Linear and Radial Conjugation in Extended π-Electron Systems
Author(s) -
Garvin M. Peters,
Girishma Grover,
Ruth L. Maust,
Curtis E. Colwell,
Haley Bates,
William A. Edgell,
Ramesh Jasti,
Miklós Kertész,
John D. Tovar
Publication year - 2020
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.9b10785
Subject(s) - chemistry , delocalized electron , arylene , intramolecular force , electronic structure , chemical physics , conjugated system , wave function , linear molecular geometry , electron , molecule , computational chemistry , molecular physics , nanotechnology , polymer , atomic physics , stereochemistry , quantum mechanics , physics , organic chemistry , aryl , alkyl , materials science
We describe the synthesis and electronic properties of new π-conjugated small molecules and polymers that combine the linear intramolecular conjugation pathways commonly associated with organic electronic materials with the emerging properties of radial conjugation found in cycloparaphenylenes (CPPs) and other curved π-surfaces. Using arylene ethynylenes as prototypical linear segments and [6]/[8]CPP as the radial segments, we demonstrate the formation of new electronic states that are not simply additive responses from the individual components. Quantum chemical calculations of model oligomeric structures reveal these electronic processes to arise from the hybrid nature of wave function delocalization over the linear and radial contributors in the photophysically relevant electronic states.
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