TY - JOUR
T1 - A photoresponsive azobenzene-bridged cubic silsesquioxane network
AU - Guo, Sufang
AU - Okubo, Tatsuya
AU - Kuroda, Kazuyuki
AU - Shimojima, Atsushi
N1 - Funding Information:
This work was supported in part by a Grant-in-Aid for Scientific Research on Innovative Areas ‘New Polymeric Materials Based on Element-Blocks (No. 2401)’ provided by The Ministry of Education, Culture, Sports, Science, and Technology, Japan.
Publisher Copyright:
© 2016, Springer Science+Business Media New York.
PY - 2016/8/1
Y1 - 2016/8/1
N2 - Abstract: An azobenzene (AZO)-bridged cubic silsesquioxane network exhibiting reversible photoisomerization behavior in nonpolar solvents has been prepared via hydrosilylation reaction between 4,4′-diallyloxy-azobenzene and octahydridosilsesquioxane (H8Si8O12; H-POSS). Approximately 70 % of the corner Si–H groups of H-POSS are reacted to form a three-dimensional gel network while maintaining the cubic siloxane structure. The dried gel has a high thermal stability, which is attributed to the highly cross-linked cubic silsesquioxane network where AZOs are covalently incorporated in the main chain. The gel exhibits reversible swelling behavior in nonpolar solvents during wetting–drying cycles. In toluene, a large extent of reversible trans–cis isomerization of the AZO moiety is observed. These results are promising for the design of a new class of photoresponsive materials applicable in host–guest chemistry. Graphical Abstract: [Figure not available: see fulltext.]
AB - Abstract: An azobenzene (AZO)-bridged cubic silsesquioxane network exhibiting reversible photoisomerization behavior in nonpolar solvents has been prepared via hydrosilylation reaction between 4,4′-diallyloxy-azobenzene and octahydridosilsesquioxane (H8Si8O12; H-POSS). Approximately 70 % of the corner Si–H groups of H-POSS are reacted to form a three-dimensional gel network while maintaining the cubic siloxane structure. The dried gel has a high thermal stability, which is attributed to the highly cross-linked cubic silsesquioxane network where AZOs are covalently incorporated in the main chain. The gel exhibits reversible swelling behavior in nonpolar solvents during wetting–drying cycles. In toluene, a large extent of reversible trans–cis isomerization of the AZO moiety is observed. These results are promising for the design of a new class of photoresponsive materials applicable in host–guest chemistry. Graphical Abstract: [Figure not available: see fulltext.]
KW - Azobenzene
KW - Inorganic–organic hybrids
KW - Photoresponsive materials
KW - Polyhedral oligomeric silsesquioxane
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U2 - 10.1007/s10971-016-4074-4
DO - 10.1007/s10971-016-4074-4
M3 - Article
AN - SCOPUS:84976640600
SN - 0928-0707
VL - 79
SP - 262
EP - 269
JO - Journal of Sol-Gel Science and Technology
JF - Journal of Sol-Gel Science and Technology
IS - 2
ER -