SYNTHESIS, STRUCTURE, AND REACTIVITY OF (PHOSPHORANYLIDENEPHOSPHINE)PENTACARBONYLTUNGSTEN COMPLEXES - ANOTHER ACCESS TO THE PHOSPHORUS CARBON DOUBLE-BOND

被引:76
作者
LEFLOCH, P [1 ]
MARINETTI, A [1 ]
RICARD, L [1 ]
MATHEY, F [1 ]
机构
[1] ECOLE POLYTECH,DCPH,CHIM PHOSPHORE & MET TRANSIT LAB,F-91128 PALAISEAU,FRANCE
关键词
D O I
10.1021/ja00162a051
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reaction of trialkylphosphines with 7-phosphanorbornadiene PW(CO)5 complexes affords the corresponding phosphoranylidenephosphine complexes R13P=P(R)→ W(CO)5. One such complex (R = CO2Et, R1 = Et) has been investigated by X-ray crystal structure analysis. It shows a zwitterionic character with a long P=P bond(2.156 (2)Å). These phosphoranylidenephosphine complexes cleanly react at room temperature with aldehydes to give the corresponding phosphaalkene complexes via a “phospha-Wittig” reaction. These phosphaalkene complexes are either isolated as such or trapped by MeOH, dimethylbutadiene, or benzoic acid. © 1990, American Chemical Society. All rights reserved.
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页码:2407 / 2410
页数:4
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