/acs.chemmater.0c03783
• Nonlinear optical properties of meso-Tetra(fluorenyl)porphyrins peripherally functionalized with one to four ruthenium alkynyl substituents
  
  Zhang, X., Shi, L., Fox, M. A., Barlow, A., Morshedi, M., Cifuentes, M. P., Humphrey, M. G., Mongin, O., Paul, F., & Paul-Roth, C. O. (2021). Nonlinear optical properties of meso-Tetra(fluorenyl)porphyrins peripherally functionalized with one to four ruthenium alkynyl substituents. Dyes and Pigments, 188, Article 109155. https://doi.org/10.1016/j.dyepig.2021.109155
• Cyclophane Molecules Exhibiting Thermally Activated Delayed Fluorescence: Linking Donor Units to Influence Molecular Conformation
  
  Hempe, M., Harrison, A. K., Ward, J. S., Batsanov, A. S., Fox, M. A., Dias, F. B., & Bryce, M. R. (2021). Cyclophane Molecules Exhibiting Thermally Activated Delayed Fluorescence: Linking Donor Units to Influence Molecular Conformation. Journal of Organic Chemistry, 86(1), 429-445. https://doi.org/10.1021/acs.joc.0c02174
• HFO-1234yf as a CF3-building block: Synthesis and Chemistry of CF3-ynones
  
  Murray, B. J., Marsh, T. G., Yufit, D. S., Fox, M. A., Harsanyi, A., Boulton, L. T., & Sandford, G. (2020). HFO-1234yf as a CF3-building block: Synthesis and Chemistry of CF3-ynones. European Journal of Organic Chemistry, 2020(39), 6236-6244. https://doi.org/10.1002/ejoc.202001071
• Unusual dual-emissive heteroleptic iridium complexes incorporating TADF cyclometalating ligands
  
  Benjamin, H., Zheng, Y., Kozhevnikov, V. N., Siddle, J. S., O’Driscoll, L. J., Fox, M. A., Batsanov, A. S., Griffiths, G. C., Dias, F. B., Monkman, A. P., & Bryce, M. R. (2020). Unusual dual-emissive heteroleptic iridium complexes incorporating TADF cyclometalating ligands. Dalton Transactions, 49(7), 2190-2208. https://doi.org/10.1039/c9dt04672k
• Exploiting trifluoromethyl substituents for tuning orbital character of singlet and triplet states to increase the rate of thermally activated delayed fluorescence
  
  Ward, J. S., Danos, A., Stachelek, P., Fox, M. A., Batsanov, A. S., Monkman, A. P., & Bryce, M. R. (2020). Exploiting trifluoromethyl substituents for tuning orbital character of singlet and triplet states to increase the rate of thermally activated delayed fluorescence. Materials Chemistry Frontiers, 4(12). https://doi.org/10.1039/d0qm00429d
• Metallacarborane Assemblies as Effective Antimicrobial Agents, Including a Highly Potent Anti-MRSA Agent
  
  Romero, I., Martinez-Medina, M., Camprubí-Font, C., Bennour, I., Moreno, D., Martínez-Martínez, L., Teixidor, F., Fox, M. A., & Viñas, C. (2020). Metallacarborane Assemblies as Effective Antimicrobial Agents, Including a Highly Potent Anti-MRSA Agent. Organometallics, 39(23), 4253-4264. https://doi.org/10.1021/acs.organomet.0c00315
• Fluorenylporphyrins functionalized by electrochromic ruthenium units as redox-triggered fluorescence switches
  
  Zhang, X., Abid, S., Shi, L., Williams, J. G., Fox, M. A., Miomandre, F., Tourbillon, C., Audibert, J., Mongin, O., Paul, F., & Paul-Roth, C. O. (2019). Fluorenylporphyrins functionalized by electrochromic ruthenium units as redox-triggered fluorescence switches. Dalton Transactions, 48(31), 11897-11911. https://doi.org/10.1039/c9dt02087j
• Unravelling the Complexities of Pseudocontact Shift Analysis in Lanthanide Coordination Complexes of Differing Symmetry
  
  Parker, D., Suturina, E., Harnden, A., Batsanov, A., Fox, M., Mason, K., Vonci, M., McInnes, E., & Chilton, N. (2019). Unravelling the Complexities of Pseudocontact Shift Analysis in Lanthanide Coordination Complexes of Differing Symmetry. Angewandte Chemie, 131(30), 10936-10400. https://doi.org/10.1002/anie.201906031
• Impact of Methoxy Substituents on Thermally Activated Delayed Fluorescence and Room-Temperature Phosphorescence in All-Organic Donor–Acceptor Systems
  
  Ward, J. S., Nobuyasu, R. S., Fox, M. A., Aguilar, J. A., Hall, D., Batsanov, A. S., Ren, Z., Dias, F. B., & Bryce, M. R. (2019). Impact of Methoxy Substituents on Thermally Activated Delayed Fluorescence and Room-Temperature Phosphorescence in All-Organic Donor–Acceptor Systems. Journal of Organic Chemistry, 84(7), 3801-3816. https://doi.org/10.1021/acs.joc.8b02848
• Synthetic, Structural, and Computational Studies on Heavier Tetragen and Chalcogen Triazenide Complexes
  
  Flanagan, K. R., Parish, J. D., Fox, M. A., & Johnson, A. L. (2019). Synthetic, Structural, and Computational Studies on Heavier Tetragen and Chalcogen Triazenide Complexes. Inorganic Chemistry, 58(24), 16660-16666. https://doi.org/10.1021/acs.inorgchem.9b02757
• Bond Rotations and Heteroatom Effects in Donor-Acceptor-Donor Molecules: Implications for Thermally Activated Delayed Fluorescence and Room Temperature Phosphorescence
  
  Ward, J. S., Nobuyasu, R. S., Fox, M. A., Batsanov, A. S., Santos, J., Dias, F. B., & Bryce, M. R. (2018). Bond Rotations and Heteroatom Effects in Donor-Acceptor-Donor Molecules: Implications for Thermally Activated Delayed Fluorescence and Room Temperature Phosphorescence. Journal of Organic Chemistry, 83(23), 14431-14442. https://doi.org/10.1021/acs.joc.8b02187
• Selective signalling of glyphosate in water using europium luminescence
  
  Jennings, L. B., Shuvaev, S., Fox, M. A., Pal, R., & Parker, D. (2018). Selective signalling of glyphosate in water using europium luminescence. Dalton Transactions, 47(45), 16145-16154. https://doi.org/10.1039/c8dt03823f
• Monitoring the ADP/ATP ratio via induced circularly‐polarised europium luminescence
  
  Parker, D., Shuvaev, S., & Fox, M. A. (2018). Monitoring the ADP/ATP ratio via induced circularly‐polarised europium luminescence. Angewandte Chemie International Edition, 57(25), 7488-7492. https://doi.org/10.1002/anie.201801248
• Enhanced selectivity for Mg2+ with a phosphinate-based chelate: APDAP versus APTRA
  
  Walter, E. R., Fox, M. A., Parker, D., & Williams, J. G. (2018). Enhanced selectivity for Mg2+ with a phosphinate-based chelate: APDAP versus APTRA. Dalton Transactions, 47(6), 1755-1763. https://doi.org/10.1039/c7dt04698g
• Role of the Diphosphine Chelate in Emissive, Charge-Neutral Iridium(III) Complexes
  
  Liao, J., Devereux, L. R., Fox, M. A., Yang, C., Chiang, Y., Chang, C., Lee, G., & Chi, Y. (2018). Role of the Diphosphine Chelate in Emissive, Charge-Neutral Iridium(III) Complexes. Chemistry - A European Journal, 24(3), 624-635. https://doi.org/10.1002/chem.201703482
• Bis-tridentate Ir(III) Metal Phosphors for Efficient Deep-Blue Organic Light-Emitting Diodes
  
  Kuo, H., Chen, Y., Devereux, L. R., Wu, C., Fox, M. A., Kuei, C., Chi, Y., & Lee, G. (2017). Bis-tridentate Ir(III) Metal Phosphors for Efficient Deep-Blue Organic Light-Emitting Diodes. Advanced Materials, 29(33), Article 1702464. https://doi.org/10.1002/adma.201702464
• Pyridylpyrazole N^N Ligands Combined with Sulfonyl-Functionalised Cyclometalating Ligands for Blue-Emitting Iridium(III) Complexes and Solution-Processable PhOLEDs
  
  Benjamin, H., Fox, M. A., Batsanov, A. S., Al-Attar, H. A., Li, C., Ren, Z., Monkman, A. P., & Bryce, M. R. (2017). Pyridylpyrazole N^N Ligands Combined with Sulfonyl-Functionalised Cyclometalating Ligands for Blue-Emitting Iridium(III) Complexes and Solution-Processable PhOLEDs. Dalton Transactions, 46, 10996-11007. https://doi.org/10.1039/c7dt02289a
• The Contributions of Molecular Vibrations and Higher Triplet Levels to the Intersystem Crossing Mechanism in Metal-Free Organic Emitters
  
  Huang, R., Avó, J., Northey, T., Chaning-Pearce, E., dos Santos, P. L., Ward, J. S., Data, P., Etherington, M. K., Fox, M. A., Penfold, T. J., Berberan-Santos, M. N., Lima, J. C., Bryce, M. R., & Dias, F. B. (2017). The Contributions of Molecular Vibrations and Higher Triplet Levels to the Intersystem Crossing Mechanism in Metal-Free Organic Emitters. Journal of Materials Chemistry C Materials for Optical and Electronic Devices, 5(25), 6269-6280. https://doi.org/10.1039/c7tc01958k
• Geometries of 11-vertex carborane monoanion radicals with 2n+3 skeletal electron counts
  
  Patel, N., Oliva-Enrich, J., & Fox, M. (2017). Geometries of 11-vertex carborane monoanion radicals with 2n+3 skeletal electron counts. European Journal of Inorganic Chemistry, 2017(38-39), 4568-4574. https://doi.org/10.1002/ejic.201700419
• New Blatter-type radicals from a bench-stable carbene
  
  Grant, J. A., Lu, Z., Tucker, D. E., Hockin, B. M., Yufit, D. S., Fox, M. A., Kataky, R., Chechik, V., & O’Donoghue, A. C. (2017). New Blatter-type radicals from a bench-stable carbene. Nature Communications, 8, Article 15088. https://doi.org/10.1038/ncomms15088
• Platinum(II) complexes of some unsymmetrical diphosphenes
  
  Dillon, K., Fox, M., Gibson, V., Goodwin, H., & Sequiera, L. (2017). Platinum(II) complexes of some unsymmetrical diphosphenes. Journal of Organometallic Chemistry, 830, 113-119. https://doi.org/10.1016/j.jorganchem.2016.10.005
• Luminescent Pt(II) complexes featuring imidazolylidene–pyridylidene and dianionic bipyrazolate: from fundamentals to OLED fabrications
  
