Insertion reactions of CS2, COS, and PhNCS at thiolate-bridged diiron centers

被引:26
作者
Chen, Yanhui [1 ]
Peng, Ying [1 ]
Chen, Pingping [1 ]
Zhao, Jinfeng [1 ]
Liu, Litao [1 ]
Li, Yang [1 ]
Chen, Shuoyi [1 ]
Qu, Jingping [1 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Sch Chem Engn, Dalian 116012, Peoples R China
基金
中国国家自然科学基金;
关键词
CRYSTAL-STRUCTURE; CARBON-DISULFIDE; BOND-CLEAVAGE; HYDRIDE BOND; CP-ASTERISK; H BOND; I-PR; COMPLEXES; HETEROCUMULENES; PH;
D O I
10.1039/b920144k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Treatment of [Cp*Fe(mu(2)-SR)(3)FeCp*] (1a, R = Et; 1b, R = Me) with CS2 obtains the insertion products [Cp*Fe(mu(2)-SR)(2)(mu-eta(2)- S2CSR)FeCp*] (2a, R = Et; 2b, R = Me) with the retained Fe2S2 subunit in excellent yield. 2a and 2b represent the first examples for the CS2 activation and incorporation at the diiron-SR bond. [Cp*Fe(mu(2)-SEt) 2(mu-eta(2)-S-2)FeCp*] (3) is prepared from COS and 1a through the decarbonylation and sulfur coupling reaction of COS resulting in the formation of S-2(2-) ligand. Addition of PhNCS into 1a affords a mononuclear complex [Cp*Fe(SEt)(eta(2)-SC(SEt)NPh)] (4). 1a is found to be unreactive towards CO2. The spectral characterization, X-ray diffraction analysis, and electrochemistry of the insertion products have also been described.
引用
收藏
页码:3020 / 3025
页数:6
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