Search results for "Transition metal complex"

showing 10 items of 10 documents

2,2′:6′,2″-Terpyridine Trimethylplatinum(IV) Iodide Complexes as Bifunctional Halogen Bond Acceptors

2016

Three new organometallic trimethylplatinum(IV) iodide complexes of 2,2′:6′,2″-terpyridines have been synthesized and characterized by 1H NMR spectroscopy, mass spectrometry, elemental analysis, and single crystal X-ray diffraction analysis. The X-ray crystal structures of PtMe3I(L) complexes 1–3 {L for 1 = 4′-chloro-2,2′:6′,2″-terpyridine, 2 = 4′-(4-cyanophenyl)-2,2′:6′,2″-terpyridine, and 3 = 4′-(4-tolyl)-2,2′:6′,2″-terpyridine} reveal distorted octahedral coordination geometry of the platinum(IV) metal centers with bidentate coordination of the terpyridine ligands. Complexation of 1–3 with iodopentafluorobenzene (IPFB) afforded single-crystal structures of halogen bond (XB) complexes 1a–3…

chemistry.chemical_classificationDenticityHalogen bond010405 organic chemistryhalogen bondsIodideGeneral ChemistryCrystal structurehalogen bond acceptors010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencestransition metal complexes0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryPyridineGeneral Materials ScienceTerpyridineBifunctionalta116Coordination geometryCrystal Growth & Design
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Studio dell'interazione di DNA con complessi di metalli di transizione

2014

G-quadruplextransition metal complexUv-ViDNACircular dichroismdicroismo circolareInorganic Chemistrymetal complexSchiff basechimica bioinorganicaintercalantiG4complessi metalliciChimica inorganicaSettore CHIM/03 - Chimica Generale E Inorganicametalli di transizioneBasi di SchiffG4-stabilizerBioinorganic Chemistryintercalator
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The Interaction of Small Molecules with Biomolecules

2014

The binding of small molecules with biological targets is associated to interesting chemical and biological properties of the resulting supramolecular systems. We have recently reported on the synthesis and characterization of cationic first row transition metal complexes and the study of their DNA binding properties, in aqueous solutions at neutral pH, essentially investigated by viscosimetry and spectroscopic techniques such as circular dichroism, absorption and fluorescence in the UV-visible wavelength range. Of course, such procedure cannot furnish atomic level details of the molecule-DNA interaction. Computational Chemistry may provide support for the interpretation of experimental dat…

Settore CHIM/03 - Chimica Generale E Inorganicatransition metal complexes DNA binding properties Molecular Dynamics G-quadruplexSettore CHIM/08 - Chimica Farmaceutica
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Flexible light-emitting electrochemical cells with single-walled carbon nanotube anodes

2016

Abstract In this work, we demonstrate flexible solution processed light emitting electrochemical cells (LECs) which use single-walled carbon nanotubes (SWCNTs) films as the substrate. The SWCNTs were synthesized by an integrated aerosol method and dry-transferred on the plastic substrates at room temperature. The addition of a screen printed poly (3,4-ethylene dioxythiophene) doped with poly (styrene sulfonate) (PEDOT:PSS) film onto the nanostructured electrode further homogenizes the surface and enlarges the work function, enhancing the hole injection into the active layer. By using an efficient phosphorescent ionic transition metal complex (iTMC) as the active material, efficacies up to 9…

Materials scienceLight-emitting electrochemical cellsFlexible devices02 engineering and technologySubstrate (electronics)Carbon nanotubeElectroluminescence010402 general chemistry01 natural sciencesElectrochemical celllaw.inventionBiomaterialsPEDOT:PSSlawSWCNTsMaterials ChemistryOLEDWork functionElectrical and Electronic Engineeringta114business.industryOLEDsGeneral ChemistryTransition metal complex021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesElectronic Optical and Magnetic MaterialsElectroluminescenceElectrodeOptoelectronics0210 nano-technologybusinessORGANIC ELECTRONICS
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DNA Binding and Biological Activity of Transition Metal Complexes

2011

DNA Transition Metal complexesSettore CHIM/03 - Chimica Generale E InorganicaSettore CHIM/08 - Chimica Farmaceutica
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New coordination polymers based on a novel polynitrile ligand: Synthesis, structure and magnetic properties of the series [M(tcnoetOH)2(4,4′-bpy)(H2O…