  Tseng, C., Fox, M., Liao, J., Ku, C., Sie, Z., Chang, C., Wang, J., Chen, Z., Lee, G., & Chi, Y. (2017). Luminescent Pt(II) complexes featuring imidazolylidene–pyridylidene and dianionic bipyrazolate: from fundamentals to OLED fabrications. Journal of Materials Chemistry C Materials for Optical and Electronic Devices, 5(6), 1420-1435. https://doi.org/10.1039/c6tc05154e
• Bright Green PhOLEDs Using Cyclometalated Diiridium(III) Complexes with Bridging Oxamidato Ligands as Phosphorescent Dopants
  
  M’hamedi, A., Fox, M. A., Batsanov, A. S., Al-Attar, H. A., Monkman, A. P., & Bryce, M. R. (2017). Bright Green PhOLEDs Using Cyclometalated Diiridium(III) Complexes with Bridging Oxamidato Ligands as Phosphorescent Dopants. Journal of Materials Chemistry C Materials for Optical and Electronic Devices, 5(27), 6777-6789. https://doi.org/10.1039/c7tc00628d
• The Role of Local Triplet Excited States and D-A Relative Orientation in Thermally Activated Delayed Fluorescence: Photophysics and Devices
  
  Dias, F., Santos, J., Graves, D., Data, P., Nobuyasu, R., Fox, M., Batsanov, A., Palmeira, T., Berberan-Santos, M., Bryce, M., & Monkman, A. (2016). The Role of Local Triplet Excited States and D-A Relative Orientation in Thermally Activated Delayed Fluorescence: Photophysics and Devices. Advanced Science, 3(12), Article 1600080. https://doi.org/10.1002/advs.201600080
• Biotransformation of fluorophenyl pyridine carboxylic acids by the model fungus Cunninghamella elegans
  
  Palmer-Brown, W., Dunne, B., Ortin, Y., Fox, M. A., Sandford, G., & Murphy, C. D. (2016). Biotransformation of fluorophenyl pyridine carboxylic acids by the model fungus Cunninghamella elegans. Xenobiotica, 47(9), 763-770. https://doi.org/10.1080/00498254.2016.1227109
• Sulfonyl-Substituted Heteroleptic Cyclometalated Iridium(III) Complexes as Blue Emitters for Solution-Processable Phosphorescent Organic Light-Emitting Diodes
  
  Benjamin, H., Zheng, Y., Batsanov, A., Fox, M., Al-Attar, H., Monkman, A., & Bryce, M. (2016). Sulfonyl-Substituted Heteroleptic Cyclometalated Iridium(III) Complexes as Blue Emitters for Solution-Processable Phosphorescent Organic Light-Emitting Diodes. Inorganic Chemistry, 55(17), 8612-8627. https://doi.org/10.1021/acs.inorgchem.6b01179
• Bis-Tridentate Iridium(III) Phosphors Bearing Functional 2-Phenyl-6-(imidazol-2-ylidene)pyridine and 2-(Pyrazol-3-yl)-6-phenylpyridine Chelates for Efficient OLEDs
  
  Lin, J., Chau, N., Liao, J., Wong, W., Lu, C., Sie, Z., Chang, C., Fox, M., Low, P., Lee, G., & Chi, Y. (2016). Bis-Tridentate Iridium(III) Phosphors Bearing Functional 2-Phenyl-6-(imidazol-2-ylidene)pyridine and 2-(Pyrazol-3-yl)-6-phenylpyridine Chelates for Efficient OLEDs. Organometallics, 35(11), 1813-1824. https://doi.org/10.1021/acs.organomet.6b00205
• Induced europium CPL for the selective signalling of phosphorylated amino-acids and O-phosphorylated hexapeptides
  
  Neil, E., Pal, R., Fox, M., & Parker, D. (2016). Induced europium CPL for the selective signalling of phosphorylated amino-acids and O-phosphorylated hexapeptides. Dalton Transactions, 45(20), 8355-8366. https://doi.org/10.1039/c6dt01212d
• Tethered N-heterocyclic carbene–carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
  
  Holmes, J., Pask, C., Fox, M., & Willans, C. (2016). Tethered N-heterocyclic carbene–carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium. Chemical Communications, 52(38), 6443-6446. https://doi.org/10.1039/c6cc01650b
• Low-melting molecular complexes: Part VII. 2,3-, 2,5- and 3,4-hexanediones and their molecular complexes with chloroform
  
  Yufit, D., & Fox, M. (2016). Low-melting molecular complexes: Part VII. 2,3-, 2,5- and 3,4-hexanediones and their molecular complexes with chloroform. Structural Chemistry, 27(1), 9-15. https://doi.org/10.1007/s11224-015-0620-x
• Substituent Effects on the Fluorescence Properties of ortho-Carbor­anes: Unusual Emission Behaviour in C-(2′-Pyridyl)-ortho-carboranes
  
  Böhling, L., Brockhinke, A., Kahlert, J., Weber, L., Harder, R., Yufit, D., Howard, J., MacBride, J., & Fox, M. (2016). Substituent Effects on the Fluorescence Properties of ortho-Carbor­anes: Unusual Emission Behaviour in C-(2′-Pyridyl)-ortho-carboranes. European Journal of Inorganic Chemistry, 2016(3), 403-412. https://doi.org/10.1002/ejic.201501284
• Ir(III)-Based Phosphors with Bipyrazolate Ancillaries; Rational Design, Photophysics, and Applications in Organic Light-Emitting Diodes
  
  Liao, J., Chi, Y., Sie, Z., Ku, C., Chang, C., Fox, M., Low, P., Tseng, M., & Lee, G. (2015). Ir(III)-Based Phosphors with Bipyrazolate Ancillaries; Rational Design, Photophysics, and Applications in Organic Light-Emitting Diodes. Inorganic Chemistry, 54(22), 10811-10821. https://doi.org/10.1021/acs.inorgchem.5b01835
• An experimental and computational approach to understanding the reactions of acyl nitroso compounds in [4+2]-cycloadditions
  
  Chaiyaveij, D., Batsanov, A., Fox, M., Marder, T., & Whiting, A. (2015). An experimental and computational approach to understanding the reactions of acyl nitroso compounds in [4+2]-cycloadditions. Journal of Organic Chemistry, 80(19), 9518-9534. https://doi.org/10.1021/acs.joc.5b01470
• Chiral probe development for circularly polarised luminescence: comparative study of structural factors determining the degree of induced CPL with four heptacoordinate europium(III) complexes
  
  Neil, E., Fox, M., Pal, R., Pålsson, L., O’Sullivan, B., & Parker, D. (2015). Chiral probe development for circularly polarised luminescence: comparative study of structural factors determining the degree of induced CPL with four heptacoordinate europium(III) complexes. Dalton Transactions, 44(33), 14937-14951. https://doi.org/10.1039/c5dt02358k
• Challenging lanthanide relaxation theory: erbium and thulium complexes that show NMR relaxation rates faster than dysprosium and terbium analogues
  
  Funk, A., Harvey, P., Finney, K., Fox, M., Kenwright, A., Rogers, N., Senanayake, P., & Parker, D. (2015). Challenging lanthanide relaxation theory: erbium and thulium complexes that show NMR relaxation rates faster than dysprosium and terbium analogues. Physical Chemistry Chemical Physics, 17(25), 16507-16511. https://doi.org/10.1039/c5cp02210j
• Syntheses and Structures of Buta-1,3-Diynyl Complexes from ‘On Complex’ Cross-Coupling Reactions
  
  Oerthel, M., Yufit, D., Fox, M., Bryce, M., & Low, P. (2015). Syntheses and Structures of Buta-1,3-Diynyl Complexes from ‘On Complex’ Cross-Coupling Reactions. Organometallics, 34(11), 2395-2405. https://doi.org/10.1021/om501186c
• Syntheses and Reductions of C-Dimesitylboryl-1,2-dicarba-closo-dodecaboranes
  
  Kahlert, J., Böhling, L., Brockhinke, A., Stammler, H., Newmann, B., Rendina, L., Low, P., Weber, L., & Fox, M. (2015). Syntheses and Reductions of C-Dimesitylboryl-1,2-dicarba-closo-dodecaboranes. Dalton Transactions, 44(21), 9766-9781. https://doi.org/10.1039/c5dt00758e
• New donor–acceptor conjugates based on a trifluorenylporphyrin linked to a redox–switchable ruthenium unit
  
  Merhi, A., Zhang, X., Yao, D., Drouet, S., Mongin, O., Paul, F., Williams, J., Fox, M., & Paul-Roth, C. (2015). New donor–acceptor conjugates based on a trifluorenylporphyrin linked to a redox–switchable ruthenium unit. Dalton Transactions, 44(20), 9470-9485. https://doi.org/10.1039/c5dt00348b
• Near infrared-emitting tris-bidentate Os(II) phosphors: control of excited state characteristics and fabrication of OLEDs
  
  Liao, J., Chi, Y., Yeh, C., Kao, H., Chang, C., Fox, M., Low, P., & Lee, G. (2015). Near infrared-emitting tris-bidentate Os(II) phosphors: control of excited state characteristics and fabrication of OLEDs. Journal of Materials Chemistry C Materials for Optical and Electronic Devices, 3(19), 4910-4920. https://doi.org/10.1039/c5tc00204d
• Why are the {Cu4N4} rings in copper(I) phosphinimide clusters [Cu{μ-N=PR3}]4 (R = NMe3 or Ph) planar?
  
  Robinson, T., Price, R., Davidson, M., Fox, M., & Johnson, A. (2015). Why are the {Cu4N4} rings in copper(I) phosphinimide clusters [Cu{μ-N=PR3}]4 (R = NMe3 or Ph) planar? Dalton Transactions, 44(12), 5611-5619. https://doi.org/10.1039/c5dt00255a
• Oligo(p-phenyleneethynylene) (OPE) Molecular Wires: Synthesis and Length Dependence of Photoinduced Charge Transfer in OPEs with Triarylamine and Diaryloxadiazole End Groups
  
  Linton, K., Fox, M., Pålsson, L., & Bryce, M. (2015). Oligo(p-phenyleneethynylene) (OPE) Molecular Wires: Synthesis and Length Dependence of Photoinduced Charge Transfer in OPEs with Triarylamine and Diaryloxadiazole End Groups. Chemistry - A European Journal, 21(10), 3997-4007. https://doi.org/10.1002/chem.201406080
• Electronic Structure and Charge Transport Properties of a Series of 3,6-(Diphenyl)-s-tetrazine Derivatives: Are They Suitable Candidates for Molecular Electronics?
  
