Search results for "guest"

showing 10 items of 122 documents

Exploring the self-assembly of resorcinarenes : from molecular level interactions to mesoscopic structures

2012

UV-vis spectroscopyresorcinareneantibacterial silverionitspektroskopiaLangmuir-Blodgett filmsolid lipid nanoparticlemolekyylitfluorescence spectroscopysupramolecular chemistrystructural chemistryNMR spectroscopyorgaaninen kemiahost-guest chemistrytoiminnalliset materiaalitpinnoitteetX-ray crystallography
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Cilvēkresursu vadība par viesu sūdzības apmierināšanas kvalitāti viesnīcu nozarē

2020

Pētījuma mērķis ir identificēt galvenos cilvēkresursu vadības elementus, kas ietekmē viesu sūdzību apmierināšanu, un izstrādāt ieteikumus, lai labāk atrisinātu sūdzības, kas pozitīvi ietekmē viesnīcas konkurētspēju. Pirmkārt, tas sniedz teorētisku pētījumu par cilvēkresursu vadības sistēmu, parāda attiecības starp HRM un viesu sūdzībām un to, kā sūdzības var rasties uzturēšanās laikā viesnīcā. Attīstības otrā nodaļa ir Uzbekistānas tūrisma nozares analīze, valsts reformas un HRM statistika šajā jomā. Pēdējā daļa no papīra ir empīrisks pētījums, kas ir darīts Hotel Uzbekistānā, kas precizē reālus jautājumus par sūdzībām un apmierinātības kvalitāti, ietekmējot uz HRM kā sviru.

Vadībzinātnehotel industryguest’s complaintsfront line employee.satisfactionhuman resources management
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Coordination Chemistry of a Bis(Tetrazine) Tweezer: A Case of Host-Guest Behavior with Silver Salts

2021

The carbon-carbon cross-coupling of phenyl s-tetrazine (Tz) units at their ortho-phenyl positions allows the formation of constrained bis(tetrazines) with original tweezer structures. In these compounds, the face-to-face positioning of the central tetrazine cores is reinforced by π-stacking of the electron-poor nitrogen-containing heteroaromatic moieties. The resulting tetra-aromatic structure can be used as a weak coordinating ligand with cationic silver. This coordination generates a set of bis(tetrazine)-silver(I) coordination complexes tolerating a large variety of counter anions of various geometries, namely, PF6−, BF4−, SbF6−, ClO4−, NTf2−, and OTf−. These compounds were characterized…

analytical_chemistrycoordinationAbsorption spectroscopyPharmaceutical ScienceCrystal structure010402 general chemistryElectrochemistryligand01 natural sciencesArticleXRD structureAnalytical ChemistryCoordination complexTetrazinechemistry.chemical_compoundQD241-441bis(tetrazine)Drug Discovery[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistrysilverPhysical and Theoretical Chemistryhost-guestchemistry.chemical_classification010405 organic chemistryLigandOrganic ChemistryCationic polymerization0104 chemical sciencesCrystallographychemistryChemistry (miscellaneous)Molecular MedicineStoichiometryMolecules
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Oligoamide Foldamers as Helical Chloride Receptors-the Influence of Electron-Withdrawing Substituents on Anion-Binding Interactions.

2019

The anion-binding properties of three closely related oligoamide foldamers were studied using NMR spectroscopy, isothermal titration calorimetry and mass spectrometry, as well as DFT calculations. The 1 H NMR spectra of the foldamers in [D6 ]acetone solution revealed partial preorganization by intramolecular hydrogen bonding, which creates a suitable cavity for anion binding. The limited size of the cavity, however, enabled efficient binding by the inner amide protons only for the chloride anion resulting in the formation of a thermodynamically stable 1:1 complex. All 1:1 chloride complexes displayed a significant favourable contribution of the entropy term. Most likely, this is due to the …

anionitreceptors010402 general chemistry01 natural sciencesBiochemistryChloridesupramolecular chemistryhost-guest systemschemistry.chemical_compoundAmidesupramolekulaarinen kemiamedicinefoldamersAnion bindingta116010405 organic chemistryChemistryHydrogen bondOrganic ChemistryFoldamerIsothermal titration calorimetryGeneral ChemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesCrystallographyProton NMRanionsmedicine.drugChemistry, an Asian journal
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Oligoamide Foldamers as Helical Chloride Receptors : the Influence of Electron-Withdrawing Substituents on Anion-Binding Interactions

