Easily Switchable 18π‐, 19π‐, and 20π‐Conjugation of Diazaporphyrin Double‐Pincer Bispalladium Complexes

Author:

Sakurai Takahiro1,Hiraoka Yuya1,Tanaka Hisaaki2ORCID,Miyake Yoshihiro1ORCID,Fukui Norihito13ORCID,Shinokubo Hiroshi1ORCID

Affiliation:

1. Department of Molecular and Macromolecular Chemistry Graduate School of Engineering and Integrated Research Consortium on Chemical Science (IRCCS) Nagoya University Furo-cho, Chikusa-ku, Nagoya 464-8603 Japan

2. Department of Applied Physics Graduate School of Engineering Nagoya University Furo-cho, Chikusa-ku, Nagoya 464-8603 Japan

3. PRESTO Japan Science and Technology Agency (JST) Kawaguchi Saitama 332-0012 Japan

Abstract

AbstractNiII 3,7,13,17‐tetrapyridyl‐5,15‐diazaporphyrin serves as a double tridentate ligand to PdII ions to provide a pincer‐type bispalladium complex. Electrochemical analysis revealed that the bispalladium complex shows excellent ability to accept electrons and reversible redox properties due to the coordination of the two cationic PdII centers to the meso‐nitrogen atoms. We isolated and characterized one‐ and two‐electron reduction species of the bispalladium complex. The 20π antiaromatic nature of the two‐electron reduction species was confirmed by 1H NMR spectroscopy, UV/Vis‐near‐IR (NIR) absorption spectra, and density functional theory (DFT) calculations. X‐ray diffraction revealed highly twisted structures for the bispalladium complexes regardless of the oxidation state.

Funder

Japan Society for the Promotion of Science

Japan Science and Technology Agency

Publisher

Wiley

Subject

General Chemistry,Catalysis

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