  Moral, M., García, G., Garzón, A., Granadino-Roldán, J., Fox, M., Yufit, D., Peñas, A., Melguizo, M., & Fernández-Gómez, M. (2014). Electronic Structure and Charge Transport Properties of a Series of 3,6-(Diphenyl)-s-tetrazine Derivatives: Are They Suitable Candidates for Molecular Electronics? Journal of Physical Chemistry C, 118(46), 26427-26439. https://doi.org/10.1021/jp5049698
• Bimetallic Cyclometalated Iridium(III) Diastereomers with Non-Innocent Bridging Ligands for High-Efficiency Phosphorescent OLEDs
  
  Zheng, Y., Batsanov, A., Fox, M., Al-Attar, H., Abdullah, K., Jankus, V., Bryce, M., & Monkman, A. (2014). Bimetallic Cyclometalated Iridium(III) Diastereomers with Non-Innocent Bridging Ligands for High-Efficiency Phosphorescent OLEDs. Angewandte Chemie International Edition, 53(43), 11616-11619. https://doi.org/10.1002/anie.201407475
• Studies on bis(1’-ortho-carboranyl)benzenes and bis(1’-ortho-carboranyl)biphenyls
  
  Harder, R., MacBride, J., Rivers, G., Yufit, D., Goeta, A., Howard, J., Wade, K., & Fox, M. (2014). Studies on bis(1’-ortho-carboranyl)benzenes and bis(1’-ortho-carboranyl)biphenyls. Tetrahedron, 70(34), 5182-5189. https://doi.org/10.1016/j.tet.2014.05.102
• Ultrafast Dynamics and Computational Studies on Diaminodicyanoquinodimethanes (DADQs)
  
  Szablewski, M., Fox, M., Dias, F., Namih, H., Snedden, E., King, S., Dai, D., & Pålsson, L. (2014). Ultrafast Dynamics and Computational Studies on Diaminodicyanoquinodimethanes (DADQs). Journal of Physical Chemistry B (Soft Condensed Matter and Biophysical Chemistry), 118(24), 6815-6828. https://doi.org/10.1021/jp411358d
• Mixed-Valence Ruthenium Complexes Rotating through a Conformational Robin–Day Continuum
  
  Parthey, M., Gluyas, J., Fox, M., Low , P., & Kaupp, M. (2014). Mixed-Valence Ruthenium Complexes Rotating through a Conformational Robin–Day Continuum. Chemistry - A European Journal, 20(23), 6895-6908. https://doi.org/10.1002/chem.201304947
• Crystal structures of the carborane dianions, [1,4-(PhCB10H10C)2C6H4]2- and [1,4-(PhCB10H10C)2C6F4]2-, and the stabilizing role of the para-phenylene unit on unusual 2n+3 SE clusters
  
  Kahlert, J., Stammler, H., Neumann, B., Harder, R., Weber, L., & Fox, M. (2014). Crystal structures of the carborane dianions, [1,4-(PhCB10H10C)2C6H4]2- and [1,4-(PhCB10H10C)2C6F4]2-, and the stabilizing role of the para-phenylene unit on unusual 2n+3 SE clusters. Angewandte Chemie International Edition, 53(14), 3702-3705. https://doi.org/10.1002/anie.201310718
• On the ambiguity of 1,3,2-benzodiazaboroles as donor/acceptor functionalities in luminescent molecules
  
  Weber, L., Halama, J., Hanke, K., Böhling, L., Brockhinke, A., Stammler, H., Neumann, B., & Fox, M. (2014). On the ambiguity of 1,3,2-benzodiazaboroles as donor/acceptor functionalities in luminescent molecules. Dalton Transactions, 43(8), 3347-3363. https://doi.org/10.1039/c3dt52836g
• 19F and 13C GIAO-NMR chemical shifts for the identification of perfluoro-quinoline and -isoquinoline derivatives
  
  Fox, M., Pattison, G., Sandford, G., & Batsanov, A. (2013). 19F and 13C GIAO-NMR chemical shifts for the identification of perfluoro-quinoline and -isoquinoline derivatives. Journal of Fluorine Chemistry, 155, 62-71. https://doi.org/10.1016/j.jfluchem.2013.05.005
• C,C′-Bis(benzodiazaborolyl)dicarba-closo-dodecaboranes: Synthesis, structures, photophysics and electrochemistry
  
  Weber, L., Kahlert, J., Brockhinke, R., Böhling, L., Halama, J., Brockhinke, A., Stammler, H., Neumann, B., Nervi, C., Harder, R., & Fox, M. (2013). C,C′-Bis(benzodiazaborolyl)dicarba-closo-dodecaboranes: Synthesis, structures, photophysics and electrochemistry. Dalton Transactions, 42(30), 10982-10996. https://doi.org/10.1039/c3dt51125a
• A novel, efficient synthesis of N-aryl pyrroles via reaction of 1-boronodienes with arylnitroso compounds
  
  Tripoteau, F., Eberlin, L., Fox, M., Carboni, B., & Whiting, A. (2013). A novel, efficient synthesis of N-aryl pyrroles via reaction of 1-boronodienes with arylnitroso compounds. Chemical Communications, 49(47), 5414-5416. https://doi.org/10.1039/c3cc42227e
• Remarkable cage deboronation and rearrangement of a closo-1,12-dicarbadodecaborane to form a neutral nido-7,9-dicarbaundecaborane
  
  Ioppolo, J., Bhadbhade, M., Fox, M., & Rendina, L. (2013). Remarkable cage deboronation and rearrangement of a closo-1,12-dicarbadodecaborane to form a neutral nido-7,9-dicarbaundecaborane. Chemical Communications, 49(32), 3312-3314. https://doi.org/10.1039/c3cc41173g
• Electrochemical and spectroelectrochemical studies of C-benzodiazaborolyl-ortho-carboranes
  
  Weber, L., Kahlert, J., Boehling, L., Brockhinke, A., Stammler, H., Neumann, B., Harder, R., Low, P., & Fox, M. (2013). Electrochemical and spectroelectrochemical studies of C-benzodiazaborolyl-ortho-carboranes. Dalton Transactions, 42(6), 2266-2281. https://doi.org/10.1039/c2dt32378h
• Some Ruthenium Derivatives of Penta-1,4-diyn-3-one
  
  Bruce, M. I., Burgun, A., Fox, M. A., Jevric, M., Low, P. J., Nicholson, B. K., Parker Christian, R., Skelton, B. W., White, A. H., & Zaitseva, N. N. (2013). Some Ruthenium Derivatives of Penta-1,4-diyn-3-one. Organometallics, 32(11), 3286-3299. https://doi.org/10.1021/om400208q
• Syntheses, structures and redox properties of tris(pyrazolyl)borate-capped ruthenium vinyl complexes
  
  Farmer, J. D., Man, W. Y., Fox, M. A., Yufit, D. S., Howard, J. A., Hill, A. F., & Low, P. J. (2012). Syntheses, structures and redox properties of tris(pyrazolyl)borate-capped ruthenium vinyl complexes. Journal of Organometallic Chemistry, 721-722, 173-185. https://doi.org/10.1016/j.jorganchem.2012.09.001
• Carboranes as model hypercarbon systems; structural and bonding patterns in selected isoelectronic closo-borane and carborane systems; [BnHn](2-), [1-CBn-1Hn](-) and 1,n-C2Bn-2Hn (n=5, 6, 7, 10 or 12)
  
  Armstrong, D., Fox, M., & Wade, K. (2012). Carboranes as model hypercarbon systems; structural and bonding patterns in selected isoelectronic closo-borane and carborane systems; [BnHn](2-), [1-CBn-1Hn](-) and 1,n-C2Bn-2Hn (n=5, 6, 7, 10 or 12). Journal of Organometallic Chemistry, 721, 130-136. https://doi.org/10.1016/j.jorganchem.2012.07.047
• Reactions of 4-substituted tetrafluoropyridine derivatives with sulfur nucleophiles: SNAr and annelation processes
  
  Fox, M. A., Sandford, G., Slater, R., Yufit, D. S., Howard, J. A., & Vong, A. (2012). Reactions of 4-substituted tetrafluoropyridine derivatives with sulfur nucleophiles: SNAr and annelation processes. Journal of Fluorine Chemistry, 143(SI), 148-154. https://doi.org/10.1016/j.jfluchem.2012.05.011
• Phosphine-alkene ligand-mediated alkyl-alkyl and alkyl-halide elimination processes from palladium(II)
  
  Tuxworth, L., Baiget, L., Phanopoulos, A., Metters, O. J., Batsanov, A. S., Fox, M. A., Howard, J. A., & Dyer, P. W. (2012). Phosphine-alkene ligand-mediated alkyl-alkyl and alkyl-halide elimination processes from palladium(II). Chemical Communications, 48(84), 10413-10415. https://doi.org/10.1039/c2cc35623f
• Diazaborolyl-boryl push–pull systems with ethynylene–arylene bridges as ‘turn-on’ fluoride sensors
  
  Weber, L., Eickhoff, D., Kahlert, J., Boehling, L., Brockhinke, A., Stammler, H., Neumann, B., & Fox, M. A. (2012). Diazaborolyl-boryl push–pull systems with ethynylene–arylene bridges as ‘turn-on’ fluoride sensors. Dalton Transactions, 41(34), 10328-10346. https://doi.org/10.1039/c2dt30438d
• Luminescence Properties of C-Diazaborolyl-ortho-Carboranes as Donor-Acceptor Systems
  
  Weber, L., Kahlert, J., Brockhinke, R., Boehling, L., Brockhinke, A., Stammler, H., Neumann, B., Harder, R., & Fox, M. (2012). Luminescence Properties of C-Diazaborolyl-ortho-Carboranes as Donor-Acceptor Systems. Chemistry - A European Journal, 18(27), 8347-8357. https://doi.org/10.1002/chem.201200390
• Experimental and Theoretical Studies on Organic D-π-A Systems Containing Three-Coordinate Boron Moieties as both π-Donor and π-Acceptor
  
  Weber, L., Eickhoff, D., Marder, T. B., Fox, M. A., Low, P. J., Dwyer, A. D., Tozer, D. J., Schwedler, S., Brockhinke, A., Stammler, H., & Neumann, B. (2012). Experimental and Theoretical Studies on Organic D-π-A Systems Containing Three-Coordinate Boron Moieties as both π-Donor and π-Acceptor. Chemistry - A European Journal, 18(5), 1369-1382. https://doi.org/10.1002/chem.201102059
• peri-Dimethylamino substituent effects on proton transfer at carbon in α-naphthylacetate esters: a model for mandelate racemase
  
  Delley, R., Bandyopadhyay, S., Fox, M., Schliehe, C., Hodgson, D., Hollfelder, F., Kirby, A., & O’Donoghue, A. (2012). peri-Dimethylamino substituent effects on proton transfer at carbon in α-naphthylacetate esters: a model for mandelate racemase. Organic and Biomolecular Chemistry, 10(3), 590-596. https://doi.org/10.1039/c1ob06525d
• Colour tuning of blue electroluminescence using bipolar carbazole-oxadiazole molecules in single-active-layer organic light emitting devices (OLEDs)
  
  Linton, K., Fisher, A., Pearson, C., Fox, M., Pålsson, L., Bryce, M., & Petty, M. (2012). Colour tuning of blue electroluminescence using bipolar carbazole-oxadiazole molecules in single-active-layer organic light emitting devices (OLEDs). Journal of Materials Chemistry, 22(23), 11816-11825. https://doi.org/10.1039/c2jm31825c
• Platinum(II) Complexes of Cyclic Triphosphenium Ions: a P-31 NMR Spectroscopic and Computational Study
  
  Coffer (nee Monks), P. K., Deng, R. M., Dillon, K. B., Fox, M. A., & Olivey, R. J. (2012). Platinum(II) Complexes of Cyclic Triphosphenium Ions: a P-31 NMR Spectroscopic and Computational Study. Inorganic Chemistry, 51(18), 9799-9808. https://doi.org/10.1021/ic3011663
• Dinuclear iridium(III) complexes of cyclometalated fluorenylpyridine ligands as phosphorescent dopants for efficient solution-processed OLEDs
  
