Search results for " theoretical"

showing 10 items of 9066 documents

Cis- and trans molybdenum oxo complexes of a prochiral tetradentate aminophenolate ligand : Synthesis, characterization and oxotransfer activity

2020

Abstract Reaction of [MoO2Cl2(dmso)2] with the tetradentate O2N2 donor ligand papy [H2papy = N-(2-hydroxybenzyl)-N-(2-picolyl)glycine] leads to formation of the dioxomolybdenum(VI) complex [MoO2(papy)] (1) as a mixture of cis and trans isomers. Recrystallization from methanol furnishes solid cis-1, whereas the use of a dichloromethane-hexane mixture allows for the isolation of the trans-1 isomer. Both isomers have been structurally characterized by X-ray crystallography and the energy difference between the isomeric pair has been investigated by electronic structure calculations. Optimization of two configurational isomers in the gas phase predicts the trans isomer to lie 2.5 kcal/mol lower…

010405 organic chemistryChemistrycomputational modellingStereoisomerism010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic ChemistrySolventvariable temperature NMRTripodal ligandepoxidationMaterials ChemistryTheoretical chemistryProton NMRtripodal ligandPhysical and Theoretical ChemistryIsomerizationOxo Atom TransferCis–trans isomerism
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Versatile behavior of conjugated diynes with zirconocene reactive species

2008

Thermal decomposition of Cp2ZrPh2 in the presence of the buta-1,3-diynes RC≡CC≡CR (R = Ph, SiMe3) can lead to seven- or five-membered metallacycles. In both cases a stable benzo-fused seven-membered zirconacyclocumulene arising from a 2-fold insertion of the triple bonds of the dialkyne in the in situ generated zirconocene benzyne is formed. In the case of Me3SiC≡CC≡CSiMe3 a second minor complex is isolated: a 3-alkynyl-substituted zirconaindene arising from a β monoinsertion of one acetylenic function of the conjugated diyne in the zirconocene benzyne. No stable 2-alkynyl-substituted zirconacycle was isolated. This α monoinsertion complex is an intermediate in the exchange of the metalated…

010405 organic chemistryChemistrycycloaddition reactionOrganic ChemistryThermal decomposition[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementmetalationConjugated system010402 general chemistryTriple bond01 natural sciencesAryne0104 chemical sciencesInorganic ChemistrycyclometalationAntimonyReagentAtomPolymer chemistryMoiety[CHIM.COOR]Chemical Sciences/Coordination chemistryzirconocene- benzyn intermediatePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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Stepwise Construction of Heterobimetallic Cages by an Extended Molecular Library Approach.

2017

Two novel heterobimetallic complexes, a trigonal-bipyramidal and a cubic one, have been synthesized and characterized using the same C3-symmetric metalloligand, prepared by a simple subcomponent self-assembly strategy. Adopting the molecular library approach, we chose a mononuclear, preorganized iron(II) complex as the metalloligand capable of self-assembly into a trigonal-bipyramidal or a cubic aggregate upon coordination to cis-protected C2-symmetric palladium(II) or unprotected tetravalent palladium(II) ions, respectively. The trigonal-bipyramidal complex was characterized by NMR and UV–vis spectroscopy, electrospray ionization mass spectrometry (ESI-MS), and single-crystal X-ray diffrac…

010405 organic chemistryChemistrytrigonal-bipyramidal and cubic heterobimetallic cagesElectrospray ionizationchemistry.chemical_element010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesIonInorganic ChemistryCrystallographyPhysical and Theoretical ChemistrySpectroscopyta116extended molecular library approachPalladiumInorganic chemistry
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Variable Cooperative Interactions in the Pressure and Thermally Induced Multistep Spin Transition in a Two-Dimensional Iron(II) Coordination Polymer

2020

Two types of experiments conducted to investigate the effect of pressure on the spin crossover (SCO) properties of the 2D Fe(II) coordination polymer formulated {Fe[bipy(ttr)2]}n are reported, namely, (1) magnetic measurements performed at variable temperature and at fixed pressure and (2) visible spectroscopy at variable pressure and fixed temperature. The magnetic experiments carried out under a hydrostatic pressure constraint of 0.04, 0.08, and 0.8 GPa reveal a two-step spin transition behavior. The characteristic critical temperatures of the spin transition are shifted upward in temperature as pressure increases. The slope of the straight-line of the Tc vs P plot, dTc/dP, is 775 K/GPa a…

010405 organic chemistryCoordination polymerHydrostatic pressureSpin transitionElastic energyThermodynamicsFlory–Huggins solution theory010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundUltraviolet visible spectroscopychemistrySpin crossoverLattice (order)Physical and Theoretical ChemistryInorganic Chemistry
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A novel two-dimensional organostannoxane coordination network promoted by phenazine: Synthesis, characterization and X-ray structure of

2009

Abstract Reaction of the dimeric hydroxo di-n-butylstannane trifluoromethanesulfonato complex [n-Bu2Sn(μ-OH)(H2O)0.5(η1-O3SCF3)]2 (1) with phenazine (C12H8N2, Phz) (2) in dichloromethane at room temperature in a 1:3 molar ratio yielded the novel two-dimensional organometallic coordination polymer 2 ∞ { [ n - Bu 2 ( μ -OH ) SnOSn ( μ - η 2 - O 3 SCF 3 ) n - Bu 2 ] 2 [ n - Bu 2 ( μ -OH ) SnOSn ( η 1 - O 3 SCF 3 ) n - Bu 2 ] 2 } (3), together with the phenazinium trifluoromethanesulfonate salt [C12H9N2]+ [CF3SO3]−, crystallographically isolated in two different structural arrangements, free 4 and in π–π aromatic stacking interaction with independent intercalated non-protonated phenazine molecu…

