Volume 58, Issue 42 p. 15031-15035
Communication

Synthesis of A Pincer‐IrV Complex with A Base‐Free Alumanyl Ligand and Its Application toward the Dehydrogenation of Alkanes

Dr. Shogo Morisako

Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8603 Aichi, Japan

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Seiya Watanabe

Department of Applied Chemistry, Faculty of Science and Engineering, Chuo University, 1-13-27, Kasuga, Bunkyo-ku, 112-8551 Tokyo, Japan

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Satoru Ikemoto

Department of Chemistry, Graduate School of Science & Research Center for Materials Science (RCMS) & Integrated Research Consortium on Chemical Science (IRCCS) & Institute for Advanced Science (IAS), Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8603 Aichi, Japan

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Prof. Dr. Satoshi Muratsugu

Corresponding Author

Department of Chemistry, Graduate School of Science & Research Center for Materials Science (RCMS) & Integrated Research Consortium on Chemical Science (IRCCS) & Institute for Advanced Science (IAS), Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8603 Aichi, Japan

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Prof. Dr. Mizuki Tada

Corresponding Author

Department of Chemistry, Graduate School of Science & Research Center for Materials Science (RCMS) & Integrated Research Consortium on Chemical Science (IRCCS) & Institute for Advanced Science (IAS), Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8603 Aichi, Japan

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Prof. Dr. Makoto Yamashita

Corresponding Author

Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8603 Aichi, Japan

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First published: 09 August 2019
Citations: 10

Abstract

A pincer‐iridium complex bearing a Lewis‐base‐free X‐type alumanyl ligand has been synthesized. X‐ray diffraction, NMR and IR spectroscopy, as well as XANES analysis confirmed its tetrahydrido‐IrV structure and Lewis acidity at the Al center as supported by DFT calculations. The resulting complex was applied as a catalyst for the transfer dehydrogenation of cyclooctane.

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