Characterization and biomimetic study of a hydroxo-bridged dinuclear phenanthroline cupric complex encapsulated in mesoporous silica: models for catechol oxidase.

We report the synthesis and characterization of a hydroxo-bridged dinuclear phenanthroline cupric complex, (phen)2Cu-OH-Cu(phen)2) (HPC, phen = phenanthroline), dispersed in molecular sieves: MCM-41's and sodium zeolite Y. We employed spectroscopic techniques (FT-IR, UV-visible, EPR, and EXAFS) to characterize and study the catalytic activities of immobilized HPC in the oxidation of 3,5-di-tert-butylcatechol (DTBC) to the corresponding quinone (3,5-di-tert-butylquinone, DTBQ) to mimic the functionality of catechol oxidases. HPC complexes can adsorb only on the outside surface of the Y zeolite due to its smaller pore size. The EXAFS spectrum gives 3.51 A for the Cu...Cu distance in HPC encapsulated in the nanochannels of Al-MCM-41 mesoporous solids, which is comparable to the O...O distance of the two hydroxyl groups of DTBC, and this made a simultaneous coordination of the diol group to the dicupric center possible. The resultant complex then allows the transfer of two electrons from DTBC to the dicupric center leading to the production of DTBQ. The nanochannels of calcined Al-MCM-41 mesoporous solids provide stability, due to confined space and surface charge, which could prevent excessive separation of the dinuclear cupric centers after removal of the hydroxo bridge in the catalytic process. A catalytic reaction scheme is proposed based on the spectroscopic data obtained in the characterization. The study demonstrates that HPC encapsulated in the nanochannels of Al-MCM-41 mesoporous materials could be a viable system for a broad range of catalytic oxidation to mimic natural occurring enzymes.