Search results for "Phene"

showing 10 items of 863 documents

Haptens, bioconjugates, and antibodies for penthiopyrad immunosensing

2014

4 pages, 1 table, 2 figures.

ImmunoconjugatesSynthetic derivativesbiologyChemistryBiosensing TechniquesThiophenesBiochemistryCombinatorial chemistryAntibodiesAnalytical ChemistryHighly sensitivePenthiopyradElectrochemistrybiology.proteinEnvironmental ChemistryPyrazolesImmunochemical analysisAntibodyHaptenHaptensSpectroscopyFungicides
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Palladium-catalyzed domino C-H/N-H functionalization: an efficient approach to nitrogen-bridged heteroacenes.

2015

Palladium-catalyzed domino C-H/N-H functionalization for the synthesis of novel nitrogen-bridged thienoacenes and 10H-benzo[4,5]thieno[3,2-b]indole derivatives from dihaloarene is reported. This domino sequence consists of initial C-H functionalization of the benzo[b]thiophene moiety, followed by Buchwald-Hartwig coupling. This transformation is also useful for the synthesis of highly π-extended compounds.

Indole testStereochemistryOrganic Chemistrychemistry.chemical_elementGeneral ChemistryMedicinal chemistryCatalysisDominoCatalysischemistry.chemical_compoundchemistryThiopheneMoietySurface modificationAminationPalladiumChemistry (Weinheim an der Bergstrasse, Germany)
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ChemInform Abstract: Palladium-Catalyzed Domino C-H/N-H Functionalization: An Efficient Approach to Nitrogen-Bridged Heteroacenes.

2015

Palladium-catalyzed domino CH/NH functionalization for the synthesis of novel nitrogen-bridged thienoacenes and 10H-benzo[4,5]thieno[3,2-b]indole derivatives from dihaloarene is reported. This domino sequence consists of initial CH functionalization of the benzo[b]thiophene moiety, followed by Buchwald–Hartwig coupling. This transformation is also useful for the synthesis of highly π-extended compounds.

Indole testchemistry.chemical_compoundChemistryThiophenechemistry.chemical_elementMoietySurface modificationGeneral MedicineMedicinal chemistryNitrogenDominoCatalysisPalladiumChemInform
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Spectroscopic and theoretical study of push-pull chromophores containing thiophene-based quinonoid structures as electron spacers

2003

Donor−acceptor chromophores containing three different types of thiophene-based electron spacers and the same donor (1,3-dithiol-2-ylidene) and acceptor (dicyanomethylene) end groups have been investigated by infrared and vis-near-IR absorption spectroscopies with the aim of elucidating the ability of the heteroquinonoid spacers as electron transmitters. Density functional theory calculations have been carried out, both within the standard and the time-dependent formalisms, to assign the most relevant electronic and infrared features of these chromophores and to assess useful information about their molecular structures. Both theoretical calculations and vibrational spectra demonstrate the …

InfraredElectronChromophorePhotochemistryAcceptorSurfaces Coatings and Filmschemistry.chemical_compoundchemistryIntramolecular forceMaterials ChemistryThiopheneDensity functional theoryPhysical and Theoretical ChemistryGround state
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Imidazo[2,1-b] [1,3,4]thiadiazoles with antiproliferative activity against primary and gemcitabine-resistant pancreatic cancer cells

2020

A new series of eighteen imidazo [2,1-b] [1,3,4]thiadiazole derivatives was efficiently synthesized and screened for antiproliferative activity against the National Cancer Institute (NCI-60) cell lines panel. Two out of eighteen derivatives, compounds 12a and 12h, showed remarkably cytotoxic activity with the half maximal inhibitory concentration values (IC50) ranging from 0.23 to 11.4 μM, and 0.29–12.2 μM, respectively. However, two additional compounds, 12b and 13g, displayed remarkable in vitro antiproliferative activity against pancreatic ductal adenocarcinoma (PDAC) cell lines, including immortalized (SUIT-2, Capan-1, Panc-1), primary (PDAC-3) and gemcitabine-resistant (Panc-1R), elici…

Inhibition of migrationAntimetabolites AntineoplasticEpithelial-Mesenchymal Transition3Modulation of EMTPTK2VimentinAntineoplastic AgentsApoptosisThiophenesAntiproliferative activity1-b][1DeoxycytidinePancreatic ductal adenocarcinomaThiadiazolesSDG 3 - Good Health and Well-beingCell MovementPancreatic cancerDrug DiscoveryThiadiazolesmedicineTumor Cells CulturedImidazo[21-b][134]thiadiazole derivativesHumansPTK2/FAKIC50Cell ProliferationImidazo[2Pharmacologybiology4]thiadiazole derivativesChemistryOrganic ChemistryDrug SynergismGeneral Medicinemedicine.diseaseGemcitabinePancreatic NeoplasmsCell cultureDrug Resistance NeoplasmImidazo[21-b][134]thiadiazole derivatives Pancreatic ductal adenocarcinoma Antiproliferative activity Inhibition of migration Spheroids shrinkage Modulation of EMT PTK2/FAKbiology.proteinCancer research/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingPhosphorylationSpheroids shrinkageTyrosine kinaseCarcinoma Pancreatic DuctalEuropean Journal of Medicinal Chemistry
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CO2 and CH2 Adsorption on Copper-Decorated Graphene: Predictions from First Principle Calculations

