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 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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
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p nucleus ever recorded in this series, and thermally decomposed with formation of a diphosphene, suggesting a phosphinidene intermediate. |
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ISSN: | 1042-6507 1563-5325 |
DOI: | 10.1080/10426509608545183 |