𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A 13C NMR study of pyridine in the presence of aqueous solutions of carbohydrates

✍ Scribed by Laurance D. Hall; Mansur Yalpani


Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
285 KB
Volume
16
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Spin‐lattice relaxation rates of the ^13^C responses of pyridine were measured in the presence of aqueous sucrose and sodium alginate solutions and calcium alginate gels. In each case the results indicated a reduction in the overall tumbling rate of pyridine compared with that in aqueous media due to molecular association with the carbohydrate. Although anisotropic motion about the C‐4:N axis of pyridine was apparent in the sucrose solutions no consistent trends were observed for the alginate samples.


📜 SIMILAR VOLUMES


Conformational study of phosphothreonine
✍ L. Pogliani; D. Ziessow 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 English ⚖ 250 KB 👁 1 views

## Abstract The 270 MHz ^1^H and 22.6 MHz ^13^C NMR spectra of DL‐phosphothreonine in D~2~O have been measured and analysed as a function of pD. The __trans__‐__trans__ conformation of the fragment H‐αC‐αC‐βOP predominates at all pD values. The C‐β—O __gauche__ contribution is notably larger fo

1H and 13C NMR studies of the self-assoc
✍ David Attwood; Roger Waigh; Ross Blundell; Debra Bloor; André Thévand; Elizabeth 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 393 KB 👁 1 views

## Abstract The ^1^H NMR spectrum of chlorpromazine hydrochloride was fully assigned at 400 MHz. Similarly, the ^13^C NMR spectrum was assigned unambiguously using two‐dimensional NMR. Measurements of chemical shift as a function of concentration in D~2~O showed appreciable changes of shift of both

13C NMR studies of tautomerism in imidaz
✍ P. Barraclough; J. C. Lindon; M. S. Nobbs; J. M. Williams 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 211 KB

A detailed analysis of the I3C NMR spectra of the 1-N-and 3-N-methyl derivatives of lH-2-(2,4-dimethoxyphenyI)imidazo[4,5-~]pyridine, utilizing long-range couplings and 2D 'H-I3C correlation experiments, has led to an unambiguous assignment of all carbons. Comparison of these definitive assignments

The tautomerism of Omeprazole in solutio
✍ Rosa M. Claramunt; Concepción López; Ibon Alkorta; José Elguero; Rong Yang; Stev 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 90 KB 👁 2 views

## Abstract The tautomerism of 5(6)‐methoxy‐2‐{[(4‐methoxy‐3,5‐dimethyl‐2‐pyridinyl)methyl] sulfinyl}‐1__H__‐benzimidazole (omeprazole) was determined in solution, __K__~__T__~ = 0.59 in THF at 195 K, in favor of the 6‐methoxy tautomer. The assignment of the signals was made by comparison with its