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Bridge-Driven Aggregation control in Dibenzofulvene-Naphthalimide Based Donor−Bridge−Acceptor Systems:  Enabling Fluorescence Enhancement, Blue to Red Emission and Solvatochromism

Abstract

Four novel 1,8-naphthalimide (NC) and mono-substituted dibenzofulvene (DBF) based structures have been designed and successfully synthesized. Two luminogens were substituted by a thiophene bridge (DT1NC and DT2NC) while the two other luminogens were substituted by a phenyl bridge (DP1NC and DP2NC) between NC and DBF units. This minor structural modification crafts striking changes in the photophysical behavior. DT1NC and DT2NC displayed aggregation induced emission enhancement (AIEE) behavior. They also showed orange and red emission (575 nm and 602 nm) respectively with large bathochromic shifts (35 nm and 112 nm) and high quantum yields (84.10% and 65.65%) in the aggregated state due to ladder type J-aggregation. DP1NC exhibited weak AIEE behavior in blue region while DP2NC showed AIE inactive nature due to the strong C-H•••π intermolecular interactions. All luminogens showed positive solvatochromism caused by intramolecular charge transfer (ICT). The DT2NC and DP2NC luminogens were substituted with two bromine atoms at 2,7 positions of the DBF moiety, but unexpectedly only the DT2NC showed strong heavy atom effect. Theoretical and experimental HOMO and LUMO energy levels were estimated by the density functional theory and cyclic voltammetry respectively. All luminogens displayed excellent thermal stabilities and good morphological behavior.

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Publication details

The article was received on 04 Aug 2017, accepted on 08 Sep 2017 and first published on 08 Sep 2017


Article type: Research Article
DOI: 10.1039/C7QM00357A
Citation: Mater. Chem. Front., 2017, Accepted Manuscript
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    Bridge-Driven Aggregation control in Dibenzofulvene-Naphthalimide Based Donor−Bridge−Acceptor Systems:  Enabling Fluorescence Enhancement, Blue to Red Emission and Solvatochromism

    P. Gopikrishna, L. R. Adil and P. K. Iyer, Mater. Chem. Front., 2017, Accepted Manuscript , DOI: 10.1039/C7QM00357A

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