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有机金属MFe2(μ3-S)2簇合物(M = Mo或Fe)的合成与结构

Synthesis and structure of the organometallic MFe2(mu3-S)2 clusters (M = Mo or Fe).

作者信息

Han Jaehong, Coucouvanis Dimitri

机构信息

Metalloenzyme Research Group, BET Research Institute and Department of Biotechnology, Chung-Ang University, Anseong, Korea.

出版信息

Dalton Trans. 2005 Apr 7(7):1234-40. doi: 10.1039/b419051c. Epub 2005 Feb 24.

Abstract

New organometallic clusters with the MFe2(mu3-S)2 core (M = Mo or Fe) have been synthesized from inorganic [MoFe3S4] or [Fe4S4] clusters under high pressure CO. The reaction of (Cl4-cat)2Mo2Fe6S8(PR3)6[R = Et, (n)Pr] with high pressure CO produced the crystalline [MoFe2S2]4+ clusters, (Cl4-cat)Mo(O)Fe2S2(CO)(n)(PR3)6-n[n= 4, Et =I, (n)Pr =II; n = 5, Et =III] after flash column chromatography. The similar [MoFe2S2]4+ cluster, (Cl4-cat)2MoFe2S2(CO)2(depe)(2)(IV), also has been achieved by the reactions of (Cl4-cat)MoFe3S3(CO)6(PEt3)2 with depe by reductive decoupling of the cluster. For the [Fe3(mu3-S)2]4+ cluster, Fe4S4(PcHex3)4 was reacted with high pressure CO to produce a new Fe3S2(CO)7(PcHex)(2)(V) compound. These reactions generalized the preparation of organometallic compounds from inorganic clusters. All the compounds have been characterized by single crystal X-ray crystallography. A possible reaction pathway for the synthesis of the MFe2(mu3-S) clusters (M = Mo or Fe) has also been suggested.

摘要

含有MFe₂(μ₃-S)₂核心(M = Mo或Fe)的新型有机金属簇合物已在高压CO条件下由无机[MoFe₃S₄]或[Fe₄S₄]簇合物合成。(Cl₄-cat)₂Mo₂Fe₆S₈(PR₃)₆[R = Et, (n)Pr]与高压CO反应,经快速柱色谱分离后得到结晶性的[MoFe₂S₂]⁴⁺簇合物,即(Cl₄-cat)Mo(O)Fe₂S₂(CO)ₙ(PR₃)₆₋ₙ[n = 4, Et = I, (n)Pr = II;n = 5, Et = III]。类似的[MoFe₂S₂]⁴⁺簇合物(Cl₄-cat)₂MoFe₂S₂(CO)₂(depe)₂(IV),也通过(Cl₄-cat)MoFe₃S₃(CO)₆(PEt₃)₂与depe反应,使簇合物发生还原解耦而制得。对于[Fe₃(μ₃-S)₂]⁴⁺簇合物,Fe₄S₄(PcHex₃)₄与高压CO反应生成了一种新的Fe₃S₂(CO)₇(PcHex)₂(V)化合物。这些反应推广了由无机簇合物制备有机金属化合物的方法。所有化合物均通过单晶X射线晶体学进行了表征。还提出了合成MFe₂(μ₃-S)簇合物(M = Mo或Fe)的可能反应途径。

相似文献

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Synthesis and structure of the organometallic MFe2(mu3-S)2 clusters (M = Mo or Fe).
Dalton Trans. 2005 Apr 7(7):1234-40. doi: 10.1039/b419051c. Epub 2005 Feb 24.

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