{"id":24932,"date":"2020-12-17T15:15:51","date_gmt":"2020-12-17T22:15:51","guid":{"rendered":"https:\/\/hepatochem.com\/the-20-must-read-photochemistry-papers-from-2020\/"},"modified":"2020-12-17T15:15:51","modified_gmt":"2020-12-17T22:15:51","slug":"the-20-must-read-photochemistry-papers-from-2020","status":"publish","type":"post","link":"https:\/\/hepatochem.com\/fr\/the-20-must-read-photochemistry-papers-from-2020\/","title":{"rendered":"The 20 Must Read Photochemistry Papers from 2020"},"content":{"rendered":"<p>[et_pb_section fb_built=\u00a0\u00bb1&Prime; _builder_version=\u00a0\u00bb4.16&Prime; global_colors_info=\u00a0\u00bb{}\u00a0\u00bb theme_builder_area=\u00a0\u00bbpost_content\u00a0\u00bb][et_pb_row _builder_version=\u00a0\u00bb4.16&Prime; background_size=\u00a0\u00bbinitial\u00a0\u00bb background_position=\u00a0\u00bbtop_left\u00a0\u00bb background_repeat=\u00a0\u00bbrepeat\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb theme_builder_area=\u00a0\u00bbpost_content\u00a0\u00bb][et_pb_column type=\u00a0\u00bb4_4&Prime; _builder_version=\u00a0\u00bb4.16&Prime; custom_padding=\u00a0\u00bb|||\u00a0\u00bb global_colors_info=\u00a0\u00bb{}\u00a0\u00bb custom_padding__hover=\u00a0\u00bb|||\u00a0\u00bb theme_builder_area=\u00a0\u00bbpost_content\u00a0\u00bb][et_pb_text _builder_version=\u00a0\u00bb4.20.4&Prime; background_size=\u00a0\u00bbinitial\u00a0\u00bb background_position=\u00a0\u00bbtop_left\u00a0\u00bb background_repeat=\u00a0\u00bbrepeat\u00a0\u00bb hover_enabled=\u00a0\u00bb0&Prime; global_colors_info=\u00a0\u00bb{}\u00a0\u00bb theme_builder_area=\u00a0\u00bbpost_content\u00a0\u00bb sticky_enabled=\u00a0\u00bb0&Prime;]<\/p>\n<p><strong>Year in review 2020. Let&rsquo;s all agree to not look back. 20 papers for 2020<\/strong><\/p>\n<div id=\"attachment_8813\" style=\"width: 310px\" class=\"wp-caption alignright\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-8813\" class=\"wp-image-8813 size-medium\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/front-image-feature-300x225.png\" alt=\"sarcastic 2020 logo\" width=\"300\" height=\"225\" \/><p id=\"caption-attachment-8813\" class=\"wp-caption-text\">Unofficially the Official Logo of 2020&#8230;<\/p><\/div>\n<p>As the year comes to the close, we thought it was time to have a little fun and look back at the year in photochemistry. 2020 was a big year for us at HepatoChem under some trying circumstances. Before we move forward to 2021 with the launch of some exciting new equipment and products, we thought that we would look back at some of our favorite photochemistry work in the literature from the past year. A quick search finds a few thousand (photoredox, photocatalysis, photochemistry, metallaphotoredox) papers so far in 2020 and with(out lifting a finger to verify) very little research effort we&rsquo;re willing to bet that this is more than in 2019. Many of the papers on the list break ground and move the field farther into unimaginable areas, while others find photochemical replacements for traditional reactions solving some unmet need. A few papers are outside the realm of topics that most of us spend any time thinking about but demonstrate the power of photochemistry. Some of the papers also include nice pictures of EvoluChem photoreactors and equipment and deserve a shout out. And a few others are just plain weird. And let&rsquo;s face it, 2020 was weird for all of us.<\/p>\n<p>If you think we&rsquo;ve missed your favorite paper or just want to send along an example of your work that you want us to recognize or recognize in the future, send us an email or respond to the tweet for this article (<a href=\"https:\/\/twitter.com\"><strong>#photoredox20for2020<\/strong><\/a>) If you disagree with the list, let us know how we screwed up by <span style=\"text-decoration: underline;\">sending us an email here<\/span>.<\/p>\n<p>To get started, a few FAQ about how we generated this list.<\/p>\n<p><strong>What are the criteria for inclusion?<\/strong><\/p>\n<p>Each paper probably uses light in some way, either a bulb, LED, laser or sunlight. We started this exercise without any particular standards or criteria, other than the goal to share the papers we enjoyed (the most) and to make it fun. It then became readily apparent that there were far more than 20 papers worthy to be included, because there was a ridiculous amount of good work put out this year. So, at a certain point we just stopped adding more. Some of the work will likely be familiar to anyone used to the photochemical field; however, in our fake scoring system bonus points were given for open access papers and work from new professors.<\/p>\n<p><strong>Why 20 papers?<\/strong><\/p>\n<p>The year is 2020, I can&rsquo;t believe you asked this question.<\/p>\n<p><strong>Are there 20 papers listed?<\/strong><\/p>\n<p>No, there are probably more or maybe less. You&rsquo;ll need to read and count the entire list to find out.<\/p>\n<p><strong>Is there a vote for best photochemistry achievement of 2020?<\/strong><\/p>\n<p>No. Awards are stupid. Do you really think we want to deal with running an internet voting poll and awarding photoredox achievement of the year to this? <a href=\"https:\/\/www.youtube.com\/watch?v=vfLZOkn0chc\">https:\/\/www.youtube.com\/watch?v=vfLZOkn0chc<strong><\/strong><\/a><\/p>\n<p><strong>Do the links for each article work?<\/strong><\/p>\n<p>Sometimes, when formatting an email or a links on website, links go to the wrong place. You can either be confused by this, email us and complain. Or use google and find the correct article. Your choice. Other times, links go to wrong place intentionally and you might find something fun.<\/p>\n<p><strong>Do I win a prize if I click on each article?<\/strong><\/p>\n<p>You&rsquo;ll have to click on each article to find out.<\/p>\n<p><strong>How do I get my work on the 21 for 2021 list?<\/strong><\/p>\n<p><a href=\"https:\/\/hepatochem.com\/fr\/photoreacteurs-accessoires-led-et-plus-encore\/\">Go here and get to work<\/a>. Send us the paper once you&rsquo;ve submitted.<\/p>\n<p><strong>In no particular order, here are our 20 favorite photochemistry papers for 2020.<\/strong><\/p>\n<h3><em><strong>1: Organocatalyzed Birch Reduction Driven by Visible Light<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>We wrote about <a href=\"https:\/\/hepatochem.com\/multi-photon-approaches-to-synthetic-photochemistry\/\"><span style=\"text-decoration: underline;\">this one back here<\/span><\/a>. Just an incredible achievement to find this much reduction potential in a photocatalytic reaction with mild conditions. Unless you prefer running reactions with liquid ammonia.<\/p>\n<p><strong>Authors: <\/strong>Justin P. Cole, Dian-Feng Chen, Max Kudisch, Ryan M. Pearson, Chern-Hooi Lim, and Garret M. Miyake<br \/><strong>Ref: <\/strong><em>J. Am. Chem. Soc.<\/em>2020, 142, 31, 13573\u201313581<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.0c05899\">https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.0c05899<\/a><\/p>\n<p><strong>Tweet:<br \/><a href=\"https:\/\/twitter.com\/J_A_C_S\/status\/1291105492627009537\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8787 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper1-tweet.png\" alt=\"\" width=\"594\" height=\"516\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper1-tweet.png 594w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper1-tweet-480x417.png 480w\" sizes=\"(min-width: 0px) and (max-width: 480px) 480px, (min-width: 481px) 594px, 100vw\" \/><\/a><\/strong><\/p>\n<p>&nbsp;<\/p>\n<h3><em><strong>2: Development of a Platform for Near-Infrared Photoredox Catalysis<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>Another paper <span style=\"text-decoration: underline;\"><a href=\"https:\/\/hepatochem.com\/red-light-applications-in-photochemistry\/\">we wrote about before<\/a><\/span>. Check this one out to discover all the reasons your favorite photochemical reaction might be better run with a red LED.<\/p>\n<p><strong>Authors: <\/strong>Benjamin D. Ravetz, Nicholas E. S. Tay, Candice L. Joe, Melda Sezen-Edmonds, Michael A. Schmidt, Yichen Tan, Jacob M. Janey, Martin D. Eastgate, and Tomislav Rovis<br \/><strong>Ref: <\/strong><em>ACS Cent. Sci.