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- W2000145354 abstract "The UV photoelectron spectra of two isomeric styrylthiophenes (5, 6) and six isomeric (thienylethenyl)pyridines (7−12) have been recorded and analyzed, making use of DFT Becke3LYP calculations. The spectra were compared with those of (E)-stilbene (1e) and the isomeric styrylpyridines (2−4), which are π-isoelectronic with 5−12. Using quantum chemical analyses, planar molecular structures were obtained for all these compounds. However, from the separation ΔIP of the ionization bands associated with the π7 and π3 MOs, it is possible to make a distinction between planar and twisted molecular structures. Accordingly in these compounds, 2-substituted pyridine rings and 3-substituted thiophene rings are nearly untwisted, whereas phenyl rings, 3- and 4-substituted pyridine, and 2-substituted thiophene rings are twisted to an extent similar to that in 1e. The apparent distortion of the molecules is probably caused by torsional vibrations, so that twisted average geometries correspond to planar equilibrium structures. The B3LYP data permit detailed conclusions to be drawn with regard to the conformational preferences of 2- and 3-substituted thiophene and pyridine rings in heterocyclic analogues of 1e, as well as the to relative stabilities of isomers 7−12. The results clearly indicate that PE spectroscopy is a powerful method for analysis of conformational properties of stilbene-like molecules." @default.
- W2000145354 created "2016-06-24" @default.
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- W2000145354 date "2001-01-01" @default.
- W2000145354 modified "2023-09-25" @default.
- W2000145354 title "Photoelectron Spectra, Electronic Structures, and Conformational Properties of (E)-Stilbene, Styrylthiophenes, and (Thienylethenyl)pyridines" @default.
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- W2000145354 doi "https://doi.org/10.1002/1099-0690(200101)2001:1<121::aid-ejoc121>3.0.co;2-r" @default.
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