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Dissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I)

With 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 vaporizati...

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Autores principales: Pintea, Maria, Mason, Nigel, Peiró-Franch, Anna, Clark, Ewan, Samanta, Kushal, Glessi, Cristiano, Schmidtke, Inga Lena, Luxford, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315492/
https://www.ncbi.nlm.nih.gov/pubmed/37405247
http://dx.doi.org/10.3389/fchem.2023.1028008
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author Pintea, Maria
Mason, Nigel
Peiró-Franch, Anna
Clark, Ewan
Samanta, Kushal
Glessi, Cristiano
Schmidtke, Inga Lena
Luxford, Thomas
author_facet Pintea, Maria
Mason, Nigel
Peiró-Franch, Anna
Clark, Ewan
Samanta, Kushal
Glessi, Cristiano
Schmidtke, Inga Lena
Luxford, Thomas
author_sort Pintea, Maria
collection PubMed
description With 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.
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spelling pubmed-103154922023-07-04 Dissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I) Pintea, Maria Mason, Nigel Peiró-Franch, Anna Clark, Ewan Samanta, Kushal Glessi, Cristiano Schmidtke, Inga Lena Luxford, Thomas Front Chem Chemistry With 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. Frontiers Media S.A. 2023-06-19 /pmc/articles/PMC10315492/ /pubmed/37405247 http://dx.doi.org/10.3389/fchem.2023.1028008 Text en Copyright © 2023 Pintea, Mason, Peiró-Franch, Clark, Samanta, Glessi, Schmidtke and Luxford. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Pintea, 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)
title Dissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I)
title_full Dissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I)
title_fullStr Dissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I)
title_full_unstemmed Dissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I)
title_short Dissociative electron attachment to gold(I)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(I)
title_sort dissociative electron attachment to gold(i)-based compounds: 4,5-dichloro-1,3-diethyl-imidazolylidene trifluoromethyl gold(i)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315492/
https://www.ncbi.nlm.nih.gov/pubmed/37405247
http://dx.doi.org/10.3389/fchem.2023.1028008
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