GRK 1626:  Chemical Photocatalysis

• Subject Area: Molecular Chemistry
• Term: from 2010 to 2019
• Project identifier: Deutsche Forschungsgemeinschaft (DFG) - Project number 134471240

• Final Report Year: 2020

Final Report Abstract

Die Verwendung von Licht in der Synthesechemie hat im letzten Jahrzehnt eine enorme Renaissance erlebt. Die klassische Photochemie hat, beflügelt durch die Fortschritte in der Beleuchtungstechnik (Licht emittierende Dioden, LEDs), in der Mikroreaktionstechnik und durch die Nutzung von sichtbarem Licht für sensibilisierte photoinduzierte Energie- und Elektronentransferprozesse ein neues Niveau erreicht. Das Graduiertenkolleg „Chemische Photokatalyse“ hat diese Entwicklung von Anfang an begleitet und durch wesentliche Beiträge mit vorangetrieben. Die Bündelung von Expertise aus der Synthesechemie, der Photochemie, der Spektroskopie und der Computerchemie in einem national und international sichtbaren Forschungsschwerpunkt ermöglichte es unter anderem neue photochemische Reaktionsprinzipien unter Verwendung mehrerer Photonen, stereoselektive photochemische Synthesen, Photoreaktionen mit Kupferkomplexen, oder auch mit heterogenen Katalysatoren und Organokatalysatoren zu etablieren. Detaillierte mechanistische Untersuchungen für die auch neue Messapparaturen und Analyseverfahren entwickelt wurden, kennzeichnen viele Arbeiten des Graduiertenkollegs. Wichtige Reaktionsprinzipien und Syntheseanwendungen wurden gefunden, die u.a. in der Wirkstoffforschung Anwendungen finden und die Grundlage für die weitere Entwicklung des Forschungsgebietes bilden. Die Bilanz von über 270 wissenschaftlichen Publikationen und 73 abgeschlossenen Promotionen dokumentieren die sehr erfolgreiche Arbeit des Graduiertenkollegs.

Publications

• Photooxidation of Benzyl Alcohols with Immobilized Flavins. Adv. Synth. Cat. 2009, 351, 163-174
  H. Schmaderer, P. Hilgers, R. Lechner, B. König
  (See online at https://doi.org/10.1002/adsc.200800576)
• Transient memory effect in the photoluminescence of InGaN single quantum wells. Optics Express 2009, 17 (25), 22855-22860
  C. Feldmeier, M. Abiko, U. T. Schwarz, Y. Kawakami and R. Micheletto
  (See online at https://doi.org/10.1364/oe.17.022855)
• [2+2]-Photocycloaddition Reactions of Tetronic Acid Esters and Amides. Synthesis 2010, 2308-2312
  J. P. Hehn, D. Gamba-Sánchez, M. Kemmler, M. Fleck, B. Basler, T. Bach
  (See online at https://doi.org/10.1055/s-0029-1218793)
• A Theoretical Study on the Repair Mechanism of the (6-4) Photolesion by the (6-4) Photolyase. J. Am. Chem. Soc. 2010, 132, 16285-16295
  K. Sadeghian, M. Bocola, T. Merz and M. Schütz
  (See online at https://doi.org/10.1021/ja108336t)
• Green-light photocatalytic reduction using dye-sensitized TiO2 and transition metal nanoparticles. Green Chem. 2010, 400-406
  Stefan Füldner, Ralph Mild, Heiko Ingo Siegmund, Josef A. Schroeder, Michael Gruber and Burkhard König
  (See online at https://doi.org/10.1039/B918140G)
• Laboratory apparatus for the accurate, facile and rapid determination of visible light photoreaction quantum yields. Photochem. Photobiol. Sci. 2010, 9, 1400-1406
  Uwe Megerle, Robert Lechner, Burkhard König and Eberhard Riedle
  (See online at https://doi.org/10.1039/c0pp00195c)
• Laboratory apparatus for the accurate, facile and rapid determination of visible light photoreaction quantum yields. Photochem. Photobiol. Sci. 2010, 9, 1400-1406
  Uwe Megerle, Robert Lechner, Burkhard König and Eberhard Riedle
  (See online at https://doi.org/10.1039/c0pp00195c)
• Mechanism of signal transduction of the LOV2-Jα photosensor from Avena sativa. Nature Communications 2010, 1, 122
  Emanuel Peter, Bernhard Dick and Stephan A. Baeurle
  (See online at https://doi.org/10.1038/ncomms1121)
• Oxidation and Deprotection of Primary Benzyl Amines by Visible Light Flavin Photocatalysis. Synthesis 2010, 1712-1718
  Robert Lechner, Burkhard König
  (See online at https://doi.org/10.1055/s-0029-1218709)
