Search results for "XY"

showing 10 items of 13736 documents

Hydrogen-bonded networks of [Fe(bpp)2]2+spin crossover complexes and dicarboxylate anions: structural and photomagnetic properties

2016

The paper reports the syntheses, crystal structures, thermal and (photo)magnetic properties of spin crossover salts of formula [Fe(bpp)2](C6H8O4)·4H2O (1·4H2O), [Fe(bpp)2](C8H4O4)·2CH3OH·H2O (2·2MeOH·H2O) and [Fe(bpp)2](C8H4O4)·5H2O (2·5H2O) (bpp = 2,6-bis(pyrazol-3yl)pyridine; C6H8O4 = adipate dianion; C8H4O4 = terephthalate dianion). The salts exhibit an intricate network of hydrogen bonds between low-spin iron(II) complexes and carboxylate dianions, with solvent molecules sitting in the voids. Desolvation is accompanied by a low-spin (LS) to high-spin (HS) transformation in the materials. The dehydrated phase 2 undergoes a two-step transition with a second step showing thermal hysteresis…

010405 organic chemistryChemistryHydrogen bondInorganic chemistryCrystal structure010402 general chemistry01 natural sciencesLIESST0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographySpin crossoverAdipatePyridineMoleculeCarboxylateDalton Trans.
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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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Effect of quaternary ammonium salts on spectral properties of zinc octacarboxyphthalocyanine

2020

Abstract The paper presents results of the research on the influence of quaternary ammonium salts on UV–vis absorption and emission spectra of zinc octacarboxyphthalocyanine (ZnPcOC). Quaternary ammonium salts which show biological activity play a crucial role. In ZnPcOC solutions with a proper concentration of tetrabutylammonium salts (TBAX), a strong bathochromic shift band (λmax = 760 nm – “R” band) showing red fluorescence appears in time. The presence of tetrabutylammonium salt causes pH increase and, consequently, a gradual dissociation of carboxyl groups in ZnPcOC molecule. It seems that –COO— anions present in the ZnPcOC complex can interact with tetraalkylammonium cations, causing …

010405 organic chemistryChemistryOrganic ChemistryInorganic chemistrySpectral propertieschemistry.chemical_elementZincUV–Vis spectraQuaternary ammonium salts010402 general chemistry01 natural sciencesFluorescenceDissociation (chemistry)Fluorescence0104 chemical sciencesAnalytical ChemistryZinc octacarboxyphthalocyanineInorganic Chemistrychemistry.chemical_compoundPDTBathochromic shiftMoleculeAmmoniumEmission spectrumSpectroscopyJournal of Molecular Structure
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Green synthesis of cavity-containing manganese oxides with superior catalytic performance in toluene oxidation

2019

10 Figuras.- 2 Tablas.- Datos suplementarios disponibles en línea en la página web del editor.-- © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

010405 organic chemistryChemistryStructural waterProcess Chemistry and TechnologyInorganic chemistryCationic polymerizationVOCs oxidationchemistry.chemical_elementNanoparticleManganeseCavities010402 general chemistry01 natural sciences7. Clean energyOxygenTolueneCatalysisHydrothermal circulationToluene oxidation0104 chemical sciencesCatalysischemistry.chemical_compoundManganese oxideToluene
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Arene C−H Activation at Aluminium(I): meta Selectivity Driven by the Electronics of S N Ar Chemistry

2020

The reactivity of the electron-rich anionic Al(I) ('aluminyl') compound K 2 [(NON)Al] 2 (NON = 4,5-bis(2,6-diisopropylanilido)-2,7-di- tert -butyl-9,9-dimethylxanthene) towards mono- and disubstituted arenes is reported. C-H activation chemistry with n -butylbenzene gives exclusively the product of activation at the arene meta position. Mechanistically, this transformation proceeds in a single step via a concerted Meisenheimer-type transition state. Selectivity is therefore based on similar electronic factors to classical S N Ar chemistry, which implies the destabilization of transition states featuring electron-donating groups in either the ortho or the para positions. In the cases of tolu…

010405 organic chemistryChemistryXyleneSubstituentGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryTolueneCatalysisTransition state0104 chemical sciences3. Good healthchemistry.chemical_compoundMeta-Nucleophilic aromatic substitutionReactivity (chemistry)SelectivityAngewandte Chemie International Edition
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Insight into the Mechanism of Water Adsorption/Desorption in Hydrophilic Viologen-Carboxylate Based PCP

2017

A water stable and highly hydrophilic porous coordination polymer based on viologen-carboxylate type ligand, the 4,4′-bipyridinium,1,1-bis(3-carboxyphenyl) (pc2), is obtained by the solvothermal method: [Cd3(pc2) (BTC)2(H2O)2]·6H2O ([1(H2O)2]·6H2O; BTC3– = 1,3,5-carboxybenzene). Its crystal structure and the ones of two partially dehydrated phases have been determined, allowing insight into the mechanism of water adsorption/desorption of this PCP material. It is shown that the dehydrated compound [1] first adsorbs two water molecules which fill the pores, leading to [1]·2H2O. On the other hand, the partial dehydration of the as-synthesized compound leads to the intermediate phase [1(H2O)]·3…

