Staff profile

• X-Ray Crystallography

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
• The Conductance and Thermopower Behavior of Pendent Trans -Coordinated Palladium(II) Complexes in Single-Molecule Junctions
  
  Bastante, P., Davidson, R. J., Al Malki, W., Salthouse, R. J., Cea, P., Martin, S., Batsanov, A. S., Lambert, C. J., Bryce, M. R., & Agrait, N. (2024). The Conductance and Thermopower Behavior of Pendent Trans -Coordinated Palladium(II) Complexes in Single-Molecule Junctions. ACS Omega, 9(36), 38303-38312. https://doi.org/10.1021/acsomega.4c06475
• Exploring the Impact of the HOMO–LUMO Gap on Molecular Thermoelectric Properties: A Comparative Study of Conjugated Aromatic, Quinoidal, and Donor–Acceptor Core Systems
  
  Blankevoort, N., Bastante, P., Davidson, R. J., Salthouse, R. J., Daaoub, A. H. S., Cea, P., Solans, S. M., Batsanov, A. S., Sangtarash, S., Bryce, M. R., Agrait, N., & Sadeghi, H. (2024). Exploring the Impact of the HOMO–LUMO Gap on Molecular Thermoelectric Properties: A Comparative Study of Conjugated Aromatic, Quinoidal, and Donor–Acceptor Core Systems. ACS Omega, 9(7), 8471-8477. https://doi.org/10.1021/acsomega.3c09760
• 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
• Quantum interference dependence on molecular configurations for cross-conjugated systems in single-molecule junctions
  
  Hurtado-Gallego, J., Davidson, R., Grace, I. M., Rincón-García, L., Batsanov, A. S., Bryce, M. R., Lambert, C. J., & Agraït, N. (2022). Quantum interference dependence on molecular configurations for cross-conjugated systems in single-molecule junctions. Molecular Systems Design & Engineering, 7(10), 1287-1293. https://doi.org/10.1039/d2me00074a
• Intramolecular Hydrogen Bonding in Thermally Activated Delayed Fluorescence Emitters: Is There Evidence Beyond Reasonable Doubt?
  
  Hempe, M., Kukhta, N. A., Danos, A., Batsanov, A. S., Monkman, A. P., & Bryce, M. R. (2022). Intramolecular Hydrogen Bonding in Thermally Activated Delayed Fluorescence Emitters: Is There Evidence Beyond Reasonable Doubt?. The Journal of Physical Chemistry Letters, 13(35), 8221-8227. https://doi.org/10.1021/acs.jpclett.2c00907
• Dominant dimer emission provides colour stability for red thermally activated delayed fluorescence emitter
  
  Cardeynaels, T., Etherington, M. K., Paredis, S., Batsanov, A. S., Deckers, J., Stavrou, K., Vanderzande, D., Monkman, A. P., Champagne, B., & Maes, W. (2022). Dominant dimer emission provides colour stability for red thermally activated delayed fluorescence emitter. Journal of Materials Chemistry C, 10(15). https://doi.org/10.1039/d1tc04913e
• Versatile Para‐Substituted Pyridine Lanthanide Coordination Complexes Allow Late Stage Tailoring of Complex Function
  
  Starck, M., Fradgley, J. D., De Rosa, D. F., Batsanov, A. S., Papa, M., Taylor, M. J., Lovett, J. E., Lutter, J. C., Allen, M. J., & Parker, D. (2021). Versatile Para‐Substituted Pyridine Lanthanide Coordination Complexes Allow Late Stage Tailoring of Complex Function. Chemistry – A European Journal, 27(71), 17921-17927. https://doi.org/10.1002/chem.202103243
• Derisking the Polymorph Landscape: The Complex Polymorphism of Mexiletine Hydrochloride
  
  Andrews, J. L., Nilsson Lill, S. O., Freitag-Pohl, S., Apperley, D. C., Yufit, D. S., Batsanov, A. S., Mulvee, M. T., Edkins, K., McCabe, J. F., Berry, D. J., Probert, M. R., & Steed, J. W. (2021). Derisking the Polymorph Landscape: The Complex Polymorphism of Mexiletine Hydrochloride. Crystal Growth & Design, 21(12), 7150-7167. https://doi.org/10.1021/acs.cgd.1c01009
• 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
• Conformational Dependence of Triplet Energies in Rotationally Hindered N‐ and S‐Heterocyclic Dimers: New Design and Measurement Rules for High Triplet Energy OLED Host Materials
  
  Wright, I. A., Danos, A., Montanaro, S., Batsanov, A. S., Monkman, A. P., & Bryce, M. R. (2021). Conformational Dependence of Triplet Energies in Rotationally Hindered N‐ and S‐Heterocyclic Dimers: New Design and Measurement Rules for High Triplet Energy OLED Host Materials. Chemistry - A European Journal, 27(21), 6545-6556. https://doi.org/10.1002/chem.202100036
• Isoniazid-Gentisic acid cocrystallization: Solubility, Stability, Dissolution rate, Antioxidant and Flowability Properties Studies
  
  Mashhadi, S. M. A., Batsanov, A. S., Sajjad, S. A., Nazir, Y., Bhatti, M. H., & Yunus, U. (2021). Isoniazid-Gentisic acid cocrystallization: Solubility, Stability, Dissolution rate, Antioxidant and Flowability Properties Studies. Journal of Molecular Structure, 1226, Article 129388. https://doi.org/10.1016/j.molstruc.2020.129388
• Carbazole isomers induce ultralong organic phosphorescence
  
