## Abstract THF solutions of the cationic chiral 1,3‐diphenylallyl bidentate phosphine complexes [Pd(η^3^‐PhCHCHCHPh)(Duphos)](CF~3~SO~3~), Duphos = 1,2‐Bis‐((2R,5R)‐2,5‐dimethylphospholano)benzene), 2, and [Pd(η^3^‐PhCHCHCHPh)(P,S)]BF~4~, 4, P,S = [8‐((__o‐__(diphenylphosphino)benzyl) thiomethyl]—
PGSE diffusion, 1H–19F HOESY and NMR studies on several [Rh(1,5-COD)(Biphemp)]X complexes: detecting positional anion effects
✍ Scribed by P. G. Anil Kumar; Paul S. Pregosin; Thomas M. Schmid; Giambattista Consiglio
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 160 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1406
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Three new salts of Rh(I), [Rh(1,5‐COD)(Biphemp)]X, Biphemp = (6,6′‐dimethylbiphenyl‐2,2′‐diyl)bis(diphenylphosphine), X = BF~4~^−^, 2a, PF~6~^−^, 2b, and CF~3~SO~3~^−^, 2c, were prepared and studied using PGSE diffusion, ^1^H–^19^F HOESY and inverse ^103^Rh (amongst other) NMR methods. Although the immediate coordination sphere of the cation does not sense the change in the anion, the PGSE diffusion and ^1^H–^19^F HOESY data suggest that, in addition to some ion pairing, each of the anions in 2 demonstrates selectivity in its approach towards the cation. Copyright © 2004 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES