Dibenzoborole-Containing π-Electron Systems: Remarkable Fluorescence Change Based on the “On/Off” Control of the pπ−π* Conjugation
Author:
Affiliation:
1. Institute for Chemical Research, Kyoto University, and PRESTO, Japan Science and Technology Corporation, Uji, Kyoto 611-0011, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja026689k
Reference25 articles.
1. Three coordinate phosphorus and boron as π-donor and π-acceptor moieties respectively, in conjugated organic molecules for nonlinear optics: crystal and molecular structures of E-Ph–CHCH–B(mes)2, E-4-MeO–C6H4–CHCH-B(mes)2, and E-Ph2P–CHCH–B(mes)2[mes = 2,4,6-Me3C6H2]
2. Synthesis and second-order nonlinear optical properties of three coordinate organoboranes with diphenylphosphino and ferrocenyl groups as electron donors: crystal and molecular structures of (E)-DCHCHB(mes)2 and DCCB(mes)2 [D P(C6H52, (η-C5H5)Fe(η-C5H4); mes = 2,4,6-(CH3)3C6H2]
3. Third-order Nonlinear Optical Properties of Organoboron Compounds: Molecular Structures and Second Hyperpolarizabilities
4. Linear and Nonlinear Optical Properties of Three-Coordinate Organoboron Compounds
5. Extension of π-Conjugation Length via the Vacant p-Orbital of the Boron Atom. Synthesis of Novel Electron Deficient π-Conjugated Systems by Hydroboration Polymerization and Their Blue Light Emission
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