• Visible light flavin photo-oxidation of methylbenzenes, styrenes and phenylacetic acids. Photochem. Photobiol. Sci. 2010, 9, 1367-1377
  R. Lechner, S. Kümmel, B. König
  (See online at https://doi.org/10.1039/c0pp00202j)
• Effect of computational methodology on the conformational dynamics of the protein photosensor LOV1 from Chlamydomonas reinhardtii. J. Chem. Biol. 2011, 4, 167-184
  E. Peter, Bernhard Dick, Stephan A. Baeurle
  (See online at https://doi.org/10.1007/s12154-011-0060-z)
• Enantioselective Intramolecular [2+2]-Photocycloaddition Reactions of 4- Substituted Quinolones Catalyzed by a Chiral Sensitizer with a Hydrogen- Bonding Motif. J. Am. Chem. Soc. 2011, 133, 16689-16697
  C. Müller, A. Bauer, M. M. Maturi, M. C. Cuquerella, M. A. Miranda, T. Bach
  (See online at https://doi.org/10.1021/ja207480q)
• Eosin Y Catalyzed Visible Light Oxidative C-C and C-P bond Formation. Org. Lett. 2011, 13, 3852-3855
  Durga Prasad Hari and Burkhard König
  (See online at https://doi.org/10.1021/ol201376v)
• Flavin-Induced DNA Photooxidation and Charge Movement Probed by Ultrafast Transient Absorption Spectroscopy. ChemBioChem 2011, 12, 703-706
  Matthias Wenninger, Danila Fazio, Uwe Megerle, Christian Trindler, Stefan Schiesser, Eberhard Riedle, and Thomas Carell
  (See online at https://doi.org/10.1002/cbic.201000730)
• Flavin-Induced DNA Photooxidation and Charge Movement Probed by Ultrafast Transient Absorption Spectroscopy. ChemBioChem 2011, 12, 703-706
  Matthias Wenninger, Danila Fazio, Uwe Megerle, Christian Trindler, Stefan Schiesser, Eberhard Riedle, and Thomas Carell
  (See online at https://doi.org/10.1002/cbic.201000730)
• Metal-Free, Cooperative Asymmetric Organophotoredox Catalysis with Visible Light. Angew. Chem. Int. Ed. 2011, 50, 951-954
  M. Neumann, S. Füldner, B. König, K. Zeitler
  (See online at https://doi.org/10.1002/anie.201002992)
• Metal-Free, Cooperative Asymmetric Organophotoredox Catalysis with Visible Light. Angew. Chem. Int. Ed. 2011, 50, 951-954. Synfacts 2010, 12, 1419 - 1419
  M. Neumann, S. Füldner, B. König, K. Zeitler
  (See online at https://doi.org/10.1002/anie.201002992)
• Polar Solvation Dynamics in Water and Methanol: Search for Molecularity. Phys. Chem. Chem. Phys. 2011, 13, 17768-17774
  M. Sajadi, M. Weinberger, H.-A. Wagenknecht, N. P. Ernsting
  (See online at https://doi.org/10.1039/C1CP21794A)
• Real-time near-field evidence of optical blinking in the photoluminescence of InGaN by scanning near-field optical microscope. Optical Materials Express 2011, 1 (2), 158 – 163
  K. Oikawa, C. Feldmeier, U. T. Schwarz, Y. Kawakami and R. Micheletto
  (See online at https://doi.org/10.1364/OME.1.000158)
• Selective Photocatalytic Reductions of Nitrobenzene Derivatives using PbBiO2X and Blue Light. Green Chem. 2011, 13, 640-643
  Stefan Füldner, Patrick Pohla, Hanna Bartling, Stephan Dankesreiter, Roland Stadler, Michael Gruber, Arno Pfitzner and Burkhard König
  (See online at https://doi.org/10.1039/C0GC00857E)
• Selective Photocatalytic Reductions of Nitrobenzene Derivatives using PbBiO2X and Blue Light. Green Chem. 2011, 13, 640-643
  Stefan Füldner, Patrick Pohla, Hanna Bartling, Stephan Dankesreiter, Roland Stadler, Michael Gruber, Arno Pfitzner and Burkhard König
  (See online at https://doi.org/10.1039/C0GC00857E)
• Selective Photocatalytic Reductions of Nitrobenzene Derivatives using PbBiO2X and Blue Light. Green Chem. 2011, 13, 640-643
  Stefan Füldner, Patrick Pohla, Hanna Bartling, Stephan Dankesreiter, Roland Stadler, Michael Gruber, Arno Pfitzner and Burkhard König
  (See online at https://doi.org/10.1039/C0GC00857E)
• Signals of LOV1: a computer simulation study on the wildtype LOV1- domain of Chlamydomonas reinhardtii and its mutants. J. Mol. Mod. 2011, 18, 1375-1388
  E. Peter, B. Dick, S. A. Baeurle
  (See online at https://doi.org/10.1007/s00894-011-1165-6)
• Unraveling the flavin-catalyzed photooxidation of benzylic alcohol with transient absorption spectroscopy from sub-pico- to microseconds. Phys. Chem. Chem. Phys. 2011, 13, 8869-8880
