Staff profile

• X-Ray Crystallography

Journal Article

• Blankevoort, N., Bastante, P., Davidson, R. J., Salthouse, R. J., Daaoub, A. H. S., Cea, P., …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
• Hurtado-Gallego, J., Davidson, R., Grace, I. M., Rincón-García, L., Batsanov, A. S., Bryce, M. R., …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
• 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?. Journal of Physical Chemistry Letters, 13(35), 8221-8227. https://doi.org/10.1021/acs.jpclett.2c00907
• Cardeynaels, T., Etherington, M. K., Paredis, S., Batsanov, A. S., Deckers, J., Stavrou, K., …Maes, W. (2022). Dominant dimer emission provides colour stability for red thermally activated delayed fluorescence emitter. Journal of Materials Chemistry C Materials for optical and electronic devices, 10(15), https://doi.org/10.1039/d1tc04913e
• Starck, M., Fradgley, J. D., De Rosa, D. F., Batsanov, A. S., Papa, M., Taylor, 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
• Andrews, J. L., Nilsson Lill, S. O., Freitag-Pohl, S., Apperley, D. C., Yufit, D. S., Batsanov, A. S., …Steed, J. W. (2021). Derisking the Polymorph Landscape: The Complex Polymorphism of Mexiletine Hydrochloride. Crystal Growth and Design, 21(12), 7150-7167. https://doi.org/10.1021/acs.cgd.1c01009
• 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
• 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
• Chen, C., Chi, Z., Chong, K. C., Batsanov, A. S., Yang, Z., Mao, 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
• 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
• 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
• 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
• 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
• Zieleniewska, A., Zhao, X., Bauroth, S., Wang, C., Batsanov, A., Calderson, C., …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
• 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
• 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
• 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
• Benjamin, H., Zheng, Y., Kozhevnikov, V. N., Siddle, J. S., O'Driscoll, L. J., Fox, M. A., …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
• 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
• 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
• 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
• 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
• Parker, D., Suturina, E., Harnden, A., Batsanov, A., Fox, M., Mason, K., …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
• 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
• 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
• Etherington, M. K., Kukhta, N. A., Higginbotham, H. F., Danos, A., Bismillah, A. N., Graves, D. 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• Huang, R., Ward, J. S., Kukhta, N. A., Avó, J., Gibson, J., Penfold, T., …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
• 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
• Congrave, D. G., Hsu, Y., 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
• Benjamin, H., Fox, M. A., Batsanov, A. S., Al-Attar, H. A., Li, C., Ren, Z., …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
• 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
• 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
• 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
• Dias, F., Pollock, S., Hedley, G., Palsson, L., Monkman, A., Perepichka, I., …Bryce, M. (2006). Intramolecular charge transfer assisted by conformational changes in the excited state of fluorene-dibenzothiophene-S,S-dioxide co-oligomers. Journal of Physical Chemistry B (Soft Condensed Matter and Biophysical Chemistry), 110(39), 19329-19339. https://doi.org/10.1021/jp0643653
• 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
• 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
• 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
• Batsanov, A., Collings, J., Ward, R., Goeta, A., Porres, L., Beeby, A., …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
• 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
• 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, 4134-4145. https://doi.org/10.1039/b605995c
• 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
• Batsanov, A., Collings, J., & Marder, T. (2006). Arene-perfluoroarene interactions in crystal engineering. XV. Ferrocene-decafluorobiphenyl (1/1). Acta crystallographica. Section C, Crystal structure communications, 62(6), M229-M231. https://doi.org/10.1107/s0108270106014090
• 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
• Fox, M., Cameron, A., Low, P., Paterson, M., Batsanov, A., Goeta, A., …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
• Amriou, S., Wang, C., Batsanov, A., Bryce, M., Perepichka, D., Orti, E., …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
• Yuan, Z., Entwistle, C., Collings, J., Albesa-Jove, D., Batsanov, A., Howard, 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
