Search results for "organometalli"

showing 10 items of 395 documents

Palladium-based catalytic systems for the synthesis of conjugated enynes by Sonogashira reactions and related alkynylations

2007

Conjugated alkynes are recurring building blocks in natural products, a wide range of industrial intermediates, pharmaceuticals and agrochemicals, and molecular materials for optics and electronics. The palladium-catalyzed cross-coupling between sp(2)-hybridized carbon atoms of aryl, heteroaryl, and vinyl halides with sp-hybridized carbon atoms of terminal acetylenes is one of the most important developments in the field of alkyne chemistry over the past 50 years. The seminal work of the 1970s has initiated an intense search for more general and reliable reaction conditions. The interest in the catalytic activation of demanding substrates, the need to minimize the consumption of depletive r…

chemistry.chemical_elementSonogashira couplingAlkyneHalideConjugated systemHeterogeneous catalysis010402 general chemistryalkynes01 natural sciencesCatalysisCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisOrganometallic Compoundscross-couplingOrganic chemistryComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationMolecular Structure010405 organic chemistryArylStereoisomerismGeneral ChemistryGeneral Medicine[CHIM.CATA]Chemical Sciences/Catalysissonogashira reactionspalladiumCombinatorial chemistry0104 chemical sciencesheterogeneous catalysischemistryCarbonPalladium
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Hexanuclear copper(ii) cage with {Cu3O⋯H⋯OCu3} core supported by a dicompartmental oxime ligand with m-xylyl spacer: synthesis, molecular structure a…

2010

A new dicompartmental dioxime ligand (H(2)L) with m-xylyl spacer between the donor sites has been synthesised by Schiff-base condensation of α,α'-diamino-m-xylene and diacetyl monooxime. The ligand reacts with copper(ii) salts giving rise to hexanuclear tricationic copper(II) cage complexes [Cu(II)(6)(μ(3)-O···H···O-μ(3))L(3)(H(2)O)(6)]X(3) (X = BF(4), 1a; X = ClO(4), 1b). The complexes have been characterised by different analytical and spectroscopic techniques and confirmed the hexanuclear structure even in solution. Single crystal X-ray diffraction studies of both the complexes revealed a very similar core structure with three dicompartmental ligands supporting two triangular Cu(3)O core…

crystal structureHydrogen bondLigandExchange interactionHexanuclear copper complexchemistry.chemical_elementCrystallography X-RayLigandsOximeHexanuclear copper complex; oxime; crystal structureoximeCopperInorganic ChemistryMagneticschemistry.chemical_compoundCrystallographychemistryUnpaired electronOximesOrganometallic CompoundsMoleculeSingle crystalCopperDalton Transactions
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Preparation of potentially porous, chiral organometallic materials through spontaneous resolution of pincer palladium conformers.

2013

Understanding the mechanism by which advanced materials assemble is essential for the design of new materials with desired properties. Here, we report a method to form chiral, potentially porous materials through spontaneous resolution of conformers of a PCP pincer palladium complex ({2,6-bis[(di-t-butylphosphino)methyl]phenyl}palladium(II)halide). The crystallisation is controlled by weak hydrogen bonding giving rise to chiral qtz-nets and channel structures, as shown by 16 such crystal structures for X = Cl and Br with various solvents like pentane and bromobutane. The fourth ligand (in addition to the pincer ligand) on palladium plays a crucial role; the chloride and the bromide primaril…

crystal structuretermoanalyysichemistry.chemical_elementCrystal structurekiderakenne010402 general chemistryjauhe röntgen diffraktioCrystallography X-Ray01 natural scienceshuokoiset materiaalitpalladium kompleksiInorganic ChemistryMolecular recognitionOrganometallic CompoundsMoleculePincer ligandta116palladium pincer complexes; hexagonal channels; self-assembly; weak interactionssingle crystal X-ray diffractionpowder X-ray diffractionorganometalliMolecular Structure010405 organic chemistryChemistryStereoisomerismpalladium complexyksikide röntgen diffraktio0104 chemical sciencesPincer movementChemistryCrystallographySelf-assemblyporous materialsPorosityPalladiumMonoclinic crystal systemPalladiumDalton transactions (Cambridge, England : 2003)
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Chalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH2)m]n (n=1-4; m=3-7)

2020

The Te…Te secondary bonding interactions (SBI) in solid heterocyclic telluroethers were explored by preparing and structurally characterizing a series of [Te(CH2)m]n (n = 1‐4; m = 3‐7) species. The SBIs in 1,7‐Te2(CH2)10, 1,8‐Te2(CH2)12, 1,5,9‐Te3(CH2)9, 1,8,15‐Te3(CH2)18, 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)28 led to the tubular packing of the molecules, as has been observed previously for related thio‐ and selenoether rings. The nature of the intermolecular interactions was explored by solid‐state PBE0‐D3/pob‐TZVP calculations involving periodic boundary conditions. The packing of molecules in 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)…

eetteritheterocyclesnoncovalent interactionskemialliset sidoksettelluuritelluriumdensity functional calculationssolid-state structurestiheysfunktionaaliteoriaorganometalliyhdisteet
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Orgaaniset ja metallo-orgaaniset epälineaariset optiset materiaalit

2017

Tässä tutkielmassa on perehdytty kirjallisuudessa raportoituihin orgaanisiin ja metallo-orgaanisiin epälineaarisiin optisiin (NLO) materiaaleihin sekä tutkittu mahdollisuutta valmistaa niitä yksinkertaisista orgaanisista molekyyleistä. Työn kirjallisessa osassa luodaan lyhyt katsaus NLO-teoriaan sekä käydään läpi orgaanisten ja metallo-orgaanisten NLO-yhdisteiden lisäksi erilaisia toisen harmonisen säteilyn (SHG) mittaustekniikoita sekä erilaisia kiteytystekniikoita. Kokeellisessa osuudessa on valmistettu polaarisista molekyyleistä heikoilla vuorovaikutuksilla sitoutuneita yhdisteitä, joista osalla on havaittu olevan SHG-ominaisuuksia.

epälineaariset optiset materiaalitorganometalliyhdisteetNLO
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Liposomes modified by mono- and bis-phthalocyanines: A comprehensive EPR study.

