Linear and bent Cp*2Si : reversible phase transition of a key molecule

dc.contributor.authorRuth, Paul Niklas
dc.contributor.authorSarcevic, Julijan
dc.contributor.authorHerbst‐Irmer, Regine
dc.contributor.authorSindlinger, Christian P.
dc.contributor.authorStalke, Dietmar
dc.date.accessioned2023-10-17T12:23:16Z
dc.date.available2023-10-17T12:23:16Z
dc.date.issued2023de
dc.date.updated2023-07-11T22:56:51Z
dc.description.abstractThe solid-state structure of decamethylsilicocene Cp*2Si with a bent and a linear molecule in the same unit cell was so far considered an exception in relation to the structures of its all-bent heavier analogues Cp*2E with E=Ge, Sn, Pb. Here, we present the solution to this conundrum by reporting a low-temperature phase, where all three symmetrically independent molecules are present in a bent formation. This reversible enantiotropic phase transition occurs in the temperature range between 80 K and 130 K and provides a rationale for the unexpected linear molecule based in entropy beyond hand-waving explanations such as electronic reasons or packing effects.en
dc.description.sponsorshipDeutsche Forschungsgemeinschaftde
dc.description.sponsorshipProjekt DEALde
dc.identifier.issn1433-7851
dc.identifier.issn1521-3773
dc.identifier.other1869737105
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-136466de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/13646
dc.identifier.urihttp://dx.doi.org/10.18419/opus-13627
dc.language.isoende
dc.relation.uridoi:10.1002/anie.202301609de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/de
dc.subject.ddc540de
dc.titleLinear and bent Cp*2Si : reversible phase transition of a key moleculeen
dc.typearticlede
ubs.fakultaetChemiede
ubs.fakultaetFakultätsübergreifend / Sonstige Einrichtungde
ubs.institutInstitut für Anorganische Chemiede
ubs.institutFakultätsübergreifend / Sonstige Einrichtungde
ubs.publikation.seiten5de
ubs.publikation.sourceAngewandte Chemie international edition 62 (2023), No. e202301609de
ubs.publikation.typZeitschriftenartikelde

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