Search results for "Radical ion"

showing 10 items of 57 documents

Understanding the local reactivity in polar organic reactions through electrophilic and nucleophilic Parr functions

2013

[EN] Building upon our recent studies devoted to the bonding changes in polar reactions [RSC Advances, 2012, 2, 1334 and Org. Biomol. Chem., 2012, 10, 3841], we propose herein two new electrophilic, P-k(+), and nucleophilic, P-k(-), Parr functions based on the spin density distribution at the radical anion and at the radical cation of a neutral molecule. These local functions allow for the characterisation of the most electrophilic and nucleophilic centres of molecules, and for the establishment of the regio- and chemoselectivity in polar reactions. The proposed Parr functions are compared with both, the Parr-Yang Fukui functions [J. Am. Chem. Soc. 1984, 106, 4049] based on frontier molecul…

ChemistryGeneral Chemical EngineeringExchangeGeneral ChemistryMoleculesDFTBond-formationDensittyIndexNucleophileRadical ionOrganic reactionComputational chemistryDiels-alder reactionElf analysisElectrophileLocalization functionMolecular orbitalChemoselectivityMulliken population analysis13-DipolarDiels–Alder reaction
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Initial Radical Cation Pathway in the Mo2Cl10-Mediated Dehydrogenative Arene Coupling

2015

Experimental (EPR) and theoretical (DFT) evidence is provided for radical cation formation as initial step in the Mo2Cl10-mediated dehydrogenative arene coupling. The initial electron transfer from methoxyarenes to molybdenum proceeds via an inner sphere mechanism.

ChemistryOrganic Chemistrychemistry.chemical_elementGeneral ChemistryInner sphere electron transferPhotochemistryCatalysislaw.inventionCoupling (electronics)Electron transferC c couplingRadical ionlawMolybdenumElectron paramagnetic resonanceChemistry - A European Journal
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Magnetic Molecular Conductors Based on Bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) and the Tris(chlorocyananilato)ferrate(III) Complex

2019

Electrocrystallization of the bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) organic donor in the presence of the [Fe(ClCNAn)3]3– tris(chlorocyananilato)ferrate(III) paramagnetic anion in different stoichiometric ratios and solvent mixtures afforded two different hybrid systems formulated as [BEDT-TTF]4[Fe(ClCNAn)3]·3H2O (1) and [BEDT-TTF]5[Fe(ClCNAn)3]2·2CH3CN (2) (An = anilato). Compounds 1 and 2 present unusual structures without the typical segregated organic and inorganic layers, where layers of 1 are formed by Λ and Δ enantiomers of the anionic paramagnetic complex together with mixed-valence BEDT-TTF tetramers, while layers of 2 are formed by Λ and Δ enantiomers of the paramagnetic…

Crystal structure010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundParamagnetismMolecular interactionsMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistry[CHIM.MATE]Chemical Sciences/Material chemistryMolecules3. Good health0104 chemical sciencesSolventCrystallographyMonomerchemistryRadical ionOligomersCrystal structuresSolventsStoichiometryTetrathiafulvaleneInorganic Chemistry
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Understanding the regioselectivity in hetero Diels–Alder reactions. An ELF analysis of the reaction between nitrosoethylene and 1-vinylpyrrolidine

2013

[EN] The regioselectivity in the hetero Diels-Alder reaction between nitrosoethylene 1 and 1-vinylpyrrolidine 2 has been studied by a comparative ELF bonding analysis along the IRC of the endo/ortho and endo/meta regioisomeric channels at the B3LYP/6-31G*. level. Along the most favorable endo/ortho regioisomeric channel, the C-C sigma bond is first formed by coupling of two pseudoradical centers located at the most electrophilic carbon of 1 and the most nucleophilic center of 2. Formation of these relevant pseudoradical centers, which depend on the total charge transfer process along the polar reaction, and not on the approach mode of each reagent, is well characterized by analysis of the a…

Electron localization functionParameterChemistryOrganic ChemistryDensityRegioselectivityPhotochemistryCycloaddition reactionBiochemistryBond-formationElectron localization functionIndexIonNucleophileRadical ionReagentDrug DiscoveryElectrophileDiels alderQuantitative characterizationElectrophilicityTopological analysis13-DipolarTetrahedron
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A crystalline radical cation derived from Thiele’s hydrocarbon with redox range beyond 1 V

2021

Thiele’s hydrocarbon occupies a central role as an open-shell platform for new organic materials, however little is known about its redox behaviour. While recent synthetic approaches involving symmetrical carbene substitution of the CPh2 termini yield isolable neutral/dicationic analogues, the intervening radical cations are much more difficult to isolate, due to narrow compatible redox ranges (typically  1 V), permitting its isolation in crystalline form. Further single-electron oxidation affords borenium dication 12+, thereby establishing an organoboron redox system fully characterized in all three redox states. We perceive that this strategy can be extended to other transient organic rad…

Electronic materialsRadicalScienceGeneral Physics and Astronomy010402 general chemistryPhotochemistryvapaat radikaalit01 natural sciencesRedoxArticleGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundhapetus-pelkistysreaktiochemistry.chemical_classificationRange (particle radiation)kemiallinen synteesiMultidisciplinary010405 organic chemistryQkationitfood and beveragesGeneral Chemistryhiilivedyt0104 chemical sciencesDicationHydrocarbonRadical ionchemistryYield (chemistry)CarbeneInorganic chemistry
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Enantiopure Conducting Salts of Dimethylbis(ethylenedithio)tetrathiafulvalene (DM‐BEDT‐TTF) with the Hexachlororhenate(IV) Anion

2014

Invited for the cover of this issue is the group of Narcis Avarvari (CIMI team) at the Laboratory MOLTECH-Anjou, UMR 6200 CNRS – Universite d'Angers, France. The cover image shows the enantiopure tetrathiafulvalene precursors used for the preparation of chiral radical cation conducting salts, together with an artwork of their packing diagrams and the suggested mirror image relationship between them.

