Staff profile
Professor Martin Bryce
Professor
Affiliation | Telephone |
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Professor in the Department of Chemistry | +44 (0) 191 33 42018 |
Biography
Martin Bryce was born near Birmingham, UK and graduated from Wolverhampton Polytechnic (B.Sc. 1st class). He obtained a D.Phil. from York University in 1978 for work on synthetic methodology for sulfur and selenium heterocycles under the guidance of John Vernon and Peter Hanson. Following postdoctoral positions at the University of British Columbia,Vancouver (in Larry Weiler’s group) and the University of Bristol (in Roger Alder’s group) he joined Durham University. He was promoted to Professor of Chemistry at Durham in 1995. He is the recipient of a Ciba-Geigy Award for academic collaboration in Europe (1990), the Royal Society of Chemistry Bader Award (1992), the Royal Society of Chemistry Interdisciplinary Award (1992), the Nuffield Foundation Science Research Fellowship (1993), the University of Durham Sir Derman Christopherson Fellowship (1995) and the Royal Society of Chemistry Heterocyclic Chemistry Award (2002). Martin has held Visiting Scientist positions at the University of California at Santa Barbara, and the University of Copenhagen. He was a Troisième Cycle Lecturer in Switzerland in 2008 and a Tarrant Visiting Professor at the University of Florida, Gainesville in 2013. He was the co-director of the Durham University Centre for Molecular and Nanoscale Electronics (1990-2018). He was the Scientific Editor of the Journal of Materials Chemistry (1995-2000). Martin coordinated the EC FP7 Marie Curie ITNs “Fundamentals of Molecular Electronic Assemblies” (FUNMOLS) (2008-2012) and “Molecular-Scale Electronics” (MOLESCO) (2014-2017) comprising 10 European partner laboratories.
Research Interests
Our work is rooted in new synthetic chemistry. Current projects include:
Materials for Optoelectronic Applications
The ability to control the optoelectronic properties of conjugated molecular and polymeric systems is a fascinating aspect in the design of new materials for organic light-emitting devices (OLEDs) and displays that offer bright colours and high stabilty. Deep-blue fluorescent and phosphorescent emitters and white-light devices (WOLEDs) are of particular current interest. Representative work concerns small molecules and polymers that possess thermaly activated delayed fluorescence (TADF), such as structures 1-3,1-3 and room temperature organic phosphorescence.4 We have reported new emitters and OLEDs based on phosphorescent cyclometallated Ir complexes.5,6 This is very interdisciplinary work, some projects involving close collaboration with colleagues in the Department of Physics in Durham (Professors Andy Monkman and Fernando Dias), and with industrial sponsors who are commercialising some of these materials for display technologies and lighting applications.
We are also studying luminescent organic and organometallic materials for sensing explosives, monitoring volatile organic compounds and for anti-conterfeiting and data encryption,7 for example iridium complex 48 and polyurethane derivative 5.9 These projects are in collaboration with Northeast Normal University, Changchun (Professor Dongxia Zhu).
Molecular and Nanoscale Electronics
Molecular electronics is attracting great attention due to potential applications in future computing technology, energy harvesting and storage, and related fields. A wide range of “molecular wires“, including structures 6-8, have been synthesised recently in our group.10-12 Their fundamenal optoelectronic, electrical and thermoelectrical properties are being developed in partnership with academic and industrial laboratories in Europe (notably IMDEA-Madrid, IBM-Zurich and Lancaster University) and China (Xiamen University) using specialised experimental techniques and theoretical expertise. Assembly and characterisation of molecules in metal | molecule | metal junctions is a prominant aspect of this work.
Related projects probe photoinduced charge transport through pi-conjugated wire-like molecules such as 913 and 1014 end-capped with electron donor and acceptor units.The techniques include cyclic voltammetry, spectroelectrochemistry, steady-state and time-resolved photolysis, X-ray crystallography, ESR spectroscopy and theoretical calculations.
Molecules for Photodynamic and Photothermal Therapy
In collaboration with laboratories in Changchun we have designed, synthesised and evaluated new molecules for photodynamic and photothermal therapy. The work is focused on red and near-infrared emitting species with high biocompatibility. In vitro and in vivo experiments have established that molecules 1115 and 1216 encapsulated in nanoparticles exhibit potent cytotoxicity towards cancer cells and effectively inhibit tumour growth with high therapeutic efficacy.
