Search results for "Complexes."

showing 10 items of 857 documents

Orbital Decomposition of the Carbon Chemical Shielding Tensor in Gold(I) N-Heterocyclic Carbene Complexes.

2020

The good performance of N‐heterocyclic carbenes (NHCs), in terms of versatility and selectivity, has called the attention of experimentalists and theoreticians attempting to understand their electronic properties. Analyses of the Au(I)–C bond in [(NHC)AuL]+/0 (L stands for a neutral or negatively charged ligand), through the Dewar–Chatt–Duncanson model and the charge displacement function, have revealed that NHC is not purely a σ‐donor but may have a significant π‐acceptor character. It turns out, however, that only the σ‐donation bonding component strongly correlates with one specific component of the chemical shielding tensor. Here, in extension to earlier works, a current density analysi…

C-13 NMR-SPECTROSCOPYElectronic structureRING CURRENTS010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundDONATION Author InformationGROUP-11MAGNETIC-PROPERTIESTensorGold(I) NHC ComplexesFull Paper010405 organic chemistryChemistryLigandElectron donationCAPTIVE INTERMEDIATEFull PapersSymmetry (physics)0104 chemical sciencesChemical shielding tensorChemistryChemical physicsElectron back‐donationElectromagnetic shieldingElectron back-donationPATTERNSDiamagnetismDONATIONGoldCarbeneCurrent densityCarbene ligandsCONTINUOUS TRANSFORMATIONBONDAPPROXIMATIONEuropean journal of inorganic chemistry
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Supramolecular Construction of Cyanide-Bridged Re I Diimine Multichromophores

2019

The reactions of labile [Re(diimine)(CO)3(H2O)]+ precursors (diimine = 2,2′-bipyridine, bpy; 1,10-phenanthroline, phen) with dicyanoargentate anion produce the dirhenium cyanide-bridged compounds [{Re(diimine)(CO)3}2CN)]+ (1 and 2). Substitution of the axial carbonyl ligands in 2 for triphenylphosphine gives the derivative [{Re(phen)(CO)2(PPh3)}2CN]+ (3), while the employment of a neutral metalloligand [Au(PPh3)(CN)] affords heterobimetallic complex [{Re(phen)(CO)3}NCAu(PPh3)]+ (4). Furthermore, the utilization of [Au(CN)2]−, [Pt(CN)4]2–, and [Fe(CN)6]4–/3– cyanometallates leads to the higher nuclearity aggregates [{Re(diimine)(CO)3NC}xM]m+ (M = Au, x = 2, 5 and 6; Pt, x = 4, 7 and 8; Fe, x…

CARBONYL-COMPLEXESSPECTROSCOPIC PROPERTIESCyanideSupramolecular chemistryEXCITED-STATECrystal structure010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundCRYSTAL-STRUCTUREPhysical and Theoretical ChemistryTriphenylphosphineta116MULTIPLE EMISSIONSDiimineDENSITY-FUNCTIONAL METHODS010405 organic chemistryLUMINESCENT RE(I)0104 chemical sciencesRHENIUM(I) TRICARBONYL COMPLEXESCrystallographychemistryExcited statePHOTOPHYSICAL PROPERTIESPhosphorescenceCOORDINATION POLYMERSDerivative (chemistry)INORGANIC CHEMISTRY
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Cobalt Electrolyte/Dye Interactions in Dye-Sensitized Solar Cells: A Combined Computational and Experimental Study

2012

We report a combined experimental and computational investigation to understand the nature of the interactions between cobalt redox mediators and TiO2 surfaces sensitized by :ruthenium and organic dyes, and their impact on. the performance of the corresponding dye-sensitized solar cells (DSSCs). We : focus: on different ruthenium dyes and fully organic dyes, to understand the dramatic loss of efficiency observed for the prototype Ru(II) N719 dye in conjunction with :Cobalt: electrolytes. Both N719- and Z907-based DSSCs showed an increased lifetime in iodine-based electrolyte compared to the cobalt-based redox-shuttle; While the organic D21L6 and D25L6 cycles endowed.With long alkoxy chains,…

