Search results for "TAXA"

showing 10 items of 268 documents

Two similar new species of Alvania Risso,1826(Caenogastropoda: Rissoidae)from the late Cenozoic of Italy

2010

Rissoidae taxonomy new taxa Pliocene Pleistocene Mediterranean area
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Formation of an interlocked double-chain from an organic-inorganic [2]rotaxane.

2019

Here we show that a structure containing a polymeric interlocking daisy chain is obtained from the reaction of an inorganic–organic [2]rotaxane [HB{CrIII7NiII(μ-F)8(O2CtBu)16}], where B is an organic thread terminated with a bi-pyridyl unit, with an oxo-centered metal carboxylate triangle [FeIII2CoII(μ3-O)(O2CtBu)6(HO2CtBu)3].

Rotaxane010405 organic chemistryChemistryMetals and AlloysGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDouble chainMetalchemistry.chemical_compoundTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYvisual_artPolymer chemistryOrganic inorganicMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumCarboxylateDaisy chainChemical communications (Cambridge, England)
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Templated synthesis of a rotaxane with a [Ru(diimine)3]2+ core.

2003

A rotaxane containing a ruthenium bisphenanthroline complex, acting as an axis, and a macrocycle incorporating a 2,2'-bipyridine (bpy) unit, threaded by the axis, has been synthesized. The bisphenanthroline ligand is such that its ruthenium(II) complexes possess a clearly identified axis, making such compounds ideal components of rotaxanes constructed around an octahedral ruthenium(II) center, which serves as a template. The ring is threaded by the axial ruthenium(II) precursor complex, to afford the corresponding pseudorotaxane in moderate yield. The X-ray structure analysis of this compound reveals the threaded nature of the complex. The length of the threaded ring (35 atoms in the periph…

Rotaxane010405 organic chemistryStereochemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciencesCatalysis0104 chemical sciencesRutheniumBipyridinechemistry.chemical_compoundCrystallographychemistryOctahedron[ CHIM.ORGA ] Chemical Sciences/Organic chemistryProton NMR[CHIM.COOR]Chemical Sciences/Coordination chemistryDiimineComputingMilieux_MISCELLANEOUSChemistry (Weinheim an der Bergstrasse, Germany)
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Fast Pirouetting Motion in a Pyridine Bisamine-Containing Copper-Complexed Rotaxane

2013

The present work reports the introduction of pyridine bisamine terdentate ligands in the structure of a pirouetting copper rotaxane. Rotaxane 2[PF6] constitutes the first example of the incorporation of imine-based dynamic covalent chemistry in the synthesis of switchable copper-complexed interlocked systems. In this rotaxane, the substitution of the classical terpyridine terdentate unit by a pyridine bisamine moiety has led to a significant stabilization of the pentacoordinated site. That fact has been evidenced by EPR spectroscopy and cyclic voltammetry. Regarding the tetracoordinated site, the congestion around the coordination sphere has been reduced to accelerate the typically slow reo…

RotaxaneCoordination sphereLigandPhenanthrolineOrganic ChemistryImineDynamic covalent chemistryGeneral ChemistryPhotochemistryCatalysischemistry.chemical_compoundchemistryPolymer chemistryPyridineTerpyridineChemistry - A European Journal
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Thermodynamic and electrochemical study of tailor-made crown ethers for redox-switchable (pseudo)rotaxanes

2020

Crown ethers are common building blocks in supramolecular chemistry and are frequently applied as cation sensors or as subunits in synthetic molecular machines. Developing switchable and specifically designed crown ethers enables the implementation of function into molecular assemblies. Seven tailor-made redox-active crown ethers incorporating tetrathiafulvalene (TTF) or naphthalene diimide (NDI) as redox-switchable building blocks are described with regard to their potential to form redox-switchable rotaxanes. A combination of isothermal titration calorimetry and voltammetric techniques reveals correlations between the binding energies and redox-switching properties of the corresponding ps…

RotaxaneSupramolecular chemistryElectrochemistryRedoxFull Research Papersupramolecular chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryComputational chemistryredox chemistrysupramolekulaarinen kemialcsh:ScienceCrown etherchemistry.chemical_classificationOrganic ChemistryIsothermal titration calorimetry540Molecular machineisothermal titration calorimetryChemistryrotaxaneschemistrycrown etherlcsh:Q500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete WissenschaftenTetrathiafulvaleneBeilstein Journal of Organic Chemistry
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Evaluation of multivalency as an organization principle for the efficient synthesis of doubly and triply threaded amide rotaxanes

2014

Mono-, di- and trivalent pseudorotaxanes with tetralactam macrocycle hosts and axles containing diamide binding stations as the guests have been synthesised. Their threading behaviour was analyzed in detail by NMR experiments and isothermal titration calorimetry. An X-ray crystal structure of the monovalent pseudorotaxane confirms the binding motif. Double mutant cycle analysis provides the effective molarities and insight into the chelate cooperativity of multivalent binding. While the second binding event in a trivalent pseudorotaxane exhibits a slightly positive cooperativity, the third binding is nearly non-cooperative. Nevertheless, the enhanced binding affinities resulting from the mu…

