[HepatoChem] Photoredox Cross-Coupling Kit: Ir/Ni Base and Ir Catalyst Screen Kit 1
(HCK1009-01-005)
2 sets of reaction conditions with 6 iridium catalysts Ir(dF-CF3–ppy)2(dtbbpy)PF6, Ir(dtbbpy)(ppy)2PF6, Ir(dF-CF3–ppy)2(bpy)PF6 Ir(dF-ppy)3, Ir(dmppy)2(dtbbpy)PF6, Ir(dF-CH3–ppy)2(dtbbpy)PF6, Ni dtbbpy , and 3 bases Cs2CO3, CsF and DBU. 36 reaction vials total.
This kit requires EvoluChem™ PhotoRedOx Box – HCK1006-01-016 and EvoluChem™ Light Source 18W-450 nm – HCK1012-01-002 as well as Syringe, decapper and reaction block included in the EvoluChem™ Starter Kit (HCK1006-01-001)
The typical protocol is performed at 0.05 mol/l using a solution containing two coupling components. Each sealed reaction vial contains 0.1 µmol of photocatalyst, 0.5 µmol Ni catalyst, 0.5 µmol ligand and 15 of µmol base (for all bases except for DBU conditions, base is added separately and shipped in a separate vial). The Ir/Ni photoredox kit contains 2 sets of vials allowing the screening of two different solvents. Sparging reaction solvents with nitrogen or argon while transferring reagents is important to achieve highest conversions of product. See protocol diagram for instructions. Recommended solvents include: MeCN, DMF, DME, dioxane and DMSO. The vial holder shipped with the kit can be placed directly on the photochemistry device.
Protocol at 100 µl volume reaction condition
- Prepare the required volume of substrate solution at 0.05 mol/L containing both coupling substrates. For example, 2.0 ml solution for 18 reaction conditions (200 µl extra to compensate potential evaporation).
- Degas substrate solution with subsurface sparging via N2 or Ar line with exit needle for 5 minutes.
- Using a clean and dry syringe, add 100 µl of the substrate solution to each reaction vial containing Cs2CO3 and CsF (excluding DBU vials for now).***
- Add remaining 800 µl of substrate solution to vial containing DBU. Stir and degas for 5 minutes.
- Transfer 100 µl substrate/DBU solution to each DBU reaction vial.
- Stir the reaction vials in the photochemical device for 18 to 24 hours.
- Remove the vial caps using a decapper.
- Prepare analytical sample for each reaction condition with 5 µl sample diluted into 200 µl in either DMSO or water/acetonitrile 50/50.
- Alternatively, reaction solvent can be evaporated in vacuo and crude mixture diluted in water/acetonitrile prior to preparation of analytical sample.
- Analyze resulting analytical samples by LC/MS.
***Alternatively, 2.24 µl of DBU can be added to each of the 6 DBU reactions separately using 10 ul ul Hamilton Syringe (not provided) instead of premixing substrate solutions and DBU base. In this case, first add 100 µl substrate solution to DBU reaction vials, followed by addition of 2.24 µl DBU and proceed to step 6.