References
- Stachelek, P. et al, ACS Appl. Mater. Interfaces 2019, 30, 27125-27133. DOI: 10.1021/acsami.9b06364.
- Li, C. et al, Adv. Opt. Mater. 2017, 5, 1700435. DOI: 10.1002/adom.201700435.
- Hempe, M. et al, J. Org. Chem. 2021, 86, 429-445. DOI: 10.1021/acs.joc.0c02174.
- Chen, C. et al, Angew. Chem., Int. Ed. 2018, 57, 16407-16411. DOI: 10.1002/anie.201809945.
- Du, M. et al, Adv. Mater., 2016, 28, 5963-5968. DOI: 10.1002/adma.201600451.
- Congrave, D. G. et al, Inorg. Chem. 2018, 57, 12836-12849. DOI: 10.1021/acs.inorgchem.8b02034.
- Jiang, Y. et al, Chem. Commun. 2017, 53, 3022-3025. DOI: 10.1039/c7cc00769h.
- Che, W. et al, Chem. Commun. 2018, 54, 1730-1733. DOI: 10.1039/c7cc08832a.
- Jiang, N. et al, Chem. Mater. 2020, 32, 5776-5784. DOI: 10.1021/acs.chemmater.0c01620.
- O’Driscoll, L. J. et al, Angew. Chem. Int. Ed. 2020, 59, 882-889. DOI 10.1002/anie.201911652.
- Liu, J. et al, Angew. Chem. Int. Ed. 2017, 56, 13061-13065. DOI: 10.1002/anie.201707710.
- Chen, H. et al, Nanoscale 2020, 12, 15150-15156. DOI: 10.1039/d0nr03303k.
- Zieleniewska, A. et al, J. Am. Chem. Soc. 2020, 142, 18769-18781. DOI: 10.1021/jacs.0c04003.
- Yzambart, G. et al, J. Phys. Chem. C 2017, 121, 13557-13569. DOI: 10.1021/acs.jpcc.7b03889.
- Zhang, L. et al, Chem. Sci. 2020, 11, 2369-2374. DOI: 10.1039/c9sc06310b.
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Zhang, L. et al, Chem. Sci. 2021, 12, 5918–5925. DOI: 10.1039/d1sc00126d.
Research interests
- Molecular Electronics
- Functional Materials
- Organic Synthesis
Publications
Conference Paper
Journal Article
- Wang, C., Batsanov, A., Bryce, M., & Sage, I. (online). An improved synthesis and structural characterisation of 2-(4-acetylthiophenylethynyl)-4-nitro-5-phenylethynylaniline: The molecule showing high negative differential resistance (NDR). Synthesis: Journal of Synthetic Organic Chemistry, 2089-2095
- Jiang, N., Meng, Y.-J., Zhu, C.-Y., Li, K.-X., Li, X., Xu, Y.-H., Xu, J.-W., & Bryce, M. R. (online). Nonconjugated Polyurethane Derivatives with Aggregation-Induced Luminochromism for Multicolor and White Photoluminescent Films. ACS Macro Letters, 1226-1232. https://doi.org/10.1021/acsmacrolett.4c00534
- Liu, S., Wang, Z., Wu, Z., Chen, H., Zhu, D., Li, G., Yan, M., Bryce, M. R., & Chang, Y. (online). Long-wavelength triggered iridium( iii ) complex nanoparticles for photodynamic therapy against hypoxic cancer. Chemical Communications, https://doi.org/10.1039/d4cc03501a
- Tavasli, M., Bettington, S., Bryce, M., Batsanov, A., & Monkman, A. (online). Practical syntheses of N-hexylcarbazol-2-yl- and -3-yl-boronic acids, their cross-coupled products and a derived tris-cyclometalated (pyridin-2-yl)carbazole iridium(III) complex. Synthesis: Journal of Synthetic Organic Chemistry, 1619-1624
- Moore, A., Batsanov, A., Bryce, M., Howard, J., Khodorkovsky, V., Shapiro, L., & Shames, A. (online). Trimethyltetrathiafulvalene bearing an N-methylpyridinium substituent: Synthesis, crystal structures, and charge transfer properties. European Journal of Organic Chemistry, 73-78
- Bryce, M., Batsanov, A., Finn, T., Hansen, T., Moore, A., Howard, J., Kamenjicki, M., Lednev, I., & Asher, S. (online). 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
- Jiang, N., Pu, X., Li, K.-X., Zhu, C.-Y., Sun, Y.-W., Xu, Y.-H., Zhu, Y.-L., & Bryce, M. R. (online). One-pot preparation of nonconventional luminescent polymer gels driven by polymerization †. Polymer Chemistry, https://doi.org/10.1039/d4py00832d
- 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. (online). 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
