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Molecular Conformation and Organic Photochemistry

by Brogaard, Rasmus Y.
Authors: SpringerLink (Online service) Series: Springer Theses, Recognizing Outstanding Ph.D. Research, 2190-5053 Physical details: XVI, 122 p. 50 illus., 19 illus. in color. online resource. ISBN: 3642293816 Subject(s): Chemistry. | Spectroscopy. | Chemistry, Physical organic. | Chemistry. | Spectroscopy/Spectrometry. | Atomic/Molecular Structure and Spectra. | Physical Chemistry.
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E-Book E-Book AUM Main Library 543.2-543.8 (Browse Shelf) Not for loan

Aspects and investigation of photochemical dynamics -- A time-resolved probing method: photoionization -- Simulation of time-resolved photoionization signals -- Simulation: the Norrish type-I reaction in acetone -- Experimental setups -- Paracyclophanes I: [2+2]cycloaddition of ethylenes -- Paracyclophanes II: The Paternò-Büchi reaction -- Probing structural dynamics by interaction between chromophores.

Rasmus Brogaard's thesis digs into the fundamental issue of how the shape of a molecules relates to its photochemical reactivity. This relation is drastically different from that of ground-state chemistry, since lifetimes of excited states are often comparable to or even shorter than the time scales of conformational changes. Combining theoretical and experimental efforts in femto-second time-resolved photoionization Rasmus Brogaard finds that a requirement for an efficient photochemical reaction is the prearrangement of the constituents in a reactive conformation. Furthermore, he is able to show that by exploiting a strong ionic interaction between two chromophores, a coherent molecular motion can be induced and probed in real-time. This way of using bichromophoric interactions provides a promising strategy for future research on conformational dynamics.

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