Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol

The reaction between [Ru3(CO)12] 1 and the pyrazolic Tröger base 5,12-dimethyl-3,10- b i s - ( p - n i t r o p h e n y l ) - 1,3,4,8,10,11-hexaazatetracyclo[ 6.6.1.02,6.09,13]-pentadeca- 2(6),4,9(13),11-tetraene (TBpz) 2 and 5-amino-3-methyl-1-(pnitrophenyl) pyrazole (amnpz) 3 was studied. Both reac...

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Autores:
Micolta, Germania
Galarza, Esperanza
Abonía, Rodrigo
Tipo de recurso:
Article of journal
Fecha de publicación:
2005
Institución:
Universidad Autónoma de Occidente
Repositorio:
RED: Repositorio Educativo Digital UAO
Idioma:
spa
OAI Identifier:
oai:red.uao.edu.co:10614/186
Acceso en línea:
http://hdl.handle.net/10614/186
Palabra clave:
Hidrogenacion
Compuestos organometálicos
Hydrogenation
Organometallic compounds
Rights
openAccess
License
Derechos Reservados - Universidad Autónoma de Occidente
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dc.title.spa.fl_str_mv Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol
title Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol
spellingShingle Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol
Hidrogenacion
Compuestos organometálicos
Hydrogenation
Organometallic compounds
title_short Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol
title_full Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol
title_fullStr Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol
title_full_unstemmed Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol
title_sort Reactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazol
dc.creator.fl_str_mv Micolta, Germania
Galarza, Esperanza
Abonía, Rodrigo
dc.contributor.author.spa.fl_str_mv Micolta, Germania
Galarza, Esperanza
Abonía, Rodrigo
dc.subject.spa.fl_str_mv Hidrogenacion
Compuestos organometálicos
Hydrogenation
Organometallic compounds
topic Hidrogenacion
Compuestos organometálicos
Hydrogenation
Organometallic compounds
description The reaction between [Ru3(CO)12] 1 and the pyrazolic Tröger base 5,12-dimethyl-3,10- b i s - ( p - n i t r o p h e n y l ) - 1,3,4,8,10,11-hexaazatetracyclo[ 6.6.1.02,6.09,13]-pentadeca- 2(6),4,9(13),11-tetraene (TBpz) 2 and 5-amino-3-methyl-1-(pnitrophenyl) pyrazole (amnpz) 3 was studied. Both reactions were carried out in refluxing toluene under inert atmosphere. From compound 2 were obtained two black and brown solids 4a and 4b respectively, being molecular formula [Ru3(TBpz)(CO)n]. From 4a were recently growth some crystals from diluted nitric acid which are currently in X-ray diffraction study. The reaction with 3 yielded the brown solid [Ru3(amnpz)(CO)m] 5. This work covered also some preliminary studies on the catalytic activity of the obtained products. The solids 4a and 4b worked as excellent pre-catalyst in the heterogeneous hydrogenation reaction of cyclohexene (100C, P(H2) 40 atm), yielding turnover of 99% and 76% respectively. The residue 4a- R obtained from the hydrogenation hydrogenation reaction with 4a was recovered and re-utilized for a new hydrogenation reaction under the same reaction conditions yielding a turnover of 89%, which makes suppose that 4a behave as a pre-catalyst more than a true catalyst. With product 5 were carried out two experiments of homogeneous hydrogenation in DMSO and THF as solvents under the same conditions, yielding only 26% and 16% of turnover respectively.
