{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T17:13:12Z","timestamp":1786122792209,"version":"build-2736575974"},"reference-count":60,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T00:00:00Z","timestamp":1786060800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T00:00:00Z","timestamp":1786060800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100001659","name":"Deutsche Forschungsgemeinschaft","doi-asserted-by":"publisher","award":["495400214"],"award-info":[{"award-number":["495400214"]}],"id":[{"id":"10.13039\/501100001659","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["chemistry-europe.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Chemistry A European J"],"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    Nitrogen\u2010centered radicals (NCRs) provide direct access to C\u2500N bonds, but their broader use remains limited by the need for strongly reducing photocatalysts, high\u2010energy irradiation, and incomplete control over competing radical transfer pathways. Here we show that nonafluoromesitylsulfonyl (Nms)\u2010substituted oxycarbamates represent a redox\u2010lowered class of amidyl\u2010radical precursors that can be activated under green light by a bichromophoric ruthenium photocatalyst. The electron\u2010deficient sulfonyl group lowers the reduction potential of the N\u2500O bond sufficiently to enable single\u2010electron cleavage under mild conditions. In DMF, the resulting amidyl radicals are trapped directly by indolizines to provide C3\u2010aminated heteroarenes. In DMSO, higher\n                    <jats:italic>N<\/jats:italic>\n                    \u2010alkyl homologues are switched via a 1,2\u2010hydrogen atom transfer (HAT) to \u03b1\u2010amino carbon\u2010centered radicals, enabling C\u2500C bond formation from the same precursor family. This solvent\u2010gated divergence provides a unified entry to aminated and alkylated indolizines and establishes redox\u2010tuned oxycarbamates as versatile radical precursors for long\u2010wavelength photoredox synthesis.\n                  <\/jats:p>","DOI":"10.1002\/chem.71550","type":"journal-article","created":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T12:25:54Z","timestamp":1786105554000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Redox\u2010Tuned Oxycarbamates Enable Divergent C\u2500N and C\u2500C Functionalization of Indolizines Under Photoredox Catalysis With Green Light"],"prefix":"10.1002","author":[{"ORCID":"https:\/\/orcid.org\/0009-0002-3212-4019","authenticated-orcid":false,"given":"Kevin Klaus","family":"Stefanoni","sequence":"first","affiliation":[{"name":"Institute of Organic Chemistry Clausthal University of Technology  Leibnizstr Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3856-2757","authenticated-orcid":false,"given":"Ren\u00e9","family":"Wilhelm","sequence":"additional","affiliation":[{"name":"Institute of Organic Chemistry Clausthal University of Technology  Leibnizstr Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,8,7]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"crossref","first-page":"8181","DOI":"10.1021\/acs.chemrev.1c00831","article-title":"Nitrogen\u2010Centered Radicals in Functionalization of sp2 Systems: Generation, Reactivity, and Applications in Synthesis","volume":"122","author":"Pratley C.","year":"2022","journal-title":"Chemical Reviews"},{"key":"e_1_2_7_3_1","doi-asserted-by":"crossref","first-page":"4999","DOI":"10.1021\/acscatal.7b01385","article-title":"Photochemical Generation of Nitrogen\u2010Centered Amidyl, Hydrazonyl, and Imidyl Radicals: Methodology Developments and Catalytic Applications","volume":"7","author":"K\u00e4rk\u00e4s M. D.","year":"2017","journal-title":"ACS