First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | |
Tipo de documento: | Artigo de conferência |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10174/5336 |
Resumo: | The search for new organometallic materials with second-order nonlinear optical (SONLO) properties is currently the subject of considerable interest due to their potential technologic applications in photonic devices for telecommunications and optical computing. Experimental systematic studies were made on half-sandwich complexes presenting nitrile and acetylide benzene and thiophene-based chromophores [1-3]. The results revealed that the combination of acetylide thiophene ligands with appropriate organometallic fragments would maximize the SONLO response. Also, recent TD-DFT studies on h5-monocyclopentadienyliron(II) complexes with substituted thienyl-acetylide ligands revealed the fundamental role played by the organometallic fragment on the corresponding SONLO properties [4]. In our continuous effort to get a better understanding on the electronic factors that may dictate the SONLO properties of η5-monocyclopentadienylmetal complexes with substituted thienyl-acetylide chromophores, we report herein the preliminary density functional theory (DFT) and time-dependent DFT (TD-DFT) results on the complexes [NiCp(PR3)(CC{SC4H2}nY)] (R=H, Ph; Y= CHO, CN, NO2; n=1,2) using the Gaussian03W program package. For instance, Figure 1 shows the optimized structure for NiCp(PH3)(CC{SC4H2}NO2. The effect of the phosphine, the Y-substituent and the conjugated length of the chromophore on the first hyperpolarizability will be evaluated. Some experimental spectroscopic data will be also explained on the basis of the TD-DFT calculations. |
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First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT StudyFIRST HYPERPOLARIZABILITYACETYLIDE COMPLEXESDFTThe search for new organometallic materials with second-order nonlinear optical (SONLO) properties is currently the subject of considerable interest due to their potential technologic applications in photonic devices for telecommunications and optical computing. Experimental systematic studies were made on half-sandwich complexes presenting nitrile and acetylide benzene and thiophene-based chromophores [1-3]. The results revealed that the combination of acetylide thiophene ligands with appropriate organometallic fragments would maximize the SONLO response. Also, recent TD-DFT studies on h5-monocyclopentadienyliron(II) complexes with substituted thienyl-acetylide ligands revealed the fundamental role played by the organometallic fragment on the corresponding SONLO properties [4]. In our continuous effort to get a better understanding on the electronic factors that may dictate the SONLO properties of η5-monocyclopentadienylmetal complexes with substituted thienyl-acetylide chromophores, we report herein the preliminary density functional theory (DFT) and time-dependent DFT (TD-DFT) results on the complexes [NiCp(PR3)(CC{SC4H2}nY)] (R=H, Ph; Y= CHO, CN, NO2; n=1,2) using the Gaussian03W program package. For instance, Figure 1 shows the optimized structure for NiCp(PH3)(CC{SC4H2}NO2. The effect of the phosphine, the Y-substituent and the conjugated length of the chromophore on the first hyperpolarizability will be evaluated. Some experimental spectroscopic data will be also explained on the basis of the TD-DFT calculations.XXI Encontro Nacional SPQ2012-10-11T11:06:10Z2012-10-112008-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjecthttp://hdl.handle.net/10174/5336http://hdl.handle.net/10174/5336engXXI Encontro Nacional SPQ, Porto, Portugal, June 2008, Book of Abstracts P238http://paginas.fe.up.pt/~xxien/documents/livro_de_resumos.pdfnaonaosimQUI - Comunicações - Em Congressos Científicos Nacionaispjgm@uevora.ptajpalace@uevora.pt306Mendes, Paulo J.Carvalho, A.J. Palaceinfo: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:RCAAP2024-01-03T18:43:58Zoai:dspace.uevora.pt:10174/5336Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:00:20.424792Repositório 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 |
First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study |
title |
First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study |
spellingShingle |
First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study Mendes, Paulo J. FIRST HYPERPOLARIZABILITY ACETYLIDE COMPLEXES DFT |
title_short |
First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study |
title_full |
First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study |
title_fullStr |
First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study |
title_full_unstemmed |
First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study |
title_sort |
First Hyperpolarizability Of Some Nickel-Acetylide Complexes: A DFT Study |
author |
Mendes, Paulo J. |
author_facet |
Mendes, Paulo J. Carvalho, A.J. Palace |
author_role |
author |
author2 |
Carvalho, A.J. Palace |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Mendes, Paulo J. Carvalho, A.J. Palace |
dc.subject.por.fl_str_mv |
FIRST HYPERPOLARIZABILITY ACETYLIDE COMPLEXES DFT |
topic |
FIRST HYPERPOLARIZABILITY ACETYLIDE COMPLEXES DFT |
description |
The search for new organometallic materials with second-order nonlinear optical (SONLO) properties is currently the subject of considerable interest due to their potential technologic applications in photonic devices for telecommunications and optical computing. Experimental systematic studies were made on half-sandwich complexes presenting nitrile and acetylide benzene and thiophene-based chromophores [1-3]. The results revealed that the combination of acetylide thiophene ligands with appropriate organometallic fragments would maximize the SONLO response. Also, recent TD-DFT studies on h5-monocyclopentadienyliron(II) complexes with substituted thienyl-acetylide ligands revealed the fundamental role played by the organometallic fragment on the corresponding SONLO properties [4]. In our continuous effort to get a better understanding on the electronic factors that may dictate the SONLO properties of η5-monocyclopentadienylmetal complexes with substituted thienyl-acetylide chromophores, we report herein the preliminary density functional theory (DFT) and time-dependent DFT (TD-DFT) results on the complexes [NiCp(PR3)(CC{SC4H2}nY)] (R=H, Ph; Y= CHO, CN, NO2; n=1,2) using the Gaussian03W program package. For instance, Figure 1 shows the optimized structure for NiCp(PH3)(CC{SC4H2}NO2. The effect of the phosphine, the Y-substituent and the conjugated length of the chromophore on the first hyperpolarizability will be evaluated. Some experimental spectroscopic data will be also explained on the basis of the TD-DFT calculations. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-01-01T00:00:00Z 2012-10-11T11:06:10Z 2012-10-11 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/conferenceObject |
format |
conferenceObject |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10174/5336 http://hdl.handle.net/10174/5336 |
url |
http://hdl.handle.net/10174/5336 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
XXI Encontro Nacional SPQ, Porto, Portugal, June 2008, Book of Abstracts P238 http://paginas.fe.up.pt/~xxien/documents/livro_de_resumos.pdf nao nao sim QUI - Comunicações - Em Congressos Científicos Nacionais pjgm@uevora.pt ajpalace@uevora.pt 306 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
XXI Encontro Nacional SPQ |
publisher.none.fl_str_mv |
XXI Encontro Nacional SPQ |
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) |
collection |
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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