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MO schemes for the isoelectronic molecules Os3i2, showing the energy relation between their MOs as three protons are removed from the Os nuclei and placed in bridging positions between the metal atoms

MO schemes for the isoelectronlc molecuies Os3 12, showing the energy relation between their MOs as three protons are removed from the Os nuclei and placed in bridging positions between the metai atoms

Mo Sdsa and Mo 3d3 2 peaks for the R025 sample calcined in nitrogen and in air

MO sketches for the NO2 molecule, a-bond skeleton is assumed to be formed by two-electrons bonds

Mo Steel Showing Internal Decarburization and Fissuring In High Temperature Hydrogen Service

MO symmetry correlation diagram for 1,3-dipolar cycloadditions.

Mo TI LEIS Intensity ratios of physical mixture of 4.1 wt M0O3 TIO2 In H2O saturated O2.

MO Triptych for the Di-n-Methane and Acyclic Bicycle Rearrangements of the Dicarbo-methoxy Compounds

Mo values in important geologic reservoirs

MO view of the depleted adjacent np lone pair orbitals

MO view of the depleted adjacent np2 lone pair orbitals

Mo W dinitrogen complex with the P N ligand N,N,N, N -tetrakis- as a target structure for a catalyst in the Chatt cycle.

MO Walsh diagram for the formation of pyramidal NaAl4

Mo were measured with

MO X-ray spectrum for he system 20 MeV on Ar for four different impact parameters. The full curve is our calculation scaled with a factor of 1.5. The experiment is from Schuch et al. I10.

MO X-ray spectrum for the system 20 MeV on Ar for four different impact parameters. The full curve is our calculation scaled by a factor of 0.5. The experiment is from Schuch et al. . b is the impact parameter.

Mo- and Ru-carbene catalysts.

Mo-0 slabs in K0.30M0O3

Mo-based catalytic olefination of aldehydes

Mo-based Schrock-type catalyst. Ar phenyl, 2,6-Me2-Cf,H3, 2,6-i-Pr2-C6H3, etc. R ethyl, phenyl, trimethylsilyl, CMejPh or t-butyl and R CMe3, CMe2CF3, CMe2, aryl, etc.

Mo-catalysed ARCM of divinylphosphinates or divinylphosphine oxides.

Mo-catalyzed ARCM of achiral trienes can be effected efficiently, enantioselectively, and in the absence of solvent

Mo-catalyzed asymmetric allylic alkylations with 3-substituted oxindoles .

Mo-catalyzed asymmetric allylic alkylations with prochiral nucleophiles .

Mo-catalyzed desymmetrization of meso tetraenes proceeds to afford optically pure heterocycles



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