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- W2783404544 endingPage "264" @default.
- W2783404544 startingPage "237" @default.
- W2783404544 abstract "Tuning the electronic states and properties of conjugated compounds by element substitution can impart organic materials with desired functionality. Replacing silicon with germanium or tin can provide an appreciable improvement in the functionalities of π-electron systems. K. Mizuno demonstrated that attaching germanium and tin substituents to pyrene suppressed the fluorescence properties. Oligomers composed of silylene- and germylene-linked diethynylfluorene units were prepared by W. Y. Wong. This was achieved by the reaction of dilithiated diethynylfluorene with dichlorogermanes, followed by separation of the oligomers from the reaction mixtures. Saito introduced germanium bridges into the triphenylene framework to form germole rings. Alternating donor-acceptor (D-A) polymers with dibenzogermole as the donor and diketopyrrolopyrrole and benzothiadiazole as the acceptor and poly(dibenzogermole-2,7-diyl) were prepared by Suzuki cross-coupling. Diselenophenogermole was prepared and recently incorporated into a D-A polymeric system, to realize photovoltaic properties." @default.
- W2783404544 created "2018-01-26" @default.
- W2783404544 creator A5005919630 @default.
- W2783404544 creator A5034576150 @default.
- W2783404544 date "2017-12-19" @default.
- W2783404544 modified "2023-09-23" @default.
- W2783404544 title "Germanium and Tin in Conjugated Organic Materials" @default.
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