1H- and 13C-NMR-Spectroscopic Study of Chemical Equilibria in Solutions of Formaldehyde in Water, Deuterium Oxide, and Methanol

1994 ◽  
Vol 33 (4) ◽  
pp. 1022-1029 ◽  
Author(s):  
Immanuel Hahnenstein ◽  
Hans Hasse ◽  
Cornelius G. Kreiter ◽  
Gerd Maurer
1991 ◽  
Vol 69 (8) ◽  
pp. 1207-1211 ◽  
Author(s):  
Paris E. Georghiou ◽  
Chi Keung (Jimmy) Ho ◽  
Chester R. Jablonski

The 1H and 13C NMR spectra of chromotropic acid (CTA) (4,5-dihydroxy-2,7-naphthalenedisulphonic acid) have been unambiguously assigned. Proton NOED spectra were used to show the proximity of both H-3 and H-6 and the hydroxyl groups. Two-dimensional 1H–13C NMR correlation spectra of CTA, of its corresponding diacetoxy derivative, and of 3-bromo- and 3,6-dibromo-CTA support the assignments. A regioselective deuterium exchange reaction of the C-3 and C-6 protons of CTA with deuterium oxide was observed during the NMR experiments. This latter finding is strongly indicative of the mode of formation, and of the nature of the chromogen formed in the reaction of CTA with formaldehyde in the well-known CTA-formaldehyde analytical reaction. Key words: chromotropic acid, 3-bromochromotropic acid, 3,6-dibromochromotropic acid.


1993 ◽  
Vol 58 (6) ◽  
pp. 1378-1387 ◽  
Author(s):  
Josef Jirman

The 1H and 13C NMR spectra of twenty-one technically important sulfonated 1- and 2-naphthylamines have been measured in deuterium oxide. The substituent chemical shifts (SCS) of a sulfonic acid group on naphthylamine skeleton have been calculated from the chemical shifts assigned.


Molecules ◽  
2000 ◽  
Vol 5 (12) ◽  
pp. 479-480
Author(s):  
Alejandra Salerno ◽  
Isabel Perillo

1987 ◽  
Vol 40 (1) ◽  
pp. 27-33 ◽  
Author(s):  
Masakazu TAKAHASHI ◽  
Masami NISHINA ◽  
Eitaro HORI ◽  
Kazuhiro MATSUSHITA ◽  
Kenzo KATO ◽  
...  

Author(s):  
George A. Olah ◽  
G. K. Surya Prakash ◽  
Massoud Arvanaghi ◽  
Frank A. L. Anet

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