ArticleRSC advances2025
From amides to thioamides: understanding enhanced anion binding in acyclic receptors.
Article in RSC advances, 2025. 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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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
6 authors.
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Abstract
We synthesized acyclic amide and thioamide-based receptors and evaluated their anion binding efficacy experimentally and computationally. Our study shows the receptors adopt favorable conformations upon chloride binding and confirms that the stronger NH donor ability of thioamides arises from sulfur's larger size relative to oxygen. Moreover, the anion size dictates selectivity.
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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.