Search results for "Azine"

showing 10 items of 1589 documents

CCDC 671674: Experimental Crystal Structure Determination

2011

Related Article: S.Shit, S.K.Dey, C.Rizzoli, E.Zangrando, G.Pilet, C.J.Gomez-Garcia, S.Mitra|2011|Inorg.Chim.Acta|370|18|doi:10.1016/j.ica.2011.01.008

(2-Hydroxy-N'-(555-trifluoro-4-(hydroxy)pent-3-en-2-ylidene)benzohydrazido)-(methanol)-(pyrazine)-copper(ii) perchlorateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1423254: Experimental Crystal Structure Determination

2015

Related Article: Diego Rota Martir, Ashu K. Bansal, Vincent Di Mascio, David B. Cordes, Adam F. Henwood, Alexandra M. Z. Slawin, Paul C. J. Kamer, Laura Martínez-Sarti, Antonio Pertegás, Henk J. Bolink, Ifor D. W. Samuel, Eli Zysman-Colman|2016|Inorg.Chem.Front.|3|218|doi:10.1039/C5QI00177C

(46-bis(Diphenylphosphino)-10H-phenoxazine)-bis(2-(pyridin-2-yl)phenyl)-iridium hexafluorophosphate dichloromethane solvate hemihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 680518: Experimental Crystal Structure Determination

2009

Related Article: A.Dobrov, V.B.Arion, S.Shova, A.Roller, E.Rentschler, B.K.Keppler|2008|Eur.J.Inorg.Chem.||4140|doi:10.1002/ejic.200800605

(M)-tris(mu~2~-methyl N-[(hydrazinyl(methylsulfanyl)methylidene]-hydrazinecarbohydrazonothioato-NN'N''N''')-di-nickel(ii)) tetra-iodide hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 164934: Experimental Crystal Structure Determination

2001

Related Article: H.Grove, J.Sletten, M.Julve, F.Lloret|2001|J.Chem.Soc.,Dalton Trans.||2487|doi:10.1039/b103588f

(mu2-23-bis(2-Pyridyl)pyrazine-NN'N''N''')-aqua-tetrachloro-(dimethylsulfoxide-O)-di-copper(ii) dimethylsulfoxide solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 247407: Experimental Crystal Structure Determination

2005

Related Article: J.Carranza, J.Sletten, C.Brennan, F.Lloret, J.Cano, M.Julve|2004|Dalton Trans.||3997|doi:10.1039/b412034p

(mu2-Croconato)-(mu2-2356-tetrakis(2-pyridyl)pyrazine)-bis(croconato)-triaqua-tri-copper(ii) heptahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 685749: Experimental Crystal Structure Determination

2009

Related Article: P.Gomez-Saiz, R.Gil-Garcia, M.A.Maestro, J.L.Pizarro, M.I.Arriortua, L.Lezama, T.Rojo, M.Gonzalez-Alvarez, J.Borras, J.Garcia-Tojal|2008|J.Inorg.Biochem.|102|1910|doi:10.1016/j.jinorgbio.2008.06.015

(mu~2~-Pyrazine)-bis(pyridine-2-aldehyde thiosemicarbazone)-di-copper(ii) diperchlorateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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A new hydrogen bonding motif involved in self-recognition in the solid state by functionalised macrocycles

2011

Self-recognition within the crystal lattices of three functionalised macrocycles results in the formation of arrays of remarkably similar hermaphroditic pairs of macrocycles. In the case of two of the macrocycles containing acylhydrazine substituents, a hitherto unknown recognition pattern is found in the interaction of the hydrazine moiety with crown-ether oxygen atoms.

010405 organic chemistryChemistryHydrogen bondStereochemistryHydrazineAcylhydrazineSolid-stateGeneral ChemistrySelf recognitionCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences3. Good health0104 chemical scienceschemistry.chemical_compoundOxygen atomPolymer chemistryMoiety[CHIM]Chemical SciencesGeneral Materials Scienceta116ComputingMilieux_MISCELLANEOUS
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Structural, photophysical and magnetic properties of transition metal complexes based on the dipicolylamino-chloro-1,2,4,5-tetrazine ligand

2015

International audience; The ligand 3-chloro-6-dipicolylamino-1,2,4,5-tetrazine (Cl-TTZ-dipica) 1, prepared by the direct reaction between 3,6-dichloro-1,2,4,5-tetrazine and di(2-picolyl)-amine, afforded a series of four neutral transition metal complexes formulated as [Cl-TTZ-dipica-MCl2]2, with M = Zn(II), Cd(II), Mn(II) and Co(II), when reacted with the corresponding metal chlorides. The dinuclear structure of the isostructural complexes was disclosed by single crystal X-ray analysis, clearly indicating the formation of [MII–(μ-Cl)2MII] motifs and the involvement of the amino nitrogen atom in semi-coordination with the metal centers, thus leading to distorted octahedral coordination geome…

010405 organic chemistryChemistryLigandStereochemistrySubstituentSupramolecular chemistry010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundTetrazineCrystallographyTransition metalvisual_artIntramolecular forceddc:540visual_art.visual_art_medium[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryIsostructuralComputingMilieux_MISCELLANEOUSDALTON TRANSACTIONS
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A Combined Experimental and Theoretical Study of the Ammonium Bifluoride Catalyzed Regioselective Synthesis of Quinoxalines and Pyrido[2,3-b]pyrazines

2015

International audience; Ammonium bifluoride was efficiently used (at a 0.5 mol % loading) to catalyze the cyclocondensation between 1,2-arylenediamines and 1,2-dicarbonyl compounds at room temperature in methanol-water, affording quinoxalines and pyrido[2,3-b]pyrazines in excellent yields. Importantly, 2,8-disubstituted quinoxalines and 3-substituted pyrido[2,3-b]pyrazines were regioselectively formed by reacting aryl glyoxals with 3-methyl-1,2-phenylenediamine and 2,3-diaminopyridine, respectively. Analysis of the DFT reactivity indices allowed to explain the catalytic role of ammonium bifluoride.

010405 organic chemistryChemistryOrganic ChemistryRegioselectivityAmmonium bifluoride010402 general chemistrypyrido[201 natural sciencesCatalysisammonium bifluoride0104 chemical sciencesCatalysischemistry.chemical_compoundregioselectivity3-b]pyrazinesDFT reactivity indices[CHIM]Chemical SciencesOrganic chemistryquinoxalinesDensity functional theoryReactivity (chemistry)Synthesis
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Radical cation and dication of a 4H-dithieno[2,3-b:3′,2′-e][1,4]-thiazine

2017

A p-tert-butylphenyl substituted 4H-dithieno[2,3-b:3′,2′-e][1,4]thiazine was synthesized by twofold Buchwald–Hartwig coupling. The electronic properties (UV/Vis, cyclic voltammetry and spectroelectrochemistry) and the DFT- and TD DFT-calculated electronic structure reveal that the parent system and the radical cation and dication oxidation products are highly polarizable π-systems with strong charge transfer contributions. The radical cation and the dication were prepared by oxidation with antimony(V) pentachloride, giving stable deeply colored salts. EPR spectroscopy of the radical cation furnishes hyperfine coupling constants with the nitrogen nucleus and the α-thienyl protons. The dicati…

010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_elementElectronic structureNuclear magnetic resonance spectroscopy010402 general chemistryPhotochemistry01 natural sciences0104 chemical scienceslaw.inventionDicationchemistry.chemical_compoundRadical ionAntimonyThiazinelawCyclic voltammetryElectron paramagnetic resonanceOrganic Chemistry Frontiers
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