Koszinowski, Konrad

[["dc.bibliographiccitation.firstpage","25"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Organometallics"],["dc.bibliographiccitation.lastpage","33"],["dc.bibliographiccitation.volume","39"],["dc.contributor.author","Auth, Thomas"],["dc.contributor.author","Koszinowski, Konrad"],["dc.contributor.author","O’Hair, Richard A. J."],["dc.date.accessioned","2020-12-10T18:09:14Z"],["dc.date.available","2020-12-10T18:09:14Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1021/acs.organomet.9b00521"],["dc.identifier.eissn","1520-6041"],["dc.identifier.issn","0276-7333"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/73577"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Dissecting Transmetalation Reactions at the Molecular Level: Phenyl Transfer in Metal Borate Complexes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","7752"],["dc.bibliographiccitation.issue","23"],["dc.bibliographiccitation.journal","Chemistry - A European Journal"],["dc.bibliographiccitation.lastpage","7762"],["dc.bibliographiccitation.volume","22"],["dc.contributor.author","Schnegelsberg, Christoph"],["dc.contributor.author","Bachmann, Sebastian"],["dc.contributor.author","Kolter, Marlene"],["dc.contributor.author","Auth, Thomas"],["dc.contributor.author","John, Michael"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Koszinowski, Konrad"],["dc.date.accessioned","2018-11-07T10:13:01Z"],["dc.date.available","2018-11-07T10:13:01Z"],["dc.date.issued","2016"],["dc.description.abstract","Grignard reagents RMgCl and their so-called turbo variant, the highly reactive RMgCl center dot LiCl, are of exceptional synthetic utility. Nevertheless, it is still not fully understood which species these compounds form in solution and, in particular, in which way LiCl exerts its reactivity-enhancing effect. A combination of electrospray-ionization mass spectrometry, electrical conductivity measurements, NMR spectroscopy (including diffusion-ordered spectroscopy), and quantum chemical calculations is used to analyze solutions of RMgCl (R=Me, Et, Bu, Hex, Oct, Dec, iPr, tBu, Ph) in tetrahydrofuran and other ethereal solvents in the absence and presence of stoichiometric amounts of LiCl. In tetrahydrofuran, RMgCl forms mononuclear species, which are converted into trinuclear anions as a result of the concentration increase experienced during the electrospray process. These trinuclear anions are theoretically predicted to adopt open cubic geometries, which remarkably resemble structural motifs previously found in the solid state. The molecular constituents of RMgCl and RMgCl center dot LiCl are interrelated via Schlenk equilibria and fast intermolecular exchange processes. A small portion of the Grignard reagent also forms anionic ate complexes in solution. The abundance of these more electron-rich and hence supposedly more nucleophilic ate complexes strongly increases upon the addition of LiCl, thus rationalizing its beneficial effect on the reactivity of Grignard reagents."],["dc.description.sponsorship","Deutsche Forschungsgmeinschaft [KO 2875/4-1]"],["dc.identifier.doi","10.1002/chem.201600699"],["dc.identifier.isi","000380267100015"],["dc.identifier.pmid","27150118"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/40354"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3765"],["dc.relation.issn","0947-6539"],["dc.title","Association and Dissociation of Grignard Reagents RMgCl and Their Turbo Variant RMgCl center dot LiCl"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

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[["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","Chemistry – A European Journal"],["dc.bibliographiccitation.volume","28"],["dc.contributor.author","Auth, Thomas"],["dc.contributor.author","Stein, Christopher J."],["dc.contributor.author","O'Hair, Richard A. J."],["dc.contributor.author","Koszinowski, Konrad"],["dc.date.accessioned","2022-12-01T08:30:33Z"],["dc.date.available","2022-12-01T08:30:33Z"],["dc.date.issued","2022"],["dc.description.sponsorship"," Deutsche Forschungsgemeinschaft https://doi.org/10.13039/501100001659"],["dc.description.sponsorship"," Alexander von Humboldt-Stiftung https://doi.org/10.13039/100005156"],["dc.identifier.doi","10.1002/chem.202103130"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/117921"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-621"],["dc.relation.eissn","1521-3765"],["dc.relation.issn","0947-6539"],["dc.rights.uri","http://creativecommons.org/licenses/by-nc-nd/4.0/"],["dc.title","Origin of the different reactivity of the high‐valent coinage‐metal complexes [RCu\r\n \r\n iii\r\n \r\n Me\r\n 3\r\n ]\r\n −\r\n and [RAg\r\n \r\n iii\r\n \r\n Me\r\n 3\r\n ]\r\n −\r\n (R=allyl)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","9797"],["dc.bibliographiccitation.issue","28"],["dc.bibliographiccitation.journal","Analytical Chemistry"],["dc.bibliographiccitation.lastpage","9807"],["dc.bibliographiccitation.volume","93"],["dc.contributor.author","Auth, Thomas"],["dc.contributor.author","Grabarics, Márkó"],["dc.contributor.author","Schlangen, Maria"],["dc.contributor.author","Pagel, Kevin"],["dc.contributor.author","Koszinowski, Konrad"],["dc.date.accessioned","2021-08-12T07:44:49Z"],["dc.date.available","2021-08-12T07:44:49Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1021/acs.analchem.1c01333"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/88301"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-448"],["dc.relation.eissn","1520-6882"],["dc.relation.issn","0003-2700"],["dc.title","Modular Ion Mobility Calibrants for Organometallic Anions Based on Tetraorganylborate Salts"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5086"],["dc.bibliographiccitation.issue","40"],["dc.bibliographiccitation.journal","Chemical Communications"],["dc.bibliographiccitation.lastpage","5089"],["dc.bibliographiccitation.volume","54"],["dc.contributor.author","Weske, Sebastian"],["dc.contributor.author","Hardin, Richard A."],["dc.contributor.author","Auth, Thomas"],["dc.contributor.author","O’Hair, Richard A. J."],["dc.contributor.author","Koszinowski, Konrad"],["dc.contributor.author","Ogle, Craig A."],["dc.date.accessioned","2021-06-01T10:50:49Z"],["dc.date.available","2021-06-01T10:50:49Z"],["dc.date.issued","2018"],["dc.description.abstract","Silver-mediated cross-coupling reactions proceed via anionic ate complexes, which have been characterized by a combination of NMR spectroscopy, ESI mass spectrometry, and quantum-chemical calculations."],["dc.description.abstract","Despite the potential of silver to mediate synthetically valuable cross-coupling reactions, the operating mechanisms have remained unknown. Here, we use a combination of rapid-injection NMR spectroscopy, electrospray-ionization mass spectrometry, and quantum chemical calculations to demonstrate that these transformations involve argentate( i ) and ( iii ) complexes as key intermediates."],["dc.identifier.doi","10.1039/C8CC01707G"],["dc.identifier.eissn","1364-548X"],["dc.identifier.issn","1359-7345"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/86795"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation.eissn","1364-548X"],["dc.relation.issn","1359-7345"],["dc.title","Argentate( i ) and ( iii ) complexes as intermediates in silver-mediated cross-coupling reactions"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]