- Chubb, R., Bryce, M., & Tarbit, B. (online). Synthesis of 2-heteroaryl-3-hydroxypyridines by ring expansion reactions of 2-acylfurans with ammonia. Journal of the Chemical Society. Perkin transactions 1, 1853-1854
- Liu, S., Chen, H., Wu, Q., Sun, Y., Pei, Y., Wang, Z., Zhu, D., Li, G., Bryce, M. R., & Chang, Y. (2024). Self-Chemiluminescence-Triggered Ir(III) Complex Photosensitizer for Photodynamic Therapy against Hypoxic Tumor. Inorganic Chemistry, 63(35), 16404-16417. https://doi.org/10.1021/acs.inorgchem.4c02399
- 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
- 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
- Jiang, N., Zhu, C.-Y., Li, K.-X., Xu, Y.-H., & Bryce, M. R. (2024). Recent Progress in Nonconventional Luminescent Macromolecules and their Applications. Macromolecules, 57(12), 5561-5577. https://doi.org/10.1021/acs.macromol.4c00186
- Liu, S., Pei, Y., Sun, Y., Wang, Z., Chen, H., Zhu, D., Bryce, M. R., Tang, B. Z., & Chang, Y. (2024). “Three birds with one stone” nanoplatform: Efficient near‐infrared‐triggered type‑I AIE photosensitizer for mitochondria‐targeted photodynamic therapy against hypoxic tumors. Aggregate, Article e547. https://doi.org/10.1002/agt2.547
- 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
- Jiang, N., Li, K.-X., Wang, J.-J., Li, C.-S., Xu, X.-Y., Xu, Y.-H., & Bryce, M. R. (2024). Cluster-induced aggregation in polyurethane derivatives with multicolour emission and ultra-long organic room temperature phosphorescence. Journal of Materials Chemistry C Materials for optical and electronic devices, 12(3), 1040-1046. https://doi.org/10.1039/d3tc04141g
- Jiang, N., Li, K.-X., Wang, J.-J., Zhu, Y.-L., Zhu, C.-Y., Xu, Y.-H., & Bryce, M. R. (2024). Amphiphilic Polyurethane with Cluster-Induced Emission for Multichannel Bioimaging in Living Cell Systems. ACS Macro Letters, 13(1), 52-57. https://doi.org/10.1021/acsmacrolett.3c00657
- 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
- Jiang, N., Li, K.-X., Xie, W., Zhang, S.-R., Li, X., Hu, Y., Xu, Y.-H., Liu, X.-M., & Bryce, M. R. (2023). Multicolor Luminescence of a Polyurethane Derivative Driven by Heat/Light-Induced Aggregation. Macromolecules, 56(19), 7721-7728. https://doi.org/10.1021/acs.macromol.3c01345
- Zhang, L., Wang, Y.-C., Liao, Y., Zhang, Q., Liu, X., Zhu, D., Feng, H., Bryce, M. R., & Ren, L. (2023). Near-Infrared Afterglow ONOO–-Triggered Nanoparticles for Real-Time Monitoring and Treatment of Early Ischemic Stroke. ACS Applied Materials and Interfaces, 15(39), https://doi.org/10.1021/acsami.3c08033
- Wang, H., Li, Q., Alam, P., Bai, H., Bhalla, V., Bryce, M. R., Cao, M., Chen, C., Chen, S., Chen, X., Chen, Y., Chen, Z., Dang, D., Ding, D., Ding, S., Duo, Y., Gao, M., He, W., He, X., Hong, X., …Tang, B. Z. (2023). Aggregation-Induced Emission (AIE), Life and Health. ACS Nano, 17(15), 14347–14405. https://doi.org/10.1021/acsnano.3c03925
- Salthouse, R. J., Hurtado-Gallego, J., Grace, I. M., Davidson, R., Alshammari, O., Agraït, N., Lambert, C. J., & Bryce, M. R. (2023). Electronic Conductance and Thermopower of Cross-Conjugated and Skipped-Conjugated Molecules in Single-Molecule Junctions. Journal of Physical Chemistry C, 127(28), 13751-13758. https://doi.org/10.1021/acs.jpcc.3c00742
- Wright, I. A., Etherington, M. K., Batsanov, A. S., Monkman, A. P., & Bryce, M. R. (2023). Oxidation State Tuning of Room Temperature Phosphorescence and Delayed Fluorescence in Phenothiazine and Phenothiazine‐5,5‐dioxide Dimers. Chemistry - A European Journal, 29(30), Article e202300428. https://doi.org/10.1002/chem.202300428
