Cocrystallization of (μ-S2)2– and (μ-S)2– and Formation of an [η2-S3N(SiMe3)2] Ligand from Chalcogen Reduction by (N2)2– in a Bimetallic Yttrium Amide Complex
Author:
Affiliation:
1. Department of Chemistry, University of California, Irvine, California 92697-2025, United States
Funder
National Science Foundation
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic501753x
Reference36 articles.
1. Reduction of Dinitrogen to Planar Bimetallic M2(μ-η2:η2-N2) Complexes of Y, Ho, Tm, and Lu Using the K/Ln[N(SiMe3)2]3 Reduction System
2. Isolation of Dysprosium and Yttrium Complexes of a Three-Electron Reduction Product in the Activation of Dinitrogen, the (N2)3− Radical
3. (N2)3− Radical Chemistry via Trivalent Lanthanide Salt/Alkali Metal Reduction of Dinitrogen: New Syntheses and Examples of (N2)2− and (N2)3− Complexes and Density Functional Theory Comparisons of Closed Shell Sc3+, Y3+, and Lu3+ versus 4f9 Dy3+
4. Influence of an Inner-Sphere K+ Ion on the Magnetic Behavior of N23– Radical-Bridged Dilanthanide Complexes Isolated Using an External Magnetic Field
5. Strong exchange and magnetic blocking in N23−-radical-bridged lanthanide complexes
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