ArticleChemical communications (Cambridge, England)2019
Rational design and synthesis of yellow-light emitting triazole fluorophores with AIE and mechanochromic properties.
Article in Chemical communications (Cambridge, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
5 citing papers in PubMed.
- Heteroaryl-Fused Triazapentalenes: Synthesis and Aggregation-Induced Emission.Molecules (Basel, Switzerland) · 2025Article
- Synthesis of Unsymmetrically Condensed Benzo- and Thienotriazologermoles.Molecules (Basel, Switzerland) · 2024Article
- Combined NMR Spectroscopy and Quantum-Chemical Calculations in Fluorescent 1,2,3-Triazole-4-carboxylic Acids Fine Structures Analysis.International journal of molecular sciences · 2023Article
- Selective Synthesis of AzoloylACS omega · 2022Article
- Construction of fluorescence active MOFs with symmetrical and conformationally rigidRSC advances · 2020Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
Previously, we reported that N-2-aryl triazoles (NATs) exhibited good fluorescence activity in the UV/blue light range. In an effort to achieve biocompetitive NAT fluorophores with green/yellow emission, a new class of 4-keto-2-(4'-N,N-diphenyl)-phenyl triazoles were designed and synthesized. Herein, we present our study on these novel fluorophores which demonstrated excellent luminescence emission both in solution (Φ up to 96%) and in the solid state (Φ up to 43%). Furthermore, these new compounds showed aggregation-induced emission (AIE) properties and reversible mechanochromic luminescence properties, which suggested their potential applications in chemical and materials science.
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Registered trials
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