Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)]
Condensation of 8-hydroxyquinoline-2-carbaldehyde with 2-aminophenol gave the (E)-2-[(2-hydroxyphenylimino)methyl]quinolin-8-ol derivative that reacted with di-n-butyltin oxide with release of H2O to yield the chelate title complex, [Sn2(C4H9)4(C16H10N2O2)2]. The compound crystallizes in th...
- Autores:
-
Camacho Camacho, Carlos
Ortiz Pastrana, Naytzé
garza-ortiz, ariadna
Rojas-Oviedo, Irma
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2017
- Institución:
- Corporación Universidad de la Costa
- Repositorio:
- REDICUC - Repositorio CUC
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.cuc.edu.co:11323/7259
- Acceso en línea:
- https://hdl.handle.net/11323/7259
https://doi.org/10.1107/S2056989016018867
https://repositorio.cuc.edu.co/
- Palabra clave:
- crystal structure
8-quinolinolates
sevenfold coordination
dialkylditin(IV) compound
- Rights
- openAccess
- License
- Attribution-NonCommercial-ShareAlike 4.0 International
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dc.title.spa.fl_str_mv |
Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)] |
title |
Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)] |
spellingShingle |
Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)] crystal structure 8-quinolinolates sevenfold coordination dialkylditin(IV) compound |
title_short |
Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)] |
title_full |
Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)] |
title_fullStr |
Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)] |
title_full_unstemmed |
Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)] |
title_sort |
Crystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)] |
dc.creator.fl_str_mv |
Camacho Camacho, Carlos Ortiz Pastrana, Naytzé garza-ortiz, ariadna Rojas-Oviedo, Irma |
dc.contributor.author.spa.fl_str_mv |
Camacho Camacho, Carlos Ortiz Pastrana, Naytzé garza-ortiz, ariadna Rojas-Oviedo, Irma |
dc.subject.spa.fl_str_mv |
crystal structure 8-quinolinolates sevenfold coordination dialkylditin(IV) compound |
topic |
crystal structure 8-quinolinolates sevenfold coordination dialkylditin(IV) compound |
description |
Condensation of 8-hydroxyquinoline-2-carbaldehyde with 2-aminophenol gave the (E)-2-[(2-hydroxyphenylimino)methyl]quinolin-8-ol derivative that reacted with di-n-butyltin oxide with release of H2O to yield the chelate title complex, [Sn2(C4H9)4(C16H10N2O2)2]. The compound crystallizes in the triclinic space group P-1, with two independent centrosymmetric dimers in the unit cell. Each features a typical pincer-type structure where the dianionic ligand is tetradentate, coordinating to the central tin atom through both phenolate oxygen atoms, as well as through the quinoline and imine N atoms. Each metal atom adopts a distorted pentagonal–bipyramidal SnC2N2O3 coordination arising from the N,N′,O,O′-tetradentate deprotonated Schiff base, one bridging phenolate O atom of the neighbouring ligand and two butyl groups in the axial sites. |
publishDate |
2017 |
dc.date.issued.none.fl_str_mv |
2017 |
dc.date.accessioned.none.fl_str_mv |
2020-11-11T16:45:21Z |
dc.date.available.none.fl_str_mv |
2020-11-11T16:45:21Z |
dc.type.spa.fl_str_mv |
Artículo de revista |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coar.spa.fl_str_mv |
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 |
dc.type.redcol.spa.fl_str_mv |
http://purl.org/redcol/resource_type/ART |
dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/acceptedVersion |
format |
http://purl.org/coar/resource_type/c_6501 |
status_str |
acceptedVersion |
dc.identifier.issn.spa.fl_str_mv |
2056-9890 |
dc.identifier.uri.spa.fl_str_mv |
https://hdl.handle.net/11323/7259 |
dc.identifier.doi.spa.fl_str_mv |
https://doi.org/10.1107/S2056989016018867 |
dc.identifier.instname.spa.fl_str_mv |
Corporación Universidad de la Costa |
dc.identifier.reponame.spa.fl_str_mv |
REDICUC - Repositorio CUC |
dc.identifier.repourl.spa.fl_str_mv |
https://repositorio.cuc.edu.co/ |
identifier_str_mv |
2056-9890 Corporación Universidad de la Costa REDICUC - Repositorio CUC |
url |
https://hdl.handle.net/11323/7259 https://doi.org/10.1107/S2056989016018867 https://repositorio.cuc.edu.co/ |
dc.language.iso.none.fl_str_mv |
eng |
language |
eng |
dc.relation.references.spa.fl_str_mv |
Rasoul-Amini, S., Khalaj, A., Shafiee, A., Daneshtalab, M., Madadkar-Sobhani, M. & Fouladdel, S. (2006). Int. J. Cancer Res. 2, 102–108. Albrecht, M., Osetska, O. & Fröhlich, R. (2005). Dalton Trans. pp. 3757–3762. Albrecht, M., Osetska, O., Fröhlich, R., Bünzli, J. G., Aebischer, A., Gumy, F. & Hamacek, J. (2007). J. Am. Chem. Soc. 129, 14178–14179. Anitha, P., Manikandan, R., Prakash, G., Pachiyappan, B., Viswanathamurthi, P. & Malecki, J. G. (2015). J. Organomet. Chem. 791, 266–273. Basu Baul, T. S., Mizar, A., Paul, A., Ruisi, G., Willem, R., Biesemans, M. & Linden, A. (2009). J. Organomet. Chem. 694, 2142–2152. Bruker (2012). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA. Charles, R. G. & Perrotto, A. (1964). Anal. Chim. Acta, 30, 131–138. Corcé, V., Renaud, S., Cannie, I., Julienne, K., Gouin, S. G., Loréal, O., Gaboriau, F. & Deniaud, D. (2014). Bioconjugate Chem. 25, 320–334. Cui, J., Qiao, Y., Yin, H. & Liu, M. Z. (2010). Z. Anorg. Allg. Chem. 636, 2508–2512. García-Santos, I., Sanmartín, J., García-Deibe, A. M., Fondo, M. & Gómez, E. (2009). Polyhedron, 28, 3055–3059. Macrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. & Wood, P. A. (2008). J. Appl. Cryst. 41, 466–470. Musiol, R., Jampilek, J., Buchta, V., Silva, L., Niedbala, H., Podeszwa, B., Palka, A., Majerz-Maniecka, K., Oleksyn, B. & Polanski, J. (2006). Bioorg. Med. Chem. 14, 3592–3598. Nasveld, P. & Kitchener, S. (2005). Trans. R. Soc. Trop. Med. Hyg. 99, 2–5. Palit, P., Paira, P., Hazra, A., Banerjee, S., Das Gupta, A., Dastidar, S. G. & Mondal, N. B. (2009). Eur. J. Med. Chem. 44, 845–853. Serda, M., Kalinowski, D., Mrozek-Wilczkiewicz, A., Musiol, R., Szurko, A., Ratuszna, A., Pantarat, N., Kovacevic, Z., Merlot, A. M., Richardson, D. R. & Polanski, J. (2012). Bioorg. Med. Chem. Lett. 22, 5527–5531. Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Sheldrick, G. M. (2015). Acta Cryst. C71, 3–8. Sousa, A. T. de, Bessler, K. E., Lemos, S. S., Ellena, J. & Gatto, C. C. (2009). Z. Anorg. Allg. Chem. 635, 106–111. Sun, W.-H., Shen, M., Zhang, W., Huang, W., Liu, S. & Redshaw, C. (2011). Dalton Trans. 40, 2645–2653. Vafaee, M., Amini, M. M. & Ng, S. W. (2010). Acta Cryst. E66, m964. Westrip, S. P. (2010). J. Appl. Cryst. 43, 920–925. Yan, Q., Sun, Z., Zhang, W., Nomura, K. & Sun, W.-H. (2014). Macromol. Chem. Phys. 215, 1744–1752. Zhang, W., Liu, S., Yang, W., Hao, X., Glaser, R. & Sun, W.-H. (2012). Organometallics, 31, 8178–8188. Zhang, H.-X., Wang, S.-Y., Wang, W.-M., Gao, H.-L. & Cui, J.-Z. (2015). Inorg. Chem. Commun. 62, 94–97. |
