Search results for "etica."

showing 10 items of 13546 documents

NMR and homology modeling studies of copper(II)-halocyanin from Natronobacterium pharaonis bacteria

2004

Abstract Halocyanin from the haloalkaliphilic archaean Natronobacterium pharaonis is a peripheral membrane type 1 blue copper protein with a single polypeptide chain of 163 amino acid residues. Halocyanin participates as putative electron carrier protein associated to an electron acceptor role for a terminal oxidase and has the lowest redox potential value reported to date for a BCP. NMR studies and homology modeling calculations were performed to evaluate the electronic properties of Cu(II)-halocyanin from Natronobacterium pharaonis . The copper coordination site properties of Cu(II)-halocyanin are discussed. The 1 H NMR spectra, isotropic chemical shifts and relaxation times for halocyani…

AmicyaninStellacyaninbiologyCopper proteinInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryProton NMRbiology.proteinHomology modelingPhysical and Theoretical ChemistryAzurinHomology (chemistry)PlastocyaninInorganica Chimica Acta
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On the formation of inclusion complexes at the solid/liquid interface of anchored temperature-responsive PNIPAAM diblock copolymers with γ-cyclodextr…

2017

The thermal responsive behavior of adsorbed layers of diblock copolymers of poly(N-isopropylacrylamide) (PNIPAAM) and poly((3-acrylamidopropyl)trimethylammonium chloride) (PAMPTMA(+)) with γ-cyclodextrin (γ-CD) at the solid/liquid interface has been investigated using three in situ techniques: null ellipsometry, quartz–crystal microbalance with dissipation monitoring, and neutron reflectometry. The measurements provided information about the adsorbed amounts, the layer thickness, hydration and viscoelastic properties, and the interfacial structure and composition. The copolymers adsorb to silica with the cationic PAMPTMA(+) blocks sitting as anchors in a flat conformation and the PNIPAAM ch…

AmidePolymers and PlasticsBlock copolymerReflectometerReflection02 engineering and technology01 natural sciencessupramolecular chemistryquartz crystal microbalancechemistry.chemical_compoundColloid and Surface ChemistryEllipsometryViscoelasticity Inclusion complexCopolymerMaterials ChemistryPoly (n isopropylacrylamide)Poly(N-isopropylacrylamide)Settore CHIM/02 - Chimica Fisicachemistry.chemical_classification/dk/atira/pure/subjectarea/asjc/1600/1606Reflectometry/dk/atira/pure/subjectarea/asjc/1500/1505Cyclodextrinunclassified drug Article021001 nanoscience & nanotechnologyThermoresponsive block copolymerpriority journalsolidpolymerizationPoly(N-isopropylacrylamide)synthesiNeutron reflectometrypolyrotaxane0210 nano-technologyellipsometryMaterials science/dk/atira/pure/subjectarea/asjc/2500/2505/dk/atira/pure/subjectarea/asjc/2500/2507poly(n isopropylacrylamide)010402 general chemistryLower critical solution temperatureAcrylic monomeratom transfer radical polymerizationAdsorptioncomplex formationPolymer chemistryCyclodextrinliquidPhysical and Theoretical ChemistrySolid/liquid interfaceThermo-responsive Hydrogels copolymerneutron reflectometryInclusion complexgamma cyclodextrinCationic polymerization0104 chemical sciencessolid liquid interfacechemistryChemical engineeringInvited ArticleColloid and Polymer Science
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Pentafulvene durch Aminomethinylierung des Cyclopentadiens

1986

Aus der Dreikomponentenreaktion von Cyclopentadien (1) mit s-Triazin (2) und einem sekundaren Amin 4 gehen die cyclisch N,N-disubstituierten Pentafulven-6-amine 5 und die cyclisch N1,N1-disubstituierten N2-(6-Pentafulvenyl)formamidine 7 hervor. Unter den biologischen Eigenschaften der neuen Verbindungen ist besonders die anthelminthische Wirkung von 5d interessant. Pentafulvenes by Aminomethynylation of Cyclopentadiene The three component reaction comprising the interaction of cyclopentadiene (1) with s-triazine (2) and a secondary amine 4 leads to the cyclic N,N-disubstituted pentafulven-6-amines 5 and the cyclic N1,N1-disubstituted N2-(6-pentafulvenyl)formamidines 7. Among the biological …

