Stalke, Dietmar

[["dc.bibliographiccitation.firstpage","14968"],["dc.bibliographiccitation.issue","24"],["dc.bibliographiccitation.journal","Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","14978"],["dc.bibliographiccitation.volume","56"],["dc.contributor.author","Koehne, Ingo"],["dc.contributor.author","Graw, Nico"],["dc.contributor.author","Teuteberg, Thorsten"],["dc.contributor.author","Herbst-Irmer, Regine"],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2020-12-10T15:22:37Z"],["dc.date.available","2020-12-10T15:22:37Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1021/acs.inorgchem.7b02276"],["dc.identifier.eissn","1520-510X"],["dc.identifier.issn","0020-1669"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/73474"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Introducing NacNac-Like Bis(4,6-isopropylbenzoxazol-2-yl)methanide in s-Block Metal Coordination"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2339"],["dc.bibliographiccitation.journal","Dalton Transactions"],["dc.bibliographiccitation.lastpage","2341"],["dc.contributor.author","Bhaduri, Sumit"],["dc.contributor.author","Gopalkrishnan, Kalpathi S."],["dc.contributor.author","Sheldrick, George M."],["dc.contributor.author","Clegg, William"],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2009-06-10T11:46:14Z"],["dc.date.accessioned","2021-10-27T13:11:50Z"],["dc.date.available","2009-06-10T11:46:14Z"],["dc.date.available","2021-10-27T13:11:50Z"],["dc.date.issued","1983"],["dc.description.abstract","Triruthenium dodecacarbonyl [Ru3(CO)12] reacts with nitrobenzene to give [Ru3(CO)10(NPh)](3) and [Ru3(CO)9(NPh)2](4) in low yields, accompanied by formation of CO2. The solution i.r. spectrum of (3) suggests the presence of triply bridging NPh and CO groups, confirmed by a single-crystal X-ray structure determination; space group P21/n, a= 12.457(1), b= 11.428(1), c= 29.234(2)Å, = 92.38(1)°, Z= 8, and R= 0.036 for 4 817 unique observed reflections. The two independent molecules differ slightly in the relative orientations of the phenyl groups. Mean bond lengths include Ru–Ru 2.746(5), Ru–µ-C 2.172(8), and Ru–µ-N 2.055(5)Å. The i.r. Spectra of complexes (3) and (4) are discussed in terms of a molecular-orbital description of M3(CO)9 moieties."],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1039/DT9830002339"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3262"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91631"],["dc.language.iso","en"],["dc.notes.intern","Migrated from goescholar"],["dc.publisher","Chemical Society"],["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","Reaction of triruthenium dodecacarbonyl with nitrobenzene and structure of µ3-phenylnitrene-triruthenium decacarbonyl, [Ru3(CO)10(µ3-NPh)] : Notes. Reaction of triruthenium dodecacarbonyl with nitrobenzene and structure of µ3-phenylnitrene-triruthenium decacarbonyl, [Ru3(CO)10(µ3-NPh) : Notes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","75"],["dc.bibliographiccitation.lastpage","99"],["dc.bibliographiccitation.seriesnr","146"],["dc.contributor.author","Flierler, Ulrike"],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2018-11-07T09:14:31Z"],["dc.date.available","2018-11-07T09:14:31Z"],["dc.date.issued","2012"],["dc.description.abstract","The focus of this chapter lies on the deduction of chemical properties from charge density studies in some interesting, mainly main group element compounds. The relationship between these numerical data and commonly accepted simple chemical concepts is unfortunately not always straightforward, and often, the researcher relies on heuristic connections, rather than rigorously defined ones. In this chapter, we demonstrate how charge density analyses can shed light on aspects of chemical bonding and the chemical reactivity resulting from the determined bonding situation."],["dc.identifier.doi","10.1007/430_2011_71"],["dc.identifier.isi","000321551700005"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/27430"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.publisher.place","New york"],["dc.relation.crisseries","Structure & Bonding"],["dc.relation.isbn","978-3-642-30802-4"],["dc.relation.ispartof","ELECTRON DENSITY AND CHEMICAL BONDING I: EXPERIMENTAL CHARGE DENSITY STUDIES"],["dc.relation.ispartofseries","Structure and Bonding; 146"],["dc.relation.issn","0081-5993"],["dc.title","Some