Chalcogen controlled redox behaviour in <i>peri</i>-substituted S, Se and Te naphthalene derivatives-Reference-Cited by-同舟云学术

Chalcogen controlled redox behaviour in peri-substituted S, Se and Te naphthalene derivatives

Published:2022 Issue:46 Volume:46 Page:22363-22383
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Roemmele Tracey L.¹,Knight Fergus R.²,Crawford Ellis²^ORCID,Robertson Stuart D.³^ORCID,Bode Bela E.²^ORCID,Bühl Michael²^ORCID,Slawin Alexandra M. Z.²^ORCID,Woollins J. Derek²⁴,Boeré René T.¹^ORCID

Affiliation:

1. Dept of Chemistry and Biochemistry and Canadian Centre for Research in Advanced Fluorine Technologies, University of Lethbridge, Lethbridge, AB, T1K 3M4, Canada

2. EaStCHEM School of Chemistry and Centre for Magnetic Resonance, University of St Andrews, St Andrews KY16 9ST, UK

3. WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow, G1 1XL, UK

4. Dept of Chemistry, Khalifa University, Abu Dhabi, United Arab Emirates

Abstract

Chemically reversible electron transfers between neutral, cation radical and dication naphthalenic peri-1,8-diphenylchalcogenides are governed by chalcogen (SS, SSe, STe, SeSe, SeTe, TeTe) contributions to the redox molecular orbitals.

Funder

Royal Society of Edinburgh

Natural Sciences and Engineering Research Council of Canada

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ04737C

Reference98 articles.

1. Noncovalent Intra‐ and Intermolecular Interactions in Peri‐Substituted Pnicta Naphthalene and Acenaphthalene Complexes

2. Nature of the E⋯E′ interactions (E, E′ = O, S, Se, and Te) at naphthalene 1,8-positions with fine details of the structures: experimental and theoretical investigations

3. Sulfur Radicals and Their Application

4. Intriguing E…E' bonding in [Nap(EPh)(E'Ph)]•+(E, E'=O, S, Se, Te)

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