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Reactivity of a Methoxido-Ruthenium Complex Bearing a Pincer-Type Bis(carbene) Ligand toward Thiocyanate, Carbon Disulfide, and Isothiocyanate

机译:带有钳形双(卡宾)配体的甲氧基钌配合物对硫氰酸盐,二硫化碳和异硫氰酸盐的反应性

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摘要

Thiocyanate linkage isomers and two insertion complexes were prepared from a methoxido–ruthenium complex bearing a 2,6-bis(3-tert-butylimidazol-2-ylidene)pyridine (CNC) and a bipyridine ligand. In the mixture of the linkage isomers obtained from the substitution reaction, a linear N-bound and a bent S-bound isomer were crystallographically determined, and the equilibrium between them at elevated temperature was revealed. On the other hand, in reactions with carbon disulfide (CS2) and phenyl isothiocyanate (PhNCS), the S=C bond was inserted into the Ru–OMe bond, and the resulting ligands are bound to the ruthenium center by the sulfur atom.
机译:硫氰酸酯键联异构体和两个插入配合物是由带有2,6-双(3-叔丁基咪唑-2-亚甲基)吡啶(CNC)和联吡啶配体的甲氧基-钌配合物制得的。在由取代反应获得的键合异构体的混合物中,通过晶体学确定线性的N-键和弯曲的S-键的异构体,并揭示了它们在高温下的平衡。另一方面,在与二硫化碳(CS2)和异硫氰酸苯酯(PhNCS)的反应中,将S = C键插入Ru-OMe键中,并且所得配体通过硫原子与钌中心键合。

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