Base de dados : MEDLINE
Pesquisa : D01.268.185 [Categoria DeCS]
Referências encontradas : 344 [refinar]
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[PMID]:28728108
[Au] Autor:Roldán-Peña JM; Alejandre-Ramos D; López Ó; Maya I; Lagunes I; Padrón JM; Peña-Altamira LE; Bartolini M; Monti B; Bolognesi ML; Fernández-Bolaños JG
[Ad] Endereço:Departamento de Química Orgánica, Facultad de Química, Universidad de Sevilla, Apartado 1203, E-41071 Seville, Spain.
[Ti] Título:New tacrine dimers with antioxidant linkers as dual drugs: Anti-Alzheimer's and antiproliferative agents.
[So] Source:Eur J Med Chem;138:761-773, 2017 Sep 29.
[Is] ISSN:1768-3254
[Cp] País de publicação:France
[La] Idioma:eng
[Ab] Resumo:We have designed a series of tacrine-based homo- and heterodimers that incorporate an antioxidant tether (selenoureido, chalcogenide) as new dual compounds: for the treatment of Alzheimer's disease and as antiproliferative agents. Symmetrical homodimers bearing a dichalcogenide or selenide-based tether, the best compounds in the series, were found to be strong and highly selective electric eel AChE inhibitors, with inhibition constants within the low nanomolar range. This high inhibitory activity was confirmed on recombinant human AChE for the most interesting derivatives. The three most promising homodimers also showed a good inhibitory activity towards amyloid-ß self aggregation. The symmetric disulfide derivative bis[5-(1',2',3',4'-tetrahydroacridin-9'-ylamino)pentyl]disulfide (19) showed the best multipotent profile and was not neurotoxic on immortalized mouse cortical neurons even at 50 µM concentration. These results represent an improvement in activity and selectivity compared to parent tacrine, the first marketed drug against Alzheimer's disease. Title compounds also exhibited excellent in vitro antiproliferative activities against a panel of 6 human tumor cell lines, with GI values within the submicromolar range for the most potent derivatives (0.12-0.95 µM); such values represent a spectacular increase compared to currently-used chemotherapeutic agents, such as 5-FU (up to 306-fold) and cisplatin (up to 162-fold). Cell cycle experiments indicated the accumulation of cells in the G phase of the cycle, a different mechanism than the reported for cisplatin. The breast cancer cell lines turned out to be the most sensitive one of the panel tested.
[Mh] Termos MeSH primário: Doença de Alzheimer/tratamento farmacológico
Antineoplásicos/farmacologia
Antioxidantes/farmacologia
Calcogênios/farmacologia
Inibidores da Colinesterase/farmacologia
Compostos Organosselênicos/farmacologia
Tacrina/farmacologia
[Mh] Termos MeSH secundário: Acetilcolinesterase/metabolismo
Peptídeos beta-Amiloides/antagonistas & inibidores
Peptídeos beta-Amiloides/metabolismo
Animais
Antineoplásicos/síntese química
Antineoplásicos/química
Antioxidantes/química
Linhagem Celular Tumoral
Proliferação Celular/efeitos dos fármacos
Calcogênios/química
Inibidores da Colinesterase/síntese química
Inibidores da Colinesterase/química
Dimerização
Relação Dose-Resposta a Droga
Ensaios de Seleção de Medicamentos Antitumorais
Seres Humanos
Camundongos
Estrutura Molecular
Compostos Organosselênicos/química
Fragmentos de Peptídeos/antagonistas & inibidores
Fragmentos de Peptídeos/metabolismo
Agregados Proteicos/efeitos dos fármacos
Relação Estrutura-Atividade
Tacrina/química
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Amyloid beta-Peptides); 0 (Antineoplastic Agents); 0 (Antioxidants); 0 (Chalcogens); 0 (Cholinesterase Inhibitors); 0 (Organoselenium Compounds); 0 (Peptide Fragments); 0 (Protein Aggregates); 0 (amyloid beta-protein (1-42)); 4VX7YNB537 (Tacrine); EC 3.1.1.7 (Acetylcholinesterase)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171002
[Lr] Data última revisão:
171002
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170721
[St] Status:MEDLINE


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[PMID]:28526476
[Au] Autor:Dardashti RN; Metanis N
[Ad] Endereço:Institute of Chemistry, The Hebrew University of Jerusalem, Safra Campus Givat Ram, Jerusalem 91904, Israel.
[Ti] Título:Revisiting ligation at selenomethionine: Insights into native chemical ligation at selenocysteine and homoselenocysteine.
[So] Source:Bioorg Med Chem;25(18):4983-4989, 2017 Sep 15.
[Is] ISSN:1464-3391
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Selenomethionine (Sem) has been incorporated recombinantly into proteins many times to elucidate their structure and function. In this paper, we revisit incorporation via chemical protein synthesis to shed light on the mechanism of native chemical ligation. The effect of chalcogen position on ligation is investigated, and selenium-containing peptide ligation is optimized. Additionally, selective methylation is performed on selenolates in a peptide in the presence of unprotected thiols.
[Mh] Termos MeSH primário: Peptídeos/síntese química
Selenocisteína/análogos & derivados
Selenocisteína/química
Selenometionina/química
[Mh] Termos MeSH secundário: Sequência de Aminoácidos
Calcogênios/química
Cromatografia Líquida de Alta Pressão
Metilação
Peptídeos/análise
Peptídeos/química
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Chalcogens); 0 (Peptides); 0CH9049VIS (Selenocysteine); 964MRK2PEL (Selenomethionine)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171009
[Lr] Data última revisão:
171009
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170521
[St] Status:MEDLINE


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[PMID]:28394585
[Au] Autor:Coughlan C; Ibáñez M; Dobrozhan O; Singh A; Cabot A; Ryan KM
[Ad] Endereço:Department of Chemical Sciences and Bernal Institute, University of Limerick , Limerick, Ireland.
[Ti] Título:Compound Copper Chalcogenide Nanocrystals.
[So] Source:Chem Rev;117(9):5865-6109, 2017 May 10.
[Is] ISSN:1520-6890
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:This review captures the synthesis, assembly, properties, and applications of copper chalcogenide NCs, which have achieved significant research interest in the last decade due to their compositional and structural versatility. The outstanding functional properties of these materials stems from the relationship between their band structure and defect concentration, including charge carrier concentration and electronic conductivity character, which consequently affects their optoelectronic, optical, and plasmonic properties. This, combined with several metastable crystal phases and stoichiometries and the low energy of formation of defects, makes the reproducible synthesis of these materials, with tunable parameters, remarkable. Further to this, the review captures the progress of the hierarchical assembly of these NCs, which bridges the link between their discrete and collective properties. Their ubiquitous application set has cross-cut energy conversion (photovoltaics, photocatalysis, thermoelectrics), energy storage (lithium-ion batteries, hydrogen generation), emissive materials (plasmonics, LEDs, biolabelling), sensors (electrochemical, biochemical), biomedical devices (magnetic resonance imaging, X-ray computer tomography), and medical therapies (photochemothermal therapies, immunotherapy, radiotherapy, and drug delivery). The confluence of advances in the synthesis, assembly, and application of these NCs in the past decade has the potential to significantly impact society, both economically and environmentally.
[Mh] Termos MeSH primário: Calcogênios/química
Cobre/química
Nanopartículas/química
Nanotecnologia/métodos
[Mh] Termos MeSH secundário: Animais
Técnicas de Química Sintética
Seres Humanos
Nanopartículas/toxicidade
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Chalcogens); 789U1901C5 (Copper)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170619
[Lr] Data última revisão:
170619
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170411
[St] Status:MEDLINE
[do] DOI:10.1021/acs.chemrev.6b00376


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[PMID]:28157170
[Au] Autor:Sánchez-Sanz G; Alkorta I; Elguero J
[Ad] Endereço:Irish Centre of High-End Computing, Grand Canal Quay, Dublin 2, Ireland.