2008

International audience; A novel polynitrile anionic ligand, tcnoetOH−(=[(NC)2CC(OCH2CH2OH)C(CN)2]−), has been synthesized by a one-pot reaction from a cyclic acetal and malononitrile. This ligand has been successfully used to prepare, with 4,4′-bpy as co-ligand, a novel series of coordination polymers formulated as [M(tcnoetOH)2(4,4′-bpy)(H2O)2] with M(II) = Fe (1), Co (2) and Ni (3). These isostructural compounds present a linear chain structure consisting of octahedrally coordinated metal ions bridged by trans 4,4′-bpy ligands. The coordination sphere of the metal ions is completed with two terminal tcnoetOH− ligand and two water molecules. The magnetic properties indicate that the three …

Transition metal complexesCoordination sphere010405 organic chemistryChemistryLigandMetal ions in aqueous solutionInorganic chemistryZero field splitting010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryParamagnetismCrystallographychemistry.chemical_compoundPolynitrileMagnetic propertiesMaterials ChemistryMolecule[CHIM]Chemical SciencesPhysical and Theoretical ChemistryIsostructuralChain complexesMalononitrile
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Role of Vibrational Dynamics in Electronic Relaxation of Cr(acac)3

2015

Ultrafast energy relaxation of Cr(acac)3 dissolved in tetrachloroethylene (TCE) is studied by time-resolved infrared (TRIR) spectroscopy by using electronic and vibrational excitation. After electronic excitation at 400 or 345 nm, the ground state recovers in two time scales: 15 ps (major pathway) and 800 ps (minor pathway), corresponding to fast electronic transition to the ground state and intermediate trapping on the long-lived (2)E state followed by intersystem crossing (ISC) to the ground state. The quantum yield for the fast recovery of the ground state depends on the excitation wavelength, being higher for 345 nm. Vibrational cooling (VC) occurs on the electronic excited states with …

ta114ChemistryRelaxation (NMR)kinetic modelsQuantum yieldMolecular physicsMolecular electronic transitiontransition metal complexesvibrationsIntersystem crossingComputational chemistryExcited statePhysical and Theoretical ChemistryGround stateSpectroscopyta116ExcitationThe Journal of Physical Chemistry A
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Sintesi di complessi metallici e studio della loro interazione con acido desossiribonucleico.

2011

transition metal complexes; deoxyribonucleic acid.transition metal complexeSettore CHIM/03 - Chimica Generale E Inorganicadeoxyribonucleic acid.
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Experimental and computational studies of transition metal complexes with polydentate amino- and amidophenolate ligands : synthesis, structure, react…

2013

Chelating polydentate ligands play a key role in several areas of modern coordination chemistry. They can be exploited, for example, in catalysis, bioinorganic chemistry, heavy metal abstraction and molecular magnetism. Furthermore, compounds of this type can be found in natural chemicals, commercial products and industrial applications. In this dissertation, several 3d, 4d and 5d transition metal complexes with polydentate amino- and amidophenolate ligands were prepared and their structure, reactivity and magnetic properties were studied with experimental and computational techniques. In the first part of the dissertation, the solid-state structure, reactivity and magnetic properties of 12…

kemiallinen synteesisynthesisx-ray diffractionmagneetiset ominaisuudetsiirtymämetallitkompleksiyhdisteetstructuremagnetic propertiesepäorgaaninen kemialaskennallinen kemiaröntgenkristallografiatransition metal complexes
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Progression of Diiminopyridines: From Single Application to Catalytic Versatility

2015

Diiminopyridyl metal complexes, first characterized several decades ago, found practical application in 1998 when they were used as precatalysts in coordinative ethylene polymerization. This discovery contributed to the so-called postmetallocene revolution and triggered the large-scale experimental and theoretical research aimed at understanding diversified diiminopyridine chemistry. The results of this quest, some of which were intriguing and difficult to anticipate, are discussed and summarized in the current Review.

redox reactiontransition metal complexChemistrySingle applicationTheoretical researchNanotechnologyGeneral ChemistryCatalysisdiiminopyridinechemistry.chemical_compoundaluminum alkylEthylene polymerizationcooperative effectsOrganic chemistryOlefin polymerizationAluminum alkylolefin polymerizationDiiminopyridineACS Catalysis
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