Conformational-induced light emission switching of N-acylhydrazone systems

August 13, 2018

Title

Conformational-induced light emission switching of N-acylhydrazone systems

Author

Mihaela Matache, Anca Gabriela Coman, Anca Paun, Codruta Paraschivescu, Niculina Daniela Hadade, Catalin C. Anghel, Augustin M Madalan, Petre Ionita

Year

2018

Journal

New Journal of Chemistry

Abstract

N-acylhydrazones have been described as responsive compounds to a wide variety of triggers that are able to induce reversible structural changes. These reversible constitutional, conformational or configurational changes caused by physical or chemical stimuli are useful tools in designing molecular switches. We report herein bis-N-acylhydrazones as new switchable-light emissive molecules triggered by light and/or solvent. The emissive properties could be explained by phototautomerisation (Excited State Intramolecular Proton Transfer) and by formation of aggregates (Aggregation-Induced Emission). We investigated influence of structural particularities brought in by electron-donor or electron-withdrawing substituents as well as the demand of several hydrazone bonds in the molecular structure for the generation of light.

Instrument

FP-8300

Keywords

Fluorescence, Chemical stability, Aggregation, Quantum yield, Organic chemistry, Materials, Optical properties