Search results for "Molecular chemistry"

showing 10 items of 1103 documents

Docetaxel-Loaded Nanoparticles Assembled from β-Cyclodextrin/Calixarene Giant Surfactants: Physicochemical Properties and Cytotoxic Effect in Prostat…

2017

Giant amphiphiles encompassing a hydrophilic β-cyclodextrin (βCD) component and a hydrophobic calix[4]arene (CA4) module undergo self-assembly in aqueous media to afford core-shell nanospheres or nanocapsules, depending on the nanoprecipitation protocol, with high docetaxel (DTX) loading capacity. The blank and loaded nanoparticles have been fully characterized by dynamic light scattering (DLS), ζ-potential measurements and cryo-transmission electron microscopy (cryo-TEM). The data are compatible with the distribution of the drug between the nanoparticle core and the shell, where it is probably anchored by inclusion of the DTX aromatic moieties in βCD cavities. Indeed, the release kinetics …

calixarenesSupramolecular chemistryNanoparticle02 engineering and technology010402 general chemistry01 natural sciencesNanocapsulesDynamic light scatteringCalixareneAmphiphiledocetaxelPharmacology (medical)Original Researchchemistry.chemical_classificationPharmacologycyclodextrinsCyclodextrinlcsh:RM1-950glioblastoma021001 nanoscience & nanotechnologyprostate cancerCombinatorial chemistry0104 chemical scienceslcsh:Therapeutics. PharmacologychemistryDrug delivery0210 nano-technologyFrontiers in pharmacology
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Hyper-reticulated calixarene polymers: a new example of entirely synthetic nanosponge materials

2018

New calixarene-based nanosponges (CaNSs), i.e., hyper-reticulated polymers constituted by calixarene monomer units joined by means of bis(1,2,3-trialzolyl)alkyl linkers, were synthesized, characterized and subjected to preliminary tests to assess their supramolecular absorption abilities towards a set of suitable organic guests, selected as pollutant models. The synthesis was accomplished by means of a CuAAC reaction between a tetrakis(propargyloxy)calix[4]arene and an alkyl diazide. The formation of the polymeric network was assessed by means of FTIR and 13C{1H} CP-MAS solid-state NMR techniques, whereas morphological characterization was provided by SEM microghaphy. The materials were pro…

calixarenesSupramolecular chemistrynanosponges02 engineering and technology010402 general chemistryNanosponge01 natural sciencesFull Research PaperHydrophobic effectlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrySmart materialCalixarenePolymer chemistryFourier transform infrared spectroscopylcsh:ScienceAlkylSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationOrganic ChemistrySettore CHIM/06 - Chimica OrganicaSettore CHIM/05 - Scienza E Tecnologia Dei Materiali PolimericiPolymer021001 nanoscience & nanotechnology0104 chemical sciencesChemistryMonomerchemistrySolid-state nuclear magnetic resonancesmart materialsCalixarenesolid-state NMRlcsh:Q0210 nano-technologyBeilstein Journal of Organic Chemistry
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Calorimetry: a Valuable Tool for Emerging Smart Nanomaterials

2012

It is well known that calorimetry is a powerful technique to determine the complete energetics (standard free energy, enthalpy and entropy) of interaction processes. We are now assisting to the increment of the use of nano-calorimetry, which appears rather versatile because it can evidence weak interactions quickly and accurately and, furthermore, needs very small amounts of material. Unfortunately, over the years the calorimetry has been applied to restricted fields so that it has been underemployed in studying smart nanomaterials (polypseudorotaxanes, polymeric aggregates, surface functionalized nanoparticles, nanocomposites, etc.) to which a tremendous scientific interest has been recent…

calorimetry supramolecular chemistry nanocompositesSettore CHIM/02 - Chimica Fisica
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Bringing a Molecular Plus One : Synergistic Binding Creates Guest-Mediated Three-Component Complexes

2020

C-Ethyl-2-Methylresorcinarene (A), pyridine (B), and a set of ten carboxylic acids (Cn) associate to form A·B·Cn ternary assemblies with 1:1:1 stoichiometry, representing a useful class of ternary systems where the guest mediates complex formation between the host and a third component. Although individually weak in solution, the combined strength of the multiple non-covalent interactions organizes the complexes even in a highly hydrogen-bond competing methanol solution as explored by both experimental and computational methods. The interactions be-tween A·B and Cn are dependent on the pKa values of carboxylic acids. The weak interactions between A and C further reinforce the interactions b…

carboxylic acidskarboksyylihapotsupramolekulaarinen kemiamolekyylitmolecular recognitionsupramolecular chemistrydiagnostic toolstunnistaminen
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Definition of the chalcogen bond (IUPAC Recommendations 2019)

2019

Abstract This recommendation proposes a definition for the term “chalcogen bond”; it is recommended the term is used to designate the specific subset of inter- and intramolecular interactions formed by chalcogen atoms wherein the Group 16 element is the electrophilic site.

chalcogen bond; IUPAC Organic and Biomolecular Chemistry Division; IUPAC Physical and Biophysical Chemistry Division; nomenclature; noncovalent interactions; self-assembly; supramolecular chemistryGeneral Chemical EngineeringChemical nomenclature010402 general chemistrynoncovalent interaction01 natural sciencessupramolecular chemistrykemialliset sidoksetnoncovalent interactionsChalcogenGroup (periodic table)supramolekulaarinen kemiaNon-covalent interactionsIUPAC Organic and Biomolecular Chemistry DivisionIUPAC Physical and Biophysical Chemistry Divisionchalcogen bondchemistry.chemical_classification010405 organic chemistryChemistryBondSolid State & Structural Chemistry Unitself-assemblyGeneral Chemistry0104 chemical sciencesTerm (time)ChemistryCrystallographyIntramolecular forcenimikkeistötnomenclaturePure and Applied Chemistry
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Kinetically Controlled Stepwise Self-Assembly of AuI-Metallopeptides in Water

