Bi- and tetranuclear tricarbido complexes:: μ,σ:σ′ and μ,σ:σ′:π⊥ coordination of bridging C3 ligands

被引:19
作者
Dewhurst, RD [1 ]
Hill, AF [1 ]
Willis, AC [1 ]
机构
[1] Australian Natl Univ, Res Sch Chem, Inst Adv Studies, Canberra, ACT 0200, Australia
关键词
D O I
10.1021/om0401152
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Fluoride-mediated desilylation of the propargylidyne [W(equivalent toCCequivalent toCSiMe(3))(CO)(2){HB(pz)(3)}] (1; pz = pyrazol-1-yl) in the presence of [RhCl(CO)(PPh3)(2)] provides the bimetallic complex [Rh(Cequivalent toCCequivalent toW(CO)(2){HB(pz)(3)})(CO)(PPh3)(2)] (2b), which reacts with iodine to give [Rh(Cequivalent toCCequivalent toW(CO)(2){HB(pz)(3)})I-2(CO)(PPh3)(2)] (3) and with [Fe-2(CO)(9)] to provide [RhFe2(mu-C3W(CO)(2){HB(pz)(3)})-(CO)(10)(PPh3)] (4), a rare example of a tricarbido ligand incorporated within a cluster framework.
引用
收藏
页码:5903 / 5906
页数:4
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