[2 + 2] light-driven cycloaddition synthesis of an organic polymer and photocatalytic activity enhancement <i>via</i> monomer truncation

[2 + 2] photocycloaddition is exploited as a tool for the synthesis of organic extended materials. As a result, polymeric semiconductors achieved are able to carry out the oxidative photocoupling of benzyl amines with versatile performance.

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Publication Details

Journal
Journal of Materials Chemistry A
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ta02288f
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

[2 + 2] light-driven cycloaddition synthesis of an organic polymer and photocatalytic activity enhancement via monomer truncation

José Alemán, M. J. Capitán, Alberto Fraile, Matı́as Blanco et al.
1 citations
Journal of Materials Chemistry A
Radical Photochemical Reactions
0.94
article

[2 + 2] light-driven cycloaddition synthesis of an organic polymer and photocatalytic activity enhancement via monomer truncation

José Alemán, M. J. Capitán, Alberto Fraile, Matı́as Blanco, Beatriz de Santos, Silvia Cabrera, J. Álvarez, Giacomo De Crescenzo
article en
1 citations

Abstract

[2 + 2] photocycloaddition is exploited as a tool for the synthesis of organic extended materials. As a result, polymeric semiconductors achieved are able to carry out the oxidative photocoupling of benzyl amines with versatile performance.

Journal of Materials Chemistry AVol. 13(29)
Instituto de Ciencia de Materiales de Madrid (ES), ORFEO-CINQA Research Network (ES), Instituto de Estructura de la Materia (ES), Universidad Autónoma de Madrid (ES)
Comunidad de Madrid, Ministerio de Ciencia e Innovación
Openalex Percentile: Top 25%
Radical Photochemical Reactions
0.94
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