  Uwe Megerle, Matthias Wenninger, Roger-Jan Kutta, Robert Lechner, Burkhard König, Bernhard Dick, Eberhard Riedle
  (See online at https://doi.org/10.1039/c1cp20190e)
• Unraveling the flavin-catalyzed photooxidation of benzylic alcohol with transient absorption spectroscopy from sub-pico- to microseconds. Phys. Chem. Chem. Phys. 2011, 13, 8869-8880
  Uwe Megerle, Matthias Wenninger, Roger-Jan Kutta, Robert Lechner, Burkhard König, Bernhard Dick, Eberhard Riedle
  (See online at https://doi.org/10.1039/c1cp20190e)
• Unraveling the flavin-catalyzed photooxidation of benzylic alcohol with transient absorption spectroscopy from sub-pico- to microseconds. Phys. Chem. Chem. Phys. 2011, 13, 8869-8880
  Uwe Megerle, Matthias Wenninger, Roger-Jan Kutta, Robert Lechner, Burkhard König, Bernhard Dick, Eberhard Riedle
  (See online at https://doi.org/10.1039/C1CP20190E)
• Urea derivatives enhance the photocatalytic activity of dye-modified titanium dioxide. Photochem. Photobiol. Sci. 2011, 10, 623-625
  Stefan Füldner, Tatiana Mitkina, Tobias Trottmann, Alexandra Frimberger, Michael Gruber and Burkhard König
  (See online at https://doi.org/10.1039/c0pp00374c)
• Visible-Light Photoredox Catalysis: Dehalogenation of Vicinal Dibromo-, α- Halo-, and α,α-Dibromocarbonyl Compounds. J. Org. Chem. 2011, 76, 736-739
  Tapan Maji, Ananta Karmakar, Oliver Reiser
  (See online at https://doi.org/10.1021/jo102239x)
• Why BLUF photoreceptors with roseoflavin cofactor loose their biological functionality. Phys. Chem. Chem. Phys. 2011, 13, 14775-14783
  Thomas Merz, Keyarash Sadeghian, Martin Schütz
  (See online at https://doi.org/10.1039/c1cp21386e)
• [Cu(dap)2Cl] As an Efficient Visible-Light-Driven Photoredox Catalyst in Carbon-Carbon Bond-Forming Reactions. Chem. Eur. J. 2012, 18, 7336-7340
  Michael Pirtsch, Suva Paria, Taisuke Matsuno, Hiroyuki Isobe, and Oliver Reiser
  (See online at https://doi.org/10.1002/chem.201200967)
• A novel computer simulation method for simulating the multiscale transduction dynamics of signal proteins. J. Chem. Phys. 2012, 136, 124112
  Emanuel Peter, Bernhard Dick, and Stephan A. Baeurle
  (See online at https://doi.org/10.1063/1.3697370)
• Application of Microflow Conditions to Visible Light Photoredox Catalysis. Org. Lett. 2012, 14, 2658-2661
  Matthias Neumann and Kirsten Zeitler
  (See online at https://doi.org/10.1021/ol3005529)
• Chemical Photocatalysis with 1-(N,N-Dimethylamino)pyrene. Synlett 2012, 23, 2803 - 2807
  A. Penner, E. Bätzner, H.-A. Wagenknecht
  (See online at https://doi.org/10.1055/s-0032-1317532)
• Enantioselective Intramolecular [2+2] Photocycloaddition Reactions of 4- Substituted Coumarins Catalyzed by a Chiral Lewis Acid. Chem. Eur. J. 2012, 18, 7552-7560
  Richard Brimioulle, Hao Guo, Thorsten Bach
  (See online at https://doi.org/10.1002/chem.201104032)
• Hermitian time-dependent coupled-cluster linear response ansätze of second-order in application to excitation energies and frequencydependent dipole polarizabilities. Phys. Rev. A, 2012, 86, 052519
  G. Wälz, D. Kats, D. Usvyat, T. Korona and M. Schütz
  (See online at https://doi.org/10.1103/PhysRevA.86.052519)
• Illuminating the early signaling pathway of a fungal LOV-photoreceptor. Proteins 2012, 80, 471-481
  Emanuel Peter, Bernhard Dick, Stephan A. Baeurle
  (See online at https://doi.org/10.1002/prot.23213)
• Kohls, Paul - Visible Light Photoredox Catalysis: Generation and Addition of N- Aryltetrahydroisoquinoline-Derived α-Amino Radicals to Michael Acceptors. Org. Lett. 2012, 14, 672-675
  Paul Kohls, Deepak Jadhav, Ganesh Pandey, Oliver Reiser
  (See online at https://doi.org/10.1021/ol202857t)
• Metal free, Visible Light Mediated Direct C-H Arylation of Heteroarenes with Aryl Diazonium salts. J. Am. Chem. Soc. 2012, 134, 2958-2961
  D. P. Hari, P. Schroll, B. König
  (See online at https://doi.org/10.1021/ja212099r)
• Metal free, Visible Light Mediated Direct C-H Arylation of Heteroarenes with Aryl Diazonium salts. J. Am. Chem. Soc. 2012, 134, 2958-2961
