Search results for "structures"

showing 10 items of 4815 documents

Inclusion complexes of Cethyl-2-methylresorcinarene and pyridine N-oxides: breaking the C–I⋯−O–N+ halogen bond by host–guest complexation

2016

C ethyl-2-Methylresorcinarene forms host–guest complexes with aromatic N-oxides through multiple intra- and intermolecular hydrogen bonds and C–H⋯π interactions. The host shows conformational flexibility to accommodate 3-methylpyridine N-oxide, while retaining a crown conformation for 2-methyl- and 4-methoxypyridine N-oxides highlighting the substituent effect of the guest. N-Methylmorpholine N-oxide, a 6-membered ring aliphatic N-oxide with a methyl at the N-oxide nitrogen, is bound by the equatorial −N–CH3 group located deep in the cavity. 2-Iodopyridine N-oxide is the only guest that manifests intermolecular N–O⋯I–C halogen bond interactions, which are broken down by the host resulting i…

StereochemistrySubstituentmacromolecular substancesCrystal structure010402 general chemistryRing (chemistry)01 natural sciencespyridine N-oxideschemistry.chemical_compoundPyridineWATERGeneral Materials ScienceCRYSTAL-STRUCTURESta116Cethyl-2-methylresorcinareneCOORDINATIONHalogen bondPACKINGta114010405 organic chemistryHydrogen bondIntermolecular forceRECOGNITIONGeneral ChemistryETHYL RESORCINARENECondensed Matter PhysicsMETHYLRESORCINARENE0104 chemical sciencesCrystallographySOLID-STATEchemistryhost–guest complexationMETALMOLECULAR CAPSULEShalogen bondSingle crystalCrystEngComm
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Preparation of trichloro- and tribromocyclopentadienyltungsten(IV)

2000

International audience; The thermal decarbonylation of (Ring)WX3(CO)2 in refluxing toluene has led to the preparation of the CO-free compounds [(Ring)WX3]2 [Ring=η5-C5H5 (Cp) and X=Cl (1a) or Br (1b); Ring=η5-C5H4Me (Cp′), X=Cl (2a) or Br (2b); Ring=η5-C5Me5 (Cp*), X=Cl (3)]. The NMR properties of these molecules are consistent with diamagnetism and thereby indicate a different structure from that of the paramagnetic molybdenum analogues. Compounds 1a and 2a react with dppe to afford mononuclear 18-electron adducts, (Ring)WCl3(dppe) (Ring=Cp (4) or Cp′ (5)). The X-ray structure of 5 shows a pseudo-fac-octahedral geometry with the dppe ligand occupying two equatorial (e.g. cis relative to Cp…

Stereochemistrychemistry.chemical_element010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryMedicinal chemistryCO-free compoundsTungstenAdductInorganic ChemistryParamagnetismchemistry.chemical_compoundMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryLigandOrganic ChemistryDecarbonylationMetal–metal bondsToluene0104 chemical sciences3. Good healthDiamagnetismchemistryMolybdenumX-ray structuresJournal of Organometallic Chemistry
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Synthesis of a labile sulfur-centred ligand, [S(H)C(PPh2S)2]−: structural diversity in lithium(i), zinc(ii) and nickel(ii) complexes

2016

A high-yield synthesis of [Li{S(H)C(PPh2S)2}]2 [Li2·(3)2] was developed and this reagent was used in metathesis with ZnCl2 and NiCl2 to produce homoleptic complexes 4 and 5b in 85 and 93% yields, respectively. The solid-state structure of the octahedral complex [Zn{S(H)C(PPh2S)2}2] (4) reveals notable inequivalence between the Zn-S(C) and Zn-S(P) contacts (2.274(1) Å vs. 2.842(1) and 2.884(1) Å, respectively). Two structural isomers of the homoleptic complex [Ni{S(H)C(PPh2S)2}2] were isolated after prolonged crystallization processes. The octahedral green Ni(ii) isomer 5a exhibits the two monoprotonated ligands bonded in a tridentate (S,S',S'') mode to the Ni(ii) centre with three distinctl…