Amidinechemistry.chemical_compoundCyclopentadienechemistryStereochemistryBiological propertyOrganic ChemistryAmine gas treatingPiperidinePhysical and Theoretical ChemistryLiebigs Annalen der Chemie
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ENANTIOSELECTIVE REDUCTION OF PROCHIRAL KETONES PROMOTED BY AMINO AMIDE RUTHENIUM COMPLEXES: A DFT STUDY

2021

International audience; The origin of enantioselectivity in the reaction of chiral Ru amino amide complexes in the asymmetric transfer hydrogenation of acetophenone was investigated using DFT calculations. For the most stable active catalysts, the full free energy profiles for the reaction were calculated according to the concerted hydrogen transfer mechanism. We succeeded in reproducing the experimentally observed enantioselectivity for the studied Ru amino amide complexes. Our results indicate that the high enantioselectivity can be explained by a stabilizing CH-π interaction existing between the phenyl group of acetophenone and the aromatic substituent of the catalyst, which plays a sign…

Amidoamide Ruthenium CatalystEnantioselective ReductionSubstituentchemistry.chemical_elementConformers010402 general chemistryTransfer hydrogenation01 natural sciencesBiochemistryDFTCatalysisInorganic Chemistrychemistry.chemical_compoundComputational chemistryMaterials ChemistryPhenyl groupPhysical and Theoretical ChemistryEnantiomeric excess010405 organic chemistryOrganic ChemistryEnantioselective synthesis3. Good health0104 chemical sciencesRuthenium[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryMechanismAcetophenone
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Thermochemical properties of small open-shell systems: experimental and high-levelab initioresults for NH2and

2006

The first adiabatic ionization energy and the first singlet–triplet splitting of the amidogen radical (NH2) have been determined by high-level ab initio quantum chemistry based on the coupled-cluster approach (90 041 and 10 319 cm−1, respectively) and by high-resolution pulsed-field-ionization zero-kinetic-energy (PFI-ZEKE) photoelectron spectroscopy (90 083.8 ± 1.0 and 10 222.0 ± 1.3 cm−1, respectively). A comparison between the theoretical and experimental values demonstrates the predictive powers of high-level ab initio theory in the derivation of the thermochemical properties of small molecular systems. The absolute accuracy of better than 100 cm−1 alleviates the experimental search for…

AmidogenAbsolute accuracyBiophysicsAb initioCondensed Matter PhysicsQuantum chemistryMolecular physicschemistry.chemical_compoundX-ray photoelectron spectroscopychemistryPhysical and Theoretical ChemistryIonization energyAdiabatic processMolecular BiologyOpen shellMolecular Physics
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Ab initio molecular orbital study of the substituent effect on ammonia and phosphine–borane complexes

2004

Abstract The complexation energies of H 3 BXH 3− n F n ( X =N, P; n =0–3) and the proton affinities of XH 3– n F n compounds have been investigated at the G2(MP2) level of theory. The G2(MP2) results show that the phosphine complexes are more stable than the corresponding ammonia ones. Increasing fluorine substitution on nitrogen atom reduces both the basicity of NH 3− n F n and the stability of ammonia complexes. For the phosphine complexes, the successive fluorine substitution on the phosphine increase the stability of H 3 BPH 3− n F n complexes although the reduction of the basicity of the PH 3– n F n ligands with this substitution. The NBO partitioning scheme shows that the stability of…

Ammonia boraneInorganic chemistrySubstituentAb initioBoraneCondensed Matter PhysicsBiochemistryMedicinal chemistryBond lengthchemistry.chemical_compoundchemistryMolecular orbitalPhysical and Theoretical ChemistryPhosphineNatural bond orbitalJournal of Molecular Structure: THEOCHEM
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Substituent effect on ammonia–borane donor–acceptor complexes: a G2(MP2) molecular orbital study

1998

Abstract H3BNHnMe3−n and Me3−nHnBNH3 (n=0–3) donor–acceptor complexes have been studied using the G2(MP2) method. Predicted equilibrium structures and dissociation energies have been correlated to the degree of substitution on the donor and the acceptor separately. It is found that successive methyl substitutions on boron reduce the dissociation energies of the complexes, contrary to the successive substitutions on nitrogen. The NBO partitioning scheme suggests that there is no correlation between the charge transfer and the dissociation energies. These results are interpreted in terms of the changes in the HOMO−LUMO gap, the type of acceptor and donor involved, and distortion of the accept…

