The Experts below are selected from a list of 999 Experts worldwide ranked by ideXlab platform
Shinsuke Takagi - One of the best experts on this subject based on the ideXlab platform.
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artificial light harvesting system with energy migration functionality in a cationic dye inorganic nanosheet complex
Journal of Physical Chemistry C, 2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra.
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Artificial Light-Harvesting System with Energy Migration Functionality in a Cationic Dye/Inorganic Nanosheet Complex
The Journal of Physical Chemistry C, 2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra.
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Artificial Light-Harvesting System with Energy Migration Functionality in a Cationic Dye/Inorganic Nanosheet Complex
2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra
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Adsorption and photochemical behaviors of the novel cationic Xanthene Derivative on the clay surface
Tetrahedron Letters, 2014Co-Authors: Yuta Ohtani, Tetsuya Shimada, Hiroshi Tachibana, Yuka Ando, Yohei Ishida, Shinsuke TakagiAbstract:Abstract Novel tetra-cationic Xanthene Derivative (Flu) was synthesized. Its adsorption and photochemical behaviors on the clay surface were investigated. Fluorescence quantum yield ( ϕ f ) and fluorescence lifetime were 0.50 and 2.9 ns for Flu/clay complex. ϕ f of Flu was enough high (>0.1) even at high density conditions (0.080 molecules nm −2 ). It is supposed that the strong interaction between clay and Flu by the ‘Size-Matching Effect’ realizes the highly emissive clay complexes at high density adsorption condition by a suppression of a molecular aggregation, which tends to decrease the photochemical activity.
Yuta Ohtani - One of the best experts on this subject based on the ideXlab platform.
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artificial light harvesting system with energy migration functionality in a cationic dye inorganic nanosheet complex
Journal of Physical Chemistry C, 2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra.
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Artificial Light-Harvesting System with Energy Migration Functionality in a Cationic Dye/Inorganic Nanosheet Complex
The Journal of Physical Chemistry C, 2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra.
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Artificial Light-Harvesting System with Energy Migration Functionality in a Cationic Dye/Inorganic Nanosheet Complex
2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra
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Adsorption and photochemical behaviors of the novel cationic Xanthene Derivative on the clay surface
Tetrahedron Letters, 2014Co-Authors: Yuta Ohtani, Tetsuya Shimada, Hiroshi Tachibana, Yuka Ando, Yohei Ishida, Shinsuke TakagiAbstract:Abstract Novel tetra-cationic Xanthene Derivative (Flu) was synthesized. Its adsorption and photochemical behaviors on the clay surface were investigated. Fluorescence quantum yield ( ϕ f ) and fluorescence lifetime were 0.50 and 2.9 ns for Flu/clay complex. ϕ f of Flu was enough high (>0.1) even at high density conditions (0.080 molecules nm −2 ). It is supposed that the strong interaction between clay and Flu by the ‘Size-Matching Effect’ realizes the highly emissive clay complexes at high density adsorption condition by a suppression of a molecular aggregation, which tends to decrease the photochemical activity.
Tetsuya Shimada - One of the best experts on this subject based on the ideXlab platform.
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artificial light harvesting system with energy migration functionality in a cationic dye inorganic nanosheet complex
Journal of Physical Chemistry C, 2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra.
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Artificial Light-Harvesting System with Energy Migration Functionality in a Cationic Dye/Inorganic Nanosheet Complex
The Journal of Physical Chemistry C, 2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra.
