Search results for "Ion pairs"

showing 9 items of 19 documents

On the Ion-Pair Recognition and Indication Features of a Fluorescent Heteroditopic Host Based on a BODIPY Core

2014

A fluorescent heteroditopic host for ion pairs and zwitterionic species has been synthesized. Its affinity towards a series of anions, cations and ion pairs in acetonitrile has been assessed, and the spectroscopic response has been evaluated. Solid–liquid extraction experiments of inorganic salts, α-amino acids and γ-aminobutyric acid (GABA) into acetonitrile solutions were performed, and the resulting complexes were analyzed by UV/Vis absorption, fluorescence and 1H NMR spectroscopy. The discrimination patterns observed have been rationalized in terms of the molecular topologies of the host and guests.

Inorganic saltschemistry.chemical_compound1h nmr spectroscopychemistryOrganic ChemistryExtraction (chemistry)Physical and Theoretical ChemistryIon pairsBODIPYAbsorption (chemistry)PhotochemistryAcetonitrileFluorescenceEuropean Journal of Organic Chemistry
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Weak alkali and alkaline earth metal complexes of low molecular weight ligands in aqueous solution

2008

This work is aimed at reviewing the chemical literature dealing with thermodynamic aspects of the weak complex formation (species with log K values less than about 3) between alkali and alkaline earth metal ions with low molecular weight inorganic and organic ligands in aqueous solution. The following ligands (up to hexavalent anions) were examined in detail: (i) hydroxide, chloride, sulfate, carbonate and phosphate as inorganic, and (ii) carboxylates, amines, amino acids, complexones and nucleotides as organic ligands. The paper also identifies the main reasons responsible for the dispersion of the stability data on ion pairs in the literature. When possible, the trend of stability for the…

Ion pairsSupporting electrolyteMetal ions in aqueous solutionInorganic chemistryAlkali metal complexeWeak complexesChlorideAlkali metal complexes; Alkaline earth metal complexes; Weak complexes; Formation and stability in aqueous solution; Ion pairs.Inorganic Chemistrychemistry.chemical_compoundAlkali metal complexesAlkaline earth metal complexesMaterials ChemistrymedicineFormation and stability in aqueous solutionSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryWeak complexeAlkaline earth metalAqueous solutionChemistryLigandAlkali metalAlkaline earth metal complexeHydroxidemedicine.drugCoordination Chemistry Reviews
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A linear Fe-O-Fe unit in bis(dibenzyldimethylammonium) mu-oxo-bis[tribromoferrate(III)].

2006

The title compound, (C 16 H 20 )N) 2 [Fe 2 Br 6 O], crystallizes with one dibenzyldimethylammonium cation and one half of a μ-oxo-bis[tribromoferrate(III)] anion in the asymmetric unit. The bridging oxo group is situated on an inversion centre, resulting in a linear conformation for the Fe-O-Fe unit. The iron(III) cations have tetrahedral geometry, with bond angles in the range 106.8 (1)-112.2 (1)°. The ion pairs are held together by Coulombic forces and C-H···Br hydrogen bonds. Each Br - anion forms one hydrogen bond. No C-H···O hydrogen bonds are found between the O atom in the Fe-O-Fe unit and surrounding counter-cations, consistent with the linear configuration of the Fe-O-Fe unit.

Models MolecularOne halfMolecular StructureHydrogen bondChemistryIronTetrahedral molecular geometryHydrogen BondingGeneral MedicineCrystal structureIon pairsCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyIonOxygenQuaternary Ammonium CompoundsCrystallographyMolecular geometryLinear configurationActa crystallographica. Section C, Crystal structure communications
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Boolean operations mediated by an ion-pair receptor of a multi-readout molecular logic gate

2013

A heteroditopic BODIPY dye that performs all basic Boolean operations with a cation (K+) and an anion (F-) as inputs and absorption, transmission and fluorescence as outputs is described. The molecular logic gate can also act as a digital comparator between the inputs.

Molecular logic gateMetal-IonsAnalytical chemistryTopologyCatalysisIonchemistry.chemical_compoundComplexDrivenMaterials ChemistryKeypad LockCrown EtherFluorescence EnhancementChemistryMetals and AlloysGeneral ChemistryIon pairsFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRecognitionTransmission (telecommunications)Ceramics and CompositesDigital comparatorInputsBoolean operations in computer-aided designBODIPY
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Complexes hétéronucléaires Cp2MM′(Cp)(CO)3 (M  Nb, Ta; M′  Mo, W) avec groupes carbonyles pontants et semi-pontants: synthèse et comportement dynam…

1991

Abstract Heteronuclear structures Cp 2 MM′(Cp)(CO) 3 (M  Nb, Ta; M′  Mo, W) are obtained by heating Cp 2 MH 3 (M  Nb, Ta) with Cp 2 M′ 2 (CO) 6 (M′  Mo, W) or starting from Cp 2 M(CO)H and Cp 2 M′ 2 (CO) 4 . These heterobimetallic complexes show three CO coordination modes: terminal, semi-bridging and bridging. The two cyclopentadienyl groups of the Cp 2 M moiety are anisochronous owing to molecular rigidity; rotation barriers around the MM′ bond have been estimated and are greatest with tantalum derivatives.

