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Nicholas J. Turro
Researcher at Columbia University
Publications - 1131
Citations - 56059
Nicholas J. Turro is an academic researcher from Columbia University. The author has contributed to research in topics: Radical & Electron paramagnetic resonance. The author has an hindex of 104, co-authored 1131 publications receiving 53827 citations. Previous affiliations of Nicholas J. Turro include University of Florence & Istanbul Technical University.
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Closed Nanocontainer Enables Thioketones to Phosphoresce at Room Temperature in Aqueous Solution
Nithyanandhan Jayaraj,Murthy V. S. N. Maddipatla,Rajeev Prabhakar,Steffen Jockusch,Nicholas J. Turro,Vaidhyanathan Ramamurthy +5 more
TL;DR: A general strategy is presented that has allowed us to record phopshorescence from a number of thioketones in aqueous solution at room temperature and is found to be the best medium to observe phosphorescence from thiocarbonyl compounds whose excited state chemistry is essentially controlled by self-quenching.
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Spin catalysis of the radical recombination reaction
TL;DR: The rate constant of the recombination of alkyl radicals with nitroxide biradicals in dioxane and ethyl benzene exceeds rate constants with parent mono radicals by 10% to 50%.
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Double Exposure Materials: Simulation Study of Feasibility
TL;DR: In this article, the authors present a feasibility study of four types of double exposure materials and their potential process windows, including double patterning, double exposure, and double exposure-based methods.
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Binding of the anti-cancer drug daunomycin to DNA probed by second harmonic generation.
Benjamin Doughty,Yi Rao,Samuel W. Kazer,Sheldon J. J. Kwok,Nicholas J. Turro,Kenneth B. Eisenthal +5 more
TL;DR: The binding constant of the anticancer drug daunomycin to a recognition triplet sequence in a 33-mer of double stranded DNA was determined and the equilibrium was found to be unaffected by the presence of free DNA in solution.
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Hammett analysis of absolute carbene addition rate constants
TL;DR: In this paper, the absolute rate constants for the addition of 5 5 -X-substituted ArCCl (X=CF 3, Cl, H, CH 3, CH 3 O) to tetramethylethylene, trimethylethsylene, trans-pentene, and 1-hexene were determined.