  D. P. Hari, P. Schroll, B. König
  (See online at https://doi.org/10.1021/ja212099r)
• Phase transition in GeF2 driven by change of type of intermolecular interaction. Phys. Rev. B, 2012, 86, 054102
  D. Usvyat, C. Yin, G. Wälz, C. Mühle, M. Schütz and M. Jansen
  (See online at https://doi.org/10.1103/PhysRevB.86.054102)
• Photocatalytic Arylation of Alkenes, Alkynes and Enones with Diazonium salts. ChemistryOpen 2012, 1, 130-133
  Peter Schroll, Durga Prasad Hari, and Burkhard König
  (See online at https://doi.org/10.1002/open.201200011)
• Photocatalytic Arylation of Alkenes, Alkynes and Enones with Diazonium salts. ChemistryOpen 2012, 1, 130-133
  P. Schroll, D. P. Hari, and B. König
  (See online at https://doi.org/10.1002/open.201200011)
• Signaling pathway of a photoactivable Rac1-GTPase in the early stages. Proteins 2012, 5, 1350-1362
  Emanuel Peter, Bernhard Dick, Stephan A. Baeurle
  (See online at https://doi.org/10.1002/prot.24031)
• Synthesis of a Benzophenone C-Nucleoside as Potential Triplet Energy and Charge Donor in Nucleic Acids. Synthesis 2012, 44, 648-652
  M. Weinberger, H.-A. Wagenknecht
  (See online at https://doi.org/10.1055/s-0031-1289672)
• The role of bridging ligand in hydrogen generation by photocatalytic Ru/Pd assemblies. Dalton Trans. 2012, 41, 13050-13059
  Gurmeet Singh Bindra, Martin Schulz, Avishek Paul, Robert Groarke, Suraj Soman, Jane L. Inglis, Wesley R. Browne, Michael G. Pfeffer, Sven Rau, Brian J. MacLean, Mary T. Pryce and Johannes G. Vos
  (See online at https://doi.org/10.1039/c2dt30948c)
• Visible Light Photocatalytic Synthesis of Benzothiophenes. Org. Lett. 2012, 14, 5334-5337
  D. P. Hari, T. Hering, B. König
  (See online at https://doi.org/10.1021/ol302517n)
• Visible Light Photocatalytic Synthesis of Benzothiophenes. Org. Lett. 2012, 14, 5334-5337
  D. P. Hari, T. Hering, B. König
  (See online at https://doi.org/10.1021/ol302517n)
• Visible-Light-Mediated α-Arylation of Enol Acetates Using Aryl Diazonium Salts. J. Org. Chem. 2012, 77, 10347-10352
  T. Hering, D. P. Hari, B. König
  (See online at https://doi.org/10.1021/jo301984p)
• Visible-Light-Mediated α-Arylation of Enol Acetates Using Aryl Diazonium Salts. J. Org. Chem. 2012, 77, 10347-10352
  T. Hering, D. P. Hari, B. König
  (See online at https://doi.org/10.1021/jo301984p)
• Visible-Light-Promoted Stereoselective Alkylation by Combining Heterogeneous Photocatalysis with Organocatalysis. Angew. Chem. Int. Ed. 2012, 17, 4062-4066
  Maria Cherevatskaya, Matthias Neumann, Stefan Füldner, Christoph Harlander, Susanne Kümmel, Stephan Dankesreiter, Arno Pfitzner, Kirsten Zeitler, and Burkhard König
  (See online at https://doi.org/10.1002/anie.201108721)
• Visible-Light-Promoted Stereoselective Alkylation by Combining Heterogeneous Photocatalysis with Organocatalysis. Angew. Chem. Int. Ed. 2012, 17, 4062-4066
  Maria Cherevatskaya, Matthias Neumann, Stefan Füldner, Christoph Harlander, Susanne Kümmel, Stephan Dankesreiter, Arno Pfitzner, Kirsten Zeitler, and Burkhard König
  (See online at https://doi.org/10.1002/anie.201108721)
• Visible-Light-Promoted Stereoselective Alkylation by Combining Heterogeneous Photocatalysis with Organocatalysis. Angew. Chem. Int. Ed. 2012, 17, 4062-4066
  Maria Cherevatskaya, Matthias Neumann, Stefan Füldner, Christoph Harlander, Susanne Kümmel, Stephan Dankesreiter, Arno Pfitzner, Kirsten Zeitler, and Burkhard König
  (See online at https://doi.org/10.1002/anie.201108721)
• Visible-Light-Promoted Stereoselective Alkylation by Combining Heterogeneous Photocatalysis with Organocatalysis. Angew. Chem. Int. Ed. 2012, 17, 4062-4066
  Maria Cherevatskaya, Matthias Neumann, Stefan Füldner, Christoph Harlander, Susanne Kümmel, Stephan Dankesreiter, Arno Pfitzner, Kirsten Zeitler, and Burkhard König
  (See online at https://doi.org/10.1002/anie.201108721)
• A Cooperative Hydrogen-Bond-Promoted Organophotoredox Catalysis Strategy for Highly Diastereoselective, Reductive Enone Cyclization. Chem. Eur. J. 2013, 19, 6950-6955
