A pyridinium salt with crystalline phase transformation under water vapor and reversible mechanochromic luminescent properties
The photophysical properties of an organic aggregate are greatly affected by molecular conformation and intermolecular packing modes. Herein, an organic pyridinium salt was synthesized by quaternization of a pyridine derivative, and the resultant CPBBr dissolved well in both water and polar organic...
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Published in | Journal of materials chemistry. C, Materials for optical and electronic devices Vol. 9; no. 35; pp. 11738 - 11744 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
21.09.2021
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Subjects | |
Online Access | Get full text |
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Summary: | The photophysical properties of an organic aggregate are greatly affected by molecular conformation and intermolecular packing modes. Herein, an organic pyridinium salt was synthesized by quaternization of a pyridine derivative, and the resultant CPBBr dissolved well in both water and polar organic solvents, with bright green emission once doped into cyclodextrin. Under water vapor, the emission color of pristine CPBBr changed from deep blue to green, accompanied by a great enhancement of fluorescence quantum efficiency. Crystal structure analysis indicated that water molecules were involved in the crystal lattice, which promotes crystalline phase transformation from CPBBr-W to CPBBr-G, and greatly inhibits the intramolecular vibration
via
stabilizing the metastable molecular conformation and strengthening the intermolecular hydrogen bonds. The sharply decreased free volume fraction also demonstrated more compact molecular arrangements in the CPBBr-G crystal. Furthermore, CPBBr exhibited reversible mechanochromic luminescent (MCL) properties, and both the fluorescence efficiency and lifetime greatly increased after mechanical grinding as a result of the formation of an intermolecular charge transfer (CT) complex.
The pyridinium salt of CPBBr undergoes crystalline phase transformation under water vapor, accompanied by emission turn-on from deep blue to green. The reversible mechanochromism luminescence indicates the formation of a charge transfer excimer. |
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Bibliography: | For ESI and crystallographic data in CIF or other electronic format see DOI 2068451 2068450 Electronic supplementary information (ESI) available: Experimental, characterization, crystal structures, photophysical data, and other additional information. CCDC and 10.1039/d1tc01540k |
ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d1tc01540k |