A multi‐stimuli‐responsive fluorescence material based on 1,8‐naphthalimide DOI

Meihui Chen,

Yi Li,

Haixia Tian

и другие.

Luminescence, Год журнала: 2024, Номер 39(8)

Опубликована: Авг. 1, 2024

Abstract A pair of 1,8‐naphthalimides (NPIs) were designed and successfully synthesized through embellishing amino‐containing NPI with 4‐diethylaminosalicyladehyde 4‐diethylaminobenzaldehyde, respectively. Their structures fully confirmed by 1 H/ 13 C NMR, HR‐MS FT‐IR spectroscopic studies. photophysical properties systematically investigated in different solvents varied polarity, THF/water mixtures varying water fractions ( f w ), THF solvent concentrations NPIs. It inferred that the distinct differences emission between two NPIs during self‐assembled process could be ascribed hydroxyl‐containing allowed excited‐state intramolecular proton transfer ‐OH CH=N units aggregation state. Interestingly, solid 4‐diethylaminosalicyladehyde‐functionalized exhibited multi‐stimuli‐responsive fluorescence changes involving mechanofluorochromism HCl/NH 3 vapor stimulus‐induced conversion. However, no remarkable change was observed photoluminescence (PL) spectra for 4‐diethylaminobenzaldehyde‐functionalized under stimuli mechanical force organic solvent.

Язык: Английский

Enhanced Photothermal Property of Dithienoindacenodithiophene Molecules by [2 + 2] Cycloaddition–Retroelectrocyclization Reaction for Efficient Solar Steam Generation DOI Creative Commons

Chia‐Yang Lin,

Shohei Shimizu, Yoshimitsu Sagara

и другие.

Solar RRL, Год журнала: 2025, Номер 9(5)

Опубликована: Фев. 23, 2025

The development of efficient photothermal materials for solar steam generation (SSG) garners significant interest as a solution to the global clean water scarcity crisis. Photothermal properties organic molecules can be fine‐tuned by molecular design. Despite this fact, use small‐molecular in SSG applications is seldom explored due their limited optical absorption range energy harvesting. In research, 6,6,12,12‐tetrakis(4‐octylphenyl)dithieno[2,3‐ d :2′,3′‐ ′]‐ s ‐indaceno[1,2‐ b :5,6‐ ′]dithiophene (DTIDT) focused upon potent conjugated core unit, and [2 + 2] cycloaddition–retroelectrocyclization (CA‐RE) reaction applied introduce additional intramolecular charge‐transfer chromophores. DTIDT derivatives exhibit broad absorption, weak photoluminescence, high nonradiative decay rates, which are useful conversion. addition, placed on top surface filter paper, devices fabricated Janus membrane enhance solar‐to‐vapor efficiency. produced CA‐RE maximum efficiency 78.3% under simulated sunlight irradiation 30 min. result suggests that an effective method synthesizing tailored applications.

Язык: Английский

Процитировано

0

A multi‐stimuli‐responsive fluorescence material based on 1,8‐naphthalimide DOI

Meihui Chen,

Yi Li,

Haixia Tian

и другие.

Luminescence, Год журнала: 2024, Номер 39(8)

Опубликована: Авг. 1, 2024

Abstract A pair of 1,8‐naphthalimides (NPIs) were designed and successfully synthesized through embellishing amino‐containing NPI with 4‐diethylaminosalicyladehyde 4‐diethylaminobenzaldehyde, respectively. Their structures fully confirmed by 1 H/ 13 C NMR, HR‐MS FT‐IR spectroscopic studies. photophysical properties systematically investigated in different solvents varied polarity, THF/water mixtures varying water fractions ( f w ), THF solvent concentrations NPIs. It inferred that the distinct differences emission between two NPIs during self‐assembled process could be ascribed hydroxyl‐containing allowed excited‐state intramolecular proton transfer ‐OH CH=N units aggregation state. Interestingly, solid 4‐diethylaminosalicyladehyde‐functionalized exhibited multi‐stimuli‐responsive fluorescence changes involving mechanofluorochromism HCl/NH 3 vapor stimulus‐induced conversion. However, no remarkable change was observed photoluminescence (PL) spectra for 4‐diethylaminobenzaldehyde‐functionalized under stimuli mechanical force organic solvent.

Язык: Английский

Процитировано

3