A catalytic system based on π-π stacking interactions between a pyrene substituted gold NHC catalyst and amphiphilic
Bengi Özgün Öztürk1, Hilal Acar1, Ayşegül Balcı1
1Hacettepe University, Faculty of Science, Chemistry Department, 06800, Beytepe, Ankara, Turkey. bengi04@hacettepe.edu.tr.
Abstract:
Pyrene-substituted amphiphilic ATRP polymers (P1) were used to stabilize the pyrene-substituted gold(I) NHC complex (Au-1) within the hydrophobic compartment of micellar structures in a methanol/water mixture through non-covalent π-π stacking interactions. The stacking interactions between pyrene groups of the polymer and the catalyst were investigated by means of fluorescence spectroscopy by comparing excimer and monomer emission signals of the pyrene moiety. The supported catalyst (Au-1@P1) formed spherical micellar structures in a water/methanol mixture with an average size of 55.6 (±13.1) nm as confirmed from TEM analysis. The performance of the catalytic system was tested on alkyne hydration reactions of alkynes. When compared to the unsupported analog, the supported catalyst showed an improved performance as a result of stabilization through π-stacking interactions within the hydrophobic compartment in the micellar structure.
Related Concept Videos
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Acid-Catalyzed Hydration of Alkenes


