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Unusual Formation of an Azaphospholene from 1,3,4,5-Tetramethylimidazol-2-ylidene and Di(isopropyl)aminophosphaalkyne
F Ekkehardt Hahn1, Duc Le Van1, Michelle C Moyes1
1Anorganisch-Chemisches Institut der Universität Wilhelm-Klemm-Strasse 8 48149 Münster (Germany) Fax: (+49) 251-833-3108.
Abstract:
Intramolecular C-H insertion into the methyl group of the amino substituent of 1 is shown by density functional theory calculations to stabilize this intermediate in the formation of the novel 1:1 carbene-phosphaalkyne adduct 2. Compound 2 is formed in near quantitative yield by reaction of 1,3,4,5-tetramethylimidazol-2-ylidene with P≡CNiPr2 .
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