Photocatalytic Production of Ethanolamines and Ethylenediamines from Bio-Polyols over a Cu/TiO2 Catalyst

被引:7
作者
Liu, Meijiang [1 ,2 ]
Li, Hongji [3 ,4 ]
Zhang, Jian [1 ]
Liu, Huifang [1 ]
Wang, Feng [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys DICP, Dalian Natl Lab Clean Energy DNL, State Key Lab Catalysis SKLC, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, 19 A Yuquan Rd, Beijing 100049, Peoples R China
[3] Zhengzhou Univ, Green Catalysis Ctr, 100 Kexue Rd, Zhengzhou 450001, Peoples R China
[4] Zhengzhou Univ, Coll Chem, 100 Kexue Rd, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomass; Heterogeneous Catalysis; Photocatalysis; Reductive Amination; REDUCTIVE AMINATION; GLYCEROL; OXIDATION; HYDROGEN; METHANOL; CONVERSION; EFFICIENT; AMINES; XPS;
D O I
10.1002/anie.202315795
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Valorization of biomass-derived polyols into high-value-added ethanolamines and ethylenediamines is highly attractive. Herein, we report a one-step photocatalytic protocol to convert bio-polyols into a 60 % yield of ethanolamines and ethylenediamines over a multifunctional Cu/TiO2 catalyst. This catalyst enables a tandem process of photocatalytic polyol C-C bond cleavage and reductive amination in one pot at room temperature, and also allows the selective conversion of various bio-polyols and amines. Mechanistic studies revealed that photogenerated holes in TiO2 promote the retro-aldol C-C bond cleavage or oxidative dehydrogenation of polyols, and photogenerated electrons accumulate on small-sized Cu clusters, which facilitate the reductive amination via hydrogen transfer and prevent the H-2 generation. This strategy provides new opportunities for the development of non-noble metal photocatalysts and methods of biomass conversion under mild conditions.
引用
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页数:8
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