## REFERENCE DATA carbons, for various substituent groups and positions were carried out by gated decoupling with NOE. ## RESULTS AND DISCUSSION The I3C NMR chemical shifts of the compounds are shown in Tables 123; 'J(CH) and long-range coupling constants of 2, 9, 13 and 18, measured by gated d
1H, 13C, 15N, 113Cd, 2D 15N1H and solid-state 13C CP/MAS NMR of Hg and Cd complexes of 4(1H)-quinazolinone-2,3-dihydro-2-thioxo
✍ Scribed by Francisco Javier Martínez-Martínez; Armando Ariza-Castolo; Victor Ramos-Nava; Norah Barba-Behrens; Rosalinda Contreras
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 323 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The Cd(II) and Hg(II) complexes of 4(1H)‐quinazolinone‐2,3‐dihydro‐2‐thioxo (1) and the free ligand were studied by 1D and 2D multinuclear magnetic resonance in solution and ^13^C cross polarization magic angle spinning NMR in the solid state. Compound 1 adopts only one of five possible tautomeric structures in solution, namely the thiouracyl‐like structure. It was found that the metal atom is linked to two molecules of deprotonated 1 by N‐1 and coordinated by the sulphur atom. The compounds retain the same structure in the solid state and in dimethyl sulphoxide solution.
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