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

Detalhes bibliográficos
Autor(a) principal: Santra, Ananyakumari
Data de Publicação: 2020
Outros Autores: Brandão, Paula, Mondal, Gopinath, Bera, Pradip, Jana, Abhimanyu, Bhattacharyya, Indranil, Pramanik, Chandana, Bera, Pulakesh
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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spelling 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
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
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