𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H and 13C n.m.r. spectra of dichloro(trans-2-chlorovinyl)arsine

✍ Scribed by Jaakko Paasivirta; Raili Versterinen; Liisa Virkki; Pekka Pyykkö


Publisher
John Wiley and Sons
Year
1977
Tongue
English
Weight
152 KB
Volume
10
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Proton and carbon magnetic resonance spectra of Lewisite or dichloro(trans‐2‐chlorovinyl)arsine have been measured and the results are compared with the n.m.r. spectral parameters of other trans‐1,2‐substituted ethylenes. The coupling constants can be rationalized by substituent electronegativity. The chemical shifts show an unusually large paramagnetic effect from the AsCl~2~ group.


📜 SIMILAR VOLUMES


13C n.m.r. spectra of some thiobenzamide
✍ C. Piccinni-Leopardi; O. Fabre; D. Zimmermann; J. Reisse; F. Cornea; C. Fulea 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 English ⚖ 254 KB

## Abstract ^13^C n.m.r. spectra of a series of __N__,__N__‐disubstituted thioamides have been recorded and signal assignments were performed. Separate signals are observed for methylene groups fixed on the nitrogen atom. Since the carbon atom __syn__ to the thiocarbonyl sulfur resonates at higher

13C n.m.r. spectra of 2-substituted pyri
✍ Christopher J. Turner; Gordon W. H. Cheeseman 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 English ⚖ 394 KB

## Abstract ^13^C n.m.r. chemical shifts and carbon‐proton coupling constants of 2‐substituted pyrimidines are reported. The carbon chemical shifts are correlated with π‐electron densities. Substituents which cause deshielding at the directly bound carbon (e.g. NH~2~, OCH~3~ and F) exert a more pow

1H, 13C and 15N NMR spectra of [1,2-15N2
✍ Alain Fruchier; Valdo Pellegrin; Rosa Maria Claramunt; Jose Elguero 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 199 KB

## 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

Effects of simultaneous 13C1H and 13C11B
✍ M. Mazurek; T. M. Mallard; P. A. J. Gorin 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 254 KB

## Abstract ^13^C FT n.m.r. spectra were obtained from borates of methyl α‐D‐glucopyranoside, triethylboron, sodium tetraphenylboron and 1‐butaneboronic acid employing a simultaneous ^1^H and ^11^B decoupling network. The effectiveness of the system was evident using the three latter organoboron co

Carbon-13 n.m.r. studies. 65—13C spectra
✍ A. K. Cheng; J. B. Stothers 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 431 KB

## Abstract The ^13^C n.m.r. spectra of 18 derivatives of the tricyclo[3.2.1.0^2,4^]octanes have been determined. This series includes methyl, hydroxyl and oxo substituted examples to compare the effects of these substituents on the skeletal carbon shieldings with those observed for the correspondi