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51.
A new and efficient method for the preparation of various phenyl esters has been achieved by a simple reaction of an acid with phenol in the presence of anhyd. ZnCl2 and a catalytic amount of AlCl3. This combined Lewis acid also catalyzes the selective phenyl esterification to different dioic acids and is very simple and high yielding. 相似文献
52.
Keiichi Tomishige Masazumi Tamura Yoshinao Nakagawa 《Chemical record (New York, N.Y.)》2014,14(6):1041-1054
The catalytic performance of ReOx‐modified Ir metal catalyst in the hydrogenolysis of C–O bonds is strongly dependent on the choice of solvent. The acidic property of the Re species becomes obvious in the alkane solvent, and the hydrogenolysis reaction proceeds mainly by acid‐catalyzed dehydration and the subsequent metal‐catalyzed hydrogenation. The acidic property of the Re species is weakened in water; however, the hydrogenolysis reaction proceeds in water via a direct mechanism involving SN2‐like attack of a hydride species at the interface between Ir and ReOx on the adsorbed Re alkoxide species. This mechanism enabled the selective dissociation of the C–O bond neighboring the CH2OH group. 相似文献
53.
《Comptes Rendus Chimie》2014,17(7-8):752-759
Single-cell and half-cell degradation test procedures were evaluated for carbon-supported Pt/C, PtCo/C and PtNi/C catalysts. Half-cell analyses were employed to understand the effect of the number of cycles and of the scan rate over the cathode catalysts degradation under potential cycling from 0.6 to 1.2 V. The data suggested a time-dependent degradation for all three catalytic systems. Single-cell measurements were used to evaluate the impact of catalyst degradation on fuel cell performance. The measurements in both setups showed similar ECSA and ORR mass activity losses. Specific degradation mechanisms related to Pt dissolution, Pt agglomeration, and transitional metal leaching were quantified and correlated with performance losses. 相似文献
54.
55.
Oleg Parenago Alexey Rybaltovsky Evgeniy Epifanov Andrey Shubnyi Galina Bragina Alexey Lazhko Dmitry Khmelenin Vladimir Yusupov Nikita Minaev 《Molecules (Basel, Switzerland)》2020,25(24)
To obtain a supported heterogeneous catalyst, laser ablation of metallic palladium in supercritical carbon dioxide was performed in the presence of a carrier, microparticles of γ-alumina. The influence of the ablation process conditions—including supercritical fluid density, ablation, mixing time of the mixture, and laser wavelength—on the completeness and efficiency of the deposition of palladium particles on the surface of the carrier was studied. The obtained composites were investigated by scanning and transmission electron microscopy using energy dispersive spectroscopy. We found that palladium particles were nanosized and had a narrow size distribution (2–8 nm). The synthesized composites revealed high activity as catalysts in the liquid-phase hydrogenation of diphenylacetylene. 相似文献
56.
57.
《Arabian Journal of Chemistry》2020,13(4):4916-4925
A nitrogen-doped carbon-supported Co catalyst (Co/N-C-800) was discovered to be highly active for the reductive amination of carbonyl compounds with NH3 and the hydrogenation of nitriles into primary amines using H2 as the hydrogen source. Structurally diverse carbonyl compounds were selectively transformed into primary amines with good to excellent yields (82.8–99.6%) under mild conditions. The Co/N-C-800 catalyst showed comparable or better catalytic performance than the reported noble metal catalysts. The Co/N-C-800 catalyst also showed high activity for the hydrogenation of nitriles, affording the corresponding primary amines with high yields (81.7–99.0%). An overall reaction mechanism is proposed for the reductive amination of benzaldehyde and the hydrogenation of benzonitrile, which involves the same intermediates of phenylmethanimine and N-benzylidenebenzylamine. 相似文献
58.
Jerzy Chrusciel Krzysztof Matyjaszewski 《Journal of polymer science. Part A, Polymer chemistry》1996,34(11):2243-2252
Ring opening of 1,2,3,4-tetramethyl-1,2,3,4-tetraphenylcyclotetrasilane in the presence of various transition metal catalysts has been studied. Pd and Pt compounds are most active. Compounds with bulky ligands [e.g., Pd(PPh3)4] lead to the formation of “dimeric” cyclooctasilanes. Compounds with less bulky groups convert monomer to dimers and mixture of oligomers and polymers. Reactions with the all-trans monomer, tttt-(MePhSi)4, result in the formation of stereoregular dimer, presumably all-trans, tttttttt-(MePhSi)8, in high yields. Reactions in the presence of oxygen lead to the formation of polymers with inserted oxygen atoms in the main chain. © 1996 John Wiley & Sons, Inc. 相似文献
59.
Bogdan Marciniec Mariusz Lewandowski 《Journal of polymer science. Part A, Polymer chemistry》1996,34(8):1443-1445
Acyclic diene polymerization (ADP) of divinyldimethylsilane in the presence of ruthenium RuCl2(PPh3)3 and rhodium [RhCl(cod)]2 catalysts led predominantly to linear silylene-vinylene oligomers (Mn = 1510 and Mw/Mn = 1.19) if the ruthenium catalyst was used or to mixture of cyclic and linear oligomers if rhodium complex was catalyst. © 1996 John Wiley & Sons, Inc. 相似文献
60.
Metakaolin-based geopolymer microspheres (MGM) with hierarchical pore structures were prepared by suspension dispersion method in dimethicone at 80 °C. The hydrothermal modification of MGM was carried out at a lower temperature of 80 °C, and a NaA molecular sieve converted from metakaolin-based geopolymer (NMGM) with good crystal structure was prepared and applied in thermal catalytic cracking of low-density polyethylene (LDPE) reaction. The one-pot two-stage thermal catalytic cracking of LDPE was carried out in a 100 mL micro-autoclave under normal pressure. In this work, the optimal proportions and optimal reaction conditions of catalysts for NMGM thermal catalytic cracking of LDPE waste to fuel oil were investigated. The NMGM catalyst showed high selectivity to the liquid product of thermal catalytic cracking of waste LDPE. Under the reaction conditions of reaction time of 1 h and reaction temperature of 400 °C, the liquid-phase yield of thermal catalytic cracking of LDPE reached a high of 88.45%, of which the content of gasoline components was 10.14% and the content of diesel components was 80.97%. 相似文献