Search results for "Pram"

showing 10 items of 1064 documents

Guest-Induced Folding and Self-Assembly of Conformationally Adaptive Macrocycles into Nanosheets and Nanotubes

2017

A conformationally adaptive macrocycle is presented, namely zorb[4]arene, which exists in multiple conformations in the uncomplexed state. The binding cavity of zorb[4]arene is concealed, either due to a collapsed conformation or by self-inclusion. The zorb[4]arene with long alkyl chains manifests itself with surprisingly low melting point and thus exist as an oil at room temperature. Binding of a guest molecule induces the folding and conformational rigidity of zorb[4]arene and leads to well-defined three-dimensional structures, which can further self-assemble into nanosheets or nanotubes upon solvent evaporation, depending on guest molecules and the conformations they can induce.

chemistry.chemical_classificationadaptive macrocyclesnanosheets010405 organic chemistryStereochemistryOrganic ChemistryLow melting pointGeneral Chemistry010402 general chemistry01 natural sciencesCatalysissupramolecular chemistryguest-induced folding0104 chemical sciencesnanotubesFolding (chemistry)Solvent evaporationchemistryMoleculeSelf-assemblyta116AlkylChemistry: A European Journal
researchProduct

Inside Cover: Efficient Self-Assembly of Di-, Tri-, Tetra-, and Hexavalent Hosts with Predefined Geometries for the Investigation of Multivalency (Ch…

2015

chemistry.chemical_classificationbiologyOrganic ChemistrySupramolecular chemistryGeneral Chemistrybiology.organism_classificationCatalysisCoordination complexchemistryComputational chemistryOrganic chemistryTetraCover (algebra)Self-assemblyChemistry - A European Journal
researchProduct

Self-instructed condensation of amino acids and the origin of biological information

1984

In contemporary cells biological information is largely stored in nucleic acids. Therefore, a prerequisite in many theories on the origin of cellular life is the pre-existence of self-replicating polynucleotides that had to be formed by abiotic processes on the prebiotic Earth. It is usually assumed that the spontaneous synthesis of a self-replicating polynucleotide could take place readily. However, serious stereochemical obstacles exist which make such a synthesis extremely improbable. Amino acids, on the other hand, which are abundantly formed in prebiotic simulation experiments, are relatively easily polymerized to macromolecules (protoproteins) that share with modern proteins many prop…

chemistry.chemical_classificationbiologyStereochemistryChemistryPrebioticmedicine.medical_treatmentSupramolecular chemistryCondensed Matter PhysicsAtomic and Molecular Physics and OpticsCellular lifeAmino acidBiochemistryPolynucleotideNucleic acidbiology.proteinmedicinePhysical and Theoretical ChemistryPolymeraseMacromoleculeInternational Journal of Quantum Chemistry
researchProduct

Hydrophilic and hydrophobic copolymers of a polyasparthylhydrazide bearing positive charges as vector for gene therapy

2008

BACKGROUND: The design of polymeric vectors for gene delivery provided with specific properties is one of the most critical aspects for a successful gene therapy. These polymers should be biocompatible as well as able to carry efficiently DNA to target tissues and to transfect it into cells. RESULTS: The formation of complexes of poly[(α,β-asparthylhydrazide)–poly(ethylene glycol)] and poly[(α,β-asparthylhydrazide)–hexadecylamine] copolymers functionalised with glycidyltrimethylammonium chloride (PAHy–PEG-GTA and PAHy–C16-GTA, respectively) with DNA was studied. The effects of the introduction of hydrophilic (PEG) or hydrophobic (C16) moieties on the chains of PAHy–GTA copolymers, such as t…

chemistry.chemical_classificationcationic polyaminoacidMaterials sciencePolymers and PlasticsPAHy-GTA copolymers polyaspartylhydrazidefungiOrganic ChemistrySupramolecular chemistryDNA protectionPolymerGene deliveryPolyelectrolytechemistry.chemical_compoundpolyion complexchemistryPolymer chemistryPEG ratioMaterials ChemistrySide chainEthylene glycolDNA
researchProduct

Derivatives of (-)-Isosteviol with Expanded Ring D and Various Oxygen Functionalities

