Search results for "ALAT"

showing 10 items of 4241 documents

Selective ortho-metallation reaction of the phosphine P(o-ClC6H4)Ph2. Synthesis and crystal structure of [Rh2(μ-O2CCH3)3(μ-(ClC6H3)PPh2(OH2)2]·CHCl3

1993

Abstract From the reaction of [Rh2(O2CCH3)4(MeOH)2] in hot acetic acid with P(o-ClC6H4)Ph2, two monometallated compounds [Rh2(O2CCH3)3(C6H4)P(o-ClC6H4)Ph(HO2CCH3)2] (1), already described, and [Rh2(O2CCH3)3{(ClC6H3)PPh2}(OH2)2] have been isolated. The new compound has been characterized by an X-ray study. It crystallizes in the triclinic space group P1. It contains three acetate groups bridging a Rh24+ unit that has a Rh-Rh bond distance of 2.426(1) A; the fourth bridging ligand is derived from one P(o-ClC6H4)Ph2 metallated in the halogenated ring. The two water molecules occupy the axial coordination sites.

StereochemistryMetalationOrganic ChemistryBridging ligandCrystal structureTriclinic crystal systemBiochemistryMedicinal chemistryInorganic ChemistryBond lengthchemistry.chemical_compoundAcetic acidchemistryMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryPhosphineJournal of Organometallic Chemistry
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Orthometalation reactions in trifluoroacetate dirhodium(II) compounds. Molecular structure of Rh2(O2CCF3)2[(C6H4)PPh2]2·(PPh3)2·2(C7H8)

1994

Abstract Rh 2 (O 2 CCF 3 ) 3 [(C 6 H 4 )PPh 2 ]·(HO 2 CCF 3 ) 2 reacts with PPh 3 yielding the doubly metalated compound Rh 2 (O 2 CCH 3 ) 2− [(C 6 H 4 )PPh 2 ] 2 ·(HO 2 CCF 3 ) 2 . The reaction proceeds via a reactive intermediate with an equatorial phosphine, Rh 2 (η 2 -O 2 CCF 3 )(μ-O 2 CCF 3 ) 2 [(C 6 H 4 )PPh 2 ](PPh 3 )·(HO 2 CCF 3 ), which can also be generated in moderate yield under photochemical conditions. The structure of the PPh 3 bis-adduct Rh 2 (O 2 CCF 3 ) 2 [(C 6 H 4 )PPh 2 ] 2 ·(PPh 3 ) 2 ·2(C 7 H 8 ) has been determined by X-ray diffraction. M r =1663.27, orthorhombic, space group Fdd 2, a =41.748(9), b =21.620(5), c =17.375(5) A, V =15683(6) A 3 , Z =8, D x =1.41 g cm −3…

StereochemistryMetalationReactive intermediateCrystal structureMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryX-ray crystallographyMaterials ChemistryMoleculeOrthorhombic crystal systemCarboxylatePhysical and Theoretical ChemistryPhosphineInorganica Chimica Acta
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Interactions of diaryl-polyamines with nucleic acids. Allosteric effects with dinuclear copper complexes

2002

Abstract A series of α,ω-diarylamines with a variable number of ethylenediamine units between terminal naphthylrings shows dramatic affinity changes towards double-stranded nucleic acids, particularly upon complexation with Cu(II) ions. Metal salts alone have under the applied conditions only a negligible effect. The affinity of the metal-free ligands towards nucleic acids shows significant differences to those of the underlying polyamines, with a reversed stabilization of DNA instead of the usually observed preference for RNA. The affinity changes and preliminary NMR studies are in line with intercalation of naphthylrings into the double-stranded nucleic acid, which is hampered by complex …

StereochemistryOrganic ChemistryAllosteric regulationIntercalation (chemistry)RNAEthylenediamineBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryNucleic acidNucleic acid structureNucleic acid analogueDNATetrahedron Letters
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Pyrimido[5,4-c]pyrrolo[2,1-a]isoquinoline: a new potential DNA-interactive ring system

2003

The acid catalyzed decomposition of the azide 9 failed to give the title compounds, which were however obtained by a Pschorr-type cyclization on reactive 1-(6-aminopyrimidin-5-yl)-pyrroles of type 13. Derivatives of type 14 and 15 were fully characterized by NMR data. Theoretical calculations demonstrated that the new compounds possess properties suitable for DNA- intercalation.

