Roesky, Herbert W.

[["dc.bibliographiccitation.firstpage","1414"],["dc.bibliographiccitation.issue","13"],["dc.bibliographiccitation.journal","Angewandte Chemie"],["dc.bibliographiccitation.lastpage","1416"],["dc.bibliographiccitation.volume","106"],["dc.contributor.author","Winkhofer, Norbert"],["dc.contributor.author","Voigt, Andreas"],["dc.contributor.author","Dorn, Hendrik"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Reller, Armin"],["dc.date.accessioned","2019-07-09T11:52:18Z"],["dc.date.available","2019-07-09T11:52:18Z"],["dc.date.issued","1994"],["dc.identifier.doi","10.1002/ange.19941061309"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3413"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60149"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject.ddc","540"],["dc.title","Stabile Silantriole als Synthesebausteine für Titanasilasesquioxane - Modellverbindungen für titandotierte Zeolithe"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","625"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Angewandte Chemie"],["dc.bibliographiccitation.lastpage","627"],["dc.bibliographiccitation.volume","105"],["dc.contributor.author","Pandey, Sushil K."],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2019-07-09T11:52:14Z"],["dc.date.available","2019-07-09T11:52:14Z"],["dc.date.issued","1993"],["dc.identifier.doi","10.1002/ange.19931050436"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3371"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60122"],["dc.language.iso","de"],["dc.notes.intern","Merged from goescholar"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject.ddc","540"],["dc.title","Die ersten solvensfreien Chelat- und Cuban-artigen Bariumkomplexe: effektive Sol-Gel-Bildner"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5444"],["dc.bibliographiccitation.issue","24"],["dc.bibliographiccitation.journal","Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","5446"],["dc.bibliographiccitation.volume","32"],["dc.contributor.author","Pandey, Sushil K."],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2019-07-09T11:52:15Z"],["dc.date.available","2019-07-09T11:52:15Z"],["dc.date.issued","1993"],["dc.description.abstract","Cyclozincaphosphazenes have been synthesized by the reaction of the bis-silylated ligand HN[P(NMe2)2NSiMe3]2 (1) with ZnR2 (2) (R = N(SiMe&, Me, Et). These complexes have been characterized by IR, NMR, and mass spectroscopy and by X-ray crystal structural analysis. X-ray analysis of [N(P(NMe2)2NSiMe3]2ZnN(SiMe3)2(]3 ) revealed that it crystallizes as a monomer in the solid state."],["dc.identifier.doi","10.1021/ic00076a007"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3394"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60133"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject.ddc","540"],["dc.title","Insertion of zinc into the cyclophosphazene skeleton: synthesis and structure of six-membered-ring complexes of zinc"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3447"],["dc.bibliographiccitation.issue","22"],["dc.bibliographiccitation.journal","Dalton Transactions"],["dc.bibliographiccitation.lastpage","3451"],["dc.contributor.author","Hasselbring, Reinhard"],["dc.contributor.author","Pandey, Sushil K."],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Steiner, Alexander"],["dc.date.accessioned","2009-07-03T11:02:11Z"],["dc.date.accessioned","2021-10-27T13:12:08Z"],["dc.date.available","2009-07-03T11:02:11Z"],["dc.date.available","2021-10-27T13:12:08Z"],["dc.date.issued","1993"],["dc.description.abstract","The reaction of HN[P(NMe2)2NSiMe3]2 with NaH and KH in 1 : 1 molar ratio yielded a dimer {NaN[P(NMe2)2NSiMe3]2}21 and a polymer {KN[P(NMe2)2NSiMe3]22 with a zigzag chain structure, respectively. The reaction of Ca[N(SiMe3)2]2·2thf (thf = tetrahydrofuran) with the phosphazene in 1 : 2 molar ratio in hexane resulted in the formation of a monomeric spirocyclic phosphazene complex Ca{N[P(NMe2)2NSiMe3]2}23 where the mode of chelation is tridentate. The crystal structures of 1–3 have been determined."],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1039/DT9930003447"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3392"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91662"],["dc.language.iso","en"],["dc.notes.intern","Migrated from goescholar"],["dc.relation.orgunit","Fakultät für Chemie"],["dc.rights","Goescholar"],["dc.rights.access","openAccess"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject","anorganische Chemie"],["dc.subject.ddc","540"],["dc.title","Metallation of the acyclic phosphazene ligand HN[P(NMe2)2NSiMe3]2. Synthesis and crystal structure