Multidentate unsymmetrically-substituted Schiff bases and their metal complexes: Synthesis, functional materials properties, and applications to catalysis

席夫碱 化学 齿合度 催化作用 高分子化学 金属 组合化学 有机化学
作者
Xiang Liu,Carolina Manzur,Néstor Novoa,Salvador Celedón,David Carrillo,Jean‐René Hamon
出处
期刊:Coordination Chemistry Reviews [Elsevier]
卷期号:357: 144-172 被引量:323
标识
DOI:10.1016/j.ccr.2017.11.030
摘要

This review focuses on the recent developments of unsymmetrically-substituted multidentate Schiff bases whose steric and electronic characteristics are easily manipulated by selecting suitable condensing aldehydes or ketones and primary amines, and on their metal complexes. After a brief historical introduction, this manuscript is divided in three main sections. In the two first parts, the synthesis, reactivity, functions, and properties of tridentate Schiff base precursors and of quadridentate Schiff base metal complexes, respectively, are discussed through a literature survey including examples of research from the authors’ groups. More specifically, the second section is formed of seven subsections with the synthesis of unsymmetrically-substituted tetradentate Schiff bases and their transition metal (V, Mn, Fe, Co, Ni, Cu, Zn, Ru, Pd, Pt) and uranyl complexes. Emphasis is given to our research work based on ferrocenyl-containing tri- and tetradentate unsymmetrically-substituted Schiff base complexes of Ni(II) and Cu(II) starting from variously substituted ferrocenyl-β-diketones. The unsymmetrically-substituted Schiff base complexes present a wide range of remarkable properties that are also summarized in this section, including structural, biocidal, magnetic, and second-order nonlinear optical properties. The third section is devoted to the catalytic activity of Schiff base metal complexes that is discussed through thirteen major organic reactions, including copper-catalyzed azide–alkyne cycloaddition (CuAAC), Henry and nitro-Mannich reactions, hydrosilylation of ketones, aldol, cyclopropanation and epoxidation reactions, among others.

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