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C CP MAS spectrum of ureido sugar, rotation speed 3 kHz.

C CP MAS TOSS NMR spectra of wool, SCMKA, SCMKA-hf, SCMKB, and HOT.

C CP NMR spectra of carbonyl carbon-labeled uniaxially draw were determined computer simulations of the observed NMR lineshapes. The structural parameters ap 90 , 3p 18 6 with the distribution of the fiber axis p 22 were found to be characteristic of the oriented component.

C CP NMR spectra of poly

C CP-MAS NMR of C 0, C and carbons from 1,2,3- CslAla-labeled bacteriorhodopsin. Reproduced with permission from the Japanese Biochemical Society.

C CP-MAS NMR spectra obtained with 50- polysiloxane-immobilized thiol-diamine ligand system. Ref. 16.

C CP-MAS NMR spectra of Ala-bR and Val-bR. Peaks designated by the asterisk from C-labeled lipids ,

C CP-MAS NMR spectra of Ala-labeled A215G of 40 pM Mn ion. The corresponding spectra of the 3- QAla-labeled wild-type bR are superimposed on the top and middle traces as dotted traces. Difference spectra between the spectra of the wild-type and mutant bRs in the presence of the Mn ion are shown as the bottom traces. Reproduced with permission from the Biophysical Society.

C CP-MAS NMR spectra of amine-based functionalized polysiloxanes. Primary

C CP-MAS NMR spectra of polysiloxane-immobilized phosphine systems. -CH2CH2PPh2. Ref. 18.

C CP-MAS NMR spectra of polysiloxane-immobilized phosphine-thiol systems. Diphenylethylphosphine-thiol. Ref. 18.

C CP-MAS NMR spectra of Pro-labeled wild-type bR from PM in the presence of 40 pM Mn ion. Reproduced with permission from Elsevier.

C CP-MAS NMR spectra of some polysiloxane-immobilized ligand systems. s -

C CP-MAS NMR spectra of some polysiloxane-immobilized ligand systems. S -CH2CH2CH2SCH2C02CH3- Asterisks indicate signals from unhydrolyzed ethoxy and methoxy groups. Ref. 15.

C CP-MAS NMR spectra of untreated polysiloxane-immobilized thiol-diamine system. Ref. 16.

C CP-MAS NMR spectra of Val-labeled wild type recorded at pH 7 and 10. It is noteworthy that the arrowed peaks from the transmembrane helices are displaced to higher frequencies by protonation of Asp 85 at neutral pH and suppressed at pH 10 taking the M-like state. The peak at 177.81 ppm is ascribed to Val 213. Reproduced with permission from the American Chemical Society.

C CP-MAS NMR spectrum of POLLG in the LC state at room temperature

C CP-MAS spectra of a Ca2Al VBS, and b Zn2Al VBS after heat treatment at different temperatures in air.

C CP-MAS spectra of APTS-mcxIified silica gel

C CP-MAS spectra of APTS-modified silica gels. Each column of spectra corresponds to the temperature of silica gel drying

C CP-MAS spectra of poly Macromolecules 1535.

C CPMAS NMR spectra of

C CPMAS NMR spectra of n-butylamine adsorbed to the surface of

C CPMAS NMR spectrum with CO in the solid state.

C CPMAS spectra at different cross-polarization times tq, of a N20 in Palatal P4 35 styrene and b H18



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