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High catalytic activity of heterometallic (Fe6Na7 and Fe6Na6) cage silsesquioxanes in oxidations with peroxides, and other alkanes, as well as alcohols, can be oxidized in acetonitrile solution to phenol—the corresponding

Prediction of the catalytic activity of Ni-Al mixed oxide in the hydroisomerization of n-alkanes mixed Ni-Al oxides as catalyst systems for the hydroisomerization of n-alkanes. A number of instrumental

First cage-like pentanuclear Co(II)-silsesquioxane in the oxidation of alkanes and alcohols. © The Royal Society of Chemistry 2016.

Palanquin-like Cu 4 Na 4 silsesquioxane synthesis (via oxidation of 1,1-bis(diphenylphosphino)methane), structure and catalytic activity in alkane or alcohol oxidation with peroxides(diphenylphosphino)methane), structure and catalytic activity in alkane or alcohol oxidation with peroxides

Solvation Properties of Triethylammonium-Based Protic Ionic Liquids-temperature DSC in order to determine the liquid range temperature. The limiting activity coefficients of alkanes

Composition of the organic compounds of different peat types from the Southern taiga subzone of Western SiberiaAcyclic (n-alkanes, n-alkan-2-ones, fatty acids, methyl esters of fatty acids, n

Thermal transformation of bitumoid of Domanic formations of Tatarstan is probably due to the decomposition of part of the kerogen. The ratio of isoprenoid alkanes (pristane

Copper(ii) complexes with 2,2′:6′,2′′-terpyridine, 2,6-di(thiazol-2-yl)pyridine and 2,6-di(pyrazin-2-yl)pyridine substituted with quinolines. Synthesis, structure, antiproliferative activity, and catalytic activity in the oxidation of alkanes and alcohols with peroxides(pyrazin-2-yl)pyridine (dppy) derivatives with n-quinolyl substituents (n = 2 and 4) was used to synthesize

Tetracopper(II) cores driven by an unexplored trifunctional aminoalcohol sulfonic acid for mild catalytic C-H functionalization of Alkanes trifunctional aminoalcohol sulfonic acid (H 3 bes, N,N-bis(2-hydroxyethyl)-2-aminoethanesulfonic acid) as a

Bis[diphenylphosphino]methane and its bridge-substituted analogues as chemically non-innocent ligands for H2 activationalkane derivative

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