Search results for "Hydrazone"

showing 10 items of 62 documents

Synthesis, X-ray structure, Hirshfeld analysis, and DFT studies of a new Pd(II) complex with an anionic s-triazine NNO donor ligand

2020

Abstract A new Pd(II) complex, [Pd(Triaz)Cl], with the hydrazono-s-triazine ligand, 2,4-di-tert-butyl-6-((2-(4-morpholino-6-(phenylamino)-1,3,5-triazin-2-yl)hydrazono)methyl)phenol (HTriaz), was synthesized by the reaction of PdCl2 with the organic ligand (1:1) in acetone under isothermal conditions. The molecular structure of the [Pd(Triaz)Cl] complex was determined using FTIR and 1H NMR spectroscopic techniques, and single-crystal X-ray diffraction. Moreover, using Hirshfeld surface analysis, the percentages of the intermolecular interactions were determined. The obtained values were 60.6%, 11.6%, 8.1%, 3.6%, and 5.0% for the H⋯H, C⋯H, O⋯H, N⋯H, and Cl⋯H interactions, respectively. Among …

chemistry.chemical_classification010405 organic chemistryChemistryLigandOrganic ChemistryIntermolecular forceHydrazone010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryCrystallographychemistry.chemical_compoundElectron transferProton NMRMoleculeSpectroscopyTriazineNatural bond orbitalJournal of Molecular Structure
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Competitive NH···Ru/Fe Hydrogen Bonding in Ferrocenyl Ruthenocenyl Tosyl Hydrazone

2016

A strong nonclassical NH···Fe intramolecular hydrogen bond (IHB) is present in the literature-known diferrocenyl tosyl hydrazone (1). Here, we confirm by NMR and IR spectroscopy as well as by XRD methods that an analogous NH···Ru IHB is present in the heavier homologue diruthenocenyl tosyl hydrazone (2). The NH···Ru IHB in 2 is stronger than the NH···Fe IHB in 1 by 6 kJ mol–1, as determined by IR spectroscopy. Further, we probed the E/Z isomer directing abilities of NH···M IHBs in the synthesis of the mixed metallocenyl compound ferrocenyl ruthenocenyl tosyl hydrazone (3). 3 is obtained as a mixture of the Z and E isomers (3a,b) with NH···Ru and NH···Fe IHBs, respectively. At 111 °C, 3a is …

chemistry.chemical_classification010405 organic chemistryHydrogen bondOrganic ChemistryInfrared spectroscopyHydrazone010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundTosylchemistryIntramolecular forcePhysical and Theoretical ChemistryOrganometallics
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Predominance of 2-arylhydrazones of 1,3-diphenylpropane-1,2,3-trione over its proton-transfer products

2001

2-Phenylhydrazones of 1,3-diphenyl-1,2,3-trione are the dominant tautomeric form detected in chloroform solution by 15N NMR chemical shifts. The substituent in the phenylhydrazone moiety does not affect this tautomeric preference. The substituent effect is transmitted effectively only to the hydrazone nitrogen and hydrogen atoms. Ab initio calculations show that the ketohydrazone tautomer is really very much favoured over its proton-transfer products in chloroform solution. The same tautomer was also detected in the crystal state by X-ray crystallography. Copyright © 2001 John Wiley & Sons, Ltd.

chemistry.chemical_classificationChloroformHydrogen bondChemical shiftOrganic ChemistrySubstituentHydrazoneTautomerchemistry.chemical_compoundchemistryComputational chemistryAb initio quantum chemistry methodsMoietyPhysical and Theoretical ChemistryJournal of Physical Organic Chemistry
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ChemInform Abstract: Gold(I)-Catalyzed Intermolecular Cycloaddition of Allenamides with α,β-Unsaturated Hydrazones: Efficient Access to Highly Substi…

2015

α,β-Unsaturated N,N-dialkyl hydrazones undergo a mild [2 + 2] cycloaddition to allenamides when treated with a suitable gold catalyst. The method, which represents the first application of N,N-dialkyl hydrazones in gold catalysis, is compatible with a wide variety of substituents at the alkenyl moiety of the hydrazone component, proceeds with excellent levels of regio- and diastereoselectivity, and provides densely substituted cyclobutanes with good to excellent yields.

chemistry.chemical_classificationCyclobutaneschemistryIntermolecular forceHydrazoneMoietyGeneral MedicineMedicinal chemistryCycloadditionCatalysisChemInform
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Method for determination of formaldehyde in air in the pptv-range by HPLC after extraction as 2,4-dinitrophenyl-hydrazone

1982

The derivatization of formaldehyde with 2,4-dinitrophenylhydrazine and the extraction of the product formalhydrazone is studied. The determination is carried out by HPLC. Applying a cryogenic sampling technique and a sampling volume of 300l of air the detection limit of formaldehyde in air is 30 pptv and this is suitable for measurements of formaldehyde in the atmosphere. (IFU)

chemistry.chemical_classificationDetection limitChromatographyChemistryClinical BiochemistryExtraction (chemistry)FormaldehydeHydrazoneGeneral MedicineHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundGeneral Materials ScienceDinitrophenylDerivatizationFresenius' Zeitschrift für analytische Chemie
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Diferrocenyl tosyl hydrazone with an ultrastrong NHFe hydrogen bond as double click switch.

