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dc.contributor.authorGuo, Yuan-Yuan
dc.contributor.authorLightfoot, Philip
dc.date.accessioned2021-08-26T23:37:50Z
dc.date.available2021-08-26T23:37:50Z
dc.date.issued2020-08-27
dc.identifier269989040
dc.identifier8983a90f-5d20-4f84-a337-bf6831cc71ce
dc.identifier85091437258
dc.identifier000571979900027
dc.identifier.citationGuo , Y-Y & Lightfoot , P 2020 , ' Structural diversity of lead halide chain compounds, APbX 3 , templated by isomeric molecular cations ' , Dalton Transactions , vol. 49 , no. 36 , pp. 12767-12775 . https://doi.org/10.1039/D0DT02782Ken
dc.identifier.issn1477-9226
dc.identifier.otherORCID: /0000-0001-7048-3982/work/79917709
dc.identifier.urihttps://hdl.handle.net/10023/23849
dc.descriptionWe acknowledge support from the University of St Andrews, the China Scholarship Council (studentship to YYG).en
dc.description.abstractThree new 1D chain structure type hybrid organic–inorganic lead(II) halides are presented: IQPbBr3, QPbBr3 and QPbI3, templated by large organic cations, isoquinolinium ([IQ+] = protonated isoquinoline) and its isomer quinolonium ([Q+] = protonated quinoline). All three compounds possess the same generic formula as cubic perovskite, ABX3, but adopt different structures. IQPbBr3 adopts a 1D face-sharing single chain hexagonal perovskite structure type, and the other two, QPbBr3 and QPbI3, adopt a non-perovskite structure which is built from 1D edge-sharing octahedral double chains. Crystal structures and preliminary photophysical properties are discussed. Two of them have lower bandgaps than the other reported materials with the same structure type, indicating the value of further exploratory studies for these types of materials.
dc.format.extent9
dc.format.extent1412240
dc.format.extent1428250
dc.language.isoeng
dc.relation.ispartofDalton Transactionsen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleStructural diversity of lead halide chain compounds, APbX3, templated by isomeric molecular cationsen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doi10.1039/D0DT02782K
dc.description.statusPeer revieweden
dc.date.embargoedUntil2021-08-27


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