σ-Coordination of a P–H Bond at a Sterically Demanding Diruthenium Site: Tautomerization between Agostic μ-Phosphane and μ-Phosphanido Complexes via an η2-P–H Bond Cleavage
Author:
Affiliation:
1. Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology, 2-12-1 O-okayama, Meguro-ku, Tokyo 152-8552, Japan
2. JST, ACT-C, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan
Funder
Japan Science and Technology Agency
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.7b00856
Reference34 articles.
1. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
2. Sterically demanding trialkylphosphines for palladium-catalyzed cross coupling reactions—alternatives to PtBu3
3. Synthesis and Properties of Diruthenium Tetrahydrides Supported by Less-substituted, Sterically Demanding Poly-tert-butylated Cyclopentadienyls
4. Synthesis, Characterization, and Reactions of Ruthenium(II), -(III), and -(IV) Complexes with Sterically Demanding 1,2,4-Tri-tert-butylcyclopentadienyl Ligands
5. Versatile and highly efficient synthesis of diruthenium tetrahydride complex
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3. A dipotassium 1,2,4-diazaphospholide dianion radical as an organometallic building block: the first 1,2-diaza-4-phosphine ruthenocene;Dalton Transactions;2018
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