{"id":25068,"date":"2022-08-06T15:39:48","date_gmt":"2022-08-06T19:39:48","guid":{"rendered":"https:\/\/hepatochem.com\/photoreactors-leds-accessories\/photoredox-box\/"},"modified":"2022-08-06T15:39:48","modified_gmt":"2022-08-06T19:39:48","slug":"photoredox-box","status":"publish","type":"page","link":"https:\/\/hepatochem.com\/euro\/photoreactors-leds-accessories\/photoredox-box\/","title":{"rendered":"PhotoRedOx Box&#x2122;"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;0|0px|0|0px|false|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_row _builder_version=&#8221;4.20.4&#8243; width=&#8221;100%&#8221; custom_padding=&#8221;0px|0px|0px|0px|false|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_text _builder_version=&#8221;4.27.2&#8243; text_font=&#8221;||||||||&#8221; text_line_height=&#8221;2em&#8221; header_font=&#8221;|700|||||||&#8221; header_4_line_height=&#8221;2em&#8221; custom_margin=&#8221;0px|15px|0px|15px|false|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h4 style=\"text-align: left;\"><strong>The EvoluChem PhotoRedOx Box&#x2122; is the photochemistry photoreactor choice for the chemist who seeks to standardize laboratory photochemical setups economically. A flexible design allows interchangeable LEDs from 365 nm to 808 nm and a wide variety of vials.<\/strong><\/h4>\n<p style=\"text-align: left;\">This photochemistry photoreactor (US Patent #10,906,022) is designed to facilitate photochemical experimentation. It is compatible with most vial formats (0.3 ml, 2 ml, 4 ml and 20 ml vials) and its compact design allows for use with any stirring plate. A built-in fan keeps the reaction conditions at room temperature.<\/p>\n<p>[\/et_pb_text][et_pb_image src=&#8221;https:\/\/hepatochem.com\/wp-content\/uploads\/2026\/04\/photobox-gray-citation-500.png&#8221; alt=&#8221;photoredox box&#8221; title_text=&#8221;photoredox box&#8221; _builder_version=&#8221;4.27.6&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;49%&#8221; module_alignment=&#8221;center&#8221; custom_margin=&#8221;|0px||0px|false|false&#8221; custom_padding=&#8221;|15px||15px|false|true&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_image][et_pb_button button_url=&#8221;\/photoreactor-order&#8221; button_text=&#8221;Order and Pricing Here&#8221; button_alignment=&#8221;center&#8221; _builder_version=&#8221;4.20.4&#8243; _module_preset=&#8221;default&#8221; custom_margin=&#8221;||3px|||&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_button][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=&#8221;3_5,2_5&#8243; _builder_version=&#8221;4.20.4&#8243; width=&#8221;100%&#8221; custom_padding=&#8221;30px|0px|27px|0px|false|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;3_5&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_blurb title=&#8221;Features&#8221; _builder_version=&#8221;4.20.4&#8243; header_level=&#8221;h3&#8243; header_font=&#8221;|700|||||||&#8221; header_font_size=&#8221;20px&#8221; body_font=&#8221;||||||||&#8221; custom_padding=&#8221;|15px|0px|15px|false|true&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<ul>\n<li style=\"list-style-type: none;\">\n<ul>\n<li>Several light sources available 365 nm to 808 nm<\/li>\n<li>Photochemistry chamber to optimize light intensity<\/li>\n<li>Flexible format vials<\/li>\n<li>Magnetic stirring on standard stirring plate<\/li>\n<li>Cooling by fan to maintain experiment at room temperature<\/li>\n<li>Pre-designed array of catalysts and reagents available<\/li>\n<li>For added efficiencies, check out the <a href=\"https:\/\/hepatochem.com\/photoreactors-leds-accessories\/photoredox-flow-reactor\/\">PhotoRedOx Flow Reactor<\/a> Accessory<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>[\/et_pb_blurb][et_pb_blurb