Deuterium Isotope Effects on 13C-NMR Chemical Shifts of 10-Hydroxybenzo[h]quinolines

Molecules

Poul Erik Hansen¹  Fadhil S. Kamounah¹ 

[1] Department of Science, Systems and Models, Roskilde University, P.O. Box 260, DK-4000 Roskilde, Denmark; E-Mail:

关键词: 10-hydroxybenzo[h]quinolones;    deuterium isotope effects on ¹³C chemical shifts;    intramolecular hydrogen bonds;    hydrogen bond potentials;    DFT calculations;   

DOI  :  10.3390/molecules18044544

来源: mdpi

【 摘 要 】

Deuterium isotope effects on ¹³C-NMR chemical shifts are investigated in a series of 10-hydroxybenzo[h]quinolines (HBQ’s) The OH proton is deuteriated. The isotope effects on ¹³C chemical shifts in these hydrogen bonded systems are rather unusual. The formal four-bond effects are found to be negative, indicating transmission via the hydrogen bond. In addition unusual long-range effects are seen. Structures, NMR chemical shifts and changes in nuclear shieldings upon deuteriation are calculated using DFT methods. Two-bond deuterium isotope effects on ¹³C chemical shifts are correlated with calculated OH stretching frequencies. Isotope effects on chemical shifts are calculated for systems with OH exchanged by OD. Hydrogen bond potentials are discussed. New and more soluble nitro derivatives are synthesized.

【 授权许可】

CC BY   
© 2013 by the authors; licensee MDPI, Basel, Switzerland.