  Matthias Neumann, Kirsten Zeitler
  (See online at https://doi.org/10.1002/chem.201204573)
• Aggregation effects in visible light flavin photocatalysts: Synthesis, structure and catalytic activity of 10-arylflavins. Chem. Eur. J. 2013, 19, 1066-1075
  Dadová J., Kümmel S., Feldmeier C., Cibulková J., Pažout R., Maixner J., Gschwind R. M., König B., Cibulka R.
  (See online at https://doi.org/10.1002/chem.201202488)
• Ambient-Light-Mediated Copper-Catalyzed C-C and C-N Bond Formation. Angew. Chem. Int. Ed. 2013, 52, 5919 - 5921
  Michal Májek, Axel Jacobi von Wangelin
  (See online at https://doi.org/10.1002/anie.201301843)
• Chemical Photocatalysis, B. König, De Gruyter 2013, pp. 139-150
  O. Reiser, G. Kachkovskyi, V. Kais, P. Kohls, S. Paria, M. Pirtsch, D. Rackl, H. Seo
  (See online at https://doi.org/10.1515/9783110269246.139 https://doi.org/10.1039/c4cc10270c)
• Conformational control of benzophenone-sensitized charge transfer in dinucleotides. Phys. Chem. Chem. Phys. 2013, 15, 18607-18619
  Thomas Merz, Matthias Wenninger, Michael Weinberger, Eberhard Riedle, Hans-Achim Wagenknecht, Martin Schütz
  (See online at https://doi.org/10.1039/c3cp52344f)
• Conformational control of benzophenone-sensitized charge transfer in dinucleotides. Phys. Chem. Chem. Phys. 2013, 15, 18607-18619
  Thomas Merz, Matthias Wenninger, Michael Weinberger, Eberhard Riedle, Hans-Achim Wagenknecht and Martin Schütz
  (See online at https://doi.org/10.1039/c3cp52344f)
• Conformational control of benzophenone-sensitized charge transfer in dinucleotides. Phys. Chem. Chem. Phys. 2013, 15, 18607-18619
  Thomas Merz, Matthias Wenninger, Michael Weinberger, Eberhard Riedle, Hans-Achim Wagenknecht and Martin Schütz
  (See online at https://doi.org/10.1039/c3cp52344f)
• Description of excited states in photocatalysis with theoretical methods. in: Chemical Photocatalysis (Ed.: B. König), Chapter 14, 263 (2013)
  T. Merz and M. Schütz
  (See online at https://doi.org/10.1515/9783110269246.263)
• Electronic transient spectroscopy from the deep UV to the NIR: unambiguous disentanglement of complex processes. Faraday Disc. 2013;163:139-58
  E. Riedle, M. Bradler, M. Wenninger, C. F. Sailer and I. Pugliesi
  (See online at https://doi.org/10.1039/c3fd00010a)
• Enantioselective Lewis Acid Catalysis of Intramolecular Enone [2+2] Photocycloaddition Reactions. Science 2013, 42, 840-843
  R. Brimioulle, T. Bach
  (See online at https://doi.org/10.1126/science.1244809)
• Heterogeneous semiconductor Photocatalysis (12. Kapitel) in Chemical Photocatalysis, 1. Ausgabe (Hrsg.: B. König), de Gruyter, Berlin, 2013
  Eisenhofer, Anna
  (See online at https://doi.org/10.1515/9783110269246.211)
• Homogeneous visible light-mediated transition metal photoredox catalysis other than ruthenium and iridium. in Chemical Photocatalysis, B. König, De Gruyter 2013, pp. 139-150
  O. Reiser, G. Kachkovskyi, V. Kais, P. Kohls, S. Paria, M. Pirtsch, D. Rackl, H. Seo
  (See online at https://doi.org/10.1515/9783110269246.139)
• Homogeneous visible light-mediated transition metal photoredox catalysis other than ruthenium and iridium. in Chemical Photocatalysis, B. König, De Gruyter 2013, pp. 139-150
  O. Reiser, G. Kachkovskyi, V. Kais, P. Kohls, S. Paria, M. Pirtsch, D. Rackl, H. Seo
  (See online at https://doi.org/10.1515/9783110269246.139)
• Influencing the conductance in biphenyl-like molecular junctions with THz radiation. Phys. Stat. Sol. (b) 2013, 250, 2408
  M. Hinreiner, D. A. Ryndyk, D. Usvyat, T. Merz, M. Schütz, K. Richter
  (See online at https://doi.org/10.1002/pssb.201349221)
• Intramolecular [2+2] Photocycloaddition of 3- and 4-(But-3- enyl)oxyquinolones: Influence of the Alkene Substitution Pattern, Photophysical Studies and Enantioselective Catalysis by a Chiral Sensitizer. Chem. Eur. J. 2013, 19, 7461 - 7472
  M. M. Maturi, M. Wenninger, R. Alonso, A. Bauer, A. Pöthig, E. Riedle, T. Bach
  (See online at https://doi.org/10.1002/chem.201300203)
