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4-十八烷氧基苯乙烯基吡啶芳基羧酸盐薄膜中单层和双层堆叠排列之间可逆的光驱动结构变化。

Reversible light-driven structural changes between the mono- and bilayer stacking alignments in 4-octadecyloxystilbazolium arylcarboxylate films.

作者信息

Ohtani Osamu, Kato Hiroki, Yui Tatsuto, Takagi Katsuhiko

机构信息

Department of Crystalline Materials Science, School of Engineering, Nagoya University, Chikusa, Nagoya 464-8603, Japan.

出版信息

J Am Chem Soc. 2003 Nov 26;125(47):14465-72. doi: 10.1021/ja030310s.

Abstract

The present investigation deals with the light-driven morphological changes in multilamella films of N-methyl-4-octadecyloxystilbazolium arylcarboxylates (C18OStz+X-) cast on glass slides. The results of XRD analysis show a photostimulated layer expansion and shrinkage of the stacked thin films along the c-axis under alternative illumination at >350 and 254 nm, respectively. It was revealed that such lamellar changes could be switched either way by a reversible transformation between the mono- and bilayer units in these stacked multilamella films. Moreover, such controlled structural adjustments in the alignment could be initiated by the photocyclodimerization of the stilbazolium moieties of the arylcarboxylate salts; i.e., a monolayer-to-bilayer transformation could be induced at a stage of only 10% cyclodimer formation. The photoinduced patterning on the surface of the films was also analyzed by SEM and fluorescence microscopic investigations.

摘要

本研究涉及在载玻片上浇铸的N-甲基-4-十八烷氧基苯乙烯基苄基芳基羧酸盐(C18OStz + X-)多层膜中光驱动的形态变化。X射线衍射分析结果表明,在分别大于350和254 nm的交替光照下,堆叠薄膜沿c轴发生光刺激层膨胀和收缩。结果表明,通过这些堆叠多层膜中单层和双层单元之间的可逆转变,这种层状变化可以双向切换。此外,这种排列中的可控结构调整可以由芳基羧酸盐的苯乙烯基苄基部分的光环二聚化引发;即,在仅10%环二聚体形成的阶段就可以诱导单层到双层的转变。还通过扫描电子显微镜和荧光显微镜研究分析了薄膜表面的光诱导图案。

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