Search results for "Pyrazine"

showing 10 items of 325 documents

Ruthenium(II) meso-tetra-(benzo-15-crown-5)-porphyrinates: synthesis and spectroscopic investigation

2007

The synthesis of novel ruthenium(II) meso-tetra-(benzo-15-crown-5)-porphyrinates, meso-[( B 15 C 5)4 Por ] Ru ( CO )( MeOH ) (1) and meso-[( B 15 C 5)4 Por ] Ru ( L )2 (2)-(4) (meso-[( B 15 C 5)4 Por ]2-= 5,10,15,20-tetrakis-(benzo-15-crown-5)-porphyrinato-dianion; L = pyridine (py), pyrazine (pyz), 4,4′-bipyridyl (4,4′-bpy)), where CO and MeOH , or two N -donor ligands are axially coordinated to the central metal, are reported. The metalation of the free ligand performed by the reaction of Ru 3( CO )12 with meso-[( B 15 C 5)4 Por ] H 2 in 1,2,4-trichlorobenzene (TCB, bp = 215°C), gives (1) in a high yield. The synthesis of (2)-(4) involves the decarbonylation of (1) with trimethylamine N …

chemistry.chemical_classificationmetalloporphyrinsPyrazineLigandMetalationInorganic chemistryDecarbonylation[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementGeneral ChemistryMedicinal chemistryRutheniumchemistry.chemical_compoundchemistry15-Crown-5Pyridine[CHIM.COOR]Chemical Sciences/Coordination chemistryrutheniumCrown etherComputingMilieux_MISCELLANEOUS
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Slow Relaxation of the Magnetization in a {Co <sup>III</sup>Mn <sup>III</sup>} Heterometallic Brick-Wall Network

2021

The use of the cyanide-bearing dicobalt(III) complex (PPh 4 ) 2 [Co 2 III (m-2,5-dpp)(CN) 8 ] as a metalloligand towards [Mn(salen)(H 2 O)]ClO 4 afforded the heterobimetallic two-dimensional compound of formula [{Mn III (salen)} 2 {(m-NC) 4 Co 2 III (m-2,5-dpp)(CN) 4 }] n (1) [PPh 4 + = teraphenylphosphonium cation, 2,5-dpp = 2,5-bis(2-pyridyl)pyrazine and H 2 salen = N,N’ -ethylenebis(salicylideneimine)] whose structure has been determined by single crystal X-ray diffraction. Compound 1 exhibits a neutral brick-wall structure, where each [Co 2 III (m-2,5-dpp)(CN) 8 ] 2- unit adopts a tetrakis-monodentate bridging mode towards four {Mn III (salen)} + fragments through four of its eight cyan…

chemistry.chemical_compoundCrystallographyMagnetizationMaterials scienceOctahedronPyrazinechemistryRelaxation (NMR)chemistry.chemical_elementMoleculeManganeseSingle crystalCobaltSSRN Electronic Journal
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Syntheses, crystal structures and magnetic properties of polynuclear 1,4,5,8,9,12-hexaazatriphenylene (hat)-bridged copper(II) complexes

2001

Three polynuclear compounds containing copper(II) and 1,4,5,8,9,12-hexaazatriphenylene (hat) as the basic building blocks have been prepared, [Cu4(hat)2Cl8]n·6nH2O 1, [Cu(hat)(H2O)2]n[NO3]2n2, and [Cu2(hat)(H2O)6]n[SO4]2n·2nH2O 3, their crystal structures determined and variable-temperature magnetic susceptibility data measured. The basic building block in 1 is the dinuclear [Cu2(hat)Cl4] entity, two such units being connected to tetranuclear units through relatively strong axial Cu–Cl bonds (out-of-plane di-μ-chloro bridges). Weaker axial Cu⋯Cl interactions link the units into a sheet structure. In 2 and 3 hat-bridged copper(II) chains extending along glide planes are present. hat serves a…

chemistry.chemical_compoundCrystallographyPyrazinechemistryOctahedronIntramolecular forceAntiferromagnetismchemistry.chemical_elementGeneral ChemistryCrystal structureMagnetic susceptibilityCopperSquare pyramidal molecular geometryJournal of the Chemical Society, Dalton Transactions
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ChemInform Abstract: Diaryldistyrylpyrazines: Solvatochromic and Acidochromic Fluorophores.

2014

Diaryldimethylpyrazines are the starting materials for the synthesis of C2-symmetric donor- or acceptor-substituted distyrylpyrazines. The optical properties of these cruciform-shaped dyes are dominated by the distyrylpyrazine units; the photophysics is controlled by the styryl substitution, the diaryl substituents on the central pyrazine only having a small effect. Protonation occurs on the pyrazine and/or lateral amines or azines, thereby altering the absorption and emission properties. Hypso- and bathochromism as well as fluorescence quenching depend on the nature of the terminal substituent. This, and a significant positive solvatochromism of the fluorescence, allow optical sensing of t…

chemistry.chemical_compoundPyrazinechemistryPolarity (physics)Optical sensingSolvatochromismSubstituentProtonationGeneral MedicineAbsorption (chemistry)PhotochemistryFluorescenceChemInform
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Synthesis of Naturally Occurring Pyrazine and Imidazole Alkaloids from Botryllus LeachiRID=?a?ID=?a? Dedicated to Prof. G . Märkl on the occasion of …

