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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 >POLYDENTATE N2S2O AND N2S2O2 LIGANDS AS ALCOHOLIC DERIVATIVES OF (N,N'-BIS(2-MERCAPTOETHYL)-1,5-DIAZACYCLOOCTANE)NICKEL(II) AND (N,N'-BIS(2-MERCAPTO-2-METHYLPROPANE)-1,5-DIAZACYCLOOCTANE)NICKEL(II)
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POLYDENTATE N2S2O AND N2S2O2 LIGANDS AS ALCOHOLIC DERIVATIVES OF (N,N'-BIS(2-MERCAPTOETHYL)-1,5-DIAZACYCLOOCTANE)NICKEL(II) AND (N,N'-BIS(2-MERCAPTO-2-METHYLPROPANE)-1,5-DIAZACYCLOOCTANE)NICKEL(II)

机译:多齿N2S2O和N2S2O2配成(N,N'-BIS(2-巯基乙基)-1,5-二氮杂环丙烷)NICKEL(II)和(N,N'-BIS(2-巯基-2-甲基丙烷)- 1,5-二氮杂环丙烷)尼科尔(II)

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The synthesis, structural characterization, spectroscopic, and electrochemical properties of N2S2-ligated Ni-II complexes, (N,N'-bis(2-mercaptoethyl)-1,5-diazacyclooctane)nickel(II), (bme-daco)Ni-II, and (N,N'-bis(2-mercapto-2-methylpropane)1, ,5-diazacyclooctane)nickel(II), (bme*-daco)Ni-II, derivatized at S with alcohol-containing alkyl functionalities, are described. Reaction of (bme-daco)Ni-II with 2-iodoethanol afforded isomers, (N,N'-bis(5-hydroxy-3-thiapentyl)-1,5-diazacyclooctane-O,N,N' iodide (halo = chloro or iodo), 1, and (N,N'-bis(5-hydroxy-3-thiapentyl)-1,5-diazacyclooctane iodide, 2, which differ in the utilization of binding sites in a potentially hexadentate N2S2O2 ligand. Blue complex 1 contains nickel in an octahedral environment of N(2)S(2)OX donors; X is best modeled as Cl. It crystallizes in the monoclinic space group P2(1) with a = 12.580(6) Angstrom, b = 12.291(6) Angstrom, c = 13.090(7) Angstrom, beta = 97.36(4)degrees, and Z = 4. In contrast, red complex 2 binds only the N2S2 donor set forming a square planar nickel complex, leaving both -CH2CH2OH arms dangling; the iodide ions serve strictly as counterions. 2 crystallizes in the orthorhombic space group Pca2(1) with a = 15.822(2) Angstrom, b = 13.171(2) Angstrom, c = 10.0390(10) Angstrom, and Z = 4. Reaction of (bme-daco)Ni-II with 1,3-dibromo-2-propanol affords another octahedral Ni species with a N2S2OBr donor set, ((5-hydroxy-3,7-dithianonadiyl)-1,5-diazacyclooctane-O,N,N',S,S')bromonick el(II) bromide, 3. Complex 3 crystallizes in the orthorhombic space group Pca2(1) with a = 15.202(5) Angstrom, b = 7.735(2) Angstrom, c = 15.443(4) Angstrom, and Z = 4. Complex 4 . 2CH(3)CN was synthesized from the reaction of (bme*-daco)Ni-II with 1,3-dibromo-2-propanol. It crystallizes in the monoclinic space group P2/c with a = 20.348(5) Angstrom, b = 6.5120(1) Angstrom, c = 20.548(5) Angstrom, and Z = 4. [References: 33]
机译:N2S2连接的Ni-II配合物(N,N'-双(2-巯基乙基)-1,5-二氮杂环辛烷)镍(II),(bme-daco)Ni的合成,结构表征,光谱学和电化学性质-II和(N,N'-双(2-巯基-2-甲基丙烷)1,,5-二氮杂环辛烷)镍(II),(bme * -daco)Ni-II,在S处用含醇烷基衍生化功能,进行了描述。 (bme-daco)Ni-II与2-碘乙醇的反应得到异构体,(N,N'-双(5-羟基-3-噻吩基)-1,5-二氮杂环辛烷-O,N,N'碘化物(卤素=氯或碘)1和(N,N'-双(5-羟基-3-噻吩基)-1,5-二氮环辛烷碘化物2,它们在潜在的六齿N2S2O2配体结合位点的利用上不同。络合物1在N(2)S(2)OX供体的八面体环境中包含镍; X最好用Cl建模。它在单斜空间群P2(1)/ n中结晶,其a = 12.580(6)埃,b = 12.291(6)埃,c = 13.090(7)埃,β= 97.36(4)度,Z =4。相比之下,红色络合物2仅与N2S2供体结合,形成一个方形的平面镍络合物,而两者都- CH2CH2OH臂悬空;碘离子严格用作抗衡离子。2在正交晶体空间群Pca2(1)中结晶,其中a = 15.822(2)埃,b = 13.171(2)埃,c = 10.0390(10)埃,和Z =4。(bme-daco)Ni-II与1,3-二溴-2-丙醇的反应得到另一个八带有N2S2OBr供体集的(a-N-SedOb)镍(a-N-Sed),((5-羟基-3,7-二硫代壬二基)-1,5-二氮杂环辛烷-O,N,N',S,S')溴化el(II)溴化物,3.复合物3在正交晶体空间群Pca2(1)中以a = 15.202(5)埃,b = 7.735(2)埃,c = 15.443(4)埃和Z = 4结晶。由(bme * -daco)Ni-II与1,3-二溴-2-丙醇的反应合成2CH(3)CN。它在a = 20.348(5)埃,b = 6.5120(1)埃,c = 20.548(5)埃和Z = 4的单斜空间群P2 / c中结晶。[参考:33]

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