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2026

75. F. Khalid, C. M. Gajendramurthy, F. F. Westermair, L. Miler, R. M. Gschwind, T. Ratajczyk, M. Urbańczyk, Analyst2026, Accepted, “Monte Carlo-like peaks assignment using a time-resolved in situ NMR approach for complex reaction monitoring: a case study of the photodegradation of retinyl acetate”

DOI: 10.1039/D6AN00072J (external link, opens in a new window)

74. M. Hecht, H. Fischer, W. Silva, V. Eichstetter, C. L. Scholtes, A. S. Ferreira, E. J. Cabrita, D. Horinek, R. M. Gschwind J. Am. Chem. Soc. 2026, Accepted “Role of 2-Hydroxyimines in Chiral Phosphoric Acid-Catalyzed Mannich-Type Reactions: Enhancing Reactivity and Selectivity via Dimerization”

DOI: 10.1021/jacs.5c22497 (external link, opens in a new window)

73. F. Gilch, J. Brossette, F. Westermair, W. Menezes da Silva, G. Balázs, R. M. Gschwind, H. Zipse, R. Wolf, Chem. Sci. 2026, Accepted, “Selective white phosphorus activation and functionalization with inorganic Grignard reagents

DOI: 10.1039/D6SC01229A (external link, opens in a new window)

2025

72. W. Wiesner, C.Wilhelm, R. C. Hoffmann, P. Stahl, K. Pellumbi, J. Jökel, I. Ivanović-Burmazović, U.-P. Apfel Angew. Chem. Int Ed. 2025, 65e25189, “Heavy is the Crown: Crown Ether Modulation of Cobalt Porphyrin CO2 Electroreduction in Zero-Gap Electrolyzers”

DOI: 10.1002/anie.202525189 (external link, opens in a new window)

71.  E. K. Taskinen, B. König J. Nat. Prod. 2025, 88, 2822–2848 “Harnessing Photochemistry in Natural Product Synthesis: From Strategy to Applications”

DOI: 10.1021/acs.jnatprod.5c00874 (external link, opens in a new window)

70.  N. A.Espinosa-Jalapa, M. Kümper, J. O. Bauer J. Am. Chem. Soc. 2025, 147, 47573–47583 „CO2 Unlocks Reactivity: Boryl Silyl Ketene Acetals Enable Mild and Direct C═C Bond Cleavage“

DOI: 10.1021/jacs.5c16770 (external link, opens in a new window)

69.  K. Vega, A, Sánchez, T. Mandal, W. Silva, R. Gschwind, B. Konig, M. Paixão, ACS Catal. 202515, 18087–18096, "Synthesis of α-Amino Acids by ConPET-mediated CO2 Fixation into Amides"

DOI: 10.1021/acscatal.5c04666 (external link, opens in a new window)

68. F. Wieberneit, N. Korber, Eur. J. Inorg. Chem. 2025, e20250040, "Carbonyl Metalates in Liquid Ammonia: Reduction of Mn2(CO)10 down to [Mn(CO)4]3−" 

DOI: 10.1002/ejic.202500401 (external link, opens in a new window)


Start of the second period (01.10.2025)


67. A. Tsutskiridze, D. Králová, I. Ghosh, B. König, Burkhard, Chem. Commun.2025, 61, 6651-6654 "Merocyanine-based photoacids as recyclable catalysts in visible-light-driven transformations." 

DOI: 10.1039/D5CC00696A (external link, opens in a new window)

66. E. K. Taskinen, D. Birnthaler, V. Kermelj, B. König, Chem. Eur. J. 2025, 31, e202500396 "Preassembly‐Controlled Radical Recombination at Bismuth: Decarboxylative C-N Coupling with Sulfonamides." 

DOI: 10.1002/chem.202500396 (external link, opens in a new window)

65. 45. 12. F. L. Pointner, J. Poll, E. K. Taskinen, V. George, T. Ruff, F. Rott, G. Mayer, N. Gessner, R. J. Kutta, B.  König, P. Nuernberger, C. Ochsenfeld, R. de Vivie-Riedle, Chem. Europe. 2025, 3, e202500133, "Mechanistic Study of the Light-Initiated Generation of Free Diazoalkanes: Towards Photo-Orthogonal Synthesis."

