Search results for "Mole"

showing 10 items of 35882 documents

Extending the halogen-bonded supramolecular synthon concept to 1,3,4-oxadiazole derivatives

2016

A series of five crystal structures of 1:1 halogen-bonded complexes were obtained from 4-[5-(4-alkoxyphenyl)-1,3,4-oxadiazole-2-yl]pyridine and 1,3,5-trifluorotriiodobenzene. Electronic structure calculations show that the N(oxadiazole)⋯I interaction in the new synthon is as strong as the classic N(pyridine)⋯I interaction. Oxygen to sulfur atom subsitution on the oxadiazole ring results in a different supramolecular packing where the N(pyridine)⋯I interaction is favored, which could be rationalized by the changes in the molecular electrostatic potential predicted from the theoretical calculations.

010405 organic chemistryStereochemistrySynthonSupramolecular chemistryOxadiazoleGeneral ChemistryCrystal structureElectronic structure010402 general chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryHalogenPyridineGeneral Materials ScienceCrystEngComm
researchProduct

Synthesis and characterization of binuclear μ-oxalato nickel(II), copper(II) and zinc(II) complexes with 3,3′-diamino-N-methyl-dipropylamine or trans…

1999

Abstract New binuclear complexes of the type [(Ni(Medpt)NO3)2ox] (1) (Medpt=3,3′-diamino-N-methyl-dipropylamine, H2ox=oxalic acid), [(Ni(dach)2)2ox]NO3·2H2O (2) (dach=trans-1,2-diaminocyclohexane), [(Cu(Medpt))2ox]X2·yH2O (X=NO3, y=2 2/3 (3); X=ClO4, y=0 (4)) and [(Zn(dach)2)2ox](ClO4)2·2H2O (5) have been prepared and characterized by IR and UV–Vis spectroscopies. Spectroscopic data are consistent with oxalate-bridged structures between six-coordinated (N3O3 or N4O2) Ni(II) (compounds 1 or 2), five-coordinated (N3O2) Cu(II) (compounds 3 and 4) or six-coordinated (N4O2) Zn(II) (compound 5). The crystal structure of [(Cu(Medpt))2ox](NO3)2·2 2/3 H2O (3) has been determined by single-crystal X-…

010405 organic chemistryStereochemistrytrans-12-Diaminocyclohexanechemistry.chemical_elementCrystal structureZinc010402 general chemistry01 natural sciencesMagnetic susceptibilityCopper0104 chemical sciences3. Good healthInorganic Chemistrychemistry.chemical_compoundCrystallographyNickelchemistryMaterials ChemistryMoleculeDipropylaminePhysical and Theoretical ChemistryPolyhedron
researchProduct

Carbon monoxide activation by a molecular aluminium imide: C-O bond cleavage and C-C bond formation

2020

Anionic molecular imide complexes of aluminium are accessible via a rational synthetic approach involving the reactions of organo azides with a potassium aluminyl reagent. In the case of K2 [(NON)Al(NDipp)]2 (NON=4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimethyl-xanthene; Dipp=2,6-diisopropylphenyl) structural characterization by X-ray crystallography reveals a short Al-N distance, which is thought primarily to be due to the low coordinate nature of the nitrogen centre. The Al-N unit is highly polar, and capable of the activation of relatively inert chemical bonds, such as those found in dihydrogen and carbon monoxide. In the case of CO, uptake of two molecules of the substrate…

010405 organic chemistrySubstrate (chemistry)General Chemistry010402 general chemistry01 natural sciencesIsocyanateCatalysis3. Good health0104 chemical scienceschemistry.chemical_compoundchemistryChemical bondReagentPolymer chemistryMoleculeImideBond cleavageCarbon monoxide
researchProduct

Long-range electronic connection in picket-fence like ferrocene–porphyrin derivatives

2012

The effects of a direct connection between ferrocene and porphyrin units have been thoroughly investigated by electrochemical and spectroscopic methods. These data not only reveal that substitution of the porphyrin macrocycle by one, two, three or four ferrocenyl groups strongly affects the electronic properties of the porphyrin and ferrocenyl moieties, they also clearly demonstrate that the metallocene centres are "connected" through the porphyrin-based electronic network. The dynamic properties of selected ferrocene-porphyrin conjugates have been investigated by VT NMR and metadynamic calculations. 1,3-Dithiolanyl protecting groups have been introduced on the upper rings of the ferrocene …

010405 organic chemistrySupramolecular chemistryCrystal structure010402 general chemistryPhotochemistryElectrochemistry01 natural sciencesPorphyrin0104 chemical sciencesDithiolaneInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistryFerrocene[CHIM]Chemical SciencesMetalloceneComputingMilieux_MISCELLANEOUS
researchProduct

Application of Rigidity-Controlled Supramolecular Affinity Materials for the Gravimetric Detection of Hazardous and Illicit Compounds.

2016

The combination of an (-)-isosteviol-derived building block and 9,9'-spirobifluorene or tetraphenylmethane generated highly potent new affinity materials for the detection of volatile organic compounds (VOCs). Comparison of their affinity behaviour with different core structures showed remarkable influence on selectivity and sensitivity due to structural rigidity and their pre-organization. Their unique supramolecular properties were investigated in an affinity assay using high fundamental frequency quartz crystal microbalances.

