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Wynberg s first enantioselective hydrophosphonylation. 0

Wynberg s model of bifunctional cinchona alkaloid catalysis.

Wyodak SRC vs, conversion

X - Growth, of diffusion-controlled structure, showing form of structure .

X - Interactions between incident light and multilayer coatings on glass

X - Ray Powder Diffractogram of Amoxicillin Trihydrate

X - T curves of 5 whisker-filled PP at different cooling rates.

X -1 curves of 5 whisker-filled PP at different cooling rates.

X -1 curves of pure PP at different cooling rates.

X -minimization frequency analysis of a generated

X -ray absorption spectra in a region including the terbium L3 edge. The spectra were taken at SSRL beam line 1-5 using a standard transmission EXAFS set up and Si 220 monochromator crystals.

X -ray absorption spectrum and its derivative of Mn ions in solution. The zero of the energy scale is fixed at the weak ls-3d excitation at threshold

X -ray absorption spectrum with absorption edges

X -ray crystal structure of a 1-naphthyl-taddol anisaldehyde complex.

X -ray crystal structure of Ar CeCeAr, Ar C6H3-2,6-Dipp2 . H atoms are not shown.

X -ray crystal structure of expanded radialene 30b H-atoms have been omitted for clarity. Atomic displacement parameters at 203 K are drawn at the 20 probability level. The perethynylated C6o-core is highlighted in bold it adopts a chair-like conformation .

X -ray crystal structure of Si66 . H atoms are not shown.

X -ray crystal structure of Snioio , H atoms are not shown.

X -ray crystal structure of the radical Ge3Ar3, Ar C6H3-2,6-Mes2 , H atoms are not shown.

X -ray diffraction diagram of the powdered magnetite from Grangesberg, Sweden. Besides magnetite ,

X -ray diffraction line broadening studies in inorganic powders by Morosin and co-workers show evidence for large plastic deformation with residual strain characteristic of cold-worked metals .

X -ray diffraction pattern, IR spectrum and electron micrograph of fer-oxyhjde.

X -ray diffraction patterns of Al65Cu20Mn15 after different milling times at milling intensity 7

X -ray diffraction patterns of the CaCC 3 halloysite composite after CaC03 formation. The first peak at 12.3 corresponds to 7.2 A . Arrows indicate peaks corresponding to the vaterite modification of CaC03. Calcite modification of CaC03 was not found. Peak assignment was made using the Powder Diffraction Database.

X -ray diffractograms of bulk and emulsified lard held isolhermally at 25 C, measured at time zero and 60 min. See Figure 1 for abbreviation.



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