z-logo
Premium
1 H, 19 F, and 31 P PGSE NMR Diffusion Studies on Chiral Organic Salts: Ion Pairing and the Dependence of a Diffusion Value on Diastereomeric Structure
Author(s) -
MartínezViviente Eloísa,
Pregosin Paul S.,
Vial Laurent,
Herse Christelle,
Lacour Jérôme
Publication year - 2004
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200305719
Subject(s) - diastereomer , chemistry , diffusion , hexacoordinate , pulsed field gradient , ion , phosphate , solvent , inorganic chemistry , organic chemistry , molecule , thermodynamics , physics , silicon
1 H, 19 F and 31 P pulsed field gradient spin‐echo (PGSE) diffusion studies on chiral organic salts that contain hexacoordinate phosphate anions, namely tris(tetrachlorobenzenediolato)phosphate( V ) (TRISPHAT) and bis(tetrachlorobenzenediolato)mono([1,1′]binaphthalenyl‐2,2′diolato)‐phosphate( V ) (BINPHAT), are reported. The first example of the dependence of a diffusion value on diastereomeric structure is presented. Marked solvent and concentration effects on the diffusion constants ( D ) of these salts are noted and the question of ion pairing is discussed.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom