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两种具有催化活性的二膦酸功能化不对称多钼酸盐,可将苄醇氧化为苯甲醛。

Two diphosphonate-functionalized asymmetric polyoxomolybdates with catalytic activity for oxidation of benzyl alcohol to benzaldehyde.

机构信息

Key Laboratory of Polyoxometalate Science of Ministry of Education Faculty of Chemistry, Northeast Normal University, Changchun, Jilin 130024, PR China.

出版信息

Dalton Trans. 2011 Sep 7;40(33):8414-8. doi: 10.1039/c0dt01729a. Epub 2011 Jul 19.

Abstract

Two asymmetric polyoxomolybdates Na(6){Mo(2)O(5)(Mo(2)O(6))NH(3)CH(2)CH(2)CH(2)C(O)(PO(3))(2)}·16H(2)O (1) and (NH(4))(7)Na{MoO(2)[(Mo(2)O(6))NH(3)CH(2)CH(2)CH(2)C(O)(PO(3))(2)]}(4)·H(2)O (2) have been synthesized by the reactions of alendronic acid with molybdate. Structure analysis revealed that the polyoxoanions 1 and 2 can be described as dimeric and tetrameric aggregates of the {MoO(3)[(Mo(2)O(6))NH(3)CH(2)CH(2)CH(2)C(O)(PO(3))(2)]} units respectively. Their tetrabutylammonium salts show efficient selective oxidation of benzyl alcohol to benzaldehyde with 72.5% and 81.5% benzyl alcohol conversion, and 87.1% and 82.4% benzaldehyde selectivity, respectively.

摘要

两种不对称的多钼酸盐 Na(6){Mo(2)O(5)(Mo(2)O(6))NH(3)CH(2)CH(2)CH(2)C(O)(PO(3))(2)}·16H(2)O(1)和(NH(4))(7)Na{MoO(2)[(Mo(2)O(6))NH(3)CH(2)CH(2)CH(2)C(O)(PO(3))(2)]}(4)·H(2)O(2)是通过丙炔酸与钼酸盐的反应合成的。结构分析表明,多氧阴离子 1 和 2 可分别描述为{MoO(3)[(Mo(2)O(6))NH(3)CH(2)CH(2)CH(2)C(O)(PO(3))(2)]}单元的二聚体和四聚体聚合体。它们的四丁基铵盐对苄醇的选择性氧化具有高效,分别得到 72.5%和 81.5%的苄醇转化率,87.1%和 82.4%的苯甲醛选择性。

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