Search results for "40"

showing 10 items of 17345 documents

Alkali Blues: Blue‐Emissive Alkali Metal Pyrrolates

2019

2-Iminopyrroles [HtBu L, 4-tert-butyl phenyl(pyrrol-2-ylmethylene)amine] are non-fluorescent π systems. However, they display blue fluorescence after deprotonation with alkali metal bases in the solid state and in solution at room temperature. In the solid state, the alkali metal 2-imino pyrrolates, M(tBu L), aggregate to dimers, [M(tBu L)(NCR)]2 (M=Li, R=CH3 , CH(CH3 )CNH2 ), or polymers, [M(tBu L)]n (M=Na, K). In solution (solv=CH3 CN, DMSO, THF, and toluene), solvated, uncharged monomeric species M(tBu L)(solv)m with N,N'-chelated alkali metal ions are present. Due to the electron-rich pyrrolate and the electron-poor arylimino moiety, the M(tBu L) chromophore possesses a low-energy intra…

010405 organic chemistryOrganic ChemistryGeneral ChemistryChromophore010402 general chemistryAlkali metal01 natural sciencesMedicinal chemistryCatalysis0104 chemical scienceschemistry.chemical_compoundMonomerDeprotonationchemistryIntramolecular forceExcited stateMoietyAmine gas treatingChemistry – A European Journal
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N-Acyl-glutarimides: Effect of Glutarimide Ring on the Structures of Fully Perpendicular Twisted Amides and N–C Bond Cross-Coupling

2020

N-Acyl-glutarimides have emerged as the most reactive precursors for N-C(O) bond cross-coupling reactions to date, wherein the reactivity is driven by ground-state destabilization of the amide bond. Herein, we report a full study on the effect of a glutarimide ring on the structures, electronic properties, and reactivity of fully perpendicular N-acyl-glutarimide amides. Most notably, this report demonstrates the generality of deploying N-acyl-glutarimides to achieve full twist of the acyclic amide bond, and results in the discovery of N-acyl-glutarimide amide with an almost perfect twist value, τ = 89.1°. X-ray structures of five new N-acyl-glutarimides are reported. Reactivity studies in t…

010405 organic chemistryOrganic ChemistryGlutarimide010402 general chemistryRing (chemistry)01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundchemistryAmideReagentPerpendicularPeptide bondReactivity (chemistry)TwistThe Journal of Organic Chemistry
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A Phenylene-Bridged Cyclohexa-meta-phenylene as Hexa-peri-hexabenzocoronene Precursor.

2018

A phenylene-bridged cyclohexa-meta-phenylene was synthesized via intramolecular Yamamoto coupling of an appropriate p-quinquephenyl derivative carrying four m-chlorophenyl substituents. The structural proof could be obtained by single-crystal X-ray diffraction analysis, which also revealed a slightly strained structure with an internal phenylene bridge. Notably, this cyclo-meta-phenylene served as a novel precursor for hexa-peri-hexabenzocoronene (HBC). The cyclodehydrogenation proceeded smoothly, providing the corresponding HBC derivative as confirmed by MALDI-TOF-MS, and UV/Vis spectroscopy.

010405 organic chemistryOrganic ChemistryHexa-peri-hexabenzocoroneneGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryPhenyleneIntramolecular forcePolymer chemistrySpectroscopyDerivative (chemistry)Chemistry (Weinheim an der Bergstrasse, Germany)
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N-Cobaltocenium Amide as Reactive Nucleophilic Reagent for Donor–Acceptor Bimetallocenes

2017

Deprotonation of the aminocobaltocenium ion [Cc-NH2]+ ([H-1]+) generates the nucleophilic imine CcNH (1). Reaction of 1 with acid chlorides R–COCl (R = Ph, Fc, and Cc+) yields the reference amide [Ph-CO-NH-Cc]+ (2+) and the amide-linked hetero- and homobimetallocenes [Fc-CO-NH-Cc]+ (3+) and [Cc-CO-NH-Cc]2+ (42+), respectively. Cation–anion interactions of charged amides 2+–42+ in the solid state and in solution are probed by single crystal X-ray diffraction and NMR and IR spectroscopy. Intramolecular metal–metal interactions in donor–acceptor heterobimetallocene 3+ and in mixed-valent homobimetallocene 4+ (prepared electrochemically) are discussed within the Marcus–Hush framework aided by s…

010405 organic chemistryOrganic ChemistryImineInfrared spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistryNucleophileIntramolecular forceReagentAmideDensity functional theoryPhysical and Theoretical ChemistryOrganometallics
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Size‐Selective Encapsulation of Hydrophobic Guests by Self‐Assembled M 4 L 6 Cobalt and Nickel Cages

2012

Subtle differences in metal-ligand bond lengths between a series of [M(4)L(6)](4-) tetrahedral cages, where M = Fe(II), Co(II), or Ni(II), were observed to result in substantial differences in affinity for hydrophobic guests in water. Changing the metal ion from iron(II) to cobalt(II) or nickel(II) increases the size of the interior cavity of the cage and allows encapsulation of larger guest molecules. NMR spectroscopy was used to study the recognition properties of the iron(II) and cobalt(II) cages towards small hydrophobic guests in water, and single-crystal X-ray diffraction was used to study the solid-state complexes of the iron(II) and nickel(II) cages.