2012

(–)-Isosteviol is a unique ex-chiral-pool building block that is readily available. Both functional groups are aligned in a concave manner. The methyl moiety on the backbone also points in this direction, creating a strong asymmetric environment close to these functional groups. The slightly divergent orientation of the keto and carboxy functions limits its use in the construction of supramolecular architectures as optically pure divalent building blocks. By selective transformations, ring D of (–)-isosteviol can be expanded and equipped with oxygen-containing functionalities, providing a variety of useful and rigid building blocks with defined stereochemistry.

chemistry.chemical_classificationchemistryBlock (programming)StereochemistryOrganic ChemistrySupramolecular chemistryMoietyPhysical and Theoretical ChemistryRing (chemistry)DivalentEuropean Journal of Organic Chemistry
researchProduct

Inside Cover: A Self-Assembled M8L6 Cubic Cage that Selectively Encapsulates Large Aromatic Guests (Angew. Chem. Int. Ed. 15/2011)

2011

chemistry.chemical_classificationchemistryPolymer chemistrySupramolecular chemistryNanotechnologyCover (algebra)General ChemistrySelf-assemblyCageCatalysisCoordination complexSelf assembledAngewandte Chemie International Edition
researchProduct

Cover Picture: Achieving Strong Positive Cooperativity through Activating Weak Non‐Covalent Interactions (Angew. Chem. Int. Ed. 3/2018)

2018

chemistry.chemical_classificationchemistryStereochemistrySupramolecular chemistryCooperative bindingNon-covalent interactionsCover (algebra)CooperativityGeneral ChemistrySelf-assemblyHost–guest chemistryCatalysisAngewandte Chemie International Edition
researchProduct

Cyclodextrins in Polymer Synthesis: Supramolecular Cyclodextrin Complexes of Pyrrole and 3,4-Ethylenedioxythiophene and Their Oxidative Polymerization

2000

chemistry.chemical_classificationchemistry.chemical_compoundMaterials sciencechemistryCyclodextrinPolymerizationMechanics of MaterialsMechanical EngineeringPolymer chemistrySupramolecular chemistryGeneral Materials SciencePolymerPyrroleAdvanced Materials
researchProduct

Tuneable pH-regulated supramolecular copolymerisation by mixing mismatched dendritic peptide comonomers

2015

Charged phenylalanine-rich dendritic peptides form highly stable and pH-switchable rod-like supramolecular copolymers, when co-assembled with a matching oppositely charged dendritic comonomer. Here, we demonstrate that by mismatching a strong with a weak β-sheet encoded comonomer, both the stability and the pH-triggered disassembly of the copolymers shifts drastically from pH 4.2 to biologically relevant pH 5.8.

chemistry.chemical_classificationchemistry.chemical_compoundPolymers and PlasticsChemistryComonomerOrganic ChemistryPolymer chemistryCopolymerSupramolecular chemistryBioengineeringPeptideBiochemistryMixing (physics)Polymer Chemistry
researchProduct

Binding abilities of new cyclodextrin-cucurbituril supramolecular hosts

2015

Various combined techniques (UV–vis spectrophotometry, isothermal titration calorimetry, thermogravimetry, ESI-MS mass spectrometry, polarimetry and 1H NMR spectroscopy) were used in order to study the interaction between a new combined supramolecular host, namely a bow-tie-structured cyclodextrin–cucurbituril association solely held by non-covalent interactions, and a suitably selected guest, namely the N-(p-nitrophenyl)-1,8-diaminooctane hydrochloride. In particular, the use of different techniques highlighted the peculiar features of the possible host–guest supramolecular interactions under different concentration conditions.

chemistry.chemical_classificationcucubiturilCyclodextrinsmedicine.diagnostic_testCyclodextrinHydrochloridecucurbiturilsSupramolecular chemistryIsothermal titration calorimetryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMass spectrometrycucurbiturilThermogravimetryCrystallographychemistry.chemical_compoundcyclodextrinchemistryComputational chemistryCucurbiturilSpectrophotometrymedicinecucurbiturils; Cyclodextrins; supramolecular co-polymerssupramolecular co-polymerscyclodextrins; cucurbiturils; supramolecular co-polymers
researchProduct