双膦配体桥联的四铁配合物的电催化产氢性能
Electrocatalytic hydrogen evolution performance of tetra-iron complexes with bridging diphosphine ligands
作者单位E-mail
朱霖洁 宁波工程学院材料与化学工程学院, 宁波 315211  
刘旭锋 宁波工程学院材料与化学工程学院, 宁波 315211 nkxfliu@126.com 
摘要: 通过配体取代反应合成了2个双膦配体桥联的四铁配合物[Fe4(CO)10(μ-SCH2CH (CH3) S)2(dppa)](1)和[Fe4(CO)10(μ-SCH2CH (CH3) S)2(trans-dppv)](2),其中dppa=双(二苯基膦)乙炔,trans-dppv=trans-1,2-双(二苯基膦)乙烯。配合物的结构经过元素分析、红外光谱、核磁共振氢谱、磷谱以及单晶X射线衍射等方法的表征。用循环伏安法研究了新配合物的电化学性质,结果表明它们均可以在乙腈溶液中催化醋酸中的质子还原产生氢气。其中配合物2的催化效率要明显优于配合物1
关键词: 四铁配合物  晶体结构  循环伏安  电催化产氢
基金项目: 浙江省自然科学基金(No.LY19B020002)资助。
Abstract: Two tetra-iron complexes with bridging diphosphine ligands, named [Fe4(CO)10(μ-SCH2CH(CH3)S)2(dppa)] (1) and [Fe4(CO)10(μ-SCH2CH(CH3)S)2(trans-dppv)] (2), where dppa=bis(diphenylphosphino)acetylene and trans-dppv= trans-1,2-bis(diphenylphosphino)ethylene, were prepared by the reaction of complex [Fe2(CO)6(μ-SCH2CH(CH3)S)] with dppa or trans-dppv. Both complexes were structurally identified by elemental analysis, FTIR spectra, 1H NMR, and 31P NMR, together with single-crystal X-ray diffraction analysis. X-ray crystallographic studies revealed that complex 1 consists of two di-iron propane-1,2-dithiolate pentacarbonyl sub-units connected by a linear dppa ligand whereas a zigzag trans-dppv ligand is found in complex 2. The electrochemical properties were probed by cyclic voltammetry, showing that two irreversible reductions and one irreversible oxidation were found for both complexes. Furthermore, electrocatalytic studies were carried out by adding acetic acid as a proton source into the solution. The results demonstrated that both complexes can catalyze proton reduction to evolve hydrogen. For comparison, the catalytic efficiency of complex 2 was better than complex 1.
Keywords: tetra-iron complex  crystal structure  cyclic voltammetry  electrocatalytic hydrogen production
投稿时间:2024-06-02 修订日期:2024-09-28
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朱霖洁,刘旭锋.双膦配体桥联的四铁配合物的电催化产氢性能[J].无机化学学报,2025,41(2):321-328.
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