13. Highly Enantioselective 6π Photoelectrocyclizations Engineered by Hydrogen Bonding
Swords, W. B.; Lee, H.; Park, Y.; Llamas, F.; Skubi, K. L.; Park, J.; Guzei, I. A.; Baik, M.-H.; Yoon, T. P. Highly Enantioselective 6π Photoelectrocyclizations Engineered by Hydrogen Bonding. J. Am. Chem. Soc. 2023, 145, 27045–27053. DOI: 10.1021/jacs.3c10782
12. Mössbauer and Nuclear Resonance Vibrational Spectroscopy Studies of Iron Species Involved in N–N Bond Cleavage
Wandzilak, A.; Grubel, K.; Skubi, K. L.; McWilliams, S. F.; Bessas, D.; Rana, A.; Hugenbruch, S.; Dey, A.; Holland, P. L.; DeBeer, S. Mössbauer and Nuclear Resonance Vibrational Spectroscopy Studies of Iron Species Involved in N–N Bond Cleavage. Inorg. Chem. 2023, 62, 18449–18464. DOI: 10.1021/acs.inorgchem.3c02594
11. Iron Complexes of a Proton-Responsive SCS Pincer Ligand with a Sensitive Electronic Structure
Skubi, K. L.*; Hooper, R. X.*; Mercado, B. Q.; Bollmeyer, M. M.; MacMillan, S. N.; Lancaster, K. M.; Holland, P. L. Iron Complexes of a Proton-Responsive SCS Pincer Ligand with a Sensitive Electronic Structure. Inorg. Chem. 2022, 61, 1644–1658. DOI: 10.1021/acs.inorgchem.1c03499
10. Synthesis and Reactivity of Iron Complexes with a Biomimetic SCS Pincer Ligand
Speelman, A. L.; Skubi, K. L.; Mercado, B. Q.; Holland, P. L. Synthesis and Reactivity of Iron Complexes with a Biomimetic SCS Pincer Ligand. Inorg. Chem. 2021, 60, 1965–1974. DOI: acs.inorgchem.0c03427
9. LED-NMR Monitoring of an Enantioselective Catalytic [2+2] Photocycloaddition
Skubi, K. L.; Swords, W. B.; Hofstetter, H.; Yoon, T. P. LED-NMR Monitoring of an Enantioselective Catalytic [2+2] Photocycloaddition. ChemPhotoChem 2020, 4, 685–690. DOI: 10.1002/cptc.202000094
8. Enantioselective Intermolecular Excited-State Photoreactions Using a Chiral Ir Triplet Sensitizer: Separating Association from Energy Transfer in Asymmetric Photocatalysis
Zheng, J.; Swords, W. B.; Jung, H.; Skubi, K. L.; Kidd, J. B.; Meyer, G. J.; Baik, M.-H.; Yoon, T. P. Enantioselective Intermolecular Excited-State Photoreactions Using a Chiral Ir Triplet Sensitizer: Separating Association from Energy Transfer in Asymmetric Photocatalysis. J. Am. Chem. Soc. 2019, 141, 13625–13634. DOI: 10.1021/jacs.9b06244
7. Photocatalytic Cycloadditions
Amador, A. G.*; Scholz, S. O.*; Skubi, K. L.*; Yoon, T. P. Photocatalytic Cycloadditions. In Science of Synthesis: Photocatalysis in Organic Synthesis; König, B., Ed.; Georg Thieme Verlag KG: New York, 2018; pp 467– 516. DOI: 10.1055/sos-SD-229-00260
6. So Close, yet Sulfur Away: Opening the Nitrogenase Cofactor Structure Creates a Binding Site.
Skubi, K. L.; Holland, P. L. So Close, yet Sulfur Away: Opening the Nitrogenase Cofactor Structure Creates a Binding Site. Biochemistry 2018, 57, 3540–3541. DOI: 10.1021/acs.biochem.8b00529
5. NRVS Detection of Fe-H Vibrations in a Bridging Hydride Model of Nitrogenase Intermediates
Pelmenschikov, V.; Gee, L. B.; Wang, H.; MacLeod, K. C.; McWilliams, S. F.; Skubi, K. L.; Cramer, S. P.; Holland, P. L. NRVS Detection of Fe-H Vibrations in a Bridging Hydride Model of Nitrogenase Intermediates. Angew. Chem. Int. Ed. 2018, 57, 9367–9371. DOI: 10.1002/anie.201804601
4. Enantioselective Excited-State Photoreactions Controlled by a Chiral Hydrogen-Bonding Iridium Sensitizer
Skubi, K. L.; Kidd, J. B.; Jung, H.; Guzei, I.; Baik, M.-H.; Yoon, T. P. Enantioselective Excited-State Photoreactions Controlled by a Chiral Hydrogen-Bonding Iridium Sensitizer. J. Am. Chem. Soc. 2017, 139, 17186–17192. DOI: 10.1021/jacs.7b10586
3. Dual Catalysis Strategies in Photochemical Synthesis
Skubi, K. L.; Blum, T. R.; Yoon, T. P. Dual Catalysis Strategies in Photochemical Synthesis. Chem. Rev. 2016, 116, 10035–10074. DOI: 10.1021/acs.chemrev.6b00018
2. Shape Control in Reactions with Light
Skubi, K. L.; Yoon, T. P. Shape Control in Reactions with Light. Nature 2014, 515, 45–46. DOI: 10.1038/515045a
1. A Dual-Catalysis Approach to Enantioselective [2+2] Photocycloadditions Using Visible Light
Du, J.*; Skubi, K. L.*; Schultz, D. M.*; Yoon, T. P. A Dual-Catalysis Approach to Enantioselective [2+2] Photocycloadditions Using Visible Light. Science2014, 344, 392–396. DOI: 10.1126/science.1251511