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首页> 外文期刊>Inorganica Chimica Acta >STUDY OF THE AQUEOUS REACTIONS OF K[PT(PH2SO)CL-3] WITH NITRILE LIGANDS AND CRYSTAL STRUCTURES OF N(C4H9)(4)[PT(PH2SO)CL-3], N(C2H5)(4)[PT(PH2SO)BR-3] AND CIS-PT(PH2SO)(C3H5CN)CL-2
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STUDY OF THE AQUEOUS REACTIONS OF K[PT(PH2SO)CL-3] WITH NITRILE LIGANDS AND CRYSTAL STRUCTURES OF N(C4H9)(4)[PT(PH2SO)CL-3], N(C2H5)(4)[PT(PH2SO)BR-3] AND CIS-PT(PH2SO)(C3H5CN)CL-2

机译:N [C4H9)(4)[PT(PH2SO)CL-3],N(C2H5)(4)[PT()(K(PT(PH2SO)CL-3)与腈配体和晶体结构的水反应)的研究PH2SO)BR-3]和CIS-PT(PH2SO)(C3H5CN)CL-2

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The aqueous reactions of K[Pt(Ph2SO)Cl-3] with nitriles were studied in different conditions of pH, mainly by Pt-195 and H-1 NMR. At normal pH (approximate to 2.4), the ligands R-CN have produced the neutral complexes Pt(Ph2SO)(R-CN)Cl-2. For acetonitrile, only the cis isomer was obtained, while for other nitriles a mixture of the two isomers was formed. The Pt-195 NMR spectra of the compounds were measured. The signals of the cis isomers were observed around -3040 ppm, while those of the trans isomers were found around -3180 ppm. The study has shown that the first product formed is the traits isomer, which then isomerizes partially to the cis compounds. The Pt-195 NMR spectra of the products obtained in neutral medium (pH adjusted to similar to 7 with NaOH) have shown several signals depending on the nitrile. Dimeric species of the type Pt(Ph2SO)Cl(mu-NHC(R)O)(2)Pt(Ph2SO)Cl are suggested to exist in solution. Head-to-head and head-to-tail isomers are probably formed. The crystal structures of N(C4H9)(4)[Pt(Ph2SO)Cl-3] (I), N(C2H5)(4)[Pt(Ph2SO)Br-3] (II) and cis-Pt(Ph2SO)(C3H5CN)Cl-2 (III) were determined. The chloro ionic complex is triclinic, P-1, with a = 10.674(2), b = 11.424(2), c = 13.731(2) Angstrom, alpha = 89.54(1), beta = 83.27(1), gamma = 80.48(1)degrees, Z = 2 and R = 0.042, while the bromo complex is monoclinic, P2(1), with a = 11.258(3), b = 19.425(4), c = 11.590(2) Angstrom, beta = 102.62(2)degrees, Z = 4 and R = 0.053. Crystal III is orthorhombic, space group P2(1)2(1)2(1), a = 9.532(3), b = 11.787(2), c = 15.464(4) Angstrom, Z = 4 and R = 0.031. The compound is the cis isomer. For crystal I, the Pt-Cl bond in trans position to the sulfoxide is 2.312(2) Angstrom. while the cis bonds are 2.282(2) and 2.299(2) Angstrom. For the bromo compound (II), the Pt-Br bonds vary between 2.397(3) and 2.421(3) Angstrom. In crystal III, the Pt-Cl bond located in trans position to the nitrile is considerably shorter (2.269(3) Angstrom) than the Pt-Cl bond in trans position to the sulfoxide ligand (2.311(3) Angstrom). The Pt-S bond distances vary between 2.201(2) and 2.228(3) Angstrom. (C) 1997 Elsevier Science S.A. [References: 36]
机译:主要通过Pt-195和H-1 NMR研究了在不同pH条件下K [Pt(Ph2SO)Cl-3]与腈的水反应。在正常pH(约2.4)下,配体R-CN产生了中性络合物Pt(Ph2SO)(R-CN)Cl-2。对于乙腈,仅获得顺式异构体,而对于其他腈,则形成两种异构体的混合物。测量了化合物的Pt-195 NMR光谱。在-3040ppm附近观察到顺式异构体的信号,而在-3180ppm附近观察到反式异构体的信号。研究表明,形成的第一个产物是性状异构体,然后部分异构化为顺式化合物。在中性介质(pH用NaOH调节至接近7的pH)中获得的产物的Pt-195 NMR谱图显示了几种信号,具体取决于腈。建议在溶液中存在Pt(Ph2SO)Cl(mu-NHC(R)O)(2)Pt(Ph2SO)Cl类型的二聚体。可能形成了头对头和头对尾的异构体。 N(C4H9)(4)[Pt(Ph2SO)Cl-3](I),N(C2H5)(4)[Pt(Ph2SO)Br-3](II)和顺式Pt(Ph2SO)的晶体结构测定了(C3H5CN)Cl-2(III)。氯离子络合物是三斜晶系的P-1,a = 10.674(2),b = 11.424(2),c = 13.731(2)埃,alpha = 89.54(1),beta = 83.27(1),gamma = 80.48(1)度,Z = 2和R = 0.042,而溴复合物是单斜晶系,P2(1)/ n,a = 11.258(3),b = 19.425(4),c = 11.590(2)埃,β= 102.62(2)度,Z = 4,R = 0.053。晶体III是正交晶体,空间群P2(1)2(1)2(1),a = 9.532(3),b = 11.787(2),c = 15.464(4)埃,Z = 4和R = 0.031。该化合物是顺式异构体。对于晶体I,与亚砜反位的Pt-Cl键为2.312(2)埃。而顺式键为2.282(2)和2.299(2)埃。对于溴化合物(II),Pt-Br键在2.397(3)和2.421(3)埃之间变化。在晶体III中,与腈亚砜配体的反式位置的Pt-Cl键(2.311(3)埃)相对于腈的反式位置的Pt-Cl键(2.269(3)埃)短得多。 Pt-S键距在2.201(2)和2.228(3)埃之间变化。 (C)1997 Elsevier Science S.A. [参考:36]

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