Table · dataset · 2026
Molecular Engineering of N–H-Type ESIPT Fluorophores Enabling Tunable Emission and ESIPT-AIE Integration
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Systematic molecular engineering of benzothiazole-based excited-state intramolecular proton transfer (ESIPT) fluorophores is achieved through complementary modulation of the <i>para</i> substituent and proton-donating N site.
Description
While <i>para</i>-substituent variation enables continuous emission tuning within the conventional ESIPT framework, N-site acylation drives the evolution toward ESIPT–aggregation-induced emission (AIE) luminogens with large Stokes shifts and bright solid-state fluorescence.
The established structure–photophysical relationships reveal the distinct roles of dual-site modulation and provide a rational design strategy for high-performance N–H-type ESIPT luminogens.
Links
Where it is published
- DOI doi.org/10.1021/acs.orglett.6c03542.s001 ↗
DOI / persistent id · from zivahub uct ac za
Catalogue records · 1
- OAI-PMH record api.figshare.com/v2/oai?verb=GetRecord&metadataPrefix=oai_dc&identifier=oai%3Af… ↗
metadata API · from zivahub uct ac za
Topics
- From keywords
- Astronomy & Astrophysics · Chemistry · Earth & Environmental Science · Ecology · Engineering · Life Sciences
Provenance · 1 source records, 11 field assertions
| Source | Key | Last seen | Raw |
|---|---|---|---|
| ZivaHub | oai:figshare.com:article/34025046 | 12 d ago | JSON v1 |
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| concepts[field].local:field:life-sciences | mapping · zivahub uct ac za | connector:zivahub_uct_ac_za@1.0.0 | |
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| license | source · zivahub uct ac za | connector:zivahub_uct_ac_za@1.0.0 | /metadata/dc/rights |
| publication_date | source · zivahub uct ac za | connector:zivahub_uct_ac_za@1.0.0 | |
| title | source · zivahub uct ac za | connector:zivahub_uct_ac_za@1.0.0 | /metadata/dc/title |