Search results for "2'-bipyridine"

showing 10 items of 377 documents

Synthesis, X‐ray Studies and Magnetic Properties of Dinuclear Ni II and Cu II Complexes Bridged by the Azo‐2,2′‐bipyridine Ligand

2003

Two new paramagnetic transition metal complexes that contain the bridging ligand azo-2,2-bipyridine (abpy) have been prepared and characterized by X-ray crystallography and magnetic susceptibility measurements. The compound [Ni2(µ-abpy)(CH3CN)2(NO3)4]·2CH3CN (1·2CH3CN) crystallizes in the triclinic space group P1 ¯ with a = 8.290(5) A u , b = 8.343(5) A u , c = 11.180(5) A u , α = 105.36(3)°, β = 94.39(3)°, γ = 107.56(3)°, V = 700.5(7) A u 3 and Z = 1. The related salt [Cu2(µ

StereochemistryChemistryLigandchemistry.chemical_elementBridging ligandTriclinic crystal systemMagnetic susceptibility22'-BipyridineInorganic ChemistryCrystallographyParamagnetismNickelchemistry.chemical_compoundTransition metalEuropean Journal of Inorganic Chemistry
researchProduct

Dimensionally controlled hydrogen-bonded nanostructures: synthesis, structure, thermal and magnetic behaviour of the tris-(chelated)nickel(II) comple…

2002

Abstract Single crystals of the compound of formula [Ni(bipy)3]Cl2·5.5H2O (bipy=2,2′-bipyridine) have been prepared and structurally characterised by X-ray diffraction. The structure analysis reveals that the complex has an approximate D3 symmetry. The coordination sphere consists of six nitrogen atoms of the three-bipyridine ligands in an octahedral arrangement about the nickel. One of the chlorine ions is surrounded by twelve CH⋯Cl hydrogen bonds. Three kinds of layers are found in the crystal structure: (i) the Λ-[Ni(bipy)3]2+ cation; (ii) the water/chloride positions (O(1w)/Cl(21) to O(7w)/Cl(27)); (iii) the Δ-[Ni(bipy)3]2+ cation and a chloride ion (Cl(1)). The layers are stacked in t…

Coordination sphereHydrogen bondchemistry.chemical_elementCrystal structureChloride22'-BipyridineInorganic Chemistrychemistry.chemical_compoundCrystallographyNickelchemistryOctahedronMaterials ChemistrymedicineMoleculePhysical and Theoretical Chemistrymedicine.drugInorganica Chimica Acta
researchProduct

Discriminating octahedral transition metal ions: highly selective tripodal tris-(2,2′-bipyridine) functionalized piperazine cyclophane receptor for C…

2011

New tripodal transition metal ion receptors, tris(5-ethoxycarbonyl-2,2'-bipyridine) and tris(5-carboxylate-2,2'-bipyridine) substituted 27-membered trimeric piperazine cyclophanes 5 and 7 as well as tetra(5-ethoxycarbonyl-2,2'-bipyridine) substituted 36-membered tetrameric piperazine cyclophane 6, have been prepared and their transition metal ion complexing properties studied in solution by UV-vis spectroscopy and in the solid state by single-crystal X-ray diffraction. The crystal structures of [H(3)5(3+)·Fe(2+)]·4(ClO(4)(-))·CF(3)COO(-) (V), [H(3)7(2+)·Fe(2+)]·2(SO(4)(2-)) (VII) and the reference complex [tris(5,5'-bis(ethoxycarbonyl)-2,2'-bipyridine)Fe(II) perchlorate] (I) showed that the…

IonsTrisStereochemistryMolecular ConformationCrystal structurePiperazines22'-BipyridineInorganic ChemistryPiperazinechemistry.chemical_compoundPerchlorateCrystallography22'-DipyridylPiperidinesTransition metalchemistryTransition ElementsSpectrophotometry UltravioletSelectivityPiperazineCopperCyclophaneDalton Transactions
researchProduct

Complexes of tetra(parasulphonatephenyl)porphyrinato ferrate(III), FeTPPs, with 1,10 phenanthroline and 2,2′ bipyridine ligands