2004

The synthesis of the naturally occurring and biologically active alkaloids 1 and 2, first isolated from the red ascidian Botryllus leachi by Duran et al. [1], is described and the structure proposed for Botryllazine B (1) is confirmed. The analytical data for 2-(p-hydroxybenzoyl)-4-(p-hydroxyphenyl)imidazole (2) are discussed and compared with the literature. With special emphasis of 1H NMR data the tautomerism of aroylimidazolemethanones is described.

chemistry.chemical_compoundbiologychemistryPyrazineStereochemistryBotryllazine BBotryllusImidazoleGeneral Chemistrybiology.organism_classificationTautomerMonatshefte f�r Chemie / Chemical Monthly
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Diaryldistyrylpyrazines: Solvatochromic and Acidochromic Fluorophores

2013

Diaryldimethylpyrazines are the starting materials for the synthesis of C2-symmetric donor- or acceptor-substituted distyrylpyrazines. The optical properties of these cruciform-shaped dyes are dominated by the distyrylpyrazine units; the photophysics is controlled by the styryl substitution, the diaryl substituents on the central pyrazine only having a small effect. Protonation occurs on the pyrazine and/or lateral amines or azines, thereby altering the absorption and emission properties. Hypso- and bathochromism as well as fluorescence quenching depend on the nature of the terminal substituent. This, and a significant positive solvatochromism of the fluorescence, allow optical sensing of t…

chemistry.chemical_compoundchemistryPyrazinePolarity (physics)Optical sensingOrganic ChemistrySolvatochromismSubstituentProtonationPhysical and Theoretical ChemistryAbsorption (chemistry)PhotochemistryFluorescenceEuropean Journal of Organic Chemistry
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Crystal Engineering Studies of the Complexes of Ethyl Resorcinarene with Aromatic Nitrogen Heterocycles

2003

Five X-ray structures of complexes of ethyl resorcinarene with aromatic nitrogen heterocycles (imidazole, 1,2,4-triazole, pyridine, pyrazine, 2-pyridylmethanol and quinoline) show that ethyl resorcinarene spontaneously forms molecular inclusion complexes with five- and six-membered aromatic nitrogen heterocycles via π π and CH π interactions. However, with 10-membered quinoline, no molecular inclusion complex is formed. Instead, quinoline manifests crystal lattice inclusion.

chemistry.chemical_compoundchemistryPyrazinePyridineQuinolineX-ray crystallographyImidazoleOrganic chemistryGeneral ChemistryCrystal structureResorcinareneCrystal engineeringMedicinal chemistrySupramolecular Chemistry
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Bidirectional Chemo-Switching of Spin State in a Microporous Framework

2009

The ins and outs of spin: Using the microporous coordination polymer {Fe(pz)[Pt(CN)(4)]} (1, pz=pyrazine), incorporating spin-crossover subunits, two-directional magnetic chemo-switching is achieved at room temperature. In situ magnetic measurements following guest vapor injection show that most guest molecules transform 1 from the low-spin (LS) state to the high-spin (HS) state, whereas CS(2) uniquely causes the reverse HS-to-LS transition.

chemo-switchingSpin statesPyrazinemicroporous materialsCoordination polymerGeneral ChemistryMicroporous materialCatalysiscoordination polymerschemistry.chemical_compoundCrystallographyspin crossoverchemistrySpin crossoverMoleculeMetal-organic frameworkSpin (physics)metal-organic frameworksAngewandte Chemie International Edition
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Iron (II) isothiocyanate complexes with substituted pyrazines: Experimental and theoretical views on their electronic structure

2015

Abstract Synthesis, structural, magnetic, Mossbauer and thermal studies of isothiocyanate iron (II) complexes with substituted pyrazines (iodo-, bromo- and amino-derivatives) are discussed here. Complexes with iodo- and bromo-derivatives were found to have the composition [Fe(Ipz)2(SCN)2(H2O)2]·2Ipz (1) and [Fe(Brpz)2(SCN)2(H2O)2]·2Brpz (2), whereas in the case of amino-functionalized pyrazine the formation of [Fe(NH2pz)4(SCN)2] (3) was observed. 3D organization of the molecular complexes is stabilized within different hydrogen, halogen and lone pair–π interactions. Spin state of iron (II) ions in 1–3 was determined as high spin by Mossbauer and magnetic measurements. DFT calculations for t…

complexesSpin statesPyrazineHydrogenspin stateMössbauer spectroscopyInorganic chemistrychemistry.chemical_elementElectronic structure3. Good healthInorganic Chemistrychemistry.chemical_compoundCrystallographyironchemistryIsothiocyanateMössbauer spectroscopyHalogenMaterials ChemistrypyrazinePhysical and Theoretical Chemistryta116Lone pairPolyhedron
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N-(Pyrazin-2-yl)adamantane-1-carboxamide

2016

Molecules of the title compound, C15H19N3O, are composed of an adamantine unit and a pyrazine ring connected to each other through an amide bond. The H—N—C=O moiety is close to planar [C—N—C—O and C—N—C—C torsion angles of 4.7 (2) and −173.8 (1)°, respectively]. The N3—C5 bond has partial double-bond character [1.370 (1) Å]. The geometries of the pyrazine ring and the adamantane substituent are normal and in good agreement with closely related structures. In the crystal, molecules are connected by N—H...O hydrogen bonds, forming zigzag chains in the [001] direction and are arranged in a herringbone fashion.

crystal structurePyrazineChemistrymedicine.drug_classHydrogen bondAdamantaneadamantaneSubstituentCarboxamideGeneral MedicineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographyantiviral activitylcsh:QD901-999medicineMoietyPeptide bondlcsh:CrystallographyIUCrData
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