Peer Reviewed

1

Document Type

Article

Publication Date

2017

Keywords

Fluorophobes, cycloadditions

Funder/Sponsor

Science Foundation Ireland grant number 11/P1/1071(T)

Comments

This article is available from the Royal Society of Chemistry at http://pubs.rsc.org

Abstract

A series of 1,2,4,5-tetrazine integrated near infrared (NIR) fluorophores based on the BF2 azadipyrromethene (NIR-AZA) class has been synthesised and their ability to modulate emission from low to high in response to Diels-Alder cycloaditions has been assessed. Substituents on the tetrazine component of the probe (Cl, OMe, p-NO2C6H4O) were seen to strongly influence quantum yields, fluorescence enhancement factors, and rates of cycloadditions. Cycloadditions between tetrazine-NIR-AZA constructs and a strained alkyne substrate were seen to be highly efficient in organic or aqueous solutions and in gels with high fluorescence enhancements of up to 48-fold observed. Real-time demonstration of the cycloaddition mediated fluorogenic property was achieved by imaging the “turn-on” reaction within a continous flow microreactor. Preliminary evidence indicates that excited state quenching involves a photoinduced electron transfer.

Disciplines

Chemistry | Medicinal-Pharmaceutical Chemistry | Medicine and Health Sciences

Citation

Wu D, O'Shea DF. Fluorogenic NIR-probes based on 1,2,4,5-tetrazine substituted BF2-azadipyrromethenes. Chem. Commun. 2017; DOI: 10.1039/C7CC06545K

DOI Link

10.1039/C7CC06545K

Creative Commons License

Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 4.0 License.

Available for download on Friday, September 14, 2018

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