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A New Design Strategy for Organic Optoelectronic Materials by Lateral Boryl Substitution
Author(s) -
Elbing Mark,
Bazan Guillermo C.
Publication year - 2008
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200703722
Subject(s) - delocalized electron , substitution (logic) , group (periodic table) , optoelectronics , materials science , nanotechnology , crystallography , chemistry , computer science , organic chemistry , programming language
Lateral thinking : Molecular solids with tunable color and excellent emission efficiencies or increased electron affinities have been obtained by lateral boryl substitution on a π‐delocalized framework (see picture, D=donor group, B=boryl group). This approach gives rise to a new design principle for organic optoelectronic materials.
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