Main Group Chemical Perceptions in the Light of Experimental Charge Density Investigations"],["dc.type","review"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","9264"],["dc.bibliographiccitation.issue","34"],["dc.bibliographiccitation.journal","Chemistry - A European Journal"],["dc.bibliographiccitation.lastpage","9278"],["dc.bibliographiccitation.volume","17"],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2018-11-07T08:53:10Z"],["dc.date.available","2018-11-07T08:53:10Z"],["dc.date.issued","2011"],["dc.description.abstract","This paper provides a short introduction to the basics of electron density investigations. The two predominant approaches for the modelling and various interpretations of electron density distributions are presented. Their potential translations into chemical concepts are explained. The focus of the article lies on the deduction of chemical properties from charge density studies in some selected main group compounds. The relationship between the obtained numerical data and commonly accepted simple chemical concepts unfortunately is not always straightforward, and often the chemist relies on heuristic connections rather than rigorously defined ones. This article tries to demonstrate how charge density analyses can shed light on aspects of chemical bonding and reactivity resulting from the determined bonding situation. Sometimes this helps to identify misconceptions and sets the scene for new unconventional synthetic approaches."],["dc.identifier.doi","10.1002/chem.201100615"],["dc.identifier.isi","000294784400001"],["dc.identifier.pmid","21717511"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/22344"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","0947-6539"],["dc.title","Meaningful Structural Descriptors from Charge Density"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2256"],["dc.bibliographiccitation.issue","21"],["dc.bibliographiccitation.journal","Angewandte Chemie"],["dc.bibliographiccitation.lastpage","2259"],["dc.bibliographiccitation.volume","106"],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2019-07-09T11:52:20Z"],["dc.date.available","2019-07-09T11:52:20Z"],["dc.date.issued","1994"],["dc.identifier.doi","10.1002/ange.19941062107"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3421"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60157"],["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","Das Lithocen-Anion und offenes Calcocen - neue Anstöße in der Chemie der Alkali- und Erdalkalimetallocene"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","no"],["dc.bibliographiccitation.issue","23"],["dc.bibliographiccitation.journal","ChemInform"],["dc.bibliographiccitation.lastpage","no"],["dc.bibliographiccitation.volume","43"],["dc.contributor.author","Leibeling, Markus"],["dc.contributor.author","Pawliczek, Martin"],["dc.contributor.author","Kratzert, Daniel"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Werz, Daniel B."],["dc.date.accessioned","2021-12-08T12:30:01Z"],["dc.date.available","2021-12-08T12:30:01Z"],["dc.date.issued","2012"],["dc.identifier.doi","10.1002/chin.201223107"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/96293"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-476"],["dc.relation.issn","0931-7597"],["dc.rights.uri","http://doi.wiley.com/10.1002/tdm_license_1.1"],["dc.title","ChemInform Abstract: A Ridge Walk Between Reaction Modes: An Unprecedented Pd-Catalyzed Domino Sequence of Diynyl-Substituted Bromoarenes."],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2343"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Organometallics"],["dc.bibliographiccitation.lastpage","2347"],["dc.bibliographiccitation.volume","29"],["dc.contributor.author","Sen, Sakya S."],["dc.contributor.author","Tavcar, Gasper"],["dc.contributor.author","Roesky, Herbert W."],["dc.contributor.author","Kratzert, Daniel"],["dc.contributor.author","Hey, Jakob"],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2018-11-07T08:43:09Z"],["dc.date.available","2018-11-07T08:43:09Z"],["dc.date.issued","2010"],["dc.description.abstract","The base-stabilized bis-silylene (LSi-SiL, L = PhC(NtBu)1) was reacted with benzophenone in a 1:2 ratio in THF, which afforded a Si2O2 four-membered ring, stabilized by bulky amidinato ligands. The most striking phenomenon is the abstraction of oxygen from benzophenone and the