title=&#8221;Benefits&#8221; _builder_version=&#8221;4.20.4&#8243; header_level=&#8221;h3&#8243; header_font=&#8221;|700|||||||&#8221; header_text_align=&#8221;left&#8221; header_font_size=&#8221;20px&#8221; body_font=&#8221;||||||||&#8221; custom_margin=&#8221;-15px||-7px|||&#8221; custom_padding=&#8221;|15px||15px|false|true&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<ul>\n<li style=\"list-style-type: none;\">\n<ul>\n<li><span>Easy setup on a standard stirring plate<\/span><\/li>\n<li><span>Perform up to 32 reaction conditions simultaneously<\/span><\/li>\n<li><span>Individually sealed vials enable flexible study design<\/span><\/li>\n<li><span>Save your substrate using low scale reaction conditions<\/span><\/li>\n<li><span>Save time on optimization<\/span><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>[\/et_pb_blurb][et_pb_video src=&#8221;https:\/\/youtu.be\/JTEza4SbtDk?si=2tvYG_r4nLCoulzd&#8221; _builder_version=&#8221;4.27.4&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_video][\/et_pb_column][et_pb_column type=&#8221;2_5&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_blurb title=&#8221;Device with blue light source&#8221; image=&#8221;https:\/\/hepatochem.com\/wp-content\/uploads\/2024\/07\/photobox-web3.png&#8221; alt=&#8221;photoreactor&#8221; image_icon_width=&#8221;100%&#8221; _builder_version=&#8221;4.20.4&#8243; header_level=&#8221;h5&#8243; header_font=&#8221;|700|||||||&#8221; header_text_align=&#8221;center&#8221; width=&#8221;100%&#8221; max_width=&#8221;100%&#8221; max_height=&#8221;100%&#8221; custom_padding=&#8221;|15px||15px|false|true&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p style=\"text-align: center;\"><span>HCK1006-01-016<\/span><br \/><span style=\"font-size: 12px; margin-top: -12px;\">(US Patent #10,906,022)<\/span><\/p>\n<p>[\/et_pb_blurb][et_pb_blurb image=&#8221;https:\/\/hepatochem.com\/wp-content\/uploads\/2016\/12\/light_mirrors-e1549406845169.png&#8221; _builder_version=&#8221;4.20.4&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;100%&#8221; custom_margin=&#8221;|15px||15px|false|false&#8221; custom_margin_tablet=&#8221;|15px||15px|false|false&#8221; custom_margin_phone=&#8221;|0px||0px|false|true&#8221; custom_margin_last_edited=&#8221;on|phone&#8221; custom_padding=&#8221;|15px||15px|false|true&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p style=\"text-align: center;\"><strong>Unique Design<\/strong><strong><\/strong><\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=&#8221;4.27.4&#8243; width=&#8221;100%&#8221; module_alignment=&#8221;center&#8221; custom_margin=&#8221;|0px||0px|false|true&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_text _builder_version=&#8221;4.20.4&#8243; header_3_font=&#8221;|700|||||||&#8221; header_3_text_align=&#8221;left&#8221; custom_padding=&#8221;|15px||15px|false|true&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3 style=\"text-align: left;\">Easy setup and compact design<\/h3>\n<p>[\/et_pb_text][et_pb_image src=&#8221;https:\/\/hepatochem.com\/wp-content\/uploads\/2023\/08\/photobox-web-4-2.png&#8221; alt=&#8221;photoreactor&#8221; title_text=&#8221;photobox web 4-2&#8243; align=&#8221;center&#8221; _builder_version=&#8221;4.27.4&#8243; _module_preset=&#8221;default&#8221; width=&#8221;100%&#8221; max_width=&#8221;100%&#8221; module_alignment=&#8221;center&#8221; custom_margin=&#8221;|0px||0px|false|true&#8221; custom_margin_tablet=&#8221;|15px||15px|false|false&#8221; custom_margin_phone=&#8221;|0px||0px|false|true&#8221; custom_margin_last_edited=&#8221;on|phone&#8221; custom_padding=&#8221;|15px||15px|false|true&#8221; custom_padding_tablet=&#8221;|0px||0px|false|false&#8221; custom_padding_phone=&#8221;|15px||15px|false|true&#8221; custom_padding_last_edited=&#8221;on|phone&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=&#8221;4.20.4&#8243; width=&#8221;100%&#8221; custom_padding=&#8221;|15px||15px|false|true&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_3_font=&#8221;|700|||||||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3 