New Strategies to Phosphino-Phosphonium Cations and Zwitterions

被引:47
作者
Geier, Stephen J. [1 ]
Dureen, Meghan A. [1 ]
Ouyang, Eva Y. [1 ]
Stephan, Douglas W. [1 ]
机构
[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
alkyne activation; hydrogen activation; main group elements; phosphino-phosphonium; phosphorus; zwitterions; FRUSTRATED LEWIS PAIRS; HETEROLYTIC DIHYDROGEN ACTIVATION; SYNTHETIC APPROACH; P BONDS; REACTIVITY; COMPLEXES; CARBENE; COORDINATION; CHEMISTRY; BORANE;
D O I
10.1002/chem.200902369
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
By employing strategies based on frustrated Lewis pair chemistry, new routes to phosphino-phosphonium cations and zwitterions have been developed. B(C6F5)(3) is shown to react with H-2 and P(2)tBu(4) to effect heterolytic hydrogen activation yielding the phosphino-phosphonium borate salt [(tBu(2)P)PHtBu(2)] [HB(C6F5)(3)] (1). Alternatively, alkenylphosphino-phosphonium borate zwitterions are accessible by reaction of B(C6F5)(3) and PhC CH with P2Ph4, P4Cy4, or P5Ph5 affording the species [(Ph2P)P(Ph)(2)C(Ph)=C(H)B(C6F5)(3)] (2), [(P3Cy3)P(Cy)-C(Ph)=C(H)B(C6F5)(3)] (3), and [(P4Ph4)P(Ph)C(Ph)=C(H)B(C6F5)(3)] (4). A related phosphino-phosphonium borate species-[(Ph4P4)P(Ph)C6F4B-(F)(C6F5)(2)] (5) is also isolated from the thermolysis of B(C6F5)(3) and P5Ph5.
引用
收藏
页码:988 / 993
页数:6
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