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Control of pi-stacking for highly emissive poly(p-phenylenevinylene)s: Synthesis and photoluminescence of new tricyclodecane substituted bulky poly(p-phenylenevinylene)s and its copolymers

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dc.contributor.author Amrutha, S R
dc.contributor.author Jayakanan, M
dc.date.accessioned 2014-04-22T11:30:27Z
dc.date.available 2014-04-22T11:30:27Z
dc.date.issued 2006
dc.identifier.citation Journal of Physical Chemistry B 110(9):4083-4091;9 Mar 2006 en_US
dc.identifier.issn 1520-6106
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/1360
dc.description.abstract In the present work, we have demonstrated a facile approach to increase the luminescence of the poly (p-phenylenevinylene)s via controlling the molecular aggregates induced by pi-stacking. We have synthesized new bulky tricyclodecane (TCD) substituted PPVs: poly(2-methoxy-5-tricyclodecanemethyleneoxy-1,4-phenylenevinylene) (MTCD-PPV), poly(bis-2,5-tricyclodecanemethyleneoxy-1,4-phenylenevinylene) (BTCD-PPV), and a series of symmetrically substituted bulky PPV copolymers (P-1-P-7) covering the entire composition range from 0 to 100 mol %. The structures of the monomers and polymers were confirmed by H-1 NMR and FTIR, and the molecular weights were determined by gel permeation chromatography. The composition analysis by NMR revealed that the bulky monomer was highly reactive and the incorporation of bulky units in MEH-PPV increased irrespective of the feed ratio. The polymers possess good solubility, high molecular weights, good thermal stability, and so forth. The molecular weights of the PPV copolymers were also significantly affected by the bulky substitution: the higher the incorporation of bulky units, the lower the molecular weight. The absorption and emission studies revealed that there was no influence on the MEH-PPV by TCD substitution in solution whereas in the solid state the photoluminescence intensity of PPV increased more than 10 times. The luminescence increase in PPV was observed throughout the entire bulk and was not confined to any particular domain in the polymer. The bulky PPV copolymers showed that both the luminescence intensity (in film) and quantum yields (in solution) increased with an increase in the extent of BTCD incorporation in the MEH-PPV and attained a maximum for 50% BTCD. The TCD unit has thus proved to be an efficient bulky susbstituent for PPV as it controls the pi-stack-induced molecular aggregates in the polymer chains by increasing the interchain distances. The new bulky PPV copolymers are highly soluble, thermally stable, and highly luminescent besides being economically cheap compared to the other materials reported so far for the bulkier approach in pi-conjugated materials. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Light-emitting polymers en_US
dc.subject Molecular aggregation en_US
dc.subject Silsesquioxane units en_US
dc.subject Conjugated polymers en_US
dc.subject Electroluminescence en_US
dc.subject Phenylenevinylene en_US
dc.title Control of pi-stacking for highly emissive poly(p-phenylenevinylene)s: Synthesis and photoluminescence of new tricyclodecane substituted bulky poly(p-phenylenevinylene)s and its copolymers en_US
dc.type Article en_US


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