An Energy-Tunable Dual Emission Mechanism of the Hybridized Local and Charge Transfer (HLCT) and the Excited State Conjugation Enhancement (ESCE)

22 November 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Molecular design of dual-fluorescent probes requires precise adjustment of the energy levels of two excited states and the energy barrier between them. While the hybridized local and charge-transfer (HLCT) state has been recently focused as an important excited state for high radiation efficiency with a tunable energy level, a dual emission involving the HLCT state has been only achieved with the excited-state intramolecular proton transfer (ESIPT) system. Here, a series of dual-fluorescent molecules involving a HLCT excited state with the excited-state conjugation enhancement (ESCE) motif is presented as the first case. The energy level of the HLCT state has been adjusted by modulating substituents and solvents, separately from the ESCE energy level. The HLCT-ESCE molecular design with tunable fluorescence properties proposes a new strategy for the development of advanced fluorescent probes.

Keywords

Excited State
Hybridized Local and Charge Transfer
Excited-State Conjugation Enhancement
Transient Absorption Spectroscopy

Supplementary materials

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Supporting Information
Description
Details for synthesis, X-ray structure analysis, photophysical properties, transient absorption measurements, and quantum chemical calculations
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