π Conjugation in 2,2‘-Bithiophene and Its Dimethyl Derivatives: Model Compounds of Organic Conducting Polymers Based on Thiophene Rings
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry
- Vol. 100 (5) , 1524-1529
- https://doi.org/10.1021/jp951592o
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- 2,2'-Bithienyl derivatives: EPR investigation of their radical ions in solution, electrochemical properties, and crystal structureThe Journal of Organic Chemistry, 1993
- Crystal structure of 4,4′,3″,4‴‐Tetramethyl2,2′:5′,2″:5″,2‴‐tetrathiophene: A comparison with the conformation in solutionAdvanced Materials, 1992
- A new strategy for the evaluation of force parameters from quantum mechanical computationsJournal of Computational Chemistry, 1991
- AB initio study of the dynamical properties of polythiopheneSynthetic Metals, 1991
- Ultraviolet photoemission study of oligothiophenes: π-band evolution and geometriesThe Journal of Chemical Physics, 1990
- An electron spin resonance study of the radical cations of pyrroles, furans, and thiophenes in liquid solutionJournal of the Chemical Society, Perkin Transactions 2, 1989
- The electron spin resonance spectra of the radical cations of furans, thiophenes, and pyrroles in liquid solutionJournal of the Chemical Society, Chemical Communications, 1987
- Conformational behaviour of isomeric bithienyls. An ab initio studyJournal of the Chemical Society, Perkin Transactions 2, 1986
- Valence effective Hamiltonian study of the electronic structure of poly(p-phenylene) and poly(p-phenylene sulfide)The Journal of Chemical Physics, 1982
- Nematic phase nuclear magnetic resonance investigations of rotational isomerism. III. Conformational preferences and interconversion barrier of 2,2'-bithienylJournal of the American Chemical Society, 1974