A versatile heterogeneous photocatalyst: nanoporous gold powder modified with a zinc(II) phthalocyanine derivative for singlet oxygen [4 + 2] cycloadditions
Autor: | Hans Hannes Doebler, Jorge Adrian Tapia Burgos, Arne Wittstock, David Steinebrunner, Günter Schnurpfeil, Dieter Wöhrle |
---|---|
Rok vydání: | 2021 |
Předmět: |
010405 organic chemistry
Nanoporous Singlet oxygen chemistry.chemical_element Zinc 010402 general chemistry Photochemistry 01 natural sciences 0104 chemical sciences Catalysis Solvent chemistry.chemical_compound Reaction rate constant chemistry Phthalocyanine Photocatalysis Physical and Theoretical Chemistry |
Zdroj: | Photochemical & Photobiological Sciences. 20:547-558 |
ISSN: | 1474-9092 1474-905X |
DOI: | 10.1007/s43630-021-00037-7 |
Popis: | Nanoporous gold was functionalized with a photosensitizer, a zinc(II) phthalocyanine derivative. Such systems are active for the generation of reactive singlet oxygen which can be used for photocatalytic oxidation reactions. This study aims to demonstrate the versatility of such an approach, in terms of substrates and the employed solvent, only possible for a truly heterogeneous catalytic system. The activity of the hybrid system was studied for [4 + 2] cycloadditions of three different types of dienes and a total of eight substrates in two organic solvents and once in water. The highest activity was measured for 1,3-diphenylisobenzofuran, which is also highest in terms of sensitivity for the reaction with 1O2. Trends in conversion could be anticipated based on reported values for the rate constant for the reaction of 1O2. In almost all cases, an amplification of the conversion by immobilization of the sensitizer onto nanoporous gold was observed. The limiting case was ergosterol, which was the largest of all substrates with a van-der-Waals radius of about 2.1 nm. Additional factors such as the limited lifetime of 1O2 in different solvents as well as the hampered diffusion of the substrates were identified. Graphic abstract |
Databáze: | OpenAIRE |
Externí odkaz: |