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A Scandium Complex Bearing Both Methylidene and Phosphinidene Ligands: Synthesis, Structure, and Reactivity

机译:带有亚甲基和亚膦基配体的Scan配合物:合成,结构和反应性

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摘要

The scandium complex bearing both methylidene and phosphinidene ligands, [(LSc)2(mu(2)-CH2)(mu(2)-PDIPP)] (L = [MeC(NDIPP)CHC(NDIPP)Me](-), DIPP = 2,6-(Pr-i)(2)C6H3) (2), has been synthesized, and its reactivity has been investigated. Reaction of scandium methyl phosphide [LSc(Me){P(H)DIPP}] with 1 equiv of scandium dimethyl complex [LScMe2] in toluene at 60 degrees C provided complex 2 in good yield, and the structure of complex 2 was determined by single-crystal X-ray diffraction. Complex 2 easily undergoes nucleophilic addition reactions with CO2, CS2, benzonitrile, and tert-butyl isocyanide. In the above reactions, the unsaturated substrates insert into the Sc-C(methylidene) bond to give some interesting dianionic ligands while the Sc-P(phosphinidene) bond remains untouched. The bonding situation of complex 2 was analyzed using DFT methods, indicating a more covalent bond between the scandium ion and the phosphinidene ligand than between the scandium ion and the methylidene ligand.
机译:带有亚甲基和次膦基配体[[LSc)2(mu(2)-CH2)(mu(2)-PDIPP)]的complex络合物(L = [MeC(NDIPP)CHC(NDIPP)Me](-),已经合成了DIPP = 2,6-(Pr-i)(2)C6H3)(2),并对其反应性进行了研究。甲基methyl磷化物[LSc(Me){P(H)DIPP}]与1当量scan二甲基络合物[LScMe2]在甲苯中的反应在60摄氏度下提供良好的收率,化合物2的结构通过单晶X射线衍射。配合物2容易与CO2,CS2,苄腈和叔丁基异氰化物发生亲核加成反应。在上述反应中,不饱和底物插入Sc-C(亚甲基)键中以产生一些有趣的双阴离子配体,而Sc-P(次膦基)键保持不变。使用DFT方法分析了配合物2的键合情况,表明the离子与次膦配体之间的共价键比than离子与亚甲基配体之间的共价键更多。

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