Schneider, Sven

[["dc.bibliographiccitation.firstpage","5511"],["dc.bibliographiccitation.issue","40"],["dc.bibliographiccitation.journal","Chemical Communications"],["dc.bibliographiccitation.lastpage","5514"],["dc.bibliographiccitation.volume","53"],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Diefenbach, Martin"],["dc.contributor.author","Bete, Sarah C."],["dc.contributor.author","Würtele, Christian"],["dc.contributor.author","Volkmann, Christian"],["dc.contributor.author","Demeshko, Serhiy"],["dc.contributor.author","Holthausen, Max C."],["dc.contributor.author","Schneider, Sven"],["dc.date.accessioned","2018-08-17T09:33:43Z"],["dc.date.accessioned","2021-10-27T13:12:42Z"],["dc.date.available","2018-08-17T09:33:43Z"],["dc.date.available","2021-10-27T13:12:42Z"],["dc.date.issued","2017"],["dc.description.abstract","Reduction of the pincer complex [OsIIICl2(PNP)] (PNP = N(CHCHPtBu2)2) affords the isolation and full characterization of an osmium(II) complex with square-planar coordination geometry, i.e. [OsIICl(PNP)]. Spectroscopic, structural and magnetic data in combination with multireference computations indicate strong temperature independent paramagnetism, which arises from an energetically well separated ground state that mixes with excited states through spin-orbit coupling."],["dc.identifier.doi","10.1039/C7CC01569K"],["dc.identifier.isi","000401602900006"],["dc.identifier.pmid","28405639"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/15307"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91714"],["dc.language.iso","en"],["dc.notes.intern","Migrated from goescholar"],["dc.notes.intern","In goescholar not merged with http://resolver.sub.uni-goettingen.de/purl?gs-1/15078 but duplicate"],["dc.relation","info:eu-repo/grantAgreement/EC/H2020/646747/EU//N2FEED"],["dc.relation.eissn","1364-548X"],["dc.relation.issn","1359-7345"],["dc.relation.orgunit","Fakultät für Chemie"],["dc.rights","Goescholar"],["dc.rights.access","openAccess"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject","Complex; Square-Planar; Osmium(II)"],["dc.subject.ddc","540"],["dc.title","A Square-Planar Osmium(II) Complex"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","submitted_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","469"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Inorganic Chemistry Frontiers"],["dc.bibliographiccitation.lastpage","477"],["dc.bibliographiccitation.volume","3"],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Finger, Markus"],["dc.contributor.author","Würtele, Christian"],["dc.contributor.author","Kasanmascheff, Müge"],["dc.contributor.author","Schneider, Sven"],["dc.date.accessioned","2016-02-15T11:46:27Z"],["dc.date.accessioned","2021-10-27T13:12:29Z"],["dc.date.available","2016-02-15T11:46:27Z"],["dc.date.available","2021-10-27T13:12:29Z"],["dc.date.issued","2016"],["dc.description.abstract","The oxidative coupling of nitride ligands (N3−) to dinitrogen and its microscopic reverse, N2-splitting to nitrides, are important elementary steps in chemical transformations, such as selective ammonia oxidation or nitrogen fixation. Here an experimental and computational evaluation is provided for the homo- and heterocoupling of our previously reported iridium(IV) and iridium(V) nitrides [IrN(PNP)]n (n = 0, +1; PNP = N(CHCHPtBu2)2). All three formal coupling products [(PNP)IrN2Ir(PNP)]n (n = 0–+2) were structurally characterized. While the three coupling reactions are all thermodynamically feasible, homocoupling of [IrN(PNP)]+ is kinetically hindered. The contributing parameters to relative coupling rates are discussed providing qualitative guidelines for the stability of electron rich transition metal nitrides."],["dc.description.sponsorship","European Research Council [646747]"],["dc.identifier.doi","10.1039/c5qi00267b"],["dc.identifier.isi","000374011600004"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/12839"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91696"],["dc.language.iso","en"],["dc.notes.intern","Migrated from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Royal Soc Chemistry"],["dc.relation","info:eu-repo/grantAgreement/EC/H2020/646747/EU/N2 as Chemical Feedstock – Synthetic Nitrogen Fixation beyond Haber-Bosch/N2FEED"],["dc.relation.issn","2052-1553"],["dc.relation.orgunit","Fakultät für Chemie"],["dc.rights","Goescholar"],["dc.rights.access","openAccess"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject","iridium nitrido complexes; Coupling"],["dc.title","Coupling of terminal iridium nitrido complexes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","802"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","Organometallics"],["dc.bibliographiccitation.lastpage","811"],["dc.bibliographiccitation.volume","37"],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Bete, Sarah C."],["dc.contributor.author","Finger, Markus"],["dc.contributor.author","Volkmann, Christian"],["dc.contributor.author","Würtele, Christian"],["dc.contributor.author","Schneider, Sven"],["dc.date.accessioned","2019-07-09T11:51:20Z"],["dc.date.available","2019-07-09T11:51:20Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1021/acs.organomet.7b00707"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16106"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/59928"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.relation","info:eu-repo/grantAgreement/EC/H2020/646747/EU//N2FEED"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject.ddc","540"],["dc.title","Four- and