DOI: 10.1002/ceur.202500133 (external link, opens in a new window)

64.  J. Wieneke, F. Cirigliano, M.Schorpp, Chem. Commun. 202561, 17601-17604, "A diazadiphospholenium cation featuring a reactive P=P bond: synthesis and reversible main-group bond activation"

DOI: 10.1039/D5CC04820F (external link, opens in a new window)

63. M. Kümper, F. F. Westermair, T. Götz, R. M. Gschwind, J. O. Bauer, Angew. Chem. Int. Ed. 2025, 64, e202517017, "Si−H Activation via Dynamic Permutational Isomerism: A Ligand-Directed Route to Dehydrogenative Coupling"

DOI: 10.1002/anie.202517017 (external link, opens in a new window)

62. M. Gawron,  J. Eder, X. Weichselgartner, R. Gschwind, R. Wolf, Organometallics. 202544, 2141–2145, "Flash Communication: A Highly Reduced Magnesium Dicobalt Complex for the Hydrogenation of Tri- and Tetra Substituted Alkenes"

DOI: 10.1021/acs.organomet.5c00246 (external link, opens in a new window)

61.  L. Zimmermann, R. Szlosek, C. Scholtes, C. Riesinger, L. Dütsch, R. M. Gschwind, M. Scheer. Chem. Europe. 2025,  "Pnictogenium Ions as a Powerful Tool for the Synthesis of Three- and Five-Membered Interpnictogen Chains"

DOI: 10.1002/ceur.202500116 (external link, opens in a new window)

60. С.L. Scholtes, J. Ilgen, R. M. Gschwind, Chem. Commun. 2025, "Efficient detection of 1H{,} 15N correlations in hydrogen bonded low molecular catalyst–substrate intermediates without selective 15N-labelling"

DOI: 10.1039/D5CC00537J (external link, opens in a new window)

59. M. Franta, A. Pattanaik, W. Silva, K. Motiram-Coral, J. Rehbein, R. M. Gschwind, J. Am. Chem. Soc. 2025, accepted “The Elusive Ternary Intermediates of Chiral Phosphoric Acids in Ion Pair Catalysis─Structures, Conformations, and Aggregation (external link, opens in a new window)

DOI: 10.1021/jacs.4c14096 (external link, opens in a new window)

58. E. K. Taskinen, D. Kolb, M. Morgenstern, B. König, Chem. Eur. J. 2025, e202404200 „Photocatalyzed Dehydration of 1-Aryl-1,2-Ethanediols to Methyl Ketones Driven by Eosin Y Fragmentation Products“

DOI: 10.1002/chem.202404200 

57. Y. Liu, F.  Westermair, I. Becker, S. Hauer, M. Bodensteiner, C. Hennig, G. Balazs, F. Meyer, R.  Gschwind, R. Wolf, J. Am. Chem. Soc. 2025, accepted “Synthesis and Reactivity of an Iron-Tin Complex with Adjacent Stannylidyne and Ferriostannylene Units”

DOI: 10.1021/jacs.4c18423 (external link, opens in a new window)

56. N. Sülzner, G. Jung, P. Nuernberger, Chemical Science “A dual experimental-theoretical perspective on ESPT photoacids and their challenges ahead”, 202516, 1560-1596

DOI: 10.1039/D4SC07148D (external link, opens in a new window)

55. 36. R. Mhanna, J. Berger, M. Jourdain, S. Muth, R.J. Kutta,  G. Jung, ChemPhysChem 202526, e202400996 “Unexpected effect of excitation wavelength in single-molecule photochemistry of terylene”

DOI: 10.1002/cphc.202400996 (external link, opens in a new window)

54. T. Huber, G. Mayer, M. Kümper, W. Silva, N. Fontana, A. Falk, S. H. F. Schreiner, J. Gramüller, A. Scrimgeour, R. M. Gschwind, D. Horinek, P. Nuernberger, J. O. Bauer, Angew. Chem. Int. Ed. 2025, e202425049. "Where Does the Proton Go? Structure and Dynamics of Hydrogen-Bond Switching in Aminophosphine Chalcogenides"

