Piotr Fita
Affiliations: | University of Warsaw, Poland |
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| Listkowski A, Kharchenko A, Ciąćka P, et al. (2021) Fluorinated Porphycenes: Synthesis, Spectroscopy, Photophysics, and Tautomerism. Chempluschem. 85: 2197-2206 |
| Kasprzycki P, Kopycki P, Listkowski A, et al. (2020) Influence of local microenvironment on the double hydrogen transfer in porphycene. Physical Chemistry Chemical Physics : Pccp |
| Ciąćka P, Fita P, Listkowski A, et al. (2016) Evidence for Dominant Role of Tunneling in Condensed Phases and at High Temperatures: Double Hydrogen Transfer in Porphycenes. The Journal of Physical Chemistry Letters. 7: 283-8 |
| Ci??ka P, Fita P, Listkowski A, et al. (2015) Tautomerism in porphycenes: analysis of rate-affecting factors. The Journal of Physical Chemistry. B. 119: 2292-301 |
| Fedoseeva M, Fita P, Vauthey E. (2013) Excited-state dynamics of charged dyes at alkane/water interfaces in the presence of salts and ionic surfactants. Langmuir : the Acs Journal of Surfaces and Colloids. 29: 14865-72 |
| Beierlein FR, Krause AM, Jäger CM, et al. (2013) Molecular dynamics simulations of liquid phase interfaces: understanding the structure of the glycerol/water-dodecane system. Langmuir : the Acs Journal of Surfaces and Colloids. 29: 11898-907 |
| Fita P, Pszona M, Orzanowska G, et al. (2012) Tautomerization in 2,7,12,17-tetraphenylporphycene and 9-amino-2,7,12,17-tetraphenylporphycene: influence of asymmetry on the direction of the transition moment. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 13160-7 |
| Fita P, Fedoseeva M, Vauthey E. (2011) Hydrogen-bond-assisted excited-state deactivation at liquid/water interfaces. Langmuir : the Acs Journal of Surfaces and Colloids. 27: 4645-52 |
| Fita P, Fedoseeva M, Vauthey E. (2011) Ultrafast excited-state dynamics of eosin B: a potential probe of the hydrogen-bonding properties of the environment. The Journal of Physical Chemistry. A. 115: 2465-70 |
| Fita P, Garbacz P, Nejbauer M, et al. (2011) Ground and excited state double hydrogen transfer in symmetric and asymmetric potentials: comparison of 2,7,12,17-tetra-n-propylporphycene with 9-acetoxy-2,7,12,17-tetra-n-propylporphycene. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 3672-8 |