Novel Tetraphosphabarrelene and -semibullvalene Derivatives by Reactions of 2,4,6-Tri-tert-butyl-1,3,5-triphosphabenzene with Phosphaalkynes☆
✍ Scribed by Paul Binger; Stefanie Stutzmann; Joachim Bruckmann; Carl Krüger; Joseph Grobe; Duc Le Van; Torsten Pohlmeyer
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 128 KB
- Volume
- 1998
- Category
- Article
- ISSN
- 1434-1948
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✦ Synopsis
6-Tri-tert-butyl-1,3,5-triphosphabenzene 4 reacts with to the 1,3,4,7-tetraphosphasemibullvalene derivative 10 as the only product. The single-crystal X-ray analysis of 10 phosphaalkynes PϵCϪR [R = tBu (5a), tPen (5b)] at room temperature in a formal [4 + 2] cycloaddition to yield the exhibits a diphosphirane unit with a very long PP distance of 2.274(1) A ˚together with a large extension of the PCP angle corresponding 1,3,5,7-tetraphosphabarrelene derivatives 8a and 8b, respectively. The analogous reaction of 4 with the in the three-membered ring to 75.3(1)°. aminophosphaethyne PϵCϪN(iPr) 2 (9) unexpectedly leads lautern, Erwin-Schrödinger-Straße, D-67663 Kaiserslautern, Germany;
📜 SIMILAR VOLUMES
A small variation in the vanadium reagent leads to a completely different product: The cyclooligomerization of phosphaalkynes 2 with tBuN=VCl ⋅DME (DME=1,2-dimethoxyethane) proceeds with incorporation of the imido fragment to give the azatetraphosphaquadricyclanes 1. In contrast, with the correspond