of {NaN[P(NMe2)2NSiMe3]2}2, {KN[P(NMe2)2NSiMe3]2} and Ca{N[P(NMe2)2NSiMe3]2}2"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","231"],["dc.bibliographiccitation.journal","Phosphorus, Sulfur, and Silicion"],["dc.bibliographiccitation.lastpage","237"],["dc.bibliographiccitation.volume","84"],["dc.contributor.author","Pandey, Sushil K."],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Schmidt, Hans Georg"],["dc.contributor.author","Noltemeyer, Mathias"],["dc.date.accessioned","2019-07-09T11:52:17Z"],["dc.date.available","2019-07-09T11:52:17Z"],["dc.date.issued","1994"],["dc.description.abstract","The reaction of the acyclic phosphazene ligand, HNP(NMe2)2NSiMe32 (1) with NH4VO3 in 1:1 molar ratio resulted in the formation of an ionic species NP(NMe2)2NH2+2 VO4(SiMe3)2- (2) in quantitative yield. The reaction shows the migration of silyl group from the terminal nitrogen atoms of the phosphazene ligand 1 to the oxygen of the vanadyl group. Compound 2 crystallizes as monomer in the solid state. The X-ray structure of the phosphazenium salt, NP(NMe2)2NH2+2Cl- (3) has also been described which crystallizes as a polymeric zig-zag chain in the solid state."],["dc.identifier.doi","10.1080/10426509308034336"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60145"],["dc.language.iso","en"],["dc.subject.ddc","540"],["dc.title","Functionalization of the Classical Oxoanion VO43- by Bissilylated Phosphazene Ligand: Syntheses and X-ray Structure"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1352"],["dc.bibliographiccitation.issue","13"],["dc.bibliographiccitation.journal","Angewandte Chemie / International Edition"],["dc.bibliographiccitation.lastpage","1354"],["dc.bibliographiccitation.volume","33"],["dc.contributor.author","Winkhofer, Norbert"],["dc.contributor.author","Voigt, Andreas"],["dc.contributor.author","Dorn, Hendrik"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Reller, Armin"],["dc.date.accessioned","2019-07-09T11:52:19Z"],["dc.date.available","2019-07-09T11:52:19Z"],["dc.date.issued","1994"],["dc.description.abstract","The first Ti4Si4 heterocubane with twelve edges bridged by O atoms was prepared in good yields and characterized by X-ray crystallography. According to the IR spectrum of 1, the characteristic band for Ti-containing zeolites at approximately 960cm-1, the assignment of which had been debated, arises from the SiOTi stretching vibration. R1 = tBu, tBu3C6H2O, iPr2C6H3N(SiMe3); R2 - MeC5H4, OiPr."],["dc.identifier.doi","10.1002/anie.199413521"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3414"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60150"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject.ddc","540"],["dc.title","Stable Silanetriols as Building Blocks for the Synthesis of Titanasilasesquioxanes - Model Compounds for Titanium-Doped Zeolites"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2941"],["dc.bibliographiccitation.issue","24"],["dc.bibliographiccitation.journal","Polyhedron"],["dc.bibliographiccitation.lastpage","2945"],["dc.bibliographiccitation.volume","12"],["dc.contributor.author","Pandey, Sushil K."],["dc.contributor.author","Hasselbring, Reinhard"],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Roesky, Herbert W."],["dc.date.accessioned","2009-07-03T11:10:27Z"],["dc.date.accessioned","2021-10-27T13:11:49Z"],["dc.date.available","2009-07-03T11:10:27Z"],["dc.date.available","2010-05-06T08:15:19Z"],["dc.date.available","2021-10-27T13:11:49Z"],["dc.date.issued","1993"],["dc.description.abstract","The monosilylated acyclic phosphazene ligand Me3SiNP(NMe2)2NP(NMe2)2 NH2 (3) has been synthesized and characterized. The reaction of 3 with antimony triacetate, Sb(OOCMe3), in refluxing toluene forms a cyclic phosphazene derivative, [N{P(NMe2)2NH}2Sb(OOCMe)2 (4), which is characterized by elemental analyses, mass, IR and NMR spectroscopy and single-crystal X-ray structural analysis. Complex 4 crystallizes in the form of a cis and trans isomeric chain in the solid state."],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1016/S0277-5387(00)80043-1"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3393"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91629"],["dc.language.iso","en"],["dc.notes.intern","Migrated from goescholar"],["dc.relation.orgunit","Fakultät für Chemie"],["dc.rights","Goescholar"],["dc.rights.access","openAccess"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.subject","anorganische Chemie"],["dc.subject.ddc","540"],["dc.title","Synthesis and x-ray structure of an isomeric cyclophosphazene complex containing antimony(III)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]