simultaneous formation of a silicon carbon bond. The four-membered Si2O2 ring is planar, and both the silicon atoms are five-coordinate. The two silicon atoms are arranged opposite each other in the four-membered Si2O2 ring. Moreover LSi-SiL was treated with N2O to afford two four-membered Si3O, rings connected with two oxygen atoms. In this structure also the silicon atoms are five-coordinate."],["dc.identifier.doi","10.1021/om100164u"],["dc.identifier.isi","000277597500017"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/19888"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0276-7333"],["dc.title","Synthesis of a Stable Four-Membered Si2O2 Ring and a Dimer with Two Four-Membered Si2O2 Rings Bridged by Two Oxygen Atoms, with Five-Coordinate Silicon Atoms in Both Ring Systems"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1365"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Angewandte Chemie"],["dc.bibliographiccitation.lastpage","1366"],["dc.bibliographiccitation.volume","106"],["dc.contributor.author","Storre, Jens"],["dc.contributor.author","Belgardt, Thomas"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Roesky, Herbert W."],["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.19941061235"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3412"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60148"],["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","Synthese und Struktur des ersten metallorganischen Galloxanhydroxids Mes6Ga6O4(OH)4"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3286"],["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","Chemistry - A European Journal"],["dc.bibliographiccitation.lastpage","3291"],["dc.bibliographiccitation.volume","18"],["dc.contributor.author","Tietze, Lutz Friedjan"],["dc.contributor.author","Hungerland, Tim"],["dc.contributor.author","Duefert, Alexander"],["dc.contributor.author","Objartel, Ina"],["dc.contributor.author","Stalke, Dietmar"],["dc.date.accessioned","2018-11-07T09:12:39Z"],["dc.date.available","2018-11-07T09:12:39Z"],["dc.date.issued","2012"],["dc.description.abstract","Helical tetrasubstituted alkenes (7) were obtained in a highly efficient way through a palladium-catalyzed domino-carbopalladation/CH-activation reaction of propargylic alcohols 6 in good to excellent yields. Electron-withdrawing- and electron-donating substituents can be introduced onto the upper and lower aromatic rings. The substrates (6) for the domino process were synthesized by addition of the lithiated alkyne (20) to various aldehydes (19); moreover, the substrates were accessible enantioselectively (in 95?% ee) by reduction of the corresponding ketone using the Noyori procedure."],["dc.identifier.doi","10.1002/chem.201103209"],["dc.identifier.isi","000300972500025"],["dc.identifier.pmid","22259072"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/26989"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","0947-6539"],["dc.title","Synthesis of Tetrasubstituted Alkenes through a Palladium-Catalyzed Domino Carbopalladation/C-H-Activation Reaction"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5513"],["dc.bibliographiccitation.issue","18"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","5517"],["dc.bibliographiccitation.volume","54"],["dc.contributor.author","Warratz, Svenja"],["dc.contributor.author","Kornhaass, Christoph"],["dc.contributor.author","Cajaraville, Ana"],["dc.contributor.author","Niepoetter, Benedikt"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2018-11-07T09:58:18Z"],["dc.date.available","2018-11-07T09:58:18Z"],["dc.date.issued","2015"],["dc.description.abstract","Aerobic oxidative C-H functionalizations of weakly coordinating benzoic acids have been accomplished with versatile ruthenium(II) biscarboxylates under ambient oxygen or air. Mechanistic studies identified the key factors controlling the elementary step of the oxidation of the ruthenium(0) complex."],["dc.identifier.doi","10.1002/anie.201500600"],["dc.identifier.isi","000354191600047"],["dc.identifier.pmid","25737001"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/37342"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3773"],["dc.relation.issn","1433-7851"],["dc.title","Ruthenium(II)-Catalyzed C-H Activation/Alkyne Annulation by Weak Coordination with O-2 as the Sole Oxidant"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]