StereochemistryOrganic ChemistryIntercalation (chemistry)Ring (chemistry)DecompositionNmr datalcsh:QD241-441chemistry.chemical_compoundchemistrylcsh:Organic chemistryAcid catalyzedAzideIsoquinolineDNAARKIVOC
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Synthesis, Structure, and Magnetic Properties of [(S)-[PhCH(CH3)N(CH3)3]][Mn(CH3CN)2/3Cr(ox)3]·(CH3CN)_(solvate), a 2D Chiral Magnet Containing a Qua…

2008

The synthesis, structure, and magnetic properties of a novel oxalate-based bimetallic magnet obtained by using the chiral (S)-trimethyl-(1-phenyl-ethyl)-ammonium, ((S)-[PhCH(CH3)N(CH3)3](+)), cation as template is reported. This compound can be formulated as [(S)-[PhCH(CH3)N(CH3)3]][Mn(CH3CN)2/3Cr(ox)3] x (CH3CN)_(solvate), and it crystallizes in the chiral trigonal space group P3. It shows a distorted two-dimensional honeycomb structure formed by Mn(II) and Cr(III) ions connected through oxalate anions with [(S)-[PhCH(CH3)N(CH3)3](+) cations and solvent molecules intercalated between the oxalate layers. Two-thirds of the Mn(II) ions of the honeycomb anionic network are heptacoordinated. Th…

StereochemistryOxalateIonInorganic ChemistrySolventHoneycomb structurechemistry.chemical_compoundCrystallographychemistryFerromagnetismMoleculeAmmoniumPhysical and Theoretical ChemistryBimetallic stripInorganic Chemistry
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Design, synthesis and biological evaluation of new oligopyrrole carboxamides linked with tricyclic DNA-intercalators as potential DNA ligands or topo…

2007

In the context of the design and synthesis of minor groove binding and intercalating DNA ligands some new oligopyrrole carboxamides were synthesized. These hybrid molecules (combilexins) possess a variable and conformatively flexible spacer at the N-terminal end. As intercalating tricyclic systems acridone, acridine, anthraquinones and in a special case iminostilbene terminate the N-terminal end of the pyrrole chain. The cytotoxicity was examined by the NCI antitumor screening, furthermore, biophysical as well as biochemical studies were performed in order to get some information about the DNA binding properties and topoisomerase inhibition effect of this new series of molecules.

Stereochemistrymedicine.drug_classTopoisomerase InhibitorsDNA FootprintingContext (language use)Antineoplastic AgentsLigandschemistry.chemical_compoundStructure-Activity RelationshipCell Line TumorDrug DiscoverymedicineStructure–activity relationshipHumansPyrrolesPharmacologybiologyMolecular StructureChemistryTopoisomeraseOrganic ChemistryDistamycinsNetropsinGeneral MedicineDNADNA Minor Groove BindingIntercalating AgentsAcridoneDrug DesignAcridinebiology.proteinTopoisomerase inhibitorDNAEuropean journal of medicinal chemistry
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Halogenomercury Salts of Sterically Crowded Triazenides - Convenient Starting Materials for Redox-Transmetallation Reactions

2010

Diaryl-substituted triazenides Ar(Ar′)N3HgX [Ar/Ar′ = Dmp/Mph, X = Cl (2a), Br (3a), I (4a); Ar/Ar′ = Dmp/Tph, X = Cl (2b), I (4b) with Mph = 2-MesC6H4, Mes = 2,4,6-Me3C6H2, Tph = 2′,4′,6′-triisopropylbiphenyl-2-yl and Dmp = 2,6-Mes2C6H3] were synthesized by salt-metathesis reactions in ethyl ether from the readily available starting materials Ar(Ar′)N3Li and HgX2. These compounds may be used for redox-transmetallation reactions with rare-earth or alkaline earth metals. Thus, reaction of 4b or 2b with magnesium or ytterbium in tetrahydrofuran afforded the triazenides Dmp(Tph)N3MX(thf) (5b: M = Mg, X = I; 6b: M = Yb, X = Cl) in good yield. All new compounds were characterized by melting poin…