[Ti] Título:Theoretical Study of Intramolecular Interactions in Peri-Substituted Naphthalenes: Chalcogen and Hydrogen Bonds.
[So] Source:Molecules;22(2), 2017 Feb 02.
[Is] ISSN:1420-3049
[Cp] País de publicação:Switzerland
[La] Idioma:eng
[Ab] Resumo:A theoretical study of the peri interactions, both intramolecular hydrogen (HB) and chalcogen bonds (YB), in 1-hydroxy-8YH-naphthalene, 1,4-dihydroxy-5,8-di-YH-naphthalene, and 1,5-dihydroxy-4,8-di-YH-naphthalene, with Y = O, S, and Se was carried out. The systems with a OH:Y hydrogen bond are the most stable ones followed by those with a chalcogen O:Y interaction, those with a YH:O hydrogen bond (Y = S and Se) being the least stable ones. The electron density values at the hydrogen bond critical points indicate that they have partial covalent character. Natural Bond Orbital (NBO) analysis shows stabilization due to the charge transfer between lone pair orbitals towards empty Y-H that correlate with the interatomic distances. The electron density shift maps and non-covalent indexes in the different systems are consistent with the relative strength of the interactions. The structures found on the CSD were used to compare the experimental and calculated results.
[Mh] Termos MeSH primário: Calcogênios/química
Ligações de Hidrogênio
Modelos Teóricos
Naftalenos/química
[Mh] Termos MeSH secundário: Modelos Químicos
Modelos Moleculares
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Chalcogens); 0 (Naphthalenes)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170509
[Lr] Data última revisão:
170509
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170204
[St] Status:MEDLINE


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[PMID]:27992115
[Au] Autor:Giroud M; Ivkovic J; Martignoni M; Fleuti M; Trapp N; Haap W; Kuglstatter A; Benz J; Kuhn B; Schirmeister T; Diederich F
[Ad] Endereço:Laboratorium für Organische Chemie, ETH Zurich, Vladimir-Prelog-Weg 3, 8093, Zurich, Switzerland.
[Ti] Título:Inhibition of the Cysteine Protease Human Cathepsin L by Triazine Nitriles: Amideâ‹…â‹…â‹…Heteroarene π-Stacking Interactions and Chalcogen Bonding in the S3 Pocket.
[So] Source:ChemMedChem;12(3):257-270, 2017 Feb 03.
[Is] ISSN:1860-7187
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:We report an extensive "heteroarene scan" of triazine nitrile ligands of the cysteine protease human cathepsin L (hCatL) to investigate π-stacking on the peptide amide bond Gly67-Gly68 at the entrance of the S3 pocket. This heteroareneâ‹…â‹…â‹…peptide bond stacking was supported by a co-crystal structure of an imidazopyridine ligand with hCatL. Inhibitory constants (K ) are strongly influenced by the diverse nature of the heterocycles and specific interactions with the local environment of the S3 pocket. Binding affinities vary by three orders of magnitude. All heteroaromatic ligands feature enhanced binding by comparison with hydrocarbon analogues. Predicted energetic contributions from the orientation of the local dipole moments of heteroarene and peptide bond could not be confirmed. Binding of benzothienyl (K =4 nm) and benzothiazolyl (K =17 nm) ligands was enhanced by intermolecular C-Sâ‹…â‹…â‹…O=C interactions (chalcogen bonding) with the backbone C=O of Asn66 in the S3 pocket. The ligands were also tested for the related enzyme rhodesain.
