Search results for "Complexes."

showing 10 items of 857 documents

Heats and Entropies of Reaction of Transition Metal Ions with Ethylenediamine

1960

THE heats of formation of complexes between ligands and metal ions are very important to further the ligand field-theory and check its implications. Until now, only the heats of hydration of the first transition group ions have been used for this purpose1 as the thermochemical data on the complexes formed by ligands other than water are very incomplete. The transition metal complexes of ethylenediamine, which have a very nearly octahedral configuration, could also be fruitfully studied in terms of ligand field-theory. Unfortunately only the thermal data on nickel (II), copper (II) and zinc (II) complexes are known2, and so the formation constants have been used instead of the values of enth…

MultidisciplinaryLigandMetal ions in aqueous solutionInorganic chemistrychemistry.chemical_elementEthylenediamineCopperStandard enthalpy of formationNickelchemistry.chemical_compoundchemistryTransition metalStability constants of complexesPhysical chemistryNature
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Conformational changes in Cmethyl-resorcinarene pyridine N -oxide inclusion complexes in the solid state

2016

Aromatic N-oxides interact with Cmethyl-resorcinarene resulting in marked changes in the conformation of the host resorcinarene. In the solid state, 2- and 3-methylpyridine N-oxides form pseudo-capsular 2 : 2 endo host-guest complexes with Cmethyl-resorcinarene stabilized by C-H⋯π interactions. The Cmethyl-resorcinarene·2-methylpyridine N-oxide complex has a C4v crown conformation, while the Cmethyl-resorcinarene·3-methylpyridine N-oxide complex has a slightly open C2v boat conformation. On the contrary, other para-substituted and benzo-fused pyridine N-oxides form only exo complexes with Cmethyl-resorcinarene. In the exo complexes, the asymmetry of the guest, conformational flexibility and…

N-oxidesHydrogenta114010405 organic chemistryChemistryStereochemistryHydrogen bondCyclohexane conformationSolid-statechemistry.chemical_elementPyridine-N-oxidemacromolecular substancesGeneral ChemistryResorcinarene010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundPyridineGeneral Materials ScienceN-oxide inclusion complexesta116CRYSTENGCOMM
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Endo-/Exo- and Halogen Bonded Complexes of Conformationally Rigid Cethyl-2-bromoresorcinarene and aromatic N-oxides

2017

The host–guest complexes of conformationally rigid C-ethyl-2-bromoresorcinarene with aromatic N-oxides were studied using single crystal X-ray crystallography. Unlike that of the conformationally more flexible C-ethyl-2-methylresorcinarene, the C-ethyl-2-bromoresorcinarene cavity forms endo-complexes only with the small pyridine-N-oxides, such as pyridine N-oxide, 2-methyl-, 3-methyl- and 4-methylpyrdine N-oxide, and quinoline N-oxide. The larger 2,4,6-trimethylpyridine, 4-phenylpyridine and isoquinoline N-oxide, and 4,4-bipyridine N,N′-dioxide and 1,3-bis(4-pyridyl)propane N,N′-dioxide do not fit into the host cavity. Instead endo-acetone complexes are formed. Remarkably, differing from th…

N-oxideshalogen bonded complexeshost-guest complexes
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Endo-/exo- and halogen-bonded complexes of conformationally rigid C-ethyl-2-bromoresorcinarene and aromatic N-oxides

2017

The host-guest complexes of conformationally rigid C-ethyl-2-bromoresorcinarene with aromatic N-oxides were studied using single crystal X-ray crystallography. Unlike that of the conformationally more flexible C-ethyl-2-methylresorcinarene, the C-ethyl-2-bromoresorcinarene cavity forms endo-complexes only with the small pyridine-N-oxides, such as pyridine N-oxide, 2-methyl-, 3-methyl- and 4-methylpyrdine N-oxide, and quinoline N-oxide. The larger 2,4,6-trimethylpyridine, 4-phenylpyridine and isoquinoline N-oxide, and 4,4-bipyridine N,N′-dioxide and 1,3-bis(4-pyridyl)propane N,N′-dioxide do not fit into the host cavity. Instead endo-acetone complexes are formed. Remarkably, differing from th…

