Search results for "Ordination"

showing 10 items of 1367 documents

Tunable Spin-Crossover Behavior of the Hofmann-like Network {Fe(bpac)[Pt(CN) 4 ]} through Host-Guest Chemistry

2013

A study of the spin-crossover (SCO) behavior of the tridimensional porous coordination polymer {Fe(bpac)[Pt(CN)4]} (bpac=bis(4-pyridyl) acetylene) on adsorption of different mono- and polyhalobenzene guest molecules is presented. The resolution of the crystal structure of {Fe(bpac)[Pt(CN) 4]}A?G (G=1,2,4-trichlorobenzene) shows preferential guest sites establishing I?A?A?A?I? stacking interactions with the host framework. These host-guest interactions may explain the relationship between the modification of the SCO behavior and both the chemical nature of the guest molecule (electronic factors) and the number of adsorbed molecules (steric factors). Copyright © 2013 WILEY-VCH Verlag GmbH & …

Steric effectsclathrates010405 organic chemistryCoordination polymerStereochemistryOrganic Chemistryhost–guest systemsStackingGeneral ChemistryCrystal structure010402 general chemistrystacking interactions01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographymetal–organic frameworkschemistryspin crossoverSpin crossoverMoleculeMetal-organic framework[CHIM.COOR]Chemical Sciences/Coordination chemistryHost–guest chemistry
researchProduct

Shedding Light on the Interactions of Hydrocarbon Ester Substituents upon Formation of Dimeric Titanium(IV) Triscatecholates in DMSO Solution

2020

Abstract The dissociation of hierarchically formed dimeric triple lithium bridged triscatecholate titanium(IV) helicates with hydrocarbyl esters as side groups is systematically investigated in DMSO. Primary alkyl, alkenyl, alkynyl as well as benzyl esters are studied in order to minimize steric effects close to the helicate core. The 1H NMR dimerization constants for the monomer–dimer equilibrium show some solvent dependent influence of the side chains on the dimer stability. In the dimer, the ability of the hydrocarbyl ester groups to aggregate minimizes their contacts with the solvent molecules. Due to this, most solvophobic alkyl groups show the highest dimerization tendency followed by…

Steric effectscoordination compoundsesteritDimersolvent effects010402 general chemistry01 natural sciencesMedicinal chemistryCatalysishelicatechemistry.chemical_compoundthermodynamicshelicate thermodynamicsSide chainMoleculeAlkylchemistry.chemical_classificationCoordination Chemistry | Hot PaperFull Paper010405 organic chemistryOrganic ChemistrykompleksiyhdisteetGeneral ChemistryFull PapersTriple bond0104 chemical sciences3. Good healthchemistrytermodynamiikkaweak interactionsSolvent effectsSolvophobicChemistry (Weinheim an Der Bergstrasse, Germany)
researchProduct

Azide Binding Controlled by Steric Interactions in Second Sphere. Synthesis, Crystal Structure, and Magnetic Properties of [Ni II 2 (L)(μ 1,1 -N 3 )]…

2016

International audience; The dinuclear Ni-II complex [Ni-2(L-2)][ClO4](2) (3) supported by the 28-membered hexaaza-dithiophenolate macro-cycle (L-2)(2-) binds the N-3(-) ion specifically end-on yielding [Ni-2(L-2)(mu(1,1)-N-3)] [ClO4] (7) or [Ni-2(L-2)(mu(1,1)-N-3)][BPh4] (8), while the previously reported complex [Ni2L1(mu(1,3)-N-3)][ClO4] (2) of the 24-membered macrocycle (L-1)(2-) coordinates it in the end-to-end fashion. A comparison of the X-ray structures of 2, 3, and 7 reveals the form-selective binding of complex 3 to be a consequence of its preorganized, channel-like binding pocket, which accommodates the azide anion via repulsive CH center dot center dot center dot pi interactions …

Steric effectsequilibrium-constantsStereochemistrytransition-metal-complexesCrystal structure010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencessolvation free-energyInorganic Chemistrychemistry.chemical_compoundtetranuclear nickel(ii) complexes[CHIM.CRIS]Chemical Sciences/CristallographyAntiferromagnetismMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistrymu-azidoEquilibrium constantmolecular-structure010405 organic chemistryChemistryLigandni-ii[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryend-to-end0104 chemical sciencesexchange interactionsCrystallographyAzideGround stateorbital interactions[ CHIM.RADIO ] Chemical Sciences/Radiochemistry
researchProduct