2016

The impact of selected metallophthalocyanines, featuring diverse molecular structure, upon the fluidity of liposome membranes was studied using the spin label EPR technique. The “mono”-type MPc’s (M = Zn, Sn; Pc = C32H16N8 is the phthalocyanine ligand) and sandwich LnPc2 complexes (Ln = Nd, Sm, Gd) were explored. Liposomes were obtained in a sonication process, from egg yolk lecithin (EYL) in water. TEMPO and 16-DOXYL spin labels were used to monitor the peripheral and central part of the lipid double layer, respectively, which allowed to localize the phthalocyanine additive within the bilayer, as well as to perform independent measurements of changes in fluidity upon addition thereof. All …

food.ingredientBiophysics02 engineering and technologyLecithinlaw.inventionCyclic N-Oxides03 medical and health scienceschemistry.chemical_compoundSonication0302 clinical medicineNuclear magnetic resonancefoodlawLecithinsOrganometallic CompoundsGeneral Materials ScienceLipid bilayerElectron paramagnetic resonanceSpin labelLiposomeChemistryLiquid crystalsBilayerElectron Spin Resonance SpectroscopySurfaces and InterfacesGeneral Chemistry021001 nanoscience & nanotechnologyCrystallographyMembraneSoft Matter030220 oncology & carcinogenesisLiposomesPhthalocyanine0210 nano-technologyBiotechnologyThe European physical journal. E, Soft matter
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Multinuclear and Solid State NMR of Gels

2020

Over the past six decades, nuclear magnetic resonance spectroscopy has been an integral part of synthetic organic and organometallic chemistry, as well as biochemistry. Beyond solution state experiments, increasing developments have opened new avenues to study materials in their solid state. Between two extremes (i.e., solution and solid), there exist several other forms of materials, especially soft materials such as gels and liquid crystals. Traditionally gels have been studied using solution state NMR spectroscopic methods. However, the viscosity of complex viscoelastic fluids such as gels affects the molecular tumbling, which in turn affects the chemical shift anisotropy and dipolar and…

geelitchemistry.chemical_classificationMaterials sciencekiinteän olomuodon kemiaNuclear magnetic resonance spectroscopyPolymerViscoelasticitychemistry.chemical_compoundSolid-state nuclear magnetic resonancechemistryChemical physicsLiquid crystalMagic angle spinningNMR-spektroskopiaAnisotropyOrganometallic chemistry
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The Monomeric Alanediyl : AlAriPr8 (AriPr8 = C6H-2,6-(C6H2-2,4,6-Pri3)2-3,5-Pri2) : An Organoaluminum(I) Compound with a One-Coordinate Aluminum Atom

2020

Reduction of the aluminum iodide AlI2AriPr8 (1; AriPr8 = C6H-2,6-(C6H2-2,4,6-Pri3)2-3,5-Pri2) with 5% w/w Na/NaCl in hexanes gave a dark red solution from which the monomeric alanediyl :AlAriPr8 (2) was isolated in ca. 28% yield as yellow-orange crystals. Compounds 1 and 2 were characterized by X-ray crystallography, electronic and NMR spectroscopy, and theoretical calculations. The Al atom in 2 is one-coordinate, and the compound displays two absorptions in its electronic spectrum at 354 and 455 nm. It reacts with H2 under ambient conditions to give the aluminum hydride {AlH(μ-H)AriPr8}2, probably via a weakly bound dimer of 2 as an intermediate. peerReviewed

kemiallinen synteesikompleksiyhdisteetalumiiniorganometalliyhdisteet
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Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes

2019

Organosilicon compounds are versatile units with a wide range of uses from medicinal chemistry to the field of organic electronics. An unprecedented method for the synthesis of novel diaryl-substituted silacyclopentenols via blue-light promoted intramolecular [2 + 2] photocycloaddition of acyl silanes is herein disclosed. Additionally, the present findings demonstrate the influence of the olefin substituents in controlling the regioselectivity of the intramolecular Paternò–Büchi reaction, providing silacycles different from previously reported ones. The high degree of functionalization of these compounds makes them attractive precursors to other synthetically challenging silacyclopentanes. …

kemiallinen synteesipiiorganometalliyhdisteet
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Extended Assemblies of Ru(bpy)(CO)2X2 (X = Cl, Br, I) Molecules Linked by 1,4-Diiodotetrafluoro-Benzene (DITFB) Halogen Bond Donors

2019

The ruthenium carbonyl compounds, Ru(bpy)(CO)2X2 (X = Cl, Br or I) act as neutral halogen bond (XB) acceptors when co-crystallized with 1,4-diiodotetrafluoro-benzene (DITFB). The halogen bonding strength of the Ru-X&sdot

kemialliset sidoksetcrystal structurebipyridinelcsh:QD901-999halogen bondcarbonyllcsh:CrystallographyorganometalliyhdisteetkiteetrutheniumCrystals
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