ArticleJournal of fluorescence2025
Conjugated Iminodibenzyl Dyes Incorporating Phenolic Hydroxyl Group and Strong Electron Donating or Accepting Groups for Facilitating ESIPT and Proton Transfer in Six- or Seven-Membered Cycles.
Article in Journal of fluorescence, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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Authors and funding
5 authors.
Funding
Abstract
In this study, a range of conjugated iminodibenzyl derivatives D1-D6 including phenolic group and strong electro donating/accepting groups (N,N-diethylamino/nitro groups) were prepared as the target dyes, which could process internal proton transfer in excited state via six-/seven membered ring transition state (TS). Furthermore, reference iminodibenzyl dyes D7-D12, devoid of the phenolic segment, were synthesized for comparative analysis of their absorption and emission spectral properties. The internal H-bond of the target dyes was analyzed by the
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.