2018

The combination of attractive supramolecular interactions of a hydrophobic AuI-metallopeptide with the shielding effect of flexible oligoethylene glycol chains provides access to a stepwise self-assembly of a AuI-metalloamphiphile in water. Kinetic control of the supramolecular polymer morphology is achieved using a temperature-dependent assembly protocol, which yields low dispersity supramolecular polymers (metastable state I) or helical bundled nanorods (state II).

chemistry.chemical_classification010405 organic chemistryChemistryDispersitySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryKinetic controlCatalysis0104 chemical sciencesSupramolecular polymersColloid and Surface ChemistryChemical engineeringMetastabilityShielding effectNanorodSelf-assemblyJournal of the American Chemical Society
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Polyaminocyclodextrin nanosponges: synthesis, characterization and pH-responsive sequestration abilities

2016

New pH-responsive nanosponges were obtained by reacting four different polyaminocyclodextrins with heptakis-(6-bromo)-(6-deoxy)-β-cyclodextrin. The materials obtained were characterized by various techniques (FT-IR, potentiometric titration, differential scanning calorimetry (DSC), porosimetry (BET), 13C{1H} CP-MAS NMR). Their adsorption abilities at different pH values were verified towards a suitable set of model guests, and seem mainly controlled by electrostatic interactions, as a function of the protonation/charge status of the polymer matrix. By contrast, data positively point out a lesser importance assumed by the induced-fit effect, important in affecting the formation of host–guest…

chemistry.chemical_classification010405 organic chemistryChemistryGeneral Chemical EngineeringPotentiometric titrationInorganic chemistryAnalytical chemistryProtonationGeneral ChemistryPolymerPorosimetrySettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciences0104 chemical sciencesMatrix (chemical analysis)Differential scanning calorimetryAdsorptionCyclodextrin Polyamine Nanosponge Polymer Supramolecular ChemistryHeteronuclear moleculeSettore CHIM/02 - Chimica Fisica
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Achieving Strong Positive Cooperativity through Activating Weak Non-Covalent Interactions

2018

Positive cooperativity achieved through activating weak non-covalent interactions is common in biological assemblies but is rarely observed in synthetic complexes. Two new molecular tubes have been synthesized and the syn isomer binds DABCO-based organic cations with high orientational selectivity. Surprisingly, the ternary complex with two hosts and one guest shows a high cooperativity factor (α=580), which is the highest reported for synthetic systems without involving ion-pairing interactions. The X-ray single-crystal structure revealed that the strong positive cooperativity likely originates from eight C-H⋅⋅⋅O hydrogen bonds between the two head-to-head-arranged syn tube molecules. Thes…

chemistry.chemical_classification010405 organic chemistryChemistryHydrogen bondStereochemistrycooperativitySupramolecular chemistrymolecular tubesCooperativityGeneral ChemistryDABCO010402 general chemistryhydorogenchemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundionsMoleculeNon-covalent interactionsmoleculesHost–guest chemistryTernary complexta116Angewandte Chemie International Edition
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Supramolecular complexes formed by dimethoxypillar[5]arenes and imidazolium salts: A joint experimental and computational investigation

2017

To gain more insights into the factors acting on the stability of complexes formed by pillar[5]arenes, we investigated the interaction of dimethoxypillar[5]arene with some 1-(n-alkyl)-3-(9-anthracenylmethyl)-imidazolium based organic salts. In particular, we used salts differing in not only the anion nature ([Cl−], [BF4−], [NTf2−] and [SbF6−]) and alkyl chain length (butyl, octyl and dodecylimidazolium derivatives), but also the presence of a hydrogenated or fluorinated tail (octyl and perfluorooctylimidazolium derivatives). Host–guest systems were analysed in solution, solid state and gas phase, using a combined approach of different techniques like fluorescence, 1H NMR, ESI-MS, DSC and DF…

chemistry.chemical_classification010405 organic chemistryChemistryInorganic chemistrySupramolecular chemistrySolid-stateGeneral ChemistrySettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesFluorescenceCatalysis0104 chemical sciencesIonSolventimidazolium salt.CrystallographyChain lengthMaterials ChemistryProton NMRpillar[5]areneAlkylSupramoleculr chemistry
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A robust nanoporous supramolecular metal–organic framework based on ionic hydrogen bonds

2014

International audience; Hydrogen-bond assembly of tripod-like organic cations [H3-MeTrip]3+ (1,2,3-tri(4′-pyridinium-oxyl)-2-methylpropane) and the hexa-anionic complex [Zr2(oxalate)7]6− leads to a structurally, thermally, and chemically robust porous 3D supramolecular framework showing channels of 1 nm in width. Permanent porosity has been ascertained by analyzing the material at the single-crystal level during a sorption cycle. The framework crystal structure was found to remain the same for the native compound, its activated phase, and after guest resorption. The channels exhibit affinities for polar organic molecules ranging from simple alcohols to aniline. Halogenated molecules and I2 …

chemistry.chemical_classification010405 organic chemistryChemistryNanoporousOrganic ChemistryInorganic chemistrySupramolecular chemistryIonic bondingGeneral Chemistry010402 general chemistryCrystal engineering01 natural sciencesCatalysis0104 chemical sciencesSupramolecular assemblySupramolecular polymersChemical engineeringMoleculeMetal-organic framework[CHIM.COOR]Chemical Sciences/Coordination chemistry
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