Catalysis"},{"key":"e_1_2_7_4_1","first-page":"1","volume-title":"Handbook of CH\u2010Functionalization","author":"Ward R. M.","year":"2026"},{"key":"e_1_2_7_5_1","doi-asserted-by":"crossref","first-page":"10617","DOI":"10.1039\/D6CC01832G","article-title":"Photocatalytic Amidyl Radical Formation: Mechanistic Insights and Reactivity Advances","volume":"62","author":"Fu H.","year":"2026","journal-title":"Chemical Communications"},{"key":"e_1_2_7_6_1","doi-asserted-by":"publisher","DOI":"10.1021\/acsorginorgau.5c00120"},{"key":"e_1_2_7_7_1","doi-asserted-by":"crossref","first-page":"12276","DOI":"10.1021\/acs.orglett.5c03828","article-title":"Photocatalytic Addition of N \u2010Oxazolidinone Radicals to Arenes and Heteroarenes in Batch and in Flow Mode","volume":"27","author":"Ferrario S.","year":"2025","journal-title":"Organic Letters"},{"key":"e_1_2_7_8_1","doi-asserted-by":"crossref","first-page":"11401","DOI":"10.1039\/D3CC03532H","article-title":"Photocatalysed C\u2013H amidation of Indoles Enabled by Tert \u2010Butyl Alkyl((perfluoropyridin\u20104\u2010yl)oxy)Carbamate","volume":"59","author":"Deng K.\u2010Y.","year":"2023","journal-title":"Chemical Communications"},{"key":"e_1_2_7_9_1","doi-asserted-by":"crossref","first-page":"2353","DOI":"10.1021\/acs.chemrev.1c00444","article-title":"Strategies to Generate Nitrogen\u2010Centered Radicals That May Rely on Photoredox Catalysis: Development in Reaction Methodology and Applications in Organic Synthesis","volume":"122","author":"Kwon K.","year":"2022","journal-title":"Chemical Reviews"},{"key":"e_1_2_7_10_1","doi-asserted-by":"crossref","first-page":"14399","DOI":"10.1002\/anie.202101775","article-title":"Three\u2010Component Aminoarylation of Electron\u2010Rich Alkenes by Merging Photoredox With Nickel Catalysis","volume":"60","author":"Jiang H.","year":"2021","journal-title":"Angewandte Chemie International Edition"},{"key":"e_1_2_7_11_1","doi-asserted-by":"crossref","first-page":"9112","DOI":"10.1021\/jacs.0c03039","article-title":"Selective Modification of Tryptophan Residues in Peptides and Proteins Using a Biomimetic Electron Transfer Process","volume":"142","author":"Tower S. J.","year":"2020","journal-title":"Journal of the American Chemical Society"},{"key":"e_1_2_7_12_1","doi-asserted-by":"crossref","first-page":"16528","DOI":"10.1002\/anie.201910926","article-title":"Carboamination of Unactivated Alkenes Through Three\u2010Component Radical Conjugate Addition","volume":"58","author":"Jiang H.","year":"2019","journal-title":"Angewandte Chemie International Edition"},{"key":"e_1_2_7_13_1","doi-asserted-by":"crossref","first-page":"12154","DOI":"10.1002\/chem.201801655","article-title":"Hydroxylamine Derivatives as Nitrogen\u2010Radical Precursors in Visible\u2010Light Photochemistry","volume":"24","author":"Davies J.","year":"2018","journal-title":"Chemistry\u2014 A European Journal"},{"key":"e_1_2_7_14_1","doi-asserted-by":"crossref","first-page":"401","DOI":"10.1021\/acs.orglett.7b03693","article-title":"Photoredox\u2010Induced Radical Relay Toward Functionalized \u03b2\u2010Amino Alcohol Derivatives","volume":"20","author":"An X.\u2010D.","year":"2018","journal-title":"Organic Letters"},{"key":"e_1_2_7_15_1","doi-asserted-by":"crossref","first-page":"2909","DOI":"10.1021\/acs.orglett.7b01145","article-title":"Photoredox\u2010Catalyzed Diamidation and Oxidative Amidation of Alkenes: Solvent\u2010Enabled Synthesis of 1,2\u2010Diamides and \u03b1\u2010Amino Ketones","volume":"19","author":"Qin Q.","year":"2017","journal-title":"Organic Letters"},{"key":"e_1_2_7_16_1","doi-asserted-by":"crossref","first-page":"5356","DOI":"10.1021\/acs.orglett.6b02711","article-title":"A Single Electron Transfer (SET) Approach to C\u2013H Amidation of Hydrazones via