Energy and electron transfer from fluorescent mesostructured organosilica framework to guest dyes

© 2012 American Chemical Society

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 28(2012), 8 vom: 28. Feb., Seite 3987-94
1. Verfasser: Mizoshita, Norihiro (VerfasserIn)
Weitere Verfasser: Yamanaka, Ken-ichi, Hiroto, Satoru, Shinokubo, Hiroshi, Tani, Takao, Inagaki, Shinji
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
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520 |a Energy and electron transfer from frameworks of nanoporous or mesostructured materials to guest species in the nanochannels have been attracting much attention because of their increasing availability for the design and construction of solid photofunctional systems, such as luminescent materials, photovoltaic devices, and photocatalysts. In the present study, energy and electron-transfer behavior of dye-doped periodic mesostructured organosilica films with different host-guest arrangements were systematically examined. Fluorescent tetraphenylpyrene (TPPy)-silica mesostructured films were used as a host donor. The location of guest perylene bisimide (PBI) dye molecules, acting as an acceptor, could be controlled on the basis of the molecular design of the PBI substituent groups. PBI dyes with bulky substituents and polar anchoring groups were located at the pore surface with low self-aggregation, which induced efficient energy or electron transfer because of the close host-guest arrangement. However, PBI dye with bulky and hydrophobic substituents was located in the center of template surfactant micelles; the fluorescence emission from the host TPPy groups was hardly quenched when the host-guest distance was longer than the critical Förster radius (ca. 4.5 nm). The relationship between the energy or electron-transfer efficiency and the location of guest species in the channels of mesostructured organosilica was first revealed by molecular design of the PBI substituents 
650 4 |a Journal Article 
700 1 |a Yamanaka, Ken-ichi  |e verfasserin  |4 aut 
700 1 |a Hiroto, Satoru  |e verfasserin  |4 aut 
700 1 |a Shinokubo, Hiroshi  |e verfasserin  |4 aut 
700 1 |a Tani, Takao  |e verfasserin  |4 aut 
700 1 |a Inagaki, Shinji  |e verfasserin  |4 aut 
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