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Artificial Light-Harvesting System with Energy Migration Functionality in a Cationic Dye/Inorganic Nanosheet Complex
2015Co-Authors: Yuta Ohtani, Tetsuya Shimada, Shinsuke TakagiAbstract:We investigated a reaction involving photochemical energy transfer between a cationic Xanthene Derivative (Flu(D)) and a cationic porphyrin (Por(A)) with an energy migration functionality, which is crucial for efficient light-harvesting on an inorganic nanosheet. Efficient energy transfer from excited Flu(D) to Por(A) took place, and the maximum energy transfer efficiency was 99%. Even under light-harvesting conditions, Por(A) concentration was much less than Flu(D) concentration (Flu(D)/Por(A) concentration ratio = 15), and the energy transfer efficiency was still 80%. Steady-state, time-resolved, anisotropic fluorescence measurements indicate energy migration between Flu(D) molecules. This system has the functionality of a light-harvesting system using a dye and having a large overlap between its absorption and fluorescence spectra
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Adsorption and photochemical behaviors of the novel cationic Xanthene Derivative on the clay surface
Tetrahedron Letters, 2014Co-Authors: Yuta Ohtani, Tetsuya Shimada, Hiroshi Tachibana, Yuka Ando, Yohei Ishida, Shinsuke TakagiAbstract:Abstract Novel tetra-cationic Xanthene Derivative (Flu) was synthesized. Its adsorption and photochemical behaviors on the clay surface were investigated. Fluorescence quantum yield ( ϕ f ) and fluorescence lifetime were 0.50 and 2.9 ns for Flu/clay complex. ϕ f of Flu was enough high (>0.1) even at high density conditions (0.080 molecules nm −2 ). It is supposed that the strong interaction between clay and Flu by the ‘Size-Matching Effect’ realizes the highly emissive clay complexes at high density adsorption condition by a suppression of a molecular aggregation, which tends to decrease the photochemical activity.
Gerhard Erker - One of the best experts on this subject based on the ideXlab platform.
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Macrocycle Formation by Cooperative Selection at a Double-Sited Frustrated Lewis Pair
Organometallics, 2019Co-Authors: Long Wang, Dongsheng Deng, Karel Škoch, Constantin G. Daniliuc, Gerald Kehr, Gerhard ErkerAbstract:Hydroboration of the 4,5-bis(allyl,mesityl)phosphanyl Xanthene Derivative 2 with Piers’ borane [HB(C6F5)2] gave the bis-P/B frustrated Lewis pair 3. In this situation, the two symmetry-equivalent P...
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Macrocycle Formation by Cooperative Selection at a Double-Sited Frustrated Lewis Pair
2019Co-Authors: Long Wang, Dongsheng Deng, Constantin G. Daniliuc, Gerald Kehr, Karel Škoch, Gerhard ErkerAbstract:Hydroboration of the 4,5-bis(allyl,mesityl)phosphanyl Xanthene Derivative 2 with Piers’ borane [HB(C6F5)2] gave the bis-P/B frustrated Lewis pair 3. In this situation, the two symmetry-equivalent P/B FLP units featured markedly different reaction modes. With resorcinol, they formed the 20-membered macrocycle 11 by a sequence of −OH deprotonation/borane-induced tautomerization. With aryl acetylenes, the 18-membered macrocyclic products 15 (three examples) were formed in a unique sequence of carbon–carbon coupling reactions
Long Wang - One of the best experts on this subject based on the ideXlab platform.
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Macrocycle Formation by Cooperative Selection at a Double-Sited Frustrated Lewis Pair
Organometallics, 2019Co-Authors: Long Wang, Dongsheng Deng, Karel Škoch, Constantin G. Daniliuc, Gerald Kehr, Gerhard ErkerAbstract:Hydroboration of the 4,5-bis(allyl,mesityl)phosphanyl Xanthene Derivative 2 with Piers’ borane [HB(C6F5)2] gave the bis-P/B frustrated Lewis pair 3. In this situation, the two symmetry-equivalent P...
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Macrocycle Formation by Cooperative Selection at a Double-Sited Frustrated Lewis Pair
2019Co-Authors: Long Wang, Dongsheng Deng, Constantin G. Daniliuc, Gerald Kehr, Karel Škoch, Gerhard ErkerAbstract:Hydroboration of the 4,5-bis(allyl,mesityl)phosphanyl Xanthene Derivative 2 with Piers’ borane [HB(C6F5)2] gave the bis-P/B frustrated Lewis pair 3. In this situation, the two symmetry-equivalent P/B FLP units featured markedly different reaction modes. With resorcinol, they formed the 20-membered macrocycle 11 by a sequence of −OH deprotonation/borane-induced tautomerization. With aryl acetylenes, the 18-membered macrocyclic products 15 (three examples) were formed in a unique sequence of carbon–carbon coupling reactions