Search results for " organic"

showing 10 items of 5145 documents

Spin Crossover and Long-Lived Excited States in a Reduced Molecular Ruby.

2020

Abstract The chromium(III) complex [CrIII(ddpd)2]3+ (molecular ruby; ddpd=N,N′‐dimethyl‐N,N′‐dipyridine‐2‐yl‐pyridine‐2,6‐diamine) is reduced to the genuine chromium(II) complex [CrII(ddpd)2]2+ with d4 electron configuration. This reduced molecular ruby represents one of the very few chromium(II) complexes showing spin crossover (SCO). The reversible SCO is gradual with T 1/2 around room temperature. The low‐spin and high‐spin chromium(II) isomers exhibit distinct spectroscopic and structural properties (UV/Vis/NIR, IR, EPR spectroscopies, single‐crystal XRD). Excitation of [CrII(ddpd)2]2+ with UV light at 20 and 290 K generates electronically excited states with microsecond lifetimes. This…

step-scan IR spectroscopychemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciencesCatalysislaw.inventionChromiumSpin crossoverlawSpin CrossoverElectron paramagnetic resonanceexcited states010405 organic chemistryChemistryCommunicationOrganic ChemistryGeneral ChemistryCommunications0104 chemical sciencesMicrosecondExcited stateElectron configurationchromiummagnetic propertiesExcitationChemistry (Weinheim an der Bergstrasse, Germany)
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Compared Binding Properties between Resveratrol and Other Polyphenols to Plasmatic Albumin: Consequences for the Health Protecting Effect of Dietary …

2014

International audience; Phytophenols are considered to have beneficial effects towards human physiology. They are food microcomponents with potent chemopreventive properties towards the most three frequent contemporary human diseases, e.g., cardiovascular alterations, cancer and neurodegenerative pathologies. Related to this, the plasmatic form and plasmatic level of plant polyphenols in the body circulation are crucial for their efficiency. Thus, determinations of the binding process of resveratrol and of common flavonoids produced by major edible plants, berries and fruits to plasma proteins are essential. The interactions between resveratrol and albumin, a major plasma protein, were comp…

structural changes[SDV]Life Sciences [q-bio]Pharmaceutical ScienceReviewResveratrolresveratrol01 natural sciencesAnalytical Chemistryquercetinchemistry.chemical_compound[ SDV.BBM.BC ] Life Sciences [q-bio]/Biochemistry Molecular Biology/Biomolecules [q-bio.BM]Resveratrol bindingDrug DiscoveryStilbenesBovine serum albuminComputingMilieux_MISCELLANEOUS0303 health sciencesbiologyfood and beveragesBlood proteins[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biomolecules [q-bio.BM]3. Good healthBiochemistryChemistry (miscellaneous)HealthMolecular MedicinefluorescencePlants EdibleQuercetinSerum albuminlcsh:QD241-44103 medical and health scienceslcsh:Organic chemistryHumans[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biochemistry [q-bio.BM]Physical and Theoretical ChemistryBinding siteSerum Albumin030304 developmental biologyFlavonoidsBinding Sites010405 organic chemistryOrganic ChemistryAlbuminPolyphenols0104 chemical sciencesDietchemistryFoodbiology.proteinaffinityMolecules
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Crystal structure and Hirshfeld surface analysis of [N(CH3)4][2,2′-Fe(1,7-closo-C2B9H11)2]

2017

Abstract This work investigates the meta -ferrabis(dicarbollide) anion that was isolated as salt of tetramethylammonium. The structure of the obtained crystal consisted of discrete [2,2′-Fe(1,7- closo -C 2 B 9 H 11 ) 2 ] − anions and disordered [N(CH 3 ) 4 ] + cations. The anion had a considerable chemical stability ensured by ionic and Van der Waals interactions. Thus, Hirshfeld surfaces and fingerprint plot were used to visualize, explore, and quantify intermolecular interactions in the crystal lattice of the title compound. This investigation proved that close contacts were dominated by H⋯H interactions.

