Structural diversity in the products formed by the reactions of 2-arylselanyl pyridine derivatives and dihalogens-Reference-Cited by-同舟云学术

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Structural diversity in the products formed by the reactions of 2-arylselanyl pyridine derivatives and dihalogens

Published:2018 Issue:13 Volume:42 Page:10592-10602
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Montis Riccardo¹²³⁴^ORCID,Arca Massimiliano¹²³⁴^ORCID,Aragoni M. Carla¹²³⁴^ORCID,Blake Alexander J.⁵⁶⁷⁸^ORCID,Castellano Carlo⁹¹⁰¹¹⁴^ORCID,Demartin Francesco⁹¹⁰¹¹⁴^ORCID,Isaia Francesco¹²³⁴^ORCID,Lippolis Vito¹²³⁴^ORCID,Pintus Anna¹²³⁴^ORCID,Lenardão Eder J.¹²¹³¹⁴¹⁵¹⁶^ORCID,Perin Gelson¹²¹³¹⁴¹⁵¹⁶^ORCID,O'Connor Alice E.⁵⁶⁷⁸,Thurow Samuel¹²¹³¹⁴¹⁵¹⁶^ORCID

Affiliation:

1. Dipartimento di Scienze Chimiche e Geologiche

2. Università degli Studi di Cagliari

3. 09042 Monserrato (CA)

4. Italy

5. School of Chemistry

6. University of Nottingham

7. Nottingham

8. UK

9. Dipartimento di Chimica

10. Università degli Studi di Milano

11. 20133 Milano

12. Laboratório de Síntese Orgânica Limpa-LASOL

13. CCQFA

14. Universidade Federal de Pelotas – UFPel

15. 96010-900 Pelotas

16. Brazil

Abstract

The presence of competing donor sites in L1–L4 influences their reactivity towards dihalogens and interhalogens.

Funder

Università di Cagliari

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C8NJ00495A

Reference60 articles.

1. The reactions of sulfur and selenium donor molecules with dihalogens and interhalogens

2. Mechanistic Aspects of the Reaction between Br2 and Chalcogenone Donors (LE; E=S, Se): Competitive Formation of 10-E-3, T-Shaped 1:1 Molecular Adducts, Charge-Transfer Adducts, and [(LE)2]2+ Dications

3. A Unique Case of Oxidative Addition of Interhalogens IX (X=Cl, Br) to Organodiselone Ligands: Nature of the Chemical Bonding in Asymmetric ISeX Polarised Hypervalent Systems

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3. Halogen-bonded liquid-crystalline complexes formed from 4-alkoxyphenylpyridines with iodine and with interhalogens;CrystEngComm;2023

4. The relationship between the crystal habit and the energy framework pattern: a case study involving halogen bonding on the edge of a covalent bond;CrystEngComm;2023

5. An unprecedented non-classical polyinterhalogen anion made of [I₂Cl]⁻ and I₂ at the 2-(p-tolyl)selenopheno[2,3-b]pyridinium cation template;New Journal of Chemistry;2022

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