73267-93-3

Upstream product

• 7758-99-8 copper(II) sulfate 
• 532-32-1 sodium benzoate 
• 12775-96-1 copper 

Downstream Products

• 1401310-31-3 Cu⁽²⁺⁾*N₃^(1-)*C₆H₅COO^(1-)*CH₃OH=Cu(N₃)(C₆H₅COO)(CH₃OH) 
• 533-01-7 copper(II) benzoate 
• 933455-72-2 [Cu(benzoato)2(semicarbazide)2] 
• 533-01-7 Copper(I); benzoate 
• 12775-96-1 copper 

Relevant academic research and scientific papers

Molecular nanoscale magnetic refrigerants: A ferrimagnetic {Cu II15GdIII7} cagelike cluster from the use of pyridine-2,6-dimethanol

The employment of pyridine-2,6-dimethanol in 3d/4f metal cluster chemistry has afforded a new {CuII15GdIII7} cagelike molecule with a beautiful structure built by fused triangular subunits; the compound exhibits

Trinuclear, tetranuclear, and polymeric CuII complexes from the first use of 2-pyridylcyanoxime in transition metal chemistry: Synthetic, structural, and magnetic studies

The first use of 2-pyridylcyanoxime, (py)C(CN)-NOH, in transition metal chemistry is described. Depending on the nature of the metal starting material and the reaction conditions employed, the CuII/(py)C(CN)NOH system has provided access to complexes [Cu3O{(py)C(CN)NO} 3(NO3)-(H2O)2(MeOH)] (1), [Cu 4O{(py)C(CN)NO}4(O2CMe)2] (2), [Cu4(OH)2{(py)C(CN)NO}2(O2CPh) 4]2n·n[Cu4(OH)2-{(py)C(CN)NO} 2(O2CPh)4](3), and [Cu{(py)C(CN)NO} 2]n (4). The molecule of 1 consists of three Cu II atoms in a strictly equilateral arrangement bridged by a central μ3-oxide group. The molecule of 2 consists of a tetrahedron of CuII atoms held together by a central μ4-oxide ion, four η1:η1:η1;;μ-(py)C(CN) NO- ligands and two η1:η1;;μ- MeCO2- groups. The crystal structure of 3 consists of [Cu4(OH)2{(py)C(CN)NO}2(O2CPh) 4]2n double chains and discrete cluster [Cu 4(OH)2{(py)C(CN)NO}2-(O2CPh) 4] molecules. The crystal structure of 4 consists of neutral polymeric chains based on centrosymmetric mononuclear [Cu{(py)C(CN)NO} 2] units. The CuII atoms are doubly bridged by the oximate groups of two η1:η1:η1:μ-(py) C(CN)NO- ligands. Variable-temperature, solid-state direct current (dc) magnetic susceptibility studies were carried out for 1-4. The data indicate very strong antiferromagnetic exchange interactions for 1-3. The obtained J values are discussed in depth on the basis of the structural parameters of the complexes, literature reports, and existing magnetostructural correlations.