Search results for " Chemical"

showing 4 items of 14084 documents

Photoluminescence properties of S2 molecule trapped in Melanophlogite

2015

We studied the photoluminescence properties of a sample of SiO2-clathrate Melanophlogite, a crystalline microporous material which is found in nature as a rare mineral. Upon β irradiation, the material displays an intense light emission under near-UV illumination. We studied in detail this optical activity by steady-state and time-resolved photoluminescence measurements as a function of temperature. The spectroscopic properties we find can be ascribed to a population of quasi-free molecules trapped within each of the two different types of cage available in the structure of this clathrate, although the spectroscopic properties of the guest molecules are affected by their interactions with t…

β IrradiationPhotoluminescenceClathrate hydratePopulation02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesGeochemistry and PetrologyMoleculeGeneral Materials ScienceClathrateeducationPhotoluminescenceeducation.field_of_studyS2 moleculeChemistryMicroporous material021001 nanoscience & nanotechnology0104 chemical sciencesChemical physicsMelanophlogiteMelanophlogiteExcited stateengineeringLight emissionMaterials Science (all)Atomic physics0210 nano-technology
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Desymmetrization of Prochiral Cyclobutanones via Nitrogen Insertion: A Concise Route to Chiral γ‐Lactams

2021

Abstract Asymmetric access to γ‐lactams is achieved via a cyclobutanone ring expansion using widely available (1S,2R)‐1‐amino‐2‐indanol for chiral induction. Mechanistic analysis of the key N,O‐ketal rearrangement reveals a Curtin–Hammett scenario, which enables a downstream stereoinduction (up to 88:12 dr) and is corroborated by spectroscopic, crystallographic, and computational studies. In combination with an easy deprotection protocol, this operationally simple sequence allows the synthesis of a range of optically pure γ‐lactams, including those bearing all‐carbon quaternary stereocenters. In addition, the formal synthesis of drug molecules baclofen, brivaracetam, and pregabalin further …

γ-lactamsChiral auxiliary010405 organic chemistryChemistryasymmetric synthesisEnantioselective synthesisCyclobutanoneGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciencesCombinatorial chemistryDesymmetrizationCatalysis0104 chemical sciencesStereocenterdesymmetrizationFormal synthesischemistry.chemical_compoundMoleculecyclobutanoneResearch ArticlesResearch ArticleAsymmetric Synthesis | Hot PaperAngewandte Chemie International Edition
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The Use of Stable Isotope Ratio Analysis to Trace European Sea Bass (D. labrax) Originating from Different Farming Systems

2020

This study aimed to determine whether isotopic ratio mass spectrometry (IRMS) can discriminate farmed European sea bass according to different farming systems and geographic origins. Dicentrarchus labrax of commercial size from three different rearing systems (concrete tank inland, sea cages, and extensive methods in valleys or salt works) were collected at the trading period (autumn&ndash

δ18Ostable isotopesgeographic origin01 natural sciencesArticle0404 agricultural biotechnologyAquacultureSettore AGR/20 - Zoocolturelcsh:ZoologyDicentrarchus labrax<i>Dicentrarchus labrax</i>lcsh:QL1-991Settore BIO/06 - Anatomia Comparata E CitologiaSea bassIsotope-ratio mass spectrometryaquaculture; Dicentrarchus labrax; stable isotopes; traceability; farming system; geographic origin; IRMS; sea bass; fish; authenticationfishaquaculture Dicentrarchus labrax stable isotopes traceability farming system geographic origin IRMS sea bass fish authenticationlcsh:Veterinary medicineGeneral Veterinaryδ13CbiologyStable isotope ratiobusiness.industry010401 analytical chemistry04 agricultural and veterinary sciencesδ15NIRMSbiology.organism_classification040401 food science0104 chemical sciencesFisherytraceabilityaquaculturelcsh:SF600-1100authenticationEnvironmental sciencefarming systemAnimal Science and ZoologyDicentrarchusbusinesssea bassAnimals
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Crystal structures of 4-chloro-pyridine-2-carbo-nitrile and 6-chloro-pyridine-2-carbo-nitrile exhibit different inter-molecular π-stacking, C-H⋯Nnitr…

2015

The crystal structures of two chloro­cyano­pyridines, namely 4-chloro­pyridine-2-carbo­nitrile and 6-chloro­pyridine-2-carbo­nitrile, exhibit unique inter­molecular C—H⋯Nnitrile, C—H⋯Npyridine and offset face-to-face π-stacking inter­actions.

π-stackingC—H...N interactionscrystal structureNitrileStereochemistrySubstituentStackingSolid-stateCrystal structureC—H⋯N inter­actions010402 general chemistryRing (chemistry)01 natural sciencesResearch Communicationschlorocyanopyridinechemistry.chemical_compoundPyridineGeneral Materials ScienceCrystallography010405 organic chemistryGeneral ChemistryCondensed Matter Physics0104 chemical sciences3. Good healthchloro­cyano­pyridineCrystallographychemistryQD901-999Acta crystallographica. Section E, Crystallographic communications
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