Visible light photoredox catalysis has emerged as a powerful tool in organic synthesis, building upon the foundation set by early pioneers in the areas of radical chemistry and photochemistry. Photoredox chemistry allows one to forge new bonds via open shell pathways and facilitates the rapid assembly of complex products en route to new areas of chemical space. Many transition-metal complexes and organocatalysts capable of initiating radical formation in the presence of visible light have been shown to facilitate a wide array of synthetic transformations including but not limited to cross-coupling, C-H functionalization, alkene and arene functionalization, and trifluoromethylation. A key aspect to visible light photoredox catalysis is the choice of light source.
Find the Photoreactor for your Experiment |
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A long-standing challenge in the field of photoredox catalysis is reproducibility between reaction setups as well as across individual reactions performed with the same setup. Our SynLED Parallel Photoreactor (Z742680) seeks to alleviate these issues by enabling small-scale photocatalysis reaction screening as well as rapid library generation while ensuring high levels of consistency across reactions and between runs. The photoreactor allows for 16 simultaneous reactions in 2 dram or smaller scintillation or microwave vials. Each well contains a 1W LED centered at 467.5 nm with a 45 degree lens. A built-in cooling fan and heat sink help maintain reaction temperatures at approximately 30 °C. The setup was designed to fit on a conventional stir plate, including a round cutout to fit firmly on IKA brand stir plates.
Figure 1.SynLED Parallel Photoreactor
SynLed Parallel Photoreactor Features and Specs:
SynLED Parallel Photoreactor in the Literature
The Penn PhD Photoreactor M2 (Z744035) is a benchtop instrument designed to facilitate consistency and reproducibility in photoredox catalysis across a wide range of reaction scales. The Photoreactor M2 combines LED illumination, mechanical stirring and cooling into one device while accepting reaction vials from 1 mL up to 40 mL. The touch screen user interface allows the chemist to precisely control temperature, intensity, stir rate and time, creating a valuable tool for repeatability, traceability, efficiency and consistency of results. The Photoreactor M2 addresses the potential to streamline synthetic sequences and create valuable strategies for addressing some of the challenges of molecule construction in drug discovery.
Figure 2.Penn PhD Photoreactor M2
Penn PhD Photoreactor M2 Features and Specs:
Penn PhD Photoreactor Accessories
These additional light sources and vial holders can be used with the Penn PhD Photoreactor M2 for chemists and researchers to accelerate chemical reactions using photoredox catalysis.
Penn PhD Photoreactor M2 in the Literature
The LightOx PhotoReact 365 (Z744061) is a benchtop instrument that provides even, directed and reproducible UV illumination at 365nm suitable for photochemical and photobiological reactions. The touch screen interface allows the user to control light intensity, energy delivery rate, and time. LED health over time is monitored using an in-built UV sensor enabling the user to produce rapid, reproducible results. This instrument is suitable for high-throughput screening in multiwell plates, providing researchers with a tool to screen high numbers of compounds and reactions essential for drug discovery.
Figure 4.LightOX Photoreact 365
LightOx PhotoReact 365 Features and Specs:
Late-Stage Functionalization (LSF) of small, pharmaceutically active molecules can provide modified potency, toxicity and pharmacokinetic profiles with altogether less effort than the ground-up syntheses of analogs. Though LSF with fluorine (and fluorinated alkyl groups) is now readily achieved through use of, amongst other technologies, the zinc sulfinates developed by the Baran Group at Scripps, the incorporation of small, non-fluorous alkyl groups like methyl and ethyl groups has remained an unmet challenge. This is especially relevant as the incorporation of small alkyl groups is likely to yield molecules with more advantageous physiochemical and safety profiles vis à vis their fluorinated brethren.
Ultimately, the late-stage incorporation of methyl, ethyl and cyclopropyl groups to pharmaceutically active small molecules was achieved through a visible light photoredox strategy. Indeed, in the presence of blue light and peroxide alkyl radical precursors, newly available [Ir{dF(CF3)ppy}2(dtbpy)]PF6 catalyst (747793) mediates the formation of the required alkyl radicals (and thus, alkyl group incorporation) typically achieved by methods not amenable to LSF1.
Figure 3.Late-Stage Incorporation of Small Alkyl Groups into Small Molecules of Biological Interest
Lignin represents over 30% of non-fossil fuel based organic carbon, and as such this biomass could be made, with the advent of chemoselective degradation processes, into a primary source of carbon-based feedstock material. The Stephenson Group has recently combined two of our innovative products to achieve the selective degradation of lignin-type model compounds in one pot. Indeed, Bobbitt’s salt was used to selectively oxidize benzyl alcohols, followed by photocatalytic reductive C-O bond cleavage to the ketone and alcohol degradation products. This last transformation was achieved without degassing and in the presence of visible light2.
Figure 3.Strategy for Room Temperature Lignin Degradation
The crossed [2 + 2] cycloaddition of styrenes was achieved in high chemoselectivity through use of an appropriately tuned Ru-based visible light photocatalyst. As demonstrated by Prof. Tehshik Yoon, unsymmetrically substituted butanes can thus be prepared on gram scale with Ru(bpm)3.
Figure 4.Crossed Intermolecular [2+2] Cycloaddition of Styrenes
Our visible light photocatalysts have been used in applications that truly span organic chemistry (and beyond). Other reactivities that have been explored include:
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