Search results for "HDI"

showing 10 items of 789 documents

Catalytic epoxidation using dioxidomolybdenum(VI) complexes with tridentate aminoalcohol phenol ligands

2019

Reaction of the tridentate aminoalcohol phenol ligands 2,4-di-tert-butyl-6-(((2 hydroxyethyl)(methyl)amino)methyl)phenol (H2L1) and 2,4-di-tert-butyl-6-(((1-hydroxybutan-2-yl)amino)methyl)phenol (H2L2) with [MoO2(acac)2] in methanol solutions resulted in the formation of [MoO2(L1)(MeOH)] (1) and [MoO2(L2)(MeOH)] (3), respectively. In contrast, the analogous reactions in acetonitrile afforded the dinuclear complexes [Mo2O2(μ-O)2(L1)2] (2) and [Mo2O2(μ-O)2(L2)2] (4). The corresponding reactions with the potentially tetradentate ligand 3-((3,5-di-tert-butyl-2-hydroxybenzyl)(methyl)amino)propane-1,2-diol (H3L3) led to the formation of the mononuclear complex [MoO2(L3)(MeOH)] (5) in methanol whi…

010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundkatalyytitepoxidationMaterials ChemistryPhenolMoietyPhysical and Theoretical ChemistryHydrogen peroxideAcetonitrileta116010405 organic chemistryLigandmolybdenum complexSubstrate (chemistry)kompleksiyhdisteettrinuclear structure0104 chemical scienceschemistrytridentate ligandMethanolmolybdeeniInorganica Chimica Acta
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Iminium Catalysis (n → π*)

2016

010402 general chemistry01 natural sciencesMedicinal chemistrycatalystsCatalysiskatalyytitepoxidationPi interactioncatalyst turnovertyppiyhdisteetDiels-Alder reactionFriedel–Crafts reactionta116cycloadditionDiels–Alder reactioncatalysis010405 organic chemistryChemistrychiral anionsIminiumnitrogen compoundsCycloaddition0104 chemical sciencesaxially chiral catalystskatalyysicocatalyst
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Interactions of a Diplumbyne with Dinuclear Transition Metal Carbonyls to Afford Metalloplumbylenes

2020

The metathesis reactions of the diplumbyne AriPr6PbPbAriPr6 (AriPr6 = −C6H3–2,6-(C6H2–2,4,6-iPr3)2) with the dinuclear metal carbonyls Mn2(CO)10, Fe2(CO)9, and Co2(CO)8 under mild conditions afforded the complexes Mn(CO)5(PbAriPr6) (1), Fe(CO)4(PbAriPr6)2 (2), and Co4(CO)9(PbAriPr6)2 (3), respectively. Complexes 1–3 were structurally characterized by single-crystal X-ray diffraction and spectroscopically characterized by 1H, 13C{1H}, 59Co{1H}, and 207Pb{1H} NMR; UV–vis; and IR methods. They are rare examples of species formed by the direct reaction of a group 14 dimetallyne with transition metal carbonyls. Complexes 1 and 2 feature Mn–Pb or Fe–Pb single bonds, whereas in 3 a Co–Pb cluster i…

010405 organic chemistryChemistryOrganic ChemistrycarbonylsmetalsMetal carbonylkompleksiyhdisteetorganometalliyhdisteet010402 general chemistry01 natural sciencescobalttransition metals0104 chemical sciencesInorganic ChemistryTransition metalPolymer chemistrySalt metathesis reactionPhysical and Theoretical Chemistrykarbonyylitnuclear magnetic resonance spectroscopy
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Halogen bonds in 2,5-dihalopyridine-copper(II) chloride complexes

2018

Ten coordination complexes obtained through a facile reaction between 2,5-dihalopyridines and copper(II) chloride (CuCl2) are characterized using single crystal X-ray diffraction. Two series of dihalopyridine complexes based on 2-chloro-5-X-pyridine and 2-bromo-5-X-pyridine (X = F, Cl, Br and I) were prepared to analyze the C–X2/X5⋯Cl–Cu halogen bonds (XB). The influence of X2- and X5-substituents on the respective interactions was examined by comparing them to the X2/X3⋯Cl–Cu XBs found in mono-substituted halopyridine complexes, (n-X-pyridine)2·CuCl2 (n = 2, 3 and X = Cl, Br and I). Varying the X5-halogens in (2,5-dihalopyridine)2·CuCl2, the C5–X5⋯Cl–Cu XBs follow the order F5 1 and they c…

