Search results for "Electronic"

showing 10 items of 17076 documents

A cyanide and hydroxo-bridged nanocage: a new generation of coordination clusters.

2013

International audience; Combining serendipitously-formed hydroxo-clusters, [CoII3(OH)(piv)4(L)]+ (where L = MeCN or Hpiv), with assembling cyanide building block, [FeIII(Tp)(CN)3]−, has led to an unprecedented architecture where polymetallic cobalt clusters and blocked tris-cyanide iron complexes define the apexes of a unique magnetic cubic nanocage.

010405 organic chemistryCyanideInorganic chemistryMetals and Alloyschemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographyNanocageschemistryBlock (telecommunications)Materials ChemistryCeramics and Composites[CHIM.COOR]Chemical Sciences/Coordination chemistryCobaltChemical communications (Cambridge, England)
researchProduct

A polar/π model of interactions explains face-to-face stacked quinoid rings: a case study of the crystal of potassium hydrogen chloranilate dihydrate

2015

International audience; The nature of interactions between face-to-face staggered stacked quinoid rings with pi-systems, observed with a short inter-ring centroid. centroid distance, is analyzed by experimental and theoretical methods. Charge density studies based on X-ray diffraction and DFT calculations, complemented by impedance spectroscopy, were employed to define the electronic and structural characteristics of the quinoid rings responsible for their interactions within the crystal packing. The crystal packing is mainly stabilized by strong electrostatic interactions between the K+ cation and the hydrogen chloranilate anion. The proximity and orientation of the stacked quinoid rings i…

010405 organic chemistryHydrogen bondChemistryStackingCharge densityGeneral ChemistryElectronic structure010402 general chemistryCondensed Matter PhysicsElectrostaticsCrystal engineeringpi-interactions ; chloranilic acid ; X-ray charge density ; periodic DFT ; intermolecular interaction01 natural sciences0104 chemical sciencesIon[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystalCrystallography[CHIM.CRIS]Chemical Sciences/CristallographyGeneral Materials Science
researchProduct

Higher MLCT lifetime of carbene iron(ii) complexes by chelate ring expansion

2021

Combining strong σ-donating N-heterocyclic carbene ligands and π-accepting pyridine ligands with a high octahedricity in rigid iron(ii) complexes increases the 3MLCT lifetime from 0.15 ps in the prototypical [Fe(tpy)2]2+ complex to 9.2 ps in [Fe(dpmi)2]2+12+. The tripodal CNN ligand dpmi (di(pyridine-2-yl)(3-methylimidazol-2-yl)methane) forms six-membered chelate rings with the iron(ii) centre leading to close to 90° bite angles and enhanced iron-ligand orbital overlap.

010405 organic chemistryLigandMetals and AlloysGeneral ChemistryOrbital overlap010402 general chemistryRing (chemistry)01 natural sciencesCatalysisPyridine ligand0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographychemistryMaterials ChemistryCeramics and CompositesChelationCarbeneChemical Communications
researchProduct

Macrocyclic complexes based on [N⋯I⋯N]+ halogen bonds

2021

New 1–2 nm macrocyclic iodine(I) complexes prepared VIA a simple ligand exchange reaction manifest rigid 0.5–1 nm cavities that bind the hexafluorophosphate anion in the gas phase. The size of the cavities and the electrostatic interactions with the iodine(I) cations influence the anion binding properties of these macrocyclic complexes.

010405 organic chemistryLigandMetals and Alloyschemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrostaticsIodine01 natural sciencesCatalysis0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonGas phasechemistry.chemical_compoundchemistryHexafluorophosphatePolymer chemistryHalogenMaterials ChemistryCeramics and CompositesAnion bindingChemical Communications
researchProduct

Electrochemical meso-functionalization of magnesium(II) porphine

2010

International audience; Regioselective meso-functionalization of the totally unsubstituted magnesium(II) porphine was performed by controlled potential electrolysis with pyridine and triphenylphosphine as nucleophiles leading to the original pyridinium and phosphonium substituted derivatives, respectively. The crystallographic structure of the latter is described as the only meso-phosphonium porphyrin reported to date.

010405 organic chemistryMagnesiumMetals and AlloysRegioselectivitychemistry.chemical_elementGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesPorphyrinCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundNucleophilechemistryPolymer chemistryPyridineMaterials ChemistryCeramics and Composites[CHIM.COOR]Chemical Sciences/Coordination chemistryPhosphoniumPyridiniumTriphenylphosphine
researchProduct

Halide-Mediated Modification of Magnetism and Electronic Structure of α-Co(II) Hydroxides: Synthesis, Characterization, and DFT+U Simulations.

