Results 211 to 220 of about 8,250 (257)
Ratiometric Detection of pH-Induced i-Motif Folding Based on a Dual Emissive Cytosine Analog. [PDF]
Barthes NPF, Le HN, Michel BY, Burger A.
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Switching on photoreactivity in Ti<sub>4</sub>-oxo clusters by increasing the size of 1,<i>n</i>-alkane diolate bridging ligands. [PDF]
Chikara A +5 more
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Boramidine: a boron-based photoacidic fluorophore.
Sucre-Rosales E +3 more
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Anion solvation in protic solvents
Journal of the Chemical Society, Chemical Communications, 1977Spectroscopic evidence is advanced in favour of the concept of continuous hydrogen-bonding from anions into bulk solvent with no intervention of an intermediate structureless region.
Susan E. Jackson +2 more
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Proton solvation in protic and aprotic solvents
Journal of Computational Chemistry, 2016Protonation pattern strongly affects the properties of molecular systems. To determine protonation equilibria, proton solvation free energy, which is a central quantity in solution chemistry, needs to be known. In this study, proton affinities (PAs), electrostatic energies of solvation, and pKA values were computed in protic and aprotic solvents.
Emanuele, Rossini, Ernst-Walter, Knapp
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Hydrogen-Bonded Encapsulation Complexes in Protic Solvents
Journal of the American Chemical Society, 2004We describe here the behavior of the hydrogen-bonded capsule 1.1 and its complexes in protic solvents. The kinetics and thermodynamics of the encapsulation process were determined through conventional (1)H NMR methods. The enthalpies and entropies of encapsulation are both positive, indicating a process that liberates solvent molecules.
Toru, Amaya, Julius, Rebek
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Solvent-mediated molar conductivity of protic ionic liquids
Physical Chemistry Chemical Physics, 2015The molar conductivity, Λm, of protic ionic liquids (PILs) in molecular solvents is measured at 298.15 K.
Sachin, Thawarkar +2 more
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Nucleofugality and Nucleophilicity of Fluoride in Protic Solvents
The Journal of Organic Chemistry, 2012A series of p-substituted benzhydryl fluorides (diarylfluoromethanes) were prepared and subjected to solvolysis reactions, which were followed conductometrically. The observed first-order rate constants k(1)(25 °C) were found to follow the correlation equation log k(1)(25 °C) = s(f)(N(f) + E(f)), which allowed us to determine the nucleofuge-specific ...
Christoph, Nolte +2 more
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