• 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
• Batsanov, A., Marder, T., & Seeler, F. (2006). Fac-Dichlorotris(trimethylphosphine)(trimethylphosphoniomethyl) rhodium(III) chloride/bromide dichloromethane benzene solvate. Acta crystallographica. Section E, 62(3), m574-m575. https://doi.org/10.1107/s1600536806005630
• Crampton, M., Emokpae, T., Isanbor, C., Batsanov, A., Howard, J., & Mondal, R. (2006). Effects of ortho- and para-ring activation on the kinetics of SNAr 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
• 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
• 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
• Batsanov, A., Clegg, W., Copley, R., Fox, M., Gill, W., Grimditch, R., …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
• 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
• Batsanov, A., Low, P., & Paterson, M. (2006). 4,4 '-Diamino-2,2 ',6,6 '-tetramethylbiphenyl. Acta crystallographica. Section E, E62, o2973-o2975. https://doi.org/10.1107/s1600536806022756
• 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
• Batsanov, A., Lightfoot, A., Twiddle, S., & Whiting, A. (2006). Bis(2,6-dimethylpyridyl)iodonium dibromoiodate. Acta crystallographica. Section E, E62, o901-o902. https://doi.org/10.1107/s1600536806003680
• Haiss, W., Wang, C., Grace, I., Batsanov, A., Schiffrin, D., Higgins, S., …Nichols, R. (2006). Precision control of single-molecule electrical junctions. Nature Materials, 5(12), 995-1002. https://doi.org/10.1038/nmat1781
• Adams, C., Baber, R., Batsanov, A., Bramham, G., Charmant, J., Haddow, M., …Orpen, A. (2006). Synthesis and reactivity of cobalt boryl complexes. Dalton Transactions, 11, 1370-1373. https://doi.org/10.1039/b516594f
• 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
• 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. Section C, Crystal structure communications, 62(5), o304-o306. https://doi.org/10.1107/s0108270106012881
• Kamtekar, K., Wang, C., Bettington, S., Batsanov, A., Perepichka, I., Bryce, 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
• 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
• Bramham, G., Batsanov, A., Marder, T., & Norman, N. (2006). 2-(p-tolyl)-1,3,2-benzodioxaborole. Acta crystallographica. Section E, E62, o972-o973. https://doi.org/10.1107/s1600536806004089
• 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
• Bettington, S., Tavasli, M., Bryce, M., Batsanov, A., Thompson, A., Al Attar, H., …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
• Collings, J., Roscoe, K., Robins, E., Batsanov, A., Stimson, L., Howard, J., …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
• Perepichka, D., Perepichka, I., Popov, A., Bryce, M., Batsanov, A., Chesney, A., …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
• 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. Section C, Crystal structure communications, 57, 1299-1302
• 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
• Moore, A., Chesney, A., Bryce, M., Batsanov, A., Kelly, J., Howard, J., …Khodorkovsky, V. (2001). 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, 2671-2687
• 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
• Bryce, M., Green, A., Moore, A., Perepichka, D., Batsanov, A., Howard, J., …Villacampa, B. (2001). Synthesis of conjugated tetrathiafulvalene (TTF)-pi-acceptor molecules - Intramolecular charge transfer and nonlinear optical properties. European Journal of Organic Chemistry, 1927-1935
• 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
• Wang, C., Jung, G., Hua, Y., Pearson, C., Bryce, M., Petty, M., …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
• 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
• Jones, A., Christensen, C., Perepichka, D., Batsanov, A., Beeby, A., Low, P., …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
• Bryce, M., Batsanov, A., Finn, T., Hansen, T., Moore, A., Howard, J., …Asher, S. (2001). 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, 933-940
• Godbert, N., Bryce, M., Dahaoui, S., Batsanov, A., Howard, J., & Hazendonk, P. (2001). Molecular saddles, 3. Hydroxymethyl-functionalised 9,10- bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene pi-electron donors as synthetic intermediates for supramolecular structures. European Journal of Organic Chemistry, 749-757
• 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
• Moore, A., Batsanov, A., Bryce, M., Howard, J., Khodorkovsky, V., Shapiro, L., & Shames, A. (2001). Trimethyltetrathiafulvalene bearing an N-methylpyridinium substituent: Synthesis, crystal structures, and charge transfer properties. European Journal of Organic Chemistry, 73-78
• Coapes, R., Souza, F., Fox, M., Batsanov, A., Goeta, A., Yufit, D., …Marder, T. (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, 1201-1209
• Batsanov, A., Bryce, M., Chesney, A., Howard, J., John, D., Moore, A., …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