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Dissertation

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|3.4 Outlook, Exploratory Investigations and Perspectives|<br />

As described for Ru(bbip),a transformation of the imidazolium salt into the corresponding<br />

carbene derivatives of different metal centers is very important. For the subsequent use as starting<br />

material in the transmetallation reactions, formation of the NHC-silver complex of Ru 2 (edip)<br />

became interesting at this stage. In this context method C2 was applied, using Ag 2 O as base<br />

for the transformation of the imidazolium salt into the corresponding metal-NHC complex (see<br />

figure 123) as discribed for Ru(bbip).<br />

N<br />

N<br />

N<br />

N<br />

Ru 2+<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

Ru 2+<br />

N<br />

N<br />

N<br />

Ru 2 (edip)<br />

Ag 2 O<br />

method C2<br />

N<br />

N<br />

N<br />

N<br />

Ru 2+<br />

N<br />

N<br />

N<br />

N<br />

Cl<br />

Ag<br />

Cl<br />

Ag<br />

N<br />

N<br />

N<br />

N<br />

N<br />

Ru 2+<br />

N<br />

N<br />

N<br />

Ru 2 (edip)Ag 2<br />

Figure 123: Preparation of the tetranuclear heterobimetallic silver NHC-complex of Ru 2 (edip).<br />

To increase the driving force the chloride salt of Ru 2 (edip) was prepared. Counter ion exchange<br />

of the [PF 6 ]-salt of Ru 2 (edip) with (Bu) 4 NCl in acetone/ethyl acetate gave the corresponding<br />

chloride salt in quantitative yield. The complexation reaction was carried out in dichloromethane.<br />

After stirring Ru 2 (edip) and Ag 2 O in the presence of molecular sieves in dichloromethane for 16<br />

hours, the solids were filtered off and the volatiles were removed from the remaining solution.<br />

Analysis of the remaining solid gave clear evidence for a complete conversion into the<br />

pure product [{(tbbpy) 2 Ru} 2 (µ-edip){AgCl} 2 ]Cl 4 (Ru 2 (edip)Ag 2 ). The disappearance of the<br />

|172|

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