Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10316/45089 https://doi.org/10.1016/j.jinorgbio.2011.11.021 |
Resumo: | A vibrational spectroscopy study (infrared and Raman) is reported for the biogenic polyamine analogues norspermidine (NSpd), N(1),N(11)-bis(ethyl)norspermine (BENSpm) and N(1)-cyclo-propylmethyl-N(11)-ethylnorspermine (CPENSpm), as well as for their newly synthesised Pt(II) and Pd(II) complexes. Attending to the potential antineoplastic properties of this kind of systems, their full conformational characterization is essential for understanding the molecular basis of their cytotoxic activity and the mechanisms through which they are transported into the cell. The all-trans geometry was found to be favoured for all the alkylated polyamines, in their totally protonated state, while their polynuclear complexes presented a stable geometry very similar to that previously obtained for the analogous chelates with spermidine (M(3)Spd(2)) and spermine (M(2)Spm), comprising two or three cisplatin-like (MCl(2)NH(2)) moieties. |
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Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysisAntineoplastic AgentsPalladiumPlatinumPlatinum CompoundsPolyaminesSpectroscopy, Fourier Transform InfraredSpectrum Analysis, RamanA vibrational spectroscopy study (infrared and Raman) is reported for the biogenic polyamine analogues norspermidine (NSpd), N(1),N(11)-bis(ethyl)norspermine (BENSpm) and N(1)-cyclo-propylmethyl-N(11)-ethylnorspermine (CPENSpm), as well as for their newly synthesised Pt(II) and Pd(II) complexes. Attending to the potential antineoplastic properties of this kind of systems, their full conformational characterization is essential for understanding the molecular basis of their cytotoxic activity and the mechanisms through which they are transported into the cell. The all-trans geometry was found to be favoured for all the alkylated polyamines, in their totally protonated state, while their polynuclear complexes presented a stable geometry very similar to that previously obtained for the analogous chelates with spermidine (M(3)Spd(2)) and spermine (M(2)Spm), comprising two or three cisplatin-like (MCl(2)NH(2)) moieties.2012info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/45089http://hdl.handle.net/10316/45089https://doi.org/10.1016/j.jinorgbio.2011.11.021https://doi.org/10.1016/j.jinorgbio.2011.11.021engSilva, T.M.Oredsson, S.Persson, L.Woster, P.Marques, M. P. M.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-09-24T10:22:39Zoai:estudogeral.uc.pt:10316/45089Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:56:08.103336Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis |
title |
Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis |
spellingShingle |
Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis Silva, T.M. Antineoplastic Agents Palladium Platinum Platinum Compounds Polyamines Spectroscopy, Fourier Transform Infrared Spectrum Analysis, Raman |
title_short |
Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis |
title_full |
Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis |
title_fullStr |
Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis |
title_full_unstemmed |
Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis |
title_sort |
Novel Pt(II) and Pd(II) complexes with polyamine analogues: Synthesis and vibrational analysis |
author |
Silva, T.M. |
author_facet |
Silva, T.M. Oredsson, S. Persson, L. Woster, P. Marques, M. P. M. |
author_role |
author |
author2 |
Oredsson, S. Persson, L. Woster, P. Marques, M. P. M. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Silva, T.M. Oredsson, S. Persson, L. Woster, P. Marques, M. P. M. |
dc.subject.por.fl_str_mv |
Antineoplastic Agents Palladium Platinum Platinum Compounds Polyamines Spectroscopy, Fourier Transform Infrared Spectrum Analysis, Raman |
topic |
Antineoplastic Agents Palladium Platinum Platinum Compounds Polyamines Spectroscopy, Fourier Transform Infrared Spectrum Analysis, Raman |
description |
A vibrational spectroscopy study (infrared and Raman) is reported for the biogenic polyamine analogues norspermidine (NSpd), N(1),N(11)-bis(ethyl)norspermine (BENSpm) and N(1)-cyclo-propylmethyl-N(11)-ethylnorspermine (CPENSpm), as well as for their newly synthesised Pt(II) and Pd(II) complexes. Attending to the potential antineoplastic properties of this kind of systems, their full conformational characterization is essential for understanding the molecular basis of their cytotoxic activity and the mechanisms through which they are transported into the cell. The all-trans geometry was found to be favoured for all the alkylated polyamines, in their totally protonated state, while their polynuclear complexes presented a stable geometry very similar to that previously obtained for the analogous chelates with spermidine (M(3)Spd(2)) and spermine (M(2)Spm), comprising two or three cisplatin-like (MCl(2)NH(2)) moieties. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10316/45089 http://hdl.handle.net/10316/45089 https://doi.org/10.1016/j.jinorgbio.2011.11.021 https://doi.org/10.1016/j.jinorgbio.2011.11.021 |
url |
http://hdl.handle.net/10316/45089 https://doi.org/10.1016/j.jinorgbio.2011.11.021 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1817551232576782336 |