StereochemistryOrganic ChemistryTantalumchemistry.chemical_elementNuclear magnetic resonance spectroscopyIon pairsBiochemistryInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryCyclopentadienyl complexHeteronuclear moleculeMaterials ChemistryMoietyPhysical and Theoretical ChemistryMetalloceneJournal of Organometallic Chemistry
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The first structurally characterized cationic lanthanide–alkyl complexesElectronic supplementary information (ESI) available: experimental and spectr…

2002

Reaction of rare earth metal–alkyl complexes [Ln(CH2SiMe3)3(THF)2] (Ln = Y, Lu) with B(C6X5)3 (X = H, F) in the presence of crown ethers gives crystallographically characterized ion pairs [Ln(CH2SiMe3)2(CE)(THF)n]+[B(CH2SiMe3)(C6X5)3]– (CE = [12]-crown-4, n = 1; CE = [15]-crown-5 and [18]-crown-6, n = 0).

chemistry.chemical_classificationLanthanideStereochemistryRare earthMetals and AlloysCationic polymerizationGeneral ChemistryIon pairsMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryMaterials ChemistryCeramics and CompositesAlkylChemical Communications
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Rate constants for ion-pair dissociation and association in the anionic two-state polymerization of styrene in THF

1965

chemistry.chemical_compoundReaction rate constantPolymerizationchemistryPolymer chemistryGeneral EngineeringIon pairsDissociation (chemistry)StyreneJournal of Polymer Science Part B: Polymer Letters
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Dynamic Refolding of Ion-Pair Catalysts in Response to Different Anions.

2019

Four distinct folding patterns were identified in two foldamer-type urea-thiourea catalysts bearing a basic dimethylamino unit by a combination of X-ray crystallography, solution NMR studies, and computational studies (DFT). These patterns are characterized by different intramolecular hydrogen bonding schemes that arise largely from different thiourea conformers. The free base forms of the catalysts are characterized by folds where the intramolecular hydrogen bonds between the urea and the thiourea units remain intact. In contrast, the catalytically relevant salt forms of the catalyst, where the catalyst forms an ion pair with the substrate or substrate analogues, appear in two entirely dif…

inorganic chemicalsBearing (mechanical)anionitcatalysis010405 organic chemistryChemistryorganic chemicalsOrganic Chemistryfolding anion bindingIon pairs010402 general chemistrykidetiede01 natural sciences0104 chemical sciencesCatalysislaw.inventionFolding (chemistry)X-rayCrystallographyconformational changelawkatalyysisolution structuresröntgenkristallografiaThe Journal of organic chemistry
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Apolar versus polar solvents: a comparison of the strength of some organic acids against different bases in toluene and in water

2010

The constants of ion-pair formation with 3-nitroaniline (3NO(2)A) for eight halogenoacetic acids (HAAs, 3a-h: TFA, TCA, TBA, DFA, DCA, DBA, MCA, and MBA), and five 2,2-dichloroalkanoic acids containing 3-8 carbon atoms (HAs, 5a-e: DCPA, DCBA, DCMBA, DCVA, and DCOA) have been determined in TOL at 298.1 K. The results obtained brought to evidence for HAAs the formation of ion-pairs with two different stoichiometries (base-acid, 1:1 or 1:2), while in contrast the HAs furnish only the 1:1 pairs. The different steric and electronic requirements of HAAs and HAs seem to be responsible for such an unlikely behavior. At the same time, the acid-catalyzed MRH of the (Z)-phenylhydrazone of 5-amino-3-be…

nitroanilinechemistry.chemical_classificationSteric effectsBase (chemistry)reazione di Boulton-Katritzskyacidi dicloroalcanoicichemistry.chemical_elementSettore CHIM/06 - Chimica Organicaacidi alogenoaceticiMedicinal chemistryTolueneMRH kinetic ion pairschemistry.chemical_compoundchemistryUreaPolarOrganic chemistryPhysical and Theoretical ChemistryCarbonreazione di Boulton-Katritzsky; nitroaniline; acidi alogenoacetici; acidi dicloroalcanoiciStoichiometry
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