style=\"text-align: left;\"><span>Fit multiple vial sizes<\/span><\/h3>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=&#8221;1_3,1_3,1_3&#8243; _builder_version=&#8221;4.20.4&#8243; width=&#8221;100%&#8221; custom_padding=&#8221;0|15px|0px|15px|false|true&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;1_3&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_blurb title=&#8221;32 X 0.3 ml vials&#8221; image=&#8221;https:\/\/hepatochem.com\/wp-content\/uploads\/2019\/03\/IMG_3764-5.jpeg&#8221; content_max_width=&#8221;470px&#8221; _builder_version=&#8221;4.20.4&#8243; header_level=&#8221;h6&#8243; header_font=&#8221;|700|||||||&#8221; header_text_align=&#8221;center&#8221; body_font_size=&#8221;12px&#8221; custom_padding=&#8221;0px||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p style=\"text-align: center;\">HCK1006-01-017<\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][et_pb_column type=&#8221;1_3&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_blurb title=&#8221;8 X 2 ml vials &#8221; image=&#8221;https:\/\/hepatochem.com\/wp-content\/uploads\/2019\/09\/2ml_holder_170x170.jpg&#8221; _builder_version=&#8221;4.20.4&#8243; header_level=&#8221;h6&#8243; header_font=&#8221;|700|||||||&#8221; header_text_align=&#8221;center&#8221; body_font_size=&#8221;12px&#8221; custom_padding=&#8221;0px||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p style=\"text-align: center;\">HCK1006-01-018<\/p>\n<p>[\/et_pb_blurb][\/et_pb_column][et_pb_column type=&#8221;1_3&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; 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Please add details or additional questions here.&#8221; field_type=&#8221;text&#8221; required_mark=&#8221;off&#8221; _builder_version=&#8221;4.20.4&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_contact_field][\/et_pb_contact_form][et_pb_text _builder_version=&#8221;4.27.6&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2 style=\"text-align: center;\">More than 500 publication since 2018<\/h2>\n<p>some examples.<\/p>\n<p>(1) \u00a0\u00a0\u00a0\u00a0 Seefeldt, P.; Villinger, A.; Brasholz, M. Photoredox-Catalyzed Carbon Radical Generation from \u03b1-Keto- N , O -Acetals\u202f: Synthesis of Functionalized Azepino [ 1 , 2- a ] Indoles and Azepino [ 1 , 2- a ] Furo [ 3 , 2- b ] Indoles. <em>Adv. Synth. Catal.<\/em> <strong>2024<\/strong>, <em>366<\/em> (1), 24\u201330.<\/p>\n<p>(2) \u00a0\u00a0\u00a0\u00a0 Adri\u00e1n Luguera Ruiz; Mariani, E.; Stefano Protti; Fagnoni, M. Photoredox Catalyzed Release of Carbon-Based Radicals from 2- Substituted-1,3-Imidazolidines. <em>Org. Chem. Front.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1039\/D3QO01856C.<\/p>\n<p>(3) \u00a0\u00a0\u00a0\u00a0 Fu-Peng Wu, Chetan C. Chintawar, Remy Lalisse, Poulami Mukherjee, Subhabrata Dutta, Jasper Tyler, Constantin G. Daniliuc, O. G. &amp; F. G. Ring Expansion of Indene by Photoredox- Enabled Functionalized Carbon-Atom Insertion. <em>Nat. Catal.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(4) \u00a0\u00a0\u00a0\u00a0 Dutta, S.; Lee, D.; Ozols, K.; Daniliuc, C. G.; Shintani, R.; Glorius, F. Photoredox-Enabled Dearomative [2\u03c0 + 2\u03c3] Cycloaddition of Phenols. <em>J. Am. Chem. Soc.<\/em> <strong>2024<\/strong>, 1\u2013116. https:\/\/doi.org\/10.1021\/jacs.3c12894.<\/p>\n<p>(5) \u00a0\u00a0\u00a0\u00a0 Revie, R. I.; Whitaker, B. J.; Paul, B.; Smith, R. C.; Anderson, E. A. Synthesis of Heterocycle-Substituted Bicyclo[3.1.1]Heptanes and Aza-Bicyclo[3.1.1]Heptanes via Photocatalytic Minisci Reaction. <em>Org. Lett.<\/em> <strong>2024<\/strong>, 10\u201313. https:\/\/doi.org\/10.1021\/acs.orglett.3c03684.<\/p>\n<p>(6) \u00a0\u00a0\u00a0\u00a0 Yadav, A. K.; Ariff, P. N. A. M.; Kawai, K.; Ochiai, S.; Narra, S. R.; Shibata, N. Cross Dehydrogenative Coupling of SF4-Alkyne with Tetrahydroisoquinolines. <em>Org. Lett.