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Exceptional dual fluorescent, excited-state intramolecular proton-transfer (ESIPT) columnar liquid crystals characterized by J-stacking and large Stokes shifts

Excited-State Intramolecular Proton-Transfer (ESIPT) fluorophores are emerging as promising future materials for electronic and biotechnological applications. ESIPT columnar (Col) liquid crystals (LCs) have been especially projected as the apt materials for advanced technological endeavors. But, the...

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Bibliographic Details
Published in:Journal of molecular liquids 2021-06, Vol.332, p.115879, Article 115879
Main Authors: Kanakala, Madhu Babu, Yelamaggad, Channabasaveshwar V.
Format: Article
Language:English
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Summary:Excited-State Intramolecular Proton-Transfer (ESIPT) fluorophores are emerging as promising future materials for electronic and biotechnological applications. ESIPT columnar (Col) liquid crystals (LCs) have been especially projected as the apt materials for advanced technological endeavors. But, there are hardly any explorations in this direction and thus, needing immediate attention. Herein we report on the synthesis, characterization, and ESIPT activity of a homologous series of novel phasmidic bis(N-salicylideneaniline) Col LCs. Optical microscopic, calorimetric and powder X-ray diffraction (XRD) studies evidence the occurrence of hexagonal columnar (Colh) phase having p6mm symmetry where the constituent slices result from the self-assembly of a pair of mesogens in a side-by-side manner facilitated by intense longitudinal π-π interactions. X-ray data confirm the absence of both directionally correlated tilting of the slices and transverse core-core interactions within the columns. Fluorescence probing clearly evidence the ESIPT occurring not only in DCM solution of the mesogens but also in their three-condensed states viz., solid, liquid crystal, and isotropic liquid phase; in general, two archetypal emission bands at ~430 nm (weak) and ~ 630 nm (strong) with large Stokes shifts (250–275 nm) of ESIPT phenomenon have been observed. The slow shift of emission maxima of the ESIPT fluorescence as a function of decreasing temperature without photoluminescence quenching coupled with the estimated tilt angle (ϴ) of the slices normal to the columnar axis (37 to 42o), from the XRD data, confirm the formation of so-called Scheibe or J-aggregates. The redox activity, metal ion sensing ability, and solvatochromism of the mesogens have also been investigated. The study suggests that these ESIPT Col LCs with band-gap of about 3 eV can be regarded as wide-bandgap semiconducting materials having the electronic characteristics falling between those of conventional semiconductors and insulators. •Novel hexacatenar liquid crystals have been synthesized and characterized.•They exhibit ESIPT activity in their three condensed states and solutions.•X-ray study confirms the columnar structure having J-aggregation.•Large stokes shift and solvatochromism have been revealed.•The metal ion sensing ability and redox activity have been witnessed.
ISSN:0167-7322
1873-3166
DOI:10.1016/j.molliq.2021.115879