publishDate 2005
dc.date.issued.spa.fl_str_mv 2005-01
dc.date.accessioned.spa.fl_str_mv 2011-09-28T22:29:33Z
dc.date.available.spa.fl_str_mv 2011-09-28T22:29:33Z
dc.type.spa.fl_str_mv Artículo de revista
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identifier_str_mv 0121-0777
url http://hdl.handle.net/10614/186
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dc.relation.ispartofseries.spa.fl_str_mv El hombre y la máquina no. 24 (ene.-jun. 2005); p. 114-121
dc.rights.spa.fl_str_mv Derechos Reservados - Universidad Autónoma de Occidente
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dc.publisher.spa.fl_str_mv Universidad Autónoma de Occidente
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spelling Micolta, Germaniaa60ef405d96711d129c04b8a1aea5af7-1Galarza, Esperanza0c5b38a961d21fa4a86c7651a56c1e70-1Abonía, Rodrigoc01de19c43af8b976f56691e322c0b11-1Universidad Autónoma de Occidente. Calle 25 115-85. Km 2 vía Cali-Jamundí2011-09-28T22:29:33Z2011-09-28T22:29:33Z2005-010121-0777http://hdl.handle.net/10614/186The reaction between [Ru3(CO)12] 1 and the pyrazolic Tröger base 5,12-dimethyl-3,10- b i s - ( p - n i t r o p h e n y l ) - 1,3,4,8,10,11-hexaazatetracyclo[ 6.6.1.02,6.09,13]-pentadeca- 2(6),4,9(13),11-tetraene (TBpz) 2 and 5-amino-3-methyl-1-(pnitrophenyl) pyrazole (amnpz) 3 was studied. Both reactions were carried out in refluxing toluene under inert atmosphere. From compound 2 were obtained two black and brown solids 4a and 4b respectively, being molecular formula [Ru3(TBpz)(CO)n]. From 4a were recently growth some crystals from diluted nitric acid which are currently in X-ray diffraction study. The reaction with 3 yielded the brown solid [Ru3(amnpz)(CO)m] 5. This work covered also some preliminary studies on the catalytic activity of the obtained products. The solids 4a and 4b worked as excellent pre-catalyst in the heterogeneous hydrogenation reaction of cyclohexene (100C, P(H2) 40 atm), yielding turnover of 99% and 76% respectively. The residue 4a- R obtained from the hydrogenation hydrogenation reaction with 4a was recovered and re-utilized for a new hydrogenation reaction under the same reaction conditions yielding a turnover of 89%, which makes suppose that 4a behave as a pre-catalyst more than a true catalyst. With product 5 were carried out two experiments of homogeneous hydrogenation in DMSO and THF as solvents under the same conditions, yielding only 26% and 16% of turnover respectively.La reacción de [Ru3(CO)12] 1 con la base de Tröger pirazólica 5,12- dimetil-3,10-bis-(p- nitrofenil)-1,3,4,8,10,11-hexaazatetraciclo[ 6.6.1.02,6.09,13]-pentadeca-2(6),4,9(13),11-tetraeno (TBpz) 2 y el 5- amino-3-metil-1-(p-nitrofenil) pirazol (amnpz) 3 se llevó a cabo en tolueno a temperatura de reflujo y bajo atmósfera inerte. A partir de (2) se obtuvieron los sólidos de color negro 4a y color café 4b de la forma [Ru3(TBpz)(CO)n]. De 4a se obtuvieron cristales en ácido nítrico diluido enviados recientemente para estudios de difracción de rayos X. La reacción de [Ru3(CO)12] con 3 proporcionó el sólido [Ru3(amnpz)(CO)m] 5. En este trabajo también se realizaron estudios preliminares de la actividad catalítica de los productos sintetizados. Los sólidos 4a y 4b actuaron como excelentes precatalizadores en la hidrogenación heterogénea del ciclohexeno a ciclohexano [100C, P(H2) 40 atm], obteniéndose porcentajes de conversión a ciclohexano de 99% y 76% respectivamente El residuo 4a-R obtenido de la reacción de hidrogenación con 4ª se recuperó y se realizó con él un nuevo ensayo de catálisis en las mismas condiciones, proporcionando un 89.7% de conversión, lo cual hace suponer que 4a es un precatalizador. Con 5 se realizaron dos ensayos de hidrogenación homogénea en DMSO y THF como solventes en las mismas condiciones, obteniéndose solo 26% y 16% respectivamente de conversión a ciclohexano.application/pdfspaUniversidad Autónoma de OccidenteEl hombre y la máquina no. 24 (ene.-jun. 2005); p. 114-121Derechos 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 UAOHidrogenacionCompuestos organometálicosHydrogenationOrganometallic compoundsReactividad del agregado dodecarboniltrirutenio con una base de Tröger de tipo pirazólico y un aminopirazolArtículo 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_970fb48d4fbd8a85PublicationTHUMBNAILT0003421.pdf.jpgT0003421.pdf.jpgGenerated Thumbnailimage/jpeg16039https://dspace7-uao.metacatalogo.com/bitstreams/7dd1fe07-5118-4fbf-9cdc-f8853d4856ed/download40682fad4637b14d36b2f60adda362dfMD54ORIGINALT0003421.pdfapplication/pdf259308https://dspace7-uao.metacatalogo.com/bitstreams/e43cd6cf-ec12-4914-a245-5f76886e6563/download16b3a1fba79f09f01549580317717a10MD51LICENSElicense.txttext/plain1849https://dspace7-uao.metacatalogo.com/bitstreams/d17bf082-6430-48bd-bd94-2e28b62bdb74/downloadc799b1f919b564a2f737c1a190b13ee9MD52TEXTT0003421.pdf.txtT0003421.pdf.txtExtracted texttext/plain25501https://dspace7-uao.metacatalogo.com/bitstreams/d935f11d-a7f9-4552-a368-3fce35455eec/download854fa27e87dde150a70cd68ef11f3153MD5310614/186oai:dspace7-uao.metacatalogo.com:10614/1862024-01-19 15:42:09.482https://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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