Search results for "steric"

showing 10 items of 476 documents

Synthesis and chemico-physical characterization of tin(IV) complexes with some crown ethers

1986

Abstract Some neutral adducts of diorganotin(IV) perchlorates and thiocyanates with three crown-ethers have been synthesised; they are of the type Me 2 SnX 2 L m · n H 2 O where m = 1 or 2, n = 2 or 4, X = ClO 4 or NCS, and L = 18-crown-6, 15-crown-5, and 12-crown-4. The values for m and n have been correlated with the coordinating ability of the two anions and with the steric hindrance by the crown ether molecules. From infrared and Mossbauer data, an octahedral coordination geometry is proposed for all the complexes. The Mossbauer parameters are discussed in terms of the electronegativity of the ligands on the tin(IV) center and of the distortions produced in the coordination polyhedra by…

Steric effectschemistry.chemical_classificationOrganic Chemistry18-Crown-6Inorganic chemistrychemistry.chemical_elementBiochemistryAdductInorganic ChemistryCrystallographychemistry.chemical_compoundchemistry15-Crown-5Materials ChemistryPhysical and Theoretical ChemistryTinHydrateCrown etherCoordination geometryJournal of Organometallic Chemistry
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Structural diversity in coordination chemistry of tridentate and tetradentate polyphosphines of Group 6 to 10 transition metal complexes

2003

Abstract Tridentate and tetradentate polyphosphines offer a huge variety of coordination modes to transition metals which lead, depending on the metal, to very different structural features in the resulting complexes. Steric effects being crucial in metal–phosphine complexes reactivity, a good knowledge of the molecular structures of the species is required both in the solid state and in solution. This article reviews from a structural point of view the monometallic and symmetrical homobimetallic complexes of the transition elements of Group 6 to 10 with tridentate and tetradentate phosphines. Concerning the classical triphosphines and tetraphosphines, emphasis was put on advances reported …

Steric effectschemistry.chemical_classificationPeriod (periodic table)LigandChemistryStereochemistryCrystal structureCoordination complexInorganic ChemistryTransition metalGroup (periodic table)Computational chemistryMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryCoordination Chemistry Reviews
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On the Adsorption Process in Polymer Brushes:  A Monte Carlo Study

1996

The adsorption process of the single polymer chain in a polymer brush of varying surface coverages is studied by means of Monte Carlo simulations of the bond-fluctuation lattice model. Only the end monomers can adsorb at the grafting surface, whereas inner monomers interact repulsively with it. The brush builds up a steric hindrance which forces the penetrating polymer to stretch strongly and which is responsible for small adsorption probabilities at surface coverages close to the overlap density. The final step of the adsorption process is determined by a fluctuation of the end monomer around its average position, which is comparable to the initial step of the desorption process.

Steric effectschemistry.chemical_classificationQuantitative Biology::BiomoleculesLattice model (finance)Polymers and PlasticsChemistryOrganic ChemistryMonte Carlo methodPolymerPolymer brushCondensed Matter::Soft Condensed MatterInorganic Chemistrychemistry.chemical_compoundAdsorptionMonomerChemical physicsDesorptionMaterials ChemistryPhysical chemistryMacromolecules
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Conformational study of N-alkyl-benzyltetrahydroisoquinolines alkaloid

2003

Abstract An exhaustive conformational study on the benzyltetrahydroisoquinolines (BTHIQ) from ab initio (RHF/6-31G(d)) calculations was carried out. The effects of different substituents at chiral C 1 atom were also considered. Our results indicate that different substituents at C 1 in BTHIQ molecules introduce a significant steric hindrance which, in turn, might be responsible for a conformational restriction favouring or disfavouring the spatial orientation of the lone pairs of N atom allowing or not the electronic attachment with the side chain of Asp residue. These results can serve as an aid for designing suitable structures of BTHIQs for better dopamine D 1 -receptor inhibitory activi…

Steric effectschemistry.chemical_classificationStereochemistryAlkaloidAb initioCondensed Matter PhysicsBiochemistryResidue (chemistry)chemistryComputational chemistrySide chainMoleculePhysical and Theoretical ChemistryLone pairAlkylJournal of Molecular Structure: THEOCHEM
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2-Acylamino-6-pyridones: breaking of an intramolecular hydrogen bond by self-association and complexation with double and triple hydrogenbonding coun…

2012

2-Acylamino-6-pyridones (acyl = RCO, where R = Me, Et, i-Pr, t-Bu, and 1-adamantyl) were previously characterized by X-ray diffractometry and solid-state NMR techniques by us. One of these compounds was used recently in organocatalysis. The series is now studied in solution and by computational methods recommended for noncovalent interactions (DFT/M05). These compounds showed interesting behavior during dilution and titration experiments monitored by (1)H NMR. 2-Acylamino-6-pyridones change their conformation at higher concentrations, forming double hydrogen-bonded dimers and trimers in which an uncommon steric effect is observed. To the best of our knowledge, this is the first example of s…

Steric effectschemistry.chemical_classificationStereochemistryHydrogen bondOrganic ChemistryIntermolecular forceTautomerCrystallographychemistryIntramolecular forceProton NMRMoleculeNon-covalent interactionsta116Journal of Organic Chemistry
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Weak Intermolecular Anion–π Interactions in Pentafluorobenzyl-Substituted Ammonium Betaines

2012

A series of ammonium–carboxylate and ammonium–sulfonate betaines was synthesized and studied by single-crystal X-ray diffraction analysis to investigate the weak intermolecular interactions as well as the intramolecular interactions in the solid state. None of the expected intramolecular anion–π interactions could be observed, probably because of the steric demands and the reduced nucleophilicity of the anionic part of the betaines. Nevertheless, a weak intermolecular anion–π interaction between the anionic part of the betaine and the pentafluorophenyl unit is present in the structure of 5a.