Inorganic ChemistryCrystallographychemistry.chemical_compoundEnantiopure drugRadical ionChemistryInorganic chemistryChirality (chemistry)TetrathiafulvaleneIonEuropean Journal of Inorganic Chemistry
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Redox-Responsive Host–Guest Chemistry of a Flexible Cage with Naphthalene Walls

2020

"Naphthocage", a naphthalene-based organic cage, reveals very strong binding (up to 1010 M-1) to aromatic (di)cationic guests, i.e., the tetrathiafulvalene mono- and dication and methyl viologen. Intercalation of the guests between two naphthalene walls is mediated by C-H···O, C-H···π, and cation···π interactions. The guests can be switched into and out of the cage by redox processes with high binding selectivity. Oxidation of the flexible cage itself in the absence of a guest leads to a stable radical cation with the oxidized naphthalene intercalated between and stabilized by the other two. Encapsulated guest cations are released from the cavity upon cage oxidation, paving the way to futur…

Intercalation (chemistry)Cationic polymerizationmacromolecular substancesGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryRedoxCatalysis0104 chemical sciencesDicationchemistry.chemical_compoundColloid and Surface ChemistrychemistryRadical ionPolymer chemistryHost–guest chemistryTetrathiafulvaleneNaphthaleneJournal of the American Chemical Society
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Electrochemically Induced Reversible and Irreversible Coupling of Triarylamines

2011

The electrochemical coupling and dimerization behavior of the low molecular compounds triphenylamine (TPA) and 9-phenylcarbazole (PHC) in comparison to tri-p-tolylamine (p-TTA) with para-blocked methyl groups has been investigated in detail. In contrast to the unsubstituted radical cations of TPA and PHC, the radical cations of p-TTA are stable in the radical cation state and do not undergo any further coupling reactions. However, we found that the dicationic state of p-TTA does undergo two different competitive reaction pathways: (1) an irreversible intramolecular coupling reaction which leads to phenylcarbazole moieties and (2) a reversible intermolecular dimerization leading to charged σ…

Intermolecular forcePhotochemistryTriphenylamineElectrochemistryCoupling reactionSurfaces Coatings and FilmsCoupling (electronics)chemistry.chemical_compoundMonomerchemistryRadical ionIntramolecular forceMaterials ChemistryPhysical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Mesomorphic and electrooptical properties of viologens based on non-symmetric alkyl/polyfluoroalkyl functionalization and on an oxadiazolyl-extended …

2019

Two different sets of ionic liquid crystals based on bistriflimide salts of non-symmetrically substituted polyfluorinated bipyridinium (viologens) and bent symmetrically substituted dialkyl-oxadiazolyl-bipyridinium have been synthesized, in order to study the effect on the mesomorphic and electrooptical properties of the non-symmetric functionalization (alkyl chain and fluoroalkyl chains of different lengths) on the two pyridinium rings and additionally the effect of a bent conjugated spacer among the two pyridinium units of the viologen. POM and DSC characterization show that the synthesized salts have a mesomorphic and, in some cases, polymesomorphic behaviour in a wide thermal range, als…

Materials sciencePHASEATALUREN02 engineering and technologySALTS010402 general chemistry01 natural scienceschemistry.chemical_compoundMaterials ChemistrymedicineBistriflimideionic liquid crystals viologens fluoroalkyl chainsviologensfluoroalkyl chainsAlkylSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationREADTHROUGHDERIVATIVESIONIC LIQUID-CRYSTALSMesophaseViologenGeneral ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographyREDUCTIONRadical ionchemistryElectrochromismIonic liquidCOMPLEXESPyridiniumionic liquid crystalsPOLYMERS0210 nano-technologyCOLUMNARmedicine.drug
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Facile formation of a meso–meso linked porphyrin dimer catalyzed by a manganese(iv)–oxo porphyrin

2011

A manganese(IV)-oxo porphyrin catalyzes C-C bond formation between zinc porphyrins at the meso-position with a two-electron oxidant to afford the meso-meso linked porphyrin dimer efficiently. The meso-meso linked dimer is formed via formation of the porphyrin radical cation, and the rate-determining step in the catalytic cycle is the formation of a manganese(IV)-oxo porphyrin with a two-electron oxidant.

MetalloporphyrinsDimerchemistry.chemical_elementManganeseZincPhotochemistryCatalysisCatalysischemistry.chemical_compoundPolymer chemistrypolycyclic compoundsMaterials Chemistryheterocyclic compoundsChemistryfungiMetals and AlloysGeneral ChemistryBond formationPorphyrinSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialscarbohydrates (lipids)Manganese CompoundsRadical ionCatalytic cycleCeramics and CompositesDimerizationChemical Communications
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