Search results for "steric"

showing 10 items of 476 documents

Linked Amido—Cyclopentadienyl Complexes of Group 3 and 4 Metals: The First “Post-Metallocenes”

1999

Linked amido—cyclopentadienyl ligands were introduced by Bercaw and Shapiro in the late eighties with the catalysts of the type Sc(η5:η1-C5Me4SiMe2N t Bu)X (X = H, alkyl) [1]. These electronically more unsaturated and sterically more accessible analogs of ansa-scandocene complexes were found to be capable of catalyzing the living oligomerization of the α-olefins propylene, 1-butene, and 1-pentene. In these complexes the steric constraint [2] of Brintzinger-type ansa-metallocenes is alleviated by the replacement of one cyclopentadienyl ligand by an amido ligand NR’ (Scheme 1). In order to explore sterically demanding derivatives of this dianionic ligand (C5R4ZNR’)2-, iron and titanium comple…

Steric effectschemistry.chemical_classificationAgostic interactionCyclopentadienyl complexLigandChemistryGroup (periodic table)chemistry.chemical_elementMedicinal chemistryAlkylCatalysisTitanium
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Mononuclear tungsten(VI) complexes with methylenebis(6-alkylphenol)s

2003

Abstract Reaction of monomeric tungsten(VI) complex [W(eg)3] (1) (eg=1,2-ethanediolate dianion) with either one or 2 equiv. of 2,2′-methylenebis(6-alkylphenol) [alkyl=Me (H2L1), iPr (H2L2), tBu (H2L3)] provides heteroleptic complexes [W(eg)2(Ln)] (2) and [W(eg)(Ln)2] (3), respectively. Sterically hindered ligand precursor H2L3, which bear bulky tert-butyl groups in ortho-positions, can form only a complex corresponding to formula 2.

Steric effectschemistry.chemical_classificationAlkylphenolLigandchemistry.chemical_elementCrystal structureTungstenMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMonomerchemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryAlkylPolyhedron
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Energy interactions in amyloid-like fibrils from NNQQNY.

2014

We use large-scale MP2 calculations to analyze the interactions appearing in amyloid fibers, which are difficult to determine experimentally. To this end, dimers and trimers of the hexapeptide NNQQNY from the yeast prion-like protein Sup35 were considered as model systems. We studied the energy interactions present in the three levels of organization in which the formation of amyloid fibrils is structured. The structural changes in the hydrogen bonds were studied too. It was found that the most energetic process is the formation of the β-sheet, which is equally due to both hydrogen bonds and van der Waals interactions. The aromatic rings help stabilize these aggregates through stacking of t…

Steric effectschemistry.chemical_classificationAmyloidHydrogen bondChemistryStereochemistryStatic ElectricityStackingGeneral Physics and AstronomyAromaticityHydrogen BondingRing (chemistry)London dispersion forceProtein Structure SecondaryPolymerizationsymbols.namesakeCrystallographysymbolsNon-covalent interactionsThermodynamicsAmino Acid SequencePhysical and Theoretical Chemistryvan der Waals forceDimerizationPhysical chemistry chemical physics : PCCP
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Molecular Recognition via Hydrogen Bonding at the Air−Water Interface:  An Isotherm and Fourier Transform Infrared Reflection Spectroscopy Study

1997

Molecular recognition in Langmuir monolayers at the air−water interface as a function of headgroup orientation and substrate using isotherms and in-situ Fourier transform infrared (FT-IR) reflection spectroscopy has been investigated. Isotherm measurements show that urea and 2,4,6-triaminopyrimidine (TAP) are specifically bound to barbituric acid lipid monolayers. As expected, TAP causes a larger shift in the limiting area of the isotherms than urea due to steric requirements. The peak positions of the CH stretching vibrations of the barbituric acid lipids indicate that the alkyl chains of barbituric acid lipids 1−3 are in a close-packed all-trans conformation both before and after the reco…

Steric effectschemistry.chemical_classificationBarbituric acidHydrogen bondtechnology industry and agricultureAnalytical chemistryInfrared spectroscopySurfaces and InterfacesCondensed Matter Physicschemistry.chemical_compoundMolecular recognitionchemistryMonolayerElectrochemistryPhysical chemistrylipids (amino acids peptides and proteins)General Materials ScienceSpectroscopySpectroscopyAlkylLangmuir
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In-Situ DRIFT Spectroscopic Investigation on the Chemical Evolution of Zinc Phosphate Acid−Base Cement

2000

Diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy has been used to follow the chemical evolution of zinc phosphate acid−base cement (ZPC), which has been prepared from unmodified, as well as from aluminum- and zinc-modified orthophosphoric acid. For the first time, amorphous dizinc cyclotetraphosphate octahydrate, Zn2P4O12·8H2O, although hydrolytically instable, has been observed as precursor phase prior to crystallization of α-hopeite, α-Zn3(PO4)2·4H2O, in both systems. Within minutes from onset of mixing the infrared spectrum of unmodified ZPC is dominated by the characteristic vibrations of α-hopeite, due to matrix crystallization. Setting of modified ZPC is strongly af…

Steric effectschemistry.chemical_classificationBase (chemistry)Diffuse reflectance infrared fourier transformGeneral Chemical EngineeringInorganic chemistryZinc phosphateGeneral Chemistrylaw.inventionAmorphous solidchemistry.chemical_compoundchemistrylawPhase (matter)Materials ChemistryCrystallizationSpectroscopyChemistry of Materials
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Ligand effects on the dimensionality of oxamato-bridged mixed-metal open-framework magnets

2012

Increasing dimensionality [from 2D (1) to 3D (2)] and T(C) [from 10 (1) to 20 K (2)] in two new oxamato-bridged heterobimetallic Mn(II)(2)Cu(II)(3) open-frameworks result from the steric hindrance provided by the different alkyl substituents of the N-phenyloxamate bridging ligands.

