dc.contributor.author |
Mahesh, S |
|
dc.contributor.author |
Anesh Gopal |
|
dc.contributor.author |
Rajasekaran, T |
|
dc.contributor.author |
Ajayaghosh, A |
|
dc.date.accessioned |
2013-07-04T06:06:01Z |
|
dc.date.available |
2013-07-04T06:06:01Z |
|
dc.date.issued |
2012-05-02 |
|
dc.identifier.citation |
Journal of the American Chemical Society 134(17):7227-7230;02 May 2012 |
en_US |
dc.identifier.uri |
http://hdl.handle.net/123456789/530 |
|
dc.description.abstract |
Ostwald ripening allows the synthesis of 1D
nanorods of metal and semiconductor nanoparticles.However, this phenomenon is unsuccessful with organic π-systems due to their spontaneous self-assembly to elongated fibers or tapes. Here we demonstrate the uses
of light as a versatile tool to control the ripening of amorphous organic nanodots (ca. 15 nm) of an azobenzene-derived molecular assembly to micrometersized supramolecular rods. A surface-confined dipole
variation associated with a low-yield (13−14%) trans−cis
isomerization of the azobenzene moiety and the
consequent dipole−dipole interaction in a nonpolar
solvent is believed to be the driving force for the ripening
of the nanodots to rods |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
American Chemical Society |
en_US |
dc.subject |
Polymers |
en_US |
dc.subject |
Azobenzene |
en_US |
dc.subject |
CDTE Nanoparticles |
en_US |
dc.subject |
Assemblies |
en_US |
dc.subject |
Chirality |
en_US |
dc.subject |
Oligo(P-phenyleneethynylene)s |
en_US |
dc.title |
Light-Induced ostwald ripening of organic nanodots to rods |
en_US |
dc.type |
Article |
en_US |
niist.citation |
|
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