CPI (complementary polytopic interaction) stabilised liquid crystal compounds formed by esters of 2-hydroxy-3,6,7,10,11-pentakis(hexyloxy)triphenylene

Citation
N. Boden et al., CPI (complementary polytopic interaction) stabilised liquid crystal compounds formed by esters of 2-hydroxy-3,6,7,10,11-pentakis(hexyloxy)triphenylene, J MAT CHEM, 11(6), 2001, pp. 1612-1617
Citations number
20
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
JOURNAL OF MATERIALS CHEMISTRY
ISSN journal
09599428 → ACNP
Volume
11
Issue
6
Year of publication
2001
Pages
1612 - 1617
Database
ISI
SICI code
0959-9428(2001)11:6<1612:C(PISL>2.0.ZU;2-K
Abstract
An improved synthesis of 2-hydroxy-3,6,7,10,11-pentakis(hexyloxy)triphenyle ne 6 is reported which is based on the oxidative coupling of 2-acetoxy-1-he xyloxybenzene 3 to 3,3',4,4'-tetrakis(hexyloxy)biphenyl 4. Most of the este rs of this phenol 7-15, give an enantiotopic Col(h) columnar liquid crystal phase, which is stable over a wide temperature interval. This can be furth er enhanced by formation of 1 :1 CPI compounds with either 2,3,6,7,10,11- h exakis(4-nonylphenyl)triphenylene {PTP9} 1 or hexakis(4-nonylphenyl)dipyraz ino[2,3-f:2',3'-h]quinoxaline {PDQ9} 2. As with other triphenylene derivati ves, these additives can also be used to induce liquid crystal behaviour in otherwise non-mesogenic esters.