Steric effectschemistry.chemical_classificationBridging (networking)Mixed metalChemistryLigandStereochemistryMetals and AlloysGeneral ChemistryOpen frameworkCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyMagnetMaterials ChemistryCeramics and CompositesAlkylCurse of dimensionalityChemical Communications
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Benzoannulated quinone-type electron acceptors: evolution of the molecular and electronic structures upon reduction

1998

Abstract The molecular and electronic structures of DCNQI and its π-extended derivatives benzo-DCNQI and DCAQI have been investigated using ab initio 6-31G ∗ calculations. The steric hindrance introduced by lateral benzoannulation determines the loss of planarity of the DCNQI moiety for DCAQI. The most stable conformation of DCAQI corresponds to a butterfly-type structure, in which the DCNQI ring adopts a boat conformation and the lateral benzene rings remain planar. This structure lies 2.75 kcal mol −1 below the fully planar conformation. MP2/6-31G ∗ calculations including full geometry optimization confirm the greater stability of the butterfly structure. The geometries of the anions and …

Steric effectschemistry.chemical_classificationChemistryCyclohexane conformationAb initioElectron acceptorCondensed Matter PhysicsRing (chemistry)BiochemistryPlanarity testingCrystallographyAb initio quantum chemistry methodsComputational chemistryMoietyPhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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A Computational Study of Ethylene C−H Bond Activation by [Cp*Ir(PR3)]

2001

It has previously been demonstrated that both [(C5Me5)Ir(PMe3)(CH=CH2)H] and [(C5Me5)Ir(PMe3)(H2C=CH2)] are formed when [(C5Me5)Ir(PMe3)] is thermolytically generated in the presence of ethylene. At higher temperatures, the vinyl hydride is converted to the eta2-ethylene adduct. Density functional theory has now been used to investigate this reaction, using the B3LYP functional, two types of basis sets (LanL2DZ and TZV*), and two models of the [(C5R5)Ir(PR3)] species (R=H and CH3). The study consists of full optimizations of local minima, first-order saddle points, and minimum energy crossing points (MECP). The experimental results are best accounted for by considering both singlet and trip…

Steric effectschemistry.chemical_classificationChemistryHydrideAlkeneOrganic ChemistryGeneral ChemistryPhotochemistry7. Clean energyCatalysisAdductKinetic isotope effectArenium ionPhysical chemistryDensity functional theorySinglet stateChemistry
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Static dielectric constant, viscosity, and structure of pure isomeric pentanols

1981

Static dielectric constants, viscosities, densitites and refractive indices of 2-pentanol, 3-pentanol, 2-methyl-1-butanol, 3-methyl-1-butanol and 2-methyl-2-butanol were measured at 15, 25, 35 and 45°C. These results together with the previous data on n-pentanol have been analyzed in terms of the Kirkwood correlation factor g k and of the energy of activiation for viscous flow. With the exception of 2-methyl-2-butanol, g k was found to be greater than unity. These results show that the monomeric units of isomeric pentanols interact by means of hydrogen bonding to form dynamic structures essentially of two types: linear chains where co-association raises the total polarizability and cyclic d…

Steric effectschemistry.chemical_classificationChemistryHydrogen bondBiophysicsThermodynamicsDielectricBiochemistryDipoleViscosityPolarizabilityComputational chemistryMoleculePhysical and Theoretical ChemistryMolecular BiologyAlkylJournal of Solution Chemistry
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Gas-phase and solution basicities of some alkyl 2,6-dialkylphenyl ketones: A comparative analysis

2000

Abstract The gas-phase basicity of a number of alkyl 2,6-dialkylphenyl ketones (2,6-R2C6H3COR′) has been found to be almost insensitive to structural variations, as a result of a compensation of steric and electronic effects associated with the bulkiness and to the polarizability, respectively, of R and/or R′. On the contrary, the basicity in concentrated sulfuric acid undergoes, along the same series of compounds, a variation of nearly 8 pK units, as a consequence of steric inhibition of solvation of the protonated carbonyl as the main effect played by R and/or R′. The results in the condensed phase agree very nicely with recent findings relevant to some 4-substituted 2,6-dimethylacetophen…

Steric effectschemistry.chemical_classificationChemistryStereochemistryArylOrganic ChemistrySolvationProtonationBiochemistryMedicinal chemistrychemistry.chemical_compoundPolarizabilityPhase (matter)Drug DiscoveryElectronic effectAlkyl
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