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This thesis investigates the transitions from one electronically excited state to another. Such processes - the fastest of events in chemistry - can be studied with femtosecond resolution, and Thomas S. Kuhlman approaches the question both with experimental and theoretical methods. His approach contributes to explain processes of high importance to all scientific fields concerned with the interaction between light and matter: the deactivation of the electronically excited states after excitation. Thomas S. Kuhlman concludes in this thesis that the electronic transition proceeds before the entire set of available degrees of freedom are active - 'It is as simple as that' !
Chemistry --- Physical Sciences & Mathematics --- Physical & Theoretical Chemistry --- Internal conversion (Nuclear physics) --- Ergodic theory. --- Ergodic transformations --- Chemistry. --- Mass spectrometry. --- Spectroscopy. --- Physical chemistry. --- Chemistry, Physical and theoretical. --- Atomic structure. --- Molecular structure. --- Spectra. --- Physical Chemistry. --- Atomic/Molecular Structure and Spectra. --- Theoretical and Computational Chemistry. --- Mass Spectrometry. --- Spectroscopy/Spectrometry. --- Continuous groups --- Mathematical physics --- Measure theory --- Transformations (Mathematics) --- Decay schemes (Radioactivity) --- Electromagnetic theory --- Electrons --- Nuclear physics --- Quantum theory --- Chemistry, Physical organic. --- Analysis, Spectrum --- Spectra --- Spectrochemical analysis --- Spectrochemistry --- Spectroscopy --- Chemistry, Analytic --- Interferometry --- Optics --- Radiation --- Wave-motion, Theory of --- Absorption spectra --- Light --- Spectroscope --- Mass spectra --- Mass spectrograph --- Mass spectroscopy --- Mass spectrum analysis --- Mass (Physics) --- Nuclear spectroscopy --- Spectrum analysis --- Physical sciences --- Chemistry, Physical organic --- Chemistry, Organic --- Chemistry, Physical and theoretical --- Qualitative --- Spectrometry --- Atomic structure . --- Molecular structure . --- Chemistry, Theoretical --- Physical chemistry --- Theoretical chemistry --- Structure, Molecular --- Chemical structure --- Structural bioinformatics --- Structure, Atomic --- Atomic theory --- Analytical chemistry
Choose an application
This thesis investigates the transitions from one electronically excited state to another. Such processes - the fastest of events in chemistry - can be studied with femtosecond resolution, and Thomas S. Kuhlman approaches the question both with experimental and theoretical methods. His approach contributes to explain processes of high importance to all scientific fields concerned with the interaction between light and matter: the deactivation of the electronically excited states after excitation. Thomas S. Kuhlman concludes in this thesis that the electronic transition proceeds before the entire set of available degrees of freedom are active - 'It is as simple as that' !
Optics. Quantum optics --- Physicochemistry --- Chemical structure --- Theoretical spectroscopy. Spectroscopic techniques --- Spectrometric and optical chemical analysis --- Organic reaction mechanisms and kinetics --- Chemistry --- Computer. Automation --- massaspectrometrie --- spectra (chemie) --- moleculaire structuur --- thermodynamica --- chemie --- informatica --- spectroscopie --- kogellagers --- fysicochemie --- spectrometrie
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