Search results for "Chemical conversion"

showing 10 items of 12 documents

On the consensus nomenclature rules for radiopharmaceutical chemistry – Reconsideration of radiochemical conversion

2021

Radiochemical conversion is an important term to be included in the "Consensus nomenclature rules for radiopharmaceutical chemistry". Radiochemical conversion should be used to define reaction efficiency by measuring the transformation of components in a crude reaction mixture at a given time, whereas radiochemical yield is better suited to define the efficiency of an entire reaction process including, for example, separation, isolation, filtration, and formulation. (C) 2020 Elsevier Inc. All rights reserved.

Cancer ResearchRadiochemistryNomenclatureRadiochemical conversionChemistryRadiochemistry610 Medicine & health10181 Clinic for Nuclear MedicineTerminology030218 nuclear medicine & medical imagingNuclear chemistryRadiochemical yield03 medical and health sciences0302 clinical medicineddc:5701313 Molecular Medicine030220 oncology & carcinogenesisYield (chemistry)2741 Radiology Nuclear Medicine and ImagingMolecular Medicine1306 Cancer ResearchRadiology Nuclear Medicine and imagingRadiopharmaceutical sciencesConsensus guidelinesNuclear Medicine and Biology
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Electrochemical conversion of carbon dioxide to formic acid: on the road to applicative scale

2018

In this context, electrochemical reduction of CO2 is considered one of the more attractive pathway to convert CO2, because the products can be selectively controlled by changing the operative conditions of the electrolysis. In the last years, an increasing attention has been devoted on the electrochemical conversion of CO2 to formic acid in water [2,3]. The main hurdle of the reduction of CO2 from water solution is the low CO2 solubility in water. In this work, the effect of some operating parameters, including pressure, current density, and flow rate, on the conversion of CO2 at tin flat cathodes to formic acid was studied using a pressurized filter-press cell with a continuous recirculati…

Electrochemical conversion reduction carbon dioxide formic acid tin pressure scale up
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Electrochemical conversion of carbon dioxide: effect of the cell and of the operating parameters on the performances of the process.

2017

Recycling technologies of CO2 allow to introduce renewable energy in the chemical and energy chain, storing a renewable energy in the chemical form. In this context, electrochemical conversion of CO2 is considered one of the more interesting approaches, using excess electric energy from intermittent renewable sources. (1) Furthermore, products can be selectively controlled by changing the operating conditions of electrolysis. In particular, in the last years, an increasing attention has been devoted to the electrochemical conversion of CO2 to formic acid or formate in water. (2,3,4) The main hurdle of the reduction of CO2 from water solution is the low CO2 solubility in water. In this work,…

Electrochemical conversion reduction pressure Sn Formic Acid CO2.
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Controlled solution-based fabrication of perovskite thin films directly on conductive substrate

2021

Abstract Organometallic perovskites are one of the most investigated materials for high-efficiency thin-film devices to convert solar energy and supply energy. In particular, methylammonium lead iodide has been used to realize thin-film perovskite solar cells, achieving an efficiency higher than 20%. Different fabrication procedures based on the spin-coating technique have been proposed, which do not ensure homogenous morphologies. In this work, we present a scalable process to fabricate methylammonium lead iodide thin films directly on conductive substrates, consisting of electrodeposition and two subsequent chemical conversions. A thorough investigation of the morphological, structural an…

FabricationMaterials scienceAbsorption spectroscopyChemical conversion Electrodeposition Organometallic perovskite Solar cell Thin filmIodide02 engineering and technologySubstrate (electronics)01 natural sciences0103 physical sciencesSettore ING-IND/17 - Impianti Industriali MeccaniciMaterials ChemistryThin filmAbsorption (electromagnetic radiation)Perovskite (structure)010302 applied physicschemistry.chemical_classificationbusiness.industrySettore FIS/01 - Fisica SperimentaleMetals and AlloysSurfaces and Interfaces021001 nanoscience & nanotechnologySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSettore ING-IND/23 - Chimica Fisica ApplicatachemistryOptoelectronics0210 nano-technologybusinessLayer (electronics)
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Synthesis of new orthometallated iridium(III) compounds by chemical and electrochemical methods

1987

Abstract Replacement of one phosphine ligand in IrCl 3 (η 2 -PCBr)(η 1 -PCBr) ( 1 ) (PCBr = P( o -BrC 6 F 4 )Ph 2 ), by various P-donor ligands has given compounds of stoichiometry IrCl 3 (η 2 -PCBr)L ( 3 : L = PMePh 2 ; 4 : L = P( p -MeC 6 H 4 ) 3 ; 5 : L = P(OMe) 3 , 6 : L = P(OPh) 3 ). All of these show two irreversible reduction peaks in the range −1.1, −1.3 and ca. −2.0 V. The electrochemical reduction of compound 1 at −1.5 V (at 0°C) leads to a very reactive iridium(I) species, probably IrCl(PCBr) 2 , which undergoes intramolecular orthometallation at room temperature. Three compounds are obtained as the results of this chemical conversion: IrBr 2 (PC)(PCBr) ( 7 ), IrCl 2 (PC)(PCBr) (…

LigandStereochemistryOrganic Chemistrychemistry.chemical_elementElectrochemistryBiochemistryMedicinal chemistryRhodiumInorganic Chemistrychemistry.chemical_compoundchemistryIntramolecular forceChemical conversionMaterials ChemistryIridiumPhysical and Theoretical ChemistryStoichiometryPhosphineJournal of Organometallic Chemistry
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Electrochemical and Spectroelectrochemical Studies of Diphosphorylated Metalloporphyrins. Generation of a Phlorin Anion Product

2015

Two series of diphosphoryl-substituted porphyrins were synthesized and characterized by electrochemistry and spectroelectrochemistry in nonaqueous media containing 0.1 M tetra-n-butylammonium perchlorate (TBAP). The investigated compounds are 5,15-bis(diethoxyphosphoryl)-10,20-diphenylporphyrins (Ph)2(P(O)(OEt)2)2PorM and 5,15-bis(diethoxyphosphoryl)-10,20-di(para-carbomethoxyphenyl)porphyrins (PhCOOMe)2(P(O)(OEt)2)2PorM where M = 2H, Co(II), Ni(II), Cu(II), Zn(II), Cd(II), or Pd(II). The free-base and five metalated porphyrins with nonredox active centers undergo two ring-centered oxidations and two ring-centered reductions, the latter of which is followed by a chemical reaction of the por…

PhotochemistryElectrochemistryMedicinal chemistryPorphyrinChemical reactionIonInorganic ChemistryPerchloratechemistry.chemical_compoundchemistryChemical conversion[CHIM]Chemical SciencesPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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STUDY OF ELECTROCHEMICAL PROCESSES FOR THE CONVERSION OF CARBON DIOXIDE TO ADDED-VALUE PRODUCTS

2020

SilverTinCO2 electrochemical conversionPressureCO2Formic acidSettore ING-IND/27 - Chimica Industriale E TecnologicaCarbon monoxide
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ChemInform Abstract: Synthesis of (+)-Isoalantolactone and (+)-Isoalloalantolactone from (-) -Santonin.

2010

Abstract This paper reports on the chemical conversion of (−)-santonin into (+)-isoalantolactone and (+)-isoalloalantolactone involving functionality transfer from C 6 to C 8 , refunctionalization of the ring A and the formation of the α-methylene-8 β,12-olide moiety.

Terpenechemistry.chemical_compoundChemistryStereochemistryChemical conversionMoietyGeneral MedicineRing (chemistry)SantoninChemInform
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Synthesis of (+)-Isoalantolactone and (+)-Isoalloalantolactone from (−)-Santonin

1992

Abstract This paper reports on the chemical conversion of (−)-santonin into (+)-isoalantolactone and (+)-isoalloalantolactone involving functionality transfer from C 6 to C 8 , refunctionalization of the ring A and the formation of the α-methylene-8 β,12-olide moiety.

chemistry.chemical_classificationStereochemistryOrganic ChemistryRing (chemistry)SesquiterpeneBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryChemical conversionMoietyEnantiomerEnoneLactoneSantoninTetrahedron
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Diels-Alder reactions of 1-phenylpyrano[3,4-b]indol-3-ones with alkynes: New functionalized carbazoles

1990

3-Indolylalkanoic acids 2 react with benzoic acid anhydride under catalysis of Et2O - ZnCl2 and mild conditions to furnish the 1-phenyl-substituted pyrano[3,4-b]indol-3-ones 1c, 1d, and 3a, 3b. Products 1c, 1d, and 3b may be converted into the novel functionalized carbazoles 4 and 5 by reaction with acceptor-substituted alkynes.

chemistry.chemical_compoundchemistryBicyclic moleculeOrganic ChemistryChemical conversionDiels alderOrganic chemistryPhysical and Theoretical ChemistryAliphatic compoundBenzoic acidCatalysisLiebigs Annalen der Chemie
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