2022

Calculations were performed using Latvian Super Cluster (LASC), located in Center of Excellence at Institute of Solid State Physics, the University of Latvia, which is supported by European Union Horizon2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under Grant Agreement No. 739508, project CAMART2. The authors would like to express their gratitude for funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 768789 (CO2EXIDE project). In the last stage of investigation and during the preparation of the publication, the authors were assisted by the postdoc D.B. with his own funding from project No. 1.1.1.2/VIAA/l/16/147 (…

Inorganic ChemistryFirst-principles calculationsGeneral Chemical EngineeringCO2 electroreductionGeneral Materials Science:NATURAL SCIENCES::Physics [Research Subject Categories]AdsorptionNanodecorationCondensed Matter Physicsgraphene; nanodecoration; first-principles calculations; adsorption; CO<sub>2</sub> electroreductionGraphen
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Graphene-type sheets of Nb(1-x)W(x)S2: synthesis and in situ functionalization.

2013

Enlightened by the discovery of graphenes, a variety of inorganic analogues have been synthesized and characterized in recent years. Solvated Nb1−xWxS2 analogues of graphene-type sheets were prepared by lithiation and exfoliation of multistacked Nb1−xWxS2 coin roll nanowires (CRNWs), followed by in situ functionalization with gold nanoparticles to synthesize gold-loaded Nb1−xWxS2/Au nanocomposites. The Nb1−xWxS2 nanosheets and the corresponding Nb1−xWxS2/Au nanocomposites were characterized by high resolution electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX), scanning transmission electron microscopy (STEM), dynamic light scattering (DLS) and scanning force microscopy …

Inorganic ChemistryMaterials scienceDynamic light scatteringColloidal goldGraphenelawScanning transmission electron microscopyNanowireNanoparticleNanotechnologyHigh-resolution transmission electron microscopyExfoliation jointlaw.inventionDalton transactions (Cambridge, England : 2003)
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Thiophen—Mangantricarbonyl-Komplexe

1967

Abstract Cationic thiophenemanganese tricabonyl complexes of the formula [C 4 (CH 3 ) x H 4- x S Mn(CO) 3 ] + have been prepared with 2-methyl-, 3-methyl-, 2,5-dimethyl-, 2,3,5-trimethyl-, tetramethylthiophene, and with thiophene by the reaction of Mn(CO) 5 Cl+AlCl 3 or AlBr 3 with the thiophenes in petrol ether, at 100–110°. The complexions give yellow solutions which are fairly stable. Their IR and some NMR spectra are given and discussed.

Inorganic ChemistryNMR spectra databasechemistry.chemical_compoundChemistryOrganic ChemistryMaterials ChemistryCationic polymerizationThiopheneOrganic chemistryEtherPhysical and Theoretical ChemistryBiochemistryMedicinal chemistryJournal of Organometallic Chemistry
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Reactive adsorption of thiophene on Ni/ZnO: role of hydrogen pretreatment and nature of the rate determining step.

2008

Abstract Reactive adsorption of thiophene on reduced and unreduced NiO/ZnO adsorbents was studied by thermal gravimetric analysis and by sulfidation in a fixed bed reactor at 330–375 °C and 10–40 mbar of thiophene in hydrogen. The adsorbents (12 wt% Ni) were prepared by co-precipitation of corresponding nitrates with sodium carbonate followed by calcination at 400 °C. We have found that such solids can react with thiophene without any prior reduction. Metallic Ni, indispensable for thiophene decomposition, is formed in this case in situ upon the contact with thiophene/H 2 reaction mixture. The reduction of NiO/ZnO in H 2 (360 °C, 6 h) results in the formation of Ni–Zn alloyed particles (as …

Inorganic chemistrySulfidation02 engineering and technologyActivation energy010402 general chemistry01 natural sciencesCatalysislaw.inventionCatalysis[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Reaction ratechemistry.chemical_compoundAdsorptionlawThiopheneCalcinationComputingMilieux_MISCELLANEOUSGeneral Environmental ScienceProcess Chemistry and Technology021001 nanoscience & nanotechnologyRate-determining step0104 chemical sciences[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]chemistry13. Climate action[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technology
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Synergetic effect of gold in Au/Pd catalysts during hydrodesulfurization reactions of model compounds

2003

Abstract The simultaneous formation of colloidal dispersions of Pd and Au metal particles protected by the organic polymer polyvinylpyrrolidone (PVP) in reducing alcohol solution was used for the synthesis of new silica-supported monometallic and bimetallic Au x Pd y catalysts with different x / y ratios. The samples, with a 2 wt% total metal loading, after air calcinations at 673 K to remove the PVP, were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and FTIR spectra of chemisorbed CO. Formation of alloyed Au x Pd y particles of different metal composition with consequent modification of their electronic and geometric properties was ascertained. The catalytic activi…

Inorganic chemistrychemistry.chemical_elementCatalysisCatalysisMetalchemistry.chemical_compoundAu-Pd catalysts; Polyvinylpyrrolidone; Hydrodesulfurization; HDS; Thiophene; DibenzothiophenechemistryTransition metalDibenzothiophenevisual_artThiophenevisual_art.visual_art_mediumPhysical and Theoretical ChemistryBimetallic stripHydrodesulfurizationPalladiumJournal of Catalysis
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