2019

The anion‐binding properties of three closely related oligoamide foldamers were studied using NMR spectroscopy, isothermal titration calorimetry and mass spectrometry, as well as DFT calculations. The 1H NMR spectra of the foldamers in [D6]acetone solution revealed partial preorganization by intramolecular hydrogen bonding, which creates a suitable cavity for anion binding. The limited size of the cavity, however, enabled efficient binding by the inner amide protons only for the chloride anion resulting in the formation of a thermodynamically stable 1:1 complex. All 1:1 chloride complexes displayed a significant favourable contribution of the entropy term. Most likely, this is due to the re…

anionitsupramolekulaarinen kemiareceptorsfoldamershost-guest systems
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Solution and solid-state studies on the halide binding affinity of perfluorophenyl-armed uranyl–salophen receptors enhanced by anion–π Interactions

2016

The enhancement of the binding between halide anions and a Lewis acidic uranyl-salophen receptor has been achieved by the introduction of pendant electron- deficient arene units into the receptor skeleton. The association and the occurrence of the elusive anion-p interaction with halide anions (as tetrabutylammonium salts) have been demonstrated in solution and in the solid state, providing unambiguous evidence on the interplay of the concerted interactions responsible for the anion binding.

anion–π interactions; halides; host–guest systems; lewis acid–base interactions; uranyl–salophen; chemistry (all)Solid-stateHalide010402 general chemistry01 natural sciencesCatalysisIonUranyl salophenPolymer chemistryOrganic chemistryReceptorAnion bindingta116Uranyl-salphenlewis acid–base interactionsanion–π interactionsuranyl–salophen010405 organic chemistryChemistryOrganic Chemistryhost–guest systemsGeneral Chemistryinteractions0104 chemical sciencesuranyl-salophen receptorshalideschemistry (all)halide recognitionanions
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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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Binding properties of heptakis-(2,6-di-O-methyl)-β-cyclodextrin and mono-(3,6-anhydro)-β-cyclodextrin: a polarimetric study

2011

The binding constants for the inclusion complexes formed between heptakis-(2,6-di-O-methyl)-β-cyclodextrin (MβCD) and mono-(3,6-anhydro)-β-cyclodextrin (AβCD) with a set of suitably selected organic guests, were measured by means of polarimetry. Measurements were carried out at various pH values in order to ensure the correct protonation state for ionizable guests. Experimental data suggest that the binding properties of MβCD may be rationalized considering the less polar and more hydrophobic character of the cavity, although similar variations in conformational/dynamic behaviour occur as for native βCD. On the other hand, AβCD shows some similarities with αCD, due to the significant distor…

chemistry.chemical_classificationCrystallographyCyclodextrins host-guest complexes polarimetric measurementsCyclodextrinChemistryBinding propertiesSupramolecular chemistryPolarProtonationSettore CHIM/06 - Chimica OrganicaGeneral ChemistryCondensed Matter PhysicsFood ScienceJournal of Inclusion Phenomena and Macrocyclic Chemistry
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Binding equilibria between beta-cyclodextrin and p-nitro-aniline derivatives: the first systematic study in mixed water-methanol solvent systems.

2009

Abstract Complexation equilibria, in mixed water–methanol solvent media, between native β-cyclodextrin and a set of suitably selected p -nitro-aniline derivatives were studied by means of polarimetry. The effects exerted by the organic co-solvent on the conditional inclusion free energies Δ G cond 0 and the differential molar optical rotations Δ Θ were thoroughly analyzed under the perspective of the enthalpy–entropy compensation effect. Experimental data suggest an intimate participation (‘dynamic co-inclusion’) of solvent molecules in the formation and in the conformational dynamics of the host–guest inclusion complex.

chemistry.chemical_classificationCyclodextrinOrganic ChemistryEnthalpyNitro compoundSettore CHIM/06 - Chimica OrganicaBiochemistryCyclodextrin host-guest complexes polarimetryInclusion compoundSolventchemistry.chemical_compoundAnilinechemistryComputational chemistryDrug DiscoveryNitroMoleculeOrganic chemistry
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Binding properties of mono-(6-deoxy-6-amino)-β-cyclodextrin towards p-nitroaniline derivatives: a polarimetric study

2009

Abstract Polarimetry was used in order to investigate the formation of supramolecular complexes between mono-6-amino-β-cyclodextrin and various p-nitroaniline derivatives at two different pH values. Comparison with the behaviour of native β-cyclodextrin gave us the opportunity to consider the effect exerted by the presence of charged groups, having different solvation requirements, on the binding equilibrium. Data offer some support to the hypothesis of ‘dynamic co-inclusion’ of solvent molecules within the host–guest complex.

chemistry.chemical_classificationCyclodextrinStereochemistryOrganic ChemistrySupramolecular chemistrySolvationNitro compoundcyclodextrins polarimetric study host-guest complexes stability constantsSettore CHIM/06 - Chimica OrganicaBiochemistryInclusion compoundSolventchemistry.chemical_compoundchemistryDrug DiscoveryMoleculeAmine gas treatingTetrahedron
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