Multisensing Emissive Pyrimidine

作者:Sinkeldam Renatus W; Marcus Paul; Uchenik Dmitriy; Tor Yitzhak*
来源:ChemPhysChem, 2011, 12(12): 2260-2265.
DOI:10.1002/cphc.201100315

摘要

Fluorescent nucleoside analogs, commonly used to explore nucleic acid dynamics, recognition and damage, frequently respond to a single environmental parameter. Herein we address the development of chromophores that can simultaneously probe more than one environmental factor while having each associated with a unique spectroscopic signature. We demonstrate that an isomorphic emissive pyridine-modified 2-deoxyuridine 1, containing multiple sensory elements, responds to changes in acidity, viscosity, and polarity. Protonation of the pyridine moiety (pK(a) 4.4) leads to enhanced emission (lambda(em) = 388 nm) and red-shifted absorption spectra (lambda(abs) = 319 nm), suggesting the formation of an intramolecular hydrogen bond with the neighboring pyrimidine carbonyl. This "locked" conformation can also be mimicked by increasing solvent viscosity, resulting in a stark enhancement of emission quantum yield. Finally, increasing solvent polarity substantially impacts the chromophore's Stokes shift [from 5.8 x 10(3) cm(-1) at E(T)(30) = 36.4 kcalmol(-1) to 9.3 x 10(3) cm(-1) at E(T)(30)= 63.1 kcalmol(-1)]. The opposite effect is seen for the impact of solvent polarity of the protonated form. The characteristic photophysical signature induced by each parameter facilitates the exploration of these environmental factors both individually and simultaneously.

  • 出版日期2011-8-22