<\/em>2020, 6, 11, 2053\u20132059<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acscentsci.0c00948\">https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acscentsci.0c00948<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/ACSCentSci\/status\/1321784516760031233\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8788 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper2-tweet.png\" alt=\"\" width=\"593\" height=\"664\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper2-tweet.png 593w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper2-tweet-480x537.png 480w\" sizes=\"(min-width: 0px) and (max-width: 480px) 480px, (min-width: 481px) 593px, 100vw\" \/><\/a><\/p>\n<h3><em><strong>3: Chemistry glows green with photoredox catalysis<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>A quick note on the efficiency and sustainability of photoredox catalysis<\/p>\n<p><strong>Authors: <\/strong>Giacomo E.M. Crisenza, Paolo Melchiorre<br \/><strong>Ref: <\/strong><em>Nature Communications<\/em>, 2020, 11, Article 803<br \/><strong>Link: <\/strong><a href=\"https:\/\/www.nature.com\/articles\/s41467-019-13887-8\">https:\/\/www.nature.com\/articles\/s41467-019-13887-8<\/a><\/p>\n<p><a href=\"https:\/\/twitter.com\/MelchiorreGroup\/status\/1225486686047612930\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8789 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper3-tweet.png\" alt=\"\" width=\"392\" height=\"780\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper3-tweet.png 392w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper3-tweet-151x300.png 151w\" sizes=\"(max-width: 392px) 100vw, 392px\" \/><\/a><\/p>\n<h3><em><strong>4: Photons as a 21st century reagent<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>Please read this paper. Everyone should treat light as a reagent like you would treat any other reagent in a chemical reaction. To repeat again, everyone should treat light as a reagent like you would treat any other reagent in your reaction.<\/p>\n<p><strong>Authors: <\/strong>Holly E. Bonfield, Thomas Knauber, Fran\u00e7ois L\u00e9vesque, Eric G. Moschetta, Flavien Susanne &amp; Lee J. Edwards<br \/><strong>Ref: <\/strong>Nature Communications, 2020, 11, Article number 804<br \/><strong>Link: <\/strong><a href=\"https:\/\/www.nature.com\/articles\/s41467-019-13988-4\">https:\/\/www.nature.com\/articles\/s41467-019-13988-4<\/a><\/p>\n<p><a href=\"https:\/\/www.nature.com\/articles\/s41467-019-13988-4\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8790 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper4-image.png\" alt=\"\" width=\"716\" height=\"457\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper4-image.png 716w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper4-image-480x306.png 480w\" sizes=\"(min-width: 0px) and (max-width: 480px) 480px, (min-width: 481px) 716px, 100vw\" \/><\/a><\/p>\n<h3><strong><em>5: Three-Component Three-Bond Forming Cascade via Palladium Photoredox Catalysis (open access)<\/em><br \/><\/strong><\/h3>\n<p><strong>Our Take<\/strong>: Look at that cool photochemical flow cell setup. I wonder who makes that?<\/p>\n<p><strong>Authors: <\/strong>Peter Bellotti, Maximilian Koy, Christian Gutheil, Steffen Heuvel and Frank Glorius<br \/><strong>Ref: <\/strong><em>Chemical Science, <\/em>2020, ASAP<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2021\/sc\/d0sc05551d#!divAbstract\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2021\/sc\/d0sc05551d#!divAbstract<\/a><\/p>\n<p><strong>Tweet: <\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/GloriusGroup\/status\/1337074033037291528\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8791 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper5-image.jpg\" alt=\"\" width=\"407\" height=\"325\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper5-image.jpg 407w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper5-image-300x240.jpg 300w\" sizes=\"(max-width: 407px) 100vw, 407px\" \/><\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-medium wp-image-8809\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/glorious-group-paper-duo-with-flow-300x201.png\" alt=\"\" width=\"300\" height=\"201\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/glorious-group-paper-duo-with-flow-300x201.png 300w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/glorious-group-paper-duo-with-flow.png 386w\" sizes=\"(max-width: 300px) 100vw, 300px\" \/><\/p>\n<h3><em><strong>6: Metallaphotoredox aryl and alkyl radiomethylation for PET ligand discovery<\/strong><\/em><\/h3>\n<p><strong>Our Take:<\/strong> Amazing work from a collaboration between the Macmillan lab at Princeton with Merck, UPenn and RTI International for last state fast radiolabeling of pharmaceutically relevant compounds.<\/p>\n<p><strong>Authors: <\/strong>Robert W. Pipal, Kenneth T. Stout, Patricia Z. Musacchio, Sumei Ren, Thomas J. A. Graham, Stefan Verhoog, Liza Gantert, Talakad G. Lohith, Alexander Schmitz, Hsiaoju S. Lee, David Hesk, Eric D. Hostetler, Ian W. Davies &amp; David W. C. MacMillan<br \/><strong>Ref: <\/strong><em>Nature, <\/em>2020, 6797<em>.<br \/><\/em><strong>Link: <\/strong><a href=\"https:\/\/www.nature.com\/articles\/s41586-020-3015-0\">https:\/\/www.nature.com\/articles\/s41586-020-3015-0<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/MacMillan_Lab\/status\/1331643372084338689\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8792 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper6-image.jpg\" alt=\"\" width=\"500\" height=\"346\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper6-image.jpg 500w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper6-image-480x332.jpg 480w\" sizes=\"(min-width: 0px) and (max-width: 480px) 480px, (min-width: 481px) 500px, 100vw\" \/><\/a><\/p>\n<h3><em><strong>7: Synthesis of azetidines via visible-light-mediated intermolecular [2+2] photocycloadditions<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>Very interesting work making highly strained four-membered ring building blocks photochemically.<\/p>\n<p><strong>Author: <\/strong>Marc R. Becker, Emily R. Wearing &amp; Corinna S. Schindler<br \/><strong>Ref: <\/strong><em>Nature Chemistry, <\/em><strong>12<\/strong>, 898-905 (2020)<br \/><strong>Link: <\/strong><a href=\"https:\/\/www.nature.com\/articles\/s41557-020-0541-1\">https:\/\/www.nature.com\/articles\/s41557-020-0541-1<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/NatureChemistry\/status\/1313031198357311493\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8793 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper7-image.jpg\" alt=\"\" width=\"363\" height=\"313\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper7-image.jpg 363w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper7-image-300x259.jpg 300w\" sizes=\"(max-width: 363px) 100vw, 363px\" \/><\/a><\/p>\n<h3><em><strong>8: U.S. Food and Drug Administration-Certified Food Dyes as Organocatalysts in the Visible Light-Promoted Chlorination of Aromatics and Heteroaromatics<\/strong><\/em><\/h3>\n<p><strong>Our Take:<\/strong> While it was the weirdness of the title that caught our eye here, being able to use non-toxic catalysts that are produced cheaply in metric ton quantities to do important chemistry is certainly valuable. There is only so much iridium out there for everyone else to use.<\/p>\n<p><strong>Authors: <\/strong>David A. Rogers, Megan D. Hopkins, Nitya Rajagopal, Dhruv Varshney, Haley A. Howard, Gabriel LeBlanc*, and Angus A. Lamar*<br \/><strong>Ref: <\/strong><em>ACS Omega<\/em>, 2020, 5, 13, 7693-7704<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.0c00631\">https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.0c00631<\/a><\/p>\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.0c00631\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8794 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper8-image.jpg\" alt=\"\" width=\"438\" height=\"293\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper8-image.jpg 438w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper8-image-300x201.jpg 300w\" sizes=\"(max-width: 438px) 100vw, 438px\" \/><\/a><\/p>\n<h3><strong><em>9: LED\u00a0\u00bbNMR Monitoring of an Enantioselective Catalytic [2+2] Photocycloaddition<\/em><\/strong><\/h3>\n<p><strong>Our Take:<\/strong> Oh, how far we&rsquo;ve come.