“…Hydrogenation of styrene, [29,31] cinnamaldehyde, [30] phenol, [32] and nitrobenzene [33] Pd/UiO-66@PDMS-60 with 100 % conversion of styrene in 65 min, 75 % reduction in reaction time compared with Pd/UiO-66 [29] Transfer hydrogenation of nitrobenzene [34] and cinnamaldehyde [35] Ni@NCF-700 with 99 % nitrobenzene conversion, 97 % aniline yield and 96 % quinoline yield [34] Oxidation of methane, [37] alcohol, [38] styrene, [39,40] cyclohexane, [41] and indene [42] AuPd@ZSM-5-C 16 with a methane conversion of 17.3 %, almost 2 times higher than that (6.3 %) of AuPd@ZSM-5 [37] Dehydrogenative coupling of organosilanes [43] Pd/XC-72-700-Ar with a TOF of 645300 h À 1 in dehydrocoupling of triethylsilane and H 2 O [43] Chemical fixation of CO 2 [44] ZIF-8/CN foam with a conversion of 100 % in the reaction of epichlorohydrin with CO 2 , higher than those of ZIF-8 (84.1 %) and CN foam (0 %) [44] Hydration of alkynes and epoxides [45] Hβ-75 with a yield of 98 % in hydration of 1,2-epoxycyclohexane [45] Hydrolysis of esters [46] Gel cat. (0.40) with 100 % conversion of silyl ether and 100 % yield of 1-octanol in desilylation of TBDPS-octyl ether [46] Transesterification of methanol with oils [47,48] N-HPC-800 with a yield of 86.1 % in the transesterification of tripalmitin with methanol, higher than those of various classical catalysts [48] Hydrophobicity Rapid diffusion of products…”