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A Two-Coordinate Cobalt(II) Imido Complex with NHC Ligation: Synthesis, Structure, and Reactivity

机译:具有NHC连接的二坐标钴(II)亚氨基配合物:合成,结构和反应活性

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The synthesis, structural characterization, and reactivity of the first two-coordinate cobalt complex featuring a metal-element multiple bond [(IPr)Co(NDmp)] (4; IPr=1,3-bis(2',6'-diisopropylphenyl)imidazole-2-ylidene; Dmp=2,6-dimesitylphenyl) is reported. Complex 4 was prepared from the reaction of [(IPr)Co(eta(2)-vtms)(2)] (vtms=vinyltrimethylsilane) with DmpN(3). An X-ray diffraction study revealed its linear C-Co-N core and a short Co-N distance (1.691(6) angstrom). Spectroscopic characterization and calculation studies indicated the high-spin nature of 4 and the multiplebond character of the Co-N bond. Complex 4 effected group-transfer reactions to CO and ethylene to form isocyanide and imine, respectively. It also facilitated E-H (E=C, Si) sigma-bond activation of terminal alkyne and hydrosilanes to produce the corresponding cobalt(II) alkynyl and cobalt(II) hydride complexes as 1,2-addition products.
机译:具有金属元素多键[(IPr)Co(NDmp)](4; IPr = 1,3-bis(2',6'-二异丙基苯基)的第一个双配位钴配合物的合成,结构表征和反应活性)咪唑-2-亚烷基; Dmp = 2,6-二甲基苯并苯基)。配合物4是由[(IPr)Co(eta(2)-vtms)(2)](vtms =乙烯基三甲基硅烷)与DmpN(3)反应制备的。 X射线衍射研究显示其线性C-Co-N核芯和较短的Co-N距离(1.691(6)埃)。光谱表征和计算研究表明4的高自旋性质和Co-N键的多重键特征。配合物4进行基团转移反应至CO和乙烯,分别形成异氰化物和亚胺。它还促进了末端炔烃和氢硅烷的E-H(E = C,Si)sigma键活化,从而生成相应的钴(II)炔基和钴(II)氢化物络合物作为1,2-加成产物。

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