Physics – Condensed Matter – Materials Science
Scientific paper
2008-03-13
Physics
Condensed Matter
Materials Science
Scientific paper
We have performed a structural analysis of the Ni K-edge XANES spectrum of a square planar coordination complex, Ni-tetramesitylporphyrin, Ni(II)TMP, in dilute toluene solution. The fit of the spectrum was carried out in the frame of the full multiple scattering (FMS) approach, via the MXAN program, starting from a muffin-tin (MT) form of the molecular potential. We have applied the MXAN analysis to the time-resolved XANES difference spectrum obtained between a 100 ps life-time photoexcited state of Ni(II)TMP (a relaxed triplet state, T1, obtained by exciting the Soret band) and the ground state, S0. From our direct simulation of the laser on/laser off difference spectrum, we obtain the fraction of T1 population (0.41-0.63) A in agreement with optical transient absorption determination, and a 0.05-0.1 A elongation of the d(Ni-N) and d(Ni-C) distances. The overall uncertainty on these results mostly depends on uncertainty on the chemical shift between the T1 and S0 state, that is assumed a priori in the differential analysis. Still our results are in good agreement with previous EXAFS data (obtained on a reconstructed absolute spectrum of the T1 state). Our best fit corresponds to no chemical shift, 54% fraction of T1 state, and either a (0.04 +/- 0.01) elongation of the average d(Ni-N) or a (0.06 +/- 0.01) elongation of the average d(Ni-pyrrol) when pyrrol rings are treated as perfectly rigid bodies. This work demonstrates that XANES spectroscopy can be used to provide structural information on square-planar transition metal compounds by analysing the metal K-edge via MS method under the MT approximation, and that XANES differential analysis can be successfully applied to study electronic/structural relationships in transient photoexcited species from time-resolved experiments.
Benfatto Maurizio
Chen Liang-Xu
Frank Peter
Hatada Keisuke
Hayakawa Kazunobu
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