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首页> 外文期刊>Journal of Organometallic Chemistry >Syntheses of the B-(8)-hydroxy- and B((8),(8)')-dihydroxy-derivatives of the bis(1,2-dicarbollido)-3-colbalt(1-)ate ion by its reductive acetoxylation and hydroxylation: molecular structure of [8,8 '-mu-CH3C(O)(2)(1,2-C2B9H10)(2)-3-Co](0) zwitterion
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Syntheses of the B-(8)-hydroxy- and B((8),(8)')-dihydroxy-derivatives of the bis(1,2-dicarbollido)-3-colbalt(1-)ate ion by its reductive acetoxylation and hydroxylation: molecular structure of [8,8 '-mu-CH3C(O)(2)(1,2-C2B9H10)(2)-3-Co](0) zwitterion

机译:双(1,2-二咔唑醇)-3-钴(1-)酸酯离子的B-(8)-羟基和B((8),(8)')-二羟基衍生物的还原反应乙酰氧基化和羟基化:[8,8'-mu-CH3C(O)(2)(1,2-C2B9H10)(2)-3-Co](0)两性离子的分子结构

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摘要

Preparative routes to 8-hydroxy-bis(1,2-dicarbollido)-3-cobalt(1-)ate (2) and 8,8'-dihydroxy-bis(1,2-dicarbollido)-3-cobalt(1-)ate (3) ions are reported by the reductive acetoxylation of the parent bis(dicarbollido)cobaltate ion (1) followed by hydrolysis of the intermediates. The essential reagent is acetic anhydride, and strong acids are required as catalysts. For the hydroxyderivative ion 2 the simultaneous presence of acetic acid brings benefit, whereas it is detrimental for the formation of the dihydroxyderivative 3. Reaction intermediate leading to the dihydroxy derivative is the already reported [8,8'-mu-CH3C(O)(2)<(1,2-C2B9H10)(2)-3-Co](0) zwitterion. This compound was adequately characterised for the first time and its molecular structure as determined by X-ray diffraction analysis is presented. Both B-hydroxylated bis(dicarbollido)-ions can be alternatively obtained on the direct hydroxylation of the parent ion by hot 60-80% sulphuric acid. Optimised synthetic procedures and the main physicochemical properties (MS, TLC, HPLC, H-1- and B-11-NMR) of the species are presented. The probable reaction course of the reductive acetoxylation is discussed. (C) 2002 Elsevier Science B.V. All rights reserved. [References: 23]
机译:制备8-羟基-双(1,2-二咔唑醇)-3-钴(1-)酸酯(2)和8,8'-二羟基-双(1,2-二咔唑醇)-3-钴(1-)的制备途径通过母体双(二咔唑基)钴酸根离子(1)的还原性乙酰氧基化,然后水解中间体,报道了)(3)离子。基本试剂是乙酸酐,需要强酸作为催化剂。对于羟基衍生物离子2,乙酸的同时存在会带来好处,而这不利于二羟基衍生物3的形成。已经报道了生成二羟基衍生物的反应中间体[8,8'-mu-CH3C(O)( 2)<(1,2-C2B9H10)(2)-3-Co](0)两性离子。首次对该化合物进行了充分的表征,并给出了通过X射线衍射分析确定的分子结构。可以通过热60-80%的硫酸直接将母体离子羟基化,从而获得两个B-羟基化的双(二咔唑基)离子。介绍了该物种的优化合成程序和主要理化性质(MS,TLC,HPLC,H-1-和B-11-NMR)。讨论了还原性乙酰氧基化的可能反应过程。 (C)2002 Elsevier Science B.V.保留所有权利。 [参考:23]

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