## Abstract Two‐dimensional H,C‐COSY spectra of some tetra‐, penta‐ and hexa‐coordinated organotin(IV) compounds were measured. The relative signs of ^__n__^__J__(^119^Sn,^13^C) and (^__n__+1^ __J__(^119^Sn,^1^H) coupling constants were determined after analysis of the orientation of the appropriat
119Sn NMR study of organotin compounds having intramolecular Sn—N coordination
✍ Scribed by Johann T. B. H. Jastrzebski; David M. Grove; J. Boersma; Gerard van Koten; Jan-Meine Ernsting
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 602 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^119^Sn NMR data are reported for organotin compounds containing potentially C,N‐chelating ligands capable of forming five‐ or six‐membered chelate rings. The ^119^Sn chemical shifts of divalent organotin compounds containing such a ligand are found at relatively high frequency. Intramolecular coordination in tetraorganotin compounds has little influence on their ^119^Sn chemical shifts. However, additional coordination in tri‐ and di‐organotin halides causes a large shift to lower frequency of about 100 ppm. Finally, for organotin compounds which exist as a diastereoisomeric mixture in solution, two well resolved ^119^Sn resonances are observed.
📜 SIMILAR VOLUMES
## Abstract The fundamental molecular aspects of trialkyltin compounds of the type R~3~SnY have been investigated in view of their applicability as ion‐selective components in solvent polymeric membranes. The interaction between these compounds and anions has been studied using ^119^Sn‐ and ^13^C‐N
## Abstract Organotin tropolonato complexes of the type R~3~Sn(trop) 1 [R = Bu (b), Ph (c)], R~2~Sn(trop)~2~ 2 [R = Me (a), Bu (b), Ph (c)] and RSn(trop)~3~ 3 [R = Bu (b), Ph (c)] were studied by single‐crystal X‐ray diffraction (1c, 2a,b, 3b), ^13^C and ^119^Sn MAS NMR and ^119^Sn NMR in solution.
## Complexes [Me 2 SnL 2 (I), Me 3 SnL (II), Et 2 SnL 2 (III), n-Bu 2 SnL 2 (IV), n-Bu 3 SnL (V), n-Oct 2 SnL 2 (VI)], where L is (E)-3-furanyl-2-phenyl-2propenoate, have been synthesized and structurally characterized by vibrational and NMR ( 1 H, 13 C and 119 Sn) spectroscopic techniques in comb