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Synlett 2016; 27(03): 355-368
DOI: 10.1055/s-0035-1560725
DOI: 10.1055/s-0035-1560725
account
Cycloadditions of Singlet Oxygen for Responsive Fluorescent Polymers
Weitere Informationen
Publikationsverlauf
Received: 30. August 2015
Accepted after revision: 21. September 2015
Publikationsdatum:
09. Dezember 2015 (online)
Abstract
This account describes progress in the author’s laboratory in the area of new fluorescent polymers that respond to the reactive oxygen species singlet oxygen (1O2). Key to the development of these materials are the [4+2] cycloaddition reactions between singlet oxygen and dienes such as acenes and furans. When covalently bound to conjugated polymer backbones, cycloadditions of these dienes with singlet oxygen can yield dramatic changes in the wavelength and intensity of luminescence: three such examples are given here. The account also summarizes our work to understand how changing the chemical structures of acenes affects reactivity with singlet oxygen as well as the cycloreversion of the resulting endoperoxides.
1 Introduction
2 Motivation
3 Organic Soluble Diene-Linked Conjugated Polymers
4 Red-Shifting Woes Lead to Reversibility
5 Building a Database
6 Integrating Other Acenes
7 Conclusion and Looking Forward
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