  M’hamedi, A., Batsanov, A. S., Fox, M. A., Bryce, M. R., Abdullah, K., Al-Attar, H. A., & Monkman, A. P. (2012). Dinuclear iridium(III) complexes of cyclometalated fluorenylpyridine ligands as phosphorescent dopants for efficient solution-processed OLEDs. Journal of Materials Chemistry, 22(27), 13529-13540. https://doi.org/10.1039/c2jm31143g
• Colour tuning from green to red by substituent effects in phosphorescent tris-cyclometalated iridium(III) complexes of carbazole-based ligands: synthetic, photophysical, computational and high efficiency OLED studies
  
  Tavasli, M., Moore, T. N., Zheng, Y., Bryce, M. R., Fox, M. A., Griffiths, G. C., Jankus, V., Al-Attar, H. A., & Monkman, A. P. (2012). Colour tuning from green to red by substituent effects in phosphorescent tris-cyclometalated iridium(III) complexes of carbazole-based ligands: synthetic, photophysical, computational and high efficiency OLED studies. Journal of Materials Chemistry, 22(13), 6419-6428. https://doi.org/10.1039/c2jm15049b
• The synthesis, molecular and electronic structure of cyanovinylidene complexes
  
  Long, E. M., Brown, N. J., Man, W. Y., Fox, M. A., Yufit, D. S., Howard, J. A., & Low, P. J. (2012). The synthesis, molecular and electronic structure of cyanovinylidene complexes. Inorganica Chimica Acta, 380, 358-371. https://doi.org/10.1016/j.ica.2011.10.067
• Substitution of Tetracyanoethene by Ethynyl-Metal Complexes Gives Tricyanovinylethynyl (Tricyanobutenynyl) Derivatives: Syntheses, Protonation, and Addition of Metal-Ligand Fragments
  
  Bruce, M. I., Fox, M. A., Low, P. J., Nicholson, B. K., Parker, C. R., Patalinghug, W. C., Skelton, B. W., & White, A. H. (2012). Substitution of Tetracyanoethene by Ethynyl-Metal Complexes Gives Tricyanovinylethynyl (Tricyanobutenynyl) Derivatives: Syntheses, Protonation, and Addition of Metal-Ligand Fragments. Organometallics, 31(7), 2639-2657. https://doi.org/10.1021/om2007503
• Synthesis and Characterization of Dithia[3.3]paracyclophane-Bridged Binuclear Ruthenium Vinyl and Alkynyl Complexes
  
  Xia, J., Man, W. Y., Zhu, X., Zhang, C., Jin, G., Schauer, P. A., Fox, M. A., Yin, J., Yu, G., Low, P. J., & Liu, S. H. (2012). Synthesis and Characterization of Dithia[3.3]paracyclophane-Bridged Binuclear Ruthenium Vinyl and Alkynyl Complexes. Organometallics, 31(15), 5321-5333. https://doi.org/10.1021/om300338j
• 1,2-Carbagerma-closo-dodecaborate as a Germanium Ligand in Coordination Chemistry - Synthesis, Structure and Reactivity
  
  Wagenpfeil, A., Nickl, C., Schubert, H., Eichele, K., Fox, M. A., & Wesemann, L. (2011). 1,2-Carbagerma-closo-dodecaborate as a Germanium Ligand in Coordination Chemistry - Synthesis, Structure and Reactivity. European Journal of Inorganic Chemistry, 2011(22), 3349-3356. https://doi.org/10.1002/ejic.201100310
• Ligand redox non-innocent behaviour in ruthenium complexes of ethynyl tolans
  
  Khairul, W., Fox, M., Schauer, P., Albesa-Jove, D., Yufit, D., Howard, J., & Low, P. (2011). Ligand redox non-innocent behaviour in ruthenium complexes of ethynyl tolans. Inorganica Chimica Acta, 374(1), 461-471. https://doi.org/10.1016/j.ica.2011.02.043
• Highly Efficient, Solution-Processed, Single-Layer, Electrophosphorescent Diodes and the Effect of Molecular Dipole Moment
  
  Al-Attar, H., Griffiths, G., Moore, T., Tavasli, M., Fox, M., Bryce, M., & Monkman, A. (2011). Highly Efficient, Solution-Processed, Single-Layer, Electrophosphorescent Diodes and the Effect of Molecular Dipole Moment. Advanced Functional Materials, 21(12), 2376-2382. https://doi.org/10.1002/adfm.201100324
• Molybdenum Complexes of C,C-Bis(ethynyl)carboranes: Design, Synthesis, and Study of a Weakly Coupled Mixed-Valence Compound
  
  Brown, N. J., Lancashire, H. N., Fox, M. A., Collison, D., Edge, R., Yufit, D. S., Howard, J. A., Whiteley, M. W., & Low, P. J. (2011). Molybdenum Complexes of C,C-Bis(ethynyl)carboranes: Design, Synthesis, and Study of a Weakly Coupled Mixed-Valence Compound. Organometallics, 30(4), 884-894. https://doi.org/10.1021/om1010353
• Simultaneous Bridge-Localized and Mixed-Valence Character in Diruthenium Radical Cations Featuring Diethynylaromatic Bridging Ligands
  
  Fox, M., Guennic, B., Roberts, R., Brue, D., Yufit, D., Howard, J., Manca, G., Halet, J., Hartl, F., & Low, P. (2011). Simultaneous Bridge-Localized and Mixed-Valence Character in Diruthenium Radical Cations Featuring Diethynylaromatic Bridging Ligands. Journal of the American Chemical Society, 133(45), 18433-18446. https://doi.org/10.1021/ja207827m
• The electronic structures of diruthenium complexes containing an oligo(phenylene ethynylene) bridging ligand, and some related molecular structures
  
  Khairul, W. M., Fox, M. A., Schauer, P. A., Yufit, D. S., Albesa-Jové, D., Howard, J. A., & Low, P. J. (2010). The electronic structures of diruthenium complexes containing an oligo(phenylene ethynylene) bridging ligand, and some related molecular structures. Dalton Transactions, 39(48), 11605-11615. https://doi.org/10.1039/c0dt00809e
• Deboronation and Deprotonation of ortho-Carborane with N-Heterocyclic Carbenes
  
  Willans, C., Kilner, C., & Fox, M. (2010). Deboronation and Deprotonation of ortho-Carborane with N-Heterocyclic Carbenes. Chemistry - A European Journal, 16(35), 10644-10648. https://doi.org/10.1002/chem.201001730
• Luminescent Platinum(II) Complexes Containing Cyclometallated Diaryl Ketimine Ligands: Synthesis, Photophysical and Computational Properties
  
  Pandya, S., Moss, K., Bryce, M., Batsanov, A., Fox, M., Jankus, V., Al Attar, H., & Monkman, A. (2010). Luminescent Platinum(II) Complexes Containing Cyclometallated Diaryl Ketimine Ligands: Synthesis, Photophysical and Computational Properties. European Journal of Inorganic Chemistry, 2010(13), 1963-1972. https://doi.org/10.1002/ejic.200901159
• Some reactions of an eta(3)-tetracyanobutadienyl-ruthenium complex
  
  Bruce, M. I., Fox, M. A., Low, P. J., Skelton, B. W., & Zaitseva, N. N. (2010). Some reactions of an eta(3)-tetracyanobutadienyl-ruthenium complex. Dalton Transactions, 39(15), 3759-3770. https://doi.org/10.1039/b921324d
• Syntheses and molecular structures of some tricobalt carbonyl clusters containing 2,4,6-trimethyl-1,3,5-trithiane
  
  Bruce, M., Zaitseva, N., Skelton, B., White, A., Fox, M., & Low, P. (2010). Syntheses and molecular structures of some tricobalt carbonyl clusters containing 2,4,6-trimethyl-1,3,5-trithiane. Dalton Transactions, 39(5), 1222-1234. https://doi.org/10.1039/b909708b
• Tuning the Intramolecular Charge Transfer Emission from Deep Blue to Green in Ambipolar Systems Based On Dibenzothiophene S S-Dioxide by Manipulation of Conjugation and Strength of the Electron Donor Units
  
  Moss, K., Bourdakos, K., Bhalla, V., Kamtekar, K., Bryce, M., Fox, M., Vaughan, H., Dias, F., & Monkman, A. (2010). Tuning the Intramolecular Charge Transfer Emission from Deep Blue to Green in Ambipolar Systems Based On Dibenzothiophene S S-Dioxide by Manipulation of Conjugation and Strength of the Electron Donor Units. Journal of Organic Chemistry, 75(20), 6771-6781. https://doi.org/10.1021/jo100898a
• The syntheses and structures of mono- and di-bromovinylidenes.
  
  Brown, N. J., Fox, M. A., Smith, M. E., Yufit, D. S., Howard, J. A., & Low, P. J. (2009). The syntheses and structures of mono- and di-bromovinylidenes. Journal of Organometallic Chemistry, 694(25), 4042-4048. https://doi.org/10.1016/j.jorganchem.2009.08.027
• From Cyclic Iminophosphoranes to -Conjugated Materials
  
  Smith, D., Batsanov, A., Fox, M., Beeby, A., Apperley, D., Howard, J., & Dyer, P. (2009). From Cyclic Iminophosphoranes to -Conjugated Materials. Angewandte Chemie International Edition, 48(48), 9109-9113. https://doi.org/10.1002/anie.200904219
• Structural, spectroscopic, electrochemical and computational studies of C,C '-diaryl-ortho-carboranes, 1-(4-XC6H4)-2-Ph-1,2-C2B10H10 (X = H, F, OMe, NMe2, NH2, OH and O-)
  
  Fox, M., Nervi, C., Crivello, A., Batsanov, A., Howard, J., Wade, K., & Low, P. (2009). Structural, spectroscopic, electrochemical and computational studies of C,C ’-diaryl-ortho-carboranes, 1-(4-XC6H4)-2-Ph-1,2-C2B10H10 (X = H, F, OMe, NMe2, NH2, OH and O-). Journal of Solid State Electrochemistry, 13(10), 1483-1495. https://doi.org/10.1007/s10008-008-0686-0
• Noninnocent Ligand Behavior in Diruthenium Complexes Containing a 1,3-Diethynylbenzene Bridge
  
  Fox, M., Farmer, J., Roberts, R., Humphrey, M., & Low, P. (2009). Noninnocent Ligand Behavior in Diruthenium Complexes Containing a 1,3-Diethynylbenzene Bridge. Organometallics, 28(17), 5266-5269. https://doi.org/10.1021/om900200n
• Trends in ortho-carboranes 1-X-2-R-1,2-C2B10H10 (R = Ph, Me) bearing an exo-CN-bonded substituent group (X = NO, N=NR ' or NHR '')
  
  Fox, M., Peace, R., Clegg, W., Elsegood, M., & Wade, K. (2009). Trends in ortho-carboranes 1-X-2-R-1,2-C2B10H10 (R = Ph, Me) bearing an exo-CN-bonded substituent group (X = NO, N=NR ’ or NHR ’’). Polyhedron, 28(12), 2359-2370. https://doi.org/10.1016/j.poly.2009.04.041
• A simple synthesis of trans-RuCl(C CR)(dppe)(2) complexes and representative molecular structures
  