• Intramolecular [2+2] Photocycloaddition of 3- and 4-(But-3- enyl)oxyquinolones: Influence of the Alkene Substitution Pattern, Photophysical Studies and Enantioselective Catalysis by a Chiral Sensitizer. Chem. Eur. J. 2013, 19, 7461 - 7472
  Maturi, M. M.; Wenninger, M.; Alonso, R.; Bauer, A.; Pöthig, A.; Riedle, E.; Bach, T.
  (See online at https://doi.org/10.1002/chem.201300203)
• Large-scale organization of ribosomal DNA chromatin is regulated by Tip5”. Nucleic Acids Research, 2013, 41, 5251-5262
  K. Zillner, M. Filarsky, K. Rachow, M. Weinberger, G. Längst, A. Németh
  (See online at https://doi.org/10.1093/nar/gkt218)
• LED based NMR Illumination Device for Mechanistic Studies on Photochemical Reactions - Versatile and Simple, yet Surprisingly Powerful. J. Mag. Res. 2013, 32, 39-44
  Christian Feldmeier, Hanna Bartling, Eberhard Riedle, Ruth M. Gschwind
  (See online at https://doi.org/10.1016/j.jmr.2013.04.011)
• LED based NMR Illumination Device for Mechanistic Studies on Photochemical Reactions - Versatile and Simple, yet Surprisingly Powerful. J. Mag. Res. 2013, 32, 39-44
  Christian Feldmeier, Hanna Bartling, Eberhard Riedle, Ruth M. Gschwind
  (See online at https://doi.org/10.1016/j.jmr.2013.04.011)
• LED based NMR illumination device for mechanistic studies on photochemical reactions – versatile and simple, yet surprisingly powerful. Journal of Magnetic Resonance 2013, 232
  C. Feldmeier, H. Bartling, E. Riedle, R. M. Gschwind
  (See online at https://doi.org/10.1016/j.jmr.2013.04.011)
• Organocatalytic Visible Light Mediated Synthesis of Aryl Sulfides. Chem. Commun. 2013, 5507-5509
  Michal Májek, Axel Jacobi von Wangelin
  (See online at https://doi.org/10.1039/c3cc41867g)
• Photocatalytic Surface Patterning of Cellulose using Diazonium Salts and Visible Light. Org. Biomol. Chem. 2013, 11, 6510-6514
  P. Schroll, C. Fehl, S. Dankesreiter, B. König
  (See online at https://doi.org/10.1039/c3ob40990b)
• Photocatalytic Surface Patterning of Cellulose using Diazonium Salts and Visible Light. Org. Biomol. Chem. 2013, 11, 6510-6514
  P. Schroll, C. Fehl, S. Dankesreiter, B. König
  (See online at https://doi.org/10.1039/c3ob40990b)
• Regulatory mechanism of the light-activable allosteric switch LOV-TAP for the control of DNA binding: A computer simulation study. Proteins 2013, 8, 394-405
  E. Peter, B. Dick, S. A. Baeurle
  (See online at https://doi.org/10.1002/prot.24196)
• Synthesis of 4-Aminophthalimide and 2,4-Diaminopyrimidine C- Nucleosides as Isosteric Fluorescent DNA Base Substitutes. J. Org. Chem. 2013, 78, 2589-2599
  M. Weinberger, F. Berndt, R. Mahrwald, N. P. Ernsting, H.-A. Wagenknecht
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• Radical Reactions Induced by Visible Light in Dichloromethane Solutions of Hünig’s Base: Synthetic Applications and Mechanistic Observation. Chem. Eur. J. 2016, 22, 15921-15928
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• Synthesis of Pyrrolo[1,2a]quinolines and Ullazines by Visible Light mediated one‐ and twofold Annulation of N-Arylpyrroles with Arylalkynes. Chem. Commun. 2016, 52 , 8695-8698
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• Visible light amination/Smiles cascade: access to phthalazine derivatives. Chem. Sci. 2016, 7, 5002-5006
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• Visible light amination/Smiles cascade: access to phthalazine derivatives. Chem. Sci. 2016, 7, 5002-5006
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• Visible Light Mediated Photoredox Catalytic Arylation Reactions. Acc. Chem. Res. 2016, 49, 1566-1577
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• Visible Light Mediated Photoredox Catalytic Arylation Reactions. Acc. Chem. Res. 2016, 49, 1566-1577
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• Visible Light Mediated Photoredox Catalytic Arylation Reactions. Acc. Chem. Res. 2016, 49, 1566-1577
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• Visible-Light Photo-Arbuzov Reaction of Aryl Bromides and Trialkyl Phosphites Yielding Aryl Phosphonates. ACS Catal. 2016, 6, 8410-8414