010405 organic chemistryChemistrySubstituentchemistry.chemical_elementGeneral Chemistrykompleksiyhdisteet010402 general chemistryCondensed Matter Physics01 natural sciencesChlorideCopperchemical bonds0104 chemical scienceschemistry.chemical_compoundCrystallographykemialliset sidoksetHalogenmedicineCopper(II) chlorideGeneral Materials Sciencecoordination complexesPolarization (electrochemistry)Single crystalta116medicine.drugCrystEngComm
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Effects of Remote Ligand Substituents on the Structures, Spectroscopic, and Magnetic Properties of Two-Coordinate Transition-Metal Thiolate Complexes

2018

The first-row transition-metal(II) dithiolates M(SAriPr4)2 [AriPr4 = C6H3-2,6-(C6H3-2,6-iPr2)2; M = Cr (1), Mn (3), Fe (4), Co (5), Ni (6), and Zn (7)] and Cr(SArMe6)2 [2; ArMe6 = C6H3-2,6-(C6H2-2,4,6-Me3)2] and the ligand-transfer reagent (NaSAriPr4)2 (8) are described. In contrast to their M(SAriPr6)2 (M = Cr, Mn, Fe, Co, Ni, and Zn; AriPr6 = C6H3-2,6-(C6H2-2,4,6-iPr3)2) congeners, which differ from 1 and 3-6 in having p-isopropyl groups on the flanking aryl rings of the terphenyl substituents, compounds 1 and 4-6 display highly bent coordination geometries with S-M-S angles of 109.802(2)° (1), 120.2828(3)° (4), 91.730(3)° (5), and 92.68(2)° (6) as well as relatively close metal-flanking …

010405 organic chemistryLigandligandsArylkompleksiyhdisteetligandit010402 general chemistryRing (chemistry)01 natural sciencesElectron spectroscopy0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryTransition metalCovalent bondvisual_artTerphenylvisual_art.visual_art_mediumcoordination complexesPhysical and Theoretical Chemistryta116
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Enantiomeric Resolution of Asymmetric-Carbon-Free Binuclear Double-Stranded Cobalt(III) Helicates and Their Application as Catalysts in Asymmetric Re…

2018

A series of double-stranded binuclear helicates [Co2(H1)2]4+, [Co2(H2)2]4+, and [Co2(H3)2]4+, derived from monodeprotonated bis-pyridyl hydrazine-based ligands of H21, H22, and H23 with one, two, and three -CH2 spacers, were obtained. These asymmetric-carbon-free racemic helicates were separated into their ΔΔ and ΛΛ enantiomers. The resolved helicates were examined for the first time as enantioselective catalysts in asymmetric benzoylation and nitroaldol reactions.

010405 organic chemistryResolution (electron density)HydrazineEnantioselective synthesischiralitychemistry.chemical_elementkompleksiyhdisteet010402 general chemistry01 natural sciencessupramolecular chemistry0104 chemical sciencesCatalysisInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryAsymmetric carbonsupramolekulaarinen kemiacoordination complexesPhysical and Theoretical ChemistryEnantiomerta116CobaltDouble strandedInorganic Chemistry
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Room-Temperature Phosphorescence and Efficient Singlet Oxygen Production by Cyclometalated Pt(II) Complexes with Aromatic Alkynyl Ligands

2020

The synthesis of five novel cyclometalated platinum(II) compounds containing five different alkynyl-chromophores was achieved by the reaction of the previously synthesized Pt–Cl cyclometalated compound (1) with the corresponding RC≡CH by a Sonogashira reaction. It was observed that the spectral and photophysical characteristics of the cyclometalated platinum(II) complexes (Pt–Ar) are essentially associated with the platinum-cyclometalated unit. Room-temperature emission of the Pt–Ar complexes was attributed to phosphorescence in agreement with DFT calculations. Broad nanosecond (ns)-transient absorption spectra were observed with decays approximately identical to those obtained from the emi…

010405 organic chemistrySinglet oxygenPhosphorescenceluminesenssichemistry.chemical_elementkompleksiyhdisteetorganometalliyhdisteetOxigen010402 general chemistryLigands01 natural sciencesCombinatorial chemistry0104 chemical sciencesInorganic ChemistryOxygenchemistry.chemical_compoundhappiLligandschemistryFosforescènciaPhysical and Theoretical ChemistryPhysics::Chemical PhysicsPhosphorescencePlatinum
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The responses of shoot-root-rhizosphere continuum to simultaneous fertilizer addition, warming, ozone and herbivory in young Scots pine seedlings in …

