𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A 13C and 1H NMR study of some aryltellurium tris(diethyldithiocarbamates)

✍ Scribed by Mohammad A. Khadim; Vijay Kumar; Peter H. Bird; Bhuvan C. Pant; Lawrence D. Colebrook


Publisher
John Wiley and Sons
Year
1982
Tongue
English
Weight
347 KB
Volume
19
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Carbon‐13 and proton NMR spectra are reported for phenyl‐,4‐methoxyphenyl‐, 4‐ethoxyphenyl‐ and 3‐methyl‐4‐methoxyphenyltellurium tris(diethyldithiocarbamate). Both the ^1^H and the ^13^C spectra are typical of compounds undergoing a fast exchange process, only the N‐methylene proton signals and the thiocarbonyl carbon signals showing evidence for exchange broadening. The phenyl C‐1 carbon signal is deshielded relative to benzene (by 12.0 ppm), and shows solvent dependence. The thiocarbonyl carbon atoms absorb at 197.5‐199.1 ppm, showing solvent dependence but little sensitivity to the aryl group substituents.


📜 SIMILAR VOLUMES


1H and 13C NMR Studies of Some Anthraqui
✍ K. Danielsen; G. W. Francis; D. W. Aksnes 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 297 KB 👁 2 views

H and lSC NMR chemical shifts are reported and assigned for 1,4,9,10-and 2,3,9,1 O-anthracenetetrone. In addition, NMR data are given for 2,3-dihydroxy-9, 1 O-anthraquinone, 2.3-dimethoxy-9.10anthraquinone and 1 -hydroxy-2-acetoxy-9,l O-anthraquinone, encountered during the preparation of the anthra

1H and 13C NMR study of some polychlorob
✍ D. Botta; E. Mantica; L. Castellani; G. Dotelli; L. Zetta 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 110 KB 👁 1 views

Because of the upsurge of interest in polychlorobuta-1,3-diene derivatives as uncommon contaminants in underground water, seven congeners, the three pentachloro-and four tetrachloro-[(Z)-and (E)-1,1,3,4tetrachloro-, 1,1,4,4-tetrachloro-and (Z,Z)-1,2,3,4-tetrachloro]buta-1,3-dienes, were synthesized

1H and 13C NMR studies of some aromatic
✍ Arlette Solladié-Cavallo; Marcel Hilbert 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 379 KB

## Abstract Carbon‐13 and proton NMR data of macrocyclic diaromatic dilactones are presented. The observed behaviour of the spectra as a function of temperature shows that the energy barrier for the re‐orientation of the side chains is lower than 49 kJ mol^−1^ (12 kcal mol^−1^) and that the energy