Synthesis and structures of tin(II) and lead(II) 1-aza-allyls;: the [N(SiMe3)C(Ph)C(SiMe3)2]- ligand

被引:31
|
作者
Hitchcock, PB [1 ]
Lappert, MF [1 ]
Layh, M [1 ]
机构
[1] Univ Sussex, Chem Lab, Brighton BN1 9QJ, E Sussex, England
基金
英国工程与自然科学研究理事会;
关键词
crystal structures; organotin complexes; organolead complexes; 1-aza-allyl complexes;
D O I
10.1016/S0020-1693(97)05788-5
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The new lithium 1-aza-allyl Li[N(R)C(Ph)CR2] (THF) (1) (Li(LL")(THF)) has been prepared in high yield from LiCR3(THF)(2) and benzonitrile (R = SiMe2; THF = tetrahydrofuran). From 1 and MCl2, the stable 1-aza-allyls [M(mu-Cl)(LL")] (2 (M = Sn); 3 (M = Pb)) and M(LL")(2) (4 (M=Sn); 5 (M=Pb)) were obtained. Each of the compounds 1-5 was fully characterised by multinuclear NMR spectroscopy (the compounds are fluxional in solution), mass spectrometry and for 3, 4 and 5 single crystal X-ray diffraction. Crystalline 3 is a centrosymmetric dimer having terminal eta(3)-1-aza-allyl ligands with one bridging Cl- strongly bonding, Pb-Cl = 2.609(3) Angstrom, and the other much less so, Pb...Cl = 3.276(3) Angstrom. Crystalline 4 and 5 are mononuclear (eta(3)-1-aza-allyl)metal(II) enamides, M[N(R)C(Ph)CR2][N(R)C(Ph):CR2]. Also reported are the synthesis and NMR spectra of PbCl[N(R)C(Bu-1)CHR] (6).
引用
收藏
页码:181 / 190
页数:10
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