Photo Click Reaction of Acylsilanes with Indoles.

Light-mediated coupling of acylsilanes with indoles is reported. This photo click reaction occurs under mild conditions (415 nm) mostly in quantitative yield and provides stable silylated N,O-acetals via light mediated siloxycarbene generation with subsequent indole-N-H insertion. We show that this very efficient and fully atom economic coupling process can be applied to conjugate complex systems, as documented by the clicking of carbohydrates with indole alkaloids.

Controlled Cellular Delivery of Amphiphilic Cargo by Redox-Responsive Nanocontainers.

The specific transport of amphiphilic compounds such as fluorescently labeled phospholipids into cells is a prerequisite for the analysis of highly dynamic cellular processes involving these molecules, e.g., the intracellular distribution and metabolism of phospholipids.

Photochemical preparation of gold nanoparticle decorated cyclodextrin vesicles with tailored plasmonic properties.

We report a photochemical strategy for the preparation of plasmonic vesicles by the in situ formation of gold nanoparticles at the surface of cyclodextrin host vesicle templates decorated with photoactive guest polymers. Upon irradiation with UV light, these carefully designed polymer shells undergo a Norrish type I reaction to generate reducing radicals for the in situ reduction of gold salts and simultaneously provide a stabilizing matrix allowing for a dense decoration with discrete gold seeds. In a highly controlled growth procedure the gold particle size can be adjusted between 3 and 28 nm resulting in an increasing interparticle plasmonic coupling as revealed by a pronounced redshift of the surface plasmon resonance (SPR) band and an enhanced absorption at wavelengths above 600 nm.

Tuning the Selectivity of AuPd Nanoalloys towards Selective Dehydrogenative Alkyne Silylation.

The cross-dehydrogenative coupling of terminal alkynes and hydrosilanes catalyzed by AuPd nanoalloys is described. Metal nanoparticles are readily prepared in 15 minutes from commercially available and cheap starting materials by using a photochemical approach. The ratio of Au and Pd in the alloys heavily influences their reactivity.

Free-Radical Carbocyanation of Olefins.

The free-radical three-component carbocyanation of electron-rich olefins was investigated with p-tosyl cyanide as cyanide source. The scope and limitations of the process were established by varying the nature of the alkene and radical precursor. Carbocyanation of chiral allylsilanes was shown to occur with high diastereocontrol, leading to syn β-silyl nitriles.