Visible\u2010Light Photoredox Catalysis","volume":"18","author":"Zhang M.","year":"2016","journal-title":"Organic Letters"},{"key":"e_1_2_7_17_1","doi-asserted-by":"crossref","first-page":"254","DOI":"10.1021\/ol503338b","article-title":"N \u2010Aminopyridinium Salts as Precursors for N\u2010Centered Radicals \u2013 Direct Amidation of Arenes and Heteroarenes","volume":"17","author":"Greulich T. W.","year":"2015","journal-title":"Organic Letters"},{"key":"e_1_2_7_18_1","doi-asserted-by":"crossref","first-page":"3504","DOI":"10.1021\/ol501457s","article-title":"Visible\u2010Light\u2010Promoted Redox Neutral C\u2013H Amidation of Heteroarenes With Hydroxylamine Derivatives","volume":"16","author":"Qin Q.","year":"2014","journal-title":"Organic Letters"},{"key":"e_1_2_7_19_1","doi-asserted-by":"crossref","DOI":"10.1002\/anie.202318304","article-title":"Deprotective Functionalization: A Direct Conversion of Nms\u2010Amides to Carboxamides Using Carboxylic Acids","volume":"63","author":"Spie\u00df P.","year":"2024","journal-title":"Angewandte Chemie International Edition"},{"key":"e_1_2_7_20_1","doi-asserted-by":"crossref","DOI":"10.1002\/chem.202301312","article-title":"Nms\u2010Amides: An Amine Protecting Group with Unique Stability and Selectivity","volume":"29","author":"Spie\u00df P.","year":"2023","journal-title":"Chemistry\u2014 A European Journal"},{"key":"e_1_2_7_21_1","doi-asserted-by":"crossref","first-page":"1326","DOI":"10.1021\/acs.orglett.3c00299","article-title":"Fluorinated 2,6\u2010Xylenesulfonyl Group: A Protective Group for Amines","volume":"25","author":"Katayama Y.","year":"2023","journal-title":"Organic Letters"},{"key":"e_1_2_7_22_1","doi-asserted-by":"publisher","DOI":"10.1039\/D5CC05424A"},{"key":"e_1_2_7_23_1","doi-asserted-by":"publisher","DOI":"10.1039\/D4QO02082K"},{"key":"e_1_2_7_24_1","doi-asserted-by":"crossref","first-page":"7804","DOI":"10.1039\/C6OB00985A","article-title":"Recent Advances in the Synthesis of Indolizines and Their \u03c0\u2010Expanded Analogues","volume":"14","author":"Sadowski B.","year":"2016","journal-title":"Organic & Biomolecular Chemistry"},{"key":"e_1_2_7_25_1","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1021\/acsorginorgau.5c00110","article-title":"C\u2013C Bond Formation via Direct Functionalization of Indolizines With a Bichromophoric Ruthenium Photocatalyst","volume":"6","author":"Stefanoni K. K.","year":"2026","journal-title":"ACS Organic & Inorganic Au"},{"key":"e_1_2_7_26_1","doi-asserted-by":"crossref","first-page":"8389","DOI":"10.1021\/acs.orglett.5c02079","article-title":"Access to SCF3 \u2010Substituted Indolizines via a Photocatalytic Late\u2010Stage Functionalization Protocol","volume":"27","author":"Stefanoni K. K.","year":"2025","journal-title":"Organic Letters"},{"key":"e_1_2_7_27_1","doi-asserted-by":"crossref","first-page":"6491","DOI":"10.1021\/acs.joc.5c00319","article-title":"Bichromophoric Ruthenium Complexes for Photocatalyzed Late\u2010Stage Synthesis of Trifluoromethylated Indolizines","volume":"90","author":"Stefanoni K. K.","year":"2025","journal-title":"Journal of Organic Chemistry"},{"key":"e_1_2_7_28_1","doi-asserted-by":"crossref","DOI":"10.1002\/chem.202203541","article-title":"Diquat Based Dyes: A New Class of Photoredox Catalysts and Their Use in Aerobic Thiocyanation","volume":"29","author":"Meier A.","year":"2023","journal-title":"Chemistry\u2014 A European Journal"},{"key":"e_1_2_7_29_1","doi-asserted-by":"crossref","first-page":"42930","DOI":"10.1039\/D0RA08749A","article-title":"A Photoredox Catalysed Heck Reaction via Hole Transfer From a Ru( ii )\u2010bis(terpyridine) Complex to Graphene Oxide","volume":"10","author":"Rosenthal M.","year":"2020","journal-title":"RSC