Fe3S2 cluster complexes containing aminodiphosphine ligand: synthesis, characterization, crystal structures and electrochemical properties

被引:0
|
作者
Yang, Jun [1 ]
Tian, Wen-Jing [1 ]
Lu, Shuang [2 ]
He, Jiao [1 ]
Hu, Kui [1 ]
Yan, Peng [1 ]
Xu, Hang [1 ]
Zeng, Mao-Xin [1 ]
Li, Yu-Long [1 ]
Li, Qian-Li [2 ]
机构
[1] Sichuan Univ Sci & Engn, Coll Chem & Environm Engn, Zigong 643000, Peoples R China
[2] Liaocheng Univ, Coll Chem & Chem Engn, Liaocheng, Shandong, Peoples R China
关键词
Fe3S2; cluster; synthesis; aminodiphosphine; crystal structure; electrochemistry; ELECTROCATALYTIC PROTON-REDUCTION; TRIIRON ENNEACARBONYL DISULFIDE; IRON HYDROGENASE; ACTIVE-SITE; MODELS; WATER; COORDINATION; DERIVATIVES; REACTIVITY; EVOLUTION;
D O I
10.1080/17415993.2022.2100702
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this article, six new Fe3S2 cluster complexes Fe-3(mu S-3)(2)(CO)(7)[(Ph2P)(2)NR] (1-6) (R = (CH2)(2)CH3, CH(CH3)(2), (CH2)(3)CH3, CH2CH(CH3)(2), p-C6H4CCH and m-C6H4CCH) were successfully synthesized by reactions of Fe3S2(CO)(9) and the corresponding aminodiphosphines under refluxing toluene. Meanwhile, treatment of Fe3S2(CO)(9) and (Ph2P)(2)NCH(CH3)Ph afforded two new Fe3S2 cluster complexes Fe-3(mu(3)-S)(2)(CO)(7)[(Ph2P)(2)NCH(CH3)Ph] (7) and Fe-3(mu(3)-S)(2)(CO)(7)[(kappa(2)-Ph2P)(2)NCH(CH3)(Ph)] (8). Complexes 1-8 were characterized by elemental analysis, FT-IR, NMR spectroscopy, and especially X-ray crystallography. The elctrochemical properties were investigated by cyclic voltammetry, showing that they all have electrocatalytic ability for the reduction of protons to H-2.
引用
收藏
页码:37 / 51
页数:15
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