010405 organic chemistryOrganic ChemistryInorganic chemistrySupramolecular chemistrychemistry.chemical_elementmacromolecular substancesGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesMetalBond lengthCrystallographyNickelchemistryTransition metalvisual_artvisual_art.visual_art_mediumMoleculeta116CobaltChemistry – A European Journal
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Synthesis, crystal structure, DFT and biological activity of E-pyrene-1-carbaldehyde oxime and E-2-naphthaldehyde oxime

2020

Abstract The aldoximes E-pyrene-1-carbaldehyde oxime 1 and E-2-naphthaldehyde oxime 2 were synthesized, in ca. 90% yield, by treatment of pyrene-1-carbaldehyde or 2-naphthaldehyde, respectively, with hydroxylamine hydrochloride and sodium carbonate in MeOH. Compounds 1 and 2 were characterized by IR, 1H and 13C{1H} NMR spectroscopies, elemental analyses and single crystal X-ray diffraction (in the case of 1). The studied system (compound 1) showed significant amounts of H⋯H (44.4%), C⋯H (25.4%) and C⋯C (13.3%) intermolecular interactions in addition to the short N⋯H (5.9%) and O⋯H (6.2%) intermolecular interactions. These interactions affect the molecular packing of the studied system in th…

010405 organic chemistryOrganic ChemistryIntermolecular forceCrystal structure010402 general chemistryOxime01 natural sciencesMedicinal chemistry0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystalchemistry.chemical_compoundchemistryYield (chemistry)PyreneSodium carbonateSingle crystalSpectroscopyJournal of Molecular Structure
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Supramolecular assemblies and photophysical properties of ionic homo- and heteronuclear metallophilic complexes

2019

Abstract The synthesis of two dinuclear ionic complexes with chemical formula [Au(PR 3 ) 2 ][Au(C ≡ CC 5 H 4 N-4) 2 ] that contain the water soluble phosphines, PR 3 , PTA (1, 3,5-triaza-7-phosphaadamantane, 1 ) and DAPTA (3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane, 2 ) is herein described. The differences on their intermolecular reorganization have been analyzed and compared with the previously reported for the neutral complexes [Au(PR 3 )(C ≡ CC 5 H 4 N-4)]. It has been evidenced that the reorganization of the ligands giving rise to the dinuclear ionic complexes produces a complete change in the properties giving rise to Au⋯Au intermolecular assemblies. These aurophilic conta…

010405 organic chemistryOrganic ChemistryIntermolecular forceSupramolecular chemistryIonic bondingOr010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryHeteronuclear moleculeHexafluorophosphateCompostos d'orMaterials ChemistryGoldPhysical and Theoretical ChemistryNonaneLuminescenceTrifluoromethanesulfonateGold compounds
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Corrosion inhibition performance of a structurally well-defined 1,2,3-triazole derivative on mild steel-hydrochloric acid interface

2021

Abstract In the present work, a new 1,4-disubstituted-1,2,3-triazole product, named 4-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-morpholine (MPTM) was successfully synthesized under click chemistry regime. The structure of the new compound that has a rigid triazole moiety and a flexible morpholine ligand has been characterized using 1H NMR, 13C NMR, HRMS, and FTIR spectroscopy. Its inhibition performance for mild steel in acidic medium 1 M HCl has been studied by utilizing a combination of experimental, spectroscopic and computational methods. The electrochemical characterization was carried out by a gravimetric study, electrochemical impedance spectroscopy (EIS), and potentiodynam…

010405 organic chemistryOrganic ChemistryLangmuir adsorption modelCarbon-13 NMR010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryDielectric spectroscopyInorganic Chemistrysymbols.namesakechemistry.chemical_compoundAdsorptionchemistryMorpholinesymbolsProton NMRFourier transform infrared spectroscopySpectroscopyDerivative (chemistry)Nuclear chemistryJournal of Molecular Structure
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A new polyketide from the bark of Hypericum roeperianum Schimp. (Hypericaceae)

2019

The isolation and spectroscopic data of a hitherto undescribed polyketide (1) from Hypericum roeperianum Schimp. (Hypericaceae) together with six known compounds (2–7) is herein reported. The struc...

010405 organic chemistryOrganic ChemistryPlant ScienceBiologyHypericaceaebiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistry010404 medicinal & biomolecular chemistryPolyketideHypericum roeperianumvisual_artBotanyvisual_art.visual_art_mediumBarkNatural Product Research
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A metal-free and regioselective approach to (Z)-β-fluorovinyl sulfones and their chemoselective hydrogenation to β-fluoroalkyl sulfones

2018

Abstract A highly regioselective, metal-free hydrofluorination reaction of alkynyl sulfones was developed using TBAF—one of the cheapest and most commonly available fluoride sources. In addition, the reactivity of the resulting β-fluorovinyl sulfones was studied, focusing on their selective hydrogenation reaction. Both β-fluorovinyl sulfones and their hydrogenation products β-fluoroalkyl sulfones may find applications in medicinal and agrochemical sciences.

010405 organic chemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryHydrogenation reactionEnvironmental ChemistryOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryFluorideJournal of Fluorine Chemistry
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