Ammonia boraneSubstituentchemistry.chemical_elementCondensed Matter PhysicsPhotochemistryBiochemistryNitrogenAcceptorDissociation (chemistry)chemistry.chemical_compoundchemistryMolecular orbitalPhysical and Theoretical ChemistryBoronNatural bond orbitalJournal of Molecular Structure: THEOCHEM
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Templated growth of smart nanocomposite thin films: Hybrid aerosol assisted and atmospheric pressure chemical vapour deposition of vanadyl acetylacet…

2009

Hybrid aerosol assisted and atmospheric pressure chemical vapour deposition methodology has been utilised to produce nanocomposite thin films of gold nanoparticles and vanadium dioxide from vanadyl acetylacetonate and auric acid. The addition of tetraoctyl ammonium bromide (TOAB) to the precursor Solution gave control of the size and distribution of gold nanoparticles in the vanadium oxide matrix. These reactions led to vanadium dioxide films with reduced crystallite sizes and enhanced thermochromic properties. The films were analysed by X-ray diffraction, scanning electron microscopy and X-ray photoelectron spectroscopy. Their optical and thermochromic behaviour was also determined, This h…

Ammonium bromideNanocompositeInorganic chemistryOxideSettore ICAR/10 - Architettura TecnicaChemical vapor depositionVanadium oxideInorganic Chemistrychemistry.chemical_compoundCVD Nanocomposite Thermochromism Aerosol HybridSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryX-ray photoelectron spectroscopyChemical engineeringColloidal goldMaterials ChemistryChemical Vapor Deposition CVD Vanadium dioxide thermochromic coatingsPhysical and Theoretical ChemistryVanadyl acetylacetonate
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Selective Extraction and Efficient Binding in a Protic Solvent of Contact Ion Triplets by Using a Thiourea-Based Bis-Calix[6]arene Receptor

2013

We report a D3h-symmetric tail-to-tail bis-calix[6]thiourea 5 that displays two divergent cavities triply connected by thiourea linkages. This calix[6]tube was efficiently synthesized through a [1+1] macrocyclization reaction and characterized by X-ray diffraction analysis. The binding properties of this heterotritopic receptor were evaluated in a protic environment (i.e., CD3OD/CDCl3) through NMR studies. Thus, bis-calix[6]thiourea 5 exhibits a remarkable ability in the cooperative complexation of an anion sandwiched between two ammonium ions, a high selectivity for ammonium sulfate salts being observed. The anion is bound through multiple hydrogen-bonding interactions at the thiourea bind…

Ammonium sulfate010405 organic chemistryOrganic ChemistryInorganic chemistrySupramolecular chemistry010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryThioureaPolymer chemistryCalixareneAmmoniumPhysical and Theoretical ChemistrySelectivityChirality (chemistry)Protic solventEuropean Journal of Organic Chemistry
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Secondary brown carbon formation via the dicarbonyl imine pathway: nitrogen heterocycle formation and synergistic effects.

2016

Dicarbonyls are known to be important precursors of so-called atmospheric brown carbon, significantly affecting aerosol optical properties and radiative forcing. In this systematic study we report the formation of light-absorbing nitrogen containing compounds from simple 1,2-, 1,3-, 1,4-, and 1,5-dicarbonyl + amine reactions. A combination of spectrophotometric and mass spectrometric techniques was used to characterize reaction products in solutions mimicking atmospheric particulates. Experiments with individual dicarbonyls and dicarbonyl mixtures in ammonium sulfate and glycine solutions demonstrate that nitrogen heterocycles are common structural motifs of brown carbon chromophores formed…

Ammonium sulfateOzonolysis010504 meteorology & atmospheric sciencesAcetylacetoneImineAcetaldehydeGeneral Physics and Astronomychemistry.chemical_element010501 environmental sciencesPhotochemistry01 natural sciencesNitrogenAbsorbancechemistry.chemical_compoundchemistryAmine gas treatingPhysical and Theoretical Chemistry0105 earth and related environmental sciencesPhysical chemistry chemical physics : PCCP
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