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首页> 外文期刊>Journal of Organometallic Chemistry >New organotin(IV) complexes of nicotinamide, isonicotinamide and some of their novel phosphoric triamide derivatives: Syntheses, spectroscopic study and crystal structures
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New organotin(IV) complexes of nicotinamide, isonicotinamide and some of their novel phosphoric triamide derivatives: Syntheses, spectroscopic study and crystal structures

机译:烟酰胺,异烟酰胺及其某些新型磷酸三酰胺衍生物的新型有机锡(IV)配合物:合成,光谱研究和晶体结构

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摘要

Three novel phosphoramidate ligands with formula RP(O)R-2', R = Nicotinamide(nia), R' = NHC(CH3)(3)(L-1), NH(C6H11)(L-2); R = isonicotinamide(iso), NH(C6H11) (L-3) and their new organotin(IV) complexes with formula SnCl2(CH3)(2)(X)(2), X = L-1 (C-1), L-2 (C-2), L-3 (C-3) plus SnCl2(CH3)(2)(L-4)(2)(C-4), L-4 = isoP(O)[NHC(CH3)(3)](2), were synthesized and characterized by H-1, C-13, P-31, Sn-119 NMR, IR, UV-Vis spectroscopy and elemental analysis. Two novel complexes of nia and iso with formula SnCl2(CH3)(2)(X)(2), X = nia (C-5), iso (C-6) were also prepared and all the complexes were spectroscopically studied in comparison to their related ligands and to each other. The crystal structure of complexes C-1, C-3, C-4, and C-5 were determined by X-ray crystallography. -Sn-Cl center dot center dot center dot H-N-major hydrogen bonds beside other electrostatic interactions produced a three dimensional polymeric cluster in the crystalline lattice of C-1, C-3, C-5 and a two dimensional polymeric chain in C-4. Results showed that coordination of the phosphoramidate ligand (L-4) to Sn in C-4 has been occurred from the nitrogen site of the pyridine ring similar to C-5, C-6 in which there is no P=O donor site; however, in C-1 and C-3 the active donor site of corresponding ligands is P=O. It seems that in these complexes there is a competition between P=O and N-pyridine donor sites and the influential factor which determines the winner site is the type of substituents on phosphorus atom.
机译:具有式RP(O)R-2'的三个新颖的氨基磷酸酯配体,R =烟酰胺(nia),R'= NHC(CH3)(3)(L-1),NH(C6H11)(L-2); R =异烟酰胺(iso),NH(C6H11)(L-3)及其新型有机锡(IV)配合物,分子式为SnCl2(CH3)(2)(X)(2),X = L-1(C-1) ,L-2(C-2),L-3(C-3)加上SnCl2(CH3)(2)(L-4)(2)(C-4),L-4 = isoP(O)[NHC合成了(CH3)(3)](2),并通过H-1,C-13,P-31,Sn-119 NMR,IR,UV-Vis光谱和元素分析对其进行了表征。还制备了两种新的nia和iso配合物,分子式为SnCl2(CH3)(2)(X)(2),X = nia(C-5),iso(C-6),并进行了光谱比较研究。它们的相关配体以及彼此。配合物C-1,C-3,C-4和C-5的晶体结构通过X射线晶体学测定。 -Sn-Cl中心点中心点中心点HN-主要氢键以及其他静电相互作用在C-1,C-3,C-5的晶格中产生三维聚合物簇,并在C-中生成二维聚合物链4。结果表明,从吡啶环的氮位点(类似于C-5,C-6),没有P = O供体位点,发生了氨基磷酸酯配体(L-4)与C-4中的Sn的配位。然而,在C-1和C-3中,相应配体的活性供体位点为P = O。似乎在这些络合物中,P = O和N-吡啶供体位点之间存在竞争,并且决定胜者位点的影响因素是磷原子上取代基的类型。

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