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首页> 外文期刊>Transition Metal Chemistry >Synthesis, ~(119)Sn Mossbauer spectroscopic studies and X-ray crystal structure determination of new seven-coordinate diorganotin(IV) complexes with S,N,N,N,S-pentadentate Schiff bases derived from 2,6-diacetylpyridine of S-methyl- and S-benzyldithiocarbazates
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Synthesis, ~(119)Sn Mossbauer spectroscopic studies and X-ray crystal structure determination of new seven-coordinate diorganotin(IV) complexes with S,N,N,N,S-pentadentate Schiff bases derived from 2,6-diacetylpyridine of S-methyl- and S-benzyldithiocarbazates

机译:合成,〜(119)Sn Mossbauer光谱研究和X射线晶体结构测定与S,N,N,N,S-五齿Schiff碱衍生自S的2,6-二乙酰基吡啶的新型七坐标二有机锡(IV)配合物-甲基-和S-苄基二硫代氨基甲酸酯

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摘要

The reactions of the ligands 2,6-diacetylpyridine bis(S-methyldithiocarbazate)] (H2dapmdtc) and 2,6-diacetylpyridine bis(S-benzyldithiocarbazate)] (H2dapbdtc) with R_(4-m)SnCl_m (R = Me, ~nBu, Ph; and m = 2) led to the formation of six seven-coordinate diorganotin(IV) complexes, which were studied by microanalysis, i.r., n.m.r (~1H, ~(119)Sn) and Mossbauer spectroscopies. The X-ray structures determination of complexes [Me2Sn(dapmdtc)], [Me2Sn(dapbdtc)] and [Ph2Sn(dapbdtc)] revealed the presence of neutral seven-coordinated complexes. The structures consist of monomeric units in which the Sn(IV) atom exhibits distorted pentagonal bipyramidal (PBP) geometry, with the S,N,N,N,S-donor systems of the ligands lying in the equatorial plane and organic groups in the apical positions. A correlation between Mossbauer and X-ray data based on the point-charge model is discussed.
机译:配体2,6-二乙酰吡啶双(S-甲基二硫代氨基甲酸酯)[H2dapmdtc)和2,6-二乙酰吡啶双(S-苄基二硫代氨基甲酸酯)](H2dapbdtc)与R_(4-m)SnCl_m(R = Me,〜 nBu,Ph;和m = 2)导致形成六种七配位的二有机锡(IV)配合物,这些配合物通过微量分析,ir,nmr(〜1H,〜(119)Sn)和Mossbauer光谱学进行了研究。配合物[Me2Sn(dapmdtc)],[Me2Sn(dapbdtc)]和[Ph2Sn(dapbdtc)]的X射线结构测定表明存在中性的7位配位配合物。该结构由单体单元组成,其中Sn(IV)原子表现出扭曲的五边形双锥体(PBP)几何形状,配体的S,N,N,N,S供体系统位于赤道平面内,而有机基团位于根尖位置。讨论了基于点电荷模型的Mossbauer与X射线数据之间的相关性。

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