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Fabrication of diverse nano-architectures through the selfassembly of a naphthalene diimide derivative bearing four carbamates

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dc.contributor.author Wagalgave, S.M.
dc.contributor.author DucLa, D.
dc.contributor.author Bhosale, R.S.
dc.contributor.author Kobaisi, M.A.
dc.contributor.author Jones, L.A.
dc.contributor.author Bhosale, Sidhanath V.
dc.contributor.author Bhosale, S.V.
dc.date.accessioned 2018-05-07T08:22:14Z
dc.date.available 2018-05-07T08:22:14Z
dc.date.issued 2018
dc.identifier.citation New Journal of Chemistry. 42(9); 2018; 6785-6793. en_US
dc.identifier.uri http://dx.doi.org/10.1039/C7NJ04503D
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/5189
dc.description.abstract A naphthalene diimide (NDI) derivative bearing four carbamate groups (coded as: W2) was synthesised using a multistep strategy, and utilizing solvophobic effects the self-assembly of this molecule was studied usingsolvent mixtures. Selfassembly led to a variety of controllable morphologies on both micro and nanoscale supramolecular structures. Nanobelts, nanospheres, nano-corals, microflowers and nanograss-like morphologies were obtained in DMF, MCH, CHCl3, THF, water and MeOH solvent mixtures. The aggregation of W2 in solution was studied using UV-vis absorption, fluorescence emission spectroscopy, FT-IR and XRD gave insight intothe mode of aggregation of W2 in various solvents. The polarity of the solvent mixtures used directed the self-organisation of W2 by drives the ?-? stacking interaction between NDI cores, and the H-bondingbetween the carbamate moieties. Our studies show that the solvent polarity guides the self-assembly process during solvent evaporation leading to the formation of supramolecular nano- and microstructures under ambient conditions. en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Chemistry en_US
dc.title Fabrication of diverse nano-architectures through the selfassembly of a naphthalene diimide derivative bearing four carbamates en_US
dc.type Journal article en_US
dc.identifier.impf y


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