Edelmann, Frank Thomas

[["dc.bibliographiccitation.firstpage","1373"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Chemische Berichte"],["dc.bibliographiccitation.lastpage","1375"],["dc.bibliographiccitation.volume","124"],["dc.contributor.author","Recknagel, Anja"],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Brooker, Sally"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Edelmann, Frank T."],["dc.date.accessioned","2019-07-09T11:52:06Z"],["dc.date.available","2019-07-09T11:52:06Z"],["dc.date.issued","1991"],["dc.description.abstract","The tetranuclear complex [Cp Sm(-OC)2FeCp ]2 (3) has been prepared by reaction of Cp 2Sm(THF)2 with [Cp Fe(CO)2]2 and structurally characterized by single-crystal X-ray diffraction."],["dc.identifier.doi","10.1002/cber.19911240611"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3329"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60098"],["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","Organolanthanid(II)-Chemie: Synthese und Struktur von [Cp2 Sm(-OC)2FeCp ]2"],["dc.title.alternative","Organolanthanide(II) Chemistry: Synthesis and Structure of [Cp*Sm(-OC)2FeCp*]2"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","217"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Journal of Organometallic Chemistry"],["dc.bibliographiccitation.lastpage","335"],["dc.bibliographiccitation.volume","414"],["dc.contributor.author","Recknagel, Anja"],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Noltemeyer, Mathias"],["dc.contributor.author","Brooker, Sally"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Edelmann, Frank T."],["dc.date.accessioned","2009-06-25T08:13:02Z"],["dc.date.accessioned","2021-10-27T13:12:33Z"],["dc.date.available","2009-06-25T08:13:02Z"],["dc.date.available","2021-10-27T13:12:33Z"],["dc.date.issued","1991"],["dc.description.abstract","Die Molekülstruktur von Li[Ph2P(NSiMe3)2](THF)2 (2) wurde durch Röntgenstrukturanalyse bestimmt. Ein viergliedriger LiNPN-Ring bildet die zentrale Einheit des monomeren Moleküls. YbI2 reagiert mit zwei Äquivalenten Li[Ph2P(NSiMe3)2] (1) zum neuartigen Ytterbium(II)diiminophosphinat [Ph2P(NSiMe3)2]2Yb(THF)2 (3). Die analoge Reaktion von 1 mit SmI2 liefert das Samarium(III)derivat [Ph2P(NSiMe3)2]2Sm(μ-I)2Li(THF)2 (4), dessen Struktur ebenfalls röntgenographisch bestimmt wurde. Abstract: The molecular structure of Li[Ph2P(NSiMe3)2](THF)2 (2) has been determined by an X-ray diffraction study. A four-membered LiNPN ring forms the central unit of the monomeric molecule. YbI2 reacts with two equivalents of Li[Ph2P(NSiMe3)2] (1) to give the novel ytterbium(II)diiminophosphinate [Ph2P(NSiMe3)2]2Yb(THF)2 (3). A similar reaction of 1 with SmI2 affords the samarium(III) derivative [Ph2P(NSiMe3)2]2Sm(μ-I)2Li(THF)2 (4) whose structure has also been determined by an X-ray diffraction study."],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1016/0022-328X(91)86331-J"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3325"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91702"],["dc.language.iso","de"],["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","Diiminophosphinate des Lithiums, Samariums und Ytterbiums: Molekülstrukturen von Li[Ph2P(NSiMe3)2](THF)2 und [Ph2P(NSiMe3)2]2Sm(μ-I)2Li(THF)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","539"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Polyhedron"],["dc.bibliographiccitation.lastpage","546"],["dc.bibliographiccitation.volume","13"],["dc.contributor.author","Edelmann, Frank T."],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Gilje, John W."],["dc.contributor.author","Jagner, Susan"],["dc.contributor.author","Håkanssons, Mikael"],["dc.date.accessioned","2009-07-03T12:01:19Z"],["dc.date.accessioned","2021-10-27T13:12:05Z"],["dc.date.available","2009-07-03T12:01:19Z"],["dc.date.available","2021-10-27T13:12:05Z"],["dc.date.issued","1994"],["dc.description.abstract","Tetracoordinate anionic neodymium(III) alkoxides and amides are obtained by adduct formation of Nd[OC(tBu)3]3 (1) and Nd[N(SiMe3)2]3 (2) with either LiCl or LiOSiMe3. The compounds (THF)3Li(μ-Cl)Nd[OC(tBu)3]3 (3), (THF)3Li(μ-Cl)Nd [N(SiMe3)2]3 (4) and [Li(THF)4][(Me3Si)2N3Nd(OSiMe3)] (5) have been characterized by single-crystal X-ray analyses."],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1016/S0277-5387(00)84729-4"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3402"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91657"],["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","Lanthanide alkoxides—III. Four-coordinate anionic neodymium(III) alkoxides