| 1 |
Nitrogen-fixing of ultrasmall Pd-based bimetallic nanoclusters on carbon supports
Wang L, Yin P, Zhang LL, Shen SC, Xu SL, Chen P, Liang HW
Journal of Catalysis, 389, 297, 2020 |
| 2 |
Semihydrogenation of phenylacetylene over nonprecious Ni-based catalysts supported on AlSBA-15
Yang L, Yu SY, Peng C, Fang XC, Cheng ZM, Zhou ZM
Journal of Catalysis, 370, 310, 2019 |
| 3 |
Semihydrogenation of phenylacetylene over nonprecious Ni-based catalysts supported on AlSBA-15
Yang L, Yu SY, Peng C, Fang XC, Cheng ZM, Zhou ZM
Journal of Catalysis, 370, 310, 2019 |
| 4 |
Catalytic hydrogen evolution and semihydrogenation of organic compounds using silicotungstic acid as an electron-coupled-proton buffer in water-organic solvent mixtures
Wu WM, Wu XY, Wang SS, Lu CZ
Journal of Catalysis, 378, 376, 2019 |
| 5 |
Visible light-induced diastereoselective semihydrogenation of alkynes to cis-alkenes over an organically modified titanium(IV) oxide photocatalyst having a metal co-catalyst
Fukui M, Omori Y, Kitagawa SY, Tanaka A, Hashimoto K, Kominami H
Journal of Catalysis, 374, 36, 2019 |
| 6 |
Design of a difunctional Zn-Ti LDHs supported PdAu catalyst for selective hydrogenation of phenylacetylene
Shen YL, Yin KJ, An CH, Xiao ZH
Applied Surface Science, 456, 1, 2018 |
| 7 |
Origin of ligand-driven selectivity in alkyne semihydrogenation over silica-supported copper nanoparticles
Kaeffer N, Larmier K, Fedorov A, Coperet C
Journal of Catalysis, 364, 437, 2018 |
| 8 |
Fabrication of hollow carbon nanospheres introduced with Fe and N species immobilized palladium nanoparticles as catalysts for the semihydrogenation of phenylacetylene under mild reaction conditions
Zhang W, Wang FS, Li XL, Liu YS, Liu Y, Ma JT
Applied Surface Science, 404, 398, 2017 |
| 9 |
Solvent-free semihydrogenation of acetylene alcohols in a capillary reactor coated with a Pd-Bi/TiO2 catalyst
Cherkasov N, Ibhadon AO, Rebrov EV
Applied Catalysis A: General, 515, 108, 2016 |
| 10 |
Scale up study of capillary microreactors in solvent-free semihydrogenation of 2-methyl-3-butyn-2-ol
Cherkasov N, Al-Rawashdeh M, Ibhadon AO, Rebrov EV
Catalysis Today, 273, 205, 2016 |