DOI: 10.1002/anie.202425049 (external link, opens in a new window)

53 V. Burger, M. Franta, A. C. O'Donoghue, A. R. Ofial, R. M. Gschwind, H. Zipse, J. Org. Chem.,  90, 2298–2306  "Pyridinamide Ion Pairs – Design Principles for Super-Nucleophiles in Apolar Organic Solvents"

DOI: 10.1021/acs.joc.4c02668 (external link, opens in a new window)

52. V. Burger, M. Franta , A. R. Ofial, R. M. Gschwind, H. Zipse, J. Am. Chem. Soc., 147, 5043–5050,

“Highly Nucleophilic Pyridinamide Anions in Apolar Organic Solvents due to Asymmetric Ion Pair Association”

DOI: 10.1021/jacs.4c14825 (external link, opens in a new window)

2024

51.  N. Schubert, J. W. Southwell, M. Vázquez-Hernández, S. Wortmann, S. Schloeglmann, A.-K. Duhme-Klair, P. Nuernberger, J. E. Bandow, N. Metzler-Nolte, RSC Chem. Biol20245, 1201-1213, „Fluorescent probes for investigating the internalisation and action of bioorthogonal ruthenium catalysts within Gram-positive bacteria”

 DOI: 10.1039/D4CB00187G (external link, opens in a new window)

50. S. Grotjahn, B. König, Chem. Commun.2024, 60, 12951-12963. “Common Ground and Divergence: OLED Emitters as Photocatalysts”

DOI: 10.1039/D4CC04409F (external link, opens in a new window)

49. F. An, J. Brossette, H. Jangra, Y. Wei, M. Shi, H. Zipse, A. R. Ofial, Chem. Sci., 2024,15, 18111-18126. "Reactivities of tertiary phosphines towards allenic, acetylenic, and vinylic Michael acceptors"

DOI: 10.1039/D4SC04852K (external link, opens in a new window)

51. Y.-M. Tian, X. Pu, A. H. Sánchez, W. Silva, R. M. Gschwind, B. König, Adv. Synth. Catal. 2024, 366, 1 – 11. „Photoinduced radical borylation of robust carbon−heteroatom bonds” 

DOI: 10.1002/adsc.202400547 (external link, opens in a new window)

47. S. Grotjahn, L. Müller, A. Pattanaik, A. Falk, G. Barison, J. O. Bauer, J. Rehbein, R. M. Gschwind,  B. König Org. Chem. Front.2024, 11, 5890-5900,  Regio-, diastereo- and enantioselectivity in the photocatalytic generation of carbanions via hydrogen atom transfer and reductive radical-polar crossover” 

DOI: 10.1039/D4QO01219D (external link, opens in a new window) 

46. A. Ratzenböck, M. Kobras, A. Rustler, O. Reiser, Chem. Eur. J., 2024, 30, e202401332,Lewis Acid Catalyzed Cyclopropane Ring-Opening-Cyclization Cascade Using Thioureas as a N,N-bisnucleophile: Synthesis of Bicyclic Furo-, Pyrano-, and Pyrrololactams via a Formal [4+1]-Addition

DOI: 10.1002/chem.202401332 (external link, opens in a new window) 

45. J. Cammarata, F. Westermair, P. Coburger, D. Duvinage, M. Janssen, M. K. Uttendorfer, J. Beckmann, R. M. Gschwind, R. Wolf, D. J. Scott, Angew. Chem. Int. Ed. 2024, 63, e202408423, „Unravelling White Phosphorus: Experimental and Computational Studies Reveal the Mechanisms of P4 Hydrostannylation”

DOI: 10.1002/anie.202408423 (external link, opens in a new window)

44. 5. S. Yakubov, B. Dauth, W. J. Stockerl, W. da Silva, R. M. Gschwind, J. P. Barham, ChemSusChem, 2024e202401057, „Protodefluorinated Selectfluor® Aggregatively Activates Selectfluor® for Efficient Radical C(sp3)−H Fluorination Reactions” 

