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Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Recommanded Product: fac-Tris(2-phenylpyridine)iridium, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 94928-86-6

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A new photoredox-catalyzed chlorotrifluoromethylation reaction of internal arylalkynes under mild conditions using visible light has been developed. The reactions proceed with high levels of regio- and stereoselectivity and utilize commercially available CF3SO2Cl as both the CF3 and Cl source. In the mechanistic pathway for this process, generation of the CF3 radical and chloride ion occurs by Ir(ppy)3-photocatalyzed reductive decomposition of CF3SO2Cl. The synthetically important trifluoromethyl-substituted vinyl chlorides produced in this process can be readily transformed to 1,1-bis-arylalkenes by using Suzuki coupling.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Recommanded Product: fac-Tris(2-phenylpyridine)iridium, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 94928-86-6

Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI