Evidence of C−H···O Hydrogen Bonds in Liquid 4-Ethoxybenzaldehyde by NMR and Vibrational Spectroscopies
Author(s) -
M. Paula M. Marques,
A. M. Amorim da Costa,
Paulo RibeiroClaro
Publication year - 2001
Publication title -
the journal of physical chemistry a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 235
eISSN - 1520-5215
pISSN - 1089-5639
DOI - 10.1021/jp0046041
Subject(s) - hydrogen bond , chemistry , ab initio , intermolecular force , ab initio quantum chemistry methods , raman spectroscopy , hydrogen , crystallography , computational chemistry , molecule , organic chemistry , physics , optics
Raman, FTIR, and NMR (both 13C and 17O) spectroscopies are used in a complementary way in order to study the occurrence of C−H···O intermolecular hydrogen bonds in liquid 4-ethoxybenzaldehyde (4EtOB). Additional information concerning the structure of the possible dimers is obtained through ab initio calculations, at the B3LYP/6-31G* level. The strongest evidences of the presence of C−H···O hydrogen bonds in the liquid phase arise from the temperature and solvent intensity dependence of the two bands observed in the νCO region of the vibrational spectra, as well as from the shift to low magnetic field detected for the carbonyl 17O NMR peak at higher dilutions. Further evidence is gathered from the changes observed in the νC-H vibrational modes, the 1JCH concentration dependence detected in the NMR spectra, and ab initio results. The experimental observations are consistent with the decrease of the C−H bond length upon hydrogen-bonding, as predicted for the nonstandard blue-shifting hydrogen bonds. Ab init...
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