Reactivity of Ln(II) Complexes Supported by (C5H4Me)1– Ligands with THF and PhSiH3: Isolation of Ring-Opened, Bridging Alkoxyalkyl, Hydride, and Silyl Products
Author:
Affiliation:
1. Department of Chemistry, University of California, Irvine, California 92697-2025, United States
Funder
Division of Chemistry
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.8b00419
Reference89 articles.
1. Lanthanum Does Form Stable Molecular Compounds in the +2 Oxidation State
2. Structural, Spectroscopic, and Theoretical Comparison of Traditional vs Recently Discovered Ln2+ Ions in the [K(2.2.2-cryptand)][(C5H4SiMe3)3Ln] Complexes: The Variable Nature of Dy2+ and Nd2+
3. Expanding Rare-Earth Oxidation State Chemistry to Molecular Complexes of Holmium(II) and Erbium(II)
4. Completing the Series of +2 Ions for the Lanthanide Elements: Synthesis of Molecular Complexes of Pr2+, Gd2+, Tb2+, and Lu2+
5. Synthesis of a Crystalline Molecular Complex of Y2+, [(18-crown-6)K][(C5H4SiMe3)3Y]
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