N-oxidesta114010405 organic chemistryStereochemistryQuinolinehalogen bonded complexesGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural scienceshost-guest complexes0104 chemical sciencesChemistrychemistry.chemical_compoundchemistryPropanePyridineHalogenGeneral Materials ScienceIsoquinolineta116Single crystalBiochemistry Biophysics and Structural BiologyCrystEngComm
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NHC-Based Iron Sensitizers for DSSCs

2018

International audience; Nanostructured dye-sensitized solar cells (DSSCs) are promising photovoltaic devices because of their low cost and transparency. Ruthenium polypyridine complexes have long been considered as lead sensitizers for DSSCs, allowing them to reach up to 11% conversion efficiency. However, ruthenium suffers from serious drawbacks potentially limiting its widespread applicability, mainly related to its potential toxicity and scarcity. This has motivated continuous research efforts to develop valuable alternatives from cheap earth-abundant metals, and among them, iron is particularly attractive. Making iron complexes applicable in DSSCs is highly challenging due to an ultrafa…

NHC ligands[CHIM.ORGA]Chemical Sciences/Organic chemistry[CHIM.COOR] Chemical Sciences/Coordination chemistry[CHIM.ORGA] Chemical Sciences/Organic chemistrylcsh:QD146-197[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryiron complexes[CHIM] Chemical Scienceslcsh:Inorganic chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryexcited statesCèl·lules fotoelèctriquesphotophysicsFerro
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Recent Advances of Spin Crossover Research

2004

Thermal spin transition (spin crossover), one of the most fascinating dynamic electronic structure phenomena occurring in coordination compounds of third row transition metal ions, mostly of iron(II), iron(III) and cobalt(II) with critical ligand field strengths competing with the spin pairing energy, has attracted increasing attention by many research groups. One of the reasons is the promising potential for practical applications. In this chapter we intend to cover essential recent work, primarily accomplished within the European research network on "Thermal and Optical Switching of Molecular Spin States (TOSS)". New spin crossover compounds and their thermal spin transition behaviour, al…

NUCLEAR INELASTIC-SCATTERINGLigand field theorySpin statescooperativitySpin transitionElectronic structurephysical propertiespressurespin crossoverSpin crossoverINTRAMOLECULAR MAGNETIC INTERACTIONlight effectsIRON(II) COMPLEXESSpin-½TRANSITION MOLECULAR MATERIALSLONG-RANGE INTERACTIONCondensed matter physicsChemistrySpin engineeringISING-LIKE SYSTEMSPairingPHOTOINDUCED PHASE-TRANSITIONSTATE TRAPPING LIESSTCondensed Matter::Strongly Correlated ElectronsX-RAY-STRUCTURELIGHT-INDUCED BISTABILITY
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Hydrolysis of Monomethyl-, Dimethyl-, and Trimethyltin(IV) Cations in Fairly Concentrated Aqueous Solutions at I = 1 mol L-1 (NaNO3) and T = 298.15 K…

2011

The hydrolysis of methyltin(IV) cations at fairly high concentrations was investigated to evaluate the formation of polynuclear species in aqueous solution. The hydrolysis of monomethyltin(IV), dimethyltin(IV), and trimethyltin(IV) was studied by potentiometry at T = 298.15 K and at I = 1 mol L-1 in NaNO3 aqueous solutions. The results obtained gave evidence for the formation of the following polynuclear species, in addition to the mononuclear species already reported, which were also considered in the models proposed for the three systems investigated: [(CH3)Sn(OH)3]0, [(CH3)Sn(OH)4]-, [((CH3)Sn)2(OH)4]2+, [((CH3)Sn)2(OH)5]+, [((CH3)Sn)2(OH)7]-, [((CH3)Sn)3(OH)5]4+, [((CH3)Sn)3(OH)7]2þ, [(…

NUCLEAR-MAGNETIC-RESONANCE; HYDROXO COMPLEXES; IONIC-STRENGTH DEPENDENCE; SN-119 NMR-SPECTROSCOPYAqueous solutionChemistryStereochemistryHYDROXO COMPLEXESGeneral Chemical EngineeringGeneral ChemistryMedicinal chemistrySN-119 NMR-SPECTROSCOPYHydrolysisIONIC-STRENGTH DEPENDENCEMolespeciation organotin hydrolysis polynuclear speciesSettore CHIM/01 - Chimica AnaliticaNUCLEAR-MAGNETIC-RESONANCE
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Polynitrile anions as ligands: From magnetic polymeric architectures to spin crossover materials