  Fox, M. A., Harris, J. E., Heider, S., Pérez-Gregorio, V., Zakrzewska, M. E., Farmer, J. D., Yufit, D. S., Howard, J. A., & Low, P. J. (2009). A simple synthesis of trans-RuCl(C CR)(dppe)(2) complexes and representative molecular structures. Journal of Organometallic Chemistry, 694(15), 2350-2358. https://doi.org/10.1016/j.jorganchem.2009.03.033
• Synthetic, structural, photophysical and computational studies on 2-arylethynyl-1,3,2-diazaboroles
  
  Weber, L., Werner, V., Fox, M. A., Marder, T. B., Schwedler, S., Brockhinke, A., Hans-Georg, S., & Neumann, B. (2009). Synthetic, structural, photophysical and computational studies on 2-arylethynyl-1,3,2-diazaboroles. Dalton Transactions, 2009(15), 2823-2831. https://doi.org/10.1039/b821208b
• New synthetic and structural studies on nitroso-ortho-carboranes RCB10H10CNO and bis(ortho-carboranyl)amines (RCB10H10C)(2)NH (R = Ph or Me)
  
  Fox, M., MacBride, J., Peace, R., Clegg, W., Elsegood, M., & Wade, K. (2009). New synthetic and structural studies on nitroso-ortho-carboranes RCB10H10CNO and bis(ortho-carboranyl)amines (RCB10H10C)(2)NH (R = Ph or Me). Polyhedron, 28(4), 789-795. https://doi.org/10.1016/j.poly.2008.12.014
• Transition metal alkynyl complexes by transmetallation from Au(C[triple bond, length as m-dash]CAr)(PPh3) (Ar = C6H5 or C6H4Me-4)
  
  Khairul, W. M., Fox, M. A., Zaitseva, N. N., Gaudio, M., Yufit, D. S., Skelton, B. W., White, A. H., Howard, J. A., Bruce, M. I., & Low, P. J. (2009). Transition metal alkynyl complexes by transmetallation from Au(C[triple bond, length as m-dash]CAr)(PPh3) (Ar = C6H5 or C6H4Me-4). Dalton Transactions, 2009(4), 610-620. https://doi.org/10.1039/b809960j
• DFT studies of the σ-donor/π-acceptor properties of [SnCB10H11]– and its relationship to [SnCl3]–, CO, PF3, [SnB11H11]2–, SnC2B9H11, and related SnC2BnHn+2 compounds
  
  Fox, M. A., Marder, T. B., & Wesemann, L. (2009). DFT studies of the σ-donor/π-acceptor properties of [SnCB10H11]– and its relationship to [SnCl3]–, CO, PF3, [SnB11H11]2–, SnC2B9H11, and related SnC2BnHn+2 compounds. Canadian Journal of Chemistry, 87(1), 63-71. https://doi.org/10.1139/v08-081
• EXPERIMENTAL AND COMPUTED DIPOLE MOMENTS IN DONOR-BRIDGE-ACCEPTOR SYSTEMS WITH p-PHENYLENE AND p-CARBORANEDIYL BRIDGES
  
  Fox, M. (2009). EXPERIMENTAL AND COMPUTED DIPOLE MOMENTS IN DONOR-BRIDGE-ACCEPTOR SYSTEMS WITH p-PHENYLENE AND p-CARBORANEDIYL BRIDGES. Collection of Czechoslovak Chemical Communications., 74(1), 131-146. https://doi.org/10.1135/cccc2008154
• Some transition metal complexes derived from mono- and di-ethynyl perfluorobenzenes.
  
  Armitt, D. J., Bruce, M. I., Gaudio, M., Zaitseva, N. N., Skelton, B. W., White, A. H., Le Guennic, B., Halet, J., Fox, M. A., Roberts, R. L., Hartl, F., & Low, P. J. (2008). Some transition metal complexes derived from mono- and di-ethynyl perfluorobenzenes. Dalton Transactions, 2008(47), 6763-6775. https://doi.org/10.1039/b808798a
• Facile photoinduced charge separation through a cyanoacetylide bridge in a heterobimetallic Fe(ii)–Re(i) complex
  
  Smith, M. E., Flynn, E. L., Fox, M. A., Trottier, A., Wrede, E., Yufit, D. S., Howard, J. A., Ronayne, K. L., Towrie, M., Parker, A. W., Hartl, F., & Low, P. J. (2008). Facile photoinduced charge separation through a cyanoacetylide bridge in a heterobimetallic Fe(ii)–Re(i) complex. Chemical Communications, 2008(44), 5845-5847. https://doi.org/10.1039/b811357b
• Ruthenium complexes of C,C '-bis(ethynyl)carboranes: An investigation of electronic interactions mediated by spherical pseudo-aromatic spacers
  
  Fox, M., Roberts, R., Baines, T., Le Guennic, B., Halet, J., Hartl, F., Yufit, D., Albesa-Jové, D., Howard, J., & Low, P. (2008). Ruthenium complexes of C,C ’-bis(ethynyl)carboranes: An investigation of electronic interactions mediated by spherical pseudo-aromatic spacers. Journal of the American Chemical Society, 130(11), 3566-3578. https://doi.org/10.1021/ja0779755
• N-Phosphino-amidines and -guanidines: synthesis, structure and P,N-chelate chemistry.
  
  Baiget, L., Batsanov, A. S., Dyer, P. W., Fox, M. A., Hanton, M. J., Howard, J. A., Lane, P. K., & Solomon, S. A. (2008). N-Phosphino-amidines and -guanidines: synthesis, structure and P,N-chelate chemistry. Dalton Transactions, 2008(8), 1043-1054. https://doi.org/10.1039/b715736c
• The preparation and characterisation of ruthenium cyanovinylidene complexes.
  
  Brown, N. J., Eckert, P. K., Fox, M. A., Yufit, D. S., Howard, J. A., & Low, P. J. (2008). The preparation and characterisation of ruthenium cyanovinylidene complexes. Dalton Transactions, 2008(4), 433-436. https://doi.org/10.1039/b714274a
• Quenched gas-phase reactions of tetraborane(10), B4H10, with substituted alkynes: new nido-dicarbapentaboranes and arachno-monocarbapentaboranes
  
  Fox, M. A., Greatrex, R., & Nikrahi, A. (2008). Quenched gas-phase reactions of tetraborane(10), B4H10, with substituted alkynes: new nido-dicarbapentaboranes and arachno-monocarbapentaboranes. Dalton Transactions, 2008(5), 676-684. https://doi.org/10.1039/b715105e
• Spectroscopic properties and electronic structures of 17-electron half-sandwich ruthenium acetylide complexes, [Ru(CCAr)(L2)Cp′]+ (Ar=phenyl, p-tolyl, 1-naphthyl, 9-anthryl; L2=(PPh3)2, Cp′=Cp; L2=dppe; Cp′=Cp∗).
  
  Fox, M. A., Roberts, R. L., Khairul, W. M., Hartl, F., & Low, P. J. (2007). Spectroscopic properties and electronic structures of 17-electron half-sandwich ruthenium acetylide complexes, [Ru(CCAr)(L2)Cp′]+ (Ar=phenyl, p-tolyl, 1-naphthyl, 9-anthryl; L2=(PPh3)2, Cp′=Cp; L2=dppe; Cp′=Cp∗). Journal of Organometallic Chemistry, 692(15), 3277-3290. https://doi.org/10.1016/j.jorganchem.2007.03.042
• Carborane radical anions: spectroscopic and electronic properties of a carborane radical anion with a 2n + 3 skeletal electron count
  
  Fox, M., Nervi, C., Crivello, A., & Low, P. (2007). Carborane radical anions: spectroscopic and electronic properties of a carborane radical anion with a 2n + 3 skeletal electron count. Chemical Communications, 23, 2372-2374. https://doi.org/10.1039/b700110j
• Elemental fluorine - Part 20. Direct fluorination of deactivated aromatic systems using microreactor techniques
  
  Fox, M. (2007). Elemental fluorine - Part 20. Direct fluorination of deactivated aromatic systems using microreactor techniques. Journal of Fluorine Chemistry, 128(1), 29-33. https://doi.org/10.1016/j.jfluchem.2006.09.010
• Improved syntheses of bis(ethynyl)-para-carboranes, 1,12-(RC C)(2)-1,12-C2B10H10 and 1,10-(RC equivalent to C)(2)-1,10-C2B8H8 (R = H or Me3Si).
  
  Fox, M., Baines, T., Albesa-Jove, D., Howard, J., & Low, P. (2006). Improved syntheses of bis(ethynyl)-para-carboranes, 1,12-(RC C)(2)-1,12-C2B10H10 and 1,10-(RC equivalent to C)(2)-1,10-C2B8H8 (R = H or Me3Si). Journal of Organometallic Chemistry, 691(18), 3889-3894. https://doi.org/10.1016/j.jorganchem.2006.05.044
• Synthetic and structural studies on C-ethynyl- and C-bromo-carboranes.
  
  Fox, M., Cameron, A., Low, P., Paterson, M., Batsanov, A., Goeta, A., Rankin, D., Robertson, H., & Schirlin, J. (2006). Synthetic and structural studies on C-ethynyl- and C-bromo-carboranes. Dalton Transactions, 29, 3544-3560. https://doi.org/10.1039/b517538k
• Reactions of Icosahedral Carboranes with Iminotris(dimethylamino)Phosphorane HNP(NMe2)3: a Deboronation Intermediate nido-C2B10H12·N(H)P(NMe2)3, Deboronation Reactions and Hydrogen-bonded Closo-carborane Systems
  
  Batsanov, A. S., Copley, R. C., Davidson, M. G., Fox, M. A., Hibbert, T. G., Howard, J. A., & Wade, K. (2006). Reactions of Icosahedral Carboranes with Iminotris(dimethylamino)Phosphorane HNP(NMe2)3: a Deboronation Intermediate nido-C2B10H12·N(H)P(NMe2)3, Deboronation Reactions and Hydrogen-bonded Closo-carborane Systems. Journal of Cluster Science, 17(1), 119-137. https://doi.org/10.1007/s10876-005-0042-9
• Preparative and structural studies on sulfur-linked carborane icosahedra: 2-phenyl-ortho-carboranyl-sulfur systems (2-Ph-1,2-C2B10H10)(2)X (X = S, S-2 or SO), and ortho-carboran-di-yl systems (1,2-C2B10H10Y)(2) (Y = S or SO)
  
  Batsanov, A., Clegg, W., Copley, R., Fox, M., Gill, W., Grimditch, R., Hibbert, T., Howard, J., MacBride, J., & Wade, K. (2006). Preparative and structural studies on sulfur-linked carborane icosahedra: 2-phenyl-ortho-carboranyl-sulfur systems (2-Ph-1,2-C2B10H10)(2)X (X = S, S-2 or SO), and ortho-carboran-di-yl systems (1,2-C2B10H10Y)(2) (Y = S or SO). Polyhedron, 25(2), 300-306. https://doi.org/10.1016/j.poly.2005.06.046
• Electronic interactions in bridged bis(cluster) assemblies - a comparison of para-CB10H10C, para-C6H4 and C-4 bridges
  
