Cyanine Modification Tuned for Amine Photorelease.

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 Photobiol

authors

Mathew JP,Greer A

doi

10.1111/php.13102

subject

Has Abstract

pub_date

2019-09-01 00:00:00

pages

1280-1282

issue

5

eissn

0031-8655

issn

1751-1097

journal_volume

95

pub_type

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