Silica nanoparticles (SNPs) are one of the most interesting materials with regard to their easy preparation, nontoxicity, and simple surface modification. Based on their various advantages, SNPs have been widely studied and used in various fields such as solid support materials in the column chromatography, 1 insulating layer and silica-polymer composite 2 in engineering fields, and bio-imaging and drug/gene delivery systems in nano-biotechnology.3-5 To make SNP work effectively in all these applications, it is necessary to synthesize size-controllable and mono-dispersed silica particles. Since Stöber showed that spherical silica particles having narrow size distribution could be prepared from tetraethyl orthosilicate (TEOS) as silica source in alcohol solvent with water and aqueous ammonia as catalyst, 6 his method has been used and modified to prepare monodispersed and regular sized SNPs.7 The size control of SNPs was possible by varying the concentration of reactants, the chain length of alkyl group in alcohol solvents and silica sources, base catalysts to primary amine instead of ammonia solution.8 It was also reported that the usage of amino acids and the control of the mixing ratio of their optical isomers could change the size of SNPs.
9Although it is known that the basic formation mechanism of SNPs is the hydrolysis-and-condensation of TEOS, interestingly, the role of solvent during the formation of SNPs has not been systematically investigated yet. When alcohols with long alkyl chains were used as solvent, the size of SNPs was increased due to the different hydrolysis-andcondensation rate to generate seeds. As an example, it was reported that the different sized SNPs were synthesized in methanol (4 nm) and ethanol (8 nm) because the supersaturation ratio of the hydrolyzed silica sources in methanol was higher than that in ethanol.10 In other words, many smaller seeds were generated in fast reaction environment in methanol and could grow to produce many smaller SNPs compared to those produced in ethanol. The reason of different reaction rates in different solvents was mainly described as the consequence of the changes of polarity, degree of hydrogen bond, and viscosity;11 the solvent having a low polarity, low hydrogen bonding ability, and high viscosity could retard the formation of seed leading to increase the final size of SNPs. It was also reported that silica sources with the long or bulky alkoxy groups resulted to generate the large sized SNPs due to the steric effect which decrease the rate of hydrolysis. 11 On the other hand, it was well known in silicon chemistry that the alkoxy groups of silicon compounds could be exchanged in alcohol solution, especially in the presence of acid or base catalysts, and the rate of hydrolysis and condensation reactions were also affected by the character of alkoxy groups.12-14 Therefore, we investigated the alkoxy exchange reactions in the conditions where SNPs were usually synthesized and found a new factor to give simpler and more precise control over their siz...