Fast Fluorescence Switching within Hydrophilic Supramolecular Assemblies

被引:34
作者
Cusido, Janet [2 ]
Battal, Mutlu [2 ]
Deniz, Erhan [2 ]
Yildiz, Ibrahim [2 ]
Sortino, Salvatore [1 ]
Raymo, Francisco M. [2 ]
机构
[1] Univ Catania, Dept Drug Sci, Lab Photochem, I-95125 Catania, Italy
[2] Univ Miami, Dept Chem, Lab Mol Photon, Coral Gables, FL 33146 USA
基金
美国国家科学基金会;
关键词
fluorescence; heterocycles; micelles; photochromism; polymers; PHOTOINDUCED ELECTRON-TRANSFER; ENERGY-TRANSFER; MOLECULES; OXAZINE; PHOTOCHROMISM; MODULATION; CHEMISTRY; DERIVATIVES; MICROSCOPY; SPIROPYRAN;
D O I
10.1002/chem.201201184
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We designed a supramolecular strategy to modulate fluorescence in water under optical control. It is based on the entrapment of fluorophorephotochrome dyads within the hydrophobic interior of an amphiphilic polymer. The polymeric envelope around the dyads protects them from the aqueous environment, while imposing hydrophilic character on the overall supramolecular construct. In the resulting assemblies, the photochromic component can be operated reversibly on a microsecond timescale under the influence of ultraviolet stimulations. In turn, the reversible transformations control the emission intensity of the adjacent fluorophore. As a result, the fluorescence of such nanostructured constructs can be photomodulated for hundreds of cycles in water with microsecond switching speeds. Thus, our protocol for fast fluorescence switching in aqueous solutions can eventually lead to the realization of functional probes for the investigation of biological samples.
引用
收藏
页码:10399 / 10407
页数:9
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