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    Polyfunctional Tetraaza-Macrocyclic Ligands: Zn(II), Cu(II) Binding and Formation of Hybrid Materials with Multiwalled Carbon Nanotubes

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    The binding properties of HL1, HL2, and HL3 ligands toward CuĀ­(II) and ZnĀ­(II) ions, constituted by tetraaza-macrocyclic rings decorated with pyrimidine pendants, were investigated by means of potentiometric and UV spectrophotometric measurements in aqueous solution, with the objective of using the related HL-MĀ­(II) (HL = HL1ā€“HL3; M = Cu, Zn) complexes for the preparation of hybrid MWCNT-HL-MĀ­(II) materials based on multiwalled carbon nanotubes (MWCNTs), through an environmentally friendly noncovalent procedure. As shown by the crystal structure of [CuĀ­(HL1)]Ā­(ClO<sub>4</sub>)<sub>2</sub>, metal coordination takes place in the macrocyclic ring, whereas the pyrimidine residue remains available for attachment onto the surface of the MWCNTs via Ļ€ā€“Ļ€ stacking interactions. On the basis of equilibrium data showing the formation of highly stable CuĀ­(II) complexes, the MWCNT-HL1-CuĀ­(II) material was prepared and characterized. This compound proved very stable toward lixiviation processes (release of HL1 and/or CuĀ­(II)); thus, it was used for the preparation of its reduced MWCNT-HL1-Cu(0) derivatives. X-ray photoelectron spectroscopy and transmission electron microscopy images showed that MWCNT-HL1-Cu(0) contains Cu(0) nanoparticles, of very small (less than 5 nm) and regular size, uniformly distributed over the surface of the MWCNTs. Also, the MWCNT-HL1-Cu(0) material proved very resistant to detachment of its components. Accordingly, both MWCNT-HL1-CuĀ­(II) and MWCNT-HL1-Cu(0) are promising candidates for applications in heterogeneous catalysis
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