2017

Abstract It is not clear how climate change in combination with increasing soil nitrogen availability and herbivory affects boreal forests, the largest terrestrial biome in the world. In this study, Scots pine ( Pinus sylvestris ) seedlings were exposed to moderate warming (ca. 1 °C), 1.5 × ambient ozone (O 3 ) concentration, fertilizer addition (120 kg N ha −1 yr −1 ) and shoot herbivory by pine sawfly ( Acantholyda posticalis ) alone and in combination. We measured fine root morphology, mycorrhizal colonization level, root fungal biomass (ergosterol), rhizosphere emission of biogenic volatile organic compounds (BVOCs), and microbial biomass (PLFAs) in the rhizosphere soil as well as seedl…

0106 biological sciences010504 meteorology & atmospheric sciencesField experimentSoil Sciencebiogenic volatile organic compounds (BVOCs)engineering.material01 natural sciencesMicrobiologyectomycorrhizasoil microbesmikrobitorgaaniset yhdisteet0105 earth and related environmental sciencesAbiotic componentmaaperäRhizospherebiologyScots pinegrowth allocationilmastonmuutokset15. Life on landbiology.organism_classificationEctomycorrhizaclimate changegreat web-spinning pine sawflyAgronomy13. Climate actionSeedlingShootengineeringta1181Fertilizer010606 plant biology & botanySoil Biology and Biochemistry
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NIR-absorbing transition metal complexes with redox-active ligands

2020

Bench top stable transition metal (M = Co, Ni, Cu) complexes with a non-innocent ortho-aminophenol derivative were synthesized by the reaction of metal(II)acetates with a ligand precursor in 2:1 ratio. The solid-state structures reveal the formation of neutral molecular complexes with square planar coordination geometries. The Co(II) and Cu(II) complexes are paramagnetic, whereas the Ni complex is a diamagnetic square planar low-spin Ni(II) complex. All complexes, and Ni(II) complex in particular, show strong absorption in the near-IR region. Peer reviewed

02 engineering and technologymetal complexesredox-active ligands010402 general chemistry01 natural sciencesInorganic ChemistryMetalParamagnetismchemistry.chemical_compoundTransition metalinfrapunasäteilyMaterials ChemistryPhysical and Theoretical Chemistrynear-IR absorptionChemistryLigandnon-innocent ligandsliganditkompleksiyhdisteet021001 nanoscience & nanotechnologyNon-innocent ligand0104 chemical sciences3. Good healthabsorptioCrystallographyvisual_artvisual_art.visual_art_mediumDiamagnetismAbsorption (chemistry)0210 nano-technologyDerivative (chemistry)
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Successful aerobic bioremediation of groundwater contaminated with higher chlorinated phenols by indigenous degrader bacteria

2018

The xenobiotic priority pollutant pentachlorophenol has been used as a timber preservative in a polychlorophenol bulk synthesis product containing also tetrachlorophenol and trichlorophenol. Highly soluble chlorophenol salts have leaked into groundwater, causing severe contamination of large aquifers. Natural attenuation of higher-chlorinated phenols (HCPs: pentachlorophenol + tetrachlorophenol) at historically polluted sites has been inefficient, but a 4-year full scale in situ biostimulation of a chlorophenol-contaminated aquifer by circulation and re-infiltration of aerated groundwater was remarkably successful: pentachlorophenol decreased from 400 μg L−1 to <1 μg L−1 and tetrachlorophen…

0301 basic medicine246-TRICHLOROPHENOL DEGRADATIONTrichlorophenolDIVERSITYIn situ bioremediation010501 environmental sciences01 natural sciencesbiologinen puhdistusbakteeritBiostimulationchemistry.chemical_compoundQuantitative PCRpentachlorophenol hydroxylaseGroundwaterWaste Management and DisposalPENTACHLOROPHENOLWater Science and Technology2. Zero hungerpcpB geneEcological ModelingIon PGM amplicon sequencingin situ bioremediationContaminationPollutionAerobiosis6. Clean waterBiodegradation EnvironmentalEnvironmental chemistryPentachlorophenol hydroxylaseChlorophenolsEnvironmental Engineeringta1172030106 microbiologySphingomonas sensu latoMICROBIAL-DEGRADATION03 medical and health sciencesBioremediationbioremediationSPHINGOBIUM-CHLOROPHENOLICUMkloorifenolitta219Microbial biodegradationgeneBOREAL GROUNDWATER1172 Environmental sciences0105 earth and related environmental sciencesCivil and Structural EngineeringChlorophenolpohjavesiBacteriaorganic chemicalsion PGM amplicon sequencingSPHINGOMONADSEVOLUTIONPentachlorophenolSOILSchemistryGenes Bacterial13. Climate actionquantitative PCREnvironmental scienceWater Pollutants ChemicalGroundwater
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