Abstract:Pyrolysis of a silica gel hybrid with a starburst dendrimer gives porous silica, in which the pore-size is successfully controlled by the size of the organic component used.
“…Poly(amidoamine)dendrimers (PAMAMs), on the other hand, have been used for self-assembly purposes in oxide, hybrid (organic/inorganic), and metallic materials. [13][14][15][16][17][18] In fact, we have recently reported on the use of PAMAM 4.0 as a template to produce porous silicas. 18 However, PAMAM 4.0 collapses upon heating, which results in pores that are significantly smaller than the PAMAM template diameter.…”
Commercially available poly(propylene)imine (DAB-Am-32 and DAB-Am-64) dendrimers were used as single-molecule templates to tailor the porosity of silicas via a nonacidic sol-gel method. X-ray diffraction on both the as-prepared (oven-dried at 373 K) and the calcined (833 K) materials revealed that modest contraction took place on template removal and that the cavities created did not achieve three-dimensional ordering under the current synthesis conditions. Transmission electron microscopy of "Pt-stained" samples supported this picture. A modified Horvath-Kawazoe analysis of the argon adsorption isotherms indicated that DAB-Am-64 is a much more effective template than DAB-Am-32. Pyrolysis and oxidation protocols for template removal are also presented.
“…Poly(amidoamine)dendrimers (PAMAMs), on the other hand, have been used for self-assembly purposes in oxide, hybrid (organic/inorganic), and metallic materials. [13][14][15][16][17][18] In fact, we have recently reported on the use of PAMAM 4.0 as a template to produce porous silicas. 18 However, PAMAM 4.0 collapses upon heating, which results in pores that are significantly smaller than the PAMAM template diameter.…”
Commercially available poly(propylene)imine (DAB-Am-32 and DAB-Am-64) dendrimers were used as single-molecule templates to tailor the porosity of silicas via a nonacidic sol-gel method. X-ray diffraction on both the as-prepared (oven-dried at 373 K) and the calcined (833 K) materials revealed that modest contraction took place on template removal and that the cavities created did not achieve three-dimensional ordering under the current synthesis conditions. Transmission electron microscopy of "Pt-stained" samples supported this picture. A modified Horvath-Kawazoe analysis of the argon adsorption isotherms indicated that DAB-Am-64 is a much more effective template than DAB-Am-32. Pyrolysis and oxidation protocols for template removal are also presented.
“…7 The most simple and convenient idea for construction of transparent and homogeneous hybrid materials is to increase the affinity between organic polymer and inorganic phases. Organic-inorganic hybrid materials are generally prepared by incorporating covalent bonds [8][9][10][11][12][13] or by physical interactions [14][15][16][17][18][19][20][21] to improve the compatibility between organic and inorganic phases.…”
Highly transparent and homogeneous hybrids containing a single nano-sized inorganic oxide domain were synthesized from poly(methyl methacrylate) (PMMA) and aqueous dispersed zirconium oxide nanocrystals (ZrO 2 -NCs) in the presence of a coupling agent, 3-(methacryloxy)propyl-trimethoxysilane (MPTS), which was grafted onto the surface of ZrO 2 -NCs by zirconium hydroxide (Zr-OH) surface groups. The surface-functionalized ZrO 2 -NCs were used as macromonomers in the process of grafting from polymerization of methyl methacrylate (MMA). The densities of surface Zr-OH groups and MPTS surface modifications were determined using thermogravimetric analysis. Fourier transform infrared analysis indicated successful bonding between organic and inorganic moieties. The morphology of the obtained hybrid films was investigated by scanning electron microscopy and tapping-mode atomic force microscopy. Hybrid films possess interesting thermal stability and optical transparency characteristics because of the uniform incorporation of networks between organic polymer chains and inorganic nanocrystals.
“…This interaction due to hydrogen bonding can be confirmed by the fact that, in FT-IR measurement, compared to the case of only organic polymer, the stretching vibrations of the amidocarbonyl group shifts to the low wavenumber side due to hybridization 4), 5) . Further, the fact that the organic polymer is uniformly dispersed in the hybrid can also be confirmed by the fact that by sintering the polymer hybrid it is possible to obtain porous silica having very small holes of molecular order 6) . Apart from the amide group which is the repeting unit in the organic polymer in [1] to [3], it is possible to consider various types as the functional group that acts as the acceptor group of hydrogen bonding.…”
Section: Organic-inorganic Polymer Hybrids Using Hydrogen Bondingmentioning
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