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Merging of the photocatalysis and copper catalysis in metal–organic frameworks for oxidative C–C bond formation

机译:金属-有机骨架中光催化和铜催化的合并形成氧化碳键

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摘要

The direct formation of new C–C bonds through photocatalytic oxidative coupling from low reactive sp3 C–H bonds using environmentally benign and cheap oxygen as oxidant is an important area in sustainable chemistry. By incorporating the photoredox catalyst [SiW11O39Ru(H2O)]5– into the pores of Cu-based metal–organic frameworks, a new approach for merging Cu-catalysis/Ru-photocatalysis within one single MOF was achieved. The direct CuII–O–W(Ru) bridges made the two metal catalyses being synergetic, enabling the application on the catalysis of the oxidative coupling C–C bond formation from acetophenones and N-phenyl-tetrahydroisoquinoline with excellent conversion and size-selectivity. The method takes advantage of visible light photoredox catalysis to generate iminium ion intermediate from N-phenyl-tetrahydroisoquinoline under mild conditions and the easy combination with Cu-catalyzed activation of nucleophiles. Control catalytic experiments using similar Cu-based sheets but with the photoredox catalytic anions embedded was also investigated for comparison.
机译:低反应性的sp 3 C–H键通过光催化氧化偶联直接形成新的C–C键,使用环境友好的廉价氧气作为氧化剂,是可持续化学的重要领域。通过将光氧化还原催化剂[SiW11O39Ru(H2O)] 5-掺入铜基金属有机骨架的孔中,实现了在单个MOF中合并铜催化/ Ru光催化的新方法。直接的Cu II –O–W(Ru)桥使两种金属催化协同作用,从而使该方法可用于催化由苯乙酮和N-苯基-四氢异喹啉形成的氧化偶联C–C键具有出色的转化率和尺寸选择性。该方法利用可见光光氧化还原催化,在温和的条件下由N-苯基-四氢异喹啉生成亚胺离子中间体,并且易于与Cu催化的亲核试剂结合使用。还对使用相似的基于铜的薄板但嵌入了光氧化还原催化阴离子的对照催化实验进行了比较。

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