  Le Guennic, B., Costuas, K., Halet, J., Nervi, C., Paterson, M., Fox, M., Roberts, R., Albesa-Jove, D., Puschmann, H., Howard, J., & Low, P. (2005). Electronic interactions in bridged bis(cluster) assemblies - a comparison of para-CB10H10C, para-C6H4 and C-4 bridges. Comptes Rendus Chimie, 8(11-12), 1883-1896. https://doi.org/10.1016/j.crci.2005.03.016
• Elemental fluorine - Part 18. Selective direct fluorination of 1,3-ketoesters and 1,3-diketones using gas/liquid microreactor technology
  
  Chambers, R., Fox, M., & Sandford, G. (2005). Elemental fluorine - Part 18. Selective direct fluorination of 1,3-ketoesters and 1,3-diketones using gas/liquid microreactor technology. Lab on a Chip, 5(10), 1132-1139. https://doi.org/10.1039/b504675k
• Versatile gas/liquid microreactors for industry
  
  Chambers, R., Fox, M., Holling, D., Nakano, T., Okazoe, T., & Sandford, G. (2005). Versatile gas/liquid microreactors for industry. Chemical Engineering and Technology, 28(3), 344-352. https://doi.org/10.1002/ceat.200407123
• Gas-phase electron diffraction studies of the icosahedral carbaboranes, ortho-, meta- and para-C2B10H12
  
  Turner, A. R., Robertson, H. E., Borisenko, K. B., Rankin, D. W. H., & Fox, M. A. (2005). Gas-phase electron diffraction studies of the icosahedral carbaboranes, ortho-, meta- and para-C2B10H12. Dalton Transactions, 2005(7), 1310-1318. https://doi.org/10.1039/B418276F
• Elemental fluorine - Part 16. Versatile thin-film gas-liquid multi-channel microreactors for effective scale-out
  
  Chambers, R., Fox, M., Holling, D., Nakano, T., Okazoe, T., & Sandford, G. (2005). Elemental fluorine - Part 16. Versatile thin-film gas-liquid multi-channel microreactors for effective scale-out. Lab on a Chip, 5(2), 191-198. https://doi.org/10.1039/b416400h
• Sulfur, tin and gold derivatives of 1-(2′-pyridyl)-ortho-carborane, 1-R-2-X-1,2-C2B10H10 (R = 2′-pyridyl, X = SH, SnMe3 or AuPPh3)
  
  Batsanov, A., Fox, M., Hibbert, T., Howard, J., Kivekäs, R., Laromaine, A., Sillanpää, R., Viñas, C., & Wade, K. (2004). Sulfur, tin and gold derivatives of 1-(2′-pyridyl)-ortho-carborane, 1-R-2-X-1,2-C2B10H10 (R = 2′-pyridyl, X = SH, SnMe3 or AuPPh3). Dalton Transactions, 2004(22), 3822-3828. https://doi.org/10.1039/b411099d
• Exo-π-bonding to an ortho-carborane hypercarbon atom: systematic icosahedral cage distortions reflected in the structures of the fluoro-, hydroxy- and amino-carboranes, 1-X-2-Ph-1,2-C2B10H10 (X = F, OH or NH2) and related anions
  
  Boyd, L., Clegg, W., Copley, R., Davidson, M., Fox, M., Hibbert, T., Howard, J., Mackinnon, A., Peace, R., & Wade, K. (2004). Exo-π-bonding to an ortho-carborane hypercarbon atom: systematic icosahedral cage distortions reflected in the structures of the fluoro-, hydroxy- and amino-carboranes, 1-X-2-Ph-1,2-C2B10H10 (X = F, OH or NH2) and related anions. Dalton Transactions, 2004(17), 2786-2799. https://doi.org/10.1039/b406422d
• Cage C---H...X interactions in solid-state structures of icosahedral carboranes
  
  Fox, M., & Hughes, A. (2004). Cage C---H...X interactions in solid-state structures of icosahedral carboranes. Coordination Chemistry Reviews, 248(5-6), 457-476. https://doi.org/10.1016/j.ccr.2003.10.002
• Two contrasting ethynyl hydroboration pathways in the formation of a novel tris-hydroboration product from reaction of dimesitylborane with 2,5-diethynylpyridine
  
  Entwistle, C. D., Batsanov, A. S., Howard, J. A. K., Fox, M. A., & Marder, T. B. (2004). Two contrasting ethynyl hydroboration pathways in the formation of a novel tris-hydroboration product from reaction of dimesitylborane with 2,5-diethynylpyridine. Chemical Communications, 2004(6), 702-703. https://doi.org/10.1039/B316250H
• The synthesis and molecular and crystal structures of 1-methyl-2-carboxy-1,2-dicarba-closo-dodecaborane(12), 1-phenyl-2-carboxy-1,2-dicarba-closo-dodecaborane(12) and 1-phenyl-2-benzoyl-1,2-dicarba-closo-dodecaborane(12)
  
  Venkatasubramanian, U., Donohoe, D., Ellis, D., Giles, B., Macgregor, S., Robertson, S., Rosair, G., Welch, A., Batsanov, A., Boyd, L., Copley, R., Fox, M., Howard, J., & Wade, K. (2004). The synthesis and molecular and crystal structures of 1-methyl-2-carboxy-1,2-dicarba-closo-dodecaborane(12), 1-phenyl-2-carboxy-1,2-dicarba-closo-dodecaborane(12) and 1-phenyl-2-benzoyl-1,2-dicarba-closo-dodecaborane(12). Polyhedron, 23(4), 629-636.
• Gas-phase electron diffraction studies on two 11-vertex dicarbaboranes, closo-2,3-C2B9H11 and nido-2,9-C2B9H13
  
  Fox, M. (2004). Gas-phase electron diffraction studies on two 11-vertex dicarbaboranes, closo-2,3-C2B9H11 and nido-2,9-C2B9H13. Inorganic Chemistry, 43(17), 5387-5392.
• Evolving patterns in boron cluster chemistry
  
  Fox, M., & Wade, K. (2003). Evolving patterns in boron cluster chemistry. Pure and Applied Chemistry, 75(9), 1315-1323. https://doi.org/10.1351/pac200375091315
• Dimesitylborane monomer-dimer equilibrium in solution, and the solid-state structure of the dimer by single crystal neutron and X-ray diffraction.
  
  Entwistle, C., Marder, T., Smith, P., Howard, J., Fox, M., & Mason, S. (2003). Dimesitylborane monomer-dimer equilibrium in solution, and the solid-state structure of the dimer by single crystal neutron and X-ray diffraction. Journal of Organometallic Chemistry, 680(1-2), 165-172. https://doi.org/10.1016/s0022-328x%2803%2900316-4
• Big macrocyclic assemblies of carboranes (big MACs): synthesis and crystal structure of a macrocyclic assembly of four carboranes containing alternate ortho- and meta-carborane icosahedra linked by para-phenylene units.
  
  Fox, M., Howard, J., MacBride, J., Mackinnon, A., & Wade, K. (2003). Big macrocyclic assemblies of carboranes (big MACs): synthesis and crystal structure of a macrocyclic assembly of four carboranes containing alternate ortho- and meta-carborane icosahedra linked by para-phenylene units. Journal of Organometallic Chemistry, 680(1-2), 155-164. https://doi.org/10.1016/s0022-328x%2803%2900313-9
• Synthesis and crystal structure of an assembly of three ortho-carborane cages linked via para-phenylene units: effect of aryl orientation on cage C-C bond lengths in C-aryl-ortho-carboranes
  
  Alekseyeva, E., Fox, M., Howard, J., MacBride, J., & Wade, K. (2003). Synthesis and crystal structure of an assembly of three ortho-carborane cages linked via para-phenylene units: effect of aryl orientation on cage C-C bond lengths in C-aryl-ortho-carboranes. Applied Organometallic Chemistry, 17(6-7), 499-508. https://doi.org/10.1002/aoc.467
• 9,12-Di­iodo-1,2-dicarba-closo-dodecaborane(12)
  
  Batsanov, A., Fox, M., Howard, J., Hughes, A., Johnson, A., & Martindale, S. (2003). 9,12-Di­iodo-1,2-dicarba-closo-dodecaborane(12). Acta Crystallographica Section C: Structural Chemistry, 59(2), O74-O76. https://doi.org/10.1107/s0108270102023582
• Alkynyl gold(I) rigid-rod molecules from 1,12-bis(ethynyl)-1,12-dicarba-closo-dodecaborane(12)
  
  Fox, M. (2003). Alkynyl gold(I) rigid-rod molecules from 1,12-bis(ethynyl)-1,12-dicarba-closo-dodecaborane(12). Organometallics, 22(23), 4792-4797.
• Synthesis and characterisation of some new boron compounds containing the 2,4,6-(CF₃)₃C₆H₂(fluoromes = Ar), 2,6-(CF₃)₂C₆H₃ (fluoroxyl = Ar '), or 2,4-(CF₃)₂C₆H₃ (Ar '') ligands
  
  Cornet, S., Dillon, K., Entwistle, C., Fox, M., Goeta, A., Goodwin, H., Marder, T., & Thompson, A. (2003). Synthesis and characterisation of some new boron compounds containing the 2,4,6-(CF₃)₃C₆H₂(fluoromes = Ar), 2,6-(CF₃)₂C₆H₃ (fluoroxyl = Ar ’), or 2,4-(CF₃)₂C₆H₃ (Ar ’’) ligands. Dalton Transactions, 2003(23), 4395-4405. https://doi.org/10.1039/b309820f
• Intra- and inter-molecular carboranyl C-H center dot center dot center dot N hydrogen bonds in pyridyl-containing ortho-carboranes
  
  Alekseyeva, E. S., Batsanov, A. S., Boyd, L. A., Fox, M. A., Hibbert, T. G., Howard, J. A. K., MacBride, J. A. H., Mackinnon, A., & Wade, K. (2003). Intra- and inter-molecular carboranyl C-H center dot center dot center dot N hydrogen bonds in pyridyl-containing ortho-carboranes. Dalton Transactions, 2003(3), 475-482. https://doi.org/10.1039/B209931D
• Unexpected formation of new fluoroboranes from the reaction of NMe4B3H8 with BF3 and MeC CH: exo-2-FB4H9 and trans-MeCH CHBF2
  
  Fox, M. A., Greatrex, R., & Ormsby, D. L. (2002). Unexpected formation of new fluoroboranes from the reaction of NMe4B3H8 with BF3 and MeC CH: exo-2-FB4H9 and trans-MeCH CHBF2. Chemical Communications, 2002(18), 2052-2053. https://doi.org/10.1039/B206102C
• A new nido-5-vertex cluster, phosphacarba-nido-pentaborane, 2-Bu-t-1,2-PCB3H5
  
  Condick, P. N., Fox, M. A., Greatrex, R., Jones, C., & Ormsby, D. L. (2002). A new nido-5-vertex cluster, phosphacarba-nido-pentaborane, 2-Bu-t-1,2-PCB3H5. Chemical Communications, 14, 1448-1449. https://doi.org/10.1039/B204409A
• Synthesis of a new boron carbonitride with a B4C-like structure from the thermolysis of N-alkylated borazines
  
  Brydson, R., Daniels, H., Fox, M. A., Greatrex, R., & Workman, C. (2002). Synthesis of a new boron carbonitride with a B4C-like structure from the thermolysis of N-alkylated borazines. Chemical Communications, 2002(7), 718-719. https://doi.org/10.1039/B110856P
• Carbon-boron-nitrogen alloys from borazarene-derived mesophase pitches.
  
