Search results for "Molecule"

showing 10 items of 5162 documents

Methyl 3',4',5'-trimethoxybiphenyl-4-carboxylate

2013

In the title compound, C17H18O5, the dihedral angle between the benzene rings is 31.23 (16)°. In the crystal, the mol­ecules are packed in an anti­parallel fashion in layers along the a axis. In each layer, very weak C-H...O hydrogen bonds occur between the meth­oxy and methyl ester groups. Weak C-H...[pi] inter­actions between the 4'- and 5'-meth­oxy groups and neighbouring benzene rings [meth­oxy-C-ring centroid distances = 4.075 and 3.486 Å, respectively] connect the layers.

röntgendiffraktiocrystal structuredendrimeeriprekursorikiderakenneDihedral angle010402 general chemistry010403 inorganic & nuclear chemistryAntiparallel (biochemistry)01 natural sciencesOrganic PapersCrystalchemistry.chemical_compoundMoleculeGeneral Materials ScienceCarboxylateBenzeneta116ChemistryHydrogen bondGeneral ChemistryCondensed Matter Physics3. Good health0104 chemical sciencesX-ray diffractionCrystallographydendrimer precursorSingle crystal
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Formation, Structural Characterization, and Calculated NMR Chemical Shifts of Selenium-Nitrogen Compounds from SeCl4 and ArNHLi (Ar = supermesityl, m…

2004

Supermesityl selenium diimide [Se{N(C6H2tBu3-2, 4, 6)}2; Se{N(mes*)}2] can be prepared in a good yield from the reaction of SeCl4 and (mes*)NHLi. The molecule adopts an unprecedented anti, anti-conformation, as deduced by DFT calculations at PBE0/TZVP level of theory and supported by 77Se NMR spectroscopy and a crystal structure determination. An analogous reaction involving (C6H2Me3-2, 4, 6)NHLi [(mes)NHLi] unexpectedly lead to the reduction of selenium and afforded the selenium diamide Se{NH(mes)}2 that was characterized by X-ray crystallography and 77Se NMR spectroscopy. The Se-N bonds of 1.847(3) and 1.852(3) A show normal single bond lengths. The <NSeN bond angle of 109.9(1)° also indi…

seleeni(II) diamiditselenium(IV) diimidesselenium(II) diamidesChemistryHydrogen bondStereochemistryChemical shiftNuclear magnetic resonance spectroscopyCrystal structureInorganic ChemistryCrystallographychemistry.chemical_compoundseleeni(IV) di-imiditMolecular geometryDiimideSingle bondMolecule
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Influence of a Thiolate Chemical Layer on GaAs (100) Biofunctionalization: An Original Approach Coupling Atomic Force Microscopy and Mass Spectrometr…

2013

International audience; Widely used in microelectronics and optoelectronics; Gallium Arsenide (GaAs) is a III-V crystal with several interesting properties for microsystem and biosensor applications. Among these; its piezoelectric properties and the ability to directly biofunctionalize the bare surface, offer an opportunity to combine a highly sensitive transducer with a specific bio-interface; which are the two essential parts of a biosensor. To optimize the biorecognition part; it is necessary to control protein coverage and the binding affinity of the protein layer on the GaAs surface. In this paper; we investigate the potential of a specific chemical interface composed of thiolate molec…

self-assembled thiolate monolayersMaterials scienceAnalytical chemistryproteins grafting02 engineering and technology010402 general chemistryMass spectrometrylcsh:Technology01 natural sciencesArticleGallium arsenideGaAs; self-assembled thiolate monolayers; proteins grafting; AFM; MALDI-TOF MSchemistry.chemical_compoundMonolayerMALDI-TOF MSMoleculeMicroelectronicsGeneral Materials Science[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronicslcsh:Microscopylcsh:QC120-168.85lcsh:QH201-278.5lcsh:Tbusiness.industryGaAs021001 nanoscience & nanotechnology0104 chemical sciencesMatrix-assisted laser desorption/ionizationchemistryChemical engineeringlcsh:TA1-2040Docking (molecular)lcsh:Descriptive and experimental mechanics[ SPI.NANO ] Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronicslcsh:Electrical engineering. Electronics. Nuclear engineeringAFMlcsh:Engineering (General). Civil engineering (General)0210 nano-technologybusinesslcsh:TK1-9971BiosensorMaterials
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Optical hybrid nanocomposite sensors for selective explosive detection