  Chen, C., Chi, Z., Chong, K. C., Batsanov, A. S., Yang, Z., Mao, Z., Yang, Z., & Liu, B. (2021). Carbazole isomers induce ultralong organic phosphorescence. Nature Materials, 20(February 2021), 175-180. https://doi.org/10.1038/s41563-020-0797-2
• Discovery of a photochemical cascade process by flow-based interception of isomerising alkenes
  
  Di Filippo, M., Trujillo, C., Sánchez-Sanz, G., Batsanov, A. S., & Baumann, M. (2021). Discovery of a photochemical cascade process by flow-based interception of isomerising alkenes. Chemical Science, 12(29). https://doi.org/10.1039/d1sc02879k
• Development of a Continuous Photochemical Benzyne-Forming Process
  
  Baumann, M., Bracken, C., & Batsanov, A. S. (2021). Development of a Continuous Photochemical Benzyne-Forming Process. SynOpen, 05(01), 29-35. https://doi.org/10.1055/s-0040-1706016
• 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
• Resonance-enhanced charge delocalization in carbazole-oligoyne-oxadiazole conjugates
  
  Zieleniewska, A., Zhao, X., Bauroth, S., Wang, C., Batsanov, A., Calderson, C., Kahnt, A., Clark, T., Bryce, M., & Guldi, D. (2020). Resonance-enhanced charge delocalization in carbazole-oligoyne-oxadiazole conjugates. Journal of the American Chemical Society, 142(44), 18769-18781. https://doi.org/10.1021/jacs.0c04003
• Electronic conductance and thermopower of single-molecule junctions of oligo(phenyleneethynylene) derivatives
  
  Dekkiche, H., Gemma, A., Tabatabaei, F., Batsanov, A. S., Niehaus, T., Gotsmann, B., & Bryce, M. R. (2020). Electronic conductance and thermopower of single-molecule junctions of oligo(phenyleneethynylene) derivatives. Nanoscale, 12(36), 18908-18917. https://doi.org/10.1039/d0nr04413j
• Nitrogen Fixation and Biological Behavior of Nanodiamond Colloidal Solutions
  
  Kurakov, A. V., Batsanov, A. S., Gavrilkin, S. M., & Batsanov, S. S. (2020). Nitrogen Fixation and Biological Behavior of Nanodiamond Colloidal Solutions. ChemPlusChem, 85(8), 1905-1911. https://doi.org/10.1002/cplu.202000437
• Phosphorescent mono- and diiridium(III) complexes cyclometalated by fluorenyl- or phenyl-pyridino ligands with bulky substituents, as prospective OLED dopants
  
  M’hamedi, A., & Batsanov, A. S. (2020). Phosphorescent mono- and diiridium(III) complexes cyclometalated by fluorenyl- or phenyl-pyridino ligands with bulky substituents, as prospective OLED dopants. Acta Crystallographica Section E: Crystallographic Communications, 76(3), 392-399. https://doi.org/10.1107/s2056989020001784
• 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
• Excitation modulation of Eu:BPEPC based complexes as low-energy reference standards for circularly polarised luminescence (CPL)
  
  Starck, M., MacKenzie, L. E., Batsanov, A. S., Parker, D., & Pal, R. (2019). Excitation modulation of Eu:BPEPC based complexes as low-energy reference standards for circularly polarised luminescence (CPL). Chemical Communications, 55(94), 14115-14118. https://doi.org/10.1039/c9cc07290j
• Achieving Conformational Control in RTP and TADF Emitters by Functionalization of the Central Core
  
  Kukhta, N., Huang, R., Batsanov, A., Bryce, M., & Dias, F. (2019). Achieving Conformational Control in RTP and TADF Emitters by Functionalization of the Central Core. Journal of Physical Chemistry C, 123(43), 26536-26546. https://doi.org/10.1021/acs.jpcc.9b08238
• Balancing charge-transfer strength and triplet states for deep-blue thermally activated delayed fluorescence with an unconventional electron rich dibenzothiophene acceptor
  
  Huang, R., Kukhta, N., Ward, J., Danos, A., Batsanov, A., Bryce, M., & Dias, F. (2019). Balancing charge-transfer strength and triplet states for deep-blue thermally activated delayed fluorescence with an unconventional electron rich dibenzothiophene acceptor. Journal of Materials Chemistry C Materials for Optical and Electronic Devices, 7(42), 13224-13234. https://doi.org/10.1039/c9tc02175b
• Molecular Design Strategies for Color Tuning of Blue TADF Emitters
  
  Stachelek, P., Ward, J. S., dos Santos, P. L., Danos, A., Colella, M., Haase, N., Raynes, S. J., Batsanov, A. S., Bryce, M. R., Monkman, A. P., & Brook, P. (2019). Molecular Design Strategies for Color Tuning of Blue TADF Emitters. ACS Applied Materials and Interfaces, 11(30), 27125-27133. https://doi.org/10.1021/acsami.9b06364
• 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
• Temperature-Induced Single-Crystal-to-Single-Crystal Transformations with Consequential Changes in the Magnetic Properties of Fe(III) Complexes
  
  Adhikary, A., Akhtar, S., Pariyar, A., Batsanov, A. S., & Mondal, R. (2019). Temperature-Induced Single-Crystal-to-Single-Crystal Transformations with Consequential Changes in the Magnetic Properties of Fe(III) Complexes. ACS Omega, 4(5), 8731-8738. https://doi.org/10.1021/acsomega.8b03400
• Delayed Blue Fluorescence via Upper-triplet State Crossing from C-C Bonded Donor-Acceptor Charge-Transfer Molecules with Azatriangulene cores
  
