| Literature DB >> 14695550 |
Richard A van Delden1, Tommaso Mecca, Carlo Rosini, Ben L Feringa.
Abstract
Two new structurally related photoswitches are described, in which azobenzene photochromism is combined with the chirality of a 2,2'-dihydroxy-1,1'-binaphthyl unit. In system 1 the chiral binaphthyl moiety is bridged by a methylene tether, locking the biaryl chirality while in system 2 the biaryl core is unbridged and has considerable conformational flexibility. Both compound are capable of inducing cholesteric liquid crystalline phases and proved to be good photoswitches both in solution and in a liquid crystalline matrix. Compound 2 is capable of completely reversing the liquid crystalline chirality which is unique for a chiroptical molecular switch where the switching unit and the chiral moiety are separate entities.Entities:
Year: 2004 PMID: 14695550 DOI: 10.1002/chem.200305276
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236