1985

Abstract Iron(III) porphyrin, FeTPPS, gives high-spin 1:1 monomeric complexes with the ligands 1,10 phenanthroline, 2,9 dimethylphenanthroline and 2,2 bipyridine in aqueous solution. Absorption spectrum of the complexes is very different to the one of the monomer metalloporphyrin, but nearly identical to the visible spectrum of the μ-oxo dimer Fe2(TPPS)2O. A spectrophotometric study of the formation equilibria yields the following values of the stability constants: Me2phen 4.3 × 104, phen 1.1 × 104, bipy 2.0 × 102 (25 °C, 0.1 M NaNO3). Analysis of the experimental data strongly suggest that the ligands are hydrogen bonded to one coordinated water molecule (TPPS)FeOH2 → (LL). Although the …

Aqueous solutionDimerPhenanthrolinePhotochemistryMedicinal chemistryPorphyrin22'-BipyridineInorganic Chemistrychemistry.chemical_compoundBipyridineMonomerchemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistryInorganica Chimica Acta
researchProduct

Enantiomer Separation of Tris(2,2′-bipyridine)ruthenium(II): Interaction of a D3-Symmetric Cation with a C2-Symmetric Anion

2015

A compound widely used in the separation of the enantiomers of Δ,Λ-[Ru(bipy)3]2+ (bipy = 2,2′-bipyridine) and originally described as “a curious lattice compound” with the formula Δ-[Ru(bipy)3]3[Sb2(R,R-tart)2]2I2·18H2O (tart = tetradeprotonated, carboxyl and hydroxyl, tartaric acid anion) has been crystallographically characterized as this species with a slightly higher degree of hydration (19.5H2O). The crystal lattice has a layered structure in which sheets containing Δ-[Ru(bipy)3]2+ cations and iodide anions alternate with those containing [Sb2(R,R-tart)2]2– anions and water. The role of the iodide ions, which lie in pseudohexagonal cavities formed by the array of three inequivalent but…

chemistry.chemical_classificationTrisStereochemistryIodidechemistry.chemical_elementGeneral ChemistryCrystal structureCondensed Matter Physics22'-BipyridineRutheniumIonchemistry.chemical_compoundCrystallographyruthenium compoundschemistryTartaric acidGeneral Materials ScienceEnantiomercrystallographyta116Crystal Growth & Design
researchProduct

Photomagnetic properties of an Fe(ii) spin-crossover complex of 6-(3,5-diamino-2,4,6-triazinyl)-2,2'-bipyridine and its insertion into 2D and 3D bime…

2017

International audience; The Fe(ii) complex of the L1 ligand (L1 = 6-(3,5-diamino-2,4,6-triazinyl)-2,2'-bipyridine) has been used as a templating cation for the growth of oxalate-based networks. The magnetic characterization of the [Fe(II)(L1)2](ClO4)2·CH3CN (1) precursor in the solid state has been performed for the first time showing that the low-spin (LS) state is predominating from 2 to 400 K with 10% of Fe(ii), which undergoes a gradual and irreversible spin-crossover above 350 K. 1 presents the LIESST effect with a photo-conversion close to 25% and a T(LIESST) of 49 K. During the preparation of 1, a secondary product of the formula [Fe(II)(L1)(CH3CN)2(H2O)](ClO4)2·CH3CN (2) has been ob…

010405 organic chemistryLigandStereochemistrySolid-state[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry01 natural sciencesOxalateLIESST22'-Bipyridine0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySpin crossoverBimetallic strip
researchProduct

Synthesis, crystal structure and magnetic properties of [Cu(bipy)2(CH3COO)][Cu(bipy)2(Cr(C2O4)3)]·∼10.5H2O, the first compound containing the [Cr(C2O…

2001

Abstract The reaction between copper(II) acetate with 2,2′-bipyridine and K3[Cr(C2O4)3] leads to the novel salt [Cu(bipy)2(CH3COO)][Cu(bipy)2(Cr(C2O4)3)]·∼10.5H2O, 1 (bipy=2,2′-bipyridine). The crystal structure of 1 consists of mononuclear cationic species [Cu(bipy)2(CH3COO)]+ and heterobinuclear anionic units, [Cu(bipy)2(Cr(C2O4)3)]−. The tris-oxalato-chromium entity behaves as a monodentate ligand toward the copper(II) ion within the complex anion. The distance between Cr(III) and Cu(II) across the bridging oxalato group is 5.056(2) A. The copper(II) ions exhibit a distorted trigonal bipyramidal surrounding in both cationic and anionic species. The π–π stacking interaction between bipy l…

