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Photochemistry and Photophysics of Coordination Compounds

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52 N.A.P. Kane-Maguire<br />

Fig. 13 Qualitative potential energy level diagram for Oh Cr(III) complexes showing possible<br />

radiationless 2 Eg relaxation processes, including a direct deactivation to the ground<br />

state, b back-intersystem crossing (BISC), c direct doublet reaction, or d surface crossing<br />

to a ground state intermediate surface (GSI)<br />

be minimal). The proposed mechanism for this photodeuteration is shown in<br />

Fig. 14.<br />

Fig. 14 Possible mechanism for photoinitiated macrocyclic N – H deuteration in acidic<br />

aqueous solution<br />

A related paper on the corresponding difluorosystems has recently been<br />

published [75].<br />

6<br />

Energy Transfer Studies<br />

Cr(III) complexes were employed as acceptor species in room temperature<br />

energy transfer experiments between transition metal complexes as early as<br />

1972 [21, 76], <strong>and</strong> several years later the first cases appeared where the donor<br />

<strong>and</strong> acceptor were both Cr(III) compounds [77, 78]. In the survey since 1999,<br />

eight articles were identified where energy transfer studies involving Cr(III)<br />

species were the primary research activity [79–86]. The paper chosen for<br />

discussion in Sect. 6.1 describes the first report <strong>of</strong> electronic energy selfexchange<br />

between Cr(III) complexes [81].

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