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首页> 外文期刊>Indian Journal of Chemistry, Section A. Inorganic, Physical, Theoretical & Analytical >Synthesis and characterization of complexes of Fe(III), Co(III), Ni(II), Cu(II),Zn(II) and UO_2~(2+) with p-tert-butylcalix[4]arene bearing two imine pendants linked through salicylyl moiety at the lower rim
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Synthesis and characterization of complexes of Fe(III), Co(III), Ni(II), Cu(II),Zn(II) and UO_2~(2+) with p-tert-butylcalix[4]arene bearing two imine pendants linked through salicylyl moiety at the lower rim

机译:Fe(III),Co(III),Ni(II),Cu(II),Zn(II)和UO_2〜(2+)与带有两个亚胺的对叔丁基杯[4]芳烃的配合物的合成和表征通过下缘的水杨基部分连接的侧基

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摘要

Metal ion complexes of the double-armed p-tert-butylcalix[4]arene derivative possessing imine functionality linked through salicylyl moiety at the lower rim has been synthesized for the first time and characterized by analytical, spectral and magnetic methods. The 1,-3- di-calix[4]arene-imine conjugate exhibits variable coordination behavior, from tetradentate to hexadentate, depending upon the metal ion to which it is bound, by always acting as di-anionic. While it uses both the ether oxygens of the pendants to coordinate in the case of Fe(III), Co(III) and Ni(II) complexes, it uses only the pendant salicylidene moieties in the case of Cu(II) and Zn(II) complexes. The Zn(II) complex catalysis ester hydrolysis through the formation of Zn(II)-hydroxo species.
机译:首次合成了具有亚胺官能团的双官能对叔丁基杯杯[4]芳烃衍生物的金属离子配合物,该亚胺官能团通过下边缘的水杨基部分连接,并通过分析,光谱和磁性方法表征。 1,-3-二杯[4]芳烃-亚胺共轭物表现出从四齿到六齿的可变配位行为,这取决于它所键合的金属离子,始终充当二阴离子。在Fe(III),Co(III)和Ni(II)配合物的情况下,虽然使用了侧链的两个醚氧进行配位,但在Cu(II)和Zn( II)复合物。通过形成Zn(II)-羟基物种,Zn(II)络合物催化酯水解。

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