首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Silver(I)-mediated isomerisation of trans-[RuCl2(P-P)(2)] (P-P = four-membered ring chelate diphosphine ligand) to cis-[{Ru(P-P)(2)(mu-Cl)(2)}(n)Ag](+) species, and applications in stereoselective syntheses of cis- and trans-[RuCl(L)(P-P)(2)](+) (L =
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Silver(I)-mediated isomerisation of trans-[RuCl2(P-P)(2)] (P-P = four-membered ring chelate diphosphine ligand) to cis-[{Ru(P-P)(2)(mu-Cl)(2)}(n)Ag](+) species, and applications in stereoselective syntheses of cis- and trans-[RuCl(L)(P-P)(2)](+) (L =

机译:银(I)介导的反式-[RuCl2(PP)(2)](PP =四元环螯合物二膦配体)异构化为顺式-[{Ru(PP)(2)(mu-Cl)(2) }(n)Ag](+)物种及其在顺式和反式[RuCl(L)(PP)(2)](+)的立体选择性合成中的应用(L =

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When complexes trans-[RuCl2(diphos)(2)] (diphos=(Ph2P)(2)C=CH2, Ph2PCH2PPh2 or Ph2PNHPPh2) were treated with silver salts of poorly coordinating anions (e.g. AgBF4, AgO3SCF3) in 1,2-dichloroethane halide abstraction was slow, even at reflux, and the reaction proceeded by an interesting mechanism involving a trans to cis isomerisation. At room temperature, a complex, characterized as [RuCl(diphos)(2)(mu -Cl)Ag](+), forms. When heated to reflux for 5-10 min this reacts to give a mixture, which includes cis-[RuCl2(diphos)(2)], and species of the type [{Ru(diphos)(2)(mu -Cl)(2)}(n)Ag](+) (n=1 or 2) in which the exact coordination geometry at Ag-I is unknown. The reactions have been followed by P-31-{H-1} NMR spectroscopy, and electronic spectroscopy results also support the isomerisation. The ruthenium and silver K-edge EXAFS spectra of the solid isolated from the reaction of trans-[RuCl2(dppm)(2)] and AgO3SCF3 lend support to this formulation; in particular, the best fit for the silver(I) environment includes coordination to one oxygen (from the -O3SCF3; Ru-O 2.43 Angstrom), two Cl (2.79 Angstrom) and between one and two Ru (3.94 Angstrom). Over 30-40 min at reflux, AgCl precipitates, the signals due to cis-[RuCl2(diphos)(2)] disappear from the P-31-{H-1} NMR spectra, those due to the [{Ru(diphos)(2)(mu -Cl)(2)}(n)Ag](+) mixture diminish, and new resonances, attributed to five-coordinate [RuCl(diphos)(2)](+), appear. This reaction has been investigated for stereoselective ligand substitution. Treatment of trans-[RuCl2(diphos)(2)] with AgBF4 or AgO3SCF3 in DCE in the presence of CH3CN or CO yields exclusively trans-[RuCl(L)(diphos)(2)](+) (L=CH3CN or CO), but treatment of trans-[RuCl2(diphos)(2)] with AgBF4 or AgO3SCF3 in DCE, followed by treatment with L, usually gave exclusively cis-[RuCl(L)(diphos)(2)](+) (L=CH3CN or CO). [References: 47]
机译:当将反式[RuCl2(diphos)(2)](diphos =(Ph2P)(2)C = CH2,Ph2PCH2PPh2或Ph2PNHPPh2)的络合物在1,2-中用配位不佳的阴离子的银盐(例如AgBF4,AgO3SCF3)处理。即使在回流下,二氯乙烷卤化物的提取也很慢,并且反应是通过有趣的机理进行的,该机理涉及反式至顺式异构化。在室温下,形成特征为[RuCl(diphos)(2)(mu -Cl)Ag](+)的配合物。加热至回流5-10分钟后,其反应生成混合物,其中包括顺式[RuCl2(diphos)(2)]和[{Ru(diphos)(2)(mu -Cl)( 2)}(n)Ag](+)(n = 1或2),其中Ag-1的确切配位几何是未知的。反应之后进行了P-31- {H-1} NMR光谱分析,电子光谱结果也支持了异构化反应。从反式[RuCl2(dppm)(2)]和AgO3SCF3的反应中分离出的固体的钌和银K边缘EXAFS光谱为该配方提供了支持;特别是,最适合银(I)环境的化合物包括与一个氧(来自-O3SCF3; Ru-O为2.43埃),两个Cl(2.79埃)以及一到两个Ru(3.94埃)之间的配位。在回流下超过30-40分钟,AgCl沉淀,由顺式[RuCl2(diphos)(2)]引起的信号从P-31- {H-1} NMR光谱中消失,而由[{Ru(diphos) )(2)(mu -Cl)(2)}(n)Ag](+)混合物减少,并且出现了归因于五坐标[RuCl(diphos)(2)](+)的新共振。已经研究了该反应的立体选择性配体取代。在存在CH3CN或CO的情况下,在DCE中用AgBF4或AgO3SCF3处理反式[RuCl2(diphos)(2)]时,仅产生反式[[RuCl(L)(diphos)(2)](+)(L = CH3CN或CO),但在DCE中用AgBF4或AgO3SCF3处理反式[RuCl2(diphos)(2)],然后用L处理,通常只得到顺式[RuCl(L)(diphos)(2)](+) (L = CH3CN或CO)。 [参考:47]

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