Search results for "Effects"

showing 10 items of 2634 documents

Asymmetric synthesis of bicyclic amino acid derivatives by Aza-Diels-Alder reactions in aqueous solution

1991

Derivatives 7–10 and 13–16 of methyl and ethyl 2-azabicyclo[2.2.1]heptane-3-carboxylates are synthesized by Aza-Diels-Alder reactions of chiral iminium ions, formed in situ from glyoxylic acid and chiral amines, with cyclopentadiene. Whereas the heterodienophiles derived from phenylglycinol and esters of sterically more demanding amino acids fail to undergo asymmetric cycloadditions, with alanine methyl ester and (R)-1-phenylethylamine hydrochoride the cycloadducts are formed in yields of 15 and 52%, respectively, reaching de values of up to 90:10 for the exo isomers.

Steric effectschemistry.chemical_classificationCyclopentadieneBicyclic moleculeOrganic ChemistryEnantioselective synthesisIminiumAmino acidchemistry.chemical_compoundchemistryOrganic chemistryAza-Diels–Alder reactionPhysical and Theoretical ChemistryGlyoxylic acidLiebigs Annalen der Chemie
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Understanding the selectivity in the formation of δ-lactams vs. β-lactams in the Staudinger reactions of chloro-cyan-ketene with unsaturated imines. …

2014

The reactions of chloro-cyan-ketene with two phenyl substituted unsaturated imines yielding β- or δ-lactams have been investigated using DFT methods at the MPWB1K/6-311G(d,p) level in diethyl ether. The reactions are initialised by the nucleophilic attack of the unsaturated imines on the ketene with formation of zwitterionic intermediates. The subsequent C–C single bond formation at the imine carbon or at the β-conjugated position enables the formation of β- or δ-lactams. Analysis of the energies involved in the two competitive channels explains the selectivity experimentally observed; in the absence of any steric hindrance, formation of δ-lactams is favoured over the formation of β-lactams…

Steric effectschemistry.chemical_classificationDouble bondStereochemistryGeneral Chemical EngineeringImineKeteneGeneral ChemistryMedicinal chemistrychemistry.chemical_compoundchemistryNucleophileSingle bondSelectivityLone pairRSC Adv.
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A theoretical study of carbon-carbon bond formation by a Michael-type addition.

2012

A theoretical study of the Michael-type addition of 1,3-dicarbonyl compounds to α,β-unsaturated carbonyl compounds has been performed in the gas phase by means of the AM1 semiempirical method and by density functional theory (DFT) calculations within the B3LYP and M06-2X hybrid functionals. A molecular model has been selected to mimic the role of a base, which is traditionally used as a catalyst in Michael reactions, an acetate moiety to modulate its basicity, and point charges to imitate the stabilization of the negative charge developed in the substrate during the reaction when taking place in enzymatic environments. Results of the study of six different reactions obtained at the three di…

Steric effectschemistry.chemical_classificationHammond's postulateAcetylacetoneMichael-type additionOrganic ChemistryProtonationAcetylacetoneRate-determining stepMichael reactionsBiochemistrychemistry.chemical_compoundNucleophilechemistryComputational chemistryCarbon–carbon bondOrganic chemistryPhysical and Theoretical ChemistryOxyanion holeαβ-unsaturated carbonylOrganicbiomolecular chemistry
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Lanthanide Discrimination with Hydroxyl-Decorated Flexible Metal–Organic Frameworks

2018

We report two new highly crystalline metal-organic frameworks (MOFs), derived from the natural amino acids serine (1) and threonine (2), featuring hexagonal channels densely decorated with hydroxyl groups belonging to the amino acid residues. Both 1 and 2 are capable of discriminating, via solid-phase extraction, a mixture of selected chloride salts of lanthanides on the basis of their size, chemical affinity, and/or the flexibility of the network. In addition, this discrimination follows a completely different trend for 1 and 2 because of the different locations of the hydroxyl groups in each compound, which is evocative of steric complementarity between the substrate and receptor. Last bu…