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(7) \u00a0\u00a0\u00a0\u00a0 Kim, S. F.; Schwarz, H.; Jurczyk, J.; Nebgen, B. R.; Hendricks, H.; Park, H.; Radosevich, A.; Zuerch, M. W.; Harper, K.; Lux, M. C.; Yeung, C. S.; Sarpong, R. Mechanistic Investigation, Wavelength-Dependent Reactivity, and Expanded Reactivity of N-Aryl Azacycle Photomediate Ring Contractions. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/jacs.3c13982.<\/p>\n<p>(8) \u00a0\u00a0\u00a0\u00a0 Subhabrata Dutta, Yi-Lin Lu, Johannes E. Erchinger, Huiling Shao, Emanuel Studer, Felix Sch\u00e4fer, Huamin Wang, Debanjan Rana, Constantin G. Daniliuc, K. N. Houk,* and Frank Glorius Shao, Emanuel Studer, Felix Sch\u00e4fer, Huamin Wang, Debanjan Rana, Constantin, and F. G. Double Strain-Release[2\u03c0+2\u03c3]-Photocycloaddition. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>, No. 1, 1\u20135.<\/p>\n<p>(9) \u00a0\u00a0\u00a0\u00a0 Dam, D.; Lagerweij, N. R.; Janmaat, K. M.; Kok, K.; Bouwman, E.; Cod, J. D. C. Organic Dye-Sensitized Nitrene Generation: Intermolecular Aziridination of Unactivated Alkenes. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>, 1\u201387. https:\/\/doi.org\/10.1021\/acs.joc.3c02709.<\/p>\n<p>(10) \u00a0\u00a0 Igor A. Lavrinchenko , Egor A. Nikiforov , Timofey D. Moseev , Mikhail V. Varaksin \u2217 , Anton N. Tsmokalyuk , Thomas V. Nechaev , Valery N. Charushin, O. N. Synthesis, Photophysical, and AIE Properties of 2H-Imidazole-Derived Push-Pull Fluorophores. <em>Synthesis (Stuttg).<\/em> <strong>2024<\/strong>.<\/p>\n<p>(11) \u00a0\u00a0 Hervieu, C.; Kirillova, M. S.; Hu, Y.; Cuesta-galisteo, S.; Merino, E.; Nevado, C. Chiral Arylsulfinylamides as Reagents for Visible Light-Mediated Asymmetric Alkene Aminoarylations. <em>Nat. Chem.<\/em> <strong>2024<\/strong>, 1\u201318. https:\/\/doi.org\/10.1038\/s41557-023-01414-8.<\/p>\n<p>(12) \u00a0\u00a0 Gesmundo, N. J.; Rago, A. J.; Young, J. M.; Keess, S.; Wang, Y. At the Speed of Light: The Systematic Implementation of Photoredox Cross-Coupling Reactions for Medicinal Chemistry Research. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, 1\u201328. https:\/\/doi.org\/10.1021\/acs.joc.3c02351.<\/p>\n<p>(13) \u00a0\u00a0 Seefeldt, P.; Edelmann, L.; Prudlik, A.; Villinger, A.; Francke, R.; Brasholz, M. Photoinduced Tandem C-O Bond Reduction \/ Ketyl Radical Addition Reactions of \u03b1 -Keto- N , O -Acetals Enabled by Proton-Coupled Electron Transfer. <em>ChemPhotoChem<\/em> <strong>2024<\/strong>.<\/p>\n<p>(14) \u00a0\u00a0 Han, G.; You, J.; Choi, J.; Joo, E. N -Iminopyridinium Compounds in Giese Reaction\u202f: Photoinduced Homolytic N-N and C-C Bond Cleavage for Cyanoalkyl Radical Generation. <em>Org. Lett.<\/em> <strong>2024<\/strong>, 1\u201399.<\/p>\n<p>(15) \u00a0\u00a0 Bonfils, P. De; Nun, P.; Coeffard, V. Unsymmetrical Anthracene Platforms as Singlet Oxygen Batteries\u202f: Effects of Substituents on Photooxygenation and Endoperoxide Thermolysis. <em>European J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>202400099<\/em> (1), 4\u20135. https:\/\/doi.org\/10.1002\/ejoc.200490000.<\/p>\n<p>(16) \u00a0\u00a0 Tagami, T.; Kawamura, S.; Sodeoka, M. Aerobic Photoredox Catalyzed Oxamate Ester Synthesis from Bromodifluoroacetate Esters. <em>European J. Org. Chem.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(17) \u00a0\u00a0 Laskar, R.; Dutta, S.; Spies, J. C.; Mukherjee, P.; Renter\u00eda-g\u00f3mez, \u00c1. \u0393\u2011Amino Alcohols via Energy Transfer Enabled Brook Rearrangement. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>.<\/p>\n<p>(18) \u00a0\u00a0 Magkoev, T. T.; Demidov, O. P.; Abaev, V. T.; Uchuskin, M. G.; Chalikidi, P. N. Unveiling Orthogonal Reactivity of Substituted 2\u2011(2- Azidostyryl)Furans: Thermolysis and Photolysis versus Catalysis. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, 1\u201368. https:\/\/doi.org\/10.1021\/acs.joc.4c00355.<\/p>\n<p>(19) \u00a0\u00a0 Ramos, A. L.; Goedken, E. R.; Frank, K. E.; Argiriadi, M. A.; Bazzaz, S.; Bian, Z.; Brown, J. T. C.; Centrella, P. A.; Chen, H.; Disch, J. S.; Donner, P. L.; Duignan, D. B.; Gikunju, D.; Greszler, S. N.; Gui, M.; Habeshian, S.; Hartl, H. E.; Hein, C. D.; Hutchins, C. W.; Jetson, R.; Keefe, A. D.; Khan, H.; Li, H.; Olszewski, A.; Cardona, B. J. O.; Osuma, A.; Panchal, S. C.; Phelan, R.; Qiu, W.; Shotwell, J. B.; Shrestha, A.; Srikumaran, M.; Su, Z.; Sun, C.; Upadhyay, A. K.; Wood, M. D.; Wu, H.; Zhang, R.; Zhang, Y.; Zhao, G.; Zhu, H.; Webster, M. P. Discovery of Small Molecule Interleukin 17A Inhibitors with Novel Binding Mode and Stoichiometry: Optimization of DNA-Encoded Chemical Library Hits to In Vivo Active Compounds. <em>J. Med. Chem.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/acs.jmedchem.3c02397.<\/p>\n<p>(20) \u00a0\u00a0 Chintawar, C. C.; Laskar, R.; Rana, D.; Wyngaerden, N. Van; Dutta, S.; Daniliuc, C. G.; Glorius, F. Photoredox-Catalyzed Amidyl Radical Insertion to Bicyclo[1.1.0]. <em>ChemRxiv. Prepr.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(21) \u00a0\u00a0 Krax, R.; Menneking, K.; Sajapin, J.; Hellwig, M. Identification of \u03b2-Aspartic Semialdehyde and Homocysteine as Major Reaction Products of Riboflavin-Sensitized Photooxidation of Peptide-Bound Methionine. <em>Eur. Food Res. Technol.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1007\/s00217-024-04540-w.<\/p>\n<p>(22) \u00a0\u00a0 Jonathan Da Luz , Michaela \u010cierna , Bradley D. Cooper , Thomas D. Harris , Ethan R. X. Lim , Jonathan R. Carney, M. J. J. Denitrative Sulfonylation of Nitroarenes with Sodium Sulfinates. <em>Synthesis (Stuttg).<\/em> <strong>2024<\/strong>.<\/p>\n<p>(23) \u00a0\u00a0 Lilian Geniller, Marc Taillefer, Eric Clot, Florian Jaroschik, and A. P. Photocatalyzed Formation of Gem\u2010difluoroalkenes Using Oxime Esters. <em>Adv. Synth. Catal.<\/em> <strong>2024<\/strong>, 1\u201323.<\/p>\n<p>(24) \u00a0\u00a0 Karlsson, S.; Leonori, D.; Plesniak, M. P. Mild Strategy for the Preparation of Alkyl Sulfonyl Fluorides from Alkyl Bromides and Alcohols Using Photoredox Catalysis and Flow Chemistry. <em>Org. Lett.<\/em> <strong>2024<\/strong>, <em>2<\/em> (1), 1\u20135. https:\/\/doi.org\/10.1021\/acs.orglett.4c01216.<\/p>\n<p>(25) \u00a0\u00a0 Ortalli, S.; Ford, J.; Trabanco, A. A.; Tredwell, M.; Gouverneur, V. Photoredox Nucleophilic ( Radio ) Fluorination of Alkoxyamines. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>, 0\u20135. https:\/\/doi.org\/10.1021\/jacs.4c02474.<\/p>\n<p>(26) \u00a0\u00a0 Mocny, P.; Lin, T.; Parekh, R.; Zhao, Y.; Czarnota, M.; Urban, M.; Majidi, C.; Matyjaszewski, K. Selective and Controlled Grafting from PVDF-Based Materials by Oxygen-Tolerant Green-Light-Mediated ATRP \u0301. <em>Appl. Mater. Interfaces<\/em> <strong>2024<\/strong>, 1\u201334. https:\/\/doi.org\/10.1021\/acsami.4c03369.<\/p>\n<p>(27) \u00a0\u00a0 Hu, T.; Fagu\u00e9, V.; Bouyssi, D.; Monteiro, N.; Amgoune, A. Hydride-Free Reduction of Propargyl Electrophiles: A Nickel-Catalyzed Photoredox Strategy for Allene Synthesis. <em>Green Chem.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1039\/d4gc00984c.<\/p>\n<p>(28) \u00a0\u00a0 Alcaraz, M.; Lyonnais, S.; Ghosh, C.; Aguilera-correa, J. J.; Richeter, S.; Ulrich, S.; Kremer, L.; Alcaraz, M.; Lyonnais, S.; Ghosh, C.; Aguilera-correa, J. J.; Richeter, S.; Ulrich, S.; Kremer, L. Evaluation and Activity of New Porphyrin-Peptide Cage-Type Conjugates for the Photoinactivation of Mycobacterium Abscessus. <em>Microbiol. Spectr.<\/em> <strong>2024<\/strong>, No. April.<\/p>\n<p>(29) \u00a0\u00a0 Hu, X.; Yin, R.; Jeong, J.; Matyjaszewski, K.; Information, S.; Hu, X.; Yin, R.; Jeong, J.; Matyjaszewski, K. Robust Miniemulsion PhotoATRP Driven by Red and Near-Infrared Light. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/jacs.4c02553.<\/p>\n<p>(30) \u00a0\u00a0 El-Arid, S.; Lenihan, J.; Jacobsen, A.; Beeler, A.; Grinstaff, M. Accessing Cyclobutane Polymers: Overcoming Synthetic Challenges via Efficient Continuous Flow [2+2] Photopolymerization. <em>ACS MacroLetters<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/acsmacrolett.4c00083.<\/p>\n<p>(31) \u00a0\u00a0 Kechiche, A.; Shaymaa Al Shehimy, L. K.; Monnereau, C.; Christophe Bucher, S. P.; Alla Bessmertnykh-Lemeune, Y. R.; Nasri, A. V. C. and H. Phosphonate-Substituted Porphyrins as Efficient, Cost-Effective and Reusable Photocatalysts. <em>Dalt. Trans.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(32) \u00a0\u00a0 Tambe, S. D.; Hwang, H. S.; Park, E.; Cho, E. J. Dual Photoredox and Nickel Catalysis in Regioselective Diacylation\u202f: Exploring the Versatility of Nickel Oxidation States in Allene Activation. <em>Org. Lett.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(33) \u00a0\u00a0 Yoshida, Y.; Takeuchi, H.; Arichi, N.; Oishi, S.; Ohno, H.; Inuki, S. Approach to Spirocyclohexadienes via Visible Light-Mediated Ipso -Cyclization of Amino Acid Derivatives with N &#8211; ( 2-Phenyl ) Benzoyl Groups. <em>Asian J. Chem.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(34) \u00a0\u00a0 Frances R. Smith, Declan Meehan, Rhys C. Griffiths, Harriet J. Knowles, Peiyu Zhang, Huw E. L. Williams, Andrew J. Wilson, and N. J. M. Peptide Macrocyclisation via Intramolecular Interception of Visible-Light-Mediated Desulfurisation. <em>Chem. Sci.<\/em> <strong>2024<\/strong>, <em>2<\/em> (100 mL), 2\u20136. https:\/\/doi.org\/10.1038\/scientificamerican10271883-6511csupp.<\/p>\n<p>(35) \u00a0\u00a0 Lasky, M. R.; Liu, E.; Remy, M. S.; Sanford, M. S. Visible-Light Photocatalytic C \u2212 H Amination of Arenes Utilizing Acridine \u2212 Lewis Acid Complexes. <em>J. Am. Chem. Soc<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/cm504475k.<\/p>\n<p>(36) \u00a0\u00a0 Tyler, J. L.; Sch\u00e4fer, F.; Shao, H.; Stein, C.; Wong, A.; Daniliuc, C. G.; Houk, K. N.; Glorius, F. Bicyclo[1.1.0]Butyl Radical Cations: Synthesis and Application to [2\u03c0+2\u03c3] Cycloaddition Reactions. <em>J. Am. Chem. Soc.<\/em> <strong>2024<\/strong>.<\/p>\n<p>(37) \u00a0\u00a0 Guselnikova, O.; Trelin, A.; Kang, Y.; Postnikov, P.; Kobashi, M.; Suzuki, A.; Shrestha, L. K.; Henzie, J.; Yamauchi, Y. Pretreatment-Free SERS Sensing of Microplastics Using a Self-Attention-Based Neural Network on Hierarchically Porous Ag Foams. <em>Nat. Commun.<\/em> <strong>2024<\/strong>, <em>15<\/em>, 4351. https:\/\/doi.org\/10.1038\/s41467-024-48148-w.<\/p>\n<p>(38) \u00a0\u00a0 Hynek, J.; Payne, D. T.; Shrestha, L. K.; Chahal, M. K.; Ma, R.; Dong, J.; Ariga, K.; Yamauchi, Y.; Hill, J. P. Mild Selective Photochemical Oxidation of an Organic Sulfide Using OxP-Polyimide Porous Polymers as Singlet Oxygen Generators. <em>Sci. Technol. Adv. Mater.<\/em> <strong>2024<\/strong>, <em>25<\/em> (1). https:\/\/doi.org\/10.1080\/14686996.2024.2322458.<\/p>\n<p>(39) \u00a0\u00a0 Nugent, J.; L\u00f3pez-franc\u00e9s, A.; Sterling, A. J.; Yi, M.; Frank, N.; James, J.; Anderson, E. A. \u03b1-Amino Bicycloalkylation through Organophotoredox Catalysis. <em>Chem. Sci.<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1039\/D4SC01368A.<\/p>\n<p>(40) \u00a0\u00a0 Photoreactor, Si. of E. into Z. U. a R. Mayuko Suga, Saki Fukushima, Kosho Makino, Kayo Nakamura, Hidetsugu Tabata, Tetsuta Oshitari, Hideaki Natsugari, Noritaka Kuroda, Kunio Kanemaru, Yuji Oda, and Hideyo Takahashi *. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>11<\/em> (1), 1\u20135. https:\/\/doi.org\/10.1021\/acs.joc.4c00721.