<i>meso</i>-Aryl substituents modify the electrochemical profile and palladium(<scp>ii</scp>) coordination of redox-active tripyrrin ligands-Reference-Cited by-同舟云学术

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meso-Aryl substituents modify the electrochemical profile and palladium(ii) coordination of redox-active tripyrrin ligands

Published:2024 Issue:6 Volume:11 Page:1789-1798
ISSN:2052-1553
Container-title:Inorganic Chemistry Frontiers
language:en
Short-container-title:Inorg. Chem. Front.

Author:

Habenšus Iva¹,Tomat Elisa¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, The University of Arizona, 1306 E. University Blvd., Tucson, AZ 85721-0041, USA

Abstract

The synthesis of meso-aryl 1,14-dimethoxytripyrrin and tripyrrin-1,14-dione allows isolation of palladium(ii) complexes presenting aliphatic C–H bond activation reactivity and multiple ligand-based redox processes.

Funder

Division of Chemistry

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QI/D3QI02597G

Reference57 articles.

1. H.Falk , The Chemistry of Linear Oligopyrroles and Bile Pigments , Springer-Verlag , Vienna , 1989

2. Synthetic Expanded Porphyrin Chemistry

3. Chemistry of meso-Aryl-Substituted Expanded Porphyrins: Aromaticity and Molecular Twist

4. Porphyrinoid Drug Conjugates

5. Lanthanide porphyrinoids as molecular theranostics

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1. Gold Tripyrrindione: Redox Chemistry and Reactivity with Dichloromethane;Inorganic Chemistry;2024-08-31

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