Dhakshinamoorthy Amarajothi, Asiri Abdullah M, Garcia Hermenegildo
School of Chemistry, Madurai Kamaraj University, Tamil Nadu, 625 021, India.
Instituto Universitario de Tecnología Química CSIC-UPV, Av. De los Naranjos s/n, 46022, Valencia, Spain.
Chemistry. 2016 Jun 6;22(24):8012-24. doi: 10.1002/chem.201505141. Epub 2016 Apr 26.
This Concept is aimed at describing the current state of the art in metal-organic frameworks (MOFs) as heterogeneous catalysts for liquid-phase oxidations, focusing on three important substrates, namely, alkenes, alkanes and alcohols. Emphases are on the nature of active sites that have been incorporated within MOFs and on future targets to be set in this area. Thus, selective alkene epoxidation with peroxides or oxygen catalyzed by constitutional metal nodes of MOFs as active sites are still to be developed. Moreover, no noble metal-free MOF has been reported to date that can act as a general catalyst for the aerobic oxidation of primary and secondary aliphatic alcohols. In contrast, in the case of alkanes, a target should be to tune the polarity of MOF internal pores to control the outcome of the autooxidation process, resulting in the selective formation of alcohol/ketone mixtures at high conversion.
本概念旨在描述金属有机框架(MOF)作为液相氧化多相催化剂的当前技术水平,重点关注三种重要底物,即烯烃、烷烃和醇类。重点在于MOF中所含活性位点的性质以及该领域未来的目标设定。因此,以MOF的结构金属节点作为活性位点,用过氧化物或氧气催化烯烃选择性环氧化仍有待开发。此外,迄今为止,尚未有报道称有无贵金属的MOF可作为伯醇和仲醇有氧氧化的通用催化剂。相比之下,对于烷烃,目标应是调节MOF内部孔的极性,以控制自氧化过程的结果,从而在高转化率下选择性地形成醇/酮混合物。