2022

Durant l'última dècada, la detecció d'artefactes explosius improvisats (IEDs) tant en l'àmbit militar com civil s'ha convertit en una prioritat estratègica en la seguretat nacional a causa de la creixent amenaça terrorista. Encara que les tècniques convencionals, com la cromatografia de gasos acoblada a espectrometria de masses o la difracció de raigs X mostren notables avantatges degut a la seua elevada sensibilitat i selectivitat, una gran part d’aquestes presenten inconvenients, com per exemple processos de mesura lents, instrumentació cara, complexa i voluminosa, que limiten el mostreig en continu i en temps real. Per aquesta raó, existeix una recerca constant per trobar una plataforma …

silver nanoparticlesUNESCO::QUÍMICA::Química analítica::Espectroscopía de infrarrojosnanocompositeperovskite nanocrystalsUNESCO::QUÍMICA::Química inorgánicatemplate moleculequantum dotsmolecularly imprinted polymergas sensor3-nitrotoluenemultichannelsensorexplosive taggantlsprfluorescenceUNESCO::QUÍMICA::Química analítica::Análisis cromatográficoUNESCO::QUÍMICA::Química analítica::Espectroscopía de emisiónUNESCO::QUÍMICA::Química analítica::Análisis de polímeros
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Electronic Structures and Molecular Properties of Chalcogen Nitrides Se2N2 and SeSN2

2006

The electronic structures and molecular properties of S2N2 as well as the currently unknown chalcogen nitrides Se2N2 and SeSN2 have been studied using various ab initio and density functional methods. All molecules share a qualitatively similar electronic structure and can be primarily described as 2π-electron aromatics having minor singlet diradical character of 6−8% that can be attributed solely to the nitrogen atoms. This diradical character is manifested in the prediction of their molecular properties, in which coupled cluster and multiconfigurational approaches, as well as density functional methods, show the best performance. The conventional ab initio methods RHF and MP2 completely f…

singletti diradikaaliChemistryDiradicalChemical shiftAb initioE2N2General MedicineElectronic structureMolecular physicssinglet diradicalsymbols.namesakeCoupled clusterChemical physicssymbolsMoleculeSinglet statePhysical and Theoretical ChemistryRaman spectroscopy
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Carbon Monoxide Activation by a Molecular Aluminium Imide: C−O Bond Cleavage and C−C Bond Formation

2020

Anionic molecular imide complexes of aluminium are accessible via a rational synthetic approach involving the reactions of organo azides with a potassium aluminyl reagent. In the case of K 2 [( NON )Al(NDipp)] 2 ( NON = 4,5‐bis(2,6‐di iso propylanilido)‐2,7‐di‐tert‐butyl‐9,9‐dimethyl‐xanthene; Dipp = 2,6‐di iso propylphenyl) structural characterization by X‐ray crystallography reveals a short Al‐N distance, which is thought to be due primarily to the low coordinate nature of the nitrogen centre. The Al‐N unit is highly polar, and capable of the activation of relatively inert chemical bonds, such as those found in dihydrogen and carbon monoxide. In the case of CO, uptake of two molecules of …

small molecule activation010405 organic chemistryaluminiumkompleksiyhdisteetGeneral Medicine010402 general chemistry01 natural sciencescarbon monoxide3. Good health0104 chemical sciencesaktivointiimidealuminylalumiinihiilimonoksidiAngewandte Chemie
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Addition of Ethylene or Hydrogen to a Main-Group Metal Cluster under Mild Conditions

