A novel azobenzene derivative modified magadiite has been prepared by the reaction between the interlayer hydroxyl groups of magadiite and the azobenzene derivative using dodecyltrimethylammonium-exchanged magadiite as the intermediate. The formation of the silylated magadiite-azobenzene system was confirmed by X-ray diffraction, IR and MAS NMR spectroscopies. The organic groups of the azobenzene molecules are grafted onto the interlayer surface of magadiite by covalent bonding, affording compounds different from those derived by ion exchange. The orientation and reorientation of the azobenzene derivative in the magadiite have been examined through observing its photoinduced anisotropy behavior. (C) 2004 Elsevier SAS. All rights reserved.
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MIT, Dep of Chemical Engineering,, Cambridge, MA, USA, MIT, Dep of Chemical Engineering, Cambridge, MA, USAMIT, Dep of Chemical Engineering,, Cambridge, MA, USA, MIT, Dep of Chemical Engineering, Cambridge, MA, USA
Merrill, E.W.
Mahmud, N.A.
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MIT, Dep of Chemical Engineering,, Cambridge, MA, USA, MIT, Dep of Chemical Engineering, Cambridge, MA, USAMIT, Dep of Chemical Engineering,, Cambridge, MA, USA, MIT, Dep of Chemical Engineering, Cambridge, MA, USA
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Univ Lille, Univ Polytech Hauts De France, CNRS, UMR 8520,IEMN,Inst Electron Microelect & Nanotechn, F-59000 Lille, FranceUniv Lille, Univ Polytech Hauts De France, CNRS, UMR 8520,IEMN,Inst Electron Microelect & Nanotechn, F-59000 Lille, France
Godey, Sylvie
Therssen, Hugo
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Univ Lille, Univ Polytech Hauts De France, CNRS, UMR 8520,IEMN,Inst Electron Microelect & Nanotechn, F-59000 Lille, FranceUniv Lille, Univ Polytech Hauts De France, CNRS, UMR 8520,IEMN,Inst Electron Microelect & Nanotechn, F-59000 Lille, France
Therssen, Hugo
Guerin, David
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Univ Lille, Univ Polytech Hauts De France, CNRS, UMR 8520,IEMN,Inst Electron Microelect & Nanotechn, F-59000 Lille, FranceUniv Lille, Univ Polytech Hauts De France, CNRS, UMR 8520,IEMN,Inst Electron Microelect & Nanotechn, F-59000 Lille, France