Advances"},{"key":"e_1_2_7_30_1","doi-asserted-by":"crossref","first-page":"142","DOI":"10.1016\/j.tet.2017.11.053","article-title":"New Pyridinium Based Ionic Dyes for the Hydrogen Evolution Reaction","volume":"74","author":"Konieczna D. D.","year":"2018","journal-title":"Tetrahedron"},{"key":"e_1_2_7_31_1","doi-asserted-by":"crossref","first-page":"38","DOI":"10.31635\/ccschem.019.20180026","article-title":"Chemistry With N\u2010Centered Radicals Generated by Single\u2010Electron Transfer\u2010Oxidation Using Photoredox Catalysis","volume":"1","author":"Jiang H.","year":"2019","journal-title":"CCS Chemistry"},{"key":"e_1_2_7_32_1","doi-asserted-by":"crossref","first-page":"412","DOI":"10.1039\/D5SC00268K","article-title":"1,2\u2010Hydrogen Atom Transfer of Aminyl Radicals Under Photoredox Catalysis for the Synthesis of \u03b1\u2010Amino Phosphine Oxides","volume":"17","author":"Pan A.","year":"2026","journal-title":"Chemical Science"},{"key":"e_1_2_7_33_1","doi-asserted-by":"crossref","first-page":"16045","DOI":"10.1021\/jacs.3c04376","article-title":"Net\u20101,2\u2010Hydrogen Atom Transfer of Amidyl Radicals: Toward the Synthesis of 1,2\u2010Diamine Derivatives","volume":"145","author":"Jiang Y.","year":"2023","journal-title":"Journal of the American Chemical Society"},{"key":"e_1_2_7_34_1","doi-asserted-by":"crossref","first-page":"1346","DOI":"10.1039\/D1CC06688A","article-title":"Photoredox Catalyzed C\u2013H Trifluoroethylamination of Heteroarenes","volume":"58","author":"Wang J.","year":"2022","journal-title":"Chemical Communications"},{"key":"e_1_2_7_35_1","doi-asserted-by":"crossref","first-page":"19146","DOI":"10.1039\/D5CC05422B","article-title":"Photoinduced C(sp3 )\u2013H Functionalization via the Photocatalyst\u2010Free Hydrogen Atom Transfer Pathway","volume":"61","author":"Wei Y.","year":"2025","journal-title":"Chemical Communications"},{"key":"e_1_2_7_36_1","doi-asserted-by":"crossref","first-page":"981","DOI":"10.1021\/jm00084a002","article-title":"A Novel Class of Calcium\u2010Entry Blockers: The 1\u2010[[4\u2010(aminoalkoxy)phenyl]sulfonyl]Indolizines","volume":"35","author":"Gubin J.","year":"1992","journal-title":"Journal of Medicinal Chemistry"},{"key":"e_1_2_7_37_1","doi-asserted-by":"publisher","DOI":"10.1021\/acs.orglett.6c00406"},{"key":"e_1_2_7_38_1","doi-asserted-by":"crossref","first-page":"7049","DOI":"10.1021\/acs.joc.5c00635","article-title":"Visible\u2010Light\u2010Induced C\u2013H Alkylation of 1,2,4\u2010Triazine\u20103,5(2 H ,4 H )\u2010diones via Infrequent 1,2\u2010Hydrogen\u2010Atom Transfer","volume":"90","author":"Wang M.","year":"2025","journal-title":"Journal of Organic Chemistry"},{"key":"e_1_2_7_39_1","doi-asserted-by":"crossref","DOI":"10.1002\/ejoc.202500819","article-title":"Photocatalysis 1,6\u2010Addition for Site\u2010Selective Alkylation of Para\u2010Quinone Methides ( p \u2010QMs) via Amidyl Radical 1,2\u2010Hydrogen Atom Transfer","volume":"28","author":"Yang Z.","year":"2025","journal-title":"European Journal of Organic Chemistry"},{"key":"e_1_2_7_40_1","doi-asserted-by":"crossref","first-page":"5823","DOI":"10.1021\/acs.orglett.5c01633","article-title":"Photoexcited Copper\u2010Catalyzed Difunctionalization of Alkenes for the Synthesis of 2,5\u2010Diamino Acid Derivatives via Uncommon 1,2\u2010Hydrogen Atom Transfer of Amidyl Radicals","volume":"27","author":"Zhang X.","year":"2025","journal-title":"Organic Letters"},{"key":"e_1_2_7_41_1","doi-asserted-by":"crossref","first-page":"962","DOI":"10.1039\/D4SC04997G","article-title":"Visible\u2010Light\u2010Driven Net\u20101,2\u2010Hydrogen Atom Transfer of Amidyl Radicals to Access \u03b2\u2010Amido Ketone Derivatives","volume":"16","author":"Jiang Y.","year":"2025","journal-title":"Chemical