Steric effectschemistry.chemical_classificationLanthanideSubstrate (chemistry)02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesChloride0104 chemical sciencesAmino acidInorganic ChemistryCrystallographychemistryChemical affinitymedicineMetal-organic frameworkPhysical and Theoretical Chemistry0210 nano-technologymedicine.drugInorganic Chemistry
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Syntheses and Crystal Structures of two Non-isostructural Copper(I) Chloride and Bromide π-Complexes with (2-Allylthio)benzimidazole of 1:1 Compositi…

2002

By alternating-current electrochemical synthesis crystals of C10H10N2S · CuCl (I) and C10H10N2S · CuBr (II) π-complexes have been obtained and structurally investigated. The symmetry of I is orthorhombic, space group Pbcn, a = 16.799(2) A, b = 7.302(2) A, c = 18.214(2) A, V = 2234.1(9) A3, Z = 8 for C10H10N2S · CuCl composition, R = 0.0635, Rw = 0.0683 for 970 reflections. Crystals of II are monoclinic, space group P21/n, a = 7.4439(5) A, b = 17.6952(3) A, c = 17.0420(7) A, s = 94.662(2)°, V = 2237.4(2) A<3, Z = 4 for (Cu · C10H10N2S)2Br2 composition, R = 0.0463 for 4123 reflections. (2-Allylthio)benzimidazole moiety acts in both structures discussed as a bidentate ligand, chelating the cop…

Steric effectschemistry.chemical_classificationLigandchemistry.chemical_elementCrystal structureCopperCoordination complexInorganic Chemistrychemistry.chemical_compoundCrystallographychemistry13. Climate actionPolymer chemistryCopper(I) chlorideOrthorhombic crystal systemIsostructuralZeitschrift für anorganische und allgemeine Chemie
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Comparison of linear and hyperbranched polyether lipids for liposome shielding by 18F-radiolabeling and positron emission tomography

2018

Multifunctional and highly biocompatible polyether structures play a key role in shielding liposomes from degradation in the bloodstream, providing also multiple functional groups for further attachment of targeting moieties. In this work hyperbranched polyglycerol (hbPG) bearing lipids with long alkyl chain anchor are evaluated with respect to steric stabilization of liposomes. The branched polyether lipids possess a hydrophobic bis(hexadecyl)glycerol membrane anchor for the liposomal membrane. hbPG was chosen as a multifunctional alternative to PEG, enabling the eventual linkage of multiple targeting vectors. Different hbPG lipids (Mn = 2900 and 5200 g mol-1) were examined. A linear bis(h…

Steric effectschemistry.chemical_classificationLiposomePolymers and PlasticsChemistryBioengineering02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryCycloaddition0104 chemical sciencesBiomaterialsMembranePEG ratioMaterials ChemistryAlkoxy grouplipids (amino acids peptides and proteins)0210 nano-technologyAlkyl
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Spectral and structural studies on Ni(II) dithiocarbamates: Nickel sulfide nanoparticles from a dithiocarbamate precursor

2015

Abstract Three new planar Ni(II) dithiocarbamate complexes; [Ni(4-dpmpzdtc)2] (1), [Ni(4-dpmpzdtc)(PPh3)(NCS)] (2) and [Ni(bupcbzdtc)(PPh3)(NCS)] (3) (where, 4-dpmpzdtc = 4-(diphenylmethyl)piperazinecarbodithioato anion, bupcbzdtc = N-butyl-N-(4-chlorobenzyl))dithiocarbamato anion and PPh3 = triphenylphosphine) with “NiS4” and “NiS2PN” chromophore units were synthesized and characterized by single crystal X-ray structural analysis as well as UV–Vis, IR and NMR (1H, 13C and 31P) spectroscopy. For 2, 1H–1H COSY spectrum was also recorded. Single crystal X-ray structural analysis of 1–3, reveals a slightly distorted square planar geometry in all three complexes wherein the steric and electroni…

Steric effectschemistry.chemical_classificationNickel sulfidesynthesisChemistrySolvothermal synthesisInorganic chemistryNanoparticlesingle crystal XRDChromophoreInorganic ChemistrydithiocarbamateCrystallographychemistry.chemical_compoundSEMTEMMaterials Chemistrynickel sulfidePhysical and Theoretical ChemistrySpectroscopyDithiocarbamateta116Single crystalInorganica Chimica Acta
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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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