and amides 1"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","C6"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Journal of Organometallic Chemistry"],["dc.bibliographiccitation.lastpage","C10"],["dc.bibliographiccitation.volume","439"],["dc.contributor.author","Gornitzka, Heinz"],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Kilimann, Ulrike"],["dc.contributor.author","Edelmann, Frank T."],["dc.contributor.author","Jacob, Klaus"],["dc.contributor.author","Thiele, Karl-Heinz"],["dc.date.accessioned","2009-06-30T05:20:06Z"],["dc.date.accessioned","2021-10-27T13:11:59Z"],["dc.date.available","2009-06-30T05:20:06Z"],["dc.date.available","2021-10-27T13:11:59Z"],["dc.date.issued","1992"],["dc.description.abstract","Dark red crystalline [(FcN)2Yb(μ-Cl)2 Li(THF)2] (2) has been prepared by treatment of anhydrous YbCl3 with 2-(dimethylaminome"],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1016/0022-328X(92)80059-7"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3351"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91647"],["dc.language.iso","de"],["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","Ferrocenliganden in der lanthanid-chemie: Chelatstabilisierung des ersten diorganyllanthanid(III)-halogenids"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","315"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Journal of Organometallic Chemistry"],["dc.bibliographiccitation.lastpage","326"],["dc.bibliographiccitation.volume","415"],["dc.contributor.author","Recknagel, Anja"],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Brooker, Sally"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Edelmann, Frank T."],["dc.date.accessioned","2009-06-25T08:07:43Z"],["dc.date.accessioned","2021-10-27T13:11:55Z"],["dc.date.available","2009-06-25T08:07:43Z"],["dc.date.available","2021-10-27T13:11:55Z"],["dc.date.issued","1991"],["dc.description.abstract","Li[Me2Si(OtBu)(NtBu)] (1) reagiert mit YbI2 zum Ytterbium(II)alkoxysilylamid [Me2Si(OtBu(NtBu)]2Yb(THF)2 (2). Die analoge Reaktion von 1 mit SmI2 liefert das Samarium(III)derivat [Me2Si(OtBu)(NtBu)]2Sm(μ-I)2Li(THF)2 (3). Däruber hinaus wird die Darstellung von [Me2Si(O)tBu)(NtBu)] Nd (4) und [Me2Si(OtBu)(NtBu)]2Yb(μ-Cl)2Li(THF)2 (5) beschrieden. Die Molekülstrukturen von 4 und 5 wurden röntgenographisch bestimmt. Abstract: Li[Me2Si(OtBu)(NtBu)](1) reacts with YbI2 to give the ytterbium(II)alkoxysilylamide [Me2Si(OtBu)-(NtBu)]2Yb (THF)2 (2). The analogous reactio of 1 with SmI2 yields the samarium(III) derivative [Me2Si(OtBu)(NtBu)]2Sm(μ-I)2Li(THF)2 (3). Moreover, the preparation of [Me2Si(OtBu)(NtBu)]3Nd (4) and [Me2Si(OtBu)(NtBu)]2Yb(μ-Cl)2Li(THF)2 (5) is described. The molecular structures of 4 and 5 have been determined by X-ray crystallography."],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1016/0022-328X(91)80131-3"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3324"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91639"],["dc.language.iso","de"],["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","Alkoxysilylamide des Neodyms, Samariums und Ytterbiums: Viergliedrige anorganische Ringsysteme in der Lanthanidchemie"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","C21"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Journal of Organometallic Chemistry"],["dc.bibliographiccitation.lastpage","C25"],["dc.bibliographiccitation.volume","431"],["dc.contributor.author","Steiner, Alexander"],["dc.contributor.author","Gornitzka, Heinz"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Edelmann, Frank T."],["dc.date.accessioned","2009-06-30T05:15:03Z"],["dc.date.accessioned","2021-10-27T13:12:23Z"],["dc.date.available","2009-06-30T05:15:03Z"],["dc.date.available","2021-10-27T13:12:23Z"],["dc.date.issued","1992"],["dc.description.abstract","The molecular structure of di-μ-carbonyl-bis[carbonyl(η5-pentamethylcyclopentadienyl)ruthenium] (Ru---Ru) has been determined by a single-crystal X-ray diffraction study (monoclinic, space group P21/n,a = 979.90(9), b = 831.91(7), c = 1427.75(12) pm, β = 100.026(9)°, R = 0.018). In the solid state the complex exists solely as the trans-carbonyl bridged isomer. The Ru---Ru bond length is 275.2(1) pm."],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1016/0022-328X(92)83295-S"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3350"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91687"],["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","Struktur von [CPRu(C0)2]2 (Cp = η5-pentamethylcyclopentadienyl)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]