Reactions of zinc dialkyls with (perfluorophenyl)boron compounds:: Alkylzinc cation formation vs C6F5 transfer

被引:91
作者
Walker, DA
Woodman, TJ
Hughes, DL
Bochmann, M [1 ]
机构
[1] Univ E Anglia, Sch Chem Sci, Wolfson Mat & Catalysis Ctr, Norwich NR4 7TJ, Norfolk, England
[2] John Innes Ctr Plant Sci Res, Dept Biol Chem, Norwich NR4 7UH, Norfolk, England
关键词
D O I
10.1021/om0103557
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reaction between ZnR2 and [H(OEt2)(2)] [B(C6F5)(4)] in ether leads to the salts [RZn(OEt2)(3)]-[B(C6F5)(4)], while mixtures of ZnR2 (R = Me, Et) and B(C6F5)(3) in toluene-d(8) undergo facile alkyl/C6F5 group exchange to give Zn(C6F5)(2). (toluene). Mixtures of ZnR2 and B(C6F5)(3) in hydrocarbon/diethyl ether solvent mixtures react with alkyl transfer to afford the ion pairs [RZn(OEt2)(3)] [RB(C6F5)(3)], whereas the reaction of ZnEt2 with [Ph3C] [B(C6F5)(4)] in toluene-d(8) proceeds with beta -H abstraction to give ethene and Ph3CH, with the subsequent rapid formation of Zn(C6F5)(2).
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页码:3772 / 3776
页数:5
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