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| Designed synthesis of zeolites with tailored microporosity and functionality has been impossible, partly due to a lack of understanding of their crystallization mechanisms. In addition,although they are formed as thermodynamically metastable phases, their phase selection occurs under kinetic control. Thus, the products that crystallize under particular conditions are hardly predictable. On the contrary, the surfactant-directed self-assembly process has been well studied as a route to control mesostructures of sol¨Cgel-derived mesoporous silica, which can be achieved under both thermodynamic and kinetic control. Sol¨Cgel-derived silica can be functionalized by introduction of organosilanes containing organic moieties with desired functionality. However,there are still difficulties in controlling local or atomic structures of sol¨Cgel-derived silica networks, because such amorphous networks are formed randomly on the hydrolysis and polycondensation of the precursors.Progress toward locally ordered structures has been made in recent years, mainly by self-assembly of well-defined oligomers as molecular building units. |
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