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Synthesis, spectral, thermal, and a crystalline structure of complexes containing [MeC(CH_2PPh_2)_3Cu(I)]

机译:含[MeC(CH_2PPh_2)_3Cu(I)]的配合物的合成,光谱,热和晶体结构

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摘要

The preparation of new [MeC(CH_2PPh_2)_3CuCl] 1 and its derivatives was carried out directly by mixing of CuCl and MeC(CH_2PPh_2)_3 ligand in dry THF, the neutral precursor 1 served to prepare [MeC(CH_2PPh_2) _3Cu(NCCH_3)]BF_4 2 and [MeC(CH _2PPh_2)_3Cu(PCH_2Ph) _3]BF_4 3. These complexes are characterized on the basis of elemental analysis, IR, EDS, ~1H, ~(13)C and ~(31)P{~1H}NMR, FAB-MS, TG/DTA and single-crystal X-ray diffraction studies. Complex 1 crystallizes in the Orthorhombic unit cells with the space group Pna2(1). The structural behavior of MeC(CH_2PPh _2)_3 ligand in the formed complexes during the coordination reaction was monitored by ~(31)P{~1H}NMR in CDCl_3 at room temperature for the first time.
机译:通过在干燥的THF中混合CuCl和MeC(CH_2PPh_2)_3配体直接进行新的[MeC(CH_2PPh_2)_3CuCl] 1及其衍生物的制备,中性前体1用于制备[MeC(CH_2PPh_2)_3Cu(NCCH_3) ] BF_4 2和[MeC(CH _2PPh_2)_3Cu(PCH_2Ph)_3] BF_4 3.基于元素分析,IR,EDS,〜1H,〜(13)C和〜(31)P {〜 1 H NMR,FAB-MS,TG / DTA和单晶X射线衍射研究。配合物1在正交晶胞中以空间群Pna2(1)结晶。首次在室温下于CDCl_3中通过〜(31)P {〜1H} NMR监测配位反应过程中MeC(CH_2PPh _2)_3配体在形成的配合物中的结构行为。

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