Stereochemistrychemistry.chemical_elementmetal complexes010402 general chemistry01 natural sciencesisomerizationelectronic structuresInorganic Chemistrychemistry.chemical_compoundelektronirakenteetrikkipohjaiset liganditStructural isomerSinglet stateTriplet stateHomolepticta116010405 organic chemistryLigandsulphur-centered ligands0104 chemical sciencesBond lengthNickelCrystallographyOctahedronchemistryisomerisaatiometallikompleksitDalton Transactions
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<title>Assessment of ocular stereovision prevalence and eye dominance stability</title>

2005

The paper reports on the development of the equipment for studies of the eye dominance and ocular stereoprevalence by using black-and-white and color stereostimuli. The stereostimuli are separated either by color-filter goggles or phase separating liquid-crystal-shutter goggles. The stability of the stereoprevalence is studied by artificial step-by-step deterioration of the retinal image quality, particularly in the dominant eye. The stimuli are blurred using spatial Gaussian filtering. The polymer-dispersed-liquid-crystal cell placed in front of the dominant eye induces a controllable light scattering. The stimuli-blurring and light-scattering methods exhibit different influence on the eye…

Stereopsisgenetic structuresbusiness.industryMedicineOptometryComputer visionsense organsArtificial intelligencebusinesseye diseasesRetinal imageOcular dominanceSPIE Proceedings
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Insertion Reactions of Neutral Phosphidozirconocene Complexes as a Convenient Entry into Frustrated Lewis Pair Territory

2016

International audience; Neutral phosphidozirconocene complexes [Cp2Zr(PR2)Me] (Cp=cyclopentadienyl; 1a: R=cyclohexyl (Cy); 1b: R=mesityl (Mes); 1c: R=tBu) undergo insertion into the Zr-P bond by non-enolisable carbonyl building blocks (O=CRR), such as benzophenone, aldehydes, paraformaldehyde or CO2, to give [Cp2Zr(OCRRPR2)Me] (3-7). Depending on the steric bulk around P, complexes 3-7 react with B(C6F5)(3) to give O-bridged cationic zirconocene dimers that display typical frustrated Lewis pair (FLP)/ambiphilic ligand behaviour. Thus, the reaction of {[Cp2Zr(-OCHPhPCy2)][MeB(C6F5)(3)]}(2) (10a) with chalcone results in 1,4 addition of the Zr+/P FLP, whereas the reaction of {[Cp2Zr(-OCHFcPCy…

Steric effectsChalconeStereochemistryzirconiumc-h activation010402 general chemistry01 natural sciencesMedicinal chemistry[ CHIM ] Chemical SciencesCatalysisFrustrated Lewis pairinsertionchemistry.chemical_compoundCyclopentadienyl complexx-ray structuresphosphinidene complexesBenzophenone[CHIM]Chemical SciencesParaformaldehydezr-p bondzirconocene-phosphido complexesmolecular-structure010405 organic chemistryLigandphosphidesOrganic ChemistryCationic polymerizationcrystal-structureGeneral Chemistry0104 chemical sciencesfunctionalized ligandsbis(trimethylsilyl)phosphido complexeschemistryfrustrated Lewis pairsphosphinoaryloxide complexesambiphilic ligands
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Self-assembly in surfactant-based mixtures driven by acid–base reactions: bis(2-ethylhexyl) phosphoric acid–n-octylamine systems

2013

Structural and dynamic features of bis(2-ethylhexyl) phosphoric acid (HDEHP)-n-octylamine (NOA) mixtures as a function of the NOA mole fraction (X-NOA) have been investigated by SAXS, WAXS, IR, dielectric spectroscopy and polarized optical microscopy. In the 0 <= X-NOA < 0.5 range, mixtures are transparent liquids, while the abrupt formation of a waxy solid characterized by an hexagonal bidimensional structure occurs at X-NOA = 0.5. Such a composition-induced phase transition results from the synergetic effect of the progressive increase in number density of ordered HDEHP-NOA nanodomains with X-NOA. Mainly driven by an HDEHP to NOA proton transfer, the increase of structural order with X-NO…

Steric effectsPhase transitionself-assembly surfactant mixtures nanostructures dynamical propertiesReversed micelles liquid crystals phosphate dielectric spectroscopyChemistrySmall-angle X-ray scatteringGeneral Chemical EngineeringReversed micellesGeneral ChemistryMole fractionDielectric spectroscopychemistry.chemical_compoundCrystallographyliquid crystalsChemical engineeringPulmonary surfactantSelf-assemblydielectric spectroscopyPhosphoric acidSettore CHIM/02 - Chimica FisicaphosphateRSC Advances
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Stacking of Sterically Congested Trifluoromethylated Aromatics in their Crystals – The Role of Weak F···π or F···F Contacts

