Catalytic Transfer Hydrogenation of Furfural to Furfuryl Alcohol under Mild Conditions over Zr-MOFs: Exploring the Role of Metal Node Coordination and Modification

被引:222
作者
Valekar, Anil H. [2 ]
Lee, Minhui [1 ]
Yoon, Ji Woong [2 ]
Kwak, Jaesung [2 ]
Hong, Do-Young [2 ,3 ]
Oh, Kyung-Ryul [2 ,4 ]
Cha, Ga-Young [2 ,3 ]
Kwon, Young-Uk [4 ,5 ]
Jung, Jaehoon [1 ]
Chang, Jong-San [2 ,4 ]
Hwang, Young Kyu [2 ,3 ]
机构
[1] Univ Ulsan, Dept Chem, Ulsan 44776, South Korea
[2] Korea Res Inst Chem Technol, Res Ctr Nanocatalysts, Daejeon 34114, South Korea
[3] Univ Sci & Technol, Dept Adv Mat & Chem Engn, Daejeon 34113, South Korea
[4] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
[5] Tianjin Polytech Univ, Sch Mat Sci Engn, Tianjin 300387, Peoples R China
来源
ACS CATALYSIS | 2020年 / 10卷 / 06期
基金
新加坡国家研究基金会;
关键词
catalytic transfer hydrogenation; zirconium-based metal-organic frameworks; metal node coordination and modification; methanol activation; density functional theory; PONNDORF-VERLEY REDUCTION; GAMMA-VALEROLACTONE; ORGANIC FRAMEWORKS; ETHYL LEVULINATE; METHANOL SYNTHESIS; ROOM-TEMPERATURE; ACID SITES; BIOMASS; CONVERSION; ZEOLITE;
D O I
10.1021/acscatal.9b05085
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The catalytic transfer hydrogenation (CTH) reaction is considered as a potential route for upgrading bio-based carbonyls to their corresponding alcohols. Herein, a series of Zr-based metal-organic frameworks (Zr-MOFs) containing various types of metal node to ligand coordinations were synthesized and tested for CTH of furfural (FUR) to furfuryl alcohol (FOL). It was found that metal node coordination plays a more important role than porosity in Zr-MOFs. MOF-808 (synthesized using a scaled-up approach to achieve a higher batch yield), with the lowest metal node to ligand coordination (coordination number 6), was found to be the most active catalyst among the various tested Zr-MOFs. Furthermore, M-MOF-808, modified by simple methanol activation (M), outperformed the pristine MOF-808 in CTH of FUR to FOL even at 30 degrees C in the presence of 2-propanol (IPA) as the hydrogen source. The simple modification of the metal node in the Zr-MOF changed the acid-base properties of the MOF-808 surface through the development of coordinatively unsaturated sites (CUS), hydroxyl and methoxy groups in the framework of the Zr-MOF, which probably help to facilitate the adsorption of FUR and IPA onto the metal node surfaces of the catalyst. To evaluate the versatility of methanol activation in CTH, further substrates, including other types of biomass and representative carbonyl compounds over M-MOF-808, were tested. To demonstrate heterogeneous catalysis, the catalyst was recycled for five consecutive cycles, with little loss after the first cycle, and was fully characterized to observe any changes in its structure. Mechanistic insights were provided by isotopically labeled 2-propanol-d(8) experiments, indicating FUR reduction through transfer hydrogenation. Finally, the reaction mechanism for CTH of FUR to FOL was proposed in detail using density functional theory (DFT) calculations over metal node modified model systems of a 6-connected Zr-MOF.
引用
收藏
页码:3720 / 3732
页数:13
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