Results 271 to 280 of about 2,359,589 (295)
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Dalton Trans., 2006
In this work we report the first example of a trinuclear Pt(II) complex with Pt-Pt-Pt bonds that are not facilitated by direct intervention of bridging ligands but are partially held by the attractive pi-pi stacking interaction between the phenyl units of the 4,4'-dimethyl-2,2'-bipyridyl ligands.
Albert, Poater +6 more
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In this work we report the first example of a trinuclear Pt(II) complex with Pt-Pt-Pt bonds that are not facilitated by direct intervention of bridging ligands but are partially held by the attractive pi-pi stacking interaction between the phenyl units of the 4,4'-dimethyl-2,2'-bipyridyl ligands.
Albert, Poater +6 more
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Monomeric Pt(II) and dimeric Pt-Pt and Pt-Pd complexes of a triazolo pyrimidine derivative
Journal of Inorganic Biochemistry, 1995The ligand 5-methyl-[1,2,4]tr iazolo-[1,5-a]pyrimidine-7-ol (mtpOH) reacts wi th K2[PtCI 4] in 0.5 M hydrochloric acid yielding cis-[PtCI2(mtpOH)2].H20 (I). Dissolving this compound in a NaOH solution causes its decomposition and, from this solution, the dimeric complex [Pt2(mtpO)4].4H20 (11) crystallizes out. On the other hand, the reaction at 45°C of
J. Rodríguez +4 more
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Dalton Trans., 2017
An intermediate compound of a tetranuclear Pt–Fe⋯Fe–Pt complex in the synthetic process to form a trinuclear Pt–Fe–Pt complex by mixing the “amidate-hanging” Pt mononuclear complex and iron sources was successfully isolated and characterized by single-crystal X-ray analysis and several physical measurements.
Kazuhiro Uemura, Masahiro Taoka
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An intermediate compound of a tetranuclear Pt–Fe⋯Fe–Pt complex in the synthetic process to form a trinuclear Pt–Fe–Pt complex by mixing the “amidate-hanging” Pt mononuclear complex and iron sources was successfully isolated and characterized by single-crystal X-ray analysis and several physical measurements.
Kazuhiro Uemura, Masahiro Taoka
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Ethylene Adsorption on Al2O3-Supported Pt, Pt–Sn, and Pt–In Catalysts
Journal of Catalysis, 1996Abstract Ethylene adsorption on a family of Al2O3-supported Pt, Pt–Sn, and Pt–In catalysts was investigated at 300 K. The presence of Sn and In caused a decrease in ethylene uptake, similar to that observed in H2chemisorption measurements. Integral, isothermal heats of adsorption were measured and the heat of adsorption (Qad) values for C2H4on small ...
Fabio B. Passos +2 more
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Oxidation of glucose and gluconate on Pt, Pt Bi, and Pt Au catalysts
Recueil des Travaux Chimiques des Pays-Bas, 1996AbstractGlucose and gluconate aqueous solutions (2 mol/l) were oxidized with air (atmospheric pressure, 333K, pH 7) on active charcoal‐supported, platinum catalysts (catalytic ratios substrate/Pt ≥ 787); some catalysts were promoted with bismuth or gold. The activity of unpromoted Pt/C catalysts for glucose oxidation was comparable with that of Pd‐Bi/C
Besson, M. +4 more
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Comparison of methanol oxidations on Pt, Pt|Ru and Pt|Sn electrodes
Journal of Electroanalytical Chemistry, 1998Abstract Electrochemical oxidations of methanol were compared on smooth or high area platinum, platinum|tin and platinum|ruthenium electrodes. On smooth platinum, while ruthenium promoted the catalytic activities steadily according to the coverage, tin showed an enhancing effect only for a short period of time because of the dissolution of tin from ...
Yu Morimoto, Ernest B Yeager
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Journal of Electroanalytical Chemistry, 1999
The kinetics of HCOOH oxidation via a reactive intermediate on Pt(100), Pt(110), Pt(111), Pt(510) and Pt(911) single crystal electrodes were studied quantitatively. The difficulty due to the self-poisoning involved in HCOOH oxidation has been overcome successfully by designing a programmed potential step procedure, which is based on results of kinetic ...
Sun, SG, Yang, YY
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The kinetics of HCOOH oxidation via a reactive intermediate on Pt(100), Pt(110), Pt(111), Pt(510) and Pt(911) single crystal electrodes were studied quantitatively. The difficulty due to the self-poisoning involved in HCOOH oxidation has been overcome successfully by designing a programmed potential step procedure, which is based on results of kinetic ...
Sun, SG, Yang, YY
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The function of zeolite on Pt autoreduction and dispersion in Pt/L and Pt/? catalysts
Catalysis Letters, 1996TPR, CO-FTIR and129Xe NMR spectroscopic techniques were used to measure the distribution of platinum species after the calcination of Pt/L and Pt/Β zeolites. Autoreduction which occurred in Pt/Β zeolite was avoided in the channel of L zeolite. Pt particles dispersed well and exhibited excellent reactivity for the aromatization ofn-hexane in L zeolite.
Jian Zheng +3 more
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Effect of oxygen on the diffusion of Ni in Pt in Pt-Ni-Pt films
Journal of Applied Physics, 1981We have studied the effect of oxygen on the diffusion of Ni into Pt in the Pt-Ni-Pt films. Below 400 °C, the diffusion rates of Ni into both Pt layers are greatly reduced by oxygen. Above 500 °C, however, Ni rapidly mixes with Pt layers, which leads to the formation of Ni oxide on the Pt surface in the presence of oxygen.
Chin-An Chang, W. K. Chu
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Theoretical study on the methane activation reactions by Pt, Pt+, and Pt− atoms
Journal of Molecular Structure: THEOCHEM, 1993Abstract The oxidative additions of CH4 to the ground and excited states of Pt, Pt−, and Pt+ species are studied by the symmetry-adapted cluster (SAC) and SAC-CI methods. The reaction path is examined by calculating the Hellmann-Feynman forces acting on C and H atoms of CH4. It involves the transition state and/or the activated complex.
M. Hada +4 more
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