Steric effectschemistry.chemical_classificationStereochemistryIntermolecular forceSupramolecular chemistryChemieMedicinal chemistryIonInorganic Chemistrychemistry.chemical_compoundBetainechemistryNucleophileIntramolecular forceNon-covalent interactionsta116EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
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Intramolecular Nitrone Cycloaddition of α-(Trifluoromethyl)styrenes. Role of the CF3 Group in the Regioselectivity

2017

The intramolecular 1,3-dipolar cycloaddition of ortho-substituted 1,1,1-trifluoromethylstyrene-derived nitrones is described. Tricyclic fused isoxazolidines were obtained as major or exclusive products, in contrast to the case for nonfluorinated substrates, which rendered the bridged derivatives. This change in the regioselectivity was attributed to the electronic and, particularly, steric requirements of the trifluoromethyl group in comparison to the methyl group. It is worth mentioning that trifluoromethylstyrenes have been employed for the first time as dipolarophiles in a 1,3-dipolar intramolecular cycloaddition reaction, leading to the corresponding isoxazolidines bearing a quaternary …

Steric effectschemistry.chemical_classificationTrifluoromethylBicyclic molecule010405 organic chemistryStereochemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesCycloaddition0104 chemical sciencesNitronechemistry.chemical_compoundchemistryIntramolecular forceMoietyThe Journal of Organic Chemistry
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Improvement of charge-transfer indices for multifunctional amino acids: Application to lysozyme

2008

Valence topological Charge-Transfer (CT) indices are applied to the calculation of pH at the isoelectric point (pI). The model is generalized for molecules with heteroatoms. The ability of the indices for the description of molecular charge distribution is established by comparing them with the pI of 21 amino acids. Linear correlation models are obtained. The CT indices improve multivariable regression equations for pI. The variance decreases by 95%. No superimposition of the corresponding G(k)-J(k) and G(k)(V)-J(k)(V) pairs is observed in most fits, which diminishes the risk of collinearity. The inclusion of heteroatoms in pi-electron system is beneficial for the description of pI, the bec…

Steric effectschemistry.chemical_classificationValence (chemistry)ChemistryStereochemistryStatic ElectricityHeteroatomCharge densityBioengineeringGeneral MedicineHydrogen-Ion ConcentrationAmino acidCrystallographychemistry.chemical_compoundIsoelectric pointModels ChemicalDrug DiscoveryPiMolecular MedicineMuramidaseIsoelectric PointAmino AcidsLysozymeSAR and QSAR in Environmental Research
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Molecular association in water-isomeric pentanol mixtures at 25�C

1982

The results of static dielectric constant and viscosity measurements on solutions of water (concentration range 0 to 0.3 mole fraction) in 2-pentanol, 3-pentanol, 2-methyl-1-butanol, 3-methyl-1-butanol, and 2-methyl-2-butanol together with previous results for solutions of water in n-pentanol are discussed in terms of the information that they provide on the nature and the extent of molecular association in these solutions. We conclude that in most systems this association leads to the formation of tetrahedral complexes such as H2O(ROH)4. Evidences of the correlation of water-alcohol interactions with molecular parameters (position of OH group, steric hindrance of alkyl chain) of alcohols a…

Steric effectschemistry.chemical_classificationViscosityChemistryStatic dielectric constantBiophysicsPhysical chemistryOrganic chemistryPhysical and Theoretical ChemistryMole fractionMolecular BiologyBiochemistryAlkylJournal of Solution Chemistry
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Steric Constraints Induced Frustrated Growth of Supramolecular Nanorods in Water.

2015

A unique example of supramolecular polymerisation in water based on monomers with nanomolar affinities, which yield rod-like materials with extraordinarily high thermodynamic stability, yet of finite length, is reported. A small library of charge-neutral dendritic peptide amphiphiles was prepared, with a branched nonaphenylalanine-based core that was conjugated to hydrophilic dendrons of variable steric demand. Below a critical size of the dendron, the monomers assemble into nanorod-like polymers, whereas for larger dendritic side chains frustrated growth into near isotropic particles is observed. The supramolecular morphologies observed by electron microscopy, X-ray scattering and diffusio…

Steric effectschemistry.chemical_classificationamphiphilesIsodesmic reaction010405 organic chemistryOrganic ChemistrySupramolecular chemistryNanotechnologyGeneral ChemistryPolymerself-assembly010402 general chemistry01 natural sciencesCatalysissupramolecular chemistry0104 chemical sciencesSupramolecular polymerschemistryChemical physicsDendrimerNanorodSelf-assemblynanomaterialspolymersChemistry (Weinheim an der Bergstrasse, Germany)
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