期刊
CATALYSIS TODAY
卷 352, 期 -, 页码 227-236出版社
ELSEVIER
DOI: 10.1016/j.cattod.2019.12.038
关键词
DUT; CO(2)cyclic carbonates; DFT
资金
- National Research Foundation of Korea through the Basic Research Program [2019-057644]
- Korea Electric Power Corporation
- Korea Research Fellowship Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2016H1D3A1936765]
- National Research Foundation of Korea [2016H1D3A1936765] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
Two aluminum-based DUT (Dresden University of Technology) metal organic frameworks were synthesized, and their structural and chemical properties were exploited for the cycloaddition reaction of CO2 and epoxide under solvent-free condition. Both the catalysts have the same supramolecular architecture but different ligands. DUT-5 (Al(OH)(bpdc), bpdc = 4,4'-biphenyldicarboxylate) has a higher number of acidic and basic sites and larger BET surface area and specific pore volume compared with DUT-4 (Al(OH)(ndc), ndc = 2,6-naphthalenedicarboxylate). The highly porous DUT-5 exhibited better catalytic conversion of epichlorohydrin (ECH) than DUT-4, with > 99 % selectivity in the presence of tetrabutylammonium bromide (TBAB). Short linkered MIL-53 (MIL = Materials Institute Lavoisier) (Al(OH)(bdc), bdc = 1,4-benzenedicarboxylate) exhibited lower ECH conversion compared with DUT-4 and DUT-5, even though all the catalysts possessed the same crystal structure. DUT catalyst could be recycled at least five times without any noticeable loss in the ECH conversion. In addition, the mechanism for the DUT-5/TBAB mediated cycloaddition of CO2 to ECH, affording the five-membered ECH carbonate, has been investigated in detail using the density functional theory. The energy barrier for the ECH ring opening in the presence of DUT-5/TBAB (15.14 kcal/mol) is significantly lower than those of un-catalyzed (61.96 kcal/mol) and TBAB-catalyzed (39.60 kcal/mol) reactions, clearly showing the vital role of the Al3+/Br(-)bifunctional catalyst system.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据