- O’Driscoll, L. J., Jay, M., Robinson, B. J., Sadeghi, H., Wang, X., Penhale-Jones, B., Bryce, M. R., & Lambert, C. J. (2023). Planar aromatic anchors control the electrical conductance of gold|molecule|graphene junctions. Nanoscale Advances, 5(8), 2299-2306. https://doi.org/10.1039/d2na00873d
- L. dos Santos, P., de Sa Pereira, D., Eng, J., Ward, J. S., Bryce, M. R., Penfold, T. J., & Monkman, A. P. (2023). Fine‐Tuning the Photophysics of Donor‐Acceptor (D‐A 3 ) Thermally Activated Delayed Fluorescence Emitters Using Isomerisation. ChemPhotoChem, 7(2), Article e202200248. https://doi.org/10.1002/cptc.202200248
- Wang, Z., Li, L., Wang, W., Wang, R., Li, G., Bian, H., Zhu, D., & Bryce, M. R. (2023). Self-assembled nanoparticles based on cationic mono-/AIE tetra-nuclear Ir(III) complexes: long wavelength absorption/near-infrared emission photosensitizers for photodynamic therapy. Dalton Transactions, 52(6), 1595-1601. https://doi.org/10.1039/d2dt03809a
- Oner, S., & Bryce, M. R. (2023). A review of fused-ring carbazole derivatives as emitter and/or host materials in organic light emitting diode (OLED) applications. Materials Chemistry Frontiers, 7(19), 4304–4338. https://doi.org/10.1039/d3qm00399j
- Gemma, A., Tabatabaei, F., Drechsler, U., Zulji, A., Dekkiche, H., Mosso, N., Niehaus, T., Bryce, M. R., Merabia, S., & Gotsmann, B. (2023). Full thermoelectric characterization of a single molecule. Nature Communications, 14(1), Article 3868. https://doi.org/10.1038/s41467-023-39368-7
- 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
- Wang, X., Ismael, A., Ning, S., Althobaiti, H., Al-Jobory, A., Girovsky, J., Astier, H. P., O'Driscoll, L. J., Bryce, M. R., Lambert, C. J., & Ford, C. J. (2022). Electrostatic Fermi level tuning in large-scale self-assembled monolayers of oligo(phenylene–ethynylene) derivatives. Nanoscale Horizons, 7(10), 1201-1209. https://doi.org/10.1039/d2nh00241h
- 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
- Li, C., Harrison, A. K., Liu, Y., Zhao, Z., Zeng, C., Dias, F. B., Ren, Z., Yan, S., & Bryce, M. R. (2022). Asymmetrical‐Dendronized TADF Emitters for Efficient Non‐doped Solution‐Processed OLEDs by Eliminating Degenerate Excited States and Creating Solely Thermal Equilibrium Routes. Angewandte Chemie International Edition, 61(19), Article e202115140. https://doi.org/10.1002/anie.202115140
- Li, C., Harrison, A. K., Liu, Y., Zhao, Z., Dias, F. B., Zeng, C., Yan, S., Bryce, M. R., & Ren, Z. (2022). TADF dendronized polymer with vibrationally enhanced direct spin-flip between charge-transfer states for efficient non-doped solution-processed OLEDs. Chemical Engineering Journal, 435, Article 134924. https://doi.org/10.1016/j.cej.2022.134924
- Liu, S., Han, J., Chang, Y., Wang, W., Wang, R., Wang, Z., Li, G., Zhu, D., & Bryce, M. R. (2022). AIE-active iridium(iii) complex integrated with upconversion nanoparticles for NIR-irradiated photodynamic therapy. Chemical Communications, 58(72), 10056 - 10059. https://doi.org/10.1039/d2cc03622c
- Liu, S., Han, J., Wang, W., Chang, Y., Wang, R., Wang, Z., Li, G., Zhu, D., & Bryce, M. R. (2022). AIE-active Ir(iii) complexes functionalised with a cationic Schiff base ligand: synthesis, photophysical properties and applications in photodynamic therapy. Dalton Transactions, 51(42), 16119-16125. https://doi.org/10.1039/d2dt02960j
- Wang, X., Sangtarash, S., Lamantia, A., Dekkiche, H., Forcieri, L., Kolosov, O. V., Jarvis, S. P., Bryce, M. R., Lambert, C. J., Sadeghi, H., & Robinson, B. J. (2022). Thermoelectric properties of organic thin films enhanced by π–π stacking. JPhys Energy, 4(2), https://doi.org/10.1088/2515-7655/ac55a3