  Westwood, A., Brydson, R., Coult, R., Fox, M., Rand, B., & Wade, K. (2002). Carbon-boron-nitrogen alloys from borazarene-derived mesophase pitches. Carbon, 40(12), 2157-2167. https://doi.org/10.1016/s0008-6223%2802%2900064-7
• Crystal and molecular structures of the nido-carborane anions, 7,9- and 2,9 C₂B₉H₁₂
  
  Fox, M., Goeta, A., Hughes, A., & Johnson, A. (2002). Crystal and molecular structures of the nido-carborane anions, 7,9- and 2,9 C₂B₉H₁₂. Dalton Transactions, 10, 2132-2141. https://doi.org/10.1039/b108937d
• Do the discrete dianions C2B9H112- exist? Characterisation of alkali metal salts of the 11-vertex nido dicarboranes, C2B9H112-, in solution
  
  Fox, M., Hughes, A., Johnson, A., & Paterson, M. (2002). Do the discrete dianions C2B9H112- exist? Characterisation of alkali metal salts of the 11-vertex nido dicarboranes, C2B9H112-, in solution. Dalton Transactions., 2002(9), 2009-2019. https://doi.org/10.1039/b109804g
• Solution and solid-state structure of the anion [Ag-2closo-CB11H12(4)](2-)
  
  Fox, M. (2002). Solution and solid-state structure of the anion [Ag-2closo-CB11H12(4)](2-). Inorganic Chemistry, 41(17), 4567-4573.
• A convenient cyanide-free "one-pot" synthesis of nido-Me3N-7-CB10H12 and nido-7-CB10H13-
  
  Batsanov, A. S., Fox, M. A., Goeta, A. E., Howard, J. A. K., Hughes, A. K., & Malget, J. M. (2002). A convenient cyanide-free "one-pot" synthesis of nido-Me3N-7-CB10H12 and nido-7-CB10H13-. Dalton Transactions., 2002(13), 2624-2631. https://doi.org/10.1039/B200930G
• Cage-closing reactions of the nido-carborane anion 7,9-C2B9H12− and derivatives; formation of neutral 11-vertex carboranes by acidification.
  
  Fox, M., Hughes, A., & Malget, J. (2002). Cage-closing reactions of the nido-carborane anion 7,9-C2B9H12− and derivatives; formation of neutral 11-vertex carboranes by acidification. Dalton Transactions., 2002(18), 3505-3517. https://doi.org/10.1039/b203920f
• Model compounds and monomers for phenylene ether carboranylene ketone (PECK) polymer synthesis: preparation and characterization of boron-arylated ortho-carboranes bearing carboxyphenyl, phenoxyphenyl or benzoylphenyl substituents
  
  Fox, M., & Wade, K. (2002). Model compounds and monomers for phenylene ether carboranylene ketone (PECK) polymer synthesis: preparation and characterization of boron-arylated ortho-carboranes bearing carboxyphenyl, phenoxyphenyl or benzoylphenyl substituents. Journal of Materials Chemistry, 12(5), 1301-1306.
• Halogenation of tris(amido)tantalacarboranes with dihalomethanes CH2X2 (X = Cl, Br)
  
  Fox, M., Goeta, A., Hughes, A., Malget, J., & Wade, K. (2002). Halogenation of tris(amido)tantalacarboranes with dihalomethanes CH2X2 (X = Cl, Br). Collection of Czechoslovak Chemical Communications., 67(6), 791-807.
• Electrochemical evidence for electronic interactions through the para-carborane skeleton in the novel tricluster [{Co2C2(SiMe3)(CO)4(dppm)}2(μ-CB10H10C)]
  
  Fox, M., Paterson, M., Nervi, C., Galeotti, F., Puschmann, H., Howard, J., & Low, P. (2001). Electrochemical evidence for electronic interactions through the para-carborane skeleton in the novel tricluster [{Co2C2(SiMe3)(CO)4(dppm)}2(μ-CB10H10C)]. Chemical Communications, 2001(17), 1610-1611. https://doi.org/10.1039/b104307m
• Synthesis of isomeric B-methylated tantalum carboranes, (Me₂N)₃TaC₂B₉H₁₀Me
  
  Fox, M., Howard, J., Hughes, A., Malget, J., & Yufit, D. (2001). Synthesis of isomeric B-methylated tantalum carboranes, (Me₂N)₃TaC₂B₉H₁₀Me. Dalton Transactions, 2001(15), 2263-2269. https://doi.org/10.1039/b103353k
• Phosphine promoted substituent redistribution reactions of B- chlorocatechol borane: Molecular structures of ClBcat, BrBcat and L center dot ClBcat (cat=1,2-O2C6H4; L = PMe3, PEt3, PBu3t, PCy3, NEt3)
  
  Coapes, R. B., Souza, F. E. S., Fox, M. A., Batsanov, A. S., Goeta, A. E., Yufit, D. S., Leech, M., Howard, J. A. K., Scott, A. J., Clegg, W., & Marder, T. B. (2001). Phosphine promoted substituent redistribution reactions of B- chlorocatechol borane: Molecular structures of ClBcat, BrBcat and L center dot ClBcat (cat=1,2-O2C6H4; L = PMe3, PEt3, PBu3t, PCy3, NEt3). Dalton Transactions., 2001(8), 1201-1209. https://doi.org/10.1039/B010025K
• Empirical and ab initio energy/architectural patterns for 73 nido-6 < V >-carborane isomers, from B6H9- to C4B2H6
  
  Fox, M. (2001). Empirical and ab initio energy/architectural patterns for 73 nido-6 < V >-carborane isomers, from B6H9- to C4B2H6. Inorganic Chemistry, 40(8), 1790-1801.
• The molecular structure of (PSH+)(nido-7,8-C2B9H12-) determined by neutron diffraction (PS = proton sponge, 1,8- bis(dimethylamino)naphthalene)
  
  Fox, M., Goeta, A., Howard, J., Hughes, A., Johnson, A., Keen, D., Wade, K., & Wilson, C. (2001). The molecular structure of (PSH+)(nido-7,8-C2B9H12-) determined by neutron diffraction (PS = proton sponge, 1,8- bis(dimethylamino)naphthalene). Inorganic Chemistry, 40(1), 173-+.
• Why are B2O2 rings rare?
  
  Burke, J. M., Fox, M. A., Goeta, A. E., Hughes, A. K., & Marder, T. B. (2000). Why are B2O2 rings rare? Chemical Communications, 2000(22), 2217-2218. https://doi.org/10.1039/B006685K
• First structural characterisation of a 2,1,12-MC2B9 metallacarborane, [2,2,2-(NMe2)(3)-closo-2,1,12-TaC2B9H11]. Trends in boron NMR shifts on replacing a BH vertex with a metal MLn vertex in icosahedral carboranes
  
  Batsanov, A. S., Eva, P. A., Fox, M. A., Howard, J. A. K., Hughes, A. K., Johnson, A. L., Martin, A. M., & Wade, K. (2000). First structural characterisation of a 2,1,12-MC2B9 metallacarborane, [2,2,2-(NMe2)(3)-closo-2,1,12-TaC2B9H11]. Trends in boron NMR shifts on replacing a BH vertex with a metal MLn vertex in icosahedral carboranes. Dalton Transactions., 2000(20), 3519-3525. https://doi.org/10.1039/B005294I
• 1,2-Ph2-9-1-1,2-closo-C2B10H9 - Steric effects in heteroboranes. Part 24
  
  Fox, M. (2000). 1,2-Ph2-9-1-1,2-closo-C2B10H9 - Steric effects in heteroboranes. Part 24. Acta Crystallographica C: Crystal Structure Communications, 56, 487-488. https://doi.org/10.1107/s0108270100000743
• Synthesis and structure of 1,12-diethynyl-para-carborane
  
  Fox, M. (2000). Synthesis and structure of 1,12-diethynyl-para-carborane. Journal of Organometallic Chemistry, 610(1-2), 20-24.
• Syntheses and reactions of some new C-pentafluorophenyl and tetrafluorophenylene carborane systems
  
  Fox, M. (2000). Syntheses and reactions of some new C-pentafluorophenyl and tetrafluorophenylene carborane systems. Journal of Organometallic Chemistry, 597(1-2), 157-163.
• Gas-phase reactions of nido-1-methylpentaborane with propyne and 2-pentyne. Formation of B-alkyl nido and close carbaboranes
  
  Fox, M. (2000). Gas-phase reactions of nido-1-methylpentaborane with propyne and 2-pentyne. Formation of B-alkyl nido and close carbaboranes. Journal of Organometallic Chemistry, 614, 262-268.
• Deboronation of 9-substituted-ortho- and -meta-carboranes
  
  Fox, M. (1999). Deboronation of 9-substituted-ortho- and -meta-carboranes. Journal of Organometallic Chemistry, 573(1-2), 279-291.
• Deboronation of ortho-carborane by an iminophosphorane: crystal structures of the novel carborane adduct nido-C2B10H12 center dot HNP(NMe2)(3) and the borenium salt [(Me2N)(3)PNHBNP(NMe2)(3)](2)O2+(C2B9H12-)(2)
  
  Davidson, M. G., Fox, M. A., Hibbert, T. G., Howard, J. A. .K., Mackinnon, A., Neretin, I. S., & Wade, K. (1999). Deboronation of ortho-carborane by an iminophosphorane: crystal structures of the novel carborane adduct nido-C2B10H12 center dot HNP(NMe2)(3) and the borenium salt [(Me2N)(3)PNHBNP(NMe2)(3)](2)O2+(C2B9H12-)(2). Chemical Communications, 1999(17), 1649-1650. https://doi.org/10.1039/A903030A
• Gas-phase flash reactions of diborane, triborane carbonyl and tetraborane with alkynes
  
  Fox, M. (1999). Gas-phase flash reactions of diborane, triborane carbonyl and tetraborane with alkynes. Collection of Czechoslovak Chemical Communications., 64(5), 806-818. https://doi.org/10.1135/cccc19990806
• Six-vertex nido-carborane structures with unusual CHB bridges or endo-CH hydrogens
  
  Fox, M. (1998). Six-vertex nido-carborane structures with unusual CHB bridges or endo-CH hydrogens. Journal of Organometallic Chemistry, 550(1-2), 331-340.
• Molecular structures of 1,12-B12H10(CO)(2) and its dihydrate 1,12-B12H10[C(OH)(2)](2) - a novel bis-carbene complex
  
