Study of the self-association of methylated pyrimidines in aqueous solutions by1H NMR chemical shifts

1990 ◽  
Vol 28 (3) ◽  
pp. 246-249 ◽  
Author(s):  
Ferenc Aradi
1983 ◽  
Vol 38 (3) ◽  
pp. 317-321 ◽  
Author(s):  
E. Haid ◽  
D. Köhnlein ◽  
G. Kössler ◽  
O. Lutz ◽  
W. Messner ◽  
...  

Abstract45Sc NMR chemical shifts, linewidths, and longitudinal relaxation rates have been measured in aqueous solutions of scandium chloride and sulphate as a function of the appropriate acid. A common typical behaviour of these parameters without sudden changes has been observed. Also signals in the basic range have been obtained. H2O -D2O solvent isotope effects on Larmor frequency and relaxation rates are presented.


2017 ◽  
Vol 19 (18) ◽  
pp. 11011-11016 ◽  
Author(s):  
Pedro P. Madeira ◽  
Helena Passos ◽  
Joana Gomes ◽  
João A. P. Coutinho ◽  
Mara G. Freire

The alternative probe pyridine-N-oxide allows the determination of the hydrogen-bond acidity of both neat ionic liquids and their aqueous solutions based on 13C NMR chemical shifts.


1990 ◽  
Vol 55 (2) ◽  
pp. 446-451 ◽  
Author(s):  
Josef Jirman ◽  
Antonín Lyčka

The 33S NMR spectra of 11 naphthalenesulfonates, 11 hydroxynaphthalenesulfonates, two dihydroxynaphthalenesulfonates, and their anions have been measured in aqueous solutions. The 33S NMR chemical shifts of these compounds exhibit upfield shifts when related to ammonium sulfate as the standard. Introduction of a further sulfonic group causes a small upfield shift (up to 3 ppm). Introduction of a hydroxyl group causes a downfield shift (up to 5 ppm) unless the ring is further substituted. Formation of the anion from hydroxyl group causes an additional downfield shift (up to 6 ppm). The half-width of 33S NMR signals of sulfonated naphthalenes, naphthols, and their anions vary from 10 to 400 Hz.


1961 ◽  
Vol 35 (5) ◽  
pp. 1911-1912 ◽  
Author(s):  
Charles F. Jumper ◽  
Merle T. Emerson ◽  
Bentz B. Howard

1984 ◽  
Vol 18 (9) ◽  
pp. 643-648
Author(s):  
E. V. Komarov ◽  
L. G. Kardo-Sysoeva ◽  
V. P. Mikhailova

Sign in / Sign up

Export Citation Format

Share Document