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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.
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页码:37 / 51
页数:15
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