DOI: 10.1002/cssc.20240105 (external link, opens in a new window)

43. 25 J. Eder, A. Antonov, E. Tupiklia, R. M. Gschwind, Chem. Eur. J., 2024, 30, e202401793,„Chiral Diselenophosphoric Acids for Ion Pair Catalysis: A Novel Approach to Enhance Both Proton Donating and Proton Accepting Properties”

DOI: 10.1002/chem.202401793 (external link, opens in a new window)

42. 24 4. M. Hecht, P. Dullinger, W. Silva, D. Horinek, R. M. Gschwind, Chem. Sci., 2024, 15, 9104-9111,„Highly Acidic N-Triflylphosphoramides as Chiral Brønsted Acid Catalysts: The Effect of Weak Hydrogen Bonds and Multiple Acceptors on Complex Structures and Aggregation”

DOI: 10.1039/D4SC01939C (external link, opens in a new window)

41.  T. Huber, J. Bauer, Chem. Eur. J. 2024, 30, e202303760, „A Powerful P−N Connection: Preparative Approaches, Reactivity, and Applications of P-Stereogenic Aminophosphines” 

DOI: 10.1002/chem.202303760 (external link, opens in a new window)

40. V. R. Landaeta*, T. M. Horsley Downie, R. Wolf, Chem. Rev. 2024, 124, 1323-1463, „Low-Valent Transition Metalate Anions in Synthesis, Small Molecule Activation, and Catalysis” 

DOI: 10.1021/acs.chemrev.3c00121 (external link, opens in a new window)

39. M. Gawron, F. Gilch, D. Schmidhuber, J. A. Kelly, T. M. Horsley Downie, A. Jacobi von Wangelin, J. Rehbein, R. Wolf, Angew. Chem. Int. Ed. 2024, 63,e202315381, „Counterion Effect in Cobaltate-Catalyzed Alkene Hydrogenation”

DOI: 10.1002/anie.202315381 (external link, opens in a new window)

38.S. Grotjahn, C. Graf, J. Zelenka, A. Pattanaik, L. Müller, R. J. Kutta, J. Rehbein, J. Roithová, R. M. Gschwind, P. Nuernberger, B. König, Angew. Chem. Int. Ed. 2024, 63,e202400815, „Reactivity of Superbasic Carbanions Generated via Reductive Radical-Polar Crossover in the Context of Photoredox Catalysis”

DOI: 10.1002/anie.202400815 (external link, opens in a new window)

37. 21. Y.-M. Tian, W. Silva, R. M. Gschwind, B. König, Science 2024, 383, 750-756, „Accelerated Photochemical Reactions at Oil-Water Interface Exploiting Melting Point Depression”

DOI: 10.1126/science.adl3092 (external link, opens in a new window) 

https://doi.org/10.1002/nadc.20244142714 (external link, opens in a new window) Nachr. Chem. 2024, 72, 48

Water boosts light-driven coupling chemistry (acs.org) (external link, opens in a new window)

Chemical Reactins on the Water Surface - Researchers develop a new synthesis method: Manufacturing chemical products more efficiently and environmentally friendly (chemeurope.com) (external link, opens in a new window)

New synthesis method uses light reaction on a water surface - Today Headline (external link, opens in a new window)

New synthesis method uses light reaction on a water surface (phys.org) (external link, opens in a new window)

Chemische Reaktionen auf der Wasseroberfläche (idw-online.de) (external link, opens in a new window)

2023

36.  P. Dullinger, D. Horinek, J. Am. Chem. Soc. 2023, 145, 24922–24930, „Solvation of Nanoions in Aqueous Solutions”

DOI: 10.1021/jacs.3c09494 (external link, opens in a new window)

35. 19. B. N. Baumann, H. Lange, F. Seeberger, P. Büschelberger, R. Wolf, M. Hapke, Mol. Catal. 2023, 550, 113482,„Cobalt and iron metallates as catalysts for cyclization reactions of diynes and triynes: [2+2+2] Cycloaddition vs. Garratt-Braverman reaction”

DOI: 10.1016/j.mcat.2023.113482 (external link, opens in a new window)

