Hydrogen bonding controlled catalysis of a porous organic framework containing benzimidazole moieties
KAUST Grant NumberCRG-1-2012-LAI-009
Permanent link to this recordhttp://hdl.handle.net/10754/598532
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AbstractA microporous organic framework (JUC-Z12) was synthesized quantitatively from tetra(4-formylphenyl)methane and 3,3′-diaminobenzidine. JUC-Z12 shows high thermal stability (>400 °C), a large surface area (SBET = 750 m2 g-1), a well-defined uniform micropore distribution (1.09 nm) and high Qst for H2 (-8.1 kJ mol-1), CO2 (-29.5 kJ mol-1), and CH 4 (-22.2 kJ mol-1). It also exhibits selective catalytic activities in the Knoevenagel reaction, which is supposed to be controlled by hydrogen bonding between substrates and JUC-Z12. The JUC-Z12 catalyst can be easily isolated from the reaction mixture by simple filtration and reused with high activity. This journal is © the Partner Organisations 2014.
CitationLiu B, Ben T, Xu J, Deng F, Qiu S (2014) Hydrogen bonding controlled catalysis of a porous organic framework containing benzimidazole moieties. New Journal of Chemistry 38: 2292. Available: http://dx.doi.org/10.1039/c4nj00053f.
SponsorsThis work was supported by National Natural Science Foundation of China (21390394), the National Basic Research Program of China (2012CB821700, 2011CB808703), NSFC (21261130584, 91022030), "111" project (B07016), Award Project of KAUST (CRG-1-2012-LAI-009) and Ministry of Education, Science and Technology Development Center Project (20120061130012).
PublisherRoyal Society of Chemistry (RSC)
JournalNew Journal of Chemistry