Distinct Photophysics of the Isomers of B18H22 Explained

0377475 - ÚACH 2013 RIV US eng J - Článek v odborném periodiku
Londesborough, Michael Geoffrey Stephen - Hnyk, Drahomír - Bould, Jonathan - Serrano-Andrés, L. - Sauri, V. - Oliva, J. M. - Kubát, Pavel - Polívka, T. - Lang, Kamil
Distinct Photophysics of the Isomers of B18H22 Explained.
Inorganic Chemistry. Roč. 51, č. 3 (2012), s. 1471-1479. ISSN 0020-1669. E-ISSN 1520-510X
Grant CEP: GA ČR(CZ) GAP207/11/1577; GA ČR GAP208/10/1678
Výzkumný záměr: CEZ:AV0Z40320502; CEZ:AV0Z40400503
Klíčová slova: photodynamic therapy * molecular structure * absorption * oxygen
Kód oboru RIV: CA - Anorganická chemie; CF - Fyzikální chemie a teoretická chemie (UFCH-W)
Impakt faktor: 4.593, rok: 2012

The photophysics of the two isomers of octadecaborane(22), anti- and syn-B18H22, have been studied by UV-vis spectroscopic techniques and theoretical computational methods. In air-saturated hexane, anti-B18H22 shows fluorescence with a high quantum yield, Phi(F) = 0.97, and singlet oxygen O-2((1)Delta(g)) production (Phi(Delta) similar to 0.008). Conversely, isomer syn-B18H22 shows no measurable fluorescence, instead displaying much faster, picosecond non-adiative decay of excited singlet states. Computed potential energy hypersurfaces (PEHs) for both isomers rationalize these data, pointing to a deep S-1 minimum for anti-B18H22 and a conical intersection (CI) between its S-0 and S-1 states that lies 0.51 eV higher in energy. Such an energy barrier to nonradiative relaxation is not present in the PEH of syn-B18H22, and the system therefore has sufficient initial energy on excitation to reach the (S-0/S-1) CI and to then decay to the ground state without fluorescence. The computational analysis of the geometries at stationary points along the PEH of both isomers shows that the determining factor for the dissimilar photophysics of anti- and syn-B18H22 may be due to the significant differences in the geometrical rearrangements at their respective conical intersections. Thus, the syn isomer shows one very large, B B elongation of 1.2 angstrom from 1.8 angstrom in the ground state to 3.0 angstrom at the CI, whereas the anti isomer shows smaller elongations (below 1 angstrom) in several B-B connectivities at its (S-0/S-1)(CI). The absorbed energy in SI for the anti-B18H22 is therefore redistributed vibrationally into several regions of the molecule rather than almost completely into a single vibrational mode as in the case for the syn isomer. The consequent prolonged S-1 lifetime for the anti isomer allows for relaxation via fluorescence.
Trvalý link: http://hdl.handle.net/11104/0007009