dc.contributor.author |
Yamauchi, M |
|
dc.contributor.author |
Kubota, S |
|
dc.contributor.author |
Karatsu, T |
|
dc.contributor.author |
Kitamura, A |
|
dc.contributor.author |
Ajayaghosh, A |
|
dc.contributor.author |
Yagai, S |
|
dc.date.accessioned |
2013-08-19T06:34:43Z |
|
dc.date.available |
2013-08-19T06:34:43Z |
|
dc.date.issued |
2013 |
|
dc.identifier.citation |
Chemical Communications 49(43):4941-4943;2013 |
en_US |
dc.identifier.uri |
http://hdl.handle.net/123456789/580 |
|
dc.description.abstract |
Bismelamines 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.iso |
en |
en_US |
dc.publisher |
Royal Society of Chemistry. |
en_US |
dc.subject |
Hydrogen-bonding interactions |
en_US |
dc.subject |
Nanotapes |
en_US |
dc.subject |
Organogels |
en_US |
dc.subject |
Chromophores |
en_US |
dc.title |
Guided supramolecular polymerization of oligo(p-phenylenevinylene) functionalized bismelamines. |
en_US |
dc.type |
Article |
en_US |