[Mh] Termos MeSH primário: Catepsina L/metabolismo
Calcogênios/química
Nitrilos/metabolismo
Triazinas/química
[Mh] Termos MeSH secundário: Amidas/química
Sítios de Ligação
Catepsina L/antagonistas & inibidores
Cristalografia por Raios X
Seres Humanos
Ligantes
Simulação de Dinâmica Molecular
Nitrilos/síntese química
Nitrilos/química
Ligação Proteica
Estrutura Terciária de Proteína
Teoria Quântica
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Amides); 0 (Chalcogens); 0 (Ligands); 0 (Nitriles); 0 (Triazines); EC 3.4.22.15 (Cathepsin L)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170630
[Lr] Data última revisão:
170630
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161220
[St] Status:MEDLINE
[do] DOI:10.1002/cmdc.201600563


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[PMID]:27866619
[Au] Autor:Mareeswari P; Brijitta J; Harikrishna Etti S; Meganathan C; Kaliaraj GS
[Ad] Endereço:Department of Electronics and Communication Engineering, G.K.M. College of Engineering and Technology, Chennai 600 063, Tamil Nadu, India.
[Ti] Título:Rhizopus stolonifer mediated biosynthesis of biocompatible cadmium chalcogenide quantum dots.
[So] Source:Enzyme Microb Technol;95:225-229, 2016 Dec.
[Is] ISSN:1879-0909
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:We report an efficient method to biosynthesize biocompatible cadmium telluride and cadmium sulphide quantum dots from the fungus Rhizopus stolonifer. The suspension of the quantum dots exhibited purple and greenish-blue luminescence respectively upon UV light illumination. Photoluminescence spectroscopy, X-ray diffraction, and transmission electron microscopy confirms the formation of the quantum dots. From the photoluminescence spectrum the emission maxima is found to be 424 and 476nm respectively. The X-ray diffraction of the quantum dots matches with results reported in literature. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay for cell viability evaluation carried out on 3-days transfer, inoculum 3×10 cells, embryonic fibroblast cells lines shows that more than 80% of the cells are viable even after 48h, indicating the biocompatible nature of the quantum dots. A good contrast in imaging has been obtained upon incorporating the quantum dots in human breast adenocarcinoma Michigan Cancer Foundation-7 cell lines.
[Mh] Termos MeSH primário: Compostos de Cádmio/química
Compostos de Cádmio/metabolismo
Calcogênios/química
Calcogênios/metabolismo
Pontos Quânticos/química
Pontos Quânticos/metabolismo
Rhizopus/metabolismo
[Mh] Termos MeSH secundário: Animais
Biotecnologia
Química Verde
Seres Humanos
Células MCF-7
Camundongos
Células NIH 3T3
Nanotecnologia
Pontos Quânticos/ultraestrutura
Sulfetos/química
Sulfetos/metabolismo
Telúrio/química
Telúrio/metabolismo
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Cadmium Compounds); 0 (Chalcogens); 0 (Sulfides); 057EZR4Z7Q (cadmium sulfide); NQA0O090ZJ (Tellurium); STG188WO13 (cadmium telluride)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170515
[Lr] Data última revisão:
170515
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161122
[St] Status:MEDLINE


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[PMID]:27866608
[Au] Autor:Dahoumane SA; Wujcik EK; Jeffryes C
[Ad] Endereço:School of Life Science and Biotechnology, Yachay Tech University, San Miguel de Urcuquí, Ecuador.
[Ti] Título:Noble metal, oxide and chalcogenide-based nanomaterials from scalable phototrophic culture systems.
[So] Source:Enzyme Microb Technol;95:13-27, 2016 Dec.