structures: crystalsIonic bondingCrystal structure010402 general chemistrychemistry01 natural sciencesBiochemistryIonInorganic ChemistryCrystalchemistry.chemical_compoundsymbols.namesakeComputational chemistrymeta-carboraneMaterials ChemistryPhysical and Theoretical Chemistryta116x-ray crystallographyTetramethylammoniummetallabis(dicarbollide)010405 organic chemistryOrganic ChemistryIntermolecular forcex-ray technology0104 chemical sciencesCrystallographydihydrogen bondschemistrysymbolsChemical stabilityvan der Waals forceHirshfeld studyJournal of Organometallic Chemistry
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Rola efektu podstawnikowego w sprzężeniu π-elektronowym w N-podstawionym karbazolu

2019

Modyfikacja właściwości optoelektronowych materiałów organicznych w wielu przypadkach sprowadza się do wywołania zmian w ich strukturze elektronowej, a w szczególności w π-elektronowej delokalizacji w obrębie całej molekuły. Dużą uwagę zajmują w tych badaniach układy skondensowane zawierające pierścienie aromatyczne, niearomatyczne oraz hetero atomy. Do układów tych można zaliczyć, między innymi, karbazol i jego pochodne, który znajduje zastosowanie w organicznych materiałach optycznych i elektronowych. W niniejszej publikacji zaprezentowano wyniki z przeprowadzonych badań nad wpływem podstawienia pierścienia fulwenowego na atomie azotu oraz podstawników o zróżnicowanym charakterze elektron…

struktura π-elektronowanowe materiały optoelektroniczne na bazie związków organicznychilościowe indeksy aromatycznościpochodne karbazoluprzerwa energetyczna pomiędzy orbitalami HOMO-LUMO
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Chemical composition of the essential oil of Centaurea grinensis Reuter and Centaurea apiculata Ledeb: Growing wild in Croatia and Bulgaria, respecti…

2016

AbstractIn the present study, the chemical composition of the essential oils from aerial parts of Centaurea grinensis Reuter (K) collected at Žuta Lova, near Senj (Croatia), and aerial parts (L1) and flowers (L2) of C. apiculata Ledeb. collected near Rebro village, near Breznik town, Znepole Region (Bulgaria), both belonging to subgenus Lopholoma (Cass.) Dobrocz, was evaluated by GC and GC-MS. The main components of K were 4-vinyl guaiacol (21.5%), hexadecanoic acid (16.2%), acetophenone (12.5%). Caryophyllene oxide (15.8%) together with sphathulenol (14.5%) and humulene epoxide II (9.4%) were recognized as the main constituent of both the aerial part (L1) and flowers (L2) of C. apiculata. …

subgenus Lopholomacaryophyllene oxidePlant ScienceBiology01 natural scienceslaw.invention4-vinyl guaiacolchemistry.chemical_compoundPlant scienceCentaurea grinensilawBotanyChemical compositionEcology Evolution Behavior and SystematicsEssential oilHumuleneCentaurea apiculata010405 organic chemistrybiology.organism_classificationEcology Evolution Behavior and Systematic0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryCaryophyllene oxideCentaureaSubgenusPCA analysi
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Classical and reverse substituent effects in meta- and para-substituted nitrobenzene derivatives

2017

Electron-accepting properties of the nitro group were studied in a series of meta- and para-X-substituted nitrobenzene derivatives (X = NMe2, NH2, OH, OMe, CH3, H, F, Cl, CF3, CN, CHO, COMe, CONH2, COOH, COCl, NO2, NO). For this purpose Hammett-like approaches were applied based on quantum chemistry modeling; the B3LYP/6-311++ G(d,p) method was used. The substituent effect (SE) was characterized by the mutually interrelated descriptors: the charge of the substituent active region, cSAR(X), and substituent effect stabilization energy, SESE, as well as substituent constants, σ. Classical SE is realized by dependences of the structural parameters of the nitro group (ONO angle and NO bond lengt…

substituent effectsMolecular modelmolecular modeling010405 organic chemistryDinitrobenzeneStereochemistrySubstituentelectronic structure010402 general chemistryCondensed Matter Physics01 natural sciencesQuantum chemistry0104 chemical sciencesNitroanilineBond lengthNitrobenzenechemistry.chemical_compoundchemistrysubstituent effect stabilization energyNitroPhysical and Theoretical Chemistrycharge of the substituent active regionStructural Chemistry
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Substituent effects on the mechanism changeover in a multipathway reaction: A model for the behavior of biological systems?

