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Journal ArticleDOI

Designer magnets containing cyanides and nitriles.

Joel S. Miller, +1 more
- 02 May 2001 - 
- Vol. 34, Iss: 7, pp 563-570
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TLDR
Three-dimensional network solids exhibiting magnetic ordering have been made from several first-row metal ions and bridging unsaturated cyanide, tricyanomethanide, and/or dicyanamide ligands, which possess several different structural motifs, and the shorter the bridge, the stronger the interaction.
Abstract
Magnets synthesized from molecules have contributed to the renaissance in the study of magnetic materials. Three-dimensional network solids exhibiting magnetic ordering have been made from several first-row metal ions and bridging unsaturated cyanide, tricyanomethanide, and/or dicyanamide ligands. These materials possess several different structural motifs, and the shorter the bridge, the stronger the interaction (i.e., C⋮N > N⋮CN ≫ N⋮CNC⋮N = N⋮CCC⋮N). Cyanide additionally has the ability to discriminate between C- and N-bonding to form ordered heterobimetallic magnets, and the strong coupling can lead to ferro- or ferrimagnetic ordering substantially above room temperature. Tricoordination of tricyanomethanide results in spin-frustrated systems, which possess interpenetrating rutile-like networks. In contrast, single rutile-like frameworks are formed by μ3-bonded dicyanamide, which leads to ferromagnetics and weak ferromagnetics.

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Citations
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Synthesis, Crystal Structures, and Magnetism of Cobalt Coordination Polymers Based on Dicyanamide and Pyrazine-dioxide Derivatives

TL;DR: Three coordination polymers of Co(II) with dicyanamide (dca) were obtained by adding coligands of 2,5-dimethylpyrazine-dioxide (2,3-dmpdo) or 2,3,5,6-tetramethylpyazine-Dioxide (3) to the binary system of Co-dca, which displays antiferromagnetic ordering below 10.8 K.
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Two 3D Triazolate―Tricarboxylate-Bridged CuII/I Frameworks by One-Pot Hydrothermal Synthesis Exhibiting Spin-Canted Antiferromagnetism and Strong Antiferromagnetic Couplings

TL;DR: Two 3D coordination polymers with the same components but different structures, obtained together by a one-pot hydrothermal reaction of Cu(OAc)(2), are observed, displaying a 3,6-connected topological network and spin-canted antiferromagnetism and overall strong antiferromeagnetic couplings up to -147.1 cm(-1).
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TEMPO in Chemical Transformations: From Homogeneous to Heterogeneous

TL;DR: The TEMPO (2,2,6,6-tetramethylpiperidine-Noxyl) radical is an organic radical that finds a variety of industrial applications for chemical transformations.
Journal ArticleDOI

Chemoselective Schmidt Reaction Mediated by Triflic Acid: Selective Synthesis of Nitriles from Aldehydes

TL;DR: The reaction of aldehydes with NaN(3) and TfOH furnishes the corresponding nitriles in near quantitative yields and tolerates a variety of electron-withdrawing and electron-donating substituents on the substrates.
Journal ArticleDOI

Copper-catalyzed aerobic oxidative synthesis of aryl nitriles from benzylic alcohols and aqueous ammonia

TL;DR: Copper-catalyzed direct conversion of benzylic alcohols to aryl nitriles was realized using NH3(aq.) as the nitrogen source, O2 as the oxidant and TEMPO as the co-catalyst.
References
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Journal ArticleDOI

Sol−Gel Synthesis of KVII[CrIII(CN)6]·2H2O: A Crystalline Molecule-Based Magnet with a Magnetic Ordering Temperature above 100 °C

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