[Is] ISSN:1879-0909
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Phototrophic cell or tissue cultures can produce nanostructured noble metals, oxides and chalcogenides at ambient temperatures and pressures in an aqueous environment and without the need for potentially toxic solvents or the generation of dangerous waste products. These "green" synthesized nanobiomaterials can be used to fabricate biosensors and bio-reporting tools, theranostic vehicles, medical imaging agents, as well as tissue engineering scaffolds and biomaterials. While successful at the lab and experimental scales, significant barriers still inhibit the development of higher capacity processes. While scalability issues in traditional algal bioprocess engineering are well known, such as the controlled delivery of photons and gas-exchange, the large-scale algal synthesis of nanomaterials introduces additional parameters to be understood, i.e., nanoparticle (NP) formation kinetics and mechanisms, biological transport of metal cations and the effect of environmental conditions on the final form of the NPs. Only after a clear understanding of the kinetics and mechanisms can the strain selection, photobioreactor type, medium pH and ionic strength, mean light intensity and other relevant parameters be specified for an optimal bioprocess. To this end, this mini-review will examine the current best practices and understanding of these phenomena to establish a path forward for this technology.
[Mh] Termos MeSH primário: Nanoestruturas
Fotobiorreatores
[Mh] Termos MeSH secundário: Materiais Biocompatíveis
Técnicas Biossensoriais
Calcogênios
Diagnóstico por Imagem
Química Verde
Seres Humanos
Nanopartículas Metálicas
Microalgas/metabolismo
Nanoestruturas/química
Nanotecnologia
Óxidos
Engenharia Tecidual
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Biocompatible Materials); 0 (Chalcogens); 0 (Oxides)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170515
[Lr] Data última revisão:
170515
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161122
[St] Status:MEDLINE


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[PMID]:27845568
[Au] Autor:Marset A; Begines P; López Ó; Maya I; García-Aranda N; Schwartz S; Abasolo I; Fernández-Bolaños JG
[Ad] Endereço:Departamento de Química Orgánica, Facultad de Química, Universidad de Sevilla, Apartado 1203, 41071, Seville, Spain.
[Ti] Título:Design of chalcogen-containing norepinephrines: efficient GPx mimics and strong cytotoxic agents against HeLa cells.
[So] Source:Future Med Chem;8(18):2185-2195, 2016 Dec.
[Is] ISSN:1756-8927
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:AIM: Numerous chronic diseases exhibit multifactorial etiologies, so focusing on a single therapeutic target is usually an inadequate treatment; instead, multi-target drugs are preferred. Herein, a panel of phenolic thioureas and selenoureas were designed as new prototypes against multifactorial diseases concerning antioxidation and cytotoxicity, as a pro-oxidant environment is usually found in such diseases. RESULTS: Selenoureas were excellent antiradical agents and biomimetic catalysts of glutathione peroxidase for the scavenging of H O . They were also potent and selective cytotoxic agents against cancer cells, in particular HeLa (IC 2.77-6.13 µM), apoptosis being involved. Selenoureas also reduced oxidative stress in HeLa cells (IC = 3.76 µM). CONCLUSION: Phenolic selenoureas are promising lead structures for the development of drugs targeting multifactorial diseases like cancer.
[Mh] Termos MeSH primário: Antioxidantes/farmacologia
Calcogênios/farmacologia
Citotoxinas/farmacologia
Desenho de Drogas
Norepinefrina/farmacologia
Compostos Organosselênicos/farmacologia
[Mh] Termos MeSH secundário: Antioxidantes/síntese química
Antioxidantes/química
Apoptose/efeitos dos fármacos
Proliferação Celular/efeitos dos fármacos
Calcogênios/química
Citotoxinas/síntese química
Citotoxinas/química
Células HeLa
Seres Humanos
Norepinefrina/química
Compostos Organosselênicos/síntese química
Compostos Organosselênicos/química
Estresse Oxidativo/efeitos dos fármacos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antioxidants); 0 (Chalcogens); 0 (Cytotoxins); 0 (Organoselenium Compounds); X4W3ENH1CV (Norepinephrine)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170808
[Lr] Data última revisão:
170808
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161116
[St] Status:MEDLINE


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[PMID]:27598123
[Au] Autor:Groh MF; Wolff A; Grasser MA; Ruck M
[Ad] Endereço:Department of Chemistry and Food Chemistry, Technische Universität Dresden, 01062 Dresden, Germany. matthias.groh@chemie.tu-dresden.de.
