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Dissertation

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|3.2 Bisphenanthroline: A Suitable Molecular Bridge?|<br />

process can only be observed in the oxygen free samples which gives rise to the speculation, that<br />

possible slow radical reaction or irreversible bridging ligand transformation might occur.<br />

0.05<br />

0.04<br />

0.02<br />

0.00<br />

O.D.<br />

O.D.<br />

0.00<br />

-0.05<br />

-0.02<br />

-0.10<br />

363-382 nm<br />

432-485 nm<br />

569-696 nm<br />

-0.04<br />

0-0.3 µs<br />

0.5-0.9 µs<br />

0.0 0.2 0.4 0.6 0.8 1.0<br />

t / µs<br />

400 500 600 700<br />

/ nm<br />

0.01<br />

0.01<br />

0.00<br />

0.00<br />

O.D.<br />

-0.01<br />

.O.D.<br />

-0.01<br />

-0.02<br />

-0.03<br />

363-382 nm<br />

435-466 nm<br />

518-531 nm<br />

575-596 nm<br />

-0.02<br />

-0.03<br />

0-3 µs<br />

18-80 µs<br />

0 20 40 60 80<br />

t / µs<br />

400 500 600 700<br />

/ nm<br />

Figure 73: Derived time resolved (left) and wavelength resolved (right) excited state absorption<br />

spectra of Ru(phenphen)Ru in oxygen saturated (top) and degassed (bottom) acetonitrile, λ exc =<br />

355 nm (∼3 mJ/pulse); mean over 100 shots (compare figure 72). The denoted brackets indicate<br />

the regions that were used for corresponding decay kinetics and differential spectra.<br />

|103|

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