首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Lower rim substituted tert-butylcalix[4]arenes (II). Complexing ability of 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetrakis-O-(piperidinylcarbonyl)me thylenecalix[4]arene. The crystal structures of the ligand and its sodium complex
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Lower rim substituted tert-butylcalix[4]arenes (II). Complexing ability of 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetrakis-O-(piperidinylcarbonyl)me thylenecalix[4]arene. The crystal structures of the ligand and its sodium complex

机译:下缘取代的叔丁基杯[4]芳烃(II)。 5,11,17,23-四叔丁基-25,26,27,28-四-O-(哌啶基羰基)对亚乙基杯[4]芳烃的络合能力。配体及其钠配合物的晶体结构

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摘要

The sodium(I) chloride and yttrium(III), lanthanum(III), samarium(III) and gadolinium(III) nitrate complexes of 5,11,17,23-tetra-tert-butyl-25,26,27,28-tetrakis(piperidinylcarbonyl)methy lene)calix[4]arene were prepared in direct reaction of the ligand and appriopriate metal salts and characterized by spectral data (IR, UV-Vis, H-1 NMR, FAB MS), and elemental analysis. The transmetallation reactions of the sodium complex by the lanthanide ions was also achieved. The crystal structures of the ligand and its sodium complex were determinated by single X-ray analysis. (C) 2002 Published by Elsevier Science Ltd. [References: 15]
机译:5,11,17,23-四叔丁基25,26,27,28的氯化钠(I)和钇(III),镧(III),sa(III)和ado(III)硝酸盐络合物在配体和适当的金属盐直接反应中制备了四(哌啶基羰基)甲基芳基杯[4]芳烃,并通过光谱数据(IR,UV-Vis,H-1 NMR,FAB MS)和元素分析进行​​了表征。也实现了镧系元素离子对钠配合物的金属转移反应。配体及其钠配合物的晶体结构通过单X射线分析确定。 (C)2002由Elsevier Science Ltd.发布[参考:15]

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