Search results for "ROS"

showing 10 items of 59694 documents

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
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

Cis versus Trans: The Coordination Environment about the Tin(IV) Atom in Spirocyclic Amino Alcohol Derivatives.

2018

The syntheses of amino alcohols MeN(CH2 CH2 CMe2 OH)2 (1), MeN(CMe2 CH2 OH)(CH2 CMe2 OH) (2), MeN(CH2 CH2 CH2 OH)(CH2 CMe2 OH) (3), MeN(CH2 CH2 CMe2 OH)(CH2 CMe2 OH) (4), MeN(CH2 CH2 CMe2 OH)(CH2 CH2 OH) (5), and MeN(CH2 CH2 OH) (CH2 CH2 CH2 OH) (6) as well as spirocyclic tin(IV) alkoxides spiro-[nBuN(CH2 CMe2 O)2 ]2 Sn (7), spiro-[MeN(CH2 CH2 CMe2 O)2 ]2 Sn (8), spiro-[para-FC6 H4 N (CH2 CMe2 O)2 ]2 Sn (9), spiro-[MeN(CMe2 CH2 O)(CH2 CMe2 O)]2 Sn (10), spiro-[MeN(CH2 CH2 CH2 O)(CH2 CMe2 O)]2 Sn (11), spiro-[MeN(CH2 CH2 CMe2 O)(CH2 CMe2 O)]2 Sn (12), spiro-[MeN(CH2 CH2 CMe2 O)(CH2 CH2 O)]2 Sn (13) and spiro-[MeN(CH2 CH2 O)(CH2 CH2 CH2 O)]2 Sn (14) are reported. The compounds were characteri…

010405 organic chemistryOrganic Chemistrychemistry.chemical_elementInfrared spectroscopyAlcoholGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryAtomTinChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

2020

Teraryl-based alpha-helix mimetics have resulted in efficient inhibitors of protein-protein interactions (PPIs). Extending the concept to even longer oligoarene systems would allow for the mimicking of even larger interaction sites. We present a highly efficient synthetic modular access to quateraryl alpha-helix mimetics, in which, at first, two phenols undergo electrooxidative dehydrogenative cross-coupling. The resulting 4,4′-biphenol is then activated by conversion to nonaflates, which serve as leaving groups for iterative Pd-catalyzed Suzuki-cross-coupling reactions with suitably substituted pyridine boronic acids. This work, for the first time, demonstrates the synthetic efficiency of …

010405 organic chemistryPeptidomimetic010402 general chemistryElectrosynthesis01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesProtein–protein interactionCatalysischemistry.chemical_compoundchemistryPyridinePhenolsPhysical and Theoretical ChemistryTrifluoromethanesulfonateAlpha helixCatalysts
researchProduct

Electrosynthesis and X‐ray Crystallographic Structure of Zn II meso ‐Triaryltriphenylphosphonium Porphyrin and Structural Comparison with Mg II meso …

2018

010405 organic chemistryPhosphorusX-raychemistry.chemical_elementCrystal structure010402 general chemistryElectrosynthesis01 natural sciencesPorphyrin0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryEuropean Journal of Inorganic Chemistry
researchProduct

[Bis(phosphonio)isophosphindolide]silver complexes

1996

The outcome of reactions of bis(phosphonio)isophosphindolide salts 1[X] and 6[X] (X- Cl-, Br-, CF3SO3-) with silver salts AgY (Y- = CF3SO3-, CF3CO2-, CH3CO2-, 1/2 SO4-) depends strongly on the available anions X, Y. If X-, Y- CF3SO3-, both mononuclear and dinuclear silver complexes are formed which exhibit either μ1,μ1(P) or μ2,η1(P) coordination of the cations 1, 6 to one or to both metals. In solution, dynamic equilibria between both types of products and free 1, 6 were detected by 31P-NMR spectroscopy. Mononuclear (4a, 7) and dinuclear (5a, 8) complexes were isolated as solvates with CHCl3 or THF. If X-, Y- = CF3CO2, only equilibrium mixtures between the free ligands and silver complexes…

010405 organic chemistryPrecipitation (chemistry)ChemistryStereochemistryBridging ligand010402 general chemistryMetathesis01 natural sciences0104 chemical sciencesIonInorganic ChemistrySilver saltsCrystallographyMoleculeSpectroscopySingle crystal
researchProduct

Substitution of the laser borane anti-B18H22 with pyridine: a structural and photophysical study of some unusually structured macropolyhedral boron h…

2018

Reaction of anti-B18H221 with pyridine in neutral solvents gives sparingly soluble B16H18-3',8'-Py23a as the major product (ca. 53%) and B18H20-6',9'-Py22 (ca. 15%) as the minor product, with small quantities of B18H20-8'-Py 4 (ca. 1%) also being formed. The three new compounds 2, 3a and 4 are characterized by single-crystal X-ray diffraction analyses and by multinuclear multiple-resonance NMR spectroscopy. Compound 2 is of ten-vertex nido:ten-vertex arachno two-atoms-in-common architecture, long postulated for a species with borons-only cluster constitution, but previously elusive. Compound 3a is of unprecedented ten-vertex nido:eight-vertex arachno two-atoms-in-common architecture. The si…

010405 organic chemistryQuantum yieldNuclear magnetic resonance spectroscopyBorane010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographysymbols.namesakechemistryPyridinesymbolsPicolinevan der Waals forcePhosphorescenceDerivative (chemistry)Dalton Transactions
researchProduct

Cathodic Corrosion of Metal Electrodes—How to Prevent It in Electroorganic Synthesis

2021

The critical aspects of the corrosion of metal electrodes in cathodic reductions are covered. We discuss the involved mechanisms including alloying with alkali metals, cathodic etching in aqueous and aprotic media, and formation of metal hydrides and organometallics. Successful approaches that have been implemented to suppress cathodic corrosion are reviewed. We present several examples from electroorganic synthesis where the clever use of alloys instead of soft neat heavy metals and the application of protective cationic additives have allowed to successfully exploit these materials as cathodes. Because of the high overpotential for the hydrogen evolution reaction, such cathodes can contri…

010405 organic chemistrySide reactionchemistry.chemical_elementReviewGeneral ChemistryOverpotential010402 general chemistryElectrochemistryElectrosynthesis01 natural sciences0104 chemical sciencesCorrosionCathodic protectionMetalchemistryChemical engineeringvisual_artvisual_art.visual_art_mediumPlatinumChemical Reviews
researchProduct