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P MAS NMR spectrum of TMPO adsorbed on S04 Ti02. Asterisks denote spinning sidebands ,

P MAS NMR spectrum of was the most active and selective so all the experiment were done using this catalyst afterwards.

P MAS single-pulse spectra

P MAS spectra of cyclophosphamide rotation speed 2300 Hz upper

P MAS spectrum of the TMPO loaded on various solid acid catalysts. Except forsulphated zirconia,all porous substrates haveaSi Al ofca. 15. The dashed curves are results obtained from spectral analysis by Gaussian deconvolution and the shaded peaks represent presence of Lewis acidity .

P MR spectra obtained during chemotherapy of a rhabdo-myosarcoma of the hand, b osteosarcoma of the femur. Signal intensities are given in arbitrary units, spectra are plotted as a function of time origin of the time axis, scaled in days, is the first day of chemotherapy

P NMR coordination shifts .

P NMR of the products of hydrolysis of cyclic-AMP by NjCotOHitOH, after reduction of Co.

P NMR spectium of IIIF-8

P NMR spectra and phosphate assignments of dithiophosphate decamer d.

P NMR spectra at 109.3 MHz of sonicated alternating purine—pyrimidine hairpin duplexes. Key

P NMR spectra for lOOmM solutions of THAsalt of PWnCo in toluene as water content changes from 29mM to 1222mM.

P NMR spectra from solutions of

P NMR spectra of cyclic trimeric and high polymeric phenyl-fluoro phosphazenes. Note the chemical shift and splitting pattern that results from phosphorus coupling to the two fluorine atoms or to one fluorine. Spectra provided by W. D. Coggio.

P nmr spectra of H3PM012O40 after addition of t-BuOOH.

P nmr spectra of H5PV2M010O40 after addition of H2OJ

P NMR spectra of N3P3

P NMR spectra of nucleosome core particles in 5 wiM tris-Cl, 0.1 mM EOT A, pH 8,19 C at three observing frequencies. The line widths are

P NMR spectra of Zn2 five equivalents DPP

P NMR spectra of Zn22 in CD3CN the presence of a 1 equivalent DPP. b 2 equivalents DPP. c 5 equivalents DPP at room temperature. Gaussian deconvolution of the phosphorous signal of spectrum with d one equivalent DPP. e two equivalents DPP and f five equivalents DPP

P NMR spectroscopic course of the reaction of Ph3PAuCl and Au55

P NMR spectrum of a used catalyst after washing with large amounts of EtOH in dg-DMSO .

P NMR spectrum of ATP S, showing resonances from different isotopic arrangements. 0 is represented by .

P NMR spectrum of C6 glioma cells grown in a hollow fibre bioreactor. Note the important contribution of the GPC and GPE resonances. Inset

P NMR spectrum of Chinese hamster ovary cells . The assignments are



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