  Ward, J., Kukhta, N., Dos Santos, P., Congrave, D., Batsanov, A., Monkman, A., & Bryce, M. (2019). Delayed Blue Fluorescence via Upper-triplet State Crossing from C-C Bonded Donor-Acceptor Charge-Transfer Molecules with Azatriangulene cores. Chemistry of Materials, 31(17), 6684-6695. https://doi.org/10.1021/acs.chemmater.9b01184
• Persistent Dimer Emission in Thermally Activated Delayed Fluorescence Materials
  
  Etherington, M. K., Kukhta, N. A., Higginbotham, H. F., Danos, A., Bismillah, A. N., Graves, D. R., McGonigal, P. R., Haase, N., Morherr, A., Batsanov, A. S., Pflumm, C., Bhalla, V., Bryce, M. R., & Monkman, A. P. (2019). Persistent Dimer Emission in Thermally Activated Delayed Fluorescence Materials. Journal of Physical Chemistry C, 123(17), 11109-11117. https://doi.org/10.1021/acs.jpcc.9b01458
• ­­Paramagnetic Lanthanide NMR Probes Signalling Changes in Zinc Concentration by Emission and Chemical Shift: A Proof of Concept Study
  
  Parker, D., Harnden, A. C., & Batsanov, A. S. (2019). ­­Paramagnetic Lanthanide NMR Probes Signalling Changes in Zinc Concentration by Emission and Chemical Shift: A Proof of Concept Study. Angewandte Chemie, 25(24), 6212-6225. https://doi.org/10.1002/chem.201900609
• Activated niobium and tantalum imido complexes: from tuneable polymerization to selective ethylene dimerization systems
  
  Messinis, A., Batsanov, A., Howard, J., Hanton, M., & Dyer, P. W. (2019). Activated niobium and tantalum imido complexes: from tuneable polymerization to selective ethylene dimerization systems. ChemCatChem, 11(6), 1756-1764. https://doi.org/10.1002/cctc.201801849
• Highly luminescent 2-phenylpyridine-free diiridium complexes with bulky 1,2-diarylimidazole cyclometalating ligands
  
  Congrave, D. G., Batsanov, A. S., & Bryce, M. R. (2018). Highly luminescent 2-phenylpyridine-free diiridium complexes with bulky 1,2-diarylimidazole cyclometalating ligands. Dalton Transactions, 47(46), 16524-16533. https://doi.org/10.1039/c8dt04043e
• Importance of Chromophore Rigidity on the Efficiency of Blue Thermally Activated Delayed Fluorescence Emitters
  
  Kukhta, N. A., Batsanov, A. S., Bryce, M. R., & Monkman, A. P. (2018). Importance of Chromophore Rigidity on the Efficiency of Blue Thermally Activated Delayed Fluorescence Emitters. Journal of Physical Chemistry C, 122(50), 28564-28575. https://doi.org/10.1021/acs.jpcc.8b10867
• Approaches to Styrenyl Building Blocks for the Synthesis of Polyene Xanthomonadin and its Analogues
  
  Madden, K., Laroche, B., David, S., Batsanov, A., Thompson, D., Knowles, J., & Whiting, A. (2018). Approaches to Styrenyl Building Blocks for the Synthesis of Polyene Xanthomonadin and its Analogues. European Journal of Organic Chemistry, 2018(38), 5312-5322. https://doi.org/10.1002/ejoc.201800540
• Intramolecular Pi-Pi Interactions with a Chiral Auxiliary Ligand Control Diastereoselectivity in a Cyclometalated Ir(III) Complex
  
  Congrave, D. G., Batsanov, A. S., Du, M., Liu, Y., Zhu, D., & Bryce, M. R. (2018). Intramolecular Pi-Pi Interactions with a Chiral Auxiliary Ligand Control Diastereoselectivity in a Cyclometalated Ir(III) Complex. Inorganic Chemistry, 57(20), 12836-12849. https://doi.org/10.1021/acs.inorgchem.8b02034
• Bis(imido) tungsten complexes: efficient pre-catalysts for the homogeneous dimerization of ethylene
  
  Messinis, A., Batsanov, A. S., Wright, W. R., Howard, J. A., Hanton, M. J., & Dyer, P. W. (2018). Bis(imido) tungsten complexes: efficient pre-catalysts for the homogeneous dimerization of ethylene. ACS Catalysis, 8(12), 11249-11263. https://doi.org/10.1021/acscatal.8b02202
• Synthesis of Tetracyclic 2,3-Dihydro-1,3-diazepines from a Dinitrodibenzothiophene Derivative
  
  Montanaro, S., Wright, I. A., Batsanov, A. S., & Bryce, M. R. (2018). Synthesis of Tetracyclic 2,3-Dihydro-1,3-diazepines from a Dinitrodibenzothiophene Derivative. Journal of Organic Chemistry, 83(19), 12320-12326. https://doi.org/10.1021/acs.joc.8b02029
• The influence of molecular conformation on the photophysics of organic room temperature phosphorescent luminophores
  
  Huang, R., Ward, J. S., Kukhta, N. A., Avó, J., Gibson, J., Penfold, T., Lima, J. C., Batsanov, A. S., Berberan-Santos, M. N., Bryce, M. R., & Dias, F. B. (2018). The influence of molecular conformation on the photophysics of organic room temperature phosphorescent luminophores. Journal of Materials Chemistry C Materials for Optical and Electronic Devices, 10(34), 9238-9247. https://doi.org/10.1039/c8tc02987c
• Weak interactions in crystals: old concepts, new developments
  
  Batsanov, A. S. (2018). Weak interactions in crystals: old concepts, new developments. Acta Crystallographica Section E: Crystallographic Communications, 74(5), 570-574. https://doi.org/10.1107/s2056989018005339
• Sky-blue emitting bridged diiridium complexes: beneficial effects of intramolecular π–π stacking
  
  Congrave, D. G., Hsu, Y.-T., Batsanov, A. S., Beeby, A., & Bryce, M. R. (2018). Sky-blue emitting bridged diiridium complexes: beneficial effects of intramolecular π–π stacking. Dalton Transactions, 47(6), 2086-2098. https://doi.org/10.1039/c7dt04201a
• 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
• Bipolar Molecules with High Triplet Energies: Synthesis, Photophysical, and Structural Properties.
  
