C−H···O Bonded Dimers in Liquid 4-Methoxybenzaldehyde: A Study by NMR, Vibrational Spectroscopy, and ab Initio Calculations
- 1 October 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry A
- Vol. 103 (43) , 8672-8677
- https://doi.org/10.1021/jp990908f
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Evidence of dimerization through C—H···O interactions in liquid 4-methoxybenzaldehyde from Raman spectra andab initio calculationsJournal of Raman Spectroscopy, 1997
- Rules governing the orientation of the 2′-hydroxyl group in RNAJournal of Molecular Biology, 1997
- Role of the C−H···O Hydrogen Bonds in Liquids: A Monte Carlo Simulation Study of Liquid Formic Acid Using a Newly Developed Pair-PotentialThe Journal of Physical Chemistry B, 1997
- Unrolling the hydrogen bond properties of C–H···O interactionsChemical Communications, 1997
- How does basis set superposition error change the potential surfaces for hydrogen-bonded dimers?The Journal of Chemical Physics, 1996
- (His)Cε-H···O=C< Hydrogen Bond in the Active Sites of Serine HydrolasesJournal of Molecular Biology, 1994
- The crystal structure of 2-methoxy-1,4-benzoquinone: molecular recognition involving intermolecular dipole–dipole- and C–H ⋯ O hydrogen bond interactionsJournal of the Chemical Society, Chemical Communications, 1994
- Molecular orbital study of acetic acid aggregation. 1. Monomers and dimersThe Journal of Physical Chemistry, 1993
- 17O NMR study of isomeric monochloro- and monohydroxy-benzaldehydes and chlorinated salicylaldehydesMagnetic Resonance in Chemistry, 1991
- Oxygen-17 NMR studies of substituent and hydrogen-bonding effects in substituted acetophenones and benzaldehydesJournal of the American Chemical Society, 1981