2022
DOI: 10.1016/j.fuel.2022.125085
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Defect-engineered MOF-808 with highly exposed Zr sites as highly efficient catalysts for catalytic transfer hydrogenation of furfural

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Cited by 42 publications
(22 citation statements)
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“…The difference in final mass is mainly caused by the difference in the number of carboxyl groups between TPA and BA. The final mass decreased with increasing BA content, indicating that BA was successfully introduced into the prepared materials …”
Section: Resultsmentioning
confidence: 99%
“…The difference in final mass is mainly caused by the difference in the number of carboxyl groups between TPA and BA. The final mass decreased with increasing BA content, indicating that BA was successfully introduced into the prepared materials …”
Section: Resultsmentioning
confidence: 99%
“…4b). 59 HBC was introduced as a temporary ligand and as a terminating agent to modulate the particle size. The degree of ligand deficiency and the number of exposed Zr sites can be well-regulated by varying the amount of HBC.…”
Section: Catalytic Hydrogenation Of Furfural To Furfuryl Alcoholmentioning
confidence: 99%
“…[19][20][21][22][23] Notably, MOF-based catalysts have enabled the regulation of many catalytic reactions via metal node variation, 24,25 organic linker functionalization, 26,27 pore size adjustment, 28,29 and defect engineering. 30,31 For example, by changing the metal node from Zr to Hf, Hf-NU-1000 [Hf 6 (OH) 16 (TBAPy) 2 , H 4 TBAPy = 1,3,6,8-tetrakis(p-benzoic acid)pyrene] showed higher conversion rate than the isoreticular Zr-NU-1000 in the catalytic activation of epoxides due to its weaker Lewis acidity. 16 Moreover, defect engineering was recently proposed as a workable way for catalytic activity improvement.…”
Section: Introductionmentioning
confidence: 99%