<strong> <\/strong>So, we&rsquo;re using LED&rsquo;s inside of NMRs now to study enantioselective photochemical reaction mechanisms for rapid reactions that are complete in under 5 minutes? WTF. It&rsquo;s a shame that everyone says all this photochemistry stuff won&rsquo;t scale up or else this field might really catch on&#8230;.<\/p>\n<p><strong>Authors: <\/strong>Kazimer L. Skubi, Wesley B. Swords, Heike Hofstetter, and Tehshik P. Yoon<br \/><strong>Ref: <\/strong><em>ChemPhotoChem<\/em> 2020, (4), 685-690.<br \/><strong>Link: <\/strong><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cptc.202000094\">https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cptc.202000094<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/TehshikYoon\/status\/1266216444896972800\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8795 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper9-image.jpg\" alt=\"\" width=\"372\" height=\"289\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper9-image.jpg 372w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper9-image-300x233.jpg 300w\" sizes=\"(max-width: 372px) 100vw, 372px\" \/><\/a><\/p>\n<h3><em><strong>10: Upscaling Photoredox Cross-Coupling Reactions in Batch Using Immersion-Well Reactors<\/strong><\/em><\/h3>\n<p><strong>Our Take:<\/strong> Ok, fine. You&rsquo;ve made a few tens of grams of your product with LED&rsquo;s. Are you sure you can really scale up this thing for something useful?<\/p>\n<p><strong>Authors: <\/strong>Isabelle Grimm, Simone T. Hauer, Tim Schulte, Gina Wycich, Karl D. Collins, Kai Lovis, and Lisa Candish<br \/><strong>Ref: <\/strong><em>Org. Process Res. Dev. <\/em>2020, 24, 6, 1185-1193.<br \/><strong>Link: <\/strong><a href=\"https:\/\/dx.doi.org\/10.1021\/acs.oprd.0c00070\">https:\/\/dx.doi.org\/10.1021\/acs.oprd.0c00070<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/OPRD_ACS\/status\/1256268734978613250\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8796 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper10-image.jpg\" alt=\"\" width=\"397\" height=\"281\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper10-image.jpg 397w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper10-image-300x212.jpg 300w\" sizes=\"(max-width: 397px) 100vw, 397px\" \/><\/a><\/p>\n<h3><strong><em>11: Development and Execution of a Production-Scale Continuous [2 + 2] Photocycloaddition<\/em><br \/><\/strong><\/h3>\n<p><strong>Our Take:<\/strong> 5 kg\/day. We good now? Have we settled this yet? If not convinced, you can find many more scale up success stories.<\/p>\n<p><strong>Authors: <\/strong>Matthew G. Beaver, En-xuan Zhang, Zhi-qing Liu, Song-yuan Zheng, Bin Wang, Jiang-ping Lu, Jian Tao, Miguel Gonzalez, Si\u00e2n Jones, and Jason S. Tedrow<br \/><strong>Ref: <\/strong><em>Org. Process Res. Dev.<\/em>2020, 24, 10, 2139\u20132146<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.0c00185\">https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.0c00185<\/a><\/p>\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.0c00185\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8797 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper11-image.jpg\" alt=\"\" width=\"343\" height=\"230\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper11-image.jpg 343w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper11-image-300x201.jpg 300w\" sizes=\"(max-width: 343px) 100vw, 343px\" \/><\/a><\/p>\n<h3><strong><em>12: C(sp3)\u2013H functionalizations of light hydrocarbons using decatungstate photocatalysis in flow<\/em><\/strong><\/h3>\n<p><strong>Our Take:<\/strong> Very cool work using a cheap photocatalyst for activation of light alkanes including methane.<\/p>\n<p><strong>Authors: <\/strong>Gabriele Laudadio, Yuchao Deng, Klaas van der Wal, Davide Ravelli, Manuel Nu\u00f1o, Maurizio Fagnoni, Duncan Guthrie, Yuhan Sun, Timothy No\u00ebl<br \/><strong>Ref: <\/strong><em>Science, <\/em>2020, (369), 92-96.<br \/><strong>Link: <\/strong><a href=\"https:\/\/science.sciencemag.org\/content\/369\/6499\/92\/tab-pdf\">https:\/\/science.sciencemag.org\/content\/369\/6499\/92\/tab-pdf<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/NoelGroupUvA\/status\/1328417129755004929\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8798 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper12-image.jpg\" alt=\"\" width=\"400\" height=\"182\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper12-image.jpg 400w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper12-image-300x137.jpg 300w\" sizes=\"(max-width: 400px) 100vw, 400px\" \/><\/a><\/p>\n<h3><strong><em>13: Organocatalytic Approach to Photochemical Lignin Fragmentation<\/em><\/strong><\/h3>\n<p><strong>Our Take: <\/strong>Metal-free reductive cleavage of lignin using an organic photocatalyst.<\/p>\n<p><strong>Authors <\/strong>Cheng Yang, Markus D. K\u00e4rk\u00e4s, Gabriel Magallanes, Kimberly Chan, and Corey R. J. Stephenson<br \/><strong>Ref: <\/strong><em>Org. Lett.<\/em> 2020, 22, 20, 8082\u20138085<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c03029\"><strong>https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c03029<\/strong><\/a><\/p>\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c03029\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8799 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper13-image.gif\" alt=\"\" width=\"500\" height=\"137\" \/><\/a><\/p>\n<h3><strong><em>14: Discovery of Key TIPS\u00a0\u00bbNaphthalene for Efficient Visible\u00a0\u00bbto\u00a0\u00bbUV Photon Upconversion under Sunlight and Room Light<\/em><\/strong><\/h3>\n<p><strong>Our Take:<\/strong> Harvesting low energy sunlight and turning it into localized higher energy UV light. I&rsquo;m sure we can find a few applications for this technology. Just a guess.<\/p>\n<p><strong>Authors: <\/strong>Naoyuki Harada, Yoichi Sasak, Masanori Hosoyamada, Nobuo Kimizuka and Nobuhiro Yanai<br \/><strong>Ref: <\/strong><em>Angewandte Int. Ed., <\/em>2020, ASAP.<br \/><strong>Link: <\/strong><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202012419\">https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202012419<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/NobuhiroYanai\/status\/1316975376070049792\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8800 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper14-image.jpg\" alt=\"\" width=\"311\" height=\"407\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper14-image.jpg 311w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper14-image-229x300.jpg 229w\" sizes=\"(max-width: 311px) 100vw, 311px\" \/><\/a><\/p>\n<h3><strong><em>15: Potent Reductants via Electron-Primed Photoredox Catalysis: Unlocking Aryl Chlorides for Radical Coupling<\/em><\/strong><\/h3>\n<p><strong>Our Take: <\/strong>Electrochemistry and Photochemistry, together? That&rsquo;s two things in this paper for old-school chemists to complain about.<\/p>\n<p><strong>Authors: <\/strong>Nicholas G. W. Cowper, Colleen P. Chernowsky, Oliver P. Williams, and Zachary K. Wickens<br \/><strong>Ref: <\/strong><em>J. Am. Chem. Soc.<\/em>2020, 142, 5, 2093\u20132099<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.9b12328\">https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.9b12328<\/a><\/p>\n<p><strong>Tweet: <\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/ZachWickens\/status\/1218277248681144320\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8801 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper15-image.jpg\" alt=\"\" width=\"414\" height=\"351\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper15-image.jpg 414w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper15-image-300x254.jpg 300w\" sizes=\"(max-width: 414px) 100vw, 414px\" \/><\/a><\/p>\n<h3><em><strong>16: Efficient Photoredox-Mediated C\u2013C Coupling Organic Synthesis and Hydrogen Production over Engineered Semiconductor Quantum Dots<\/strong><\/em><\/h3>\n<p><strong>Our Take:<\/strong> The title could use more buzzwords, but the technology is very cool.<\/p>\n<p><strong>Authors:<\/strong> Ming-Yu Qi, Yue-Hua Li, Masakazu Anpo, Zi-Rong Tang, and Yi-Jun Xu<br \/><strong>Ref:<\/strong><em> ACS Catal.