2010

International audience; The use of polynitrile anions as ligands (L) either alone or in combination with neutral co-ligands (L′) is a very promising and appealing strategy to get molecular architectures with different topologies and dimensionalities thanks to their ability to coordinate and bridge metal ions in many different ways. The presence of several potentially coordinating nitrile groups (or even other donor groups as –OH, –SH or –NH2), their rigidity and their electronic delocalization allow the synthesis of original magnetic high dimensional coordination polymers with transition metals ions. Furthermore, these ligands have shown coordinating and bridging capabilities in novel discr…

NitrileMetal ions in aqueous solutionMetal(II) complexesInorganic chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesCoordination complexInorganic ChemistryDelocalized electronchemistry.chemical_compoundTransition metalSpin crossoverMagnetic propertiesMagnetic transitionMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistrychemistry.chemical_classificationThermochromismThermochromism010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryPolymer0104 chemical sciencesCoordination polymersCrystallographyPolynitrilechemistryStructural transitionNitrile ligandCyano ligand
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Pt(II) nitrile complexes: New insights on old complexes from a combined experimental and theoretical study

2017

Abstract The spectroscopic characterization of cis - and trans -[PtCl 2 (NCR) 2 ] (R = CH 3 , Ph, CH 2 Ph) was reported in solid state and solution phase. Moreover, the X-ray structures of cis -[PtCl 2 (NCCH 3 ) 2 ], cis - and trans -[PtCl 2 (NCPh) 2 ] were redetermined at low temperature. FT-IR and NMR showed a blue-shift and a slight shielding of the νCN and δ ( 13 C CN ) values, respectively, in a counterintuitive way with respect to the well known improved reactivity towards nucleophiles of nitriles ligands coordinated to platinum(II), when compared to their free forms. These spectroscopic behaviors were also confirmed by theoretical experiments at DFT level. Moreover, DFT approach show…

NitrileStereochemistrySolid-statechemistry.chemical_elementTheoretical calculations010402 general chemistry01 natural sciencesMedicinal chemistryCP MAS NMR studyInorganic Chemistrychemistry.chemical_compoundNucleophilePlatinum nitrile complexesMaterials ChemistryOrbital controlReactivity (chemistry)Platinum nitrile complexePhysical and Theoretical Chemistry010405 organic chemistrySolution phase0104 chemical sciencesBenzonitrilechemistrySettore CHIM/03 - Chimica Generale E InorganicaCP MAS NMR study; Platinum nitrile complexes; Spectroscopic characterization; Theoretical calculationsSpectroscopic characterizationPlatinum
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Half-sandwich Mo(III) complexes with asymmetric diazadiene ligands

2006

The asymmetric 1,4-diazadiene ligands R ∗ N CHCH NR ∗ [R ∗  = ( S )-CH(CH 3 )Ph], R 2 ∗ dad , and 2,2′-bis(4-ethyloxazoline), as-ox, have been used to generate half-sandwich Mo III derivatives by addition to Cp 2 Mo 2 Cl 4 . Ligand R 2 ∗ dad affords a mononuclear, paramagnetic 17-electron product, CpMoCl 2 ( R 2 ∗ dad ) , whereas as-ox leads to the isolation of a dinuclear compound where only one molecule of ligand has been added per two Mo atoms, Cp 2 Mo 2 Cl 4 (as-ox). In the presence of free as-ox, this compound coexists with the paramagnetic mononuclear complex in solution. Both products are capable of controlling the radical polymerization of styrene under typical atom transfer radical…

Nitroxide mediated radical polymerizationRadical polymerizationHalf-sandwich complexesDiazadiene010402 general chemistry01 natural sciencesMedicinal chemistryStyreneInorganic Chemistrychemistry.chemical_compoundTacticityPolymer chemistryMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryPolystyreneAtom transfer radical polymerizationMolybdenum010405 organic chemistryLigandAtom-transfer radical-polymerization[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymerschemistryPolystyreneInorganica Chimica Acta
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