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Your search keyword '"Khuyen, Hoang Thi"' showing total 3 results
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3 results on '"Khuyen, Hoang Thi"'

1. Characterization of Gd2O3:Eu3+ Nanocomplexes Conjugate with IgG for the Identification of CEA Tumor Cells

Author

Lien, Pham Thi, Tu, Vu Duc, Diep, Lai Ngoc, Huong, Nguyen Thanh, Khuyen, Hoang Thi, Anh, Nguyen Thi Ngoc, Nghia, Vu Xuan, Anh, Tran Kim, Tomala, Robert, Minh, Le Quoc, Laboratoire Lumière, Matière et Interfaces (LuMIn), and CentraleSupélec-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Ecole Normale Supérieure Paris-Saclay (ENS Paris Saclay)

Subjects
[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics], [PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph], ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2020

2. Efficient Photoswitching of the Nonlinear Optical Properties of Dipolar Photochromic Zinc(II) Complexes

Author

Keitaro Nakatani, Véronique Guerchais, Hubert Le Bozec, Vincent Aubert, Khuyen Hoang-Thi, Eléna Ishow, Isabelle Ledoux, Institut des Sciences Chimiques de Rennes (ISCR), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées (INSA), Laboratoire de Photophysique et Photochimie Supramoléculaires et Macromoléculaires (PPSM), École normale supérieure - Cachan (ENS Cachan)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Photonique Quantique et Moléculaire (LPQM), École normale supérieure - Cachan (ENS Cachan)-CentraleSupélec-Centre National de la Recherche Scientifique (CNRS), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), and Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

Subjects
Molecular switch, 010405 organic chemistry, Chemistry, Nonlinear optics, chemistry.chemical_element, General Medicine, General Chemistry, Zinc, 010402 general chemistry, Photochemistry, 01 natural sciences, Catalysis, 0104 chemical sciences, Dipole, Photochromism, Nonlinear optical, [CHIM.COOR]Chemical Sciences/Coordination chemistry, ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2008

3. Donor-Acceptor-Donor Tetrazines Containing a Ferrocene Unit: Synthesis, Electrochemical and Spectroscopic Properties

Author

Fabien Miomandre, Janusz Zakrzewski, Izabela Janowska, Isabelle Ledoux-Rak, Gilles Clavier, Khuyen Hoang Thi, Pierre Audebert, Department of Organic Chemistry, Łódź University of Technology, Laboratoire de Photophysique et Photochimie Supramoléculaires et Macromoléculaires (PPSM), École normale supérieure - Cachan (ENS Cachan)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Photonique Quantique et Moléculaire (LPQM), and École normale supérieure - Cachan (ENS Cachan)-CentraleSupélec-Centre National de la Recherche Scientifique (CNRS)

Subjects
chemistry.chemical_compound, Ferrocene, chemistry, 010405 organic chemistry, Polymer chemistry, [PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph], Physical and Theoretical Chemistry, 010402 general chemistry, Electrochemistry, Photochemistry, Donor acceptor, 01 natural sciences, 0104 chemical sciences
Abstract

International audience; Donor-acceptor-donor tetrazines containing ferrocene moieties and phenyl unit as a ð-bridge have been synthesized and characterized. UV-vis spectroscopic and cyclic voltamperometric results indicate sizable intramolecular charge transfer interactions in the ground state when the ferrocene is directly bound to the tetrazine. On the other hand, the results show reduction of the electron-donor strength of ferrocene moieties when there is a phenyl linkage. Both tetrazines display a high reduction potential. The role of ferrocenyl groups appear to be detrimental to maximize the cubic hyperpolarizability ç of tetrazines, as compared to purely organic groups such as thiophene. A possible explanation for this behavior may originate from metalto- ligand charge transfer processes.

Published
2006

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