Tautomeric and conformational switching in a new versatile N-rich heterocyclic ligand-Reference-Cited by-同舟云学术

Tautomeric and conformational switching in a new versatile N-rich heterocyclic ligand

Published:2020 Issue:41 Volume:49 Page:14452-14462
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Parisi Emmanuele¹²³⁴^ORCID,Capasso Domenica⁵²⁶⁴^ORCID,Capobianco Amedeo⁷⁸⁹⁴^ORCID,Peluso Andrea⁷⁸⁹⁴^ORCID,Di Gaetano Sonia¹⁰¹¹⁴^ORCID,Fusco Sandra¹²³⁴,Manfredi Carla¹²³⁴^ORCID,Mozzillo Rosaria¹²³⁴,Pinto Gabriella¹²³⁴^ORCID,Centore Roberto¹²³⁴^ORCID

Affiliation:

1. Department of Chemical Sciences

2. University of Naples Federico II

3. I-80126 Naples

4. Italy

5. CESTEV

6. 80145 Naples

7. Department of Chemistry and Biology

8. University of Salerno

9. I-84084 Fisciano

10. CNR–Institute of Biostructures and Bioimaging

11. 80134 Naples

Abstract

The dancing of protons: five different tautomers/conformers of a new N-rich heterocyclic ligand were isolated and characterized.

Funder

European Cooperation in Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/DT/D0DT02572K

Reference30 articles.

1. Entry “tautomerism” in IUPAC, Compendium of Chemical Terminology, 2nd ed. (the “Gold Book”) , Compiled by A. D. McNaught and A. Wilkinson, Blackwell Scientific Publications , Oxford , 1997

2. Let’s not forget tautomers

3. Genetical Implications of the Structure of Deoxyribonucleic Acid

4. Mutations caught in the act

5. Structural evidence for the rare tautomer hypothesis of spontaneous mutagenesis

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