Synthesis 13C NMR, λmax and MMP2 calculations of two ‘tailor-made’ α-conjugated hexamethylsexithiophenes.
- 1 January 1992
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 48 (32) , 6701-6708
- https://doi.org/10.1016/s0040-4020(01)80015-6
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Crystal structure of 4,4′,3″,4‴‐Tetramethyl2,2′:5′,2″:5″,2‴‐tetrathiophene: A comparison with the conformation in solutionAdvanced Materials, 1992
- Electrochemical coupling of dialkylated sexithiopheneAdvanced Materials, 1992
- Conformation and optical absorption properties of thiophene oligomers: 13C‐NMR, UV, and MMP2 calculations of Di‐ and tetramethyl‐quaterthiophenesAdvanced Materials, 1991
- A molecular mechanics (MM2) study of Furan, Thiophene, and related compoundsJournal of Computational Chemistry, 1989
- Characteristics of conducting polymer as optical active elementSynthetic Metals, 1989
- Optical properties of conducting polymersChemical Reviews, 1988
- Use of the Pariser-Parr-Pople approximation to obtain practically useful predictions for electronic spectral properties of conducting polymersMacromolecules, 1987
- Organic polymers based on aromatic rings (polyparaphenylene, polypyrrole, polythiophene): Evolution of the electronic properties as a function of the torsion angle between adjacent ringsThe Journal of Chemical Physics, 1985
- Nickel-phosphine complex-catalyzed Grignard coupling—IITetrahedron, 1982
- The Carbon-13 Nuclear Magnetic Resonance Spectra of Furan, Pyrrole, Thiophene, and Some of Their Methyl Derivatives1aJournal of the American Chemical Society, 1965