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Photophysics and photochemistry of a BODIPY-based photosensitizerquantumchemical simulations /
Record Type:
Electronic resources : Monograph/item
Title/Author:
Photophysics and photochemistry of a BODIPY-based photosensitizerby Karl Michael Ziems.
Reminder of title:
quantumchemical simulations /
Author:
Ziems, Karl Michael.
Published:
Wiesbaden :Springer Fachmedien Wiesbaden :2019.
Description:
xiii, 139 p. :ill., digital ;24 cm.
Contained By:
Springer eBooks
Subject:
Photosensitizing compounds.
Online resource:
https://doi.org/10.1007/978-3-658-26188-7
ISBN:
9783658261887$q(electronic bk.)
Photophysics and photochemistry of a BODIPY-based photosensitizerquantumchemical simulations /
Ziems, Karl Michael.
Photophysics and photochemistry of a BODIPY-based photosensitizer
quantumchemical simulations /[electronic resource] :by Karl Michael Ziems. - Wiesbaden :Springer Fachmedien Wiesbaden :2019. - xiii, 139 p. :ill., digital ;24 cm. - BestMasters,2625-3577. - BestMasters..
Theoretical Background of Quantum Chemistry -- Computational Details -- Results for Heavy Atom Mechanism -- Results for Chemical Reduction Mechanism.
Karl Michael Ziems investigates a meso-mesityl-2,6-Iodine substituted Boron Dipyrromethene (BODIPY) dye regarding its functionality as photosensitizer in a two-component light-driven hydrogen evolution. The author uses quantum chemical calculations performed at the time-dependent density functional (TDDFT) and multi-state restricted active space perturbation theory through second-order (MS-RASPT2) level of theory. The light-induced processes associated with the formation of the active photosensitizer, i.e., by means of charge separation, as well as the population of undesired degradative pathways are elucidated. Hereby, the two proposed and investigated mechanisms are based on a heavy atom effect of iodine in the (excited) singlet/triplet manifold and preliminary reduction (of the dye) by a sacrificial electron donor and subsequent photoexcitation. Contents Theoretical Background of Quantum Chemistry Computational Details Results for Heavy Atom Mechanism Results for Chemical Reduction Mechanism Target Groups Academics, researchers, and students in the fields of chemistry, especially computational chemistry, and physics The Author Karl Michael Ziems obtained his Master of Science in chemistry at the Friedrich Schiller University Jena, and conducted his Master's thesis in the field of quantum chemistry. Currently, he studies theoretical and computational chemistry at the University of Oxford.
ISBN: 9783658261887$q(electronic bk.)
Standard No.: 10.1007/978-3-658-26188-7doiSubjects--Topical Terms:
559609
Photosensitizing compounds.
LC Class. No.: QD708.2 / .Z546 2019
Dewey Class. No.: 541.35
Photophysics and photochemistry of a BODIPY-based photosensitizerquantumchemical simulations /
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Theoretical Background of Quantum Chemistry -- Computational Details -- Results for Heavy Atom Mechanism -- Results for Chemical Reduction Mechanism.
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Karl Michael Ziems investigates a meso-mesityl-2,6-Iodine substituted Boron Dipyrromethene (BODIPY) dye regarding its functionality as photosensitizer in a two-component light-driven hydrogen evolution. The author uses quantum chemical calculations performed at the time-dependent density functional (TDDFT) and multi-state restricted active space perturbation theory through second-order (MS-RASPT2) level of theory. The light-induced processes associated with the formation of the active photosensitizer, i.e., by means of charge separation, as well as the population of undesired degradative pathways are elucidated. Hereby, the two proposed and investigated mechanisms are based on a heavy atom effect of iodine in the (excited) singlet/triplet manifold and preliminary reduction (of the dye) by a sacrificial electron donor and subsequent photoexcitation. Contents Theoretical Background of Quantum Chemistry Computational Details Results for Heavy Atom Mechanism Results for Chemical Reduction Mechanism Target Groups Academics, researchers, and students in the fields of chemistry, especially computational chemistry, and physics The Author Karl Michael Ziems obtained his Master of Science in chemistry at the Friedrich Schiller University Jena, and conducted his Master's thesis in the field of quantum chemistry. Currently, he studies theoretical and computational chemistry at the University of Oxford.
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based on 0 review(s)
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EB QD708.2 .Z668 2019 2019
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https://doi.org/10.1007/978-3-658-26188-7
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