TY  - THES
A1  - Lämmermann, Anica
T1  - Anwendung von Substituenteneffekten zur Strukturaufklärung mittels NMR-Spektroskopie und Moleculare Modelling
Y1  - 2010
CY  - Potsdam
ER  - 
TY  - JOUR
A1  - Lämmermann, Anica
A1  - Szatmári, István
A1  - Fulop, Ferenc
A1  - Kleinpeter, Erich
T1  - Inter- or intramolecular N···H-O or N-H···O Hydrogen bonding in 1,3-Amino-alpha/beta-naphthols : an experimental NMR and computational study
N2  - The existence of intermolecular or intramolecular N···H;O or N;H···O hydrogen bonding in three series (series 1, substituted 1-aminoalkyl-2-naphthols: R = H, Me, Et, Pr, i-Pr; series 2, substituted 1-;- aminobenzyl-2-naphthols: H, p-OMe, p-F, p-Cl, p-Br, p-NO2, p-Me; series 3, substituted 2-;-aminobenzyl-1-naphthols: R = H, p-Me, p-F, p-Br, p-OMe, m-NO2, m-Br) are studied by NMR spectroscopy and computed at the DFT level of theory [B3LYP/6-311+G(d,p)]. The correct nature of the H-bond was assigned unequivocally both experimentally and computationally by potential energy scans rotating the involved dihedral angles. We investigated the effects of substituents on the strength of the H-bond by evaluating the corresponding hyperconjugative stabilization energy nlonepair ; ;*X;H and Hammett substituent constant plots. By this means, steric and electronic substituent effects could be easily quantified and separated.
Y1  - 2009
UR  - http://pubs.acs.org/journal/jpcafh
U6  - https://doi.org/10.1021/Jp902731n
SN  - 1089-5639
ER  -