RotaxaneTandemStereochemistryOrganic ChemistryCooperative bindingIsothermal titration calorimetryCooperativityNuclear magnetic resonance spectroscopyCrystal structure540Crystallographychemistry.chemical_compoundchemistryAmideta116Organic Chemistry Frontiers: an international journal of organic chemistry
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Directional Shuttling of a Stimuli-Responsive Cone-Like Macrocycle on a Single-State Symmetric Dumbbell Axle

2018

Rotaxane-based molecular shuttles are often operated using low-symmetry axles and changing the states of the binding stations. A molecular shuttle capable of directional shuttling of an acid-responsive cone-like macrocycle on a single-state symmetric dumbbell axle is now presented. The axle contains three binding stations: one symmetric di(quaternary ammonium) station and two nonsymmetric phenyl triazole stations arranged in opposite orientations. Upon addition of an acid, the protonated macrocycle shuttles from the di(quaternary ammonium) station to the phenyl triazole binding station closer to its butyl groups. This directional shuttling presumably originates from charge repulsion and an …

RotaxaneeducationTriazoleProtonation010402 general chemistry01 natural sciencessupramolecular chemistryCatalysischemistry.chemical_compoundbutyl groupssupramolekulaarinen kemiahost-guest chemistryrotaxanemoleculesta116Physicsmolecular machine010405 organic chemistrymolekyylitGeneral MedicineGeneral ChemistryMolecular machine0104 chemical sciencesMechanism (engineering)CrystallographyAxleMolecular shuttlechemistryDumbbellmacrocycleAngewandte Chemie International Edition
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Photoinduced Electron Transfer in Multiporphyrinic Interlocked Structures: The Effect of Copper(I) Coordination in the Central Site

2004

Photoinduced processes have been determined in a [2]catenane containing a zinc(II) porphyrin, a gold(III) porphyrin, and two free phenanthroline binding sites, Zn-Au(+), and in the corresponding copper(I) phenanthroline complex, Zn-Cu(+)-Au(+). In acetonitrile solution Zn-Au(+) is present in two different conformations: an extended one, L, which accounts for 40 % of the total, and a compact one, S. In the L conformation, the electron transfer from the excited state of the Zn porphyrin to the gold-porphyrin unit (k = 1.3x10(9) s(-1)) is followed by a slow recombination (k = 8.3x10(7) s(-1)) to the ground state. The processes in the S conformation cannot be clearly resolved but a charge-separ…

RotaxanesMetalloporphyrinsPhotochemistryPhenanthrolineCatenaneMolecular Conformationchemistry.chemical_elementElectronsPhotochemistryCatalysisPhotoinduced electron transferElectron Transportchemistry.chemical_compoundElectron transferChemistryOrganic ChemistryGeneral ChemistryPorphyrinCopperZincCrystallographyEnergy TransferSpectrophotometryExcited stateGoldGround stateCopperChemistry - A European Journal
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Studies on the Quercus hybrids in Sicily: leaf micromorphology and xylem structure in Quercus × fontanesii Guss.

2000

In order to find new suitable characters in the taxonomic delimitation of the genus Quercus, whose hardness is well known, Quercus x fontanesii, endemic to Sicily, has been studied in comparison with its parents, i.e. Q. gussonei, wich is close to Q. cerris, and Q. suber. These taxa are here delimited as far as taxonomy, ecology, and Sicilian distribution are concerned. Furthermore, the results of SEM microstructure analysis of leaves and xylem anatomy are illustrated and commented. The analysis of the leaf microstructures shows that there is a remarkable similarity between the stomata and stellata trichomes of Q. x fontanesii and both the parental species, as the trichome rays are numerica…

Settore AGR/05 - Assestamento Forestale E Selvicolturaleaf structurexylem anatomymorphological analysinothotaxaQuercus hybrid
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Protective Effect of Astaxanthin on Primary Retinal Cells of the Gerbil Psammomys Obesus Cultured in Diabetic Milieu

2017

Astaxanthin is a major marine carotenoid with powerful antioxidant and neuroprotective properties. The in vitro protective effect of astaxanthin in adult retinal cells of the type-2 diabetic model Psammomys obesus in hyperglycemic conditions was investigated. Primary retinal cells were cultured in normal (5 mM) or high concentrations of glucose (25 and 40 mM) for 5 days and treated with 1-20 μM astaxanthin for the last 48 h of culturing. Mitochondrial dehydrogenase activity and cell viability were assessed using MTT test and trypan blue exclusion dye. Retinal cells were characterized by immunohistochemistry. The results showed that mitochondrial function increased significantly (P<0.05) …

Settore AGR/20 - ZoocoltureASTAXANTHIN PRIMARY RETINAL CELLS GERBIL PSAMMOMYS OBESUS DIABETSettore BIO/06 - Anatomia Comparata E Citologia
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