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• "Trojan Horse" Effect in Photocatalysis - How Anionic Silver Impurities Influence Apparent Catalytic Activity. Chem. Eur. J. 2017, 23, 2271-2274
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• A systematic study of the influence of mesoscale structuring on the kinetics of a chemical reaction. Phys. Chem. Chem. Phys. 2017, 19, 23773-23780
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• Aromatic Chlorosulfonylation by Photoredox Catalysis. ChemSusChem 2017, 10, 151-155
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• Carboxylation of Aromatic and Aliphatic Bromides and Triflates with CO2 by Dual Visible-Light-Nickel Catalysis. Angew. Chem. Int. Ed. 2017, 56, 13426-13430
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• Desyl and Phenacyl as Versatile, Photocatalytically Cleavable Protecting Groups: A Classic Approach in a Different (Visible) Light. ACS Catal. 2017, 7, 6821-6826
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• Lanthanide Ions Coupled with Photoinduced Electron Transfer Generate Strong Reduction Potentials from Visible Light. Chem. Eur. J. 2017, 23, 7900-7904
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• Molecular polygons probe the role of intramolecular strain in the photophysics of pi-conjugated chromophores. Angew. Chem. Int. Ed. 2017, 56, 1234
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• Photocatalytic N-Formylation of Amines via a Reductive Quenching Cycle in the Presence of Air. Org. Biomol. Chem. 2017, 15, 2536-2540
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• Photocatalytic N-Formylation of Amines via a Reductive Quenching Cycle in the Presence of Air. Org. Biomol. Chem. 2017, 15, 2536-2540
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• Photocatalytic oxidation of sulfinates to vinyl sulfones with cyanamidefunctionalised carbon nitride. Eur. J. Org. Chem. 2017, 15, 2179-2185
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• Photocatalytic Phenol-Arene C-C and C-O Cross-Dehydrogenative Coupling. Eur. J. Org. Chem. 2017, 15, 2194-2204
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• Photosensitised regioselective [2+2]-cycloaddition of cinnamates and related alkene. Chem. Commun. 2017, 53, 12072-12075
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• Photosensitised regioselective [2+2]-cycloaddition of cinnamates and related alkenes. Chem. Commun. 2017, 53, 12072-12075
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• Photosensitised regioselective [2+2]-cycloaddition of cinnamates and related alkenes. Chem. Commun. 2017, 53, 12072-12075
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• Quantum dots in visible light photoredox catalysis: Reductive dehalogenations and C-H arylation reactions using aryl bromides. Chemistry of Materials 2017, 29, 5225-5231
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• Radical Aromatic Trifluoromethylthiolation: Photoredox Catalysis vs. Base Mediation. Eur. J. Org. Chem. 2017, 6722-6725
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• Selective Single C(sp3)-F Bond Cleavage in Trifluoromethylarenes: Merging Visible-Light Catalysis with Lewis Acid Activation. J. Am. Chem. Soc. 2017, 139, 18444-18447
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• Sensitization-Initiated Electron Transfer for Photoredox Catalysis. Angew. Chem. Int. Ed. 2017, 56, 8544-8549
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• Switching from adduct formation to electron transfer in a light–oxygen–voltage domain containing the reactive cysteine. PCCP 2017, 19(17), 10808-10819
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• Synthesis of Arylated Nucleobases by Visible Light Photoredox Catalysis. J. Org. Chem. 2017, 82, 3552-3560
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• Visible-light photoredox-catalyzed desulfurization of thiol- and disulfidecontaining amino acids and small peptides. J. Pept. Sci. 2017, 23, 556-562
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• Visible-Light-Accelerated C–H Sulfinylation of Heteroarenes. Angew. Chem. Int. Ed. 2017, 56, 409-412C–H. Sulfinylierung von Heteroaromaten beschleunigt durch sichtbares Licht.A. U. Meyer, A. Wimmer, B. König. Angew. Chem. 2017, 129, 420-423
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• Visible-Light-Driven Aerobic Photooxidation of Aldehydes to Methyl Esters Catalyzed by Riboflavin Tetraacetate. ChemCatChem 2017, 9, 920-923
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• Visible-Light-Mediated Radical Arylation of Anilines with Acceptor- Substituted (Hetero)aryl Halides. Org. Lett. 2017, 19, 5976-5979
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• Visible-Light-Mediated Synthesis of Pyrazines from Vinyl Azides Utilizing a Photocascade Process. Synlett 2017, 28, 1707-1714 (special issue Heterocycles)
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• 1,10-Phenanthroline-dithiine iridium and ruthenium complexes: synthesis, characterization and photocatalytical dihydrogen evolution. Photochemistry & Photobiological Sciences 2018, 17, 1056-1067
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• A synergistic LUMO lowering strategy using Lewis acid catalysis in water to enable photoredox catalytic, functionalizing C–C cross-coupling of styrenes. Chem. Sci.2018, 9, 7096–7103
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• Air-sensitive Photoredox Catalysis Performed under Aerobic Conditions in Gel Networks. J. Org. Chem. 2018, 83, 7828-7938
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• Catalytic deracemization of chiral allenes by sensitized excitation with visible light. Nature 2018, 564, 240-243
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• Chemical Photocatalysis with Rhodamine 6G: Investigation of 2 Photoreduction by Simultaneous Fluorescence Correlation 3 Spectroscopy. J. Phys. Chem. B 2018, 122, 10728-10735
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• Dichromatic Photocatalytic Substitutions of Aryl Halides with a Small Organic Dye. Chem. Eur. J. 2018, 24, 105-108
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• Ligand-Controlled Regioselective Hydrocarboxylation of Styrenes with CO2 by Combining Visible Light and Nickel Catalysis. J. Am. Chem. Soc. 2018, 140, 3198-3201
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• Mechanism and cis/trans Selectivity of Vinylogous Nazarov-Type [6π] Photocyclizations. J. Org. Chem. 2018, 83, 964-972
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• Molecular excitonic seesaw. PNAS 2018, 115, E3626-E3634
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• Photocatalysis with Nucleic Acids and Peptides. Physical Sciences Reviews, 2018, 3
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• Photocatalytic Barbier Reaction - Visible-Light induced Allylation and Benzylation of Aldehydes and Ketones. Chem. Sci. 2018, 9, 7230-7235
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• Photocatalytic Barbier Reaction - Visible-Light induced Allylation and Benzylation of Aldehydes and Ketones. Chem. Sci. 2018, 9, 7230-7235
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• Photocatalytic formation of carbon-sulfur bonds. J. Org. Chem. 2018, 14, 54-83
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• Photocatalytic Oxidative Bromination of Electron-Rich Arenes and Heteroarenes by Anthraquinone. Adv. Synth. Catal. 2018, 360, 626-630
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• Reinventing the De Mayo Reaction: Synthesis of 1,5-Diketones or 1,5- Ketoesters via Visible Light [2+2] Cycloaddition of β-Diketones or β- Ketoesters with Styrenes. Chem. Commun. 2018, 54, 11602-11605
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• Temperature Controlled Selective C-S or C-C Bond Formation: Photocatalytic Sulfonylation versus Arylation of Unactivated Heterocycles Utilizing Aryl Sulfonyl Chlorides. Org. Lett. 2018, 20, 648-651
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