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Camacho Camacho, CarlosOrtiz Pastrana, Naytzégarza-ortiz, ariadnaRojas-Oviedo, Irma2020-11-11T16:45:21Z2020-11-11T16:45:21Z20172056-9890https://hdl.handle.net/11323/7259https://doi.org/10.1107/S2056989016018867Corporación Universidad de la CostaREDICUC - Repositorio CUChttps://repositorio.cuc.edu.co/Condensation of 8-hydroxyquinoline-2-carbaldehyde with 2-aminophenol gave the (E)-2-[(2-hydroxyphenylimino)methyl]quinolin-8-ol derivative that reacted with di-n-butyltin oxide with release of H2O to yield the chelate title complex, [Sn2(C4H9)4(C16H10N2O2)2]. The compound crystallizes in the triclinic space group P-1, with two independent centrosymmetric dimers in the unit cell. Each features a typical pincer-type structure where the dianionic ligand is tetradentate, coordinating to the central tin atom through both phenolate oxygen atoms, as well as through the quinoline and imine N atoms. Each metal atom adopts a distorted pentagonal–bipyramidal SnC2N2O3 coordination arising from the N,N′,O,O′-tetradentate deprotonated Schiff base, one bridging phenolate O atom of the neighbouring ligand and two butyl groups in the axial sites.Camacho Camacho, CarlosOrtiz Pastrana, Naytzégarza-ortiz, ariadna-will be generated-orcid-0000-0003-2585-1285-600Rojas-Oviedo, Irma-will be generated-orcid-0000-0003-2807-5402-600application/pdfengCorporación Universidad de la CostaAttribution-NonCommercial-ShareAlike 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Acta Crystallogr E Crystallogr Communhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5209758/crystal structure8-quinolinolatessevenfold coordinationdialkylditin(IV) compoundCrystal structure of bis{mu-(E)-2-[(2-oxidophenyl-imino)methyl]quinolin-8-olato-kappa O-4,N,N ',O '}-bis[dibutyltin(IV)]Artículo 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/ARTinfo:eu-repo/semantics/acceptedVersionRasoul-Amini, S., Khalaj, A., Shafiee, A., Daneshtalab, M., Madadkar-Sobhani, M. & Fouladdel, S. (2006). Int. J. Cancer Res. 2, 102–108.Albrecht, M., Osetska, O. & Fröhlich, R. (2005). Dalton Trans. pp. 3757–3762.Albrecht, M., Osetska, O., Fröhlich, R., Bünzli, J. G., Aebischer, A., Gumy, F. & Hamacek, J. (2007). J. Am. Chem. Soc. 129, 14178–14179.Anitha, P., Manikandan, R., Prakash, G., Pachiyappan, B., Viswanathamurthi, P. & Malecki, J. G. (2015). J. Organomet. Chem. 791, 266–273.Basu Baul, T. S., Mizar, A., Paul, A., Ruisi, G., Willem, R., Biesemans, M. & Linden, A. (2009). J. Organomet. Chem. 694, 2142–2152.Bruker (2012). APEX2, SAINT and SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.Charles, R. G. & Perrotto, A. (1964). Anal. Chim. Acta, 30, 131–138.Corcé, V., Renaud, S., Cannie, I., Julienne, K., Gouin, S. G., Loréal, O., Gaboriau, F. & Deniaud, D. (2014). Bioconjugate Chem. 25, 320–334.Cui, J., Qiao, Y., Yin, H. & Liu, M. Z. (2010). Z. Anorg. Allg. Chem. 636, 2508–2512.García-Santos, I., Sanmartín, J., García-Deibe, A. M., Fondo, M. & Gómez, E. (2009). Polyhedron, 28, 3055–3059.Macrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. & Wood, P. A. (2008). J. Appl. Cryst. 