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Microemulsions are thermodynamically stable, macroscopically isotropic, nanostructured

mixtures of at least three components: a polar, a non-polar and an amphiphilic; in general

water, oil and surfactant. The surfactant, if optimally selected, generates an ultra-low

interfacial tension and a large internal interface. Both properties are of central relevance in

this thesis. In the first part, the new fluorescent surfactant class NaC

X,Y

ANS was synthesized,

comprehensively characterized and first application-relevant studies in the field of cell

labeling were carried out. The efficiency – namely the reduction of the interfacial tension – of

this new surfactant class was demonstrated at the phase behaviour of non-ionic

microemulsions in comparison with common ionic surfactants. As companion product, the

highly efficient surfactant class NaC

X,Y

ABS was developed, which shows great potential for

the independent formation of microemulsions without further co-surfactant. Since

microemulsions can completely solubilize hydrophilic and lipophilic components, these

systems are outstandingly suitable as reaction medium in organic synthesis across the internal

interface. This was closer investigated in decomposition experiments of glucose by an

N-heterocyclic carbene (NHC). Moreover, extensive complexation reactions of aldehyde

adducts of NHCs (Breslow intermediates) with transition metal compounds provided initial

insights into their coordination behaviour. In particular, the high reactivity of cobalt towards

Breslow intermediates has been highlighted.

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