首页> 外文期刊>Journal of the American Chemical Society >Metallosupramolecular chemistry with bis(benzene-o-dithiolato) ligands - art. no. JA063655U
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Metallosupramolecular chemistry with bis(benzene-o-dithiolato) ligands - art. no. JA063655U

机译:具有双(苯-邻-二硫代巯基)配体的金属超分子化学-艺术。没有。 JA063655U

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摘要

The bis(benzene-o-dithiol) ligands H-4-1, H-4-2, and H-4-3 react with [Ti(OC2H5)(4)] to give dinuclear triple-stranded helicates [Ti2L3](4-) (L = 1(4-), 2(4-), 3(4-)). NMR spectroscopic investigations revealed that the complex anions possess C-3 symmetry in solution. A crystal structure analysis for (PNP)(4)[Ti-2(2)(3)] ((PNP)(4)-[14]) confirmed the C-3 symmetry for the complex anion in the solid state. The complex anion in Li(PNP)(3)[Ti-2(1)(3)] (Li(PNP)(3)[13]) does not exhibit C-3 symmetry in the solid state due to the formation of polymeric chains of lithium bridged complex anions. Complexes [13](4-) and [14](4-) were obtained as racemic mixtures of the Delta, Delta and Lambda, Lambda isomers. In contrast to that, complex (PNP)(4)[Ti-2(3)(3)] ((PNP)(4)[15]) with the enantiomerically pure chiral ligand 3(4-) shows a strong Cotton effect in the CD spectrum, indicating that the chirality of the ligands leads to the formation of chiral metal centers. The o-phenylene diamine bridged bis(benzene-o-dithiol) ligand H-4-4 reacts with Ti4+ to give the dinuclear double-stranded complex Li-2[Ti-2(4)(2)(mu-OCH3)(2)] containing two bridging methoxy ligands between the metal centers. The crystal structure analysis and the H-1 NMR spectrum of (Ph4As)(2)[Ti-2(4)(2)(mu-OCH3)(2)] ((Ph4As)(2)[(16]) reveal C-2 symmetry for the anion [Ti-2(4)(2)(mu-OCH3)(2)](2-). For a comparative study the dicatechol ligand H-4-5, containing the same o-phenylene diamine bridging group as the bis(benzene-o-dithiol) ligands H-4-4, was prepared and reacted with [TiO(acac)(2)] to give the dinuclear complex anion [Ti-2(5)(2)(mu-OCH3)(2)](2-). The molecular structure of (PNP)(2)[Ti-2(5)(2)(mu-OCH3)(2)] ((PNP)(2)[17]) contains a complex anion which is similar to [16](2-), with the exception that strong N-H center dot center dot center dot O hydrogen bonds are formed in complex anion [17](2-), while N-H center dot center dot center dot S hydrogen bonds are absent in complex anion [16](2-).
机译:双(苯-邻-二硫醇)配体H-4-1,H-4-2和H-4-3与[Ti(OC2H5)(4)]反应,生成双核三链螺旋结构[Ti2L3]( 4-)(L = 1(4-),2(4-),3(4-))。 NMR光谱研究表明,该复合阴离子在溶液中具有C-3对称性。 (PNP)(4)[Ti-2(2)(3)]((PNP)(4)-[14])的晶体结构分析证实了固态阴离子的C-3对称性。 Li(PNP)(3)[Ti-2(1)(3)](Li(PNP)(3)[13])中的配位阴离子由于形成锂桥接的复合阴离子的聚合物链。以δ,δ和λ,λ异构体的外消旋混合物的形式得到络合物[13](4-)和[14](4-)。与此相反,具有对映体纯手性配体3(4-)的复合物(PNP)(4)[Ti-2(3)(3)]((PNP)(4)[15])显示出很强的棉花效应在CD光谱中,表明配体的手性导致手性金属中心的形成。邻苯二胺桥联的双(苯-邻二硫醇)配体H-4-4与Ti4 +反应生成双核双链络合物Li-2 [Ti-2(4)(2)(mu-OCH3)( 2)]在金属中心之间包含两个桥接的甲氧基配体。 (Ph4As)(2)[Ti-2(4)(2)(mu-OCH3)(2)]((Ph4As)(2)[(16])的晶体结构分析和H-1 NMR光谱揭示阴离子[Ti-2(4)(2)(mu-OCH3)(2)](2-)的C-2对称性为了进行比较研究,二邻苯二酚配体H-4-5含有相同的邻亚苯基制备了二胺桥联基作为双(苯-邻-二硫醇)配体H-4-4,并与[TiO(acac)(2)]反应生成双核络合物阴离子[Ti-2(5)(2) (mu-OCH3)(2)](2-)。(PNP)(2)[Ti-2(5)(2)(mu-OCH3)(2)]((PNP)(2)的分子结构[17])包含与[16](2-)相似的配位阴离子,不同之处在于在复合阴离子[17](2-)中形成了强NH中心点中心点中心点O氢键。中心阴离子中心阴离子中心点中心点S不存在氢键[16](2-)。

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