Steric effectsAlkaline earth metalMagnesiumInorganic chemistrychemistry.chemical_elementInfrared spectroscopyEtherMedicinal chemistryRedoxInorganic ChemistryTransmetalationchemistry.chemical_compoundchemistryTetrahydrofuranZeitschrift für anorganische und allgemeine Chemie
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Synthesis and Structure of a Potassium Potassiochromate: A Bis-Chromium(II) Molecule Held Together by Near-Square-Planar Potassium−Ligand Bridges

2010

No Cr-Cr bonding is found in a new type of mixed-metal ate complex having two coordinatively unsaturated but sterically saturated bisamido-monoalkyl Cr(II) groups linked via an unusual near-square-planar-coordinated K atom in the moiety of the ate, while the cationic moiety is a separated iris-tmeda solvated second potassium atom.

Steric effectsLigandMetalationChemistryPotassiumOrganic ChemistryCationic polymerizationchemistry.chemical_elementAte complexPhotochemistryInorganic ChemistryCrystallographyMoietyMoleculePhysical and Theoretical ChemistryOrganometallics
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DNA interaction of new copper(II) complexes with sulfonamides as ligands

2007

New copper(II) complexes with sulfonamide ligands have been prepared and characterized. Sulfonamide ligands were prepared through a reaction between 8-aminoquinoline and either 2-mesitylene (Hqmesa), 4-tert-butylbenzene (Hqtbsa), or alpha-toluene (Halphaqtsa) sulfonyl chlorides. The structural analysis carried out for complex [Cu(alphaqtsa)(2)] indicated that the local environment of the Cu(II) cation is between a square planar and a tetrahedral geometry, with stacking of the benzene rings of the sulfonyl ligands between neighbor molecules. Powder EPR spectra at room temperature gave rhombic spectra for the [Cu(alphaqtsa)(2)] and [Cu(qmesa)(2)] complexes and an axial spectrum for the [Cu(qt…

Steric effectsMolecular Conformationchemistry.chemical_elementAscorbic AcidCrystallography X-RayPhotochemistryBiochemistryMedicinal chemistrylaw.inventionInorganic ChemistrylawOrganometallic CompoundsMoleculeSinglet stateElectron paramagnetic resonancechemistry.chemical_classificationSulfonylSulfonamidesMolecular StructureTetrahedral molecular geometryDNACopperIntercalating AgentsSulfonamidechemistryReactive Oxygen SpeciesCopperPlasmidsJournal of Inorganic Biochemistry
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Impact of the use of sterically congested Ir(III) complexes on the performance of light-emitting electrochemical cells

2018

International audience; The synthesis, structural and optoelectronic characterization of a family of sterically congested cyclometalated cationic Ir(iii) complexes of the form [Ir(C^N)2(dtBubpy)]PF6 (with dtBubpy = 4,4′-di-tert-butyl-2,2′-bipyridine and C^N = a cyclometalating ligand decorated at the 4-position of the pyridine ring and/or the 3-position of the phenyl ring with a range of sterically bulky substituents) are reported. This family of complexes is compared to the unsubstituted analogue complex R1 bearing 2-phenylpyridinato as cyclometalating ligand. The impact of sterically bulky substituents on the C^N ligands on both the solid state photophysics and light-emitting electrochemi…

Steric effectsPhotoluminescenceMaterials scienceSterically congested02 engineering and technology010402 general chemistryRing (chemistry)Ligands01 natural sciencesElectrochemical cellchemistry.chemical_compoundPyridineMaterials ChemistryOptoelectronic characterization[CHIM.COOR]Chemical Sciences/Coordination chemistryLight-emitting electrochemical cell[PHYS]Physics [physics]X ray powder diffractionLigandChelationYellow luminescenceCationic polymerizationDevice performancePhotoluminescence quantum yieldsGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCyclometalating ligandCrystallographychemistrySynthesis (chemical)Iridium compounds0210 nano-technologyLuminescence[CHIM.OTHE]Chemical Sciences/OtherInternuclear distances
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