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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 >Syntheses, reactivity, and crystal structures of molybdenum complexes with pyridine-2-thionate (pyS)-containing ligands: Crystal structures of [Mo(eta(3)-C3H5)(CO)(2)](2)(mu-eta(1),eta(2)-pyS)(2), exo-[Mo(eta(3)-C3H5)(CO)(eta(2)-pyS)(eta(2)-dppe)], [
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Syntheses, reactivity, and crystal structures of molybdenum complexes with pyridine-2-thionate (pyS)-containing ligands: Crystal structures of [Mo(eta(3)-C3H5)(CO)(2)](2)(mu-eta(1),eta(2)-pyS)(2), exo-[Mo(eta(3)-C3H5)(CO)(eta(2)-pyS)(eta(2)-dppe)], [

机译:含吡啶-2-硫酸酯(pyS)配体的钼配合物的合成,反应性和晶体结构:[Mo(eta(3)-C3H5)(CO)(2)](2)(mu-eta)的晶体结构(1),eta(2)-pyS)(2),exo- [Mo(eta(3)-C3H5)(CO)(eta(2)-pyS)(eta(2)-dppe)],[

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摘要

The doubly bridged pyridine-2-thionate (pyS) dimolybdenum complex [Mo(eta(3)-C3H5)(CO)(2)](2)(mu-eta(1),eta(2)-pyS)(2) (1) is accessible by the reaction of [Mo(eta(3)-C3H5)(CO)(2)(CH3CN)(2)Br] with pySK in methanol at room temperature. Complex I reacts with piperidine in acetonitrile to give the complex [Mo(eta(3)-C3H5)(CO)(2)(eta(2)-pyS) (C5H10NH)] (2). Treatment of I with 1,10-phenanthroline (phen) results in the formation of complex [Mo(eta(3)-C3H5)(CO)2(eta(1)-pyS)(phen)] (3), in which the pyS ligand is coordinated to Mo through the sulfur atom. Four conformational isomers, endo,exo-complexes [Mo(eta(3)-C3H5)(CO)(eta(2)-pyS)(eta(2)-diphos)] (diphos = dppm, 4a-4d; dppe, 5a-5d), are accessible by the reactions of 1 with dppm and dppe in refluxing acetonitrile. Homonuclear shift-correlated 2-D P-31{H-1}-P-31{H-1} NMR experiments of the mixtures 4a-4d have been employed to elucidate the four stereoisomers. The reaction of 4 and pySK or [MO(CO)(3)(eta(1)-SC5H4NH)(eta(2)-dppm)] (6) and O-2 affords allyl-displaced seven-coordinate bis(pyridine-2-thionate) complex [MO(CO)(eta(2)-PYS)(2)(eta(2)-dppm)] (7). All of the complexes are identified by spectroscopic methods, and complexes 1, 5d, 6, and 7 are determined by single-crystal X-ray diffraction. Complexes 1 and 5d crystallize in the orthorhombic space groups Pbcn and Pbca with Z = 4 and 8, respectively, whereas 6 belongs to the monoclinic space group C2/c with Z = 8 and 7 belongs to the triclinic space group P (1) over bar with Z = 2. The cell dimensions are as follows: for 1, a = 8.3128(1) Angstrom, b = 16.1704(2) Angstrom, c = 16.6140(2) Angstrom; for 5d, a = 17.8309(10) Angstrom, b = 17.3324(10) Angstrom, c = 20.3716(11) Angstrom; for 6, a = 18.618(4) Angstrom, b 16.062(2) Angstrom, c 27.456(6) Angstrom, p = 96.31(3)degrees; for 7, a = 9.1660(2) Angstrom, b = 12.0854(3) Angstrom, c = 15,9478(4) Angstrom, alpha = 78.4811(10)degrees, beta = 80.3894(10)degrees, gamma = 68.7089(11)degrees. [References: 30]
机译:双桥吡啶-2-硫代吡啶(pyS)二钼配合物[Mo(eta(3)-C3H5)(CO)(2)](2)(mu-eta(1),eta(2)-pyS)(2 )(1)可在室温下通过[Mo(eta(3)-C3H5)(CO)(2)(CH3CN)(2)Br]与pySK在甲醇中的反应获得。配合物I与哌啶在乙腈中反应生成配合物[Mo(eta(3)-C3H5)(CO)(2)(eta(2)-pyS)(C5H10NH)](2)。用1,10-菲咯啉(phen)处理I会形成复合物[Mo(eta(3)-C3H5)(CO)2(eta(1)-pyS)(phen)](3),其中pyS配体通过硫原子与Mo配位。四个构象异构体,内,外复合物[Mo(eta(3)-C3H5)(CO)(eta(2)-pyS)(eta(2)-diphos)](diphos = dppm,4a-4d; dppe, 1与dppm和dppe在回流乙腈中的反应可得到5a-5d)。混合物4a-4d的同核位移相关的2-D P-31 {H-1} -P-31 {H-1} NMR实验已用于阐明这四种立体异构体。 4与pySK或[MO(CO)(3)(eta(1)-SC5H4NH)(eta(2)-dppm)](6)和O-2的反应提供了烯丙基取代的七坐标双(吡啶- 2-硫酸酯)络合物[MO(CO)(η(2)-PYS)(2)(η(2)-dppm)](7)。所有配合物均通过光谱法鉴定,配合物1、5d,6和7通过单晶X射线衍射测定。配合物1和5d分别在Z = 4和8的正交空间群Pbcn和Pbca中结晶,而6属于Z = 8的单斜空间群C2 / c,7属于三斜晶空间群P(1)。 Z = 2的条形。单元格尺寸如下:对于1,a = 8.3128(1)埃,b = 16.1704(2)埃,c = 16.6140(2)埃;对于5d,a = 17.8309(10)埃,b = 17.3324(10)埃,c = 20.3716(11)埃;对于6,a = 18.618(4)埃,b 16.062(2)埃,c 27.456(6)埃,p = 96.31(3)度;对于7,a = 9.1660(2)埃,b = 12.0854(3)埃,c = 15,9478(4)埃,alpha = 78.4811(10)度,beta = 80.3894(10)度,γ= 68.7089(11 )度。 [参考:30]

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