The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Solid‐State Emission of the Anthracene‐o‐Carborane Dyad from the Twisted‐Intramolecular Charge Transfer in the Crystalline State
Abstract
The emission process of the o‐carborane dyad with anthracene originating from the twisted intramolecular charge transfer (TICT) state in the crystalline state is described. The anthracene‐o‐carborane dyad was synthesized and its optical properties were investigated. Initially, the dyad had aggregation‐ and crystallization‐induced emission enhancement (AIEE and CIEE) properties via the intramolecular charge transfer (ICT) state. Interestingly, the dyad presented the dual‐emissions assigned to both locally excited (LE) and ICT states in solution. From the mechanistic studies and computer calculations, it was indicated that the emission band from the ICT should be attributable to the TICT emission. Surprisingly, even in the crystalline state, the TICT emission was observed. It was proposed from that the compact sphere shape of o‐carborane would allow for rotation even in the condensed state.
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Cites
Aggregation-Induced Emission: Together We Shine, United We Soar!
Mei, J., Leung, N. L. C., Kwok, R. T. K., Lam, J. W. Y., & Tang, B. Z. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00263 · Cited by 8,270
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New sensing mechanisms for design of fluorescent chemosensors emerging in recent years
Wu, J., Liu, W., Ge, J., Zhang, H., & Wang, P. (2011) · Chemical Society Reviews · doi:10.1039/c0cs00224k · Cited by 1,858
Twisted Intramolecular Charge Transfer and Aggregation-Induced Emission of BODIPY Derivatives
Hu, R., Lager, E., Aguilar-Aguilar, A., Liu, J., Lam, J. W. Y., Sung, H. H. Y., Williams, I. D., Zhong, Y., Wong, K. S., Peña-Cabrera, E., et al. (2009) · The Journal of Physical Chemistry C · doi:10.1021/jp902962h · Cited by 1,023
Dicarba-closo-dodecaboranes C2B10H12 and their derivatives
Bregadze, V. I. (1992) · Chemical Reviews · doi:10.1021/cr00010a002 · Cited by 800
Carbaboranes as Pharmacophores: Properties, Synthesis, and Application Strategies
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Furue, R., Nishimoto, T., Park, I. S., Lee, J., & Yasuda, T. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201603232 · Cited by 464
New Polymeric Materials Based on Element-Blocks
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Self-citationBoron clusters in luminescent materials
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Cited by
Visible‐Light‐Excited Ultralong Organic Phosphorescence by Manipulating Intermolecular Interactions
Cai, S., Shi, H., Li, J., Gu, L., Ni, Y., Cheng, Z., Wang, S., Xiong, W., Li, L., An, Z., et al. (2017) · Advanced Materials · doi:10.1002/adma.201701244 · Cited by 437
Wang, J., Gu, X., Zhang, P., Huang, X., Zheng, X., Chen, M., Feng, H., Kwok, R. T. K., Lam, J. W. Y., & Tang, B. Z. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b10150 · Cited by 284
Metadata
- Authors
- Naito, H., Nishino, K., Morisaki, Y., Tanaka, K., & Chujo, Y.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2016-12
- Volume
- 56
- Issue
- 1
- Pages
- 254-259
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2558822712
- Cited by
- 386
- References
- 42
- FWCI
- 20.08
- Type
- journal article
- Language
- en
- Open access
- closed
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- Naito, H., Nishino, K., Morisaki, Y., Tanaka, K., & Chujo, Y. (2017). Solid‐State Emission of the Anthracene‐o‐Carborane Dyad from the Twisted‐Intramolecular Charge Transfer in the Crystalline State. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201609656
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