Quinolin‐8‐aminium toluene‐4‐sulfonate
Author(s) -
Smith Graham,
Wermuth Urs D.,
Healy Peter C.
Publication year - 2004
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s1600536804014898
Subject(s) - quinoline , sulfonate , toluene , protonation , chemistry , hydrogen bond , cationic polymerization , crystal structure , proton , sulfonic acid , medicinal chemistry , hydrogen atom , group (periodic table) , photochemistry , polymer chemistry , organic chemistry , molecule , sodium , ion , physics , quantum mechanics
The crystal structure of the 1:1 proton‐transfer compound of 8‐aminoquinoline with toluene‐4‐sulfonic acid, viz . quinolin‐8‐aminium toluene‐4‐sulfonate, C 9 H 9 N 2 + ·C 7 H 7 O 3 S − , is different from previously characterized proton‐transfer compounds of 8‐aminoquinoline, in that the 8‐amino group rather than the quinoline N atom is protonated. All H atoms of this aminium group are subsequently involved in intermolecular hydrogen‐bonding interactions with sulfonate O‐atom acceptors, linking the cationic and anionic species and forming a linear polymer structure.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom