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dc.contributor.authorPrasanthkumar, S-
dc.contributor.authorSaeki, A-
dc.contributor.authorSeki, S-
dc.contributor.authorAjayaghosh, A-
dc.date.accessioned2014-03-31T08:19:31Z-
dc.date.available2014-03-31T08:19:31Z-
dc.date.issued2010-
dc.identifier.citationJournal of the American Chemical Society 132(26):8866-8867;7Jul 2010en_US
dc.identifier.issn0002-7863-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1250-
dc.description.abstractTrithienylenevinylenes having amide end functional groups form supramolecular gels in nonpolar solvents, comprised of self-assembled nanowires. These gels exhibit the unique property of solution phase epitaxy leading to the alignment of fibers on mica surface. FP-TRMC studies revealed high charge carrier mobility for xerogels from decane-chloroform whereas films obtained from chloroform solutions showed less mobility, highlighting the role of self-assembly and gelation on the electronic properties of semiconducting molecular gelators. This study opens the window for a new class of conducting gelators which may find wide application in organic electronic devices.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectPI-conjugated systemsen_US
dc.subjectThienylenevinylene oligomersen_US
dc.subjectQuaterthiopheneen_US
dc.subjectNanowiresen_US
dc.subjectOrganogelsen_US
dc.titleSolution phase epitaxial self-assembly and high charge-carrier mobility nanofibers of semiconducting molecular gelatorsen_US
dc.typeArticleen_US
Appears in Collections:2010

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