PICOSECOND SPECTROSCOPY OF SOME METALLOPORPHYRINS
Academic Article
Overview
Identity
Additional Document Info
Other
View All
Overview
abstract
The energy relaxation process of metal-free protoporphyrin IX dimethyl ester and its compounds with Cu(II), Ag(II), Ni(II), Pd(II), Pt(II), Zn(II), Fe(III) and the heme proteins myoglobin, hemoglobin and cytochrome c were studied by dual-beam picosecond spectroscopy. Excitation at 530 nm, which is in the visible absorption band for these compounds, revealed that both the metal-free porphyrin and the Zn(II) porphyrin have lifetimes for S1 which are longer than 1 ns, in keeping with their known fluorescence properties. From the time-resolved spectra after excitation, absorption due to S1, T1 and S0 could be identified. In addition, a low-lying singlet d-d level was seen for the Ni(II) porphyrin. While the Pt(II) and Pd(II) compounds have intersystem crossing times of less than 8 ps and 20 ps respectively, the Ni(II) compound relaxes from S1 to Sd in about 10 ps and from Sd to S0 in 260 ps. The paramagnetic Cu(II) and Ag(II) species have intersystem crossing from 2S1 to 2T1 in less than 8 ps followed by an equilibrium of the 2T1 and 4T1 states, requiring about 450 ps for the Cu(II) compound and about 12 ps for the Ag(II) compound. An anomalous lengthening of the decay time with increasing excitation intensity was observed for the copper but not for the silver porphyrin. The Fe(III) porphyrins relax with rates faster than 6 ps, which was the resolving time of this experiment. No differences between heme proteins and Fe(III) protoporphyrins in solution were observable within this time resolution. 1981.