41, 466–470.Musiol, R., Jampilek, J., Buchta, V., Silva, L., Niedbala, H., Podeszwa, B., Palka, A., Majerz-Maniecka, K., Oleksyn, B. & Polanski, J. (2006). Bioorg. Med. Chem. 14, 3592–3598.Nasveld, P. & Kitchener, S. (2005). Trans. R. Soc. Trop. Med. Hyg. 99, 2–5.Palit, P., Paira, P., Hazra, A., Banerjee, S., Das Gupta, A., Dastidar, S. G. & Mondal, N. B. (2009). Eur. J. Med. Chem. 44, 845–853.Serda, M., Kalinowski, D., Mrozek-Wilczkiewicz, A., Musiol, R., Szurko, A., Ratuszna, A., Pantarat, N., Kovacevic, Z., Merlot, A. M., Richardson, D. R. & Polanski, J. (2012). Bioorg. Med. Chem. Lett. 22, 5527–5531.Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122.Sheldrick, G. M. (2015). Acta Cryst. C71, 3–8.Sousa, A. T. de, Bessler, K. E., Lemos, S. S., Ellena, J. & Gatto, C. C. (2009). Z. Anorg. Allg. Chem. 635, 106–111.Sun, W.-H., Shen, M., Zhang, W., Huang, W., Liu, S. & Redshaw, C. (2011). Dalton Trans. 40, 2645–2653.Vafaee, M., Amini, M. M. & Ng, S. W. (2010). Acta Cryst. E66, m964.Westrip, S. P. (2010). J. Appl. Cryst. 43, 920–925.Yan, Q., Sun, Z., Zhang, W., Nomura, K. & Sun, W.-H. (2014). Macromol. Chem. Phys. 215, 1744–1752.Zhang, W., Liu, S., Yang, W., Hao, X., Glaser, R. & Sun, W.-H. (2012). Organometallics, 31, 8178–8188.Zhang, H.-X., Wang, S.-Y., Wang, W.-M., Gao, H.-L. & Cui, J.-Z. (2015). Inorg. Chem. Commun. 62, 94–97.PublicationORIGINALCrystal structure of bis{[mu]-(E)-2-[(2-oxidophenylimino)methyl]quinolin-8-olato-[kappa]4O,N,N',O'}bis[dibutyltin(IV)] _ Enhanced Reader.pdfCrystal structure of bis{[mu]-(E)-2-[(2-oxidophenylimino)methyl]quinolin-8-olato-[kappa]4O,N,N',O'}bis[dibutyltin(IV)] _ Enhanced Reader.pdfapplication/pdf8128835https://repositorio.cuc.edu.co/bitstreams/c941f254-9b4f-41b8-ae2b-4af2b92f151a/downloade7bc022eb817a2ab0816535d46cc8267MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-81031https://repositorio.cuc.edu.co/bitstreams/a165552a-425c-4663-9fb2-58d7c68b00b0/download934f4ca17e109e0a05eaeaba504d7ce4MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-83196https://repositorio.cuc.edu.co/bitstreams/f415ce66-1017-41c7-9f6d-f78f9de51a17/downloade30e9215131d99561d40d6b0abbe9badMD53THUMBNAILCrystal structure of bis{[mu]-(E)-2-[(2-oxidophenylimino)methyl]quinolin-8-olato-[kappa]4O,N,N',O'}bis[dibutyltin(IV)] _ Enhanced Reader.pdf.jpgCrystal structure of bis{[mu]-(E)-2-[(2-oxidophenylimino)methyl]quinolin-8-olato-[kappa]4O,N,N',O'}bis[dibutyltin(IV)] _ Enhanced Reader.pdf.jpgimage/jpeg62315https://repositorio.cuc.edu.co/bitstreams/316fb63e-c2e2-4415-9766-7ec4f23af168/download9eaf53f1f22e8d848a25168ccabeba18MD54TEXTCrystal structure of bis{[mu]-(E)-2-[(2-oxidophenylimino)methyl]quinolin-8-olato-[kappa]4O,N,N',O'}bis[dibutyltin(IV)] _ Enhanced Reader.pdf.txtCrystal structure of bis{[mu]-(E)-2-[(2-oxidophenylimino)methyl]quinolin-8-olato-[kappa]4O,N,N',O'}bis[dibutyltin(IV)] _ Enhanced Reader.pdf.txttext/plain17https://repositorio.cuc.edu.co/bitstreams/5a8bf11b-579c-4e1c-b55d-c19c2cc13d75/download24e648839aa31918bceb936aff170ec0MD5511323/7259oai:repositorio.cuc.edu.co:11323/72592024-09-17 12:48:23.272http://creativecommons.org/licenses/by-nc-sa/4.0/Attribution-NonCommercial-ShareAlike 4.0 Internationalopen.accesshttps://repositorio.cuc.edu.coRepositorio de la Universidad de la Costa 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