ArticleRSC advances2021
Disulfide-yne reaction: controlling the reactivity of a surface by light.
Article in RSC advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 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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Who cites it
2 citing papers in PubMed, 5 citations in OpenAlex.
- Dual-Stimuli Chromogenic Membranes for Optical Security: Photochromic and Halochromic Anti-Counterfeiting Applications.Small (Weinheim an der Bergstrasse, Germany) · 2025Article
- Transition-Metal-Free Thioboration of Terminal Alkynes.JACS Au · 2024Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In this paper we provide new insight into the disulfide-yne photo reaction, which is similar but different from the well-known thiol-yne photoclick reaction. We show that, unlike the stable product generated from thiol-yne chemistry, the vinyl dithioether structure obtained from disulfide-yne reaction exhibits unique reactivity with thiols and disulfides, which can be used for surface photochemistry to fabricate reactive and dynamic surfaces. The possible mechanism for the unique reactivity of vinyl dithioether structure was discussed. We demonstrated that disulfide-yne reactions are highly compatible with thiol-yne chemistry, but offer the flexibility and dynamic nature that is lacking in thiol-yne chemistry, thus could be a good replenishment for the existing thiol-yne toolbox.
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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.