2020

European journal of organic chemistry : EurJOC 2020(38), 6073-6077 (2020). doi:10.1002/ejoc.202001008

Steric effectsaromaattiset yhdisteetChemistryOrganic ChemistryStackingstacking interactionskiteet540fluoriCrystallographyddc:540solid-state structurescrystalssupramolekulaarinen kemiafluorinated compoundsPhysical and Theoretical Chemistryröntgenkristallografiatrifluoromethyl substituents
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Thiophene based imino-pyridyl palladium(II) complexes : Synthesis, molecular structures and Heck coupling reactions

2017

Abstract The new compounds (5-methyl-2-thiophene-2-pyridyl(R))imine [R = methyl (L1); R = ethyl (L2)] and (5-bromo-2-thiophene-2-pyridyl(R)imine [R = methyl (L3); R = ethyl (L4)] were successfully synthesized via Schiff base condensation reaction and obtained in good yields. These potential ligands were reacted with [PdCl2(COD)] and [PdClMe(COD)] to give the corresponding complexes [PdCl2(L)] (L = L1-L4; 1–4) and [PdClMe(L)] (L = L1-L4; 5–8). All compounds were characterized by IR, 1H and 13C NMR spectroscopy, elemental analysis and mass spectrometry. The molecular structures of 1, 2, 6 and 8 were confirmed by X-ray crystallography. The complexes were evaluated as catalyst precursors for st…

Steric effectssynthesisStereochemistryIminechemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryCatalysismolecular structuresInorganic Chemistrychemistry.chemical_compoundHeck reactionMaterials ChemistryThiophenePhysical and Theoretical Chemistryta116heck reactionsSchiff base010405 organic chemistryOrganic ChemistryCondensation reactionpalladium0104 chemical sciencesimino-pyridylchemistryPalladiumJournal of Organometallic Chemistry
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Registration and fusion of segmented left atrium CT images with CARTO electrical maps for the ablative treatment of atrial fibrillation

2005

This study aims to extract the interior surface of the left atrium (LA) and pulmonary veins (PVs) from threedimensional tomographic data and to integrate it with LA CARTO electrical maps. The separation of LA and PVs from other overlapping structures of the heart was performed processing 3D CT data by marker-controlled watershed segmentation and surface extraction. CARTO maps were then registered on the L A internal surface by a stochastic optimization algorithm based on simulated annealing. The residual registration error resulted inferior to 3 mm. The integration between electrophysiological and high resolved anatomic information of LA results feasible and may constitute a significant sup…

Stochastic optimization algorithmmedicine.medical_specialtybusiness.industryLeft atriumImage registrationAtrial fibrillationImage segmentationmedicine.diseasemedicine.anatomical_structureAblative caseSettore ING-INF/06 - Bioingegneria Elettronica E Informaticacardiovascular systemmedicineRadiologyOverlapping structuresbusinessCardiology and Cardiovascular MedicineSoftwareBiomedical engineering
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Micro- to macro-scale internal structures, diagenesis and petrophysical evolution of injectite networks in the Vocontian Basin (France): implications…

2015

27 pages; International audience; This study discusses the characteristics of two Lower Cretaceous injectite networks in the Vocontian Basin (SE France) using combined structural, sedimentary, diagenetic, and petrophysical analyses. Internal structures, at both the macro- and micro-scale, and diagenetic phases characterising these injectite networks have been described. Simultaneously, precementation porosity values were estimated and parameters controlling the geographical distributions of these values were analysed and statistically tested. All of the data were integrated so as to reconstruct the spatial evolution of the porosity from the time of injection to modern times through five maj…

StratigraphyMineralogyCataclastic rockOceanography[ SDU.STU.ST ] Sciences of the Universe [physics]/Earth Sciences/StratigraphyCretaceousDiagenesischemistry.chemical_compoundPetrologyPorosityLithificationDeformation structures[ SDU.STU.PE ] Sciences of the Universe [physics]/Earth Sciences/PetrographyPetrophysicsGeologyDiagenesisVocontian BasinGeophysicschemistryFluid flowMinus-cement porosityCarbonateEconomic GeologyDeformation bandsSedimentary rockInjectitesGeology
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