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DC Field | Value | Language |
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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 |
Appears in Collections: | 2013 |
Files in This Item:
File | Description | Size | Format | |
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2013_0017.pdf Restricted Access | 1.66 MB | Adobe PDF | View/Open Request a copy |
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