  Fox, M. A., Howard, J. A. K., Moloney, J. M., & Wade, K. (1998). Molecular structures of 1,12-B12H10(CO)(2) and its dihydrate 1,12-B12H10[C(OH)(2)](2) - a novel bis-carbene complex. Chemical Communications, 1998(22), 2487-2488. https://doi.org/10.1039/A806898D
• Studies on tetraborane(8) carbonyl, B4H8.CO: its isomeric composition in the gas phase and in solution, and its reactions with alkenes
  
  Fox, M. (1998). Studies on tetraborane(8) carbonyl, B4H8.CO: its isomeric composition in the gas phase and in solution, and its reactions with alkenes. Journal of Organometallic Chemistry, 550(1-2), 207-212.
• Transmission of electronic effects by icosahedral carboranes: skeletal carbon-13 chemical shifts and ultraviolet-visible spectra of substituted aryl-p-carboranes (1,12-dicarba-closo-dodecaboranes)
  
  Wade, K., Fox, M., McBride, J., & Peace, R. (1998). Transmission of electronic effects by icosahedral carboranes: skeletal carbon-13 chemical shifts and ultraviolet-visible spectra of substituted aryl-p-carboranes (1,12-dicarba-closo-dodecaboranes). Dalton Transactions, 1998(3), 401-411.
• Gas-phase reaction of tetraborane(10) and ethyne: Molecular structure of nido-1,2-C2B3H7 in the gas phase
  
  Fox, M. (1998). Gas-phase reaction of tetraborane(10) and ethyne: Molecular structure of nido-1,2-C2B3H7 in the gas phase. Inorganic Chemistry, 37(9), 2166-2176.
• 2,4-Ethanotetraborane derivatives. 3. Determination of the molecular structure of 2,4-(t-butylethano)tetraborane(10), 2,4-((BuCHCH2)-C-t)B4H8, in the gas phase by electron diffraction
  
  Fox, M. (1998). 2,4-Ethanotetraborane derivatives. 3. Determination of the molecular structure of 2,4-(t-butylethano)tetraborane(10), 2,4-((BuCHCH2)-C-t)B4H8, in the gas phase by electron diffraction. Journal of Molecular Structure, 445(1-3), 319-334.
• Cage-fluorination during deboronation of meta-carboranes
  
  Fox, M. (1997). Cage-fluorination during deboronation of meta-carboranes. Polyhedron, 16(14), 2517-2525.
• Fluoride-ion deboronation of p-fluorophenyl-ortho- and -meta-carboranes. NMR evidence for the new fluoroborate, HOBHF2-
  
  Fox, M. (1997). Fluoride-ion deboronation of p-fluorophenyl-ortho- and -meta-carboranes. NMR evidence for the new fluoroborate, HOBHF2-. Polyhedron, 16(14), 2499-2507.
• Convenient direct syntheses of novel fused-ring CB4N5 systems by nitrile hydroboration
  
  Coult, R., Fox, M. A., Rand, B., Wade, K., & Westwood, A. V. K. (1997). Convenient direct syntheses of novel fused-ring CB4N5 systems by nitrile hydroboration. Dalton Transactions., 1997(19), 3411-3413. https://doi.org/10.1039/A705523D
• Molecular structure of trifluorophosphine tetraborane(8), B4H8PF3, as determined in the gas phase by electron diffraction and ab initio computations
  
  Fox, M. (1997). Molecular structure of trifluorophosphine tetraborane(8), B4H8PF3, as determined in the gas phase by electron diffraction and ab initio computations. Inorganic Chemistry, 36(6), 1048-1054.
• Gas-phase reaction of tetrahorane(10) with allene: The fluxional arachno-1-carbapentaborane(10) isomeric system and derivatives 1,2- and 1,3-Me-2-1-CB4H8; analogies in 1-CB4H10, MeB5H10, and B5H10-
  
  Fox, M. (1997). Gas-phase reaction of tetrahorane(10) with allene: The fluxional arachno-1-carbapentaborane(10) isomeric system and derivatives 1,2- and 1,3-Me-2-1-CB4H8; analogies in 1-CB4H10, MeB5H10, and B5H10-. Angewandte Chemie International Edition, 36(13-14), 1498-1501. https://doi.org/10.1002/anie.199714981
• Some boron-containing ring systems
  
  Fox, M. (1997). Some boron-containing ring systems. Phosphorus, Sulfur, and Silicon and the Related Elements, 125, 73-82.
• Crystallographic evidence for the diene character of C2B10H10C4H4 ('benzocarborane') and a Diels-Alder reaction of its anionic nido-analogue, [C2B9H10C4H4](-): Crystal structures of C2B10H10C4H4 and C2B10H10C4H6
  
  Copley, R. C. B., Fox, M. A., Gill, W. R., Howard, J. A. K., MacBride, J. A. H., Peace, R. J., Rivers, G. P., & Wade, K. (1996). Crystallographic evidence for the diene character of C2B10H10C4H4 (’benzocarborane’) and a Diels-Alder reaction of its anionic nido-analogue, [C2B9H10C4H4](-): Crystal structures of C2B10H10C4H4 and C2B10H10C4H6. Chemical Communications, 1996(17), 2033-2034. https://doi.org/10.1039/CC9960002033
• Gas-phase reactions of tetraborane(10) with 1-en-3-ynes: Syntheses of the parent tricarbahexaborane, nido-2,3,4-C3B3H7, and its derivatives
  
  Fox, M. A., Greatrex, R., & Nikrahi, A. (1996). Gas-phase reactions of tetraborane(10) with 1-en-3-ynes: Syntheses of the parent tricarbahexaborane, nido-2,3,4-C3B3H7, and its derivatives. Chemical Communications, 1996(2), 175-176. https://doi.org/10.1039/CC9960000175
• Existence of C,3-Me(2)-closo-1,2-C2B3H3 refuted by the ab initio IGLO, GIAO-MP2/NMR method. Attempted repetition of the synthesis
  
  Fox, M. (1996). Existence of C,3-Me(2)-closo-1,2-C2B3H3 refuted by the ab initio IGLO, GIAO-MP2/NMR method. Attempted repetition of the synthesis. Inorganic Chemistry, 35(21), 6170-6178.
• Deboronation of C-substituted ortho- and meta-closo-carboranes using ''wet'' fluoride ion solutions
  
  Fox, M. (1996). Deboronation of C-substituted ortho- and meta-closo-carboranes using ’’wet’’ fluoride ion solutions. Polyhedron, 15(4), 565-571.
• Re-identification of the major volatile carbaboranes from the gas-phase reactions of tetraborane(10) and alkynes at 50 °C
  
  Fox, M. A., & Greatrex, R. (1995). Re-identification of the major volatile carbaboranes from the gas-phase reactions of tetraborane(10) and alkynes at 50 °C. Journal of the Chemical Society, Chemical Communications, 1995(6), 667-668. https://doi.org/10.1039/C39950000667
• 2,4-ETHANOTETRABORANE DERIVATIVES .2. SYNTHESIS, CHARACTERIZATION, AND GAS-PHASE STRUCTURES OF 2,4-(MECHCH(2))B4H8, 2,4-(TRANS-MECHCHME)B4H8, AND 2-PR-2,4-(MECHCH(2))B4H7 AND 4-PR-2,4-(MECHCH(2))B4H7
  
  Fox, M. (1995). 2,4-ETHANOTETRABORANE DERIVATIVES .2. SYNTHESIS, CHARACTERIZATION, AND GAS-PHASE STRUCTURES OF 2,4-(MECHCH(2))B4H8, 2,4-(TRANS-MECHCHME)B4H8, AND 2-PR-2,4-(MECHCH(2))B4H7 AND 4-PR-2,4-(MECHCH(2))B4H7. Inorganic Chemistry, 34(11), 2841-2849.
• THE STRUCTURES OF ALKYL DERIVATIVES OF ARACHNO-1-CB4H10 FROM REACTIONS OF B4H10 WITH ALKYNES
  
  Fox, M. (1994). THE STRUCTURES OF ALKYL DERIVATIVES OF ARACHNO-1-CB4H10 FROM REACTIONS OF B4H10 WITH ALKYNES. Angewandte Chemie International Edition, 33(22), 2298-2300. https://doi.org/10.1002/anie.199422981
• The true identity of the ‘bare-carbon’ cluster, closo-C3B5H7
  
  Fox, M. A., & Greatrex, R. (1994). The true identity of the ‘bare-carbon’ cluster, closo-C3B5H7. Dalton Transactions., 1994(21), 3197-3198. https://doi.org/10.1039/DT9940003197
• X-RAY STRUCTURE AND BONDING OF 1-PHENYLETHYNYL-2-PHENYL-1,2-DICARBADODECABORANE(12), [1-(PHC=C)-2-PH-1,2-C2B10H10], A MODEL ALKYNE COMPLEX CONTAINING A RICH VARIETY OF CARBON-CARBON BOND TYPES
  
  Fox, M. (1993). X-RAY STRUCTURE AND BONDING OF 1-PHENYLETHYNYL-2-PHENYL-1,2-DICARBADODECABORANE(12), [1-(PHC=C)-2-PH-1,2-C2B10H10], A MODEL ALKYNE COMPLEX CONTAINING A RICH VARIETY OF CARBON-CARBON BOND TYPES. Polyhedron, 12(22), 2711-2717.
• Even more reliable NMR chemical shift computations by the GIAO-MP2 method
  
  Schleyer, P. von R., Gauss, J., Bühl, M., Greatrex, R., & Fox, M. A. (1993). Even more reliable NMR chemical shift computations by the GIAO-MP2 method. Journal of the Chemical Society, Chemical Communications, 1993(23), 1766-1768. https://doi.org/10.1039/C39930001766
• C-ARYLATION AND C-HETEROARYLATION OF ICOSAHEDRAL CARBORANES VIA THEIR COPPER(I) DERIVATIVES
  
  Fox, M. (1993). C-ARYLATION AND C-HETEROARYLATION OF ICOSAHEDRAL CARBORANES VIA THEIR COPPER(I) DERIVATIVES. Journal of Organometallic Chemistry, 462(1-2), 19-29.
• PROPOSED STRUCTURE OF THE 1ST HYPHO CARBABORANE, C3B4H12
  
  Fox, M. (1993). PROPOSED STRUCTURE OF THE 1ST HYPHO CARBABORANE, C3B4H12. Polyhedron, 12(15), 1849-1853.
• A PENTUPLY-BRIDGING THIOCARBONYL GROUP - X-RAY CRYSTAL-STRUCTURE OF A SALT OF THE 1-THIO-2-PHENYL-1,2-DICARBADODECABORATE(12) ANION, [LH]+[S(PH)C2B10H10]- (L = 1,8-N,N,N1,N1-TETRAMETHYLNAPHTHALENE DIAMINE)
  
  Fox, M. (1992). A PENTUPLY-BRIDGING THIOCARBONYL GROUP - X-RAY CRYSTAL-STRUCTURE OF A SALT OF THE 1-THIO-2-PHENYL-1,2-DICARBADODECABORATE(12) ANION, [LH]+[S(PH)C2B10H10]- (L = 1,8-N,N,N1,N1-TETRAMETHYLNAPHTHALENE DIAMINE). Polyhedron, 11(20), 2717-2721.