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Synthesis, Structure, and Reactions of the First Rotational Isomers of Stable Thiobenzaldehydes, 2,4,6-Tris[bis(trimethylsilyl)methyl]thiobenzaldehydes

โœ Scribed by Nobuhiro Takeda; Prof. Dr. Norihiro Tokitoh; Prof. Dr. Renji Okazaki


Book ID
102792865
Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
996 KB
Volume
3
Category
Article
ISSN
0947-6539

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โœฆ Synopsis


The first rotational isomers of thiobenzaldehydes, TbtCH=S (2a and 2b: Tbt = 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl), were synthesized and isolated as stable crystalline compounds by the desulfurization of the corresponding overcrowded cyclic polysulfides TbtCHS, (n = 5 or 8) with phosphine reagents. The molecular structures of 2a and 2 b in the solid state, determined by X-ray crystallographic analysis, differed in their confor-mations, which were essentially identical with those in solution as revealed by 'H('H} nuclear Overhaus,er effect (NOE) experiments. The isomeric thiobenzalde-Keywords competition experimentsconformation determinationisomerizationsrotamersthioaldehydes

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