  Zheng, Y., Batsanov, A., Jankus, V., Dias, F., Bryce, M., & Monkman, A. (2011). Bipolar Molecules with High Triplet Energies: Synthesis, Photophysical, and Structural Properties. Journal of Organic Chemistry, 76(20), 8300-8310. https://doi.org/10.1021/jo201488v
• A Catalytic Aldol Reaction and Condensation through In Situ Boron “Ate” Complex Enolate Generation in Water
  
  Aelvoet, K., Batsanov, A. S., Blatch, A. J., Grosjean, C., Patrick, L. G. F., Smethurst, C. A., & Whiting, A. (2008). A Catalytic Aldol Reaction and Condensation through In Situ Boron “Ate” Complex Enolate Generation in Water. Angewandte Chemie International Edition, 47(4), 768-770. https://doi.org/10.1002/anie.200704293
• Calix 6 arene derivatives selectively functionalized at alternate sites on the smaller rim with 2-phenylpyridine and 2-fluorenylpyridine substituents to provide deep cavities
  
  Zeng, X., Batsanov, A., & Bryce, M. (2006). Calix 6 arene derivatives selectively functionalized at alternate sites on the smaller rim with 2-phenylpyridine and 2-fluorenylpyridine substituents to provide deep cavities. Journal of Organic Chemistry, 71(26), 9589-9594. https://doi.org/10.1021/jo0614341
• Convergent synthesis of 10 nm aryleethynylene molecular wires by an iterative regioselective deprotection/sonogashira coupling protocol
  
  Wang, C., Batsanov, A., & Bryce, M. (2006). Convergent synthesis of 10 nm aryleethynylene molecular wires by an iterative regioselective deprotection/sonogashira coupling protocol. Journal of Organic Chemistry, 71(1), 108-116. https://doi.org/10.1021/jo051711o
• Synthesis of new axially-disubstituted silicon-phthalocyanine derivatives : optical and structural characterisation.
  
  Barker, C., Findlay, K., Bettington, S., Batsanov, A., Perepichka, I., Bryce, M., & Beeby, A. (2006). Synthesis of new axially-disubstituted silicon-phthalocyanine derivatives : optical and structural characterisation. Tetrahedron, 62(40), 9433-9439. https://doi.org/10.1016/j.tet.2006.07.046
• Synthesis and structure of an unusual di-rhodium diarylbutadiyne pi-complex featuring a mu-(1,2-eta(2)):(3,4-eta(2))-p-CF3C6H4-C C-C C-C6H4-p-CF3 moiety.
  
  Ward, R., Batsanov, A., Howard, J., & Marder, T. (2006). Synthesis and structure of an unusual di-rhodium diarylbutadiyne pi-complex featuring a mu-(1,2-eta(2)):(3,4-eta(2))-p-CF3C6H4-C C-C C-C6H4-p-CF3 moiety. Inorganica Chimica Acta, 359(11), 3671-3676. https://doi.org/10.1016/j.ica.2005.12.018
• The dihydrofuran template approach to furofuran synthesis
  
  Aldous, D., Batsanov, A., Yufit, D., Dalencon, A., Dutton, W., & Steel, P. (2006). The dihydrofuran template approach to furofuran synthesis. Organic and Biomolecular Chemistry, 4(15), 2912-2927. https://doi.org/10.1039/b604952d
• Extreme conformational constraints in pi-extended tetrathiafulvalenes : Unusual topologies and redox behavior of doubly and triply bridged cyclophanes.
  
  Christensen, C., Batsanov, A., & Bryce, M. (2006). Extreme conformational constraints in pi-extended tetrathiafulvalenes : Unusual topologies and redox behavior of doubly and triply bridged cyclophanes. Journal of the American Chemical Society, 128(32), 10484-10490. https://doi.org/10.1021/ja062358m
• Crystal engineering with ethynylbenzenes Part 2. Structures of 4-trimethylsilylethynyl-N,N-dimethylaniline, and 4-ethynyl-N,N-dimethylaniline with Z '=12 and a single-crystal to single-crystal phase transition at 122.5 +/- 2 K
  
  Batsanov, A., Collings, J., Ward, R., Goeta, A., Porres, L., Beeby, A., Howard, J., Steed, J., & Marder, T. (2006). Crystal engineering with ethynylbenzenes Part 2. Structures of 4-trimethylsilylethynyl-N,N-dimethylaniline, and 4-ethynyl-N,N-dimethylaniline with Z ’=12 and a single-crystal to single-crystal phase transition at 122.5 +/- 2 K. CrystEngComm, 8, 622-628. https://doi.org/10.1039/b606327f
• Arene-perfluoroarene interactions in crystal engineering. XV. Ferrocene-decafluorobiphenyl (1/1)
  
  Batsanov, A., Collings, J., & Marder, T. (2006). Arene-perfluoroarene interactions in crystal engineering. XV. Ferrocene-decafluorobiphenyl (1/1). Acta Crystallographica C: Crystal Structure Communications, 62(6), M229-M231. https://doi.org/10.1107/s0108270106014090
• Nanoscale aryleneethynylene oligomers incorporating fluorenone units as electron-dopable molecular wires.
  