<\/em>2020, 10, 23, 14327\u201314335<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c04237\">https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c04237<\/a><\/p>\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c04237\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-8802 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper16-image.gif\" alt=\"\" width=\"500\" height=\"279\" \/><\/a><\/p>\n<h3><strong><em>17: Hydroarylation of Arenes via Reductive Radical-Polar Crossover<\/em><br \/><\/strong><\/h3>\n<p><strong>Our Take: <\/strong>Very useful reaction for dearomatization without H2, metals or low temperatures.<\/p>\n<p><strong>Authors: <\/strong>Autumn R. Flynn, Kelly A. McDaniel, Meredith E. Hughes, David B. Vogt, and Nathan T. Jui<br \/><strong>Ref:<\/strong><em> J. Am. Chem. Soc.<\/em>2020, 142, 20, 9163\u20139168<br \/><strong>Link:<\/strong> <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c03926\">https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c03926<\/a><\/p>\n<p><strong>Tweet: <\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/TotalSyntheses\/status\/1260421923734982656\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-8803\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper17-image.png\" alt=\"\" width=\"474\" height=\"402\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper17-image.png 474w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper17-image-300x254.png 300w\" sizes=\"(max-width: 474px) 100vw, 474px\" \/><\/a><\/p>\n<h3><em><strong>18: Development of a Large-Enrollment Course-Based Research Experience in an Undergraduate Organic Chemistry Laboratory: Structure\u2013Function Relationships in Pyrylium Photoredox Catalysts<\/strong><\/em><\/h3>\n<p><strong>Comment: <\/strong>Adding photochemistry to the undergraduate curriculum is incredibly important, specifically experiments for undergraduate lab.<\/p>\n<p><strong>Authors: <\/strong>Cole L. Cruz, Natalie Holmberg-Douglas, Nicholas P. R. Onuska, Joshua B. McManus, Ian A. MacKenzie, Bryant L. Hutson, Nita A. Eskew, and David A. Nicewicz<br \/><strong>Ref: <\/strong>J. <em>Chem. Educ<\/em>. 2020, 97, 6, 1572\u20131578<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jchemed.9b00786\">https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jchemed.9b00786<\/a><\/p>\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jchemed.9b00786\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-8804\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper18-image.gif\" alt=\"\" width=\"500\" height=\"307\" \/><\/a><\/p>\n<h3><em><strong>19: High-throughput Synthesis and Screening of Iridium(III) Photocatalysts for the Fast and Chemoselective Dehalogenation of Aryl Bromides<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>A rapid assay for screening over 1,000 unique iridium catalysts from the lab that first synthesized several of the most commonly used Iridium catalysts used today over a decade ago.<\/p>\n<p><strong>Authors: <\/strong>Velabo Mdluli, Stephen Diluzio, Jacqueline Lewis, Jakub F. Kowalewski, Timothy U. Connell, David Yaron, Tomasz Kowalewski, and Stefan Bernhard<br \/><strong>Ref: <\/strong><em>ACS Catal<\/em>. 2020, 10, 13, 6977\u20136987<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c02247\">https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c02247<\/a><\/p>\n<p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c02247\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-8805\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper19-image.gif\" alt=\"\" width=\"500\" height=\"243\" \/><\/a><\/p>\n<h3><em><strong>20: UV Light Generation and Challenging Photoreactions Enabled by Upconversion in Water<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>Blue to UV-upconversion in water. Water-soluble iridium catalysts. Degradation of some pretty nasty contaminants. Much more to come from this technology.<\/p>\n<p><strong>Author: <\/strong>Bj\u00f6rn Pfund, Debora M. Steffen, Mirjam R. Schreier, Maria-Sophie Bertrams, Chen Ye, Karl B\u00f6rjesson, Oliver S. Wenger, and Christoph Kerzig<br \/><strong>Ref:<\/strong> <em>J. Am. Chem. Soc.<\/em>2020, 142, 23, 10468\u201310476<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c02835\">https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c02835<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/J_A_C_S\/status\/1267497445954633729\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-8806\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper-20-image.jpg\" alt=\"\" width=\"437\" height=\"299\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper-20-image.jpg 437w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper-20-image-300x205.jpg 300w\" sizes=\"(max-width: 437px) 100vw, 437px\" \/><\/a><\/p>\n<p>&nbsp;<\/p>\n<h4><em>So many great papers like we said earlier, so we thought we&rsquo;d be like 2020 and have this article seemingly never end&#8230;<\/em><\/h4>\n<h3><em><strong>21: Rapid High-Resolution Visible Light 3D Printing<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>Some of us use 3D printers to make photoreactors to run photocatalysis. Some people using photoredox to 3D print. The circle of life.<\/p>\n<p><strong>Authors: <\/strong>Dowon Ahn, Lynn M. Stevens, Kevin Zhou, and Zachariah A. Page<br \/><strong>Ref:<em> <\/em><\/strong><em>ACS Cent. Sci.<\/em>2020, 6, 9, 1555\u20131563<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.0c00929\">https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.0c00929<\/a><\/p>\n<h3><em><strong>22: Photocatalytic \u03b1-Tertiary Amine Synthesis via C\u2013H Alkylation of Unmasked Primary Amines<\/strong><\/em><\/h3>\n<p><strong>Our Take<\/strong>: First paper from the Cresswell group early this year. Congrats. Check out their photo page (<a href=\"https:\/\/cresswell-lab.wixsite.com\/cresswellgroup\/photos\">https:\/\/cresswell-lab.wixsite.com\/cresswellgroup\/photos<\/a>). Also, we retroactively assign Photochemistry Achievement of the Year for 2019 to this&#8230;<a href=\"https:\/\/twitter.com\/Cresswellgroup\/status\/1194636451071180801\"> incredible, edible lab diorama<\/a>.<\/p>\n<p><strong>Authors: <\/strong>Alexander James Cresswell, Alison Ryder, William Cunningham, George Ballantyne, Tom Mules, Anna Kinsella, Jacob Turner-Dore, Catherine Alder, Lee Edwards, Blandine McKay, and Matthew Grayson<br \/><strong>Ref: <\/strong><em>Angew. Chem. Int. Ed.,<\/em> 2020, 59, 14986-14991.<br \/><strong>Link: <\/strong><a href=\"https:\/\/doi.org\/10.1002\/anie.202005294\">https:\/\/doi.org\/10.1002\/anie.202005294<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/Cresswellgroup\/status\/1259884607513780226\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-8808\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper22-image.jpg\" alt=\"\" width=\"399\" height=\"338\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper22-image.jpg 399w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper22-image-300x254.jpg 300w\" sizes=\"(max-width: 399px) 100vw, 399px\" \/><\/a><\/p>\n<h3><em><strong>And to close, a few reviews for the year&#8230;<\/strong><\/em><\/h3>\n<h3><em><strong>Visible-Light Photocatalysis as an Enabling Technology for Drug Discovery: A Paradigm Shift for Chemical Reactivity<\/strong><\/em><\/h3>\n<p><strong>Our Take:<\/strong> Nice review with a summary of photocatalysis platforms within drug discovery programs.<\/p>\n<p><strong>Authors: <\/strong>Peijun LiPeijun Li, Jack A. Terrett, and Jason R. Zbieg<br \/><strong>Ref:<em> <\/em><\/strong><em>ACS Med. Chem. Lett.<\/em>2020, 11, 11, 2120\u20132130<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsmedchemlett.0c00436\">https:\/\/pubs.acs.org\/doi\/10.1021\/acsmedchemlett.0c00436<\/a><\/p>\n<p><strong>Tweet:<\/strong><\/p>\n<p><a href=\"https:\/\/twitter.com\/J2_Mousseau\/status\/1319272028986314752\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-8811\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/review.jpg\" alt=\"\" width=\"351\" height=\"372\" srcset=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/review.jpg 351w, https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/review-283x300.jpg 283w\" sizes=\"(max-width: 351px) 100vw, 351px\" \/><\/a><\/p>\n<h3><em>Stereoinduction in Metallaphotoredox Catalysis<\/em><\/h3>\n<p><strong>Our Take:<\/strong> Summary of the state of art in chiral photoredox reactions.