Chromoselective Synthesis of Sulfonyl Chlorides and Sulfonamides with Potassium Poly(heptazine imide) Photocatalyst.

carbon nitride chromoselective catalysis organic synthesis photoredox catalysis sulfonyl chloride

Journal

Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543

Informations de publication

Date de publication:
06 Sep 2021
Historique:
revised: 22 06 2021
received: 07 05 2021
pubmed: 6 7 2021
medline: 6 7 2021
entrez: 5 7 2021
Statut: ppublish

Résumé

Among external stimuli used to promote a chemical reaction, photocatalysis possesses a unique one-light. Photons are traceless reagents that provide an exclusive opportunity to alter chemoselectivity of the photocatalytic reaction varying the color of incident light. This strategy may be implemented by using a sensitizer capable to activate a specific reaction pathway depending on the excitation light. Herein, we use potassium poly(heptazine imide) (K-PHI), a type of carbon nitride, to generate selectively three different products from S-arylthioacetates simply varying the excitation light and otherwise identical conditions. Namely, arylchlorides are produced under UV/purple, sulfonyl chlorides with blue/white, and diaryldisulfides at green to red light. A combination of the negatively charged polyanion, highly positive potential of the valence band, presence of intraband states, ability to sensitize singlet oxygen, and multi-electron transfer is shown to enable this chromoselective conversion of thioacetates.

Identifiants

pubmed: 34223699
doi: 10.1002/anie.202106183
pmc: PMC8457082
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

20543-20550

Subventions

Organisme : Max-Planck-Gesellschaft

Informations de copyright

© 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.

Références

Angew Chem Int Ed Engl. 2016 Jun 27;55(27):7676-9
pubmed: 27198967
Curr Top Med Chem. 2016;16(11):1200-16
pubmed: 26369815
Nat Commun. 2019 Jun 14;10(1):2634
pubmed: 31201327
Chemistry. 2016 Jan 26;22(5):1704-13
pubmed: 26742657
ChemSusChem. 2017 Jan 10;10(1):151-155
pubmed: 27863070
Angew Chem Int Ed Engl. 2020 Aug 24;59(35):15061-15068
pubmed: 32412175
Pharmacology. 2008;82(3):171-9
pubmed: 18679046
Angew Chem Int Ed Engl. 2021 Mar 22;60(13):7436-7443
pubmed: 33259655
Top Curr Chem (Cham). 2017 Oct 9;375(6):82
pubmed: 28993992
Angew Chem Int Ed Engl. 2021 Mar 22;60(13):6965-6969
pubmed: 33529432
Angew Chem Int Ed Engl. 2018 Aug 6;57(32):10034-10072
pubmed: 29457971
Angew Chem Int Ed Engl. 2021 Sep 6;60(37):20543-20550
pubmed: 34223699
Nat Commun. 2018 Jan 4;9(1):60
pubmed: 29302040

Auteurs

Yevheniia Markushyna (Y)

Department of Colloid Chemistry, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.

Christoph M Schüßlbauer (CM)

Department of Chemistry and Pharmacy, Interdisciplinary Center for Molecular Materials(ICMM), Friedrich-Alexander University of Erlangen-Nürnberg, Egerlandstrasse 3, 91058, Erlangen, Germany.

Tobias Ullrich (T)

Department of Chemistry and Pharmacy, Interdisciplinary Center for Molecular Materials(ICMM), Friedrich-Alexander University of Erlangen-Nürnberg, Egerlandstrasse 3, 91058, Erlangen, Germany.

Dirk M Guldi (DM)

Department of Chemistry and Pharmacy, Interdisciplinary Center for Molecular Materials(ICMM), Friedrich-Alexander University of Erlangen-Nürnberg, Egerlandstrasse 3, 91058, Erlangen, Germany.

Markus Antonietti (M)

Department of Colloid Chemistry, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.

Aleksandr Savateev (A)

Department of Colloid Chemistry, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.

Classifications MeSH