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reaction suitability
reaction type: Photocatalysis
reagent type: catalyst
Related Categories
General description
Features and Benefits of Penn PhD Photoreactor M2
- Modular design allows for use with a variety of wavelengths 365nm – 450nm
- 360 degree reflective environment maximizes surface area photon capture
- Light shield interlock prevents user exposure to harmful light rays
- Interactive touch screen controls reaction parameters
- Intertek ETL, CE, and CB approved
- User defined parameters including temperature, light intensity, fan speed and stirring
- Auto stop, pause and reset options
- Supports vial sizes gc, 4, 8, 20, 40 ml
- Temp feedback using a k-type thermocouple
Photocatalysis Technology Spotlight
related product
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (example: T1503).
Example:
Additional examples:
705578-5MG-PW
PL860-CGA/SHF-1EA
MMYOMAG-74K-13
1000309185
enter as 1.000309185)
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How to Find a Lot/Batch Number for COA
Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.
Aldrich Products
For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').
For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').
For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.
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In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.
Articles
Photoredox catalysis is a powerful synthetic methodology to form challenging covalent bonds using light irradiation. It is effective for light-driven polymer and small molecule synthesis.
Csp2- and Csp-hybridized coupling reactions are established catalytic approaches. However, multi-step Csp3- and Csp2-coupling reactions of boronic acids and related derivatives are still limited by ineffective two-electron transmetalation reactions.
While Markovnikov alkene reactivity is very well developed and utilized commonly in the synthesis of commodity and research chemicals, catalytic access to the anti-Markovnikov-selective adducts is a much less-developed endeavor.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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