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American Chemical Society, Organic Letters, 21(16), p. 5528-5531, 2014

DOI: 10.1021/ol502003a

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TMIO-PyrImid Hybrids are Profluorescent, Site-Directed Spin Labels for Nucleic Acids

This paper is available in a repository.
This paper is available in a repository.

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Abstract

We report the synthesis of a new class of molecules which are hybrids of long-lived tetramethylisoindolinoxyl (TMIO) radicals and the pyrido[1,2-a]benzimidazole (PyrImid) scaffold. These compounds represent a new lead for noncovalently binding nucleic acid probes, as they interact with nucleic acids with previously unreported C (DNA) and C/U (RNA) complementarity, which can be detected by electron paramagnetic resonance (EPR) techniques. They also have promising properties for fluorimetric analysis, as their fluorescent spin-quenched derivatives exhibit a significant Stokes shift.