152
Views
6
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis, characterization and catalytic oxidation of cyclohexene with molecular oxygen over host (nanopores of zeolite-Y)/guest ([Ni([R]2-N2X2)]2+ (R = H, CH3; X = NH, O, S) nanocatalyst

Pages 980-995 | Received 27 Feb 2008, Accepted 23 May 2008, Published online: 30 Jan 2009
 

Abstract

Nickel(II) complexes of 12-membered macrocyclic ligands with different donating atoms (N2O2, N2S2 and N4) in the macrocyclic ring have been encapsulated in the nanocavity of zeolite-Y by the fexible-ligand method. Nickel(II) complexes with macrocyclic ligands were entrapped in the nanocavity of zeolite-Y by a two-step process in the liquid phase: (i) adsorption of precursor ligand; 1,2-di(o-aminophenyl-, amino, oxo, thio)ethane, N2X2; in the supercages of the Ni(II)–NaY, and (ii) in situ condensation of the Ni(II) precursor complex; [Ni(N2X2)]2+; with glyoxal or biacetyl. The new host–guest nanocatalysts (HGNM), [Ni([R]2-N2X2)]2+–NaY (R = H, CH3; X = NH, O, S), have been characterized by FT-IR, DRS and UV–Vis spectroscopic techniques, XRD and elemental analysis, as well as nitrogen adsorption, and were used for oxidation of cyclohexene with molecular oxygen.

Acknowledgement

Author is grateful to Council of University of Kashan for providing financial support to undertake this work.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.