Cu(II) complexes bearing the 2,2,2-tris(1-pyrazolyl)ethanol or 2,2,2-tris(1-pyrazolyl)ethyl methanesulfonate scorpionates. X-Ray structural characterization and application in the mild catalytic peroxidative oxidation of cyclohexane

• Published in: Dalton transactions : an international journal of inorganic chemistry no. 42; pp. 9207 - 9215
• Main Authors: Silva, Telma F S, Mishra, Gopal S, da Silva, M Fátima Guedes, Wanke, Riccardo, Martins, Luísa M D R S, Pombeiro, Armando J L
• Format: Journal Article
• Language: English
• Published: England 14.11.2009
• Subjects: Catalysis; Coordination Complexes - chemical synthesis; Coordination Complexes - chemistry; Copper - chemistry; Crystallography, X-Ray; Cyclohexanes - chemistry; Hydrogen Bonding; Mesylates - chemistry; Molecular Conformation; Oxidation-Reduction; Pyrazoles - chemistry
• ISSN: 1477-9234
• DOI: 10.1039/b911990f

Reactions between CuCl2 and the functionalized scorpionate 2,2,2-tris(1-pyrazolyl)ethanol HOCH2C(pz)3 1 (pz = pyrazolyl) or 2,2,2-tris(1-pyrazolyl)ethyl methanesulfonate CH3SO2OCH2C(pz)3 2 yield the corresponding water soluble CuII complexes [CuCl2{HOCH2C(pz)3}] 3 or [CuCl2{CH3SO2OCH2C(pz)3}]2 4. In 3 the scorpionate ligand shows the typical N,N,N-coordination mode, whereas in the dinuclear complex 4 it binds the metal as a bidentate species. Compounds 1-4 have been characterized by IR, far-IR, elemental analysis and (for 2-4) single crystal X-ray diffraction. The new scorpionate complexes 3 and 4 are shown to act as catalyst precursors for the peroxidative oxidation of cyclohexane to cyclohexanol (main product) and cyclohexanone, under mild conditions (at room temperature and using an aqueous solution of H2O2) reaching TON values up to 186 in NCMe/H2O. Their hydrosolubility allows them to operate also in pure aqueous media (without any organic solvent, although less effectively), a rare feature of significance towards a green alkane oxidation process.