Stereochemistry-dependent hydrogen bonds stabilise stacked conformations in jet-cooled cyclic dipeptides: (LD) vs. (LL) cyclo tyrosine

Stereochemistry-dependent hydrogen bonds stabilise stacked conformations in jet-cooled cyclic dipeptides: (LD) vs. (LL) cyclo tyrosine–tyrosine

Published:2018 Issue: Volume:212 Page:399-419
ISSN:1359-6640
Container-title:Faraday Discussions
language:en
Short-container-title:Faraday Discuss.

Author:

BenNasr Feriel¹²³⁴⁵,Pérez-Mellor Ariel¹²³⁴⁵,Alata Ivan¹²³⁴⁵,Lepere Valeria¹²³⁴⁵,Jaïdane Nejm-Eddine⁶⁷⁸⁹,Zehnacker Anne¹²³⁴⁵^ORCID

Affiliation:

1. Institut des Sciences Moléculaires d’Orsay (ISMO)

2. CNRS

3. Univ. Paris-Sud

4. Université Paris-Saclay

5. F-91405 Orsay

6. Laboratoire de Spectroscopie Atomique, Moléculaire et Applications (LSAMA)

7. Université de Tunis El Manar

8. Tunis 1060

9. Tunisia

Abstract

Changing the chirality of one residue prevents the formation of an OH⋯O intramolecular hydrogen bond in cyclo di-tyrosine.

Funder

Agence Nationale de la Recherche

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/FD/C8FD00079D

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