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   <subfield code="a">Time-Resolved Continuous-Wave and Pulse EPR Investigation of Photoinduced States of Zinc Porphyrin Linked with an Ethylenediamine Copper Complex</subfield>
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   <subfield code="c">[A. Sukhanov, K. Konov, K. Salikhov, V. Voronkova, E. Mikhalitsyna, V. Tyurin]</subfield>
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   <subfield code="a">Electron spin dynamics of the photoexcited state of a new porphyrin system built of a zinc porphyrin molecule with a linked complex of copper ion (ZnPCu) was studied using electron paramagnetic resonance (EPR) methods. The time-resolved continuous-wave and echo-detected EPR data show that electron spins of the ZnPCu system are polarized. The shape of the EPR spectrum and the echo-detected nutation spectroscopy data indicate that there is a relatively small spin-spin interaction between two subunits, namely, less than the zero-field splitting parameter of the excited triplet ZnP molecule. Results have been interpreted assuming that the S=1 Zn porphyrin subunit electron spins are polarized via the triplet mechanism and this polarization is transferred to the S=1/2 copper subunit via a flip-flop process induced by the exchange interaction between these subunits. The formation of the integral spin polarization in the triplet-doublet system as a function of the value and type of the triplet-doublet interaction was analyzed.</subfield>
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