## 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
Pyridine and aminide derivatives as ligands in 1 : 1 Rh2[tfa]4 adducts: 1H, 13C and 15N NMR study
✍ Scribed by Jarosław Jaźwiński; Helmut Duddeck
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 143 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1263
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✦ Synopsis
Abstract
^1^H, ^13^C and ^15^N chemical shifts of some pyridines and mesoionic oxatriazole aminides were recorded in the absence and presence of the complex dirhodium tetrakis(trifluoroacetate). The adduct formation shifts prove that the nitrogen atom in the pyridine derivatives and the N‐6 atom of the aminides are the binding sites in the adducts. At low temperature, adduct species can be identified separately by their individual signals. The ^15^N chemical shift responds very sensitively even to small concentration changes in the adduct. Copyright © 2003 John Wiley & Sons, Ltd.
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