Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study
Autor(a) principal: | |
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Data de Publicação: | 2020 |
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/10773/37671 |
Resumo: | The reaction of S-alkyl/aryl dithiocarbazate functionalized with 2-acetyl pyridine ligands and cadmium chloride in ethanol leads to the formation of a mono nuclear cadmium(II) complex, [Cd(L1)2] (SP1), (HL1 is S-methyl-2-(1-(pyridine-2-yl)ethylidene)hydrazine-1-carbodithioate) and a dinuclear dichloro bridged complex, [(L2)Cd(μ-Cl)2Cd(L2)] (SP2), (L2 is S-benzyl-2-(1-(pyridine-2-yl)ethylidene)hydrazine-1-carbodithioate). The complexes are characterized by FTIR, single X-ray crystallography and thermogravimetry analysis. Density functional calculations indicate that different coordination patterns of the complexes with HL1 and HL2 ligands relate with the available space of the dissociation of CdCl2 in their solutions. Thermochemical destruction of the precursor complexes at the molecular level fabricated hexagonal CdS nanoparticles where the morphology is guided by the precursor. In situ generated thiols e.g., CH3SH in case of SP1, and PhCH2SH in case of SP2, internally stabilized the flower-like and rod shaped CdS structures, respectively. The synthesized nanoparticles were characterized by powder X-ray diffraction (XRD), scanning electronic microscope (SEM) and energy-dispersive X-ray spectroscopy (EDAX). The UV–Vis spectroscopic study shows a prominent quantum confinement effect in CdS with a band gap energy of 2.4 eV and 2.5 eV for SP1 and SP2, respectively. The CdS nanocrystals under investigation degrade Rose Bengal (RB) dye (96%) under visible light irradiation. A reusability study shows that the CdC nanoparticles retain their catalytic activity (86%). |
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Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation studyPyridinyl dithiocarbazatesSingle-source precursorX-ray crystallographySolvothermalCdS nanocrystalsPhotocatalytic activityThe reaction of S-alkyl/aryl dithiocarbazate functionalized with 2-acetyl pyridine ligands and cadmium chloride in ethanol leads to the formation of a mono nuclear cadmium(II) complex, [Cd(L1)2] (SP1), (HL1 is S-methyl-2-(1-(pyridine-2-yl)ethylidene)hydrazine-1-carbodithioate) and a dinuclear dichloro bridged complex, [(L2)Cd(μ-Cl)2Cd(L2)] (SP2), (L2 is S-benzyl-2-(1-(pyridine-2-yl)ethylidene)hydrazine-1-carbodithioate). The complexes are characterized by FTIR, single X-ray crystallography and thermogravimetry analysis. Density functional calculations indicate that different coordination patterns of the complexes with HL1 and HL2 ligands relate with the available space of the dissociation of CdCl2 in their solutions. Thermochemical destruction of the precursor complexes at the molecular level fabricated hexagonal CdS nanoparticles where the morphology is guided by the precursor. In situ generated thiols e.g., CH3SH in case of SP1, and PhCH2SH in case of SP2, internally stabilized the flower-like and rod shaped CdS structures, respectively. The synthesized nanoparticles were characterized by powder X-ray diffraction (XRD), scanning electronic microscope (SEM) and energy-dispersive X-ray spectroscopy (EDAX). The UV–Vis spectroscopic study shows a prominent quantum confinement effect in CdS with a band gap energy of 2.4 eV and 2.5 eV for SP1 and SP2, respectively. The CdS nanocrystals under investigation degrade Rose Bengal (RB) dye (96%) under visible light irradiation. A reusability study shows that the CdC nanoparticles retain their catalytic activity (86%).Elsevier2023-05-11T09:49:34Z2020-02-01T00:00:00Z2020-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/37671eng0020-169310.1016/j.ica.2019.119315Santra, AnanyakumariBrandão, PaulaMondal, GopinathBera, PradipJana, AbhimanyuBhattacharyya, IndranilPramanik, ChandanaBera, Pulakeshinfo: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:RCAAP2024-02-22T12:12:53Zoai:ria.ua.pt:10773/37671Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:08:16.415329Repositório 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 |
Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study |
title |
Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study |
spellingShingle |
Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study Santra, Ananyakumari Pyridinyl dithiocarbazates Single-source precursor X-ray crystallography Solvothermal CdS nanocrystals Photocatalytic activity |
title_short |
Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study |
title_full |
Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study |
title_fullStr |
Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study |
title_full_unstemmed |
Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study |
title_sort |
Monomeric and dimeric cadmium(II) complexes of S-alkyl/aryl dithiocarbazate as single-source precursors for cadmium sulfide nanoparticles: an experimental, theoretical interpretation in the stability of precursor and visible light dye degradation study |
author |
Santra, Ananyakumari |
author_facet |
Santra, Ananyakumari Brandão, Paula Mondal, Gopinath Bera, Pradip Jana, Abhimanyu Bhattacharyya, Indranil Pramanik, Chandana Bera, Pulakesh |
author_role |
author |
author2 |
Brandão, Paula Mondal, Gopinath Bera, Pradip Jana, Abhimanyu Bhattacharyya, Indranil Pramanik, Chandana Bera, Pulakesh |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Santra, Ananyakumari Brandão, Paula Mondal, Gopinath Bera, Pradip Jana, Abhimanyu Bhattacharyya, Indranil Pramanik, Chandana Bera, Pulakesh |
dc.subject.por.fl_str_mv |
Pyridinyl dithiocarbazates Single-source precursor X-ray crystallography Solvothermal CdS nanocrystals Photocatalytic activity |
topic |
Pyridinyl dithiocarbazates Single-source precursor X-ray crystallography Solvothermal CdS nanocrystals Photocatalytic activity |
description |
The reaction of S-alkyl/aryl dithiocarbazate functionalized with 2-acetyl pyridine ligands and cadmium chloride in ethanol leads to the formation of a mono nuclear cadmium(II) complex, [Cd(L1)2] (SP1), (HL1 is S-methyl-2-(1-(pyridine-2-yl)ethylidene)hydrazine-1-carbodithioate) and a dinuclear dichloro bridged complex, [(L2)Cd(μ-Cl)2Cd(L2)] (SP2), (L2 is S-benzyl-2-(1-(pyridine-2-yl)ethylidene)hydrazine-1-carbodithioate). The complexes are characterized by FTIR, single X-ray crystallography and thermogravimetry analysis. Density functional calculations indicate that different coordination patterns of the complexes with HL1 and HL2 ligands relate with the available space of the dissociation of CdCl2 in their solutions. Thermochemical destruction of the precursor complexes at the molecular level fabricated hexagonal CdS nanoparticles where the morphology is guided by the precursor. In situ generated thiols e.g., CH3SH in case of SP1, and PhCH2SH in case of SP2, internally stabilized the flower-like and rod shaped CdS structures, respectively. The synthesized nanoparticles were characterized by powder X-ray diffraction (XRD), scanning electronic microscope (SEM) and energy-dispersive X-ray spectroscopy (EDAX). The UV–Vis spectroscopic study shows a prominent quantum confinement effect in CdS with a band gap energy of 2.4 eV and 2.5 eV for SP1 and SP2, respectively. The CdS nanocrystals under investigation degrade Rose Bengal (RB) dye (96%) under visible light irradiation. A reusability study shows that the CdC nanoparticles retain their catalytic activity (86%). |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-02-01T00:00:00Z 2020-02-01 2023-05-11T09:49:34Z |
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/10773/37671 |
url |
http://hdl.handle.net/10773/37671 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
0020-1693 10.1016/j.ica.2019.119315 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
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 |
institution |
RCAAP |
reponame_str |
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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