NMR Relaxation Study of the Protonated Form of 1,8-Bis(dimethylamino)naphthalene in Isotropic Solution: Anisotropic Motion outside of Extreme Narrowing and Ultrafast Proton Transfer
Author:
Affiliation:
1. Physical Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91 Stockholm, Sweden
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp045454n
Reference49 articles.
1. Temperature-jump study of proton transfer from protonated 1,8-bis-(dialkylamino)naphthalenes to hydroxide ion in water and aqueous dioxan
2. Strain effects on amine basicities
3. Review: Strong hydrogen bonding in molecules and enzymatic complexes
4. Ab Initio Quantum Mechanical Study on the Origin of the pKa Differences of the Proton Sponges 1,8-Bis(dimethylamino)naphthalene, 1,8-Bis(dimethylamino)-2,7-dimethoxynaphthalene, 1,6-Dimethyl-1,6-diazacyclodecane, and 1,6-Diazabicyclo[4.4.4]tetradecane
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3. Effect of solvent on proton location and dynamic behavior in short intramolecular hydrogen bonds studied by molecular dynamics simulations and NMR experiments;Chemical Physics;2015-09
4. “Zwitterionic Proton Sponge” Hydrogen Bonding Investigations on the Basis of Car–Parrinello Molecular Dynamics;Journal of Chemical Information and Modeling;2015-05-19
5. Effects of Counterion and Solvent on Proton Location and Proton Transfer Dynamics of N–H···N Hydrogen Bond of Monoprotonated 1,8-Bis(dimethylamino)naphthalene;The Journal of Physical Chemistry A;2013-10-03
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