4-Hydroxy-1-naphthaldehydes: proton transfer or deprotonation-Reference-Cited by-同舟云学术

4-Hydroxy-1-naphthaldehydes: proton transfer or deprotonation

Published:2015 Issue:15 Volume:17 Page:10238-10249
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Manolova Y.¹²³⁴,Kurteva V.¹²³⁴,Antonov L.¹²³⁴^ORCID,Marciniak H.⁵⁶⁷⁸,Lochbrunner S.⁵⁶⁷⁸,Crochet A.⁹¹⁰¹¹¹²,Fromm K. M.⁹¹⁰¹¹¹²,Kamounah F. S.¹³¹⁴¹⁵¹⁶,Hansen P. E.¹³¹⁴¹⁵¹⁶

Affiliation:

1. Institute of Organic Chemistry with Centre of Phytochemistry

2. Bulgarian Academy of Sciences

3. Sofia 1113

4. Bulgaria

5. Institut für Physik

6. Universität Rostock

7. 18051 Rostock

8. Germany

9. Department of Chemistry

10. University of Fribourg

11. 1700 Fribourg

12. Switzerland

13. Department of Science, Systems and Models

14. Roskilde University

15. DK-4000 Roskilde

16. Denmark

Abstract

Proton captured/proton lost: in 4-hydroxy-1-naphthaldehyde concentration dependent deprotonation is observed, while when a piperidine unit is attached the proton is captured.

Funder

Schweizerische Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CP/C5CP00870K

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