2014

The intramolecular NH⋯Fe hydrogen bond in diferrocenyl hydrazone 2 raises the barrier for intramolecular electron transfer in its mixed-valent cation 2+ and is only disrupted by double oxidation to 22+.

chemistry.chemical_classificationHydrogen bondMetals and AlloysHydrazoneGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferchemistryTosylIntramolecular forceMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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The synthesis of thienocycloheptenoindoles

1984

A synthesis of the methylthieno[3,2-c]cyclohepteno[b]indole 7 from 2-methylthieno[3,2-b]cycloheptanone 3 is described. Unsuccessful attempts to prepare the isomeric thienocycloheptenoindole system present in formula 2, from the dihydrobenzothiophenone 8, and from derivatives of 5-(2-thienyl)-4-oxopentanoic acid, 17 and 18, and from N-benzylcycloheptindol-1-one 22 were unsuccessful. The preparation of 4,5-dihydro-2-phenyl-1-thienylmethyl-3H-pyridazin-3-one 20 and of the 5-aminopyrazole 21 are reported.

chemistry.chemical_classificationIndole testchemistry.chemical_compoundchemistryOrganic ChemistryOrganic chemistryHydrazoneCycloheptanoneJournal of Heterocyclic Chemistry
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A novel mixed valent Cu(II)-Cu(I) 2D framework made of a hydrazone and μ-SCN bridged metallacyclic loops cross-linked by μ3-SCN chains.

2012

A mixed valent copper complex [Cu(II)Cu(I)(L)(μ-SCN)(μ(3)-SCN)](n) (LH = N'-((pyridin-2-yl)methylene)acetohydrazide) has been synthesized and characterized. It is a unique example of a 2D mixed valent Cu(II)-Cu(I) interlinked molecular assembly with a very unusual bridging property of the hydrazone ligand. An extraordinary in situ partial Cu(II)→ Cu(I) reduction is observed in this system at room temperature.

chemistry.chemical_classificationIonsCopper complexStereochemistryPyridinesHydrazonesMolecular ConformationTemperatureHydrazoneCrystallography X-RayLigandsInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMixed valentCoordination ComplexesHydrazone ligandMethyleneCopperDalton transactions (Cambridge, England : 2003)
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Five-to-Six Membered Ring-rearrangements in the Reaction of 5-Perfluoroalkyl-1,2,4-oxadiazoles with Hydrazine and Methylhydrazine

2006

The hydrazinolysis reaction of 5-perfluoroalkyl-1,2,4-oxadiazoles with hydrazine or methylhydrazine as bidentate nucleophiles has been investigated. The reaction occurred through the addition of the bidentate nucleophile to the C(5)-N(4) double bond of the 1,2,4-oxadiazole followed by ring-opening and ring-closure (ANRORC) involving the second nucleophilic site of the reagent. This ring-closure step could involve either the original C(3) of the 1,2,4-oxadiazole (giving a five-to-five membered ring rearrangement) or an additional electrophilic center linked to it (exploiting a five-to-six membered ring rearrangement). An alternative initial nucleophilic attack may involve the additional elec…

chemistry.chemical_classificationMethylhydrazineKetoneDouble bondChemistryStereochemistryTRANSFORMATIONS15N-NMR SPECTROSCOPYCHEMICAL SHIFT CALCULATIONSOrganic ChemistryFLUORINATED HETEROCYCLIC-COMPOUNDSHydrazoneRegioselectivityBKR REARRANGEMENTRing (chemistry)EXPEDIENT ROUTEMOLECULAR-REARRANGEMENTSNucleophileAROMATICITY INDEXElectrophileATTACKFIVE TO SIX REAGGANGEMENT
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On the Dichotomic Behavior of the Z-2,4-Dinitrophenylhydrazone of 5-Amino-3-benzoyl-1,2,4-oxadiazole with Acids in Toluene and in Dioxane/Water:  Rea…

2004

The mononuclear rearrangement (MRH) of the Z-2,4-dinitrophenylhydrazone (4a) and of the Z-phenylhydrazone (4b) of 5-amino-3-benzoyl-1,2,4-oxadiazole into the relevant triazoles 5a and 5b in toluene has been quantitatively investigated in the presence of trichloroacetic acid (TCA) and of piperidine at 313.1 K. While the behavior in the presence of piperidine recalls the one previously evidenced for some Z-hydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole, the study of the reactivity in the presence of TCA has most interestingly evidenced a general-acid-catalyzed rearrangement for “both” 4a and 4b. Thus, 4a offers the first example of a solvent-dependent dichotomic behavior in MRH processes o…

chemistry.chemical_classificationReaction mechanismOrganic Chemistryacid catalysiOxadiazoleHydrazoneMedicinal chemistryToluenechemistry.chemical_compoundHydrolysisAcid catalysischemistryOrganic chemistrymononuclear rearrangement of heterocycleReactivity (chemistry)Piperidinebase catalysisThe Journal of Organic Chemistry
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