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首页> 外文期刊>Organometallics >Stabilizing the RSn(μ_2-O)SnR motif through intramolecular N→Sn coordination. synthesis and characterization
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Stabilizing the RSn(μ_2-O)SnR motif through intramolecular N→Sn coordination. synthesis and characterization

机译:通过分子内N→Sn配位稳定RSn(μ_2-O)SnR基序。合成和表征

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摘要

The reactions of RSnCl_3 (1; R = 2-(phenylazo)phenyl) with FcCOOH or di-tert-butyl phosphate in refluxing THF afforded the monoorganodistannoxanes (RSn)_2(μ_2-O)(μ_2- FcCOO)_2(η-FcCOO)_2·THF (2) and {(RSn)_2(μ_2-O)(t-BuO)_2PO_2_2Cl_2}·THF·2H_2O (3). The molecular structure of 2 contains seven-coordinate tin centers in a distorted-pentagonal- bipyramidal geometry, while 3 contains six-coordinate tin centers in a distorted-octahedral geometry. In the dinuclear compounds 2 and 3 the two tin centers are bridged by a μ_2-O unit, affording a rare Sn-O-Sn motif among monoorganostannoxanes. In addition, each tin is also intramolecularly coordinated to the nitrogen atom of the 2-phenylazophenyl substituent (N→Sn). Further, in 2, the two tin centers are bridged by two isobidentate ferrocenecarboxylate ligands; each tin center also is bound to a chelating ferrocenecarboxylate ligand. On the other hand, in 3, while the two tin centers are bridged by two isobidentate di-tert-butyl phosphate ligands, each tin center also has a terminal chloride ligand.
机译:RSnCl_3的反应(1;R = 2-(苯偶氮)苯基)与FcCOOH或磷酸二叔丁酯在回流THF中得到单有机二烟烷[(RSn)_2(μ_2-O)(μ_2-FcCOO)_2(η-FcCOO)_2]·THF (2) 和 {(RSn)_2(μ_2-O)[(t-BuO)_2PO_2]_2Cl_2}·THF·2H_2O (3).2 的分子结构在扭曲的五边形双锥体几何中包含七配位锡中心,而 3 在扭曲的八面体几何中包含六配位锡中心。在双核化合物 2 和 3 中,两个锡中心由 μ_2-O 单元桥接,在单有机单烷中提供了罕见的 Sn-O-Sn 基序。此外,每个锡还与2-苯基偶氮苯取代基(N→Sn)的氮原子进行分子内配位。此外,在图2中,两个锡中心由两个异二烯酸二茂铁羧酸配体桥接;每个锡中心也与螯合二茂铁羧酸配体结合。另一方面,在3中,虽然两个锡中心由两个异二烯酸二叔丁基磷酸配体桥接,但每个锡中心也有一个末端氯化物配体。

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