<\/p>\n<p><strong>Authors: <\/strong>Alexander Lipp, Shorouk O. Badir, and Gary A. Molander<br \/><strong>Ref: <\/strong><em>Angewandte Chemie Int. Ed. <\/em>2020, ASAP<br \/><strong>Link: <\/strong><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202007668\">https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202007668<\/a><\/p>\n<h3><em><strong>Light-Triggered Click Chemistry<\/strong><\/em><\/h3>\n<p><strong>Comment: <\/strong>A good summary of the current state of the art in light activated click chemistry<\/p>\n<p><strong>Authors: <\/strong>Gangam Srikanth Kumar and Qing Lin<br \/><strong>Ref: <\/strong><em>Chem. Rev. <\/em>2020, ASAP<br \/><strong>Link: <\/strong><a href=\"https:\/\/dx.doi.org\/10.1021\/acs.chemrev.0c00799\">https:\/\/dx.doi.org\/10.1021\/acs.chemrev.0c00799<\/a><\/p>\n<h3><strong><em>Light-Promoted Organic Transformations Utilizing Carbon-Based Gas Molecules as Feedstocks<\/em><\/strong><\/h3>\n<p><strong>Our Take: <\/strong>Summary of the state of the art in photochemical reactions using feedstocks.<\/p>\n<p><strong>Authors: <\/strong>Bin Cai, Han Wen Cheo, Tao Liu, and Jie Wu<br \/><strong>Ref: <\/strong><em>Angewandte Chemie Int. Ed., <\/em>2020, ASAP<br \/><strong>Link: <\/strong><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202010710\">https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202010710<\/a><\/p>\n<h3><em><strong>New Redox Strategies in Organic Synthesis by Means of Electrochemistry and Photochemistry<\/strong><\/em><\/h3>\n<p><strong>Our Take: <\/strong>A good review combining the topics of electrochemistry and photochemistry.<\/p>\n<p><strong>Authors: <\/strong>Jinjian Liu, Lingxiang Lu, Devin Wood, and Song Lin<br \/><strong>Ref: <\/strong><em>ACS Cent. Sci.<\/em>2020, 6, 8, 1317\u20131340<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.0c00549\">https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.0c00549<\/a><\/p>\n<h3><em><strong>If you made it this far, thanks for reading and hope you enjoyed! <\/strong><\/em><\/h3>\n<h3><em><strong>Hope everyone out there has a great end of 2020 and we look forward to hearing from you in 2021.<\/strong><\/em><\/h3>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Many of these papers move the field farther into unimaginable areas, while others find photochemical replacements for traditional reactions solving an unmet need.<\/p>\n","protected":false},"author":1,"featured_media":24934,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"<p><strong>Year in review 2020.\u00a0 Let\u2019s all agree to not look back.\u00a0 20 papers for 2020<\/strong><\/p>[caption id=\"attachment_8813\" align=\"alignright\" width=\"300\"]<img class=\"wp-image-8813 size-medium\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/front-image-feature-300x225.png\" alt=\"sarcastic 2020 logo\" width=\"300\" height=\"225\" \/> Unofficially the Official Logo of 2020...[\/caption]<p>As the year comes to the close, we thought it was time to have a little fun and look back at the year in photochemistry.\u00a0 2020 was a big year for us at HepatoChem under some trying circumstances.\u00a0 Before we move forward to 2021 with the launch of some exciting new equipment and products, we thought that we would look back at some of our favorite photochemistry work in the literature from the past year.\u00a0 A quick search finds a few thousand (photoredox, photocatalysis, photochemistry, metallaphotoredox) papers so far in 2020 and with(out lifting a finger to verify) very little research effort we\u2019re willing to bet that this is more than in 2019.\u00a0 \u00a0Many of the papers on the list break ground and move the field farther into unimaginable areas, while others find photochemical replacements for traditional reactions solving some unmet need. \u00a0\u00a0A few papers are outside the realm of topics that most of us spend any time thinking about but demonstrate the power of photochemistry. \u00a0Some of the papers also include nice pictures of EvoluChem photoreactors and equipment and deserve a shout out.\u00a0 And a few others are just plain weird.\u00a0 And let\u2019s face it, 2020 was weird for all of us.<\/p><p>If you think we\u2019ve missed your favorite paper or just want to send along an example of your work that you want us to recognize or recognize in the future, send us an email or respond to the tweet for this article (<a href=\"https:\/\/twitter.com\"><strong>#photoredox20for2020<\/strong><\/a>)\u00a0 If you disagree with the list, let us know how we screwed up by <span style=\"text-decoration: underline;\">sending us an email here<\/span>.<\/p><p>To get started, a few FAQ about how we generated this list.<\/p><p><strong>What are the criteria for inclusion?<\/strong><\/p><p>Each paper probably uses light in some way, either a bulb, LED, laser or sunlight.\u00a0 We started this exercise without any particular standards or criteria, other than the goal to share the papers we enjoyed (the most) and to make it fun. \u00a0\u00a0It then became readily apparent that there were far more than 20 papers worthy to be included, because there was a ridiculous amount of good work put out this year.\u00a0 So, at a certain point we just stopped adding more. \u00a0Some of the work will likely be familiar to anyone used to the photochemical field; however, in our fake scoring system bonus points were given for open access papers and work from new professors.<\/p><p><strong>Why 20 papers?<\/strong><\/p><p>The year is 2020, I can\u2019t believe you asked this question.<\/p><p><strong>Are there 20 papers listed?<\/strong><\/p><p>No, there are probably more or maybe less.\u00a0 You\u2019ll need to read and count the entire list to find out.<\/p><p><strong>Is there a vote for best photochemistry achievement of 2020?<\/strong><\/p><p>No.\u00a0 Awards are stupid.\u00a0 Do you really think we want to deal with running an internet voting poll and awarding photoredox achievement of the year to this?\u00a0 <a href=\"https:\/\/www.youtube.com\/watch?v=vfLZOkn0chc\">https:\/\/www.youtube.com\/watch?v=vfLZOkn0chc<strong>\u00a0<\/strong><\/a><\/p><p><strong>Do the links for each article work?<\/strong><\/p><p>Sometimes, when formatting an email or a links on website, links go to the wrong place.\u00a0 You can either be confused by this, email us and complain.\u00a0 Or use google and find the correct article.\u00a0 Your choice.\u00a0 Other times, links go to wrong place intentionally and you might find something fun.<\/p><p><strong>Do I win a prize if I click on each article?<\/strong><\/p><p>You\u2019ll have to click on each article to find out.<\/p><p><strong>How do I get my work on the 21 for 2021 list?<\/strong><\/p><p><a href=\"\/photoreactors-leds-accessories\/\">Go here and get to work<\/a>. \u00a0\u00a0Send us the paper once you\u2019ve submitted.<\/p><p><strong>In no particular order, here are our 20 favorite photochemistry papers for 2020.<\/strong><\/p><h3><em><strong>1: Organocatalyzed Birch Reduction Driven by Visible Light<\/strong><\/em><\/h3><p><strong>Our Take:\u00a0 <\/strong>We wrote about <a href=\"https:\/\/hepatochem.com\/multi-photon-approaches-to-synthetic-photochemistry\/\"><span style=\"text-decoration: underline;\">this one back here<\/span><\/a>.\u00a0 Just an incredible achievement to find this much reduction potential in a photocatalytic reaction with mild conditions.\u00a0 Unless you prefer running reactions with liquid ammonia.<\/p><p><strong>Authors:\u00a0 <\/strong>Justin P. Cole, Dian-Feng Chen, Max Kudisch, Ryan M. Pearson, Chern-Hooi Lim, and Garret M. Miyake<br \/><strong>Ref:\u00a0 <\/strong><em>J. Am. Chem. Soc.<\/em>\u00a02020, 142, 31, 13573\u201313581<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.0c05899\">https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.0c05899<\/a><\/p><p><strong>Tweet:<br \/><a href=\"https:\/\/twitter.com\/J_A_C_S\/status\/1291105492627009537\"><img class=\"aligncenter wp-image-8787 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper1-tweet.png\" alt=\"\" width=\"594\" height=\"516\" \/><\/a><\/strong><\/p><p>\u00a0<\/p><h3><em><strong>2: Development of a Platform for Near-Infrared Photoredox Catalysis<\/strong><\/em><\/h3><p><strong>Our Take:\u00a0 <\/strong>Another paper <span style=\"text-decoration: underline;\"><a href=\"https:\/\/hepatochem.com\/red-light-applications-in-photochemistry\/\">we wrote about before<\/a><\/span>.