Science"},{"key":"e_1_2_7_42_1","doi-asserted-by":"crossref","first-page":"8693","DOI":"10.1021\/acs.orglett.3c03594","article-title":"Visible\u2010Light\u2010Driven C,N \u2010Selective Heteroarylation of N \u2010Fluoroalkyl Hydroxylamine Reagents With Quinoxalin\u20102(1 H )\u2010ones","volume":"25","author":"Liu Y.","year":"2023","journal-title":"Organic Letters"},{"key":"e_1_2_7_43_1","doi-asserted-by":"crossref","first-page":"1876","DOI":"10.1021\/jacsau.5c01732","article-title":"Nickel\u2010Catalyzed \u03b1\u2010Arylation and Alkenylation of \u03b1\u2010Trifluoromethyl Amines via 1,2\u2010HAT Assisted by DMSO","volume":"6","author":"Bilal M.","year":"2026","journal-title":"JACS Au"},{"key":"e_1_2_7_44_1","doi-asserted-by":"crossref","first-page":"3277","DOI":"10.1039\/jr9630003277","article-title":"609. Indolizines. Part II. Preparation From Ethyl 2\u2010Pyridylacetate and Related Compounds","volume":"609","author":"Bragg D. R.","year":"1963","journal-title":"Journal of the Chemical Society (Resumed)"},{"key":"e_1_2_7_45_1","doi-asserted-by":"crossref","first-page":"3291","DOI":"10.1021\/acs.orglett.8b01168","article-title":"Transition\u2010Metal\u2010Free Regioselective Cross\u2010Coupling: Controlled Synthesis of Mono\u2010 or Dithiolation Indolizines","volume":"20","author":"Li B.","year":"2018","journal-title":"Organic Letters"},{"key":"e_1_2_7_46_1","doi-asserted-by":"crossref","first-page":"15973","DOI":"10.1021\/acs.joc.1c00873","article-title":"Oxidation Potential\u2010Guided Electrochemical Radical\u2013Radical Cross\u2010Coupling Approaches to 3\u2010Sulfonylated Imidazopyridines and Indolizines","volume":"86","author":"Kim W.","year":"2021","journal-title":"Journal of Organic Chemistry"},{"key":"e_1_2_7_47_1","doi-asserted-by":"crossref","first-page":"3018","DOI":"10.1002\/jhet.4000","article-title":"6\u2010(Hetero)arylindolizino[1,2\u2010 c ]quinolines as Highly Fluorescent Chemical Space: Synthesis and Photophysical Properties","volume":"57","author":"Singh D. K.","year":"2020","journal-title":"Journal of Heterocyclic Chemistry"},{"key":"e_1_2_7_48_1","doi-asserted-by":"crossref","first-page":"1733","DOI":"10.1055\/s-2000-8195","article-title":"A Novel and Practical Synthesis of 3\u2010Unsubstituted Indolizines","volume":"2000","author":"Zhang L.","year":"2000","journal-title":"Synthesis"},{"key":"e_1_2_7_49_1","doi-asserted-by":"crossref","first-page":"5605","DOI":"10.1021\/jacs.3c14195","article-title":"Catalytic Intermolecular Deoxygenative Coupling of Carbonyl Compounds With Alkynes by a Cp*Mo(II)\u2010Catalyst","volume":"146","author":"Wang J.\u2010L.","year":"2024","journal-title":"Journal of the American Chemical Society"},{"key":"e_1_2_7_50_1","doi-asserted-by":"crossref","first-page":"7189","DOI":"10.1021\/acs.joc.9b00871","article-title":"Regioselective Synthesis of 1\u2010Sulfanyl\u2010 and 1\u2010Selanylindolizines","volume":"84","author":"Penteado F.","year":"2019","journal-title":"Journal of Organic Chemistry"},{"key":"e_1_2_7_51_1","doi-asserted-by":"crossref","DOI":"10.1039\/c1cc13683f","article-title":"Efficient Electron Transfer Through a Triazole Link in Ruthenium(II) Polypyridine Type Complexes","volume":"47","author":"Baron A.","year":"2011","journal-title":"Chemical Communications"},{"key":"e_1_2_7_52_1","doi-asserted-by":"crossref","first-page":"12492","DOI":"10.1021\/ic4014976","article-title":"Synthesis of Phosphonic Acid Derivatized Bipyridine Ligands and Their Ruthenium Complexes","volume":"52","author":"Norris M. R.","year":"2013","journal-title":"Inorganic Chemistry"},{"key":"e_1_2_7_53_1","doi-asserted-by":"crossref","DOI":"10.1002\/wcms.1493","article-title":"Extended Tight\u2010Binding Quantum Chemistry Methods","volume":"11","author":"Bannwarth