34. J. Gramüller, R. M. Gschwind*, Acc. Chem. Res. 2023, 56, 2968-2979,„An NMR Spectroscopy View on London Dispersion in Catalysis: Detection, Quantification and Application in Ion Pair and Transition Metal Catalysis”

DOI: 10.1021/acs.accounts.3c00431 (external link, opens in a new window)

33.  V. GeorgeB. König*, Chem. Commun. 2023, 59, 11835-11838, „Photogenerated donor–donor diazo compounds enable facile access to spirocyclopropanes” 

DOI: 10.1039/D3CC03581F (external link, opens in a new window)

32.  P. A. Braun, F. Westermair, R. M. Gschwind, N. Korber, Z. Anorg. Allg. Chem. 2023, 649, e20230017, „(K,Rb)@([2.2.2]crypt)]2(K,Rb)4[Si9W(CO)4] ⋅ 13.4 NH3 – The First Tungsten Functionalized Silicon Zintl Cluster”

DOI: 10.1002/zaac.202300117 (external link, opens in a new window)

31. L. Wylie, J. P. Barham, B. Kirchner, ChemPhysChem 2023e202300470, „Solvent Dependency of Catalyst-Substrate Aggregation Through π-π Stacking in Photoredox Catalysis” 

DOI: 10.1002/cphc.202300470 (external link, opens in a new window)

30. S. Fischer, T-T. H. Nguyen, A. Ratzenboeck, H. M. L. Davies, O. Reiser, Org. Lett. 2023, 25, 4411–4415, „Stereoselective Synthesis of Highly Functionalized Cyclohexenes via Strong-Acid-Mediated Endocyclic C–C Bond Cleavage of Monocyclopropanated Cyclopentadienes” 

DOI: 10.1021/acs.orglett.3c00935 (external link, opens in a new window)

29. A. M. Arnold, P. Dullinger, A. Biswas, C. Jandl, D. Horinek, T. Gulder, Nat. Commun. 2023, 14, 813,„Enzyme-like polyene cyclizations catalyzed by dynamic, self-assembled, supramolecular fluoro alcohol-amine clusters” 

DOI: 10.1038/s41467-023-36157-0 (external link, opens in a new window)

28. W. Stockerl, R. M. Gschwind, Chem. Commun. 2023, 59, 1325-1328, „Photo enhancement reveals (E,Z) and (Z,Z) configurations as additional intermediates in iminium ion catalysis”

DOI: 10.1039/D2CC05976B (external link, opens in a new window)

27.  Y.-M. Tian, E. Hofmann, W. Silva, D. Touraud, R. M. Gschwind, W. Kunz, B. König*, Angew. Chem. Int. Ed. 2023, 62,e202218775,„Enforced Electronic-Donor-Acceptor Complex formation in Water for Photochemical Cross-Coupling”

DOI: 10.1002/anie.202218775 (external link, opens in a new window)

26. S. M. Tiefenthaler, N. Korber, Z. Anorg. Allg. Chem. 2023, 649, e202200286, „[K([2.2.2]-crypt)]K[Pt32-CO)3(PPh3)3]∙3 NH3 – A New Chini-Type Platinum Carbonyl Complex”

DOI: 10.1002/zaac.202200286 (external link, opens in a new window)

2022

25. J. O. Bauer, Organometallics 2022, 41, 321–327, „Influence of Amino Functions on the Coordination Ability of Silyl Ethers and Disiloxanes”

DOI: 10.1021/acs.organomet.1c00663 (external link, opens in a new window)

24. S. M. Tiefenthaler, F. Kleemiss, N. Korber, Z. Anorg. Allg. Chem.2022, 648, e202100378,„[A([18]crown-6)]2[Pt(CO)3] ⋅ 10 NH(A=K, Rb) – A crystal structure containing the long postulated [Pt(CO)3]2− 

DOI: 10.1002/zaac.20210037 (external link, opens in a new window)

23. S. Yakubov, W. J. Stockerl, X. Tian, A. Shahin, M. J. P. Mandigma, R. M. Gschwind, J. P. Barham, Chem. Sci. 2022, 13, 14041-14051, „Benzoates as photosensitization catalysts and auxiliaries in efficient, practical, light-powered direct C(sp3)–H fluorinations” 