\u00a0 Check this one out to discover all the reasons your favorite photochemical reaction might be better run with a red LED.<\/p><p><strong>Authors:\u00a0 <\/strong>Benjamin D. Ravetz, Nicholas E. S. Tay, Candice L. Joe, Melda Sezen-Edmonds, Michael A. Schmidt, Yichen Tan, Jacob M. Janey, Martin D. Eastgate, and Tomislav Rovis<br \/><strong>Ref:\u00a0 <\/strong><em>ACS Cent. Sci.<\/em>\u00a02020, 6, 11, 2053\u20132059<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acscentsci.0c00948\">https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acscentsci.0c00948<\/a><\/p><p><strong>Tweet:\u00a0<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/ACSCentSci\/status\/1321784516760031233\"><img class=\"aligncenter wp-image-8788 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper2-tweet.png\" alt=\"\" width=\"593\" height=\"664\" \/><\/a><\/p><h3><em><strong>3: Chemistry glows green with photoredox catalysis\u00a0<\/strong><\/em><\/h3><p><strong>Our Take:\u00a0 <\/strong>A quick note on the efficiency and sustainability of photoredox catalysis<\/p><p><strong>Authors:\u00a0 <\/strong>Giacomo E.M. Crisenza, Paolo Melchiorre<br \/><strong>Ref:\u00a0 <\/strong><em>Nature Communications<\/em>, 2020, 11, Article 803<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/www.nature.com\/articles\/s41467-019-13887-8\">https:\/\/www.nature.com\/articles\/s41467-019-13887-8<\/a><\/p><p><a href=\"https:\/\/twitter.com\/MelchiorreGroup\/status\/1225486686047612930\"><img class=\"aligncenter wp-image-8789 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper3-tweet.png\" alt=\"\" width=\"392\" height=\"780\" \/><\/a><\/p><h3><em><strong>4: Photons as a 21st century reagent<\/strong><\/em><\/h3><p><strong>Our Take: \u00a0<\/strong>Please read this paper. \u00a0Everyone should treat light as a reagent like you would treat any other reagent in a chemical reaction.\u00a0 To repeat again, everyone should treat light as a reagent like you would treat any other reagent in your reaction.<\/p><p><strong>Authors:\u00a0 <\/strong>Holly E. Bonfield, Thomas Knauber, Fran\u00e7ois L\u00e9vesque, Eric G. Moschetta, Flavien Susanne & Lee J. Edwards<br \/><strong>Ref:\u00a0 <\/strong>Nature Communications, 2020, 11, Article number 804<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/www.nature.com\/articles\/s41467-019-13988-4\">https:\/\/www.nature.com\/articles\/s41467-019-13988-4<\/a><\/p><p><a href=\"https:\/\/www.nature.com\/articles\/s41467-019-13988-4\"><img class=\"aligncenter wp-image-8790 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper4-image.png\" alt=\"\" width=\"716\" height=\"457\" \/><\/a><\/p><h3><strong><em>5: Three-Component Three-Bond Forming Cascade via Palladium Photoredox Catalysis (open access)<\/em><br \/><\/strong><\/h3><p><strong>Our Take<\/strong>:\u00a0 Look at that cool photochemical flow cell setup.\u00a0 I wonder who makes that?<\/p><p><strong>Authors:\u00a0 <\/strong>Peter Bellotti, Maximilian Koy, Christian Gutheil, Steffen Heuvel and Frank Glorius<br \/><strong>Ref:\u00a0 <\/strong><em>Chemical Science, <\/em>2020, ASAP<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2021\/sc\/d0sc05551d#!divAbstract\">https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2021\/sc\/d0sc05551d#!divAbstract<\/a><\/p><p><strong>Tweet:\u00a0 <\/strong><\/p><p><a href=\"https:\/\/twitter.com\/GloriusGroup\/status\/1337074033037291528\"><img class=\"aligncenter wp-image-8791 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper5-image.jpg\" alt=\"\" width=\"407\" height=\"325\" \/><\/a><\/p><p><img class=\"aligncenter size-medium wp-image-8809\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/glorious-group-paper-duo-with-flow-300x201.png\" alt=\"\" width=\"300\" height=\"201\" \/><\/p><h3><em><strong>6: Metallaphotoredox aryl and alkyl radiomethylation for PET ligand discovery<\/strong><\/em><\/h3><p><strong>Our Take:<\/strong>\u00a0 Amazing work from a collaboration between the Macmillan lab at Princeton with Merck, UPenn and RTI International for last state fast radiolabeling of pharmaceutically relevant compounds.<\/p><p><strong>Authors: <\/strong>Robert W. Pipal, Kenneth T. Stout, Patricia Z. Musacchio, Sumei Ren, Thomas J. A. Graham, Stefan Verhoog, Liza Gantert, Talakad G. Lohith, Alexander Schmitz, Hsiaoju S. Lee, David Hesk, Eric D. Hostetler, Ian W. Davies & David W. C. MacMillan<br \/><strong>Ref:\u00a0 <\/strong><em>Nature, <\/em>2020, 6797<em>.<br \/><\/em><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/www.nature.com\/articles\/s41586-020-3015-0\">https:\/\/www.nature.com\/articles\/s41586-020-3015-0<\/a><\/p><p><strong>Tweet:<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/MacMillan_Lab\/status\/1331643372084338689\"><img class=\"aligncenter wp-image-8792 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper6-image.jpg\" alt=\"\" width=\"500\" height=\"346\" \/><\/a><\/p><h3><em><strong>7: Synthesis of azetidines via visible-light-mediated intermolecular [2+2] photocycloadditions<\/strong><\/em><\/h3><p><strong>Our Take:\u00a0\u00a0 <\/strong>Very interesting work making highly strained four-membered ring building blocks photochemically.<\/p><p><strong>Author:\u00a0 <\/strong>Marc R. Becker, Emily R. Wearing & Corinna S. Schindler<br \/><strong>Ref:\u00a0 <\/strong><em>Nature Chemistry, <\/em><strong>12<\/strong>, 898-905 (2020)<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/www.nature.com\/articles\/s41557-020-0541-1\">https:\/\/www.nature.com\/articles\/s41557-020-0541-1<\/a><\/p><p><strong>Tweet:<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/NatureChemistry\/status\/1313031198357311493\"><img class=\"aligncenter wp-image-8793 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper7-image.jpg\" alt=\"\" width=\"363\" height=\"313\" \/><\/a><\/p><h3><em><strong>8: U.S. Food and Drug Administration-Certified Food Dyes as Organocatalysts in the Visible Light-Promoted Chlorination of Aromatics and Heteroaromatics<\/strong><\/em><\/h3><p><strong>Our Take:<\/strong>\u00a0 While it was the weirdness of the title that caught our eye here, being able to use non-toxic catalysts that are produced cheaply in metric ton quantities to do important chemistry is certainly valuable.\u00a0 There is only so much iridium out there for everyone else to use.<\/p><p><strong>Authors:\u00a0 <\/strong>David A. Rogers, Megan D. Hopkins, Nitya Rajagopal, Dhruv Varshney, Haley A. Howard, Gabriel LeBlanc*, and Angus A. Lamar*<br \/><strong>Ref:\u00a0 <\/strong><em>ACS Omega<\/em>, 2020, 5, 13, 7693-7704<br \/><strong>Link: <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.0c00631\">https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.0c00631<\/a><\/p><p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.0c00631\"><img class=\"aligncenter wp-image-8794 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper8-image.jpg\" alt=\"\" width=\"438\" height=\"293\" \/><\/a><\/p><h3><strong><em>9: LED\u2010NMR Monitoring of an Enantioselective Catalytic [2+2] Photocycloaddition<\/em>\u00a0<\/strong><\/h3><p><strong>Our Take:<\/strong>\u00a0 Oh, how far we\u2019ve come.<strong>\u00a0 <\/strong>So, we\u2019re using LED\u2019s inside of NMRs now to study enantioselective photochemical reaction mechanisms for rapid reactions that are complete in under 5 minutes?\u00a0 WTF.\u00a0 It\u2019s a shame that everyone says all this photochemistry stuff won\u2019t scale up or else this field might really catch on\u2026.<\/p><p><strong>Authors:\u00a0 <\/strong>Kazimer L. Skubi, Wesley B. Swords, Heike Hofstetter, and Tehshik P. Yoon<br \/><strong>Ref:\u00a0 <\/strong><em>ChemPhotoChem<\/em> 2020, (4), 685-690.<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cptc.202000094\">https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cptc.202000094<\/a><\/p><p><strong>Tweet:\u00a0<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/TehshikYoon\/status\/1266216444896972800\"><img class=\"aligncenter wp-image-8795 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper9-image.jpg\" alt=\"\" width=\"372\" height=\"289\" \/><\/a><\/p><h3><em><strong>10: Upscaling Photoredox Cross-Coupling Reactions in Batch Using Immersion-Well Reactors<\/strong><\/em><\/h3><p><strong>Our Take:<\/strong>\u00a0 Ok, fine.