2015

Reaction of the tin cluster Sn8(Arinline image)4 (Arinline image=C6H2-2,6-(C6H3-2,4,6-Me3)2) with excess ethylene or dihydrogen at 25 °C/1 atmosphere yielded two new clusters that incorporated ethylene or hydrogen. The reaction with ethylene yielded Sn4(Arinline image)4(C2H2)5 that contained five ethylene moieties bridging four aryl substituted tin atoms and one tin–tin bond. Reaction with H2 produced a cyclic tin species of formula (Sn(H)Arinline image)4, which could also be synthesized by the reaction of {(Arinline image)Sn(μ-Cl)}2 with DIBAL-H. These reactions represent the first instances of direct reactions of isolable main-group clusters with ethylene or hydrogen under mild conditions…

small molecule activationEthyleneHydrogenInorganic chemistrychemistry.chemical_elementInfrared spectroscopyCatalysisetyleeniklusteritchemistry.chemical_compoundtinPolymer chemistryCluster (physics)ethyleneclustersta116ArylmetalliklusteritGeneral ChemistryGeneral MedicinechemistryMain group elementvetyhydrogenpienmolekyylien aktivointiDensity functional theorytinaTinAngewandte Chemie
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Trapping and Reactivity of a Molecular Aluminium Oxide Ion

2019

Aluminium oxides constitute an important class of inorganic compound that are widely exploited in the chemical industry as catalysts and catalyst supports. Due to the tendency for such systems to aggregate via Al‐O‐Al bridges, the synthesis of well‐defined, soluble, molecular models for these materials is challenging. Here we show that reactions of the potassium aluminyl complex K 2 [( NON )Al] 2 ( NON = 4,5‐bis(2,6‐diiso‐propylanilido)‐2,7‐di‐tert‐butyl‐9,9‐dimethylxanthene) with CO 2 , PhNCO and N 2 O all proceed via a common aluminium oxide intermediate. This highly reactive species can be trapped by coordination of a THF molecule as the anionic oxide complex [( NON )AlO(THF)] ‐ , which …

small molecule activationOxidereduction010402 general chemistry01 natural sciencesHeterolysisCatalysischemistry.chemical_compoundPolymer chemistryMoleculeReactivity (chemistry)alumiiniBond cleavageAluminium oxides010405 organic chemistryaluminiumpelkistysGeneral MedicineGeneral Chemistrykompleksiyhdisteet0104 chemical sciencesHyponitritechemistryoksiditAluminium oxidealuminyloxide
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Synthesis, characterization, and reactivity of heavier group 13 and 14 metallylenes and metalloid clusters : small molecule activation and more

2015

small molecule activationkemiallinen synteesipienmolekyylitsynthesispuolimetallitmolekyylitmain group chemistrylaskennallinen kemiacomputational chemistrykemialliset sidoksetmetalloid clustersmetallylenesnanohiukkasetröntgenkristallografiaX-ray crystallography
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Low‐Valent Germanylidene Anions: Efficient Single‐Site Nucleophiles for Activation of Small Molecules

2021

Abstract Rare mononuclear and helical chain low‐valent germanylidene anions supported by cyclic (alkyl)(amino)carbene and hypermetallyl ligands were synthesised by stepwise reduction from corresponding germylene precursors via stable and isolable germanium radicals. The electronic structures of the anions can be described with ylidene and ylidone resonance forms with the Ge−C π‐electrons capable of binding even weak electrophiles. The germanylidene anions reacted with CO2 to give μ‐CO2‐κC:κO complexes, a rare coordination mode for low‐valent germanium and inaccessible for the related neutral germylones. These results implicate low‐valent germanylidene anions as efficient single‐site nucleop…

small molecule activationkemialliset yhdisteetdonor-acceptor systemsRadical010402 general chemistry01 natural sciencesMedicinal chemistryCatalysischemistry.chemical_compoundsub-valent compoundsNucleophilemain group elementsAlkylchemistry.chemical_classificationkemialliset reaktiot010405 organic chemistryChemistryCommunicationOrganic ChemistrymolekyylitGeneral ChemistryResonance (chemistry)Small moleculeCommunications0104 chemical sciences3. Good healthgermaniumaktivointiMain group elementElectrophileCarbenevalenssi (kemia)Chemistry – A European Journal
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