COLLOIDAL TIO2 FILMSinorganic chemicalsLOW QUANTUM YIELDSInorganic chemistrychemistry.chemical_element02 engineering and technologyElectrolyte010402 general chemistryPhotochemistry01 natural sciencesBiochemistryRedoxREDOX COUPLECatalysisEFFECTIVE CORE POTENTIALSDENSITY-FUNCTIONAL THEORYColloid and Surface ChemistryDENSITY-FUNCTIONAL THEORY; EFFECTIVE CORE POTENTIALS; INTRAMOLECULAR ELECTRON-TRANSFER; TRANSITION-METAL-COMPLEXES; COLLOIDAL TIO2 FILMS; LOW QUANTUM YIELDS; MOLECULAR CALCULATIONS; REDOX COUPLE; MAGNETIC-PROPERTIES; PHOTOVOLTAIC CELLSMAGNETIC-PROPERTIESPHOTOVOLTAIC CELLSLigandGeneral Chemistry021001 nanoscience & nanotechnologyMOLECULAR CALCULATIONSTRANSITION-METAL-COMPLEXES0104 chemical sciencesMarcus theoryRutheniumDye-sensitized solar cellchemistryAlkoxy groupINTRAMOLECULAR ELECTRON-TRANSFER0210 nano-technologyCobalt
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Pulse EPR methods for studying chemical and biological samples containing transition metals

2006

This review discusses the application of pulse EPR to the characterization of disordered systems, with an emphasis on samples containing transition metals. Electron nuclear double-resonance (ENDOR), electron-spin-echo envelope-modulation (ESEEM), and double electron-electron resonance (DEER) methodologies are outlined. The theory of field modulation is outlined, and its application is illustrated with DEER experiments. The simulation of powder spectra in EPR is discussed, and strategies for optimization are given. The implementation of this armory of techniques is demonstrated on a rich variety of chemical systems: several porphyrin derivatives that are found in proteins and used as model s…

CONTINUOUS-WAVEAnalytical chemistryElectronBiochemistryResonance (particle physics)CatalysisSpectral linelaw.inventionInorganic ChemistryELECTRON-PARAMAGNETIC-RESONANCEchemistry.chemical_compoundTransition metallawDrug DiscoveryPhysical and Theoretical ChemistryElectron paramagnetic resonanceENVELOPE MODULATIONChemistryPulsed EPROrganic ChemistryPorphyrinSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)COENZYME-M-REDUCTASECharacterization (materials science)Chemical physicsRADICAL COMPLEXESSPIN SYSTEMSHELVETICA CHIMICA ACTA
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Spectroscopic, crystal structural, theoretical and biological studies of phenylacetohydrazide Schiff base derivatives and their copper complexes

2020

Two phenylacetohydrazide Schiff base derivatives: N’-(1-(2-hydroxyphenyl)ethylidene)-2-phenylacetohydrazide, HL1, and N’-((1-hydroxynaphthalen-2-yl)methylene)-2-phenylacetohydrazide, HL2, were synthesized. HL1 dimerizes in presence of HCl, probably via radical mechanism to give (2,2’-((1E)-hydrazine-1,2-diylidenebis(ethan-1-yl-1-ylidene))diphenol (DIM). Thermal reactions of Cu(II) ions with the two Schiff base ligands resulted in formation of the binuclear complexes [(CuL1)2] and [(CuL2)2]. The stoichiometry and structures of the reported compounds were investigated by several spectroscopic and analytical techniques. The structure of the HL1 ligand and its complex [(CuL1)2] as well as the D…

CT-DNA bindingantioxidant activitychemistry.chemical_elementkupari010402 general chemistry01 natural sciencesAnalytical ChemistryInorganic Chemistrykemialliset sidoksetchemistry.chemical_compoundDFT studiesReactivity (chemistry)copper complexesMethyleneSpectroscopyantioksidantitSchiff base010405 organic chemistryLigandtiheysfunktionaaliteoriaOrganic Chemistrymolecular dockingkompleksiyhdisteetCopper0104 chemical sciencesCrystallographyMolecular geometrychemistrySingle crystalröntgenkristallografiaStoichiometryX-ray analysisJournal of Molecular Structure
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Chemical speciation of nucleotide 5′-monophosphates in the presence of biogenic amines

2001

The interaction of adenosine-, uridine-, inosine- and guanosine-5’-monophosphates with protonated ethylenediamine, putrescine, cadaverine, spermidine and spermine, was studied potentiometrically, a...

