Diastereo-specific conformational properties of neutral, protonated and radical cation forms of (1R,2S)-cis- and (1R,2R)-trans-amino-indanol by gas phase spectroscopy-Reference-Cited by-同舟云学术

Diastereo-specific conformational properties of neutral, protonated and radical cation forms of (1R,2S)-cis- and (1R,2R)-trans-amino-indanol by gas phase spectroscopy

Published:2015 Issue:39 Volume:17 Page:25809-25821
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Bouchet Aude¹²³⁴,Klyne Johanna¹²³⁴,Piani Giovanni⁵⁶⁷⁸⁹,Dopfer Otto¹²³⁴,Zehnacker Anne⁵⁶⁷⁸⁹

Affiliation:

1. Institut für Optik und Atomare Physik

2. Technische Universität Berlin

3. D-10623 Berlin

4. Germany

5. CNRS

6. Institut des Sciences Moléculaires d’Orsay (ISMO/UMR8214) and Univ. Paris Sud

7. Orsay

8. France

9. CLUPS (Centre Laser de l’Université Paris Sud/LUMAT FR 2764)

Abstract

The effects of ionisation and protonation on the geometric and electronic structure of a prototypical aromatic amino-alcohol with two chiral centres are revealed by IR and UV spectroscopy.

Funder

Research Executive Agency

German Academic Exchange Service

Deutsche Forschungsgemeinschaft

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/C5CP00576K

Reference92 articles.

1. Chirality Recognition between Neutral Molecules in the Gas Phase