\u00a0 You\u2019ve made a few tens of grams of your product with LED\u2019s.\u00a0 Are you sure you can really scale up this thing for something useful?<\/p><p><strong>Authors:\u00a0 <\/strong>Isabelle Grimm, Simone T. Hauer, Tim Schulte, Gina Wycich, Karl D. Collins, Kai Lovis, and Lisa Candish<br \/><strong>Ref:\u00a0 <\/strong><em>Org. Process Res. Dev. <\/em>2020, 24, 6, 1185-1193.<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/dx.doi.org\/10.1021\/acs.oprd.0c00070\">https:\/\/dx.doi.org\/10.1021\/acs.oprd.0c00070<\/a><\/p><p><strong>Tweet:<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/OPRD_ACS\/status\/1256268734978613250\"><img class=\"aligncenter wp-image-8796 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper10-image.jpg\" alt=\"\" width=\"397\" height=\"281\" \/><\/a><\/p><h3><strong><em>11: Development and Execution of a Production-Scale Continuous [2 + 2] Photocycloaddition<\/em><br \/><\/strong><\/h3><p><strong>Our Take:<\/strong>\u00a0 5 kg\/day.\u00a0 We good now?\u00a0 Have we settled this yet?\u00a0 If not convinced, you can find many more scale up success stories.<\/p><p><strong>Authors:\u00a0 <\/strong>Matthew G. Beaver, En-xuan Zhang, Zhi-qing Liu, Song-yuan Zheng, Bin Wang, Jiang-ping Lu, Jian Tao, Miguel Gonzalez, Si\u00e2n Jones, and Jason S. Tedrow<br \/><strong>Ref: <\/strong><em>Org. Process Res. Dev.<\/em>\u00a02020, 24, 10, 2139\u20132146<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.0c00185\">https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.0c00185<\/a><\/p><p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.0c00185\"><img class=\"aligncenter wp-image-8797 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper11-image.jpg\" alt=\"\" width=\"343\" height=\"230\" \/><\/a><\/p><h3><strong><em>12: C(sp3)\u2013H functionalizations of light hydrocarbons using decatungstate photocatalysis in flow<\/em><\/strong><\/h3><p><strong>Our Take:<\/strong>\u00a0 Very cool work using a cheap photocatalyst for activation of light alkanes including methane.<\/p><p><strong>Authors:\u00a0 <\/strong>Gabriele Laudadio, Yuchao Deng, Klaas van der Wal, Davide Ravelli, Manuel Nu\u00f1o, Maurizio Fagnoni, Duncan Guthrie, Yuhan Sun, Timothy No\u00ebl<br \/><strong>Ref:\u00a0 <\/strong><em>Science, <\/em>2020, (369), 92-96.<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/science.sciencemag.org\/content\/369\/6499\/92\/tab-pdf\">https:\/\/science.sciencemag.org\/content\/369\/6499\/92\/tab-pdf<\/a><\/p><p><strong>Tweet:<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/NoelGroupUvA\/status\/1328417129755004929\"><img class=\"aligncenter wp-image-8798 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper12-image.jpg\" alt=\"\" width=\"400\" height=\"182\" \/><\/a><\/p><h3><strong><em>13: Organocatalytic Approach to Photochemical Lignin Fragmentation<\/em><\/strong><\/h3><p><strong>Our Take:\u00a0 <\/strong>Metal-free reductive cleavage of lignin using an organic photocatalyst.<\/p><p><strong>Authors <\/strong>Cheng Yang, Markus D. Ka\u0308rka\u0308s, Gabriel Magallanes, Kimberly Chan, and Corey R. J. Stephenson<br \/><strong>Ref:\u00a0 <\/strong><em>Org. Lett.<\/em>\u00a0 2020, 22, 20, 8082\u20138085<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c03029\"><strong>https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c03029<\/strong><\/a><\/p><p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c03029\"><img class=\"aligncenter wp-image-8799 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper13-image.gif\" alt=\"\" width=\"500\" height=\"137\" \/><\/a><\/p><h3><strong><em>14: Discovery of Key TIPS\u2010Naphthalene for Efficient Visible\u2010to\u2010UV Photon Upconversion under Sunlight and Room Light<\/em><\/strong><\/h3><p><strong>Our Take:<\/strong>\u00a0 Harvesting low energy sunlight and turning it into localized higher energy UV light.\u00a0 I\u2019m sure we can find a few applications for this technology.\u00a0 Just a guess.<\/p><p><strong>Authors:\u00a0 <\/strong>Naoyuki Harada, Yoichi Sasak, Masanori Hosoyamada, Nobuo Kimizuka and Nobuhiro Yanai<br \/><strong>Ref:\u00a0 <\/strong><em>Angewandte Int. Ed., <\/em>2020, ASAP.<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202012419\">https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202012419<\/a><\/p><p><strong>Tweet:<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/NobuhiroYanai\/status\/1316975376070049792\"><img class=\"aligncenter wp-image-8800 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper14-image.jpg\" alt=\"\" width=\"311\" height=\"407\" \/><\/a><\/p><h3><strong><em>15: Potent Reductants via Electron-Primed Photoredox Catalysis: Unlocking Aryl Chlorides for Radical Coupling<\/em><\/strong><\/h3><p><strong>Our Take:\u00a0 <\/strong>Electrochemistry and Photochemistry, together?\u00a0 That\u2019s two things in this paper for old-school chemists to complain about.<\/p><p><strong>Authors:\u00a0 <\/strong>Nicholas G. W. Cowper, Colleen P. Chernowsky, Oliver P. Williams, and Zachary K. Wickens<br \/><strong>Ref:\u00a0 <\/strong><em>J. Am. Chem. Soc.<\/em>\u00a02020, 142, 5, 2093\u20132099<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.9b12328\">https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.9b12328<\/a><\/p><p><strong>Tweet: <\/strong><\/p><p><a href=\"https:\/\/twitter.com\/ZachWickens\/status\/1218277248681144320\"><img class=\"aligncenter wp-image-8801 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper15-image.jpg\" alt=\"\" width=\"414\" height=\"351\" \/><\/a><\/p><h3><em><strong>16: Efficient Photoredox-Mediated C\u2013C Coupling Organic Synthesis and Hydrogen Production over Engineered Semiconductor Quantum Dots<\/strong><\/em><\/h3><p><strong>Our Take:<\/strong>\u00a0 The title could use more buzzwords, but the technology is very cool.<\/p><p><strong>Authors:<\/strong>\u00a0 Ming-Yu Qi, Yue-Hua Li, Masakazu Anpo, Zi-Rong Tang, and Yi-Jun Xu<br \/><strong>Ref:<\/strong><em> ACS Catal.<\/em>\u00a02020, 10, 23, 14327\u201314335<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c04237\">https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c04237<\/a><\/p><p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c04237\"><img class=\"aligncenter wp-image-8802 size-full\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper16-image.gif\" alt=\"\" width=\"500\" height=\"279\" \/><\/a><\/p><h3><strong><em>17: Hydroarylation of Arenes via Reductive Radical-Polar Crossover<\/em><br \/><\/strong><\/h3><p><strong>Our Take:\u00a0 <\/strong>Very useful reaction for dearomatization without H2, metals or low temperatures.<\/p><p><strong>Authors:\u00a0 <\/strong>Autumn R. Flynn, Kelly A. McDaniel, Meredith E. Hughes, David B. Vogt, and Nathan T. Jui<br \/><strong>Ref:<\/strong><em> J. Am. Chem. Soc.<\/em>\u00a02020, 142, 20, 9163\u20139168<br \/><strong>Link:<\/strong>\u00a0 <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c03926\">https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c03926<\/a><\/p><p><strong>Tweet:\u00a0 <\/strong><\/p><p><a href=\"https:\/\/twitter.com\/TotalSyntheses\/status\/1260421923734982656\"><img class=\"aligncenter size-full wp-image-8803\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper17-image.png\" alt=\"\" width=\"474\" height=\"402\" \/><\/a><\/p><h3><em><strong>18: Development of a Large-Enrollment Course-Based Research Experience in an Undergraduate Organic Chemistry Laboratory: Structure\u2013Function Relationships in Pyrylium Photoredox Catalysts<\/strong><\/em><\/h3><p><strong>Comment:\u00a0 <\/strong>Adding photochemistry to the undergraduate curriculum is incredibly important, specifically experiments for undergraduate lab.<\/p><p><strong>Authors:\u00a0 <\/strong>Cole L. Cruz, Natalie Holmberg-Douglas, Nicholas P. R. Onuska, Joshua B. McManus, Ian A. MacKenzie, Bryant L. Hutson, Nita A. Eskew, and David A. Nicewicz<br \/><strong>Ref:\u00a0 <\/strong>J. <em>Chem. Educ<\/em>. 