The combination of continuum and ultrafast pump–probe spectroscopy with DFT and TDDFT calculations, in viscous and non-viscous environments, is effective in unraveling important features of the twisted intramolecular charge transfer mechanism in a new push–pull molecule that possesses aggregation induced emission properties. Long-living optical gain is found when this mechanism is inhibited, highlighting the importance of the environment rigidity in the design of materials for photonic applications.

Long-living optical gain induced by solvent viscosity in a push-pull molecule

PASINI, DARIO;
2016-01-01

Abstract

The combination of continuum and ultrafast pump–probe spectroscopy with DFT and TDDFT calculations, in viscous and non-viscous environments, is effective in unraveling important features of the twisted intramolecular charge transfer mechanism in a new push–pull molecule that possesses aggregation induced emission properties. Long-living optical gain is found when this mechanism is inhibited, highlighting the importance of the environment rigidity in the design of materials for photonic applications.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1172546
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