Five-Coordinate Osmium(IV) Nitrides and Imides: Circumventing the “Nitrido Wall”"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","submitted_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","9290"],["dc.bibliographiccitation.issue","19"],["dc.bibliographiccitation.journal","Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","9302"],["dc.bibliographiccitation.volume","54"],["dc.contributor.author","Scheibel, Markus G."],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Kinauer, Markus"],["dc.contributor.author","Heinemann, Frank W."],["dc.contributor.author","Wuertele, Christian"],["dc.contributor.author","de Bruin, Bas"],["dc.contributor.author","Schneider, Sven"],["dc.date.accessioned","2018-11-07T09:50:22Z"],["dc.date.available","2018-11-07T09:50:22Z"],["dc.date.issued","2015"],["dc.description.abstract","The redox series [Ir-n(NHx)(PNP)] (n = II-IV, x = 3-0; PNP = N(CHCHPtBu2)(2)) was examined with respect to electron, proton, and hydrogen atom transfer steps. The experimental and computational results suggest that the Ir-III imido species [Ir(NH) (PNP)] is not stable but undergoes to the respective Ir-II amido and Ir-III nitrido species. N-H bond strengths are estimated upon reaction with hydrogen atom transfer reagents to rationalize this observation and are used to discuss the reactivity of these compounds toward E-H bond activation."],["dc.identifier.doi","10.1021/acs.inorgchem.5b00829"],["dc.identifier.isi","000362460800008"],["dc.identifier.pmid","26192601"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/12282"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/35691"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","1520-510X"],["dc.relation.issn","0020-1669"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Homolytic N-H Activation of Ammonia: Hydrogen Transfer of Parent Iridium Ammine, Amide, lmide, and Nitride Species"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","6338"],["dc.bibliographiccitation.issue","19"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","6341"],["dc.bibliographiccitation.volume","58"],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Delony, Daniel"],["dc.contributor.author","Neben, Marc C."],["dc.contributor.author","Würtele, Christian"],["dc.contributor.author","de Bruin, Bas"],["dc.contributor.author","Schneider, Sven"],["dc.date.accessioned","2019-07-09T11:51:54Z"],["dc.date.available","2019-07-09T11:51:54Z"],["dc.date.issued","2019"],["dc.description.abstract","The isolable complex [Os(PHMes )H(PNP)] (Mes =2,4,6-t Bu3 C6 H3 ; PNP=N{CHCHPt Bu2 }2 ) exhibits high phosphinyl radical character. This compound offers access to the phosphinidene complex [Os(PMes )H(PNP)] by P-H proton coupled electron transfer (PCET). The P-H bond dissociation energy (BDE) was determined by isothermal titration calorimetry and supporting DFT computations. The phosphinidene product exhibits electrophilic reactivity as demonstrated by intramolecular C-H activation."],["dc.identifier.doi","10.1002/anie.201901470"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16225"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60037"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.relation","info:eu-repo/grantAgreement/EC/H2020/646747/EU//N2FEED"],["dc.relation.issn","1433-7851"],["dc.rights","CC BY-NC-ND 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by-nc-nd/4.0"],["dc.subject.ddc","540"],["dc.title","Interconversion of Phosphinyl Radical and Phosphinidene Complexes by Proton Coupled Electron Transfer"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","830"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","834"],["dc.bibliographiccitation.volume","58"],["dc.contributor.author","Schendzielorz, Florian"],["dc.contributor.author","Finger, Markus"],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Würtele, Christian"],["dc.contributor.author","Krewald, Vera"],["dc.contributor.author","Schneider, Sven"],["dc.date.accessioned","2020-01-14T13:35:36Z"],["dc.date.accessioned","2021-10-27T13:12:51Z"],["dc.date.available","2020-01-14T13:35:36Z"],["dc.date.available","2021-10-27T13:12:51Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1002/anie.201812125"],["dc.identifier.doi","10.1002/ange.201812125"],["dc.identifier.eissn","1521-3773"],["dc.identifier.issn","1433-7851"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17095"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91728"],["dc.language.iso","en"],["dc.notes.intern","Migrated from goescholar"],["dc.relation","info:eu-repo/grantAgreement/EC/H2020/646747/EU//N2FEED"],["dc.relation.issn","1433-7851"],["dc.relation.orgunit","Fakultät für Chemie"],["dc.rights","Goescholar"],["dc.rights.access","openAccess"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject","N2FEED"],["dc.subject.ddc","540"],["dc.title","Metal-Ligand Cooperative Synthesis of Benzonitrile by Electrochemical Reduction and Photolytic Splitting of Dinitrogen"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","submitted_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","10275"],["dc.bibliographiccitation.issue","44"],["dc.bibliographiccitation.journal","Chemical