Search results for "Helical Structures"

showing 4 items of 4 documents

Corrosion of Heritage Objects: Collagen‐Like Triple Helix Found in the Calcium Acetate Hemihydrate Crystal Structure

2020

Abstract Helical motifs are common in nature, for example, the DNA double or the collagen triple helix. In the latter proteins, the helical motif originates from glycine, the smallest amino acid, whose molecular confirmation is closely related to acetic acid. The combination of acetic acid with calcium and water, which are also omnipresent in nature, materializing as calcium acetate hemihydrate, was now revealed to exhibit a collagen‐like triple helix structure. This calcium salt is observed as efflorescence phase on calcareous heritage objects, like historic Mollusca shells, pottery or marble reliefs. In a model experiment pure calcium acetate hemihydrate was crystallized on the surface of…

Collagen helixchemistry.chemical_elementSalt (chemistry)Crystal structureCalcium010402 general chemistry01 natural sciencesCatalysisAcetic acidchemistry.chemical_compoundchemistry.chemical_classificationcalcium010405 organic chemistryChemistryCommunicationstructure elucidationHelical StructuresGeneral Chemistrycarboxyalate ligandsCommunications0104 chemical sciencesAmino acidX-ray diffractionEfflorescenceCrystallographyTriple helixAngewandte Chemie (International Ed. in English)
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Kinetic control in the chiral recognition of three-bladed propellers

2010

The ion pair of the stereolabile C(3)-symmetric, i(+)o proton complex [1H](+) of diaza-macropentacycle 1 and the configurationally stable Delta-TRISPHAT ([Delta-3](-)) anion exists in the form of two diastereomers, namely, [Delta-(1.H)][Delta-3] and [Lambda-(1.H)][Delta-3], the ratio of which, in terms of diastereomeric excess (de) decreases in the order [D(8)]THF (28%)CD(2)Cl(2) (22%)CDCl(3) (20%)[D(8)]toluene (16%)C(6)D(6) (7%)[D(6)]acetone (0%) at thermodynamic equilibrium. Except in the case of [D(6)]acetone, the latter is reached after a period of time that increases from 1 h ([D(8)]THF) to 24 h (CDCl(3)). Moreover, the initial value of the de of [1.H][Delta-3] in CDCl(3), before the t…

CryptandsIon pairsProtonStereochemistryOrganic ChemistryKineticsDiastereomerProtonationGeneral ChemistryNuclear magnetic resonance spectroscopyTolueneCatalysischemistry.chemical_compoundCrystallographyKineticsDeprotonationchemistryddc:540Solvent effectsSolvent effectsHelical structures
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Functionalized lipid tubules as tools for helical crystallization of proteins

1997

The development of functional supramolecular devices built by self-assembly of elementary molecules and with bioactive properties arouses considerable interest in the field of nanotechnology and new materials. We report here the formation of a new class of lipid tubules exhibiting both properties of molecular recognition and crystal formation for the protein streptavidin. These lipid tubules, made of biotin-containing dioctadecylamine molecules, are straight hollow cylinders with a constant diameter of 27 nm and variable length up to several micrometers. They are unilamellar with an inner diameter of about 16 nm, as shown by cryoelectron microscopy. Streptavidin binds to the biotinylated tu…

StreptavidinliposomesSupramolecular chemistryTWO-DIMENSIONAL CRYSTALSMEMBRANESCatalysisACETYLCHOLINE-RECEPTORVESICLESlipidschemistry.chemical_compoundTOXIN B-SUBUNITMolecular recognition2-DIMENSIONAL CRYSTALLIZATIONELECTRON-MICROSCOPYLiposomeChemistryVesicleOrganic Chemistrytechnology industry and agricultureCHOLERA-TOXINGeneral ChemistryCrystallographyMembranehelical structuresRESOLUTIONBiotinylationSelf-assemblyself-assembly tubulesMICROSTRUCTURESChemistry – A European Journal
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A Hydrogen-Bonded Supramolecular meso-Helix

2003

[EN] A new one-dimensional hydrogen-bonded polymer with a unique meso-helical structure has been prepared from the spontaneous self-assembly in the solid-state of meta-substituted phenylene dioxamic acid diethyl ester monomers. The helical nature of this molecule and its self-complementary character, through intermolecular hydrogen bonding between oxamic acid ester functions, are the two main factors responsible for the crystalline aggregation process, as confirmed by both experimental X-ray crystallographic data and theoretical ab initio calculations.

StereochemistryHydrogen bondOrganic ChemistrySupramolecular chemistryCrystal engineeringCrystal engineeringAmidesHydrogen bondschemistry.chemical_compoundCrystallographyDensity functional calculationsMonomerchemistryAb initio quantum chemistry methodsPhenyleneFISICA APLICADAHelixMoleculePhysical and Theoretical ChemistryHelical structures
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