DOI: 10.1039/D2SC05735B (external link, opens in a new window)

22.  A. Falk, J. O. Bauer, Inorg. Chem. 2022, 61, 15576–15588,„Structural and Electronic Effects on Phosphine Chalcogenide Stabilized Silicon Centers in Four-Membered Heterocyclic Cations” 

DOI: 10.1021/acs.inorgchem.2c02360 (external link, opens in a new window)

21. F. Babawale, K. Murugesan, R. Narobe, B. König, Org. Lett. 2022, 24, 4793–4797, „Synthesis of Unnatural α-Amino Acid Derivatives via Photoredox Activation of Inert C(sp3)–H Bonds” 

DOI: 10.1021/acs.orglett.2c01822 (external link, opens in a new window)

20. J. Gramüller, P. Dullinger, D. Horinek, R. M. Gschwind, Chem. Sci. 2022, 13, 14366-14372, „Bidentate Substrate Binding in Brønsted Acid Catalysis: Structural Space, Hydrogen Bonding and Dimerization” 

DOI: 10.1039/D2SC05076E (external link, opens in a new window)

19.  S. Wortmann, R. J. Kutta, P. Nuernberger, Front. Chem. 2022, 10:983342, „Monitoring the photochemistry of a formazan over 15 orders of magnitude in time”

DOI: 10.3389/fchem.2022.983342 (external link, opens in a new window)

18.  J. Gramüller, M. Franta, R. M. Gschwind, J. Am. Chem. Soc. 2022, 144, 19861–19871, „Tilting the Balance: London Dispersion Systematically Enhances Enantioselectivities in Brønsted Acid Catalyzed Transfer Hydrogenation of Imines”

DOI: 10.1021/jacs.2c07563 (external link, opens in a new window)

17. T. E. Schirmer, B. König, J. Am. Chem. Soc. 2022, 144, 19207–19218, „Ion-Pairing Catalysis in Stereoselective, Light-Induced Transformations” 

DOI: 10.1021/jacs.2c04759 (external link, opens in a new window)

16.  P. Denk, A. El Maangar, S. Prévost, W. Silva, R. M. Gschwind, T. Zemb, W. Kunz, J. Colloid Interface Sci. 2022, 621, 470–488, „Cloud point, auto-coacervation, and nematic ordering of micelles formed by ethylene oxide containing carboxylate surfactants”

DOI: 10.1016/j.jcis.2022.04.046 (external link, opens in a new window)

15.  A. K. Dutta, S. Park, C. Allacher, A. Abramov, P. Dullinger, K. Kuzmanoska, D. Fritsch, P. Hitzfeld, D. Horinek, J. Rehbein, P. Nuernberger, R. M. Gschwind, A. Breder, Angew. Chem. Int. Ed., 2022, 61, e202208611, ”Hydrogen bond-modulated nucleofugality of SeIII species to enable photoredox catalytic semipinacol manifolds”

DOI: 10.1002/anie.202208611 (external link, opens in a new window)

14. K. Kristinaityte, A. Mames, M. Pietrzak, F. F. Westermair, W. Silva, R. M. Gschwind, T. Ratajczyk, M. Urba´nczyk, J. Am. Chem. Soc. 2022, 144, 13938–13945, „Deeper insight into photopolymerization: The Synergy of Time-Resolved Non-Uniform Sampling and Diffusion NMR”

DOI: 10.1021/jacs.2c05944 (external link, opens in a new window)

13.  J. A. Kelly, V. Streitferdt, M. Dimitrova, F. F. Westermair, R. M. Gschwind, R. Berger, R. Wolf, J. Am. Chem. Soc. 2022, 144, 20434–20441, „Transition-Metal-Stabilised Heavy Tetraphospholide Anions”

DOI: 10.1021/jacs.2c08754 (external link, opens in a new window)

