TY - JOUR
T1 - Development of tethered dual catalysts
T2 - synergy between photo- and transition metal catalysts for enhanced catalysis
AU - Wang, Danfeng
AU - Malmberg, Robert
AU - Pernik, Indrek
AU - Prasad, Shyamal K. K.
AU - Roemer, Max
AU - Venkatesan, Koushik
AU - Schmidt, Timothy W.
AU - Keaveney, Sinead T.
AU - Messerle, Barbara A.
N1 - Copyright the Publisher 2020. Version archived for private and non-commercial use with the permission of the author/s and according to publisher conditions. For further rights please contact the publisher.
PY - 2020/6/28
Y1 - 2020/6/28
N2 - While dual photocatalysis–transition metal catalysis strategies are extensively reported, the majority of systems feature two separate catalysts, limiting the potential for synergistic interactions between the catalytic centres. In this work we synthesised a series of tethered dual catalysts allowing us to investigate this underexplored area of dual catalysis. In particular, Ir(I) or Ir(III) complexes were tethered to a BODIPY photocatalyst through different tethering modes. Extensive characterisation, including transient absorption spectroscopy, cyclic voltammetry and X-ray absorption spectroscopy, suggest that there are synergistic interactions between the catalysts. The tethered dual catalysts were more effective at promoting photocatalytic oxidation and Ir-catalysed dihydroalkoxylation, relative to the un-tethered species, highlighting that increases in both photocatalysis and Ir catalysis can be achieved. The potential of these catalysts was further demonstrated through novel sequential reactivity, and through switchable reactivity that is controlled by external stimuli (heat or light).
AB - While dual photocatalysis–transition metal catalysis strategies are extensively reported, the majority of systems feature two separate catalysts, limiting the potential for synergistic interactions between the catalytic centres. In this work we synthesised a series of tethered dual catalysts allowing us to investigate this underexplored area of dual catalysis. In particular, Ir(I) or Ir(III) complexes were tethered to a BODIPY photocatalyst through different tethering modes. Extensive characterisation, including transient absorption spectroscopy, cyclic voltammetry and X-ray absorption spectroscopy, suggest that there are synergistic interactions between the catalysts. The tethered dual catalysts were more effective at promoting photocatalytic oxidation and Ir-catalysed dihydroalkoxylation, relative to the un-tethered species, highlighting that increases in both photocatalysis and Ir catalysis can be achieved. The potential of these catalysts was further demonstrated through novel sequential reactivity, and through switchable reactivity that is controlled by external stimuli (heat or light).
UR - http://purl.org/au-research/grants/arc/CE170100026
UR - http://www.scopus.com/inward/record.url?scp=85089573270&partnerID=8YFLogxK
U2 - 10.1039/D0SC02703K
DO - 10.1039/D0SC02703K
M3 - Article
SN - 2041-6520
VL - 11
SP - 6256
EP - 6267
JO - Chemical Science
JF - Chemical Science
IS - 24
ER -