2009

By studying the rearrangement in dioxane/water of a series of (Z)-arylhydrazones of 5-amino-3- benzoyl-1,2,4-oxadiazole (1a-k) into the relevant (2-aryl-5-phenyl-2H-1,2,3-triazol-4-yl)ureas (2a-k) in a wide range of pS + (an operational scale of proton concentration in the mixed solvent used; dioxane/water, 1:1, v:v), the occurrence of three different reaction pathways (specific-acid- catalyzed, uncatalyzed, and general-base-catalyzed) for the relevant SNi process has been recently enlightened. The significantly different substituent effects on the three pathways cause some crossovers in the log kA,R versus pS + plots. Both the pS + value at which the crossover occurs and the width of the u…

substituents effectbase-catalysiProtonStereochemistryChemistryOrganic ChemistrySubstituentChangeoverSettore CHIM/06 - Chimica OrganicaCatalysisSolventTurn (biochemistry)chemistry.chemical_compoundComputational chemistryMechanism (philosophy)Reactivity (chemistry)mononuclear rearrangement
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1,2,6-Thiadiazine 1-Oxides: Unsaturated Three-Dimensional S,N-Heterocycles from Sulfonimidamides.

2020

Unprecedented three-dimensional 1,2,6-thiadiazine 1-oxides have been prepared by an aza-Michael-addition/cyclization/condensation reaction sequence starting from sulfonimidamides and propargyl ketones. The products have been further functionalized by standard cross-coupling reactions, selective bromination of the heterocyclic ring, and conversion into a β-hydroxy substituted derivative. A representative product was characterized by single-crystal X-ray structure analysis. peerReviewed

sulfonimidamidessingle-crystal X-raybioaktiiviset yhdisteet010405 organic chemistryStereochemistryChemistryOrganic ChemistryOxideHalogenation010402 general chemistryCondensation reaction01 natural sciencesBiochemistryCoupling reaction0104 chemical scienceschemistry.chemical_compoundPropargylPhysical and Theoretical ChemistrySequence (medicine)Organic letters
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Electronic shell structures in bare and protected metal nanoclusters

2016

This short review discusses the concept of the electronic shell structure in the context of metal nanoclusters. Electronic shell structure is a natural consequence of quantization of fermionic states in a quantum confinement, where the symmetry of the confining potential creates energetically close-lying sets of states that reflect the symmetry of the potential. It was introduced in cluster physics in early 1980s and initially influenced greatly by the related model of nuclear shell structure from 1950’s. Three application areas are discussed consisting of free gas phase clusters, clusters supported by insulating oxides or oxide thin films, and clusters that are synthesized by wet chemistry…

superatomligand-stabilized nanoclusterNuclear TheoryShell (structure)General Physics and AstronomyNanotechnologynanoclusterengineering.material010402 general chemistry01 natural sciencesNanoclustersMetalQuantization (physics)Physics::Atomic and Molecular Clustersnoble metalta116ta114simple metal010405 organic chemistryChemistrySuperatom0104 chemical sciencesChemical physicsmagic numbersvisual_artvisual_art.visual_art_mediumengineeringNoble metalAdvances in Physics: X
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Structural Motifs of Alkali Metal Superbases in Non‐coordinating Solvents

2020

Abstract Lochmann–Schlosser superbases (LSB) are a standard reagent in synthetic chemistry to achieve an exchange of a proton on an organic framework with an alkali metal cation, which in turn can be replaced by a wide range of electrophilic groups. In standard examples, the deprotonating reagent consists of an equimolar mixture of n‐butyllithium and potassium t‐butoxide. However, the nature of the reactive species could not be pinned down either for this composition or for similar mixtures with comparable high reactivity. Despite the poor solubility and the fierce reactivity, some insights into this mixture were achieved by some indirect results, comparison with chemically related systems,…

superbasealkali metalschemistry.chemical_element010402 general chemistry01 natural sciencesChemical synthesisCatalysisReactivity (chemistry)Solubility010405 organic chemistrypotassiumOrganic ChemistrySuperbaseaggregationMinireviewsGeneral ChemistryAlkali metalCombinatorial chemistry0104 chemical scienceschemistrylithiumReagentElectrophileLithiumMinireviewOrganometallic Chemistry | Reviews ShowcaseChemistry – A European Journal
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