Search results for "High selectivity"

showing 6 items of 16 documents

Molecular Sensors for Moisture Detection by Mössbauer Spectroscopy

2002

A parameter of importance in various industrial and commercial applications is sensitivity to moisture. A new class of molecular sensors which enable the qualitative and quantitative determination of air moisture (high selectivity and sensitivity) by application of Mossbauer spectroscopy as the probe technique has been investigated. The electronic properties of the iron-containing sensor depend upon the presence of moisture which is taken up by it and this process is accompanied by a change in electronic spin ground state which can be detected by Mossbauer spectroscopy. The sensor is suitable for in-field and industrial application using the recently developed Mossbauer spectrometer MIMOS I…

MoistureSpectrometerChemistryMolecular sensorHigh selectivityMössbauer spectroscopyAnalytical chemistryElectronic spinSensitivity (control systems)Ground statePhysics::Atmospheric and Oceanic Physics
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Synthesis of hexahydrocyclopenta[ij]isoquinolines as a new class of dopaminergic agents.

2014

In this study, we have described the synthesis of the tricyclic 1,2,3,7,8,8a-hexahydrocyclopenta [ij]isoquinoline (HCPIQ). Herein, six differently substituted 5,6-dioxygenated-7-phenyl-HCPIQs have been synthesized using a new methodology via (E)-1-styryl-THIQ by Friedel-Crafts cyclization with Eaton's reagent. Results showed that HCPIQs (3, 3a-e) displayed a moderate affinity for D1 dopamine receptors (DR) in the micromolar range, furthermore the catecholic HCPIQs 3a (NH), 3c (NCH3) and 3e (NCH2CHCH2) exhibited outstanding affinity and high selectivity towards D2 DR. Indeed, 3a, 3c and 3e showed Ki values of 29 nM, 13 nM and 18 nM, respectively, and HCPIQs 3a (NH) and 3c (NCH3) displayed a …

Pharmacologychemistry.chemical_classificationDose-Response Relationship DrugMolecular StructureChemistryStereochemistryReceptors Dopamine D2Receptors Dopamine D1Organic ChemistryHigh selectivityDopaminergicDopamine AgentsGeneral MedicineIsoquinolineschemistry.chemical_compoundStructure-Activity RelationshipDopamine receptorReagentDrug DiscoveryHumansIsoquinolineCytotoxicitySelectivityTricyclicEuropean journal of medicinal chemistry
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In-beam spectroscopic studies of shape coexistence and collectivity in the neutron-deficientZ≈ 82 nuclei

2016

In the present paper we focus on studies of shape coexistence in even-mass nuclei in the neutron-deficient Pb region. They are based on experiments carried out using tagging techniques in the Accelerator Laboratory of the University of Jyväskylä, Finland. Excited states in many of these nuclei can only be accessed via fusion-evaporation reactions employing high-intensity stable-ion beams. The key features in these experiments are high selectivity, clean spectra and instrumentation that enables high count rates. We review three spectroscopic highlights in this region. peerReviewed

PhysicsNuclear and High Energy Physicsquadrupole momentrecoil distance Doppler-shift method010308 nuclear & particles physicsHigh selectivitydeformationshape coexistenceKey features01 natural sciencesSpectral lineNuclear physicsJUROGAMydinreaktiotExcited state0103 physical sciencesNeutronin-beam γ-ray spectroscopyAtomic physicsNuclear Experiment010306 general physicsBeam (structure)Journal of Physics G: Nuclear and Particle Physics
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Electrochemically triggered iodide-vacancy BiOI film for selective extraction of iodide ion from aqueous solutions

2021

Abstract The effective extraction and regeneration of radioactive iodide remains an urgent concern for safe nuclear energy utilization. Herein, we developed a novel electrochemically triggered iodide-vacancy BiOI film, which exhibited excellent I− ion extraction capacity of 328.3 mg·g−1. Especially, due to the ion vacancy trap effect, the film showed high selectivity towards I− ions in the existence of a large number of competitive anions. Additionally, the electrochemically switched ion extraction (ESIE) process with this iodide-vacancy BiOI film possessed fast extraction kinetics and high stability. More importantly, the trapped I− ions were easily desorbed from the film without the secon…

chemistry.chemical_classificationAqueous solutionChemistryExtraction (chemistry)KineticsHigh selectivityInorganic chemistryIodideFiltration and Separation02 engineering and technologySettore ING-IND/27 - Chimica Industriale E Tecnologica021001 nanoscience & nanotechnologyIodide ions Iodide-vacancy BiOI film Electrochemically switched ion extraction Selective extraction Radioactive waterAnalytical ChemistryIonIodide ion020401 chemical engineeringVacancy defect0204 chemical engineering0210 nano-technology
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Homocalixpyridines: Ligands Exhibiting High Selectivity in Extraction and Sensor Processes

1998

A novel spherical host architecture, based on pyridine subunits, has been created. It exhibits selective complexing properties toward soft metal ions (right), which have been tested in extraction and sensor processes. The complex-forming behaviour can be tailored by variation of the size of the cavity and by substitution. Homocalixpyridines are interesting in view of their application as selective carriers in separation and sensing techniques.

chemistry.chemical_compoundchemistryMolecular modelOrganic ChemistryPyridineHigh selectivitySoft metalInorganic chemistryGeneral ChemistryHost–guest chemistryCombinatorial chemistryCatalysisIonChemistry - A European Journal
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“One Ring to Bind Them All”—Part II: Identification of Promising G-Quadruplex Ligands by Screening of Cyclophane-Type Macrocycles

2010

A collection of 26 polyammonium cyclophane-type macrocycles with a large structural diversity has been screened for G-quadruplex recognition. A two-step selection procedure based on the FRET-melting assay was carried out enabling identification of macrocycles of high affinity (ΔT1/2up to30°C) and high selectivity for the human telomeric G-quadruplex. The four selected hits possess sophisticated architectures, more particularly the presence of a pendant side-arm as well as the existence of a particular topological arrangement appear to be strong determinants of quadruplex binding. These compounds are thus likely to create multiple contacts with the target that may be at the origin of their h…

lcsh:QH426-470Article SubjectHigh selectivityStructural diversityBiology010402 general chemistryRing (chemistry)G-quadruplexBioinformatics01 natural sciencesBiochemistrylcsh:Biochemistry03 medical and health scienceschemistry.chemical_compound[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular Biology[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biologylcsh:QD415-436Molecular Biology030304 developmental biology0303 health sciencesCombinatorial chemistry0104 chemical scienceslcsh:GeneticschemistryIdentification (biology)CyclophaneResearch ArticleJournal of Nucleic Acids
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