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dc.contributor.authorLy, Hanh
dc.contributor.authorTuononen, Heikki
dc.contributor.authorParvez, Masood
dc.contributor.authorRoesler, Roland
dc.date.accessioned2015-11-19T12:43:50Z
dc.date.available2015-11-19T12:43:50Z
dc.date.issued2007
dc.identifier.citationLy, H., Tuononen, H., Parvez, M., & Roesler, R. (2007). Assembly of a planar, tricyclic B4N8 framework with s-indacene structure. <i>Chemical Communications</i>, (43), 4522-4524. <a href="https://doi.org/10.1039/B709270A" target="_blank">https://doi.org/10.1039/B709270A</a>
dc.identifier.otherCONVID_17431831
dc.identifier.otherTUTKAID_28497
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/47753
dc.description.abstractA neutral, formally 16π-electron, tricyclic tetrahydrazidotetraborane was obtained in a two-step procedure involving self-assembly of a dilithiodiborate with B4N8 framework and subsequent oxidation of the phenylborate moieties to boranes and biphenyl using Fe(II) as an oxidant.
dc.language.isoeng
dc.publisherRSC
dc.relation.ispartofseriesChemical Communications
dc.subject.otherboori-typpi yhdisteet
dc.subject.otherboron-nitrogen compounds
dc.titleAssembly of a planar, tricyclic B4N8 framework with s-indacene structure
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201511183712
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2015-11-18T13:15:33Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange4522-4524
dc.relation.issn1359-7345
dc.relation.numberinseries43
dc.type.versionacceptedVersion
dc.rights.copyright© The Royal Society of Chemistry 2007. This is a final draft version of an article whose final and definitive form has been published by RSC. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1039/B709270A
dc.type.okmA1


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