Search results for "terpyridine"

showing 10 items of 128 documents

Synthesis and structural characterization of new transition metal complexes of a highly luminescent amino-terpyridine ligand

2020

Abstract The synthesis, NMR and UV–Vis spectroscopy measurements and X-ray diffraction analysis of four new metal complexes of the amino terpyridine ligand 4′-[4-(4-aminophenyl)phenyl]-2,2′:6′,2″-terpyridine L, namely [FeL2](ClO4)2 (1), [ZnL2](ClO4)2 (2), [CdL2](ClO4)2 (3) and [PtMe3IL] (4), are reported. The X-ray crystal structures of complexes 1–3 are 1:2 metal:ligand structures with tridentate ligands decorated around the octahedral metal centers. In complex 4, with L in a bidentate coordination mode, the Pt(IV) coordinated methyl and iodine groups form a fac-arrangement. The 1H NMR spectrum of 4 shows three 195Pt-1H resonances for the methyl groups incorporating the fac-arrangement, wh…

Denticity010405 organic chemistryLigandSolvatochromismCrystal structure010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryTransition metalPyridineMaterials ChemistryProton NMRPhysical and Theoretical ChemistryTerpyridinePolyhedron
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Bis(terpyridyl)-ruthenium(II) units attached to polyazacycloalkanes as sensing fluorescent receptors for transition metal ions

2000

A synthetic strategy has been devised for the preparation of new compounds in which terpyridyl fragments are linked to 1,4,8,11-tetraazacyclotetradecane (cyclam). Reaction of excess cyclam with 4′-[(4-bromomethyl)phenyl]-2,2′:2″,6′-terpyridine afforded the ligand 1-[4′-p-tolyl-(2,2′:6′,2″-terpyridyl)]-1,4,8,11-tetraazacyclotetradecane (L1) in which the tetraaza macrocycle was covalently attached to one benzyl-terpyridyl fragment. Under similar conditions reaction of cyclam with excess 4′-[(4-bromomethyl)phenyl]-2,2′:2″,6′-terpyridine gave the tetra substituted cyclam derivative 1,4,8,11-[4′-p-tolyl-(2,2′:6′,2″-terpyridyl)]-1,4,8,11-tetraazacyclotetradecane (L2). The multidentate ligand L2 w…

DenticityAqueous solutionLigandInorganic chemistryPotentiometric titrationchemistry.chemical_elementRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryCyclamTerpyridineMethylene
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Red emitting [Ir(C^N)2(N^N)]+ complexes employing bidentate 2,2':6,2''-terpyridine ligands for light-emitting electrochemical cells

2014

2,2':6',2''-Terpyridine (tpy), 4'-(4-HOC6H4)-2,2':6',2''-terpyridine (1), 4'-(4-MeOC6H4)-2,2':6',2''-terpyridine (2), 4'-(4-MeSC6H4)-2,2':6',2''-terpyridine (3), 4'-(4-H2NC6H4)-2,2':6',2''-terpyridine (4) and 4'-(4-pyridyl)-2,2':6',2''-terpyridine (4) act as N^N chelates in complexes of the type [Ir(C^N)2(N^N)][PF6] in which the cyclometallating ligand, C^N, is derived from 2-phenylpyridine (Hppy) or 3,5-dimethyl-1-phenyl-1H-pyrazole (Hdmppz). The single crystal structures of eight complexes have been determined, and in each iridium(III) complex cation, the non-coordinated pyridine ring of the tpy unit is involved in a face-to-face π-stacking interaction with the cyclometallated ring of an …

DenticityChemistryHydrogen bondLigandAnalytical chemistrychemistry.chemical_elementInorganic ChemistryNMR spectra databasechemistry.chemical_compoundCrystallographyPyridineIridiumTerpyridineSingle crystal
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Dynamic chemical devices: photoinduced electron transfer and its ion-triggered switching in nanomechanical butterfly-type bis(porphyrin)terpyridines.

2005

A series of butterfly-type molecular constructs has been prepared in good yield by using a double Stille coupling synthetic protocol. They are composed of a terpyridine (terpy) scaffold and two wings composed of appended porphyrins that are capable of switching from an extended W geometry to a compact U geometry upon cation coordination of the terpy unit. The porphyrin moieties exist in the constructs either as free bases or they can be sequentially metallated, thus giving rise to wings of different "colours". Stationary and time-resolved emission studies of the HZn, ZnAu and Zn2Au constructs show that the electronic properties are strongly dependent on the geometry. In the extended W confo…

DenticityMagnetic Resonance SpectroscopyPorphyrinsChemical PhenomenaPhotochemistryPyridinesMolecular ConformationElectronsPhotochemistryCrystallography X-RayLigandsCatalysisPhotoinduced electron transferchemistry.chemical_compoundElectron transferLigandHydrogen bondChemistry PhysicalOrganic ChemistryTemperatureGeneral ChemistryHydrogen-Ion ConcentrationPorphyrinZincSpectrometry FluorescencechemistryExcited stateSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIndicators and ReagentsSpectrophotometry UltravioletTerpyridineChemistry (Weinheim an der Bergstrasse, Germany)
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Fast redox-triggered shuttling motions in a copper rotaxane based on a phenanthroline–terpyridine conjugate

