INTERCONVERSION OF ETA(1)-PROPARGYL, ETA(1)-ALLENYL, AND ETA(3)-PROPARGYL ALLENYL LIGANDS ON PLATINUM - SYNTHESIS, STRUCTURE, AND REACTIVITY OF [(PH3P)2PT(ETA(3)-CH2CCPH)]O3SCF3

被引：91

作者：

BLOSSER, PW ^{[1
]}

SCHIMPFF, DG ^{[1
]}

GALLUCCI, JC ^{[1
]}

WOJCICKI, A ^{[1
]}

机构：

[1] OHIO STATE UNIV,DEPT CHEM,COLUMBUS,OH 43210

来源：

ORGANOMETALLICS | 1993年 / 12卷 / 06期

关键词：

D O I：

10.1021/om00030a001

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The eta3-propargyl/allenyl complex [(Ph3-P)2Pt(eta3-CH2CCPh)]+ (4), formed by reaction of trans-(PPh3)2PtBr(eta1-CH2C=CPh) with AgO3SCF3 or (Ph3-P)2Pt(eta2-PhC=CCH2OMe) with BF3.OEt2, reacts with Br-to yield 9:1 cis-/trans-(Ph3P)2PtBr(eta1-CH2C=CPh), with excess PMe3 to give [(Me3P)3Pt(eta1-C(Ph)=C=CH2)]+, and with CO to afford 1:1 [trans-(Ph3P)2Pt(CO)(eta1-CH2C=CPh)]+/[trans- (Ph3P)2Pt(CO) (eta1-C(Ph)=C=CH2)]+. With Et2NH, ROH (R = Me, Et), and CH(CO2Me)2-, 4 undergoes nucleophilic addition to the central C atom with transfer of hydrogen to the CPh atom of eta3-CH2CCPh to produce eta3-allyl complexes as single syn or anti isomers.

引用

页码：1993 / 1995

页数：3

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