## Abstract High‐resolution ^1^H{^14^N} and proton‐coupled natural‐abundance ^13^C{^14^N} double resonance spectra have been recorded for pyridinium tetrafluoroborate dissolved in CD~3~CN. Iterative analysis of these spectra has provided the accurate values and relative signs of all possible long
High resolution NMR spectroscopy of heteroaromatic cations. II—pyrylium, thiapyrylium and seleninium cations
✍ Scribed by P. Sándor; L. Radics
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 892 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
High resolution ^1^H, proton coupled ^13^C and broad‐band decoupled ^13^C{^1^H} spectra have been recorded for pyrylium, thiapyrylium and seleninium tetrafluoroborates in CD~3~CN. Analysis of these spectra has provided accurate values and relative signs of all ^1^H,^1^H and ^13^C,^1^H coupling constants, as well as the magnitudes of all one‐ and three‐bond ^13^C,^13^C couplings observable in naturally occurring doubly‐labelled isotopomers. For the seleninium cation, the magnitudes and relative signs of all ^77^Se,^1^H and ^77^Se,^13^C coupling constants were also obtained. The chemical shifts and coupling data are compared, on a qualitative basis, with existing theoretical predictions.
📜 SIMILAR VOLUMES
The proton (H) attached to the bold structure at the nitrogen atom of the acylthiourea ligand in Scheme 2 in the printed paper [1] was present in error. These ligands are actually deprotonated, and the proton (H) has been removed in the corrected Scheme 2 shown in this document.