Staff profile
Overview
https://apps.dur.ac.uk/biography/image/1407
Dr Patrycja Brook
Royal Society University Research Fellow
Affiliation |
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Royal Society University Research Fellow in the Department of Chemistry |
Publications
Journal Article
- De Rosa, D. F., Brook, P., Black, D. J., & Pal, R. (2023). Rapid handheld time-resolved circularly polarised luminescence photography camera for life and material sciences. Nature Communications, 14, Article 1537. https://doi.org/10.1038/s41467-023-37329-8
- Algoazy, N., Clarke, R. G., Penfold, T. J., Waddell, P. G., Probert, M. R., Aerts, R., …Knight, J. G. (2022). Near-Infrared Circularly Polarised Luminescence from Helically Extended Chiral N,N,O,O -Boron Chelated Dipyrromethenes. ChemPhotoChem, 6(9), Article e202200090. https://doi.org/10.1002/cptc.202200090
- Penty, S. E., Zwijnenburg, M. A., Orton, G. R., Stachelek, P., Pal, R., Xie, Y., …Barendt, T. A. (2022). The Pink Box: Exclusive Homochiral Aromatic Stacking in a Bis-perylene Diimide Macrocycle. Journal of the American Chemical Society, 144(27), 12290-12298. https://doi.org/10.1021/jacs.2c03531
- Stachelek, P., MacKenzie, L., Parker, D., & Pal, R. (2022). Circularly polarised luminescence laser scanning confocal microscopy to study live cell chiral molecular interactions. Nature Communications, 13(1), Article 533. https://doi.org/10.1038/s41467-022-28220-z
- ]phenazine‐Cored Donor–Acceptor–Donor Triads. Chemistry - A European Journal, 27(53), 13390-13398. https://doi.org/10.1002/chem.202101654
- Haase, N., Danos, A., Pflumm, C., Stachelek, P., Brütting, W., & Monkman, A. P. (2021). Are the Rates of Dexter Transfer in TADF Hyperfluorescence Systems Optically Accessible?. Materials Horizons, 8(6), 1805-1815. https://doi.org/10.1039/d0mh01666g
- MacKenzie, L. E., & Brook, P. (2021). The twists and turns of chiral chemistry. Nature Chemistry, 13(6), 521-522. https://doi.org/10.1038/s41557-021-00729-8
- Nyga, A., Izumi, S., Higginbotham, H. F., Stachelek, P., Pluczyk, S., de Silva, P., …Data, P. (2020). Electrochemical and Spectroelectrochemical Comparative Study of Macrocyclic Thermally Activated Delayed Fluorescent Compounds: Molecular Charge Stability vs OLED EQE Roll‐Off. Asian Journal of Organic Chemistry, 9(12), 2153-2161. https://doi.org/10.1002/ajoc.202000475
- Izumi, S., Higginbotham, H. F., Nyga, A., Stachelek, P., Tohnai, N., Silva, P. D., …Minakata, S. (2020). Thermally Activated Delayed Fluorescent Donor–Acceptor–Donor–Acceptor π-Conjugated Macrocycle for Organic Light-Emitting Diodes. Journal of the American Chemical Society, 142(3), 1482-1491. https://doi.org/10.1021/jacs.9b11578
- 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
- Stachelek, P., Ward, J. S., dos Santos, P. L., Danos, A., Colella, M., Haase, N., …Monkman, A. 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
- Itai, Y., Nishii, Y., Stachelek, P., Data, P., Takeda, Y., Minakata, S., & Miura, M. (2018). Syntheses of Diverse Donor-Substituted Bisbenzofuro[2,3-b:3’,2’- e]pyridines (BBZFPys) via Pd Catalysis, and Their Photophysical Properties. Journal of Organic Chemistry, 83(17), 10289-10302. https://doi.org/10.1021/acs.joc.8b01451
- Ziessel, R., Stachelek, P., Harriman, A., Hedley, G. J., Roland, T., Ruseckas, A., & Samuel, I. D. (2018). Ultrafast Through-Space Electronic Energy Transfer in Molecular Dyads Built around Dynamic Spacer Units. The Journal of Physical Chemistry A, 122(18), 4437-4447. https://doi.org/10.1021/acs.jpca.8b02415
- Woodford, O. J., Stachelek, P., Ziessel, R., Algoazy, N., Knight, J. G., & Harriman, A. (2018). End-to-end communication in a linear supermolecule with a BOPHY centre and N,N-dimethylanilino-based terminals. New Journal of Chemistry, 42(7), https://doi.org/10.1039/c7nj04654e
- Stachelek, P., Alsimaree, A. A., Alnoman, R. B., Harriman, A., & Knight, J. G. (2017). Thermally-Activated, Delayed Fluorescence in O,B,O- and N,B,O-Strapped Boron Dipyrromethene Derivatives. The Journal of Physical Chemistry A, 121(10), 2096-2107. https://doi.org/10.1021/acs.jpca.6b11131
- Stachelek, P., & Harriman, A. (2016). Electronic Communication in Closely Connected BODIPY-Based Bichromophores. The Journal of Physical Chemistry A, 120(41), 8104-8113. https://doi.org/10.1021/acs.jpca.6b08284
- Thakare, S., Stachelek, P., Mula, S., More, A. B., Chattopadhyay, S., Ray, A. K., …Harriman, A. (2016). Solvent-Driven Conformational Exchange for Amide-Linked Bichromophoric BODIPY Derivatives. Chemistry - A European Journal, 22(40), 14356-14366. https://doi.org/10.1002/chem.201602354
- Harriman, A., Stachelek, P., Sutter, A., & Ziessel, R. (2015). A bifurcated molecular pentad capable of sequential electronic energy transfer and intramolecular charge transfer. Physical Chemistry Chemical Physics, 17(39), 26175-26182. https://doi.org/10.1039/c5cp03932k
- Harriman, A., Stachelek, P., Sutter, A., & Ziessel, R. (2015). Stepwise photoconversion of an artificial light-harvesting array built from extended BODIPY units. Photochemical & Photobiological Sciences, 14(6), 1100-1109. https://doi.org/10.1039/c5pp00021a
- Bahaidarah, E., Harriman, A., Stachelek, P., Rihn, S., Heyer, E., & Ziessel, R. (2014). Fluorescent molecular rotors based on the BODIPY motif: effect of remote substituents. Photochemical & Photobiological Sciences, 13(10), 1397-1401. https://doi.org/10.1039/c4pp00204k
- Nano, A., Ziessel, R., Stachelek, P., Alamiry, M. A., & Harriman, A. (2014). Exciplex Emission from a Boron Dipyrromethene (Bodipy) Dye Equipped with a Dicyanovinyl Appendage. ChemPhysChem, 15(1), 177-186. https://doi.org/10.1002/cphc.201300805
- Nano, A., Ziessel, R., Stachelek, P., & Harriman, A. (2013). Charge-Recombination Fluorescence from Push-Pull Electronic Systems Constructed around Amino-Substituted Styryl-BODIPY Dyes. Chemistry - A European Journal, 19(40), 13528-13537. https://doi.org/10.1002/chem.201301045