ArticleACS omega2026
Photochromism of Dicyanorhodanine-Pyrrole Conjugates: Substituent and Solvent Effects.
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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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
Dicyanorhodanine (RCN)-pyrrole conjugates are a relatively new class of photochromic compounds capable of highly efficient reversible photoisomerization upon visible-light excitation in both solution and solid-state, and understanding the factors governing their photophysical behavior is essential for designing reliable photoswitches. In this study, a library of RCN-pyrrole chromophores is investigated to elucidate the influence of substituents with varying electronic and steric properties on their π-π* absorption characteristics in solution. Solvent polarity affects the frontier molecular orbital energies, resulting in a negative solvatochromic effect. Even so, (near)-quantitative bidirectional
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