Izvorni znanstveni članak

Ultrafast Excited-state Proton Transfer Processes: Energy Surfaces and On-the-fly Dynamics Simulations

Adélia J. A. Aquino ; Institute for Theoretical Chemistry, University of Vienna, Waehringerstrasse 17, A-1090 Vienna, Austria
Felix Plasser ; Institute for Theoretical Chemistry, University of Vienna, Waehringerstrasse 17, A-1090 Vienna, Austria
Mario Barbatti ; Institute for Theoretical Chemistry, University of Vienna, Waehringerstrasse 17, A-1090 Vienna, Austria
Hans Lischka ; Institute for Theoretical Chemistry, University of Vienna, Waehringerstrasse 17, A-1090 Vienna, Austria

Sažetak

The excited-state intramolecular proton transfer (ESIPT) is reviewed for several benchmark systems [o-hydroxybenzaldehyde (OHBA), salicylic acid and 2-(2′-hydroxyphenyl)-benzothiazole (HBT)] in order to verify the applicability of the time-dependent density functional theory (TDDFT) and the resolution-of-the-identity approximate second-order coupled cluster (RI-CC2) methods. It was found that these approaches are very well suited for the description of ESIPT processes. A comparative investigation of previous and new excited-state dynamics simulations is performed for HBT, 10-hydroxybenzo[h]quinoline (HBQ), and [2,2′-bipyridyl]-3,3′-diol (BP(OH)₂). The time scale for the ESIPT process in these systems ranges in the time interval of 30−40 fs for HBT and HBQ and amounts to about 10 fs for the first proton transfer step in BP(OH)₂. The dynamics simulations also show that the proton transfer in HBT is strongly supported by skeletal modes and the proton plays a rather passive role, whereas in HBQ a semipassive mechanism is found due to its increased rigidity in comparison to HBT. The special role of the double proton transfer in BP(OH)₂ is discussed as well.

Ključne riječi

density functional theory; on-the-fly dynamics; excited states; proton transfer mechanism

Hrčak ID:

38627

URI

https://hrcak.srce.hr/38627

Datum izdavanja:

30.6.2009.

Posjeta: 3.029 *