An Electron‐Deficient CpE Iridium(III) Catalyst: Synthesis, Characterization, and Application to Ether‐Directed C−H Amidation

Author:

Tomita Eiki1,Kojima Masahiro1ORCID,Nagashima Yuki2ORCID,Tanaka Ken2ORCID,Sugiyama Haruki34ORCID,Segawa Yasutomo34ORCID,Furukawa Atsushi15ORCID,Maenaka Katsumi16ORCID,Maeda Satoshi789ORCID,Yoshino Tatsuhiko16ORCID,Matsunaga Shigeki16ORCID

Affiliation:

1. Faculty of Pharmaceutical Sciences Hokkaido University Kita-ku Sapporo 060-0812 Japan

2. Department of Chemical Science and Engineering Tokyo Institute of Technology O-okayama, Meguro-ku Tokyo 152-8550 Japan

3. Institute for Molecular Science Okazaki 444-8787 Japan

4. Department of Structural Molecular Science SOKENDAI (The Graduate University for Advanced Studies) Myodaiji Okazaki 444-8787 Japan

5. Current address: Faculty of Pharmaceutical Sciences Institute of Medical Pharmaceutical and Health Sciences Kanazawa University Kanazawa 920-1192 Japan

6. Global Station for Biosurfaces and Drug Discovery Hokkaido University Kita-ku Sapporo 060-0812 Japan

7. Institute for Chemical Reaction Design and Discovery (WPI-ICReDD) Hokkaido University Kita-ku Sapporo 001-0021 Japan

8. Department of Chemistry Faculty of Science Hokkaido University Kita-ku Sapporo 060-0810 Japan

9. JST ERATO Maeda Artificial Intelligence for Chemical Reaction Design and Discovery Project Kita-ku Sapporo 060-0810 Japan

Abstract

AbstractThe synthesis, characterization, and catalytic performance of an iridium(III) catalyst with an electron‐deficient cyclopentadienyl ligand ([CpEIrI2]2) are reported. The [CpEIrI2]2 catalyst was synthesized by complexation of a precursor of the CpE ligand with [Ir(cod)OAc]2, followed by oxidation, desilylation, and removal of the COD ligand. The electron‐deficient [CpEIrI2]2 catalyst enabled C−H amidation reactions assisted by a weakly coordinating ether directing group. Experimental mechanistic studies and DFT calculations suggested that the high catalytic performance of [CpEIrI2]2 is due to its electron‐deficient nature, which accelerates both C−H activation and IrV‐nitrenoid formation.

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Chemistry,Catalysis

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