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dc.date.accessioned2024-03-05T21:04:35Z
dc.date.available2024-03-05T21:04:35Z
dc.date.created2023-07-26T11:00:07Z
dc.date.issued2023
dc.identifier.citationPintea, Maria Mason, Nigel Peiró-Franch, Anna Clark, Ewan Samanta, Kushal Glessi, Cristiano Schmidtke, Inga Lena Luxford, Thomas . Dissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I). Frontiers in Chemistry. 2023, 11
dc.identifier.urihttp://hdl.handle.net/10852/109195
dc.description.abstractWith the use of proton-NMR and powder XRD (XRPD) studies, the suitability of specific Au-focused electron beam induced deposition (FEBID) precursors has been investigated with low electron energy, structure, excited states and resonances, structural crystal modifications, flexibility, and vaporization level. 4,5-Dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I) is a compound that is a uniquely designed precursor to meet the needs of focused electron beam-induced deposition at the nanostructure level, which proves its capability in creating high purity structures, and its growing importance in other AuIm x and AuCl n B (where x and n are the number of radicals, B = CH, CH 3 , or Br) compounds in the radiation cancer therapy increases the efforts to design more suitable bonds in processes of SEM (scanning electron microscopy) deposition and in gas-phase studies. The investigation performed of its powder shape using the XRPD XPERT 3 panalytical diffractometer based on CoK α lines shows changes to its structure with change in temperature, level of vacuum, and light; the sensitivity of this compound makes it highly interesting in particular to the radiation research. Used in FEBID, though its smaller number of C, H, and O atoms has lower levels of C contamination in the structures and on the surface, it replaces these bonds with C–Cl and C–N bonds that have lower bond-breaking energy. However, it still needs an extra purification step in the deposition process, either H 2 O, O 2 , or H jets.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleDissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I)
dc.title.alternativeENEngelskEnglishDissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I)
dc.typeJournal article
dc.creator.authorPintea, Maria
dc.creator.authorMason, Nigel
dc.creator.authorPeiró-Franch, Anna
dc.creator.authorClark, Ewan
dc.creator.authorSamanta, Kushal
dc.creator.authorGlessi, Cristiano
dc.creator.authorSchmidtke, Inga Lena
dc.creator.authorLuxford, Thomas
cristin.unitcode185,15,12,0
cristin.unitnameKjemisk institutt
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2163623
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Frontiers in Chemistry&rft.volume=11&rft.spage=&rft.date=2023
dc.identifier.jtitleFrontiers in Chemistry
dc.identifier.volume11
dc.identifier.pagecount0
dc.identifier.doihttps://doi.org/10.3389/fchem.2023.1028008
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2296-2646
dc.type.versionPublishedVersion
cristin.articleid1288


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