2014

Fast shuttling motions in solution have been observed by cyclic voltammetry in a Cu(I/II)-based [2] rotaxane. In the reported system, the different coordination preferences of both copper oxidation states are exploited to promote the electrochemically-triggered gliding of the ring from a tetra to a pentacoordinated site and vice versa. The thread of this rotaxane consists of a tridentate 2,2':6',2''-terpyridine chelating unit directly bonded through its 5-position to the 3-position of the bidentate 1,10-phenanthroline unit. This distribution reduces to a minimum the distance between the two coordination sites and lessens the congestion around the tetrahedral environment. These two factors h…

DenticityRotaxaneRotaxanesPyridinesPhenanthrolineOrganic Chemistrychemistry.chemical_elementPhotochemistryElectrochemistryBiochemistryRedoxCopperKineticsMotionchemistry.chemical_compoundchemistryElectrochemistryPhysical and Theoretical ChemistryTerpyridineCyclic voltammetryOxidation-ReductionCopperPhenanthrolinesOrg. Biomol. Chem.
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Synthesis and properties of dinuclear Ru(II)/Os(II) complexes based on a heteroditopic phenanthroline-terpyridine bridging ligand.

2010

The synthesis and characterization of a series of mono- and dinuclear ruthenium(II) and osmium(II) polypyridyl complexes based on the heteroditopic bridging ligand PT are reported. This ligand incorporates bidentate phen (1,10-phenanthroline) and terdentate tpy (2,2':6',2''-terpyridine) units directly connected by their 3 and 5 positions, respectively. The dinuclear complexes have been synthesized via a Pd(0) catalyzed cross-coupling reaction between a bromo-substituted Ru-phen complex and a tpy derivative incorporating a boronate ester, followed by Ru(II) or Os(II) complexation. The compounds obtained are fully characterized using spectroscopic and electrochemical measurements. The electro…

DenticityStereochemistryLigandPhenanthrolinechemistry.chemical_elementBridging ligandRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMoietyOsmiumPhysical and Theoretical ChemistryTerpyridineInorganic chemistry
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Efficiency range of the Belousov-Zhabotinsky reaction to induce the self-organization of transient bonds in metallo-supramolecular polymeric systems.

2020

The periodic change of the oxidation state of the metal catalyst in the oscillating Belousov-Zhabotinsky (BZ) reaction has been reported to establish a periodic organization of metallo-supramolecular bonds in polymeric systems, which results in autonomous viscosity oscillations. To appraise the possible extent of quantitative control on the viscosity oscillation features, we assess how the kinetics of the BZ reaction affects the periodic self-organization of the metal-ligand coordination, and vice versa. Our model system includes mono-, bis-, and tetra-functional polyethyleneglycol (PEG) precursors end grafted with terpyridine ligands that are complexed with ruthenium ions, which oscillate …

DiffusionKineticsGeneral Physics and Astronomy02 engineering and technologyReaction intermediate010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesReaction rateViscositychemistry.chemical_compoundBelousov–Zhabotinsky reactionchemistryChemical physicsOxidation statePhysical and Theoretical ChemistryTerpyridine0210 nano-technologyPhysical chemistry chemical physics : PCCP
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Synthesis and Structure of Trimethylplatinum(IV) Iodide Complex of 4'-(4-Methoxyphenyl)-2,2':6',2''-terpyridine Ligand and its Halogen Bonding Proper…

2020

Inorganic Chemistrychemistry.chemical_classificationNMR spectra databasechemistry.chemical_compoundHalogen bondchemistryChemical bondLigandIodideX-ray crystallographyPolymer chemistryMoleculeTerpyridineZeitschrift für anorganische und allgemeine Chemie
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Observation of electroluminescence at room temperature from a ruthenium(II) bis-terpyridine complex and its use for preparing light-emitting electroc…

2005

A terpyridine ruthenium (II) complex containing a substituted and an unsubstituted terpyridine ligand was synthesized, and its luminescence properties were studied in a solid-state single-layer light-emitting electrochemical cell. The obtained devices emitted light of a very deep red color (CIE, x = 0.717 y = 0.282) at low external applied bias. It is the first example of an electroluminescence device based on a bis-chelated ruthenium complex. Its ambient atmosphere decay is remarkably different from analogous devices using tris-chelated ruthenium complexes.

Inorganic Chemistrychemistry.chemical_compoundchemistryLigandchemistry.chemical_elementPhysical and Theoretical ChemistryTerpyridineElectroluminescenceLuminescencePhotochemistryRed ColorElectrochemical cellRutheniumInorganic chemistry
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CO 2 Fixation and Activation by Cu II Complexes of 5,5″‐Terpyridinophane Macrocycles

2007

An aza-terpyridinophane receptor containing the polyamine 4,7,10,13-tetraazahexadecane-1,16-diamine linked through methylene groups to the 5,5″ positions of a terpyridine unit has been prepared and characterized (L). The acid-base behaviour, CuII speciation and ability to form ternary complexes (CuII-L-carbonate) have been explored by potentiometric titrations in 0.15 M NaClO4 and by UV/Vis and paramagnetic NMR spectroscopy. Comparisons are made with a previously reported terpyridinophane containing the polyamine 4,7,10-triazatridecane-1,13-diamine (L1). For this latter receptor, reductive coupling between indigo and carbon dioxide at indigo-modified electrodes produces carboxylated derivat…

Inorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryCarbon fixationPotentiometric titrationInorganic chemistryNuclear magnetic resonance spectroscopyMethyleneTerpyridineTernary operationElectrochemistryPolyamineEuropean Journal of Inorganic Chemistry
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