010405 organic chemistryCoordination polymerLigandInorganic chemistryGeneral ChemistryCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundAdsorptionchemistryDesorptionPolymer chemistryMoleculeGeneral Materials ScienceCarboxylatePyridiniumComputingMilieux_MISCELLANEOUSCrystal Growth & Design
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Tetracationic and Tetraanionic Manganese Porphyrins: Electrochemical and Spectroelectrochemical Characterization

2017

International audience; The electrochemistry and spectroelectrochemistry of four tetrapositively charged and two tetranegatively charged porphyrins were characterized in two nonaqueous solvents (dimethyl sulfoxide and N,N-dimethylformamide) containing 0.1 M tetra-n-butylammonium perchlorate. The tetrapositively charged compounds are represented by the tetrapyridylporphyrins [TRPyPM]4+(X-)4, where R is a methyl or [2-[2-(2-methoxy)ethoxy]ethoxy]ethyl group, M = MnIIII, MnIIICl, CuII, or PdII, and X = I- or Cl-. The tetranegatively charged porphyrins are represented by the tetrasulfonato derivatives [TPPSMn(OAc)]4-(NH4+)4 and [TArPSMn(OAc)]4-(NH4+)4, where Ar = 4-O-[2-[2-(2-methoxy)ethoxy]eth…

010405 organic chemistryDimethyl sulfoxidechemistry.chemical_element[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryManganese[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundPerchloratechemistry13. Climate actionAlkoxy groupPyridiniumEthyl groupPhysical and Theoretical Chemistry
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Structure and properties of a novel staircase-like decanuclear [CuII10] cluster supported by carbonate and carboxylate bridges

2018

This article describes a novel staircase-like decanuclear copper(II) cluster [CuII10(cpdp)4(CO3)4(CH3OH)2]·3.33CH3OH·7.83H2O (1) (H3cpdp = N,N′-bis[2-carboxybenzomethyl]-N,N′-bis[2-pyridylmethyl]-1,3-diaminopropan-2-ol) composed of a pair of [CuII5] pentamers. In methanol, the reaction of H3cpdp with Cu(NO3)2·3H2O in the presence of K2CO3 leads to the isolation of complex 1. This complex has been characterized by various analytical techniques including single crystal X-ray crystallography. Structural analysis reveals that the two [CuII5] pentameric units are bridged together exclusively by two μ2:η2:η1 carbonate groups. Complex 1 shows a rare μ3:η2:η1:η1 bridging coordination mode of four b…

010405 organic chemistryLigandInorganic chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCopperCatalysis0104 chemical scienceslaw.inventionMetalchemistry.chemical_compoundCrystallographychemistrylawvisual_artMaterials Chemistryvisual_art.visual_art_mediumCarboxylateCyclic voltammetryElectron paramagnetic resonanceSingle crystalNew Journal of Chemistry
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Zinc(ii), cobalt(ii) and manganese(ii) networks with phosphoserine ligand: synthesis, crystal structures and magnetic and proton conductivity propert…

2017

A series of zinc(II), cobalt(II) and manganese(II) coordination networks with phosphoserine ligand (H3PSer) are synthesized and characterized. Whereas in compounds 1 and 2 with the general formula [M(HPser)]n [M = Zn (1) and Co (2)], the metal(II) ion presents a tetrahedral geometry, in [Co(HPSer)(H2O)2]n (3) and [Mn(HPSer)(H2O)]n (4), the metal(II) ions are in a distorted octahedral geometry. The 3D frameworks are formed by inorganic layers built up from MO4 or MO6 polyhedra and phosphate groups. These layers are linked by the carboxylate groups of the phosphoserine ligand. The presence of extended hydrogen bonding stabilizes the 3D network and favours the proton transfer leading to modera…

010405 organic chemistryLigandInorganic chemistrychemistry.chemical_elementTetrahedral molecular geometryZincManganese010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artOctahedral molecular geometryvisual_art.visual_art_mediumCarboxylateCobaltDalton Transactions
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Titanocene–gold complexes containing N-heterocyclic carbene ligands inhibit growth of prostate, renal, and colon cancers in vitro

2016

We report on the synthesis, characterization, and stability studies of new titanocene complexes containing a methyl group and a carboxylate ligand (mba = −OC(O)-p-C6H4-S−) bound to gold(I)−N-heterocyclic carbene fragments through the thiolate group: [(η5 -C5H5)2TiMe(μ-mba)Au(NHC)]. The cytotoxicities of the heterometallic compounds along with those of novel monometallic gold−N-heterocyclic carbene precursors [(NHC)Au(mbaH)] have been evaluated against renal, prostate, colon, and breast cancer cell lines. The highest activity and selectivity and a synergistic effect of the resulting heterometallic species was found for the prostate and colon cancer cell lines. The colocalization of both tita…

010405 organic chemistryLigandStereochemistryOrganic Chemistry010402 general chemistrymedicine.disease01 natural sciencesArticleIn vitro3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundProstate cancermedicine.anatomical_structurechemistryProstatemedicineCarboxylatePhysical and Theoretical ChemistryQD0146SelectivityCarbeneMethyl group
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