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H NMR chemical shift changes .

H NMR chemical shift of sulfamidites and sulfamidates.

H NMR chemical shift ranges X Halogen. -N . -S-. -0-

H NMR chemical shifts extracted from spectra of binary mixtures of and as function of molar ratio .

H NMR chemical shifts for 1-alkyl- and 2-alkyl-pyrazolopyridines

H NMR chemical shifts for carboxonium ions from chrysene derivatives .

H NMR chemical shifts for cyclopentadiene, pyrrole, furan, and 35, the last computed at PW91 IGLO-III B3LYP 6-311-l-G.

H NMR chemical shifts for dications from cyclopentaphenan-threne derivatives .

H NMR chemical shifts for fluoropyrenium ions .

H NMR chemical shifts for persistent 9-alkylanthracenium ions.

H NMR chemical shifts for quinolizinium bromide

H NMR chemical shifts interacting with the zeolite surface.

H NMR chemical shifts of annulene and its dianion . Ring currents are indicated in blue. The magnetic field B points toward the viewer. Particularly the dianion is a floppy structure, which

H NMR chromatogram of an SFC separation of five plasticisers

H NMR chromatogram of an SPE-HPLC separation of naproxen, fenoprofen and ibuprofen.

H NMR contour plot of a solvent mixture over the range from 100 ACN to

H NMR coupling constant data of keto-acetonide 49.

H NMR data demonstrating the formation of 47a to 51 and the conversion of 51 to 52 over time. Structural assignments were independently confirmed by ReactIR technology

H NMR data for benzophenanthrenium ions, benzochrysenium ions, and related carboxonium ions.

H NMR data for carbocations derived from benzopyrene and dibenzopyrene.

H NMR data for dynamic phenanthrenium ions .

H NMR data for methylphenanthrenium dications.

H NMR data for methylphenanthrenium ions.

H NMR data for persistent carbocations from the benzanthracene derivatives and for related a-substituted carbocations and a-carboxonium ions .

H NMR data for pyrene-dicarboxonium dications.



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