CadaverineChemical Health and SafetyStereochemistryHealth Toxicology and MutagenesisSpermineEthylenediamineToxicologyMedicinal chemistryBiogenic PolyaminesUridineSpermidinechemistry.chemical_compoundchemistrynucleotide 5′-monophosphates; biogenic polyamines; nucleotide 5′-monophosphate-polyammonium cation complexes; speciationmedicinePutrescineInosinemedicine.drug
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Interactions of Dioxouranium(VI) with Amines in Aqueous Solution

2010

The interaction of the dioxouranium(VI) ion with five low molecular weight polyamines (ethylenediamine, putrescine, cadaverine, spermidine, and spermine) and with poly(allyl)amine (15 kDa) was studied potentiometrically (ISE-H + glass electrode) at T ) 298.15 K. Investigations were carried out in NaNO3 ionic medium, at I ) 0.1 mol · L -1 (and 0.5 mol · L -1 for poly(allyl)amine only), in the pH range 3.5 to 5.5, before the formation of uranyl insoluble species. The results gave evidence for the formation of two species, namely, UO2L 2+ and UO2L(OH) + for the diamine systems (ethylenediamine, putrescine, cadaverine), UO2L 2+ and UO2LH 3+ for spermidine, and UO2LH 3+ and UO2LH2 4+ for spermin…

CadaverineGeneral Chemical EngineeringInorganic chemistryEthylenediamineGeneral Chemistrydioxouranium; sequestrationMedicinal chemistrySpermidinestability constantschemistry.chemical_compoundchemistryaminespeciationStability constants of complexesuranylDiaminePutrescineQualitative inorganic analysisSettore CHIM/01 - Chimica AnaliticaPolyamine
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Formation and Stability of Cadmium(II)/Phytate Complexes by Different Electrochemical Techniques. Critical Analysis of Results

2010

In the present work the stability constants of various cadmium(II)/phytate (Phy) species were determined at T = 298.15 K in NaNO3(aq) at I = 0.1 mol·L−1 by DP-ASV (Differential Pulse Anodic Stripping Voltammetry) and by potentiometric titrations using an ISE-Cd2+. Cyclic voltammograms were also recorded to check the electrochemical behavior of cadmium in the presence of phytate. The results were analyzed together with previous data determined by ISE-H+ measurements. Data obtained were used to provide an exhaustive speciation scheme for the phytate/cadmium(II) system at different conditions, as well as a comprehensive representation of the binding ability of phytate toward cadmium(II). Diffe…

CadmiumChemistryInorganic chemistryPotentiometric titrationBiophysicsAnalytical chemistrychemistry.chemical_elementElectrochemistryBiochemistryPhytate Cadmium Voltammetry ISE-Cd2+ SpeciationBinding abilityAnodic stripping voltammetryPhytate; Cadmium; Voltammetry; ISE-Cd; SpeciationStability constants of complexesSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistryMolecular BiologyVoltammetry
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Manganese carbonyl terpyridyl complexes: their synthesis, characterization and potential application as CO-release molecules

2014

MnI carbonyl terpyridyl complexes have been synthesized and characterized. The tricarbonyl derivative exhibits interesting behaviors for controlled CO-release by both thermal and photosynthetic pathways.

Carbon MonoxideManganeseLightMetals and Alloyschemistry.chemical_elementGeneral ChemistryManganesePhotosynthesisPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)chemistry.chemical_compoundchemistryCoordination ComplexesMaterials ChemistryCeramics and CompositesMolecule[CHIM]Chemical SciencesCo releaseta116Derivative (chemistry)ComputingMilieux_MISCELLANEOUSChemical Communications
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Reversible coordination of dioxygen by tripodal tetraamine copper complexes incorporated in a porous silica framework.

2010

The present study reports the synthesis and rational design of porous structured materials by using a templating method. A tetraethoxysilylated tripodal tetraamine (TREN) was covalently incorporated in a silica framework with a double imprint: A surfactant template and a metal ion imprint. The presence of a cationic surfactant (CTAB) endowed the material with a high porosity, and the tripodal or square-pyramidal topology of the ligand was preserved thanks to the use of the silylated Cu(II) complex. After removal of the surfactant and de-metalation, the incorporated tetraamine was quantitatively complexed by CuCl(2) and the material has shown after thermal activation that a reversible bindin…

Carbon MonoxideSilicon dioxideLigandNitrogenMetal ions in aqueous solutionOrganic ChemistryInorganic chemistryCationic polymerizationElectron Spin Resonance Spectroscopychemistry.chemical_elementGeneral ChemistrySilicon DioxideCopperCatalysisAdductOxygenchemistry.chemical_compoundchemistryCoordination ComplexesTripodal ligandPolymer chemistryReactivity (chemistry)AminesPorosityCopperChemistry (Weinheim an der Bergstrasse, Germany)
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