首页> 外文期刊>Journal of Organometallic Chemistry >Characterization of the mu-(eta(1)-C :eta(2)-S,S ')dithiocarboxylate complexes Cp(CO)(2)Fe-CS2-Zr(X)Cp-2 (X=Cl, OCMe3); CS2 insertion into the FeZr bond of the heterobimetallic complex Cp(CO)(2)Fe-Zr(OCMe3)Cp-2
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Characterization of the mu-(eta(1)-C :eta(2)-S,S ')dithiocarboxylate complexes Cp(CO)(2)Fe-CS2-Zr(X)Cp-2 (X=Cl, OCMe3); CS2 insertion into the FeZr bond of the heterobimetallic complex Cp(CO)(2)Fe-Zr(OCMe3)Cp-2

机译:mu-(eta(1)-C:eta(2)-S,S')二硫代羧酸酯络合物Cp(CO)(2)Fe-CS2-Zr(X)Cp-2(X = Cl,OCMe3)的表征; CS2插入异双金属配合物Cp(CO)(2)Fe-Zr(OCMe3)Cp-2的FeZr键中

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摘要

Treatment of the carbon disulfide adducts FpCS(2)K and Fp'CS2K [Fp' = (eta(5)-C5H4CH3)Fe(CO)(2)] with Cp2ZrCl2 affords the mu-(eta(1)-C: eta(2)-S,S') dithiocarboxylate complexes FpCS(2)ZrClCp(2) (1) and Fp'CS2ZrClCp2 (2). Both stable products were fully characterized. Metathesis between FpCS(2)K and Cp2ZrCl(OCMe3) provided FpCS(2)Zr(OCMe3)Cp-2 (3), which was not obtained analytically pure. This product was characterized by comparison of its IR and H-1-, C-13{H-1}-NMR spectral data with that for 1 and 2. The iron-zirconium complex FpZr(OCMe3)Cp-2 (4) was transformed by one equivalent of CS2 to 3 (75% spectroscopic yield), a reaction that did not occur for FpZrClCp(2). An insertion pathway is discussed for incorporating the CS2 into the Fe-Zr bond of FpZr(OCMe3)Cp-2. (C) 1998 Elsevier Science S.A. All rights reserved. [References: 23]
机译:用Cp2ZrCl2处理二硫化碳加合物FpCS(2)K和Fp'CS2K [Fp'=(eta(5)-C5H4CH3)Fe(CO)(2)]得到mu-(eta(1)-C:eta (2)-S,S')二硫代羧酸盐络合物FpCS(2)ZrClCp(2)(1)和Fp'CS2ZrClCp2(2)。两种稳定的产品都经过充分表征。 FpCS(2)K和Cp2ZrCl(OCMe3)之间的复分解提供了FpCS(2)Zr(OCMe3)Cp-2(3),该纯度无法通过分析获得。将该产品的红外光谱和H-1,C-13 {H-1} -NMR光谱数据与1和2进行比较。铁锆配合物FpZr(OCMe3)Cp-2(4)为通过将一当量的CS2转化为3(光谱产率为75%),对于FpZrClCp(2)不会发生此反应。讨论了将CS2掺入FpZr(OCMe3)Cp-2的Fe-Zr键的插入途径。 (C)1998 Elsevier Science S.A.保留所有权利。 [参考:23]

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