2019

The present study introduces a comprehensive exploration in terms of physicochemical characterization and calculations based on density functional theory with Hubbard's correction (DFT+U) of the whole family of α-Co(II) hydroxyhalide (F, Cl, Br, I). These samples were synthesized at room temperature by employing a one-pot approach based on the epoxide route. A thorough characterization (powder X-ray diffraction, X-ray photoelectron spectroscopy, thermogravimetric analysis/mass spectroscopy, and magnetic and conductivity measurements) corroborated by simulation is presented that analyzes the structural, magnetic, and electronic aspects. Beyond the inherent tendency of intercalated anions to …

010405 organic chemistryMagnetismepoxide routechemistry.chemical_elementHalideElectronic structure010402 general chemistrycobalt01 natural sciences0104 chemical sciencesCharacterization (materials science)//purl.org/becyt/ford/1 [https]Inorganic Chemistrychemistrymagnetism//purl.org/becyt/ford/1.4 [https]Physical chemistryDensity functional theoryPhysical and Theoretical Chemistrylayered hydroxidesCobaltFisicoquímicaInorganic chemistry
researchProduct

Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis

2018

[EN] A multicatalytic approach that combines a bifunctional Brønsted base¿squaramide organocatalyst and Ag+ as Lewis acid has been applied in the reaction of unactivated ketones with tert-butyl isocyanoacetate to give chiral oxazolines bearing a quaternary stereocenter. The formal [3+2] cycloaddition provided high yields of the corresponding cis-oxazolines with good diastereoselectivity and excellent enantioselectivity, being applied to aryl¿alkyl and alkyl¿alkyl ketones.

010405 organic chemistryMetals and AlloysEnantioselective synthesisGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCycloaddition0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundchemistryCatàlisiFISICA APLICADAOrganocatalysisMaterials ChemistryCeramics and CompositesLewis acids and basesBifunctionalQuímica orgànica
researchProduct

Unveiling the high reactivity of cyclohexynes in [3 + 2] cycloaddition reactions through the molecular electron density theory

2018

[3 + 2] cycloaddition (32CA) reactions of cyclohexyne, a cyclic strained acetylene, with methyl azide and methoxycarbonyl diazomethane have been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d) computational level. These 32CA reactions, which take place through a one-step mechanism involving highly asynchronous transition state structures, proceed with relatively low activation enthalpies of 6.0 and 4.3 kcal mol-1, respectively, both reactions being strongly exothermic. The reactions are initiated by the creation of a pseudoradical center at one of the two acetylenic carbons of cyclohexyne with a very low energy cost, 1.0 kcal mol-1, which promotes the eas…

010405 organic chemistryOrganic ChemistryRegioselectivityElectronic structure010402 general chemistry01 natural sciencesBiochemistryCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryAcetyleneComputational chemistrySingle bondReactivity (chemistry)Physical and Theoretical ChemistryGround stateMethyl azideOrganic & Biomolecular Chemistry
researchProduct

Formation and trapping of the thermodynamically unfavoured inverted-hemicucurbit[6]uril

2019

Amplification of a thermodynamically unfavoured macrocyclic product through the directed shift of the equilibrium between dynamic covalent chemistry library members is difficult to achieve. We show for the first time that during condensation of formaldehyde and cis-N,N'-cyclohexa-1,2-diylurea formation of inverted-cis-cyclohexanohemicucurbit[6]uril (i-cis-cycHC[6]) can be induced at the expense of thermodynamically favoured cis-cyclohexanohemicucurbit[6]uril (cis-cycHC[6]). The formation of i-cis-cycHC[6] is enhanced in low concentration of the templating chloride anion and suppressed in excess of this template. We found that reaction selectivity is governed by the solution-based template-a…

010405 organic chemistryPrecipitation (chemistry)Metals and AlloysDiastereomerGeneral ChemistryTrapping010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryComputational chemistryYield (chemistry)Materials ChemistryCeramics and CompositesTrifluoroacetic acidDynamic combinatorial chemistrySelectivityBinding affinitiesChemical Communications
researchProduct

Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness.

2016

The cooperative supramolecular polymerization of 1 and 2 yields P- or M-type helical aggregates depending on the absolute configuration (S or R) of the stereogenic centres attached to the side chains. The connectivity of the amide group does not affect the handedness of the helical aggregates, but determines a larger cooperativity for retroamides 1.

010405 organic chemistryStereochemistryMetals and AlloysSupramolecular chemistryAbsolute configurationCooperativityGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundCrystallographychemistryPolymerizationAmideMaterials ChemistryCeramics and CompositesSide chainChemical communications (Cambridge, England)
researchProduct