<\/p>\n<p>(41) \u00a0\u00a0 Galibert-guijarro, A.; Tronc, J.; Mouysset, D.; Siri, D.; Bertrand, M. P.; Feray, L. Investigation of UV Light-Promoted Synthesis of a -Sulfonyl Amides from N- Sulfonyl Ynamides . <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, 1\u2013166.<\/p>\n<p>(42) \u00a0\u00a0 de Blois, C.; Engel, M.; Rejou, M. A.; Molcrette, B.; Favier, A.; Montel, F. Optical Single Molecule Characterisation of Natural and Synthetic Polymers through Nanopores. <em>Nanoscale<\/em> <strong>2024<\/strong>, <em>16<\/em> (1), 138\u2013151. https:\/\/doi.org\/10.1039\/d3nr04915a.<\/p>\n<p>(43) \u00a0\u00a0 Pijper, B.; Saavedra, L. M.; Lanzi, M.; Alonso, M.; Fontana, A.; Serrano, M.; G\u00f3mez, J. E.; Kleij, A. W.; Alc\u00e1zar, J.; Ca\u00f1ellas, S. Addressing Reproducibility Challenges in High-Throughput Photochemistry. <em>JACS Au<\/em> <strong>2024<\/strong>. https:\/\/doi.org\/10.1021\/jacsau.4c00312.<\/p>\n<p>(44) \u00a0\u00a0 Morad, V.; Stelmakh, A.; Svyrydenko, M.; Feld, L. G.; Boehme, S. C.; Aebli, M.; Affolter, J.; Kaul, C. J.; Schrenker, N. J.; Bals, S.; Sahin, Y.; Dirin, D. N.; Cherniukh, I.; Raino, G.; Baumketner, A.; Kovalenko, M. V. Designer Phospholipid Capping Ligands for Soft Metal Halide Nanocrystals. <em>Nature<\/em> <strong>2024<\/strong>, <em>626<\/em> (7999), 542\u2013548. https:\/\/doi.org\/10.1038\/s41586-023-06932-6.<\/p>\n<p>(45) \u00a0\u00a0 Angeltveit, C. F.; Kommedal, E. G.; Stepnov, A. A.; Eijsink, V. G. H.; Horn, S. J. Light Exposure of Lignin Affects the Saccharification Efficiency of LPMO- Containing Cellulolytic Enzyme Cocktails. <em>ACS Sustain. Chem. Eng.<\/em> <strong>2024<\/strong>, 1\u20136. https:\/\/doi.org\/10.1021\/acssuschemeng.4c02042.<\/p>\n<p>(46) \u00a0\u00a0 Reischauer, S.; Smoljan, C. S.; Rabeah, J.; Xie, H.; Formalik, F.; Chen, Z.; Vornholt, S. M.; Sha, F.; Chapman, K. W.; Snurr, R. Q.; Notestein, J. M.; Farha, O. K. A Titanium-Based Metal\u2212Organic Framework For Tandem Metallaphotocatalysis. <em>Appl. Mater. Interfaces<\/em> <strong>2024<\/strong>.<\/p>\n<p>(47) \u00a0\u00a0 Andrews, J. A.; Woodger, R. G.; Palmer, C. F.; Poole, D. L.; Willis, M. C. 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Direct Decarboxylative Allylation and Arylation of Aliphatic Carboxylic Acids Using Flavin-Mediated Photoredox Catalysis. <em>European J. Org. Chem.<\/em> <strong>2020<\/strong>, <em>2020<\/em> (10), 1539\u20131550. https:\/\/doi.org\/10.1002\/ejoc.201900888.<\/p>\n<p>(287) Escobar, R. A.; Johannes, J. W. A Unified and Practical Method for Carbon\u2013Heteroatom Cross-Coupling Using Nickel\/Photo Dual Catalysis. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em> (23), 5168\u20135173.<\/p>\n<p>(288) Cardinale, L.; Konev, M. O.; Jacobi Von Wangelin, A. Photoredox-Catalyzed Addition of Carbamoyl Radicals to Olefins: A 1,4-Dihydropyridine Approach. <em>Chem. Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em> (37), 8239\u20138243.<\/p>\n<p>(289) Legros, F.; Fernandez-Rodriguez, P.; Mishra, A.; Weck, R.; Bauer, A.; Sandvoss, M.; Ruf, S.; Mendez, M.; Mora-Rado, H.; Rackelmann, N.; Poverlein, C.; Derdau, V. Photoredox-Mediated Hydrogen Isotope Exchange Reactions of Amino-Acids, Peptides, and Peptide-Derived Drugs. <em>Chem. Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em> (56), 12738\u201312742.<\/p>\n<p>(290) Lyu, J.; Claraz, A.; Vitale, M. R.; Allain, C.; Masson, G. Preparation of Chiral Photosensitive Organocatalysts and Their Application for the Enantioselective Synthesis of 1,2-Diamines. <em>J. Org. Chem.<\/em> <strong>2020<\/strong>, <em>85<\/em> (20), 12843\u201312855. https:\/\/doi.org\/10.1021\/acs.joc.0c01931.<\/p>\n<p>(291) Gallhof, M.; Kell, L.; Brasholz, M. Ligand Substitution of RuII\u2013Alkylidenes to Ru(Bpy)32+: Sequential Olefin Metathesis\/Photoredox Catalysis. <em>Chem. &#8211; A Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em> (8), 1772\u20131775. https:\/\/doi.org\/10.1002\/chem.201905694.