010405 organic chemistryCoordination polymerOrganic ChemistryIntermolecular forcePhenazineSupramolecular chemistryStacking010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistryTrifluoromethanesulfonateDichloromethaneJournal of Organometallic Chemistry
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New crystal structures of fluorinated α-aminophosphonic acid analogues of phenylglycine

2020

The four novel phosphonic acid analogues of phenylglycine with various substituents in phenyl ring (mostly fluorine atoms) have been synthesized by using procedure of amidoalkylation of phosphorus trichloride with aromatic aldehydes and acetamide. The NMR, ESI-MS spectroscopy, and single-crystal X-Ray diffraction methods were used to characterize unusual structures: the amino-(4-trifluoromethylbenzyl)-(1), amino-(3,4-difluorobenzyl)-(2), amino-(2,4,6-trifluorobenzyl)-(3), and amino-(2-fluoro-4-hydroxybenzyl)-(4) phosphonic acids. Since the α-aminophosphonates have a potential for biological activity and could be used as building blocks in medicinal chemistry, it is important to know their d…

010405 organic chemistryCrystal and molecular structureschemistry.chemical_elementBiological activityCrystal structure010402 general chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciencesMedicinal chemistryNMRESI-MS spectra0104 chemical sciencesTurn (biochemistry)chemistry.chemical_compoundchemistryFluorinated α-aminophosphonic acidFluorinePhosphorus trichloridePhysical and Theoretical ChemistrySpectroscopyAcetamideStructural Chemistry
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Synthesis, crystal structures and magnetic properties of picolinate-bridged copper(II) chains

2018

The paper reports the synthesis, crystal structures, and magnetic properties of two copper(II) coordination polymers, Cu2(L1)4 (1) and Cu3(L2)6 (2), based on rigid ethynylene-bridged ditopic ligands containing one picolinate subunit (L1 = 5-(pyridin-3-ylethynyl)picolinate anion; L2 = 5-((4-(methoxycarbonyl)phenyl)ethynyl)picolinate anion). Both 1 and 2 have a chain structure. In 1, the repeating unit in the chain is a doubly bridged picolinate dicopper(II) complex, whereas 2 is built upon trimeric units where the Cu2+ ions are also connected by double picolinate bridges. Both compounds exhibit antiferromagnetic interactions in the solid state. The magnetic properties of 1 and 2 were analyze…

010405 organic chemistryDimerIntermolecular forcechemistry.chemical_elementTrimerCrystal structure010402 general chemistry01 natural sciencesCopper0104 chemical sciencesIonchemistry.chemical_compoundCrystallographychemistryMaterials ChemistryAntiferromagnetismMetal-organic frameworkPhysical and Theoretical Chemistry
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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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A Generalized Semiempirical Approach to the Modeling of the Optical Band Gap of Ternary Al-(Ga, Nb, Ta, W) Oxides Containing Different Alumina Polymo…

2021

A generalization of the modeling equation of optical band gap values for ternary oxides, as a function of cationic ratio composition, is carried out based on the semiempirical correlation between the differences in the electronegativity of oxygen and the average cationic electronegativity proposed some years ago. In this work, a novel approach is suggested to account for the differences in the band gap values of the different polymorphs of binary oxides as well as for ternary oxides existing in different crystalline structures. A preliminary test on the validity of the proposed modeling equations has been carried out by using the numerous experimental data pertaining to alumina and gallia p…

010405 organic chemistryGeneralizationChemistryBand gapCationic polymerizationThermodynamicsFunction (mathematics)Aluminum oxideComposition (combinatorics)010402 general chemistry01 natural sciencesArticleMixed oxides0104 chemical sciencesInorganic ChemistryCondensed Matter::Materials ScienceSettore ING-IND/23 - Chimica Fisica ApplicataBand GapPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryTernary operation
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A family of layered chiral porous magnets exhibiting tunable ordering temperatures.

2013

A simple change of the substituents in the bridging ligand allows tuning of the ordering temperatures, Tc, in the new family of layered chiral magnets A[M(II)M(III)(X2An)3]·G (A = [(H3O)(phz)3](+) (phz = phenazine) or NBu4(+); X2An(2-) = C6O4X2(2-) = 2,5-dihydroxy-1,4-benzoquinone derivative dianion, with M(III) = Cr, Fe; M(II) = Mn, Fe, Co, etc.; X = Cl, Br, I, H; G = water or acetone). Depending on the nature of X, an increase in Tc from ca. 5.5 to 6.3, 8.2, and 11.0 K (for X = Cl, Br, I, and H, respectively) is observed in the MnCr derivative. Furthermore, the presence of the chiral cation [(H3O)(phz)3](+), formed by the association of a hydronium ion with three phenazine molecules, lead…

010405 organic chemistryHexagonal crystal systemInorganic chemistryPhenazineBridging ligand010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMagnetAcetone[CHIM]Chemical SciencesMoleculePhysical and Theoretical ChemistryPorosityComputingMilieux_MISCELLANEOUSDerivative (chemistry)Inorganic chemistry
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