Photochromic hybrid organic-inorganic liquid-crystalline materials built from nonionic surfactants and polyoxometalates:: Elaboration and structural study

被引:44
作者
Poulos, Andreas S. [1 ]
Constantin, Doru [1 ]
Davidson, Patrick [1 ]
Imperor, Marianne [1 ]
Pansu, Brigitte [1 ]
Panine, Pierre [2 ]
Nicole, Lionel [3 ]
Sanchez, Clement [3 ]
机构
[1] Univ Paris 11, Phys Solides Lab, CNRS, UMR 8502, F-91405 Orsay, France
[2] European Synchrotron Radiat Facil, F-38043 Grenoble, France
[3] Univ Paris 06, CNRS, UMR 7574, F-75005 Paris, France
关键词
D O I
10.1021/la8004322
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work reports the elaboration and structural study of new hybrid organic-inorganic materials constructed via the coupling of liquid-crystalline nonionic surfactants and polyoxometalates (POMs). X-ray scattering and polarized light microscopy demonstrate that these hybrid materials, highly loaded with POMs (up to 18 wt %), are nanocomposites of liquid-crystalline lamellar structure (L alpha), with viscoelastic properties close to those of gels. The interpretation of X-ray scattering data strongly suggests that the POMs are located close to the terminal-OH groups of the nonionic. surfactants, within the aqueous sublayers. Moreover, these materials exhibit a reversible photochromism associated to the photoreduction of the polyanion. The photoinduced mixed-valence behavior has been characterized through ESR and UV-visible-near-IR spectroscopies that demonstrate the presence of W-v metal cations and of the characteristic intervalence charge transfer band in the near-IR region, respectively. These hybrid nanocomposites exhibit optical properties that may be useful for applications involving UV-light-sensitive coatings or liquid-crystal-based photochromic switches. From a more fundamental point of view, these hybrid materials should be very helpful models for the study of both the static and dynamic properties of nano-objects confined within soft lamellar structures.
引用
收藏
页码:6285 / 6291
页数:7
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