2012
DOI: 10.1016/j.cplett.2012.02.024
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Efficient charge transfer process in Coumarin 153–nanotubolar TiO2 hybrid system

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Cited by 11 publications
(8 citation statements)
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“…As expected the optical properties strongly change as a function of the terminal group [8], revealing a high stoke shift for the 1a compound and a higher efficiency for the 1d compound. Generally, the maximum absorption peak depend on the π π* transition from the ground HOMO and HOMO-1 state to the excited LUMO bands.…”
Section: Figurementioning
confidence: 89%
“…As expected the optical properties strongly change as a function of the terminal group [8], revealing a high stoke shift for the 1a compound and a higher efficiency for the 1d compound. Generally, the maximum absorption peak depend on the π π* transition from the ground HOMO and HOMO-1 state to the excited LUMO bands.…”
Section: Figurementioning
confidence: 89%
“…A dye with lower bandgap energy would absorb light at lower frequencies, thus transferring electrons into the conductive band of ZnO. In this way much higher light utilizations are usually reached [1,7,10]. Below our main results aimed at solving this problem will be elucidated, which are based on coumarin-153.…”
Section: Resultsmentioning
confidence: 99%
“…The electron-donor group lowers significantly the S ππ* and T ππ* energies, while the electron-acceptor group shifts the peaks of optical fluorescence and absorption to longer wavelengths. Therefore the absorption peak of coumarin-153 is shifted towards 430 nm, while the same peak for coumarin is known to be located at 365 nm as [7].…”
Section: Introductionmentioning
confidence: 99%
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“…The large coumarin family (with more than 1000 derivatives) includes naturally occurring dye molecules that belong to the flavonoid class of plant secondary metabolites. Thanks to their remarkable photophysical properties, coumarins find applications in many and different areas, ranging from photonics to photochemistry and photobiology. Indeed, the coumarin unit (5,6-benzo-2-pyrone), found in many natural and synthetic drug molecules, displays strong absorption cross sections in the near-UV–green wavelength region and a large radiative quantum yield, making the coumarin compounds suitable as laser dyes, as efficient fluorescent labels and probes, or as sensitizers for solar energy collectors. , In addition, coumarin derivatives are known for their antioxidant, anticoagulant, antibacterial, and anti-HIV properties largely applied in biology, medicine, and agriculture (such as enzyme inhibitors, anticoagulant agents, , drugs with spasmolytic and anticancer activity, sun-screening additives, and pesticides ,, ). The Hymecromone (7-hydroxy-4-methyl-coumarin, Scheme a), also known as umbelliferone or coumarin 4 (C4), is often regarded as the parent molecule of this family of heterocyclic compounds and has been largely investigated as the archetype for the photochemical and photophysical properties of the coumarin family.…”
Section: Introductionmentioning
confidence: 99%