与[FeFe]-氢化酶有关的单核和双核羰基二硫烯配合物

IF 0.6 Q4 CHEMISTRY, ORGANIC Molbank Pub Date : 2023-09-06 DOI:10.3390/m1719
Mohamed Kdider, C. Elléouet, F. Pétillon, P. Schollhammer
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引用次数: 0

摘要

二羰基二亚硫铁桥接配合物[Fe2(CO)6(µ-S2C2(CO2Me)2)](1)与1当量的光气PR3(R=Ph,OMe)反应,得到作为主要产物的单取代衍生物[Fe2(CO)5L(µ-S2C2(CO2 Me)2))](L=PPh3(2),P(OMe)3(3))。在过量(3-4当量)的P(OMe)3存在的情况下,1的部分裂解发生,并获得单核物种[Fe(CO)(P(OMe)3)2(κ2-S2C2(CO2Me)2)](4)和3的混合物。化合物2-4通过红外光谱和1H,31P-{1H}NMR光谱进行了分析。通过X射线衍射分析确定了它们的固态结构,符合它们的光谱特征。
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Mono- and Dinuclear Carbonyl Dithiolene Complexes Related to the [FeFe]-Hydrogenases
The di-iron carbonyl dithiolene bridged complex [Fe2(CO)6(µ-S2C2(CO2Me)2)] (1) reacts with 1 equivalent of phosphane PR3 (R = Ph, OMe) to give, as major products, monosubstituted derivatives [Fe2(CO)5L(µ-S2C2(CO2Me)2)] (L = PPh3 (2), P(OMe)3 (3)). In the presence of an excess (3–4 equiv.) of P(OMe)3, the cleavage of 1 arises partly and a mixture of the mononuclear species [Fe(CO)(P(OMe)3)2(κ2-S2C2(CO2Me)2)] (4) and 3 is obtained. The compounds 2–4 were analyzed by IR and 1H, 31P-{1H} NMR spectroscopies. Their structures in solid state were determined by X-ray diffraction analyses, which accord with their spectroscopic characteristics.
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来源期刊
Molbank
Molbank Chemistry-Physical and Theoretical Chemistry
CiteScore
0.70
自引率
33.30%
发文量
174
审稿时长
11 weeks
期刊介绍: •organic synthesis •biosynthesis •extraction and purification •natural product derivatives •structural elucidation (X-ray crystallography, NMR, etc.)
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