<\/p>\n<p>(292) Aguilar Troyano, F. J.; Ballaschk, F.; Jaschinski, M.; \u00d6zkaya, Y.; G\u00f3mez-Su\u00e1rez, A. 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J.; Mansfield, S. J.; Caputo, D. F. J.; Owen, B.; Mousseau, J. J.; Duarte, F.; Anderson, E. A. A General Route to Bicyclo[1.1.1]Pentanes through Photoredox Catalysis. <em>ACS Catal.<\/em> <strong>2019<\/strong>, <em>9<\/em> (10), 9568\u20139574. https:\/\/doi.org\/10.1021\/acscatal.9b03190.<\/p>\n<p>(296) Meyer, C. F.; Hell, S. M.; Misale, A.; Trabanco, A. A.; Gouverneur, V. Hydrodifluoromethylation of Alkenes with Difluoroacetic Acid. <em>Angew. Chemie &#8211; Int. Ed.<\/em> <strong>2019<\/strong>, <em>58<\/em> (26), 8829\u20138833. https:\/\/doi.org\/10.1002\/anie.201903801.<\/p>\n<p>(297) Rossolini, T.; Ferko, B.; Dixon, D. J. Photocatalytic Reductive Formation of \u03b1-Tertiary Ethers from Ketals. <em>Org. Lett.<\/em> <strong>2019<\/strong>, <em>21<\/em> (17), 6668\u20136673. https:\/\/doi.org\/10.1021\/acs.orglett.9b02273.<\/p>\n<p>(298) Ramirez, N. P.; K\u00f6nig, B.; Gonzalez-Gomez, J. C. 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Radical Deoxychlorination of Cesium Oxalates for the Synthesis of Alkyl Chlorides. <em>Org. Lett.<\/em> <strong>2018<\/strong>, <em>20<\/em> (16), 4912\u20134916. https:\/\/doi.org\/10.1021\/acs.orglett.8b02045.<\/p>\n<p>(302) Leitch, J. A.; Fuentes De Arriba, A. L.; Tan, J.; Hoff, O.; Mart\u00ednez, C. M.; Dixon, D. J. Photocatalytic Reverse Polarity Povarov Reaction. <em>Chem. Sci.<\/em> <strong>2018<\/strong>, <em>9<\/em> (32), 6653\u20136658. https:\/\/doi.org\/10.1039\/c8sc01704b.<\/p>\n<p>(303) Davies, J.; Angelini, L.; Alkhalifah, M. A.; Sanz, L. M.; Sheikh, N. S.; Leonori, D. Photoredox Synthesis of Arylhydroxylamines from Carboxylic Acids and Nitrosoarenes. <em>Synth.<\/em> <strong>2018<\/strong>, <em>50<\/em> (4), 821\u2013830. https:\/\/doi.org\/10.1055\/s-003.<\/p>\n<p>(304) L\u00e4mmermann, H.; Sudau, A.; Rackl, D.; Weinmann, H.; Collins, K.; Wortmann, L.; Candish, L.; Hog, D. T.; Meier, R. 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Nickel-Catalyzed Photoredox-Mediated Cross-Coupling of Aryl Electrophiles and Aryl Azides. <em>ACS Catal.<\/em> <strong>2018<\/strong>, <em>8<\/em> (10), 9120\u20139124. https:\/\/doi.org\/10.1021\/acscatal.8b02954.<\/p>\n<p>(308) Vil\u00e9, G.; Richard-Bildstein, S.; Lhuillery, A.; Rueedi, G. Electrophile, Substrate Functionality, and Catalyst Effects in the Synthesis of \u03b1-Mono and Di-Substituted Benzylamines via Visible-Light Photoredox Catalysis in Flow. <em>ChemCatChem<\/em> <strong>2018<\/strong>, <em>10<\/em> (17), 3786\u20133794. https:\/\/doi.org\/10.1002\/cctc.201800754.<\/p>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The EvoluChem PhotoRedOx Box&#x2122; is the photochemistry photoreactor choice for the chemist who seeks to standardize laboratory photochemical setups economically. A flexible design allows interchangeable LEDs from 365 nm to 808 nm and a wide variety of vials. This photochemistry photoreactor (US Patent #10,906,022) is designed to facilitate photochemical experimentation. It is compatible with most [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":25070,"parent":25056,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"class_list":["post-25068","page","type-page","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>PhotoRedOx Box&#x2122; - HepatoChem<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/hepatochem.com\/euro\/photoreactors-leds-accessories\/photoredox-box\/\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"66 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/hepatochem.com\\\/euro\\\/photoreactors-leds-accessories\\\/photoredox-box\\\/\",\"url\":\"https:\\\/\\\/hepatochem.com\\\/euro\\\/photoreactors-leds-accessories\\\/photoredox-box\\\/\",\"name\":\"PhotoRedOx Box&#x2122; 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