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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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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. |
format | Online Article Text |
id | pubmed-10315492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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