010405 organic chemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundRigidity (electromagnetism)Molecular recognitionchemistryOrganic chemistryGravimetric analysisSelectivityStructural rigidityTetraphenylmethaneChemPlusChem
researchProduct

Bowl-shape electron donors with absorptions in the visible range of the solar spectrum and their supramolecular assemblies with C 60

2012

We describe the synthesis, electronic, optical and photophysical properties of a family of three electron-donor bowl-shaped organic molecules that absorb light in the whole range of the visible spectrum (up to 800 nm in one case), and associate C60 in solution with binding constants in the range of 104–102 M−1 as measured from both UV-vis and fluorescence titrations in several solvents. These molecules are π-extended derivatives of tetrathiafulvalene, based on a truxene core to which two or three units of dithiole are covalently attached. The inclusion of the bulky dithiole groups is responsible for their bowl-shape geometry, which allows them to associate with C60, and their electron-donor…

010405 organic chemistrySupramolecular chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesPhotoexcitationchemistry.chemical_compoundchemistryIntramolecular forceUltrafast laser spectroscopyDensity functional theoryAbsorption (chemistry)TetrathiafulvaleneVisible spectrum
researchProduct

Encapsulation of tetramethylphosphonium cations

2009

International audience; The weak interactions and capsule formation of tetramethylphosphonium (TMP) cation with resorcinarenes 1 and 2 and the corresponding pyrogallarenes 3 and 4 were studied in the solid state by single crystal X-ray diffraction, in solution by NMR and in the gas phase by mass spectrometry. In methanol-D4, the NMR titration studies reveal that the association constants for the 1:1 complexes of TMP@3 and TMP@4 are much higher (TMP@4:390±37 M-1) than for the corresponding TMP@1 and TMP@2 (TMP@2:130±10 M-1) complexes. In the gas phase both monomeric 1:1 TMP@1-TMP@4 complexes as well as the dimeric 1:2 capsule complexes, TMP@12-TMP@42 were observed. The 1:1:2 molar mixtures o…

010405 organic chemistrySupramolecular chemistrySolid-stateGeneral Chemistry010402 general chemistryMass spectrometry01 natural sciences0104 chemical sciences3. Good healthGas phasechemistry.chemical_compoundCrystallographyMonomerchemistryPhysical SciencesNmr titrationX-ray crystallographyMethanolSupramolecular Chemistry
researchProduct

Microporous Triptycene‐Based Affinity Materials on Quartz Crystal Microbalances for Tracing of Illicit Compounds

2019

Triptycene-based organic molecules of intrinsic microporosity (OMIMs) with extended functionalized π-surfaces are excellent materials for gas sorption and separation. In this study, the affinities of triptycene-based OMIM affinity materials on 195 MHz high-fundamental-frequency quartz crystal microbalances (HFF-QCMs) for hazardous and illicit compounds such as piperonal and (-)-norephedrine were determined. Both new and existing porous triptycene-based affinity materials were investigated, resulting in very high sensitivities and selectivities that could be applied for sensing purposes. Remarkable results were found for safrole - a starting material for illicit compounds such as ecstasy. A …

010405 organic chemistrySupramolecular chemistrySorptionGeneral ChemistryMicroporous material010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCrystalchemistry.chemical_compoundPiperonalchemistryTriptycenePorosityQuartzChemPlusChem
researchProduct

Modulating the DNA cleavage ability of copper(II) Schiff bases through ternary complex formation

2018

Copper(II) complexes with the potentially tridentate Schiff bases N-[(3-ethoxy-2-hydroxyphenyl)methylidene]-N′-tosylbenzene-1,2-diamine (H2L1) and N-[(2-hydroxynaphthanyl)methylidene]-N′-tosylbenzene-1,2-diamine (H2L2) have been synthesized by electrochemical oxidation of the metal in an electrochemical cell containing a solution of the corresponding ligand in acetonitrile. Adducts of these compounds with 2,2′-bipyridine (2,2′-bpy), 4,4′-bipyridine (4,4′-bpy) or 1,10-phenanthroline (phen) were also obtained. The complexes have been characterized by microanalysis, mass spectrometry, EPR, IR and UV-Vis spectroscopies, as well as DFT calculations. The ligand H2L1 and the compounds [CuL1(H2O)]·…

010405 organic chemistrySupramolecular chemistrychemistry.chemical_elementNANOPARTÍCULASGeneral Chemistry010402 general chemistry01 natural sciencesCopperCatalysisSquare pyramidal molecular geometry0104 chemical scienceslaw.inventionAdductMetalCrystallographychemistry.chemical_compoundchemistrylawvisual_artMaterials Chemistryvisual_art.visual_art_mediumElectron paramagnetic resonanceAcetonitrileTernary complex
researchProduct

A Ferrocenyl Amino Substituted Stannylene as an Intramolecular Fe→Sn Lewis Adduct

2018

010405 organic chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesAdductInorganic Chemistrychemistry.chemical_compoundchemistryFerroceneIntramolecular forceLewis acids and basesTinZeitschrift für anorganische und allgemeine Chemie
researchProduct