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dc.contributor.authorYamauchi, M-
dc.contributor.authorKubota, S-
dc.contributor.authorKaratsu, T-
dc.contributor.authorKitamura, A-
dc.contributor.authorAjayaghosh, A-
dc.contributor.authorYagai, S-
dc.date.accessioned2013-08-19T06:34:43Z-
dc.date.available2013-08-19T06:34:43Z-
dc.date.issued2013-
dc.identifier.citationChemical Communications 49(43):4941-4943;2013en_US
dc.identifier.urihttp://hdl.handle.net/123456789/580-
dc.description.abstractBismelamines end-functionalized with oligo(p-phenylenevinylene) self-aggregate in nonpolar solvent to form short nanorods by helical π–π stacking. This inherent self-aggregation can be guided to a supramolecular polymerization pathway by complexing with a cyanurate, leading to gel-forming elongated nanotapes lacking the helical sense of the π-conjugated moieties.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistry.en_US
dc.subjectHydrogen-bonding interactionsen_US
dc.subjectNanotapesen_US
dc.subjectOrganogelsen_US
dc.subjectChromophoresen_US
dc.titleGuided supramolecular polymerization of oligo(p-phenylenevinylene) functionalized bismelamines.en_US
dc.typeArticleen_US
Appears in Collections:2013

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