C.","year":"2021","journal-title":"WIREs Computational Molecular Science"},{"key":"e_1_2_7_54_1","doi-asserted-by":"crossref","first-page":"7169","DOI":"10.1039\/C9CP06869D","article-title":"Automated Exploration of the Low\u2010Energy Chemical Space With Fast Quantum Chemical Methods","volume":"22","author":"Pracht P.","year":"2020","journal-title":"Physical Chemistry Chemical Physics"},{"key":"e_1_2_7_55_1","doi-asserted-by":"crossref","first-page":"2847","DOI":"10.1021\/acs.jctc.9b00143","article-title":"Exploration of Chemical Compound, Conformer, and Reaction Space With Meta\u2010Dynamics Simulations Based on Tight\u2010Binding Quantum Chemical Calculations","volume":"15","author":"Grimme S.","year":"2019","journal-title":"Journal of Chemical Theory and Computation"},{"key":"e_1_2_7_56_1","doi-asserted-by":"crossref","DOI":"10.1002\/anie.202113905","article-title":"Hydrocarbon Macrocycle Conformer Ensembles and 13C\u2010NMR Spectra","volume":"61","author":"Bohle F.","year":"2022","journal-title":"Angewandte Chemie International Edition"},{"key":"e_1_2_7_57_1","doi-asserted-by":"crossref","first-page":"4039","DOI":"10.1021\/acs.jpca.1c00971","article-title":"Efficient Quantum Chemical Calculation of Structure Ensembles and Free Energies for Nonrigid Molecules","volume":"125","author":"Grimme S.","year":"2021","journal-title":"Journal of Physical Chemistry A"},{"key":"e_1_2_7_58_1","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1002\/wcms.81","article-title":"The ORCA Program System","volume":"2","author":"Neese F.","year":"2012","journal-title":"WIREs Computational Molecular Science"},{"key":"e_1_2_7_59_1","doi-asserted-by":"crossref","DOI":"10.1063\/1.3382344","article-title":"A Consistent and Accurate Ab Initio Parametrization of Density Functional Dispersion Correction (DFT\u2010D) for the 94 Elements H\u2010Pu","volume":"132","author":"Grimme S.","year":"2010","journal-title":"Journal of Chemical Physics"},{"key":"e_1_2_7_60_1","doi-asserted-by":"crossref","first-page":"3297","DOI":"10.1039\/b508541a","article-title":"Balanced Basis Sets of Split Valence, Triple Zeta Valence and Quadruple Zeta Valence Quality for H to Rn: Design and Assessment of Accuracy","volume":"7","author":"Weigend F.","year":"2005","journal-title":"Physical Chemistry Chemical Physics"},{"key":"e_1_2_7_61_1","doi-asserted-by":"crossref","first-page":"6515","DOI":"10.1021\/acs.orglett.5c01933","article-title":"Dearomatization of Electron\u2010Deficient Indoles with N \u2010Alkylanilines via Visible\u2010Light\u2010Induced Hydroalkylation","volume":"27","author":"Zhang Q.","year":"2025","journal-title":"Organic Letters"}],"container-title":["Chemistry \u2013 A European Journal"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/chem.71550","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full-xml\/10.1002\/chem.71550","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/chem.71550","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T12:26:01Z","timestamp":1786105561000},"score":1,"resource":{"primary":{"URL":"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.71550"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,8,7]]},"references-count":60,"alternative-id":["10.1002\/chem.71550"],"URL":"https:\/\/doi.org\/10.1002\/chem.71550","archive":["Portico"],"relation":{},"ISSN":["0947-6539","1521-3765"],"issn-type":[{"value":"0947-6539","type":"print"},{"value":"1521-3765","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,8,7]]},"assertion":[{"value":"2026-06-29","order":0,"name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-07-29","order":2,"name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-08-07","order":3,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}],"article-number":"e71550"}}