2020, 97, 6, 1572\u20131578<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jchemed.9b00786\">https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jchemed.9b00786<\/a><\/p><p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jchemed.9b00786\"><img class=\"aligncenter size-full wp-image-8804\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper18-image.gif\" alt=\"\" width=\"500\" height=\"307\" \/><\/a><\/p><h3><em><strong>19: High-throughput Synthesis and Screening of Iridium(III) Photocatalysts for the Fast and Chemoselective Dehalogenation of Aryl Bromides<\/strong><\/em><\/h3><p><strong>Our Take:\u00a0 <\/strong>A rapid assay for screening over 1,000 unique iridium catalysts from the lab that first synthesized several of the most commonly used Iridium catalysts used today over a decade ago.<\/p><p><strong>Authors:\u00a0 <\/strong>Velabo Mdluli, Stephen Diluzio, Jacqueline Lewis, Jakub F. Kowalewski, Timothy U. Connell, David Yaron, Tomasz Kowalewski, and Stefan Bernhard<br \/><strong>Ref:\u00a0 <\/strong><em>ACS Catal<\/em>. 2020, 10, 13, 6977\u20136987<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c02247\">https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c02247<\/a><\/p><p><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.0c02247\"><img class=\"aligncenter size-full wp-image-8805\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper19-image.gif\" alt=\"\" width=\"500\" height=\"243\" \/><\/a><\/p><h3><em><strong>20: UV Light Generation and Challenging Photoreactions Enabled by Upconversion in Water<\/strong><\/em><\/h3><p><strong>Our Take: <\/strong>Blue to UV-upconversion in water.\u00a0 Water-soluble iridium catalysts.\u00a0 Degradation of some pretty nasty contaminants.\u00a0\u00a0\u00a0 Much more to come from this technology.<\/p><p><strong>Author:\u00a0 <\/strong>Bj\u00f6rn Pfund, Debora M. Steffen, Mirjam R. Schreier, Maria-Sophie Bertrams, Chen Ye, Karl B\u00f6rjesson, Oliver S. Wenger, and Christoph Kerzig<br \/><strong>Ref:<\/strong>\u00a0 <em>J. Am. Chem. Soc.<\/em>\u00a02020, 142, 23, 10468\u201310476<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c02835\">https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.0c02835<\/a><\/p><p><strong>Tweet:\u00a0<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/J_A_C_S\/status\/1267497445954633729\"><img class=\"aligncenter size-full wp-image-8806\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper-20-image.jpg\" alt=\"\" width=\"437\" height=\"299\" \/><\/a><\/p><p>\u00a0<\/p><h4><em>So many great papers like we said earlier, so we thought we'd be like 2020 and have this article seemingly never end...<\/em><\/h4><h3><em><strong>21: Rapid High-Resolution Visible Light 3D Printing<\/strong><\/em><\/h3><p><strong>Our Take:\u00a0 <\/strong>Some of us use 3D printers to make photoreactors to run photocatalysis.\u00a0 Some people using photoredox to 3D print.\u00a0 The circle of life.<\/p><p><strong>Authors:\u00a0 <\/strong>Dowon Ahn, Lynn M. Stevens, Kevin Zhou, and Zachariah A. Page<br \/><strong>Ref:<em>\u00a0 <\/em><\/strong><em>ACS Cent. Sci.<\/em>\u00a02020, 6, 9, 1555\u20131563<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.0c00929\">https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.0c00929<\/a><\/p><h3><em><strong>22: Photocatalytic \u03b1-Tertiary Amine Synthesis via C\u2013H Alkylation of Unmasked Primary Amines<\/strong><\/em><\/h3><p><strong>Our Take<\/strong>: First paper from the Cresswell group early this year.\u00a0 Congrats.\u00a0 Check out their photo page (<a href=\"https:\/\/cresswell-lab.wixsite.com\/cresswellgroup\/photos\">https:\/\/cresswell-lab.wixsite.com\/cresswellgroup\/photos<\/a>).\u00a0 Also, we retroactively assign Photochemistry Achievement of the Year for 2019 to this...<a href=\"https:\/\/twitter.com\/Cresswellgroup\/status\/1194636451071180801\"> incredible, edible lab diorama<\/a>.<\/p><p><strong>Authors:\u00a0 <\/strong>Alexander James Cresswell, Alison Ryder, William Cunningham, George Ballantyne, Tom Mules, Anna Kinsella, Jacob Turner-Dore, Catherine Alder, Lee Edwards, Blandine McKay, and Matthew Grayson<br \/><strong>Ref:\u00a0 <\/strong><em>Angew. Chem. Int. Ed.,<\/em> 2020, 59, 14986-14991.<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/doi.org\/10.1002\/anie.202005294\">https:\/\/doi.org\/10.1002\/anie.202005294<\/a><\/p><p><strong>Tweet:\u00a0\u00a0<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/Cresswellgroup\/status\/1259884607513780226\"><img class=\"aligncenter size-full wp-image-8808\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/paper22-image.jpg\" alt=\"\" width=\"399\" height=\"338\" \/><\/a><\/p><h3><em><strong>And to close, a few reviews for the year...<\/strong><\/em><\/h3><h3><em><strong>Visible-Light Photocatalysis as an Enabling Technology for Drug Discovery: A Paradigm Shift for Chemical Reactivity<\/strong><\/em><\/h3><p><strong>Our Take:<\/strong>\u00a0 Nice review with a summary of photocatalysis platforms within drug discovery programs.<\/p><p><strong>Authors:\u00a0 <\/strong>Peijun LiPeijun Li, Jack A. Terrett, and Jason R. Zbieg<br \/><strong>Ref:<em>\u00a0 <\/em><\/strong><em>ACS Med. Chem. Lett.<\/em>\u00a02020, 11, 11, 2120\u20132130<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsmedchemlett.0c00436\">https:\/\/pubs.acs.org\/doi\/10.1021\/acsmedchemlett.0c00436<\/a><\/p><p><strong>Tweet:\u00a0\u00a0<\/strong><\/p><p><a href=\"https:\/\/twitter.com\/J2_Mousseau\/status\/1319272028986314752\"><img class=\"aligncenter size-full wp-image-8811\" src=\"https:\/\/hepatochem.com\/wp-content\/uploads\/2020\/12\/review.jpg\" alt=\"\" width=\"351\" height=\"372\" \/><\/a><\/p><h3><em>Stereoinduction in Metallaphotoredox Catalysis<\/em><\/h3><p><strong>Our Take:<\/strong>\u00a0 Summary of the state of art in chiral photoredox reactions.<\/p><p><strong>Authors:\u00a0 <\/strong>Alexander Lipp, Shorouk O. Badir, and Gary A. Molander<br \/><strong>Ref:\u00a0 <\/strong><em>Angewandte Chemie Int. Ed. <\/em>2020, ASAP<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202007668\">https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202007668<\/a><\/p><h3><em><strong>Light-Triggered Click Chemistry<\/strong><\/em><\/h3><p><strong>Comment:\u00a0 <\/strong>A good summary of the current state of the art in light activated click chemistry<\/p><p><strong>Authors:\u00a0 <\/strong>Gangam Srikanth Kumar and Qing Lin<br \/><strong>Ref:\u00a0 <\/strong><em>Chem. Rev. <\/em>2020, ASAP<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/dx.doi.org\/10.1021\/acs.chemrev.0c00799\">https:\/\/dx.doi.org\/10.1021\/acs.chemrev.0c00799<\/a><\/p><h3><strong><em>Light-Promoted Organic Transformations Utilizing Carbon-Based Gas Molecules as Feedstocks<\/em><\/strong><\/h3><p><strong>Our Take:\u00a0 <\/strong>Summary of the state of the art in photochemical reactions using feedstocks.<\/p><p><strong>Authors:\u00a0 <\/strong>Bin Cai, Han Wen Cheo, Tao Liu, and Jie Wu<br \/><strong>Ref:\u00a0 <\/strong><em>Angewandte Chemie Int. Ed., <\/em>2020, ASAP<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202010710\">https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.202010710<\/a><\/p><h3><em><strong>New Redox Strategies in Organic Synthesis by Means of Electrochemistry and Photochemistry<\/strong><\/em><\/h3><p><strong>Our Take:\u00a0 <\/strong>A good review combining the topics of electrochemistry and photochemistry.<\/p><p><strong>Authors:\u00a0 <\/strong>Jinjian Liu, Lingxiang Lu, Devin Wood, and Song Lin<br \/><strong>Ref:\u00a0 <\/strong><em>ACS Cent. Sci.<\/em>\u00a02020, 6, 8, 1317\u20131340<br \/><strong>Link:\u00a0 <\/strong><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.0c00549\">https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.0c00549<\/a><\/p><h3><em><strong>If you made it this far, thanks for reading and hope you enjoyed!\u00a0 <\/strong><\/em><\/h3><h3><em><strong>Hope everyone out there has a great end of 2020 and we look forward to hearing from you in 2021.<\/strong><\/em><\/h3><p>\u00a0<\/p><p>\u00a0<\/p><p>\u00a0<\/p><p>\u00a0<\/p><p>\u00a0<\/p>","_et_gb_content_width":"","_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[485,489,494,487],"tags":[500,491,493],"class_list":["post-24932","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-feature-1","category-featured-articles","category-humor","category-photoredox","tag-500","tag-photochemistry","tag-photoredox-catalysis"],"yoast_head":"<!-- This site is optimized with the Yoast SEO 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