[Ti] Título:Controlled Synthesis of Polyions of Heavy Main-Group Elements in Ionic Liquids.
[So] Source:Int J Mol Sci;17(9), 2016 Sep 01.
[Is] ISSN:1422-0067
[Cp] País de publicação:Switzerland
[La] Idioma:eng
[Ab] Resumo:Ionic liquids (ILs) have been proven to be valuable reaction media for the synthesis of inorganic materials among an abundance of other applications in different fields of chemistry. Up to now, the syntheses have remained mostly "black boxes"; and researchers have to resort to trial-and-error in order to establish a new synthetic route to a specific compound. This review comprises decisive reaction parameters and techniques for the directed synthesis of polyions of heavy main-group elements (fourth period and beyond) in ILs. Several families of compounds are presented ranging from polyhalides over carbonyl complexes and selenidostannates to homo and heteropolycations.
[Mh] Termos MeSH primário: Líquidos Iônicos/química
Poliaminas/química
Polímeros/química
[Mh] Termos MeSH secundário: Calcogênios/química
Halogênios/química
Poliaminas/síntese química
Polímeros/síntese química
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Chalcogens); 0 (Halogens); 0 (Ionic Liquids); 0 (Polyamines); 0 (Polymers); 0 (polyanions); 0 (polycations)
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170323
[Lr] Data última revisão:
170323
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160907
[St] Status:MEDLINE


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[PMID]:27583775
[Au] Autor:Novak S; Lin PT; Li C; Borodinov N; Han Z; Monmeyran C; Patel N; Du Q; Malinowski M; Fathpour S; Lumdee C; Xu C; Kik PG; Deng W; Hu J; Agarwal A; Luzinov I; Richardson K
[Ad] Endereço:Department of Materials Science and Engineering, Clemson University; spencen@g.clemson.edu.
[Ti] Título:Electrospray Deposition of Uniform Thickness Ge23Sb7S70 and As40S60 Chalcogenide Glass Films.
[So] Source:J Vis Exp;(114), 2016 Aug 19.
[Is] ISSN:1940-087X
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Solution-based electrospray film deposition, which is compatible with continuous, roll-to-roll processing, is applied to chalcogenide glasses. Two chalcogenide compositions are demonstrated: Ge23Sb7S70 and As40S60, which have both been studied extensively for planar mid-infrared (mid-IR) microphotonic devices. In this approach, uniform thickness films are fabricated through the use of computer numerical controlled (CNC) motion. Chalcogenide glass (ChG) is written over the substrate by a single nozzle along a serpentine path. Films were subjected to a series of heat treatments between 100 °C and 200 °C under vacuum to drive off residual solvent and densify the films. Based on transmission Fourier transform infrared (FTIR) spectroscopy and surface roughness measurements, both compositions were found to be suitable for the fabrication of planar devices operating in the mid-IR region. Residual solvent removal was found to be much quicker for the As40S60 film as compared to Ge23Sb7S70. Based on the advantages of electrospray, direct printing of a gradient refractive index (GRIN) mid-IR transparent coating is envisioned, given the difference in refractive index of the two compositions in this study.
[Mh] Termos MeSH primário: Antimônio/química
Arsenicais/química
Calcogênios/química
Germânio/química
Vidro/química
Espectroscopia de Infravermelho com Transformada de Fourier/métodos
Compostos de Enxofre/química
[Mh] Termos MeSH secundário: Aerossóis/química
Refratometria
Análise Espectral Raman
Difração de Raios X
[Pt] Tipo de publicação:JOURNAL ARTICLE; VIDEO-AUDIO MEDIA
[Nm] Nome de substância:
0 (Aerosols); 0 (Arsenicals); 0 (Chalcogens); 0 (Sulfur Compounds); 00072J7XWS (Germanium); 9IT35J3UV3 (Antimony)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170721
[Lr] Data última revisão:
170721
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160902
[St] Status:MEDLINE
[do] DOI:10.3791/54379



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