- Hurtado-Gallego, J., Sangtarash, S., Davidson, R., Rincón-García, L., Daaoub, A., Rubio-Bollinger, G., Lambert, C. J., Oganesyan, V. S., Bryce, M. R., Agraït, N., & Sadeghi, H. (2022). Thermoelectric Enhancement in Single Organic Radical Molecules. Nano Letters, 22(3), https://doi.org/10.1021/acs.nanolett.1c03698
- Bryce, M. R. (2021). A review of functional linear carbon chains (oligoynes, polyynes, cumulenes) and their applications as molecular wires in molecular electronics and optoelectronics. Journal of Materials Chemistry C Materials for optical and electronic devices, 9(33), 10524-10546. https://doi.org/10.1039/d1tc01406d
- Mayorga-Burrezo, P., Bejarano, F., Calbo, J., Zhao, X., De Sousa, J. A., Lloveras, V., Bryce, M. R., Ortí, E., Veciana, J., Rovira, C., & Crivillers, N. (2021). Allocation of Ambipolar Charges on an Organic Diradical with a Vinylene–Phenylenediyne Bridge. Journal of Physical Chemistry Letters, 12(26), 6159-6164. https://doi.org/10.1021/acs.jpclett.1c01565
- 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
- Zhang, L., Geng, Y., Li, L., Tong, X., Liu, S., Liu, X., Su, Z., Xie, Z., Zhu, D., & Bryce, M. R. (2021). Rational design of iridium–porphyrin conjugates for novel synergistic photodynamic and photothermal therapy anticancer agents. Chemical Science, 12(16), 5918-5925. https://doi.org/10.1039/d1sc00126d
- 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
- O'Driscoll, L. J., & Bryce, M. R. (2021). Extended curly arrow rules to rationalise and predict structural effects on quantum interference in molecular junctions. Nanoscale, 13(2), 1103-1123. https://doi.org/10.1039/d0nr07819k
- O'Driscoll, L. J., & Bryce, M. R. (2021). A review of oligo(arylene ethynylene) derivatives in molecular junctions. Nanoscale, 13(24), 10668-10711. https://doi.org/10.1039/d1nr02023d
- 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
- Jiang, N., Wang, R., You, X., Geng, Y., Zhu, D., Zhang, N., & Bryce, M. R. (2021). Supramolecular oligourethane gels as light-harvesting antennae: achieving multicolour luminescence and white-light emission through FRET. Journal of Materials Chemistry C Materials for optical and electronic devices, 9(38), https://doi.org/10.1039/d1tc03105h
- Kukhta, N. A., & Bryce, M. R. (2021). Dual emission in purely organic materials for optoelectronic applications. Materials Horizons, 8(1), 33-55. https://doi.org/10.1039/d0mh01316a
- O’Driscoll, L. J., Sangtarash, S., Xu, W., Daaoub, A., Hong, W., Sadeghi, H., & Bryce, M. R. (2021). Heteroatom Effects on Quantum Interference in Molecular Junctions: Modulating Antiresonances by Molecular Design. Journal of Physical Chemistry C, 125(31), 17385-17391. https://doi.org/10.1021/acs.jpcc.1c04242
- 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
- Feng, Y., Jiang, N., Zhu, D., Su, Z., & Bryce, M. R. (2020). Supramolecular oligourethane gel as a highly selective fluorescent “on–off–on” sensor for ions. Journal of Materials Chemistry C Materials for optical and electronic devices, 8(33), 11540-11545. https://doi.org/10.1039/d0tc02381g
- 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
- Jiang, N., Ruan, S.-H., Liu, X.-M., Zhu, D., Li, B., & Bryce, M. R. (2020). Supramolecular Oligourethane Gel with Multicolor Luminescence Controlled by Mechanically Sensitive Hydrogen-Bonding. Chemistry of Materials, 32(13), 5776-5784. https://doi.org/10.1021/acs.chemmater.0c01620
- Grace, I. M., Olsen, G., Hurtado-Gallego, J., Rincón-García, L., Rubio-Bollinger, G., Bryce, M. R., Agraït, N., & Lambert, C. J. (2020). Connectivity dependent thermopower of bridged biphenyl molecules in single-molecule junctions. Nanoscale, 12(27), 14682-14688. https://doi.org/10.1039/d0nr04001k
