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Four-Coordinate Organoboron Compounds with a π-Conjugated Chelate Ligand for Optoelectronic Applications
Abstract
Four-coordinate organoboron compounds with a π-conjugated chelate backbone have emerged recently as highly attractive materials for a number of applications including use as emitters and electron-transport materials for organic light-emitting diodes (OLEDs) or organic field transistors, photoresponsive materials, and sensory and imaging materials. Many applications of this class of boron compounds stem from the electronic properties of the π-conjugated chelate backbone. Charge-transfer transitions from an aromatic substituent attached to the boron center of the π-conjugated chelate backbone and steric congestion have also been found to play important roles in the luminescent and photochromic properties of the four-coordinate boron compounds. This article provides an update-to-date account on the application aspects of this important class of compounds in materials science with the emphasis on OLED applications and photochromic switching.
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Cites
Organic electroluminescent diodes
Tang, C. W., & VanSlyke, S. A. (1987) · Applied Physics Letters · doi:10.1063/1.98799 · Cited by 14,363
BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties
Loudet, A., & Burgess, K. (2007) · Chemical Reviews · doi:10.1021/cr078381n · Cited by 5,238
Diarylethenes for Memories and Switches
Irie, M. (2000) · Chemical Reviews · doi:10.1021/cr980069d · Cited by 4,157
Lamansky, S., Djurovich, P., Murphy, D., Abdel-Razzaq, F., Lee, H.-E., Adachi, C., Burrows, P. E., Forrest, S. R., & Thompson, M. E. (2001) · Journal of the American Chemical Society · doi:10.1021/ja003693s · Cited by 2,812
Charge Carrier Transporting Molecular Materials and Their Applications in Devices
Shirota, Y., & Kageyama, H. (2007) · Chemical Reviews · doi:10.1021/cr050143+ · Cited by 1,756
Spiropyrans and Spirooxazines for Memories and Switches
Berkovic, G., Krongauz, V., & Weiss, V. (2000) · Chemical Reviews · doi:10.1021/cr9800715 · Cited by 1,588
Recent Progresses on Materials for Electrophosphorescent Organic Light‐Emitting Devices
Xiao, L., Chen, Z., Qu, B., Luo, J., Kong, S., Gong, Q., & Kido, J. (2011) · Advanced Materials · doi:10.1002/adma.201003128 · Cited by 1,383
A dual-emissive-materials design concept enables tumour hypoxia imaging
Zhang, G., Palmer, G. M., Dewhirst, M. W., & Fraser, C. L. (2009) · Nature Materials · doi:10.1038/nmat2509 · Cited by 1,150
Fluoride Ion Complexation and Sensing Using Organoboron Compounds
Wade, C. R., Broomsgrove, A. E. J., Aldridge, S., & Gabbaï, F. P. (2010) · Chemical Reviews · doi:10.1021/cr900401a · Cited by 1,089
(2001) · Wiley eBooks · doi:10.1002/3527600329 · Cited by 957
Ultrafast Dynamics of Photochromic Systems
Tamai, N., & Miyasaka, H. (2000) · Chemical Reviews · doi:10.1021/cr9800816 · Cited by 840
Polymorphism and Reversible Mechanochromic Luminescence for Solid-State Difluoroboron Avobenzone
Zhang, G., Lu, J., Sabat, M., & Fraser, C. L. (2010) · Journal of the American Chemical Society · doi:10.1021/ja9097719 · Cited by 840
Applications of Three-Coordinate Organoboron Compounds and Polymers in Optoelectronics
Entwistle, C. D., & Marder, T. B. (2004) · Chemistry of Materials · doi:10.1021/cm0495717 · Cited by 777
Entwistle, C. D., & Marder, T. B. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020816)41:16<2927::aid-anie2927>3.0.co;2-l · Cited by 770
Metal chelates as emitting materials for organic electroluminescence
Chen, C. (1998) · Coordination Chemistry Reviews · doi:10.1016/s0010-8545(98)00022-8 · Cited by 714
You, Y., & Park, S. Y. (2009) · Dalton Trans. · doi:10.1039/b812281d · Cited by 655
Fluoride Ion Recognition by Chelating and Cationic Boranes
Hudnall, T. W., Chiu, C.-W., & Gabbaï, F. P. (2009) · Accounts of Chemical Research · doi:10.1021/ar8001816 · Cited by 519
Organic Photochromic and Thermochromic Compounds
(2002) · Topics in Applied Chemistry · doi:10.1007/b115590 · Cited by 386
Wakamiya, A., Taniguchi, T., & Yamaguchi, S. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200504391 · Cited by 331
