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Bridging homogeneous and heterogeneous catalysis with MOFs: 'Click' reactions with Cu-MOF catalysts

机译:用MOF桥接均相和异相催化:与Cu-MOF催化剂的“点击”反应

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摘要

Various copper-containing MOF catalysts, i.e., [Cu(2-pymo)_2], [Cu(im)_2], [Cu_3(BTC)_2] and [Cu(BDC)] (2-pymo: 2-hydroxypyrimidinolate; im: imidazolate; BTC: benzene tricarboxylate; BDC: benzene dicarboxylate), have shown to be highly active and fully regioselective for "click" reactions (1,3-dipolar cycloaddition reactions). The activity of the best MOF catalyst is comparable to homogeneous Cu catalysts. It has been found that the activity of Cu changes with the organic linker in the MOF, being those containing CuN_4 more active than CuO_4 centers. The controlling step of the reaction is the formation of an adduct between Cu and phenylacetylene. When using MOF catalysts, the use of alcohol or alcohol-water solvents is not required, and the catalysts can be fully recovered and recycled. Finally, Cu-MOF catalysts allow to design a one-pot two-step process, where the azide is formed "in situ" and reacted immediately with phenylacetylene.
机译:各种含铜的MOF催化剂,即[Cu(2-pymo)_2],[Cu(im)_2],[Cu_3(BTC)_2]和[Cu(BDC)](2-pymo:2-hydroxypyrimidinolate; im:咪唑盐; BTC:三羧酸苯; BDC:二羧酸苯)对“点击”反应(1,3-偶极环加成反应)具有很高的活性和区域选择性。最好的MOF催化剂的活性与均相Cu催化剂相当。已经发现,Cu的活性随MOF中的有机连接基而改变,MOB中的有机连接基比CuO_4中心的CuN_4的活性更高。反应的控制步骤是在铜和苯乙炔之间形成加合物。使用MOF催化剂时,不需要使用醇或醇-水溶剂,并且催化剂可以完全回收和再循环。最后,Cu-MOF催化剂允许设计一锅两步工艺,其中叠氮化物“就地”形成,并立即与苯乙炔反应。

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