(Strept)avidin as host for biotinylated coordination complexes: stability, chiral discrimination, and cooperativity

2005

Incorporation of a biotinylated ruthenium tris(bipyridine) [Ru(bpy)₂(Biot-bpy)]²⁺ (1) in either avidin or streptavidin-(strept)avidin-can be conveniently followed by circular dichroism spectroscopy. To determine the stepwise association constants, cooperativity, and chiral discrimination properties, diastereopure (Λ and δ)-1 species were synthesized and incorporated in tetrameric (strept)avidin to afford (δ-[Ru(bpy)₂(Biot-bpy)]²⁺)x⊂avidin, (Λ- [Ru(bpy)₂(Biot-bpy)]²⁺)x⊂avidin, (δ-[Ru(bpy)₂(Biot- bpy)]²⁺)x⊂streptavidin, and (Λ-[Ru(bpy)₂(Biot-bpy)]²⁺) x⊂streptavidin (x = 1-4) For these four systems, the overall stability constants are log β₄ = 28.6, 30.3, 36.2, and 36.4, respectively. Critical…

StreptavidinCircular dichroismProtein ConformationStereochemistryBiotinchemistry.chemical_elementCooperativity010402 general chemistry01 natural sciencesInorganic ChemistryStructure-Activity RelationshipBipyridinechemistry.chemical_compound22'-DipyridylBacterial ProteinsBiotinCoordination ComplexesBiotinylation[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSMolecular Structurebiology010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryAvidinProtein Structure Tertiary0104 chemical sciencesRuthenium[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographychemistryBiotinylation[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrybiology.proteinStreptavidinAvidin
researchProduct

Trapping Amorphous Intermediates of Carbonates – A Combined Total Scattering and NMR Study

2018

Crystallization via metastable phases plays an important role in chemical manufacturing, biomineralization, and protein crystallization, but the kinetic pathways leading from metastable phases to the stable crystalline modifications are not well understood. In particular, the fast crystallization of amorphous intermediates makes a detailed characterization challenging. To circumvent this problem, we devised a system that allows trapping and stabilizing the amorphous intermediates of representative carbonates (calcium, strontium, barium, manganese, and cadmium). The long-term stabilization of these transient species enabled a detailed investigation of their composition, structure, and morpho…

StrontiumCoordination numberchemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysisAmorphous calcium carbonate0104 chemical scienceslaw.inventionAmorphous solidCondensed Matter::Materials Sciencechemistry.chemical_compoundColloid and Surface ChemistrychemistryChemical engineeringlawMetastabilityCrystallization0210 nano-technologyProtein crystallizationBiomineralizationJournal of the American Chemical Society
researchProduct

Violence and Proximity Violence: Links and Interpretative Developments

2020

This first chapter aims to deciphering the unresolved ties that harken back to patriarchy, a category used to justify all kinds of abuse and maltreatment of women, even in recent years. The more representations legitimizing the centuries-old exercise of control by men over women’s bodies are shared socially, the more they relegate women to positions of segregation. This is a practice typical of patriarchal systems, which tend to place the weakest subject in a position of permanent subordination. In the case of migrant women, in extreme cases, patriarchy even arrives at the dehumanization, objectification, and reification of their bodies.

Subordination (finance)PatriarchySubject (philosophy)VulnerabilityGender studiesSociologyObjectificationControl (linguistics)DehumanizationReification (Marxism)
researchProduct

Old French Parataxis: syntactic variant or stylistic variation?

2012

The existence of paratactic constructions in Old French is a well-known fact, as in the following: Co sent Rollanto la veue ad perdue‘Roland feels (that) he has lost his sight’ (Chanson de Roland2297). These structures alternate with structures containing que: Co sent Rollant que s’espee li tolt‘Roland feels that his sword has been taken from him’ (Chanson de Roland2284). Although traditional philologists note that different types of asyndetic subordinate clauses exist, they do not provide an explanation of how and why such structures alternate with those introduced by que. Moreover, a detailed analysis reveals that the distribution of paratactic constructions does not seem to be homogeneou…

Subordination (linguistics)Historyancien françaisparataxe05 social sciencesOld Frenchsubordination[SHS.LANGUE] Humanities and Social Sciences/LinguisticsLinguisticslanguage.human_language030507 speech-language pathology & audiology03 medical and health sciencesParataxisPhilologyDirect speechlanguage[ SHS.LANGUE ] Humanities and Social Sciences/LinguisticsDependent clause0501 psychology and cognitive sciencesSWORD[SHS.LANGUE]Humanities and Social Sciences/Linguistics0305 other medical science050104 developmental & child psychologyRelative clause
researchProduct

