ArticleACS omega2026
Morphological Study on the Gelation-Induced Phosphorescence of All-Organic Phosphors Based on Substituted Benzil.
Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
4 authors.
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Abstract
We report gelation-induced phosphorescence at room temperature based on 4,4'-disubstituted benzils with alkyloxy and ester groups. The title compounds include five 4,4'-dialkyloxybenzils with varying alkyl chain lengths (from octyloxy to dodecyloxy) and two 4,4'-diesterbenzil (nonylester and phenyl ester). All of the title compounds showed excellent gelation properties in hydrocarbon, alcohol, and acetonitrile solvents. The room-temperature phosphorescence was turned on upon gelation, whereas no emission was observed in solution. The investigation of the photophysical properties of the dried gels (xerogels) revealed that the length of the alkyloxy side group significantly influenced the phosphorescence lifetime (τ) and quantum yield (Φ
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