Search results for "Chloroform"

showing 10 items of 414 documents

Biphenyl derivatives containing trimethylsilyl benzyl ether or oxime groups as probes for NO2 detection

2016

[EN] Four probes based in the use of a biphenyl moiety and functionalized with trimethylsilyl benzyl ether (P1 and P3) and oxime (P2 and P4) groups have been prepared and tested as optical probes for the detection of NO2. Reaction of NO2 with acetonitrile solutions of P2-P4 resulted in the formation of aldehydes 7 and 8 with a concomitant redshift of the absorption bands. Probe P2 displayed a bathochromic shift of 45 nm upon reaction with NO2 and was able to detect this poisonous gas at concentrations as low as 0.02 ppm. P2 was highly selective against NO2 and other gases (i.e. NO, CO2, H2S, SO2) and vapours of organic solvents (i.e. acetone, hexane, chloroform, acetonitrile or toluene) had…

BiphenylChloroformTrimethylsilyl010405 organic chemistryGeneral Chemical EngineeringQUIMICA INORGANICAGeneral Chemistry010402 general chemistryOxime01 natural sciencesMedicinal chemistryToluene0104 chemical scienceschemistry.chemical_compoundQUIMICA ORGANICAchemistryBathochromic shiftOrganic chemistryMoietyAcetonitrile
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Griffonianone D, an isoflavone with anti-inflammatory activity from the root bark of Millettia griffoniana.

2003

A new isoflavone, griffonianone D (1), and the previously known compounds durmillone and odorantin were isolated from a chloroform extract of the root bark of Millettia griffoniana. The structure of 1 was established as (7E)-(6",7"-dihydroxy-3",7"-dimethyloct-2"-enyl)oxy-4'-methoxyisoflavone on the basis of its spectral data. The chloroform extract of the root bark of M. griffoniana and compound 1 showed anti-inflammatory effects in different experimental models of inflammation.

Blood Plateletsmedicine.drug_classFlavonoidPharmaceutical SciencePlant RootsAnti-inflammatoryMillettiaPhospholipases AAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryBotanymedicineLeukocytesAnimalsEdemaHumansCameroonSpectral dataNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationFlavonoidsChloroformPlants MedicinalTraditional medicinebiologyMolecular StructureOrganic ChemistryAnti-Inflammatory Agents Non-SteroidalGriffonianone DEarStereoisomerismbiology.organism_classificationIsoflavonesMillettiaRatsPhospholipases AComplementary and alternative medicinechemistryProstaglandin-Endoperoxide Synthasesvisual_artvisual_art.visual_art_mediumPlant BarkMolecular MedicineBarkJournal of natural products
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Soil Carbon, Nitrogen and Phosphorus Dynamics as Affected by Solarization Alone or Combined with Organic Amendment

2006

Soil solarization, alone or combined with organic amendment, is an increasingly attractive approach for managing soil-borne plant pathogens in agricultural soils. Even though it consists in a relatively mild heating treatment, the increased soil temperature may strongly affect soil microbial processes and nutrients dynamics. This study aimed to investigate the impact of solarization, either with or without addition of farmyard manure, in soil dynamics of various C, N and P pools. Changes in total C, N and P contents and in some functionally-related labile pools (soil microbial biomass C and N, K2SO4-extractable C and N, basal respiration, KCl-exchangeable ammonium and nitrate, and water-sol…

ChemistrySoil organic matterSoil biologySettore AGR/13 - Chimica AgrariaBulk soilfood and beveragesSoil ScienceSoil solarizationPlant Sciencecomplex mixturesManureHumusSoil managementAgronomySoil fertilitychloroform fumigation–extraction labile N microbial biomass organic amendment soil organic matter soil solarization water-soluble PPlant and Soil
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Synthesis, solution behaviour and potential anticancer activity of new trinuclear organometallic palladium(II) complex of S-1-phenylethyl dithiooxami…

