Linear and Radial Conjugation in Extended $$π$$-Electron Systems
- Johns Hopkins Univ., Baltimore, MD (United States); Johns Hopkins University
- Georgetown Univ., Washington, DC (United States)
- Univ. of Oregon, Eugene, OR (United States)
- Johns Hopkins Univ., Baltimore, MD (United States)
Here 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 cyclo(para-phenylene)s (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 wavefunction delocalization over the linear and radial contributors in the photophysically relevant electronic states.
- Research Organization:
- Johns Hopkins Univ., Baltimore, MD (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
- Grant/Contract Number:
- SC0019017
- OSTI ID:
- 1595540
- Journal Information:
- Journal of the American Chemical Society, Journal Name: Journal of the American Chemical Society Journal Issue: 5 Vol. 142; ISSN 0002-7863
- Publisher:
- American Chemical Society (ACS)Copyright Statement
- Country of Publication:
- United States
- Language:
- English
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