Science"],["dc.bibliographiccitation.lastpage","10282"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","Schluschaß, Bastian"],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Demeshko, Serhiy"],["dc.contributor.author","Finger, Markus"],["dc.contributor.author","Franke, Alicja"],["dc.contributor.author","Herwig, Christian"],["dc.contributor.author","Würtele, Christian"],["dc.contributor.author","Ivanovic-Burmazovic, Ivana"],["dc.contributor.author","Limberg, Christian"],["dc.contributor.author","Schneider, Sven"],["dc.contributor.author","Telser, Joshua"],["dc.date.accessioned","2021-06-01T10:50:53Z"],["dc.date.available","2021-06-01T10:50:53Z"],["dc.date.issued","2019"],["dc.description.abstract","An N 2 -bridged ditungsten complex is presented that undergoes N 2 -splitting or hydrogen evolution upon protonation depending on the acid and reaction conditions. Spectroscopic, kinetic and computational results emphasize the impact of hydrogen bonding on the reaction selectivity."],["dc.description.abstract","Mo complexes are currently the most active catalysts for nitrogen fixation under ambient conditions. In comparison, tungsten platforms are scarcely examined. For active catalysts, the control of N 2 vs. proton reduction selectivities remains a difficult task. We here present N 2 splitting using a tungsten pincer platform, which has been proposed as the key reaction for catalytic nitrogen fixation. Starting from [WCl 3 (PNP)] (PNP = N(CH 2 CH 2 P t Bu 2 ) 2 ), the activation of N 2 enabled the isolation of the dinitrogen bridged redox series [(N 2 ){WCl(PNP)} 2 ] 0/+/2+ . Protonation of the neutral complex results either in the formation of a nitride [W(N)Cl( H PNP)] + or H 2 evolution and oxidation of the W 2 N 2 core, respectively, depending on the acid and reaction conditions. Examination of the nitrogen splitting vs. proton reduction selectivity emphasizes the role of hydrogen bonding of the conjugate base with the protonated intermediates and provides guidelines for nitrogen fixation."],["dc.identifier.doi","10.1039/C9SC03779A"],["dc.identifier.eissn","2041-6539"],["dc.identifier.issn","2041-6520"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16963"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/86812"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.notes.intern","Merged from goescholar"],["dc.relation.eissn","2041-6539"],["dc.relation.issn","2041-6520"],["dc.rights","CC BY 3.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/3.0"],["dc.title","Selectivity of tungsten mediated dinitrogen splitting vs. proton reduction"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5872"],["dc.bibliographiccitation.issue","21"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","5876"],["dc.bibliographiccitation.volume","56"],["dc.contributor.author","Silantyev, Gleb A."],["dc.contributor.author","Förster, Moritz"],["dc.contributor.author","Schluschaß, Bastian"],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Würtele, Christian"],["dc.contributor.author","Volkmann, Christian"],["dc.contributor.author","Holthausen, Max C."],["dc.contributor.author","Schneider, Sven"],["dc.date.accessioned","2019-07-09T11:45:45Z"],["dc.date.available","2019-07-09T11:45:45Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1002/anie.201701504"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/15308"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/59303"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.relation","info:eu-repo/grantAgreement/EC/H2020/646747/EU//N2FEED"],["dc.relation.issn","1433-7851"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject.ddc","540"],["dc.title","Dinitrogen Splitting Coupled to Protonation"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","submitted_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","565"],["dc.bibliographiccitation.issue","13"],["dc.bibliographiccitation.journal","Zeitschrift für anorganische und allgemeine Chemie"],["dc.bibliographiccitation.lastpage","569"],["dc.bibliographiccitation.volume","646"],["dc.contributor.author","Abbenseth, Josh"],["dc.contributor.author","Schneider, Sven"],["dc.date.accessioned","2020-12-10T14:07:19Z"],["dc.date.available","2020-12-10T14:07:19Z"],["dc.date.issued","2020"],["dc.description.abstract","Terminal, electrophilic phosphinidene complexes (M=PR) are attractive platforms for PR‐transfer to organic substrates. In contrast to aryl‐ or alkylphosphinidene complexes terminal chlorophosphinidenes (M=PCl) have only been proposed as transient intermediates but isolable example remain elusive. Here we present the transfer of PCl from chloro‐substituted dibenzo‐7λ3‐phosphanorbornadiene to a square‐planar osmium(II) PNP pincer complex to give the first isolable, terminal chlorophosphinidene complex with remarkable thermal stability. Os=P bonding was examined computationally giving rise to highly covalent {OsII=PICl} double bonding."],["dc.description.abstract","image John Wiley \\u0026 Sons, Ltd."],["dc.description.sponsorship","European Research Council http://dx.doi.org/10.13039/501100000781"],["dc.identifier.doi","10.1002/zaac.202000010"],["dc.identifier.eissn","1521-3749"],["dc.identifier.issn","0044-2313"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/70169"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made."],["dc.title","A Terminal Chlorophosphinidene Complex"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]