Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals
The silicon organic compounds phenyltrimethylsilane (1), 1,4-bis(trimethylsilyl)benzene (2), diphenyldimethylsilane (3) y 1,1,2,2-dibenzobis(dimethyls ilane) (4) were synthesized and characterized by IR, NMR-1 H and elemental analysis. They were also reduced to the corresponding silicon radical anio...
- Autores:
-
Galarza, Esperanza
Micolta, Germania
Vargas, Rubén A.
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2006
- Institución:
- Universidad Autónoma de Occidente
- Repositorio:
- RED: Repositorio Educativo Digital UAO
- Idioma:
- spa
- OAI Identifier:
- oai:red.uao.edu.co:10614/262
- Acceso en línea:
- http://hdl.handle.net/10614/262
- Palabra clave:
- Silicon compounds
Aniones
Compuestos de silicio
Anions
Electrochemical analysis
- Rights
- openAccess
- License
- Derechos Reservados - Universidad Autónoma de Occidente
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dc.title.spa.fl_str_mv |
Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals |
title |
Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals |
spellingShingle |
Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals Silicon compounds Aniones Compuestos de silicio Anions Electrochemical analysis |
title_short |
Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals |
title_full |
Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals |
title_fullStr |
Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals |
title_full_unstemmed |
Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals |
title_sort |
Study of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicals |
dc.creator.fl_str_mv |
Galarza, Esperanza Micolta, Germania Vargas, Rubén A. |
dc.contributor.author.spa.fl_str_mv |
Galarza, Esperanza Micolta, Germania Vargas, Rubén A. |
dc.subject.spa.fl_str_mv |
Silicon compounds Aniones Compuestos de silicio Anions Electrochemical analysis |
topic |
Silicon compounds Aniones Compuestos de silicio Anions Electrochemical analysis |
description |
The silicon organic compounds phenyltrimethylsilane (1), 1,4-bis(trimethylsilyl)benzene (2), diphenyldimethylsilane (3) y 1,1,2,2-dibenzobis(dimethyls ilane) (4) were synthesized and characterized by IR, NMR-1 H and elemental analysis. They were also reduced to the corresponding silicon radical anions: Potassium trimethylsilylphenylide (1a), Potassium 1,4-bis(trimet hylsilylphenylide (2a), Potassium dimethylsilyl-diphenylide (3a), Potassium 1,1,2,2-bis(di methylsilylphenylide) (4a). The electronic delocalization study was made by UV spectroscopy and complex impedance. By UV spectroscopy evidence was found a bathochromic shift in the following order: silicon radical anions, organosilicon and the analogous carbonate precursors, which is consistent with the electronic delocalization. By impedance spectroscopy, information about the type of impedance and the magnitude of the dc conductivity for the carbonates and silicon com compounds, as well as their silicon radical anions were obtained. These results allowed us to identify the silicon derivatives of benzene and their corresponding reduced compounds in the range of the semiconductors and those of the analogous carbonates in the non conducting materials |
publishDate |
2006 |
dc.date.issued.spa.fl_str_mv |
2006-01 |
dc.date.accessioned.spa.fl_str_mv |
2011-09-28T22:30:06Z |
dc.date.available.spa.fl_str_mv |
2011-09-28T22:30:06Z |
dc.type.spa.fl_str_mv |
Artículo de revista |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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http://purl.org/coar/resource_type/c_6501 |
dc.type.content.spa.fl_str_mv |
Text |
dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
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http://purl.org/redcol/resource_type/ARTREF |
dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_6501 |
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publishedVersion |
dc.identifier.issn.spa.fl_str_mv |
0121-0777 |
dc.identifier.uri.spa.fl_str_mv |
http://hdl.handle.net/10614/262 |
identifier_str_mv |
0121-0777 |
url |
http://hdl.handle.net/10614/262 |
dc.language.iso.spa.fl_str_mv |
spa |
language |
spa |
dc.relation.ispartofseries.spa.fl_str_mv |
El hombre y la máquina no. 26 (ene.-jun. 2006); p. 124-129 |
dc.rights.spa.fl_str_mv |
Derechos Reservados - Universidad Autónoma de Occidente |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.uri.spa.fl_str_mv |
https://creativecommons.org/licenses/by-nc/4.0/ |
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info:eu-repo/semantics/openAccess |
dc.rights.creativecommons.spa.fl_str_mv |
Atribución-NoComercial 4.0 Internacional (CC BY-NC 4.0) |
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Derechos Reservados - Universidad Autónoma de Occidente https://creativecommons.org/licenses/by-nc/4.0/ Atribución-NoComercial 4.0 Internacional (CC BY-NC 4.0) http://purl.org/coar/access_right/c_abf2 |
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openAccess |
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application/pdf |
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Universidad Autónoma de Occidente. Calle 25 115-85. Km 2 vía Cali-Jamundí |
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Universidad Autónoma de Occidente |
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Galarza, Esperanza0c5b38a961d21fa4a86c7651a56c1e70-1Micolta, Germaniaa60ef405d96711d129c04b8a1aea5af7-1Vargas, Rubén A.224b9150dbd1b79e5b3e14765bfccf7e-1Universidad Autónoma de Occidente. Calle 25 115-85. Km 2 vía Cali-Jamundí2011-09-28T22:30:06Z2011-09-28T22:30:06Z2006-010121-0777http://hdl.handle.net/10614/262The silicon organic compounds phenyltrimethylsilane (1), 1,4-bis(trimethylsilyl)benzene (2), diphenyldimethylsilane (3) y 1,1,2,2-dibenzobis(dimethyls ilane) (4) were synthesized and characterized by IR, NMR-1 H and elemental analysis. They were also reduced to the corresponding silicon radical anions: Potassium trimethylsilylphenylide (1a), Potassium 1,4-bis(trimet hylsilylphenylide (2a), Potassium dimethylsilyl-diphenylide (3a), Potassium 1,1,2,2-bis(di methylsilylphenylide) (4a). The electronic delocalization study was made by UV spectroscopy and complex impedance. By UV spectroscopy evidence was found a bathochromic shift in the following order: silicon radical anions, organosilicon and the analogous carbonate precursors, which is consistent with the electronic delocalization. By impedance spectroscopy, information about the type of impedance and the magnitude of the dc conductivity for the carbonates and silicon com compounds, as well as their silicon radical anions were obtained. These results allowed us to identify the silicon derivatives of benzene and their corresponding reduced compounds in the range of the semiconductors and those of the analogous carbonates in the non conducting materialsSe sintetizaron y caracterizaron por IR, RMN-1H y análisis elemental los compuestos organosilados feniltrimetilsilano (1), 1,4-bis (trimetilsilil) bencen o (2), difenildimetilsilano (3) y 1,1,2,2-dibenzobis(dimetilsilan o) (4) y se redujeron a los correspondientes aniones radicales organosilados: (trimetilsilil)feniluro de potasio (1a), 1,4-bis(trimetilsilil)feniluro de potasio (2a), dimetilsilidifeniluro de potasio (3a), 1,1,2,2-bis(dimetilsililfeniluro) de potasio (4a). El estudio de deslocalización electrónica se realizó por técnicas de espectroscopía ultravioleta (UV) y de impedancia compleja. La espectroscopía UV evidenció un desplazamiento batocrómico en el siguiente orden: aniones radicales organosilados, organosilados precursores y carbonados análogos, consistente con la delocalización electrónica. Por espectroscopía de impedan cia, se obtuvo información acerca del tipo de impedancia y de la magnitud de la conductividad dc para compuestos carbonados como para organosilados y aniones radicales organosilados, ubicando a los organosilados derivados del benceno y a sus correspondientes compuestos reducidos en el rango de los semiconductores y a los carbonados análogos en el de los no conductores.application/pdfspaUniversidad Autónoma de OccidenteEl hombre y la máquina no. 26 (ene.-jun. 2006); p. 124-129Derechos Reservados - Universidad Autónoma de Occidentehttps://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccessAtribución-NoComercial 4.0 Internacional (CC BY-NC 4.0)http://purl.org/coar/access_right/c_abf2instname:Universidad Autónoma de Occidentereponame:Repositorio Institucional UAOSilicon compoundsAnionesCompuestos de silicioAnionsElectrochemical analysisStudy of the Electronic delocalization in Silicon organic derivatives of benzene and their corresponding anion radicalsArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1Textinfo:eu-repo/semantics/articlehttp://purl.org/redcol/resource_type/ARTREFinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85PublicationTHUMBNAILT0003450.pdf.jpgT0003450.pdf.jpgGenerated Thumbnailimage/jpeg14320https://dspace7-uao.metacatalogo.com/bitstreams/1020a2b7-6ffa-4ddd-9575-bec9b5e8683b/download15e7a41d92a28c4d49128a05a4eaaeb6MD54ORIGINALT0003450.pdfapplication/pdf370768https://dspace7-uao.metacatalogo.com/bitstreams/52d76f21-7dd6-47ea-8661-22c88b2ce7a9/downloadd2729b5e5fbe4d1f0f83b5e5dfd8f5b7MD51LICENSElicense.txttext/plain1849https://dspace7-uao.metacatalogo.com/bitstreams/4cc9280b-59db-470d-aba2-0b125b66d65f/downloadae8845f14fa67805d48d8e95d55559ddMD52TEXTT0003450.pdf.txtT0003450.pdf.txtExtracted texttext/plain17441https://dspace7-uao.metacatalogo.com/bitstreams/cf9b3c5c-9b1b-4298-a508-bdd65b95dac3/downloadb6f39bc16b609309475496c005a6c476MD5310614/262oai:dspace7-uao.metacatalogo.com:10614/2622024-01-19 16:34:13.577https://creativecommons.org/licenses/by-nc/4.0/Derechos Reservados - Universidad Autónoma de Occidenteopen.accesshttps://dspace7-uao.metacatalogo.comRepositorio UAOrepositorio@uao.edu.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 |