ArticleAngewandte Chemie (International ed. in English)2025
NIR-Sensitized Activated Formation of Lophyl Radicals by Heptamethine Cyanines Enables Dry Film Photoresists.
Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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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.
- Meso-electron-withdrawing pentamethine cyanines achieve large anti-Stokes blue-emitting triplet-triplet annihilation upconversion.Nature communications · 2026Article
- NIR-Sensitized Activated Formation of Lophyl Radicals by Heptamethine Cyanines Enables Dry Film Photoresists.Angewandte Chemie (International ed. in English) · 2025Article
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9 authors.
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Abstract
The near-infrared (NIR) sensitized generation of lophyl radicals (L·) by heptamethine cyanine led to initiation of radical photopolymerization of multifunctional acrylates when different hexa-arylbisimidazoles (HABIs) and N-phenylglycine (NPG) operated as coinitiator. The latter functioned as donor. For a deeper understanding, heptamethine cyanines were used following a photoinduced electron transfer (PET). HABI derivatives with electron-donating and -withdrawing substituents demonstrated that those with electron acceptors resulted in a higher photopolymerization efficiency of multifunctional acrylates. Tri-(propylene glycol) diacrylate (TPGDA) and tri-methylolpropane triacrylate (TMPTA) served as the monomers. Sensitizers (Sens) exposed with a high intense NIR-light source at 808 nm exhibiting a positive charge in the cyanine pattern significantly operate more efficiently for radical photopolymerization than a Sens without a positive charge. Differences in efficiency of PET can give an explanation for these differences. The heat generated by the cyanine's internal conversion from S
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