Issue 3, 2021

Molecular structure controlled self-assembly of pyridine appended fluorophores: multi-stimuli fluorescence responses and fabricating rewritable/self-erasable fluorescent platforms

Abstract

The fluorescence properties of organic materials are intrinsically governed by the molecular conformation and intermolecular interaction mediated aggregation. Herein, we have synthesized two sets of isomeric fluorescence molecules with a partially planar and propeller structure, (Z)-3-(4-(9H-carbazol-9-yl)phenyl)-2-(pyridinyl)acrylonitrile (1–3) and (Z)-3-(4-(diphenylamino)phenyl)-2-(pyridinyl)acrylonitrile (4–6) and explored their effect on the molecular aggregation, and tunable and switchable solid state fluorescence. Molecular aggregation studies revealed the formation of 1D nanostructures of nanoparticles with the evolution of intermolecular interactions with increasing water fraction and time. The evolution of nanostructures led to a tunable fluorescence from green to red. The subtle structural change and formation of different crystal forms/polymorphs resulted in a tunable fluorescence between 514 and 644 nm (Φf = 11.3 to 25.3%). Solid state structural studies showed relatively weak intermolecular interactions in the crystal lattice of 1, 3 and 6 that resulted in the formation of different crystal forms/polymorphs and varied molecular assemblies with tunable fluorescence. Mechanofluorochromism (MFC) studies also showed molecular structure dependent fluorescence switching. 1–3 and 6 showed crushing/heating induced reversible fluorescence switching whereas 4 and 5 did not show any MFC. Integrating an acid/base sensitive pyridine functionality has been exploited for demonstrating halochromic reversible fluorescence switching as well as fabricating rewritable/self-erasable fluorescent platforms on filter paper and glass plates.

Graphical abstract: Molecular structure controlled self-assembly of pyridine appended fluorophores: multi-stimuli fluorescence responses and fabricating rewritable/self-erasable fluorescent platforms

Supplementary files

Article information

Article type
Paper
Submitted
25 sep. 2020
Accepted
10 dic. 2020
First published
12 dic. 2020
This article is Open Access
Creative Commons BY-NC license

Mater. Adv., 2021,2, 996-1005

Molecular structure controlled self-assembly of pyridine appended fluorophores: multi-stimuli fluorescence responses and fabricating rewritable/self-erasable fluorescent platforms

P. Gayathri, M. Pannipara, A. G. Al-Sehemi, D. Moon and S. P. Anthony, Mater. Adv., 2021, 2, 996 DOI: 10.1039/D0MA00736F

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