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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis and characterization of new addition compounds of bis(substituted-salicylaldeh.ydo) cobalt(II) with 2,2 '-bipyridine (bipy). Crystal and molecular structures of [Co-II(3-methoxy-salicylaldehyde)(2)(bipy)] center dot CH3OH (1) and [Co-II(bip
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Synthesis and characterization of new addition compounds of bis(substituted-salicylaldeh.ydo) cobalt(II) with 2,2 '-bipyridine (bipy). Crystal and molecular structures of [Co-II(3-methoxy-salicylaldehyde)(2)(bipy)] center dot CH3OH (1) and [Co-II(bip

机译:双(取代-水杨醛醛.ydo)钴(II)与2,2'-联吡啶(bipy)的新加成化合物的合成与表征。 [Co-II(3-甲氧基-水杨醛)(2)(联吡啶)]中心点CH3OH(1)和[Co-II(bip)的晶体和分子结构

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摘要

The cobalt(II) addition compounds [Co(X-salo)(2)(bipy)], where X-salo is the anion of substituted salicylaldehydes (X = 3-OCH3 (1); 5-CH3 (2); 5-Cl (3); 5-NO2 (4)) and bipy the neutral 2,2'-bipyridine, were synthesized and characterized by physicochemical and spectral (IR, UV-Vis) data. Theoretical calculations (DFT, ZINDO) with GAUSSIAN-03 for the prediction of the electronic spectrum for the compound 1, gave good correlation with the experimental one in the solid state. The absorption spectra at different solvents showed that the compound is stable in CH3CN, but unstable in CH3OH and DMF solutions. The cyclic voltammetry study in CH3CN gave all the expected waves for the redox processes of the metal Co(II) and the ligands bipy and salicylaldehydes. The compound 1 is very stable at ambient temperature but unstable upon heating decomposing to Coo at 980 degrees C in nitrogen, but at 500 degrees C in oxygen atmosphere. The X-ray diffraction study of the compound 1 verified the proposed octahedral arrangement of the ligands around the cobalt(II) atom. Along with the main products (1-4), a side product (5) verified by X-ray diffraction study as [Co-II(bipy)(3)]Br-2 center dot 0.5(5-chlorosalicylaldehydeH) center dot 1.5CH(3)OH. (c) 2006 Elsevier Ltd. All rights reserved.
机译:钴(II)加成化合物[Co(X-salo)(2)(bipy)],其中X-salo是取代的水杨醛的阴离子(X = 3-OCH3(1); 5-CH3(2); 5合成了-Cl(3); 5-NO2(4))和Bipy中性2,2'-联吡啶,并通过理化和光谱(IR,UV-Vis)数据进行了表征。用GAUSSIAN-03进行的理论计算(DFT,ZINDO)用于预测化合物1的电子光谱,与固态的实验值具有良好的相关性。在不同溶剂下的吸收光谱表明,该化合物在CH3CN中稳定,但在CH3OH和DMF溶液中不稳定。 CH3CN中的循环伏安法研究给出了金属Co(II)以及配体联吡啶和水杨醛的氧化还原过程的所有预期波。化合物1在环境温度下非常稳定,但在氮气中在980℃下加热分解成Coo,而在氧气氛下在500℃下加热分解时不稳定。化合物1的X射线衍射研究验证了钴(II​​)原子周围的配体的拟八面体排列。与主要产品(1-4)一起,副产物(5)通过X射线衍射研究验证为[Co-II(bipy)(3)] Br-2中心点0.5(5-氯水杨醛H)中心点1.5 CH(3)OH。 (c)2006 Elsevier Ltd.保留所有权利。

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