2019

Abstract Addition of H2R2DTO (R = {S}-1-phenylethyl and DTO = dithiooxamide) to the bis(benzonitrile)palladium(II) chloride complex in chloroform afforded the mononuclear Pd(DTO)2·2HCl complex. The complex treated with NaHCO3 for removing of HCl and then reacted with [Pd(ƞ3-allyl)(µ-Cl)]2 for preparation of a new trimetallic organopalladium(II) complex. The molecular structure of the trimetallic complex was determined by X-ray diffraction indicating a planar geometry around each palladium center. Also, variable temperature spectroscopy for this complex was performed in CDCl3 in the range 298–390 K, and simulations of the dynamic spectra were performed using the gNMR program. A comparison be…

Chloroform010405 organic chemistryChemistryTrinuclear organometallic complex anticancer activity platinum palladium proteasome cathepsin.chemistry.chemical_element010402 general chemistry01 natural sciencesChlorideMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundBenzonitrileDithiooxamideOrganopalladiumMaterials ChemistrymedicineMoleculePhysical and Theoretical ChemistryPlatinummedicine.drugPalladium
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Cd(II) and Cu(II) coordination polymers constructed from the expanded 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene ligand: conventional and ultrasound-…

2018

Shaabani, Behrouz/0000-0001-5576-4604; Kubicki, Maciej/0000-0001-7202-9169; Grzeskiewicz, Anita M./0000-0003-0377-2260 WOS: 000447971700041 A 3D open inorganic/organic framework, {[Cd(mu-L)(mu(3)-SO4)(H2O)]center dot H2O}(n) (1) [L = 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene] was synthesized by the reaction of CdSO4 center dot 8H(2)O with L. The treatment of Cu(NO3)(2)center dot 3H(2)O with the same N,N'-donor ligand in two different solvent mixtures, methanol/ dichloromethane (2) and methanol/ chloroform (3), afforded two new ladder-like coordination polymers of formula {[Cu(mu-L)(mu-NO3)(NO3)]center dot solv}(n) [solv = CH2Cl2 (2) and CHCl3 (3)]. The non-interpenetrated ladder motifs 2 a…

Chloroform010405 organic chemistryLigand13-ButadieneGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSolventchemistry.chemical_compoundCrystallographychemistryMaterials ChemistryMoleculeLuminescenceDichloromethane
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Coordination self-assembly through weak interactions in meso-dialkoxyphosphoryl-substituted zinc porphyrinates.

2019

International audience; The self-assembly of seven zinc 10-(dialkoxyphosphoryl)-5,15-diarylporphyrinates Zn5-Zn11 containing different substituents at the phosphonate and aryl groups was investigated. Single crystals of Zn5-Zn9 complexes were grown under the same conditions and analyzed by X-ray structural analysis. A supramolecular self-assembly is observed in all crystals through weak coordinative bonding of the phosphoryl group of one porphyrin molecule to the zinc(II) ion of a second porphyrin molecule. The geometry of the porphyrin macrocycle is similar in all of the studied crystals and the central zinc atom in each case adopts a distorted tetragonal pyramidal environment. However, th…

Chloroform010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryArylSupramolecular chemistrychemistry.chemical_elementZinc010402 general chemistry01 natural sciencesPorphyrinToluene0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistrySelf-assemblyDalton transactions (Cambridge, England : 2003)
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Ab initio calculations and vibrational spectroscopy on the phenylenediamine isomers

1998

Molecular orbital calculations at HF and MP2 levels have been performed using the 6-3IG** basis set for full geometry optimization of the phenylenediamine isomers. Our results show that only a transoid conformer is found for o-phenylenediamine, whereas cis and trans conformers exist for m- and p-phenylenediamine. Vibrational normal modes have been also analyzed for the gas phase and in chloroform solution, and compared with experimental data we have obtained using FTIR spectroscopy. © 1998 Elsevier Science B.V.