DenticityChemistryInorganic chemistryStackingCationic polymerizationchemistry.chemical_elementCrystal structureMagnetic susceptibilityCopper22'-BipyridineInorganic Chemistrychemistry.chemical_compoundTrigonal bipyramidal molecular geometryCrystallographyMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
researchProduct

Heteropolymetallic Supramolecular Solid-State Architectures Constructed from [Cr(AA)(C2O4)2]- Tectons, and Sustained by Coordinative, Hydrogen Bond a…

2004

The paper reports on four novel solid-state architectures constructed by using tectons having the general formula:  [Cr(AA)(C2O4)2]- [AA = 2,2‘-bipyridine (bipy) and 1,10-phenanthroline (phen)]. These building blocks are involved in various intermolecular interactions:  coordinative, hydrogen bonds, and π−π contacts. Two new crystallohydrates in the Ba[Cr(AA)(C2O4)2]2·nH2O family have been characterized:  [BaCr2(bipy)2(C2O4)4(H2O)2]·4H2O (1) and [BaCr2(phen)2(C2O4)4(H2O)2] (2). Because of the different numbers of water molecules, their crystal structures are completely different from those of two others previously reported, [BaCr2(bipy)2(C2O4)4(H2O)]·H2O and [BaCr2(phen)2(C2O4)4(H2O)2]·4H2O…

DenticityChemistryHydrogen bondPhenanthrolineStackingSupramolecular chemistryGeneral ChemistryCrystal structureCondensed Matter Physics22'-Bipyridinechemistry.chemical_compoundCrystallographyMoleculeGeneral Materials ScienceCrystal Growth & Design
researchProduct

Crystal structure and magnetic properties of the single-μ-chloro copper(II) chain [Cu(bipy)Cl2] (bipy = 2,2′-bipyridine)

1999

Abstract The crystal and molecular structure of the copper(II) chain [Cu(bipy)Cl2] (1) (bipy = 2,2′-bipyridine) has been determined by X-ray diffraction methods. The crystal structure of 1 consists of neutral single chloro-bridged copper(II) chains with alternating short and long Cu–Cl distances through a screw axis parallel to a. The copper surrounding is best described as distorted square pyramidal, the equatorial plane being built by the two nitrogen atoms of the chelating bipy and two chlorine atoms (one terminal and the other bridging), whereas the apical position is filled by the bridging chlorine atom from the symmetry-related adjacent unit. The equatorial Cu–Cl bonds (2.291(3) and 2…

chemistry.chemical_classificationDiffractionChemistrychemistry.chemical_elementCrystal structurePolymerAtmospheric temperature rangeCopperSquare pyramidal molecular geometry22'-BipyridineInorganic ChemistryCrystallographychemistry.chemical_compoundMaterials ChemistryMoleculePhysical and Theoretical Chemistry
researchProduct

Shine bright or live long: substituent effects in [Cu(N^N)(P^P)]+-based light-emitting electrochemical cells where N^N is a 6-substituted 2,2'-bipyri…

2016

We report [Cu(P^P)(N^N)][PF6] complexes with P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 6-methyl-2,2′-bipyridine (Mebpy), 6-ethyl-2,2′-bipyridine (Etbpy), 6,6′-dimethyl-2,2′-bipyridine (Me2bpy) or 6-phenyl-2,2′-bipyridine (Phbpy). The crystal structures of [Cu(POP)(Phbpy)][PF6]·Et2O, [Cu(POP)(Etbpy)][PF6]·Et2O, [Cu(xantphos)(Me2bpy)][PF6], [Cu(xantphos)(Mebpy)][PF6]·CH2Cl2·0.4Et2O, [Cu(xantphos)(Etbpy)][PF6]·CH2Cl2·1.5H2O and [Cu(xantphos)(Phbpy)][PF6] are described; each copper(I) centre is distorted tetrahedral. In the crystallographically determined structures, the N^N domain in [Cu(xantphos)(Phbpy)]+ and [Cu(…

XantphosLigand02 engineering and technologyGeneral ChemistryCrystal structureNuclear magnetic resonance spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences22'-Bipyridine0104 chemical scienceschemistry.chemical_compoundCrystallographyElectron transferchemistryExcited stateMaterials ChemistrySinglet state0210 nano-technology
researchProduct