  Wang, C., Batsanov, A., & Bryce, M. (2006). Nanoscale aryleneethynylene oligomers incorporating fluorenone units as electron-dopable molecular wires. Faraday Discussions, 131, 221-234. https://doi.org/10.1039/b506712j
• Remarkable interplay of redox states and conformational changes in a sterically crowded, cross-conjugated tetrathiafulvalene vinylog.
  
  Amriou, S., Perepichka, I., Batsanov, A., Bryce, M., Rovira, C., & Vidal-Gancedo, J. (2006). Remarkable interplay of redox states and conformational changes in a sterically crowded, cross-conjugated tetrathiafulvalene vinylog. Chemistry - A European Journal, 12(21), 5481-5494. https://doi.org/10.1002/chem.200600244
• 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
• The interplay of inverted redox potentials and aromaticity in the oxidized states of new pi-electron donors: 9-(1,3-dithiol-2-ylidene)fluorene and 9-(1,3-dithiol-2-ylidene)thioxanthene derivatives.
  
  Amriou, S., Wang, C., Batsanov, A., Bryce, M., Perepichka, D., Orti, E., Viruela, R., Vidal-Gancedo, J., & Rovira, C. (2006). The interplay of inverted redox potentials and aromaticity in the oxidized states of new pi-electron donors: 9-(1,3-dithiol-2-ylidene)fluorene and 9-(1,3-dithiol-2-ylidene)thioxanthene derivatives. Chemistry - A European Journal, 12(12), 3389-3400. https://doi.org/10.1002/chem.200501326
• Synthesis, crystal structures, linear and nonlinear optical properties, and theoretical studies of (p-R-phenyl)-, (p-R-phenylethynyl)-, and (E)-[2-(p-R-phenyl)ethenyl]dimesitylboranes and related compounds
  
  Yuan, Z., Entwistle, C., Collings, J., Albesa-Jove, D., Batsanov, A., Howard, J., Taylor, N., Kaiser, H., Kaufmann, D., Poon, S., Wong, W., Jardin, C., Fathallah, S., Boucekkine, A., Halet, J., & Marder, T. (2006). Synthesis, crystal structures, linear and nonlinear optical properties, and theoretical studies of (p-R-phenyl)-, (p-R-phenylethynyl)-, and (E)-[2-(p-R-phenyl)ethenyl]dimesitylboranes and related compounds. Chemistry - A European Journal, 12(10), 2758-2771. https://doi.org/10.1002/chem.200501096
• 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
• Effects of ortho- and para-ring activation on the kinetics of S_NAr reactions of 1-chloro-2-nitro and 1-phenoxy-2-nitrobenzenes with aliphatic amines in acetonitrile
  
  Crampton, M., Emokpae, T., Isanbor, C., Batsanov, A., Howard, J., & Mondal, R. (2006). Effects of ortho- and para-ring activation on the kinetics of S_NAr reactions of 1-chloro-2-nitro and 1-phenoxy-2-nitrobenzenes with aliphatic amines in acetonitrile. European Journal of Organic Chemistry, 2006(5), 1222-1230. https://doi.org/10.1002/ejoc.200500774
• Fac-Dichlorotris(trimethylphosphine)(trimethylphosphoniomethyl) rhodium(III) chloride/bromide dichloromethane benzene solvate.
  
  Batsanov, A., Marder, T., & Seeler, F. (2006). Fac-Dichlorotris(trimethylphosphine)(trimethylphosphoniomethyl) rhodium(III) chloride/bromide dichloromethane benzene solvate. Acta Crystallographica. Section E, Structure Reports Online., 62(3), m574-m575. https://doi.org/10.1107/s1600536806005630
• The synthesis, structure, reactivity and electrochemical properties of ruthenium complexes featuring cyanoacetylide ligands
  
  Cordiner, R. L., Smith, M. E., Batsanov, A. S., Albesa-Jové, D., Hartl, F., Howard, J. A., & Low, P. J. (2006). The synthesis, structure, reactivity and electrochemical properties of ruthenium complexes featuring cyanoacetylide ligands. Inorganica Chimica Acta, 359(3), 946-961. https://doi.org/10.1016/j.ica.2005.06.044
• Arene-perfluoroarene interactions in crystal engineering. Part 14. 1 : 1 Complexes of octafluoronaphthalene with fluorene and 9,10-dihydrophenanthrene
  
  Collings, J., Batsanov, A., Howard, J., & Marder, T. (2006). Arene-perfluoroarene interactions in crystal engineering. Part 14. 1 : 1 Complexes of octafluoronaphthalene with fluorene and 9,10-dihydrophenanthrene. Canadian Journal of Chemistry, 84(2), 238-242. https://doi.org/10.1139/v06-007
• 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
• Ir-Catalyzed borylation of C-H bonds in N-containing heterocycles: Regioselectivity in the synthesis of heteroaryl boronate esters
  
  Ibraheem, A., Mkhalid, D., A-J. Coventry, D., Batsanov, A., Howard, J., Perutz, R., & Marder, T. (2006). Ir-Catalyzed borylation of C-H bonds in N-containing heterocycles: Regioselectivity in the synthesis of heteroaryl boronate esters. Angewandte Chemie International Edition, 45(3), 489-491. https://doi.org/10.1002/anie.200503047
• Chelating N-pyrrolylphosphino-N-arylaldimine ligands : synthesis, ligand behaviour and applications in catalysis.
  
