Assessing the effects of covalent, dative and halogen bonds on the electronic structure of selenoamides-Reference-Cited by-同舟云学术

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Assessing the effects of covalent, dative and halogen bonds on the electronic structure of selenoamides

Published:2022 Issue:22 Volume:46 Page:10568-10576
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Ciancaleoni Gianluca¹^ORCID,Marchetti Fabio¹^ORCID,Santi Claudio²^ORCID,Merlino Orsola²,Zacchini Stefano³^ORCID

Affiliation:

1. Dipartimento di Chimica e Chimica Industriale, Università degli studi di Pisa, via Giuseppe Moruzzi 13, 56124, Italy

2. Dipartimento di Scienze Farmaceutiche, Università degli studi di Perugia, via del Liceo, 06132, Perugia, Italy

3. Dipartimento di Chimica Fisica ed Inorganica, Università di Bologna, viale Risorgimento 4, 40136 Bologna, Italy

Abstract

The C–NMe2 bond rotation of a selenoamide is proposed as an experimental probe to compare different chemical interactions.

Funder

Università di Pisa

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ01421A

Reference56 articles.

1. Definition of the halogen bond (IUPAC Recommendations 2013)

2. The Halogen Bond

3. The interplay of covalency, hydrogen bonding, and dispersion leads to a long range chiral network: The example of 2-butanol

4. Electrostatics and polarization determine the strength of the halogen bond: a red card for charge transfer

5. A solvent-resistant halogen bond

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