TY - JOUR
T1 - Oligomeric alkoxysilanes with cagelike hybrids as cores
T2 - Designed precursors of nanohybrid materials
AU - Kuge, Hideki
AU - Hagiwara, Yoshiaki
AU - Shimojima, Atsushi
AU - Kuroda, Kazuyuki
PY - 2008/3/7
Y1 - 2008/3/7
N2 - Well-defined alkoxysilane oligomers containing a cagelike carbosiloxane core were synthesized and used as novel building blocks for the formation of siloxane-based hybrid networks. These oligomers were synthesized from the cagelike trimer derived from bis(triethoxysilyl)methane by silylation with mono-, di-, and triethoxychlorosilanes ((EtO)nMe3-nSiCl, n=1, 2, and 3). Hybrid xerogels were prepared by hydrolysis and polycondensation of these oligomers under acidic conditions. The structures of the products varied depending on the number of alkoxy groups (n). When n=2 and 3, microporous xerogels (BET surface areas of 820 and 510 m2g-1, respectively) were obtained, whereas a nonporous xerogel was obtained when n=1. 29̂Si NMR spectroscopic analysis suggested that partial rearrangement of the siloxane networks, which accompanied the cleavage of the Si-O-Si linkages, occurred during the polycondensation processes. By using an amphiphilic triblock copolymer surfactant as a structure-directing agent, hybrid thin films with a 2D hexagonal mesostructure were obtained when n=2 and 3. These results provide important insight into the rational synthesis of molecularly designed hybrid materials by sol-gel chemistry.
AB - Well-defined alkoxysilane oligomers containing a cagelike carbosiloxane core were synthesized and used as novel building blocks for the formation of siloxane-based hybrid networks. These oligomers were synthesized from the cagelike trimer derived from bis(triethoxysilyl)methane by silylation with mono-, di-, and triethoxychlorosilanes ((EtO)nMe3-nSiCl, n=1, 2, and 3). Hybrid xerogels were prepared by hydrolysis and polycondensation of these oligomers under acidic conditions. The structures of the products varied depending on the number of alkoxy groups (n). When n=2 and 3, microporous xerogels (BET surface areas of 820 and 510 m2g-1, respectively) were obtained, whereas a nonporous xerogel was obtained when n=1. 29̂Si NMR spectroscopic analysis suggested that partial rearrangement of the siloxane networks, which accompanied the cleavage of the Si-O-Si linkages, occurred during the polycondensation processes. By using an amphiphilic triblock copolymer surfactant as a structure-directing agent, hybrid thin films with a 2D hexagonal mesostructure were obtained when n=2 and 3. These results provide important insight into the rational synthesis of molecularly designed hybrid materials by sol-gel chemistry.
KW - Mesoporous materials
KW - Organic-inorganic hybrid composites
KW - Self-assembly
KW - Siloxanes
KW - Sol-gel processes
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U2 - 10.1002/asia.200700242
DO - 10.1002/asia.200700242
M3 - Article
C2 - 18246561
AN - SCOPUS:54549090990
SN - 1861-4728
VL - 3
SP - 600
EP - 606
JO - Chemistry - An Asian Journal
JF - Chemistry - An Asian Journal
IS - 3
ER -