Search results for "Pyramid"

showing 10 items of 410 documents

Data from: Phylogenomics of Lophotrochozoa with consideration of systematic error

2021

Phylogenomic studies have improved understanding of deep metazoan phylogeny and show promise for resolving incongruences among analyses based on limited numbers of loci. One region of the animal tree that has been especially difficult to resolve, even with phylogenomic approaches, is relationships within Lophotrochozoa (the animal clade that includes molluscs, annelids, and flatworms among others). Lack of resolution in phylogenomic analyses could be due to insufficient phylogenetic signal, limitations in taxon and/or gene sampling, or systematic error. Here, we investigated why lophotrochozoan phylogeny has been such a difficult question to answer by identifying and reducing sources of sys…

Helobdella robustaGlycera dibranchiataMytilus edulisAnnelidaEntalina tetragonaLeptochiton asellusCerebratulus marginatusLoxosomella cf. viviparaGraptacme eboreaLineus longissimusmedicine and health careClymenella torquataRuditapes philippinarumNucella lapillusHaliotis rufescenslong branch attractionPlatyzoaBarentsia gracilisPriapulus caudatusLineus ruberAlitta virenssaturationProchaetoderma californicumLife SciencesPinctada fucataSchistosoma mansoniPolyzoaCephalothrix hongkongensisRhyssoplax olivaceusLoxosoma pectinaricolaPhascolosoma agassiziiAdineta vagaDrosophila melanogasterEntoproctaBugula neritinaPhoronis vancouverensisMedicineNovocrania anomalaVillosa lienosaDaphnia pulexSagitta sp.Pectinaria gouldiiSymbion americanusNuculana pernulaSepia esculentaEnucula tenuisSolemya velumLineus lacteusTubulanus polymorphus-StruckGnathostomula paradoxaBoccardia proboscideaMacellomenia schanderiLaevipilina hyalinaTubulanus polymorphus-HalanychBryozoaPomatoceros lamarckiiSepioteuthis lessonianaParanemertes peregrinaMalacobdella grossaHemithiris psittaceaLeptochiton rugatusTrochozoaBrachionus plicatilisSpathoderma clenchiLaqueus californicusPatella vulgataLottia giganteaCrepidula fornicataPhoronidaAplysia californicaGlottidia pyramidataPhoronis psammophilaSchmidtea mediterraneaAlexandromenia crassaBrachiopodaMegadasys sp.Octopus vulgarisCapitella teletaNeomenia carinