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Nucleobase-specific quenching of fluorescent dyes. 1. nucleobase one-electron redox potentials and their correlation with static and dynamic quenching efficiencies

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TLDR
In this paper, the feasibility of photoinduced electron transfer reaction for the nucleobase-specific quenching of fluorescent dyes is investigated by the calculation of the standard free energy changes with the Rehm−Weller equation.
Abstract
Intermolecular static and dynamic fluorescence quenching constants of eight coumarin derivatives by nucleobase derivatives have been determined in aqueous media. One common sequence of the quenching efficiency has been found for the nucleobases. The feasibility of a photoinduced electron transfer reaction for the nucleobase-specific quenching of fluorescent dyes is investigated by the calculation of the standard free energy changes with the Rehm−Weller equation. A complete set of one-electron redox potential data for the nucleobases are determined electrochemically in aprotic solvents for the first time, which are compared with values obtained by various other methods. Depending on the redox properties of the fluorescent dyes, the sequences of the quenching efficiencies can be rationalized by the orders of electrochemical oxidation potentials (vs NHE) of nucleosides (dG (+1.47 V) < dA < dC ≈ dT < U (≥ +2.39 V)) and reduction potentials (dG (< −2.76 V) < dA < dC < dT < U (−2.07 V)). The correlation between...

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Citations
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Nanoparticle Probes for the Detection of Cancer Biomarkers, Cells, and Tissues by Fluorescence

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Colloquium: The quest for high-conductance DNA

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References
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Journal ArticleDOI

Molecular computation of solutions to combinatorial problems

TL;DR: This experiment demonstrates the feasibility of carrying out computations at the molecular level by solving an instance of the directed Hamiltonian path problem with standard protocols and enzymes.
Journal ArticleDOI

Kinetics of Fluorescence Quenching by Electron and H‐Atom Transfer

TL;DR: In this article, the rate constants of 60 typical electron donor-acceptor systems have been measured in de-oxygenated acetonitrile and are shown to be correlated with the free enthalpy change, ΔG23, involved in the actual electron transfer process.
Journal ArticleDOI

Reduction Potentials of One-Electron Couples Involving Free Radicals in Aqueous Solution

TL;DR: In this paper, the reduction potentials of one-electron couples are used to predict the direction or feasibility of many free-radical reactions in aqueous solutions, including those involving phenols, aromatic amines, indoles, pyrimidines, thiols and phenothiazines.
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