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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >SYNTHESIS AND NMR INVESTIGATION OF DIRHODIUM(II) FORMAMIDINATE COMPLEXES CONTAINING BIDENTATE PHOSPHORUS DONORS - X-RAY CRYSTAL STRUCTURE OF THE ORTHO-METALATED COMPLEX RH-2(FORM)(MU-O2CCF3)[(C6H4)(C6H5)P-(CH2)(2)P(C6H5)(2)](SIGMA-O2CCF3)(P-TO LUIDIN
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SYNTHESIS AND NMR INVESTIGATION OF DIRHODIUM(II) FORMAMIDINATE COMPLEXES CONTAINING BIDENTATE PHOSPHORUS DONORS - X-RAY CRYSTAL STRUCTURE OF THE ORTHO-METALATED COMPLEX RH-2(FORM)(MU-O2CCF3)[(C6H4)(C6H5)P-(CH2)(2)P(C6H5)(2)](SIGMA-O2CCF3)(P-TO LUIDIN

机译:含二齿磷酸盐供体的甲AMI二甲酸二(II)配合物的合成及NMR研究-邻位修饰的配合物RH-2(FORM)(MU-O2CCF3)[(C6H4)((C6H5))的X射线晶体结构(2)P(C6H5)(2)](SIGMA-O2CCF3)(P-LUIDIN

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The reactivity of bidentate P-donors with dirhodium(II) complexes, leading to a further example of orthometalation across the Rh-2(4+) core, is reported. The dirhodium(II) formamidinate complex Rh-2(form)(2)(O-2-CCF3)(2)(H2O)(2) (form = N,N'-di-p-tolylformamidinate anion) easily reacts with diphosphines giving products whose nature is critically dependent on the aliphatic chain length. While the short-bite dppm is able to coordinate in equatorial position across the Rh-2(4+) core, the reaction with dppe proceeds via ortho-metalation of the diphosphine giving a further evidence of the versatility of the above fragment toward ortho-metalation. [References: 24]
机译:报道了二齿P-供体与dirhodium(II)配合物的反应性,这导致了跨Rh-2(4+)核心的正金属化的另一个例子。 ho(II)甲ami酸盐络合物Rh-2(form)(2)(O-2-CCF3)(2)(H2O)(2)(form = N,N'-di-p-tolylformamimidate anion)容易与二膦类化合物,其性质严格取决于脂肪族链的长度。虽然短片段dppm能够在整个Rh-2(4+)核的赤道位置上进行配位,但与dppe的反应是通过二膦的正金属化进行的,从而进一步证明了上述片段对邻位的多功能性。金属化。 [参考:24]

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