12. R. Eckl, S. Fischer, C. M. Sonnleitner, D. Schmidhuber, J. Rehbein, O. Reiser, ACS Org. Inorg. Au 2022, 2, 169-174, „Stereoselective Synthesis of Biologically Relevant Tetrahydropyridines and Dihydro-2H-pyrans via Ring-Expansion of Monocyclopropanated Heterocycles” 

DOI: 10.1021/acsorginorgau.1c00042 (external link, opens in a new window)

11. M. Zabka, R. M. Gschwind, Eur. J. Org. Chem 2022, 26, e202200048, „Substrate Photoswitching for Rate Enhancement of an Organocatalytic Cyclization Reaction”

DOI: 10.1002/ejoc.202200048 (external link, opens in a new window)

10.  T. Götz, A. Falk, J. O. Bauer, Chem. Eur. J. 2022, 28, e202103531,„Molecular Scissors for Tailor-Made Modification of Siloxane Scaffolds” 

DOI: 10.1002/chem.202103531 (external link, opens in a new window)

9. N. Fontana, N. A. Espinosa-Jalapa, M. Seidla, J. O. Bauer, Chem. Commun., 2022, 58, 2144-2147, „Hidden silylium-type reactivity of a siloxane-based phosphonium–hydroborate ion pair” 

DOI: 10.1039/D1CC07016A (external link, opens in a new window) 

8. G. Hierlmeier, R. Wolf, Organometallics, 2022, 41, 776-784„Bulking up CpBIG: A Penta-Terphenyl Cyclopentadienyl Ligand” 

DOI: 10.1021/acs.organomet.2c00009 (external link, opens in a new window)

7.  M. Till, V. Streitferdt, D. J. Scott, M. Mende, R. M. Gschwind, R. Wolf, Chem. Commun., 2022, 58, 1100-1103„Photochemical transformation of chlorobenzenes and white phosphorus into arylphosphines and phosphonium salts” 

DOI: 10.1039/D1CC05691C (external link, opens in a new window)

6. S. Wortmann, S. Schloeglmann, P. Nuernberger, J. Org. Chem. 2022, 87, 1745-1755„Sensitivity of Isomerization Kinetics of 1,3,5-Triphenylformazan on Cosolvents Added to Toluene”

DOI: 10.1021/acs.joc.1c01928 (external link, opens in a new window)

2021

5. M. Zabka, R.M. Gschwind, Chem. Sci.2021, 12, 15263-15272"Ternary Complexes of Chiral Disulfonimides in Transfer-Hydrogenation of Imines: The Relevance of Late Intermediates in Ion Pair Catalysis" 

DOI: 10.1039/D1SC03724B (external link, opens in a new window)

4. 1. M.J. Margeson, F. Seeberger, J. A. Kelly, J. Leitl, P. Coburger, R. Szlosek, C. Müller, R Wolf, ChemCatChem 2021, 13, 3761-3764„Expedient Hydrofunctionalisation of Carbonyls and Imines Initiated by Phosphacyclohexadienyl Anions”

DOI: 10.1002/cctc.202100651 (external link, opens in a new window)

3. S. Karbalaei Khani, B. Geissler, E. Engelage, P. Nuernberger, C. Hättig, Phys. Chem. Chem. Phys. 2021, 23, 7480–7494, „Tracing absorption and emission characteristics of halogen-bonded ion pairs involving halogenated imidazolium species”

DOI: 10.1039/D1CP00009H (external link, opens in a new window)

2. N. Berg, S. Bergwinkl, P. Nuernberger, D. Horinek, R.M. Gschwind, J. Am. Chem. Soc. 2021, 143, 724-735, „Extended Hydrogen Bond Networks for Effective Proton-Coupled Electron Transfer (PCET) Reactions: The Unexpected Role of Thiophenol and Its Acidic Channel in Photocatalytic Hydroamidations” 

DOI: 10.1021/jacs.0c08673 (external link, opens in a new window)

1. J. Kelly, J. Gramüller, R.M. Gschwind, R. Wolf, Dalton Trans. 2021, 50, 13985-13992,Low-oxidation state cobalt-magnesium complexes: ion-pairing and reactivitys”

DOI: 10.1039/D1DT02621F (external link, opens in a new window)

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