Polyoxometalates (H(3)PMo(12)O(40), H(3)PW(12)O(40), H(4)PMo(11)VO(40)) supported on oxygen- and alkyl-functionalized graphene sheets were investigated. Discrete molecular species were directly observed by electron microscopy at loadings below 20 wt.%. The interaction between the polyoxometalates and the graphene surface was found to significantly impact their vibrational spectra and a linear correlation between the frequency of the M-O(c)-M vibration and the dispersion was evidenced by FTIR. While bulk-like electronic properties were observed for small aggregates (2-5 nm), UV-vis spectroscopy and cyclic voltammetry revealed changes in the electronic structure of isolated molecular species as a result of their interaction with graphene. Because of the ability to disperse alkyl-functionalized graphene in a variety of polar and nonpolar solvents, the materials synthesized in this work provide an opportunity to disperse polyoxometalates in media in which they would not dissolve if unsupported.
We have explored in this work the stability and the reactivity of multiarm cyclam-grafted mesoporous silica samples in aqueous solution. A series of hybrid materials have been prepared by grafting silylated cyclam molecules bearing one, two, or four silyl groups onto both amorphous silica gel (K60) and ordered mesoporous silica (SBA15). Under these conditions, cyclam moieties are attached to the silica walls via one, two, or four arms. Various physicochemical techniques have been applied to characterize the functionalized solids (elemental analysis, 1H-29Si and 1H-13C CPMAS NMR, and N2 adsorption-desorption isotherms). The interest in two and four arms for improving the chemical stability in solution, by comparison with the system displaying only one arm, has been demonstrated by using a set of complementary experiments involving pH measurements and silicon determination with ICP-AES. Then, the investigation of their protonation and binding properties toward copper(II) has revealed a significant decrease in the reactivity of these hybrids as a consequence of multiarm tethering. A comparison of amorphous and ordered materials has permitted us to point out the influence of mesostructuration on the reactivity of these functionalized solids, especially from a kinetic point of view.
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