Cyanine Modification Tuned for Amine Photorelease.
Journal
Photochemistry and photobiology
ISSN: 1751-1097
Titre abrégé: Photochem Photobiol
Pays: United States
ID NLM: 0376425
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
04
03
2019
accepted:
19
03
2019
pubmed:
31
3
2019
medline:
13
3
2020
entrez:
31
3
2019
Statut:
ppublish
Résumé
Cyanines are emerging as useful agents for photoreleasing biological compounds because of their capability of utilizing near-infrared (NIR) light. Another benefit is their ability to self-sensitize to produce singlet oxygen for the release of aryl amines, a process that has not been as feasible in the past. Here, we highlight the paper by Schnermann et al. (https://doi.org/10.1111/php.13090), which reports on a cyanine conjugate for heterolytic photocleavage of aryl amines. This paper is timely-delving into a photorelease mechanism involving a domino rearrangement and β-elimination triggered by NIR light.
Types de publication
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Comment
Langues
eng
Sous-ensembles de citation
IM
Pagination
1280-1282Commentaires et corrections
Type : CommentOn
Informations de copyright
© 2019 American Society for Photobiology.
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