  Anderson, C., Batsanov, A., Dyer, P., Fawcett, J., & Howard, J. (2006). Chelating N-pyrrolylphosphino-N-arylaldimine ligands : synthesis, ligand behaviour and applications in catalysis. Dalton Transactions, 45, 5362-5378. https://doi.org/10.1039/b611652c
• Bis(2,6-dimethylpyridyl)iodonium dibromoiodate
  
  Batsanov, A., Lightfoot, A., Twiddle, S., & Whiting, A. (2006). Bis(2,6-dimethylpyridyl)iodonium dibromoiodate. Acta Crystallographica. Section E, Structure Reports Online., E62, o901-o902. https://doi.org/10.1107/s1600536806003680
• 2-(p-tolyl)-1,3,2-benzodioxaborole
  
  Bramham, G., Batsanov, A., Marder, T., & Norman, N. (2006). 2-(p-tolyl)-1,3,2-benzodioxaborole. Acta Crystallographica. Section E, Structure Reports Online., E62, o972-o973. https://doi.org/10.1107/s1600536806004089
• Concise syntheses of tridentate PNE ligands and their coordination chemistry with palladium(II): a solution- and solid-state study
  
  Anderson, C., Apperley, D., Batsanov, A., Dyer, P., & Howard, J. (2006). Concise syntheses of tridentate PNE ligands and their coordination chemistry with palladium(II): a solution- and solid-state study. Dalton Transactions, 2006(34), 4134-4145. https://doi.org/10.1039/b605995c
• Are terminal aryl butadiynes stable? Synthesis and X-ray crystal structures of a series of aryl- and heteroaryl-butadiynes (Ar-C C-C C-H)
  
  West, K., Wang, C., Batsanov, A., & Bryce, M. (2006). Are terminal aryl butadiynes stable? Synthesis and X-ray crystal structures of a series of aryl- and heteroaryl-butadiynes (Ar-C C-C C-H). Journal of Organic Chemistry, 71(22), 8541-8544. https://doi.org/10.1021/jo0615697
• Synthesis and reactivity of cobalt boryl complexes.
  
  Adams, C., Baber, R., Batsanov, A., Bramham, G., Charmant, J., Haddow, M., Howard, J., Lam, W., Lin, Z., Marder, T., Norman, N., & Orpen, A. (2006). Synthesis and reactivity of cobalt boryl complexes. Dalton Transactions, 11, 1370-1373. https://doi.org/10.1039/b516594f
• Precision control of single-molecule electrical junctions
  
  Haiss, W., Wang, C., Grace, I., Batsanov, A., Schiffrin, D., Higgins, S., Bryce, M., Lambert, C., & Nichols, R. (2006). Precision control of single-molecule electrical junctions. Nature Materials, 5(12), 995-1002. https://doi.org/10.1038/nmat1781
• New electroluminescent bipolar compounds for balanced charge-transport and tuneable colour in organic light emitting diodes: triphenylamine oxadiazole-fluorene triad molecules
  
  Kamtekar, K., Wang, C., Bettington, S., Batsanov, A., Perepichka, I., Bryce, M., Ahn, J., Rabinal, M., & Petty, M. (2006). New electroluminescent bipolar compounds for balanced charge-transport and tuneable colour in organic light emitting diodes: triphenylamine oxadiazole-fluorene triad molecules. Journal of Materials Chemistry, 16(39), 3823-3835. https://doi.org/10.1039/b604543j
• Bridged diiridium complexes for electrophosphorescent OLEDs : synthesis, X-ray crystal structures, photophysics, and devices.
  
  Bettington, S., Tavasli, M., Bryce, M., Batsanov, A., Thompson, A., Al Attar, H., Dias, F., & Monkman, A. (2006). Bridged diiridium complexes for electrophosphorescent OLEDs : synthesis, X-ray crystal structures, photophysics, and devices. Journal of Materials Chemistry, 16(11), 1046-1052. https://doi.org/10.1039/b515258e
• 2-(4-Chloroanilino)- and 2-(4-methoxyanilino)-1,2-diphenyl-ethanone
  
  Batsanov, A., Goeta, A., Howard, J., Soto, B., & Au-Alvarez, O. (2006). 2-(4-Chloroanilino)- and 2-(4-methoxyanilino)-1,2-diphenyl-ethanone. Acta Crystallographica., 62(5), o304-o306. https://doi.org/10.1107/s0108270106012881
• Structural investigations on quinone methides for understanding their properties in confined media.
  
  Szarma, R., Batsanov, A., Kataky, R., & Baruah, J. (2006). Structural investigations on quinone methides for understanding their properties in confined media. Journal of Inclusion Phenomena and Macrocyclic Chemistry, 55(1-2), 1-9. https://doi.org/10.1007/s10847-005-9001-1
• 4,4 '-Diamino-2,2 ',6,6 '-tetramethylbiphenyl
  
  Batsanov, A., Low, P., & Paterson, M. (2006). 4,4 ’-Diamino-2,2 ’,6,6 ’-tetramethylbiphenyl. Acta Crystallographica. Section E, Structure Reports Online., E62, o2973-o2975. https://doi.org/10.1107/s1600536806022756
• The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid
  
  Masesane, I., Batsanov, A., Howard, J., Mondal, R., & Steel, P. (2006). The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid. Beilstein Journal of Organic Chemistry, 2(9), Article 9. https://doi.org/10.1186/1860-5397-2-9
• 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
• 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
• Arene-perfluoroarene interactions in crystal engineering 8: structures of 1 : 1 complexes of hexafluorobenzene with fused-ring polyaromatic hydrocarbons
  
