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Eosin Y Post-Decorated Metal–Organic Framework as a Selectivity Regulator for the Alcohols Oxidation

材料科学 选择性 调节器 金属有机骨架 金属 化学工程 无机化学 纳米技术 有机化学 催化作用 化学 冶金 吸附 生物化学 工程类 基因
作者
Hui Gao,Yang Tang,Songtao Liu,Cheng He,Huaqing Li,Liang Zhao,Chunying Duan
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (29): 37896-37905 被引量:17
标识
DOI:10.1021/acsami.4c05017
摘要

The selective oxidation of alcohols into aldehydes is a basic and significant procedure, with great potential for scientific research and industrial applications. However, as an important factor in the C(sp3)–H activation process, high selectivity is generally difficult to achieve due to the fact that the more easily activated properties of aldehydes are compared to alcohols. Herein, by the ingenious decoration of eosin Y into a Zr-based metal–organic framework (MOF–808), EY@MOF–808 was prepared as a selectivity regulator for the aerobic oxidation of the benzyl alcohols into corresponding aldehydes, possessing applicability for the benzylic alcohols with various substituents. By anchoring eosin Y on Zr6O4(OH)4 clusters of MOF–808 and maintaining open metal nodes with selective binding effects, the benzyl alcohol substrates were selectively coordinated to the unsaturated metal clusters adjacent to eosin Y, which ensured that the excited eosin Y rapidly activated substrates to generate carbon radicals by the hydrogen atom transfer (HAT) process. The rapid electron transfer (ET) simultaneously produced reactive oxygen species (O2•–) and then a combination of both to further promote the generation of benzaldehydes. The weak interaction of benzaldehydes with the skeleton allowed it to dissociate rapidly, thus preventing overoxidation. Under the catalysis of EY@MOF–808, the selectivity of various benzaldehydes was more than 99%. In contrast, eosin Y gave only benzoic acid products under the same conditions, which demonstrated the superiority of regulatory selectivity of EY@MOF–808. Taking advantage of the heterogeneity of the MOF, EY@MOF–808 was recycled four times without a decrease in its selectivity and avoided the quenching effect of eosin Y. The organic functional units postdecorated MOF-based photocatalyst strategy exhibits a promising new perspective approach to sustainably regulating the selectivity of inert oxidation.
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