Gomis, J., & Passerini, F. (2006) · Journal of High Energy Physics · doi:10.1088/1126-6708/2006/08/074 · Cited by 290
Chen, J., Xie, Z., Lam, J. W. Y., Law, C. C. W., & Tang, B. Z. (2003) · Macromolecules · doi:10.1021/ma0213504 · Cited by 255
Holographic Wilson LoopsPreprint
Jaume Gomis, A., & Passerini, F. (2006) · Cited by 241
Liu, S.-F., Wu, Q., Schmider, H. L., Aziz, H., Hu, N.-X., Popović, Z., & Wang, S. (2000) · Journal of the American Chemical Society · doi:10.1021/ja9944249 · Cited by 211
Self-citationCollings, J. C., Poon, S., Le Droumaguet, C., Charlot, M., Katan, C., Pålsson, L., Beeby, A., Mosely, J. A., Kaiser, H. M., Kaufmann, D., et al. (2009) · Chemistry – A European Journal · doi:10.1002/chem.200801719 · Cited by 208
Synthesis of the most intensely fluorescent azobenzene by utilizing the B–N interaction
Yoshino, J., Kano, N., & Kawashima, T. (2007) · Chem. Commun. · doi:10.1039/b615966d · Cited by 194
π-Conjugated Organoboron Polymers via the Vacant p-Orbital of the Boron Atom
Matsumi, N., & Chujo, Y. (2008) · Polymer Journal · doi:10.1295/polymj.pj2007170 · Cited by 187
Liu, Q. D., Mudadu, M. S., Thummel, R., Tao, Y., & Wang, S. (2005) · Advanced Functional Materials · doi:10.1002/adfm.200400081 · Cited by 182
Self-citationHigginson, K. A., Zhang, X., & Papadimitrakopoulos, F. (1998) · Chemistry of Materials · doi:10.1021/cm970599a · Cited by 113
Yoshino, J., Furuta, A., Kambe, T., Itoi, H., Kano, N., Kawashima, T., Ito, Y., & Asashima, M. (2010) · Chemistry - A European Journal · doi:10.1002/chem.201000258 · Cited by 110
Zhang, H., Huo, C., Zhang, J., Zhang, P., Tian, W., & Wang, Y. (2005) · Chemical Communications · doi:10.1039/b513918j · Cited by 100
Zhang, G., Lu, J., & Fraser, C. L. (2010) · Inorganic Chemistry · doi:10.1021/ic902591s · Cited by 95
Luminescent Boron-Contained Ladder-Type π-Conjugated Compounds
Zhang, Z., Bi, H., Zhang, Y., Yao, D., Gao, H., Fan, Y. H., Zhang, H., Wang, Y., Wang, Y., Chen, Z., et al. (2009) · Inorganic Chemistry · doi:10.1021/ic900673s · Cited by 95
Baik, C., Hudson, Z. M., Amarne, H., & Wang, S. (2009) · Journal of the American Chemical Society · doi:10.1021/ja906430s · Cited by 94
Self-citationNagai, A., Kokado, K., Nagata, Y., & Chujo, Y. (2008) · Macromolecules · doi:10.1021/ma801690d · Cited by 84
Zhang, G., Evans, R. E., Campbell, K. A., & Fraser, C. L. (2009) · Macromolecules · doi:10.1021/ma9019043 · Cited by 80
Job, A., Wakamiya, A., Kehr, G., Erker, G., & Yamaguchi, S. (2010) · Organic Letters · doi:10.1021/ol102282x · Cited by 79
Luminescent Organoboron Conjugated Polymers
Nagai, A., & Chujo, Y. (2010) · Chemistry Letters · doi:10.1246/cl.2010.430 · Cited by 77
Kappaun, S., Rentenberger, S., Pogantsch, A., Zojer, E., Mereiter, K., Trimmel, G., Saf, R., Möller, K. C., Stelzer, F., & Slugovc, C. (2006) · Chemistry of Materials · doi:10.1021/cm060720q · Cited by 77
BORAZANs: Tunable Fluorophores Based on 2-(Pyrazolyl)aniline Chelates of Diphenylboron
Liddle, B. J., Silva, R. M., Morin, T. J., Macedo, F. P., Shukla, R., Lindeman, S. V., & Gardinier, J. R. (2007) · The Journal of Organic Chemistry · doi:10.1021/jo0705420 · Cited by 70
Chen, K., Yang, C., Chi, Y., Liu, C., Chang, C., Chen, C.-C., Wu, C., Chung, M., Cheng, Y., Lee, G., et al. (2010) · Chemistry - A European Journal · doi:10.1002/chem.200902902 · Cited by 55
Sugar response of boronic acid-substituted azobenzene dye-modified polymer
Egawa, Y., Gotoh, R., Seki, T., & Anzai, J. (2008) · Materials Science and Engineering C · doi:10.1016/j.msec.2008.05.014 · Cited by 33
Cited by
Long, X., Ding, Z., Dou, C., Zhang, J., Liu, J., & Wang, L. (2016) · Advanced Materials · doi:10.1002/adma.201601205 · Cited by 331
Metadata
- Authors
- Rao, Y.-L., & Wang, S.
- Venue
- Inorganic Chemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 2011-05-23
- Volume
- 50
- Issue
- 24
- Pages
- 12263-12274
- ISSN
- 0020-1669 (ISSN-L)
- 1520-510X
- OpenAlex
- W1993058251
- Cited by
- 277
- References
- 41
- FWCI
- 9.73
- Type
- journal article
- Language
- en
- Open access
- closed
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