  Collings, J., Roscoe, K., Robins, E., Batsanov, A., Stimson, L., Howard, J., Clark, S., & Marder, T. (2002). Arene-perfluoroarene interactions in crystal engineering 8: structures of 1 : 1 complexes of hexafluorobenzene with fused-ring polyaromatic hydrocarbons. New Journal of Chemistry, 26(12), 1740-1746. https://doi.org/10.1039/b207102a
• 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
• Electron acceptors of the fluorene series. Part 12. 9- (Metalloceneylidene)nitrofluorene derivatives of Fc-NF, NF-Fc- NF, and NF-Rc-NF types, and the vinylogues Fc-pi-NF: synthesis, characterisation, intramolecular charge transfer, redox properties and X-
  
  Perepichka, D., Perepichka, I., Popov, A., Bryce, M., Batsanov, A., Chesney, A., Howard, J., & Sokolov, N. (2001). Electron acceptors of the fluorene series. Part 12. 9- (Metalloceneylidene)nitrofluorene derivatives of Fc-NF, NF-Fc- NF, and NF-Rc-NF types, and the vinylogues Fc-pi-NF: synthesis, characterisation, intramolecular charge transfer, redox properties and X-. Journal of Organometallic Chemistry, 637, 445-462.
• Cocrystals of 2-(2,4,5,7-tetranitrofluoren-9- ylidene)propanedinitrile and 2,4,5,7-tetranitrofluoren-9-one with chlorobenzene
  
  Batsanov, A., Perepichka, I., Bryce, M., & Howard, J. (2001). Cocrystals of 2-(2,4,5,7-tetranitrofluoren-9- ylidene)propanedinitrile and 2,4,5,7-tetranitrofluoren-9-one with chlorobenzene. Acta Crystallographica C: Crystal Structure Communications, 57, 1299-1302.
• Electron acceptors of the fluorene series. Part 13. 9-(5- Nitrofuran-2-ylidene)- and 9-(5-nitro-2-thienylidene)-2,4,5,7- tetranitrofluorenes: novel pi-extended electron acceptors. Synthesis, cyclic voltammetry and X-ray crystal structures for the acceptor
  
  Perepichka, I., Perepichka, D., Lyubchik, S., Bryce, M., Batsanov, A., & Howard, J. (2001). Electron acceptors of the fluorene series. Part 13. 9-(5- Nitrofuran-2-ylidene)- and 9-(5-nitro-2-thienylidene)-2,4,5,7- tetranitrofluorenes: novel pi-extended electron acceptors. Synthesis, cyclic voltammetry and X-ray crystal structures for the acceptor. Journal of the Chemical Society, Perkin Transactions 2, 2001(9), 1546-1551.
• Trialkyltetrathiafulvalene-sigma-tetracyanoanthraquinodimethane (R3TTF-sigma-TCNAQ) diads: Synthesis, intramolecular charge- transfer properties, and X-ray crystal structure
  
  Perepichka, D., Bryce, M., Batsanov, A., Howard, J., Cuello, A., Gray, M., & Rotello, V. (2001). Trialkyltetrathiafulvalene-sigma-tetracyanoanthraquinodimethane (R3TTF-sigma-TCNAQ) diads: Synthesis, intramolecular charge- transfer properties, and X-ray crystal structure. Journal of Organic Chemistry, 66(13), 4517-4524.
• Synthesis of conjugated tetrathiafulvalene (TTF)-pi-acceptor molecules - Intramolecular charge transfer and nonlinear optical properties
  
  Bryce, M., Green, A., Moore, A., Perepichka, D., Batsanov, A., Howard, J., Ledoux-Rak, I., Gonzalez, M., Martin, N., Segura, J., Garin, J., Orduna, J., Alcala, R., & Villacampa, B. (2001). Synthesis of conjugated tetrathiafulvalene (TTF)-pi-acceptor molecules - Intramolecular charge transfer and nonlinear optical properties. European Journal of Organic Chemistry, 10, 1927-1935.
• Molecular saddles. 7. New 9,10-bis(1,3-dithiol-2-ylidene)-9,10- dihydroanthracene cyclophanes: Synthesis, redox properties, and X-ray crystal structures of neutral species and a dication salt
  
  Christensen, C., Batsanov, A., Bryce, M., & Howard, J. (2001). Molecular saddles. 7. New 9,10-bis(1,3-dithiol-2-ylidene)-9,10- dihydroanthracene cyclophanes: Synthesis, redox properties, and X-ray crystal structures of neutral species and a dication salt. Journal of Organic Chemistry, 66(10), 3313-3320.
• An efficient pyridine- and oxadiazole-containing hole-blocking material far organic light-emitting diodes: Synthesis, crystal structure, and device performance
  
  Wang, C., Jung, G., Hua, Y., Pearson, C., Bryce, M., Petty, M., Batsanov, A., Goeta, A., & Howard, J. (2001). An efficient pyridine- and oxadiazole-containing hole-blocking material far organic light-emitting diodes: Synthesis, crystal structure, and device performance. Chemistry of Materials, 13(4), 1167-1173.
• 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
• Synthesis, crystal structure and electrochemistry of a new bimetallic nickel dithiolene complex (NBu4+)(2){C2S4 NiS2C2S2(CO) (2)}(2-). A precursor for molecular conductors
  
