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首页> 外文期刊>Angewandte Chemie >Synthesis, Electronic Structure, and Reactivity of a Planar Four-Coordinate, Cobalt-Imido Complex
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Synthesis, Electronic Structure, and Reactivity of a Planar Four-Coordinate, Cobalt-Imido Complex

机译:平面四坐标,钴-imido复合物的合成,电子结构和反应性

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摘要

A four-coordinate cobalt-imido complex, ((tBu)mPNP)Co=NMes ((tBu)mPNP=modified PNP pincer ligand) has been synthesized from addition of 2,4,6-trimethylphenylazide (Mes-N-3) to the corresponding dinitrogen complex. The solid-state structure determined by X-ray diffraction established a rare, idealized planar geometry with a Co=N bond distance of 1.716(2) angstrom. Magnetic measurements revealed an S=1 ground state with CAS-SCF calculations supporting radical character on the imide nitrogen. Thermolysis of the cobalt-imido compound induced selective insertion of the imido group into a Co-P bond and yielded a three-coordinate cobalt complex with a distorted T-shaped geometry. Transition state analysis conducted with DFT calculations established the thermodynamic stability of the P-N coupled product and provided insight into the exclusive selectivity.
机译:将2,4,6-三甲基苯基叠氮化物(Mes-N-3)加入相应的二氮络合物中,合成了一种四配位钴亚胺络合物((tBu)mPNP)Co=NMes((tBu)mPNP=修饰的PNP钳形配体)。由X射线衍射确定的固态结构建立了一种罕见的理想平面几何结构,Co=N键距为1.716(2)埃。磁性测量揭示了S=1基态,CAS-SCF计算支持酰亚胺氮的自由基特征。钴-亚氨基化合物的热分解导致亚氨基基团选择性插入Co-P键,并产生具有扭曲T形几何形状的三配位钴络合物。通过DFT计算进行的过渡态分析确定了P-N偶合产物的热力学稳定性,并提供了独家选择性的见解。

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