Synthesis, structures, and electrochemistry of diiron toluene-3,4-dithiolate complexes containing phosphine ligands

被引:6
|
作者
Lin, Hui-Min [1 ]
Mu, Chao [2 ]
Li, Ao [2 ]
Liu, Xu-Feng [1 ]
Li, Yu-Long [2 ]
Jiang, Zhong-Qing [3 ]
Wu, Hong-Ke [4 ]
机构
[1] Ningbo Univ Technol, Sch Mat & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
[2] Sichuan Univ Sci & Engn, Coll Chem & Environm Engn, Zigong 643000, Peoples R China
[3] Zhejiang Sci Tech Univ, Dept Phys, Key Lab ATMMT, Minist Educ, Hangzhou 310018, Zhejiang, Peoples R China
[4] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
FE-ONLY HYDROGENASE; ACTIVE-SITE MODELS; IRON HYDROGENASE; ETHANEDITHIOLATE COMPLEXES; AZADITHIOLATE COMPLEXES; COORDINATION SPHERE; PROTON-REDUCTION; ANALOGS; CHEMISTRY; DINUCLEAR;
D O I
10.1007/s11243-019-00342-2
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this paper, four diiron toluene-3,4-dithiolate complexes with phosphine ligands were synthesized and characterized. Treatment of complex [Fe-2(CO)(6){mu-SC6H3(CH3)S}] (1) with the corresponding phosphine ligands ethyl diphenylphosphinite, 4-(dimethylamino)phenyldiphenylphosphine, 2-(diphenylphosphino)biphenyl, or vinyldiphenylphosphine in the presence of Me3NO center dot 2H(2)O as the CO-oxidative agent afforded the products [Fe-2(CO)(5)(L){mu-SC6H3(CH3)S}] (L = Ph2POCH2CH3, 2; Ph2P(4-C6H4NMe2), 3; Ph2P(2-C6H4Ph), 4; Ph2PCH = CH2, 5) in 68-88% yields. The complexes 2-5 were characterized by elemental analysis, IR, NMR spectroscopy, as well as by X-ray diffraction analysis. Furthermore, the electrochemistry of these complexes was studied by cyclic voltammetry.
引用
收藏
页码:491 / 498
页数:8
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