Cultural Paradigm and Popular Canon: The Discourse on Nation in Nineteenth-century Music of Slavic Mitteleuropa

2016

Nacionalna identiteta slovanske Srednje Evrope je v razpravi obravnavana z novim pristopom k različnim kulturnim paradigmam, takim, ki upošteva zgodovinske dogodke, preko katerih se je ob koncu 18. stoletja na Poljskem in v 19. stoletju na Češkem, Slovenskem in na Hrvaškem uveljavil splošno priznani glasbeni kanon. Pojav kanona je treba analizirati v okviru, v katerem sta kozmopolitizem in nacionalizem soobstajala v prepletu uporabne in avtonomne glasbe, kar presega zamejevanje v kategorije podrejenosti, prirejenosti in avtonomije. The national identity of Slavic Mitteleuropa is examined by means of a new approach to different cultural paradigms, namely the historical events out of which th…

Subordination (linguistics)Literaturebusiness.industrymedia_common.quotation_subjectCanonArtnational identity music eighteenth century nineteenth century Bohemia Slovenia CroatiaNationalismPhenomenonNational identitySettore L-ART/07 - Musicologia E Storia Della MusicaSlavic languagesbusinessMusicClassicsAutonomymedia_common
researchProduct

Triggering the generation of an iron(IV)-oxo compound and its reactivity toward sulfides by RuII photocatalysis

2014

The preparation of [FeIV(O)(MePy2tacn)]2+ (2, MePy2tacn = N-methyl-N,N-bis(2-picolyl)-1,4,7-triazacyclononane) by reaction of [FeII(MePy2tacn)(solvent)]2+ (1) and PhIO in CH3CN and its full characterization are described. This compound can also be prepared photochemically from its iron(II) precursor by irradiation at 447 nm in the presence of catalytic amounts of [Ru II(bpy)3]2+ as photosensitizer and a sacrificial electron acceptor (Na2S2O8). Remarkably, the rate of the reaction of the photochemically prepared compound 2 toward sulfides increases 150-fold under irradiation, and 2 is partially regenerated after the sulfide has been consumed; hence, the process can be repeated several times.…

SulfideFotocatàlisi010402 general chemistryPhotochemistry01 natural sciencesBiochemistryChemical reactionArticleCatalysisCatalysisReaccions químiquesReaction rateColloid and Surface ChemistrySofre -- CompostosChemical reactionsSulphur compoundsOrganic chemistryWATER[CHIM.COOR]Chemical Sciences/Coordination chemistryPhotosensitizerReactivity (chemistry)Photocatalysischemistry.chemical_classificationOXYGENATION REACTIONS010405 organic chemistryChemistryGeneral ChemistryElectron acceptorSTATE0104 chemical sciencesELECTRON-TRANSFER PROPERTIESC-H OXIDATIONSPIN FE(IV) COMPLEXPhotocatalysisIRON-OXO COMPLEXESLIGANDTAURINE/ALPHA-KETOGLUTARATE DIOXYGENASENONHEME OXOIRON(IV) COMPLEXES
researchProduct

1H NMR and UV-vis spectroscopic characterization of sulfonamide complexes of nickek(II)-carbonic anhydrase. Resonance assignments based on NOE effects

1992

The binding of acetazolamide, p-fluorobenzensulfonamide, p-toluenesulfonamide, and sulfanilamide to nickel(II)-substituted carbonic anhydrase II has been studied by 1H NMR and electronic absorption spectroscopies. These inhibitors bind to the metal ion forming 1:1 complexes and their affinity constants were determined. The 1H NMR spectra of the formed complexes show a number of isotropically shifted signals corresponding to the histidine ligands. The complexes with benzene-sulfonamides gave rise to very similar 1H NMR spectra. The NMR data suggest that these aromatic sulfonamides bind to the metal ion altering its coordination sphere. In addition, from the temperature dependence of 1H NMR s…

SulfonamidesConformational changeMagnetic Resonance SpectroscopyCoordination sphereProtein ConformationCarbon-13 NMR satelliteChemistryStereochemistryCarbonic anhydrase IINuclear magnetic resonance spectroscopy of nucleic acidsNuclear magnetic resonance spectroscopyBiochemistryAdductAcetazolamideInorganic ChemistryCrystallographyNickelSpectrophotometryProton NMRAnimalsCattleSpectrophotometry UltravioletCarbonic AnhydrasesProtein BindingJournal of Inorganic Biochemistry
researchProduct