Effects of a Sterically Demanding P-Aryl Substituent in Phosphole and 7-Phosphanorbornene Chemistry

The 2,4-di-tert-butyl-6-methylphenyl substituent was placed on phosphorus of a phosphole, causing restricted rotation about the P-C bond and flattening of the phosphorus pyramid. Electron delocalization was greater in this phosphole as a result of the flattening. The 7-phosphanorbornene with this su...

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Veröffentlicht in:Phosphorus, sulfur, and silicon and the related elements sulfur, and silicon and the related elements, 1996-01, Vol.109 (1-4), p.433-436
Hauptverfasser: Quin, Louis D., Ionkin, Alexey S., Kalgutkar, Rajdeep, Keglevich, György
Format: Artikel
Sprache:eng
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Zusammenfassung:The 2,4-di-tert-butyl-6-methylphenyl substituent was placed on phosphorus of a phosphole, causing restricted rotation about the P-C bond and flattening of the phosphorus pyramid. Electron delocalization was greater in this phosphole as a result of the flattening. The 7-phosphanorbornene with this substituent had the most deshielded 31 p nucleus ever recorded in this series, and thermally decomposed with formation of a diphosphene, suggesting a phosphinidene intermediate.
ISSN:1042-6507
1563-5325
DOI:10.1080/10426509608545183