Iridium Complex Immobilized on Custom-Designed Periodic Mesoporous Organosilica as Reusable Catalyst for the Dehydrogenative Oxidation of Alcohols

被引:16
|
作者
Shimizu, Mineyuki [1 ]
Michikawa, Kumiko [1 ]
Maegawa, Yoshifumi [2 ]
Inagaki, Shinji [1 ]
Fujita, Ken-ichi [2 ]
机构
[1] Kyoto Univ, Grad Sch Human & Environm Studies, Kyoto 6068501, Japan
[2] Toyota Cent Res & Dev Labs Inc, Nagakute, Aichi 4801192, Japan
来源
ACS APPLIED NANO MATERIALS | 2020年 / 3卷 / 03期
关键词
iridium; mesoporous materials; supported catalysts; dehydrogenation; oxidation; alcohols; METAL-LIGAND COOPERATION; BOND ACTIVATION; BIPYRIDONATE LIGAND; HYDROGEN STORAGE; ORGANIC GROUPS; WATER; BEARING; LACTONIZATION; BORYLATION; OXIDE;
D O I
10.1021/acsanm.9b02607
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Over the past few decades, a number of homogeneous transition metal complex catalysts for efficient organic transformations have been developed. Some of these highly active catalysts have been designed based on the concept of "cooperativity between a transition metal atom and a custom-designed ligand molecule". In this paper, we report the synthesis of a periodic mesoporous organosilica (PMO) catalyst support (BPyOH-BP-PMO) that enables cooperativity between a transition-metal atom and the custom-designed ligand. We immobilized iridium complexes on BPyOH-BP-PMO to produce a heterogeneous catalyst that exhibits excellent catalytic activity for the dehydrogenative oxidation of a variety of alcohols and is superior to a similar previously used homogeneous catalyst. Furthermore, the immobilized catalyst (Ir@BPyOH-BP-PMO) can be recovered by simple filtration and reused without decrease of its catalytic activity. We believe that the concept for the design of the present heterogeneous catalyst would provide important guidance for the development of innovative catalysts.
引用
收藏
页码:2527 / 2535
页数:9
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