ChloroformChemistryInfrared spectroscopyCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundAb initio quantum chemistry methodsComputational chemistryPhysical chemistryFTIR spectroscopy Geometry optimization Vibrational mode analysisMolecular orbitalPhysical and Theoretical ChemistryFourier transform infrared spectroscopyConformational isomerismCis–trans isomerismBasis set
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Crystal structure of t-Butylcalix[8]arene octamethyl ether

2002

Abstract The title compound 1a crystallized with a molecule of chloroform in a triclinic lattice, space group P-1, with a=16.5215(19) A, b=17.4181(19) A, c=18.7403(18) A, α=78.328(8)°, β=64.210(8)°, γ=87.863(9)°, Z=2. The molecule assumes a not yet observed conformation with approximate (not crystallographic) C4V-symmetry with the inclusion of one molecule of chloroform in the molecular cavity. Layers of molecules are packed in alternating order in the crystal lattice.

ChloroformChemistryOrganic ChemistryEtherGeneral ChemistryCrystal structureTriclinic crystal systemInorganic Chemistrychemistry.chemical_compoundCrystallographyLattice (order)CalixareneMaterials ChemistryMoleculeJournal of Supramolecular Chemistry
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Synthesis and spectroscopic investigations (IR, NMR and Mössbauer) of tin(IV) and organotin(IV) derivatives of bis(pyrazol-1-yl) alkanes: X-ray cryst…

1995

A series of 1:1 adducts of the type [(L)R(n)SnX(4-n)] . zH(2)O (L = bis(4-methylpyrazol-1-yl)methane (L(4)), bis(3,4,5-trimethylpyrazol-1-yl)methane (L(T)), 1,2-bis(pyrazol-1-yl)ethane (L(A)) or 1,2-bis(3,5-dimethylpyrazol-1-yl)ethane (L(B)); R = Me, Et, Bu or Ph; X = I, Br or Cl; n = 0, 1 or 2; z = 1, 1.5 or 2), and the likely polynuclear [(L(A))(5)(SnCl4)(4)] . (H2O)(5) and [(L(B))(2)(SnCl4)(3)] . 1/2[Et(2)O] have been characterized in the solid state and in solution by analyses, spectral (IR, Mossbauer, and H-1, C-13 and Sn-119 NMR) data and conductivity measurements. When L(T) reacts with SnCl4, cleavage of a carbon (sp(3))-nitrogen bond was observed and the adduct [(3,4,5-trimethylpyra…

ChloroformChemistryOrganic ChemistryInorganic chemistryHexacoordinateInfrared spectroscopychemistry.chemical_elementCrystal structurePyrazoleBiochemistryMedicinal chemistryAdductInorganic ChemistryBond lengthchemistry.chemical_compoundMaterials ChemistryPhysical and Theoretical ChemistryTinJournal of Organometallic Chemistry
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Synthesis and electrochemical study of a new doubly-metallated compound with the ferrocene-labelled phosphine PPh2(C5H4)Fe(C5H5)

1993

Abstract Direct reaction of the metalled compound Rh 2 (μ 2 -O 2 CCH 3 ) 3 [μ 2 -(C 6 H 4 ) PPh 2 ]·(H 2 O) 2 with PPh 2 Fc [Fc = (C 5 H 4 )Fe(C 5 H 5 )] in chloroform solution yields the corresponding mono-adduct Rh 2 (O 2 CCH 3 ) 3 [(C 6 H 4 )PPh 2 ]·(PPh 2 Fc) ( 1 ), which has been characterized by 31 P NMR spectroscopy. Photochemical irradiation of 1 in chloroform gives the compound Rh 2 (μ-O 2 CCH 3 ) 2 (η 2 -O 2 CCH 3 )[μ 2 -(C 6 H 4 )PPh 2 ][PPh 2 Fc]·(H 2 O) ( 2 ) in practically quantitative yield. Compound 2 , by thermal treatment in chloroform solution, yields cleanly the doubly-metallated compound Rh 2 (μ 2 -O 2 CCH 3 ) 2 [μ 2 -(C 6 H 4 )PPhFc][μ 2 -(C 6 H 4 )PPh 2 ]·(H 2 O) 2 ( …

ChloroformChemistryStereochemistryNuclear magnetic resonance spectroscopyElectrochemistryMedicinal chemistryAdductInorganic Chemistrychemistry.chemical_compoundFerroceneMaterials ChemistryPhysical and Theoretical ChemistryCyclic voltammetryMetallocenePhosphinePolyhedron
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