  Batsanov, A., Bryce, M., Dhindsa, A., Howard, J., & Underhill, A. (2001). Synthesis, crystal structure and electrochemistry of a new bimetallic nickel dithiolene complex (NBu4+)(2){C2S4 NiS2C2S2(CO) (2)}(2-). A precursor for molecular conductors. Polyhedron, 20(6), 537-540.
• Photochemistry of the pi-extended 9,10-bis(1,3-dithiol-2- ylidene)-9,10-dihydroanthracene system: Generation and characterisation of the radical cation, dication, and derived products
  
  Jones, A., Christensen, C., Perepichka, D., Batsanov, A., Beeby, A., Low, P., Bryce, M., & Parker, A. (2001). Photochemistry of the pi-extended 9,10-bis(1,3-dithiol-2- ylidene)-9,10-dihydroanthracene system: Generation and characterisation of the radical cation, dication, and derived products. Chemistry - A European Journal, 7(5), 973-978. https://doi.org/10.1002/1521-3765%2820010302%297%3A5%3C973%3A%3Aaid-chem973%3E3.0.co%3B2-%23
• Molecular saddles. 4. Redox-active cyclophanes by bridging the 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene system: Synthesis, electrochemistry, and X-ray crystal structures of neutral species and a dication salt
  
  Godbert, N., Batsanov, A., Bryce, M., & Howard, J. (2001). Molecular saddles. 4. Redox-active cyclophanes by bridging the 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene system: Synthesis, electrochemistry, and X-ray crystal structures of neutral species and a dication salt. Journal of Organic Chemistry, 66(3), 713-719.
• Hydroxymethyl-Functionalised 9,10-Bis(1,3-dithiol-2-ylidene)-9,10-Dihydroanthracene π-Electron Donors as Synthetic Intermediates for Supramolecular Structures
  
  Godbert, N., Bryce, M., Dahaoui, S., Batsanov, A., Howard, J., & Hazendonk, P. (2001). Hydroxymethyl-Functionalised 9,10-Bis(1,3-dithiol-2-ylidene)-9,10-Dihydroanthracene π-Electron Donors as Synthetic Intermediates for Supramolecular Structures. European Journal of Organic Chemistry, 2001(4), 749-757. https://doi.org/10.1002/1099-0690%28200102%292001%3A4
• Synthesis and crystal engineering of new halogenated tetrathiafulvalene (TTF) derivatives and their charge transfer complexes and radical ion salts
  
  Batsanov, A., Bryce, M., Chesney, A., Howard, J., John, D., Moore, A., Wood, C., Gershtenman, H., Becker, J., Khodorkovsky, V., Ellern, A., Bernstein, J., Perepichka, I., Rotello, V., Gray, M., & Cuello, A. (2001). Synthesis and crystal engineering of new halogenated tetrathiafulvalene (TTF) derivatives and their charge transfer complexes and radical ion salts. Journal of Materials Chemistry, 11(9), 2181-2191.
• 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
• Modification Of Molecular Packing: Crystal Structures And Magnetic Properties Of Monomeric And Dimeric Difluorophenyl-1,2,3,5-dithiadiazolyl Radicals
  
  Banister, A., Batsanov, A., Dawe, O., Herbertson, P., Howard, J., Lynn, S., May, I., Smith, J., Rawson, J., Rogers, T., Tanner, B., Antorrena, G., & Palacio, F. (1997). Modification Of Molecular Packing: Crystal Structures And Magnetic Properties Of Monomeric And Dimeric Difluorophenyl-1,2,3,5-dithiadiazolyl Radicals. Dalton Transactions., 15, 2539-2541. https://doi.org/10.1039/A702881D
• Trimethyltetrathiafulvalene bearing an N-methylpyridinium substituent: Synthesis, crystal structures, and charge transfer properties
  
  Moore, A., Batsanov, A., Bryce, M., Howard, J., Khodorkovsky, V., Shapiro, L., & Shames, A. (n.d.). Trimethyltetrathiafulvalene bearing an N-methylpyridinium substituent: Synthesis, crystal structures, and charge transfer properties. European Journal of Organic Chemistry, 1, 73-78.
• Synthesis, structures and nonlinear optical properties of novel D-pi-A chromophores: Intramolecular charge transfer from 1,3- dithiole or ferrocene moieties to polynitrofluorene or dicyanomethylene moieties through conjugated linkers
  
  Moore, A., Chesney, A., Bryce, M., Batsanov, A., Kelly, J., Howard, J., Perepichka, I., Perepichka, D., Meshulam, G., Berkovic, G., Kotler, Z., Mazor, R., & Khodorkovsky, V. (n.d.). Synthesis, structures and nonlinear optical properties of novel D-pi-A chromophores: Intramolecular charge transfer from 1,3- dithiole or ferrocene moieties to polynitrofluorene or dicyanomethylene moieties through conjugated linkers. European Journal of Organic Chemistry, 14, 2671-2687.
• Crown-annelated 9,10-bis(1,3-dithiol-2-ylidene)-9,10- dihydroanthracene derivatives as cation sensors: Synthesis, X- ray crystal structures, voltammetric and spectroscopic monitoring of metal complexation
  
  Bryce, M., Batsanov, A., Finn, T., Hansen, T., Moore, A., Howard, J., Kamenjicki, M., Lednev, I., & Asher, S. (n.d.). Crown-annelated 9,10-bis(1,3-dithiol-2-ylidene)-9,10- dihydroanthracene derivatives as cation sensors: Synthesis, X- ray crystal structures, voltammetric and spectroscopic monitoring of metal complexation. European Journal of Organic Chemistry, 5, 933-940.