Abstract:
: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.
journal_name
Photochem Photobioljournal_title
Photochemistry and photobiologyauthors
Mathew JP,Greer Adoi
10.1111/php.13102subject
Has Abstractpub_date
2019-09-01 00:00:00pages
1280-1282issue
5eissn
0031-8655issn
1751-1097journal_volume
95pub_type
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