- Chen, H., Sangtarash, S., Li, G., Gantenbein, M., Cao, W., Alqorashi, A., Liu, J., Zhang, C., Zhang, Y., Chen, L., Chen, Y., Olsen, G., Sadeghi, H., Bryce, M. R., Lambert, C. J., & Hong, W. (2020). Exploring the thermoelectric properties of oligo(phenylene-ethynylene) derivatives. Nanoscale, 12(28), 15150-15156. https://doi.org/10.1039/d0nr03303k
- Jiang, N., Zhu, D., Su, Z., & Bryce, M. R. (2020). Blue-emitting thermoreversible oligourethane gelators with aggregation-induced emission properties. Journal of Materials Chemistry C Materials for optical and electronic devices, 8(15), 5137-5142. https://doi.org/10.1039/d0tc00757a
- Zhang, L., Che, W., Yang, Z., Liu, X., Liu, S., Xie, Z., Zhu, D., Su, Z., Tang, B. Z., & Bryce, M. R. (2020). Bright red aggregation-induced emission nanoparticles for multifunctional applications in cancer therapy. Chemical Science, 11(9), 2369-2374. https://doi.org/10.1039/c9sc06310b
- 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
- Li, G., Zhu, D., Wang, X., Su, Z., & Bryce, M. R. (2020). Dinuclear metal complexes: multifunctional properties and applications. Chemical Society Reviews, 49(3), 765-838. https://doi.org/10.1039/c8cs00660a
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- Bryce, M. (2002). New molecular electron-transport materials for light-emitting devices
- Kuz'mina, L., Perepichka, I., Perepichka, D., Howard, J., & Bryce, M. (2002). Supramolecular architecture of two charge-transfer complexes based on 2,7-(X,X)-4,5-dinitro-9-dicyanomethylenefluorenes (X=NO2 or CN) and tetrathiafulvalene. Crystallography Reports, 47(2), 251-261
- Kataky, R., Bryce, M., Goldenberg, L., Hayes, S., & Nowak, A. (2002). A biosensor for monitoring formaldehyde using a new lipophilic tetrathiafulvalene-tetracyanoquinodimethane salt and a polyurethane membrane. Talanta, 56(3), 451-458
- Farren, C., FitzGerald, S., Beeby, A., & Bryce, M. (2002). The first genuine observation of fluorescent mononuclear phthalocyanine aggregates. Chemical Communications, 2002(6), 572-573. https://doi.org/10.1039/B110876J
- Bryce, M., Cooke, G., Devonport, W., Duclairoir, F., & Rotello, V. (2002). A stopperless tetrathiafulvalene based 2 pseudorotaxane molecular shuttle (vol 42, pg 4223, 2001). Tetrahedron Letters, 43(3), 537-537
- Bryce, M., Batsanov, A., Godbert, N., & Christensen, C. (2002). New pi-electron rich donors and cavities and their supramolecular assemblies: Synthesis, electrochemistry and crystal structures. Molecular Crystals and Liquid Crystals, 379, 1-8
- Farren, C., FitzGerald, S., Bryce, M., Beeby, A., & Batsanov, A. (2002). Synthesis, structure and optical characterisation of silicon phthalocyanine bis-esters. Journal of the Chemical Society-Perkin Transactions 2, 2002(1), 59-66. https://doi.org/10.1039/B108778A
- Wang, C., Jung, G., Batsanov, A., Bryce, M., & Petty, M. (2002). New electron-transporting materials for light emitting diodes: 1,3,4-oxadiazole-pyridine and 1,3,4-oxadiazole-pyrimidine hybrids. Journal of materials chemistry, 12(2), 173-180
- Sutcliffe, O., Chesney, A., & Bryce, M. (2001). Voltammetric metal cation sensors based on ferrocene derivatives with oxazoline and imine substituents. Journal of Organometallic Chemistry, 637, 134-138
- 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
- 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
- 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., Cooke, G., Devonport, W., Duclairoir, F., & Rotello, V. (2001). A stopperless tetrathiafulvalene based 2 pseudorotaxane molecular shuttle. Tetrahedron Letters, 42(25), 4223-4226
- 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, 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
- Perepichka, D., Bryce, M., McInnes, E., & Zhao, J. (2001). The first tetrathiafulvalene-sigma-polynitrofluorene diads: Low HOMO-LUMO gap, amphoteric redox behavior, and charge transfer properties. Organic Letters, 3(10), 1431-1434
- 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
- Bryce, M., Christensen, C., & Godbert, N. (2001). Synthesis and redox chemistry of tetrathiafulvalene and related bis(1,3-dithiole) dendrimers
- Perepichka, D., Perepichka, I., Bryce, M., Moore, A., & Sokolov, N. (2001). Push-pull dithiole - fluorene accepters as electron transport materials for holography. Synthetic Metals, 121(1-3), 1487-1488
- Le Gall, T., Bryce, M., Moore, A., Pearson, C., & Petty, M. (2001). Spin-coated films of tetrakis-arborol-tetrathiafulvalenes. Synthetic Metals, 121(1-3), 1409-1410
- 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
- Palsson, L., Wang, C., Monkman, A., Bryce, M., Rumbles, G., & Samuel, I. (2001). Fluorene co-polymer luminescence: implications for molecular interactions. Synthetic Metals, 119(1-3), 627-628
- Bogza, S., Kobrakov, K., Malienko, A., Sujkov, S., Perepichka, I., Bryce, M., Bogdan, N., & Dulenko, V. (2001). Convenient one pot synthesis of 5-unsubstituted pyrazolo 3,4- c isoquinolines. Journal of Heterocyclic Chemistry, 38(2), 523-525
- 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
- Bryce, M., Cooke, G., Duclairoir, F., & Rotello, V. (2001). An investigation of the complexation behaviour of structurally modified tetrathiafulvalene derivatives with the electron deficient cyclophane cyclobis(paraquat-p-phenylene). Tetrahedron Letters, 42(6), 1143-1145
- Wang, C., Kilitziraki, M., Palsson, L., Bryce, M., Monkman, A., & Samuel, I. (2001). Polymeric alkoxy PBD 2-(4-biphenylyl)-5-phenyl-1,3,4- oxadiazole for light-emitting diodes. Advanced Functional Materials, 11(1), 47-50
- 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
- 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
- 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
- Perepichka, D., Perepichka, I., Bryce, M., Sokolov, N., & Moore, A. (2001). pi-Extended nitrofluorene-1,3-dithiole chromophore: enhancing the photoresponse of holographic materials through the balance of intramolecular charge transfer and electron affinity. Journal of materials chemistry, 11(7), 1772-1774
- Bryce, M. R., Batsanov, A. S., Finn, T., & Hansen, T. K. (2000). Crown-annelated 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene derivatives: a new efficient transducer in the electrochemical and spectroscopic monitoring of metal complexation. Chemical Communications, 2000, 295-296. https://doi.org/10.1039/a908716h
- Bryce, M., Chesney, A., Yoshida, S., & Perepichka, I. (2000). Synthesis and Trapping of Transient 1,2-Diselones to Yield 1,4-Diselenin Derivatives: Calculated Structures of 1,2-Diselones, 1,2-Diselenetes and Their Sulfur Analogues. Chemistry - A European Journal, 6(1), 1-7
- Bryce, M., Moore, A., Batsanov, A., & Green, A. (1998). New 1,3-dithiol-2-ylidene donor-pi-acceptor chromophores with intramolecular charge-transfer properties, and related donor-pi-donor molecules: synthesis, electrochemistry, X-ray crystal structures, non-linear optical properties and theoretical calculation. Journal of materials chemistry, 8(5), 1173-1184
- Bryce, M., Wang, C., Batsanov, A., & Howard, J. (1997). Synthesis of Pyrazinoporphyrazine Derivatives Functionalised with Tetrathiafulvalene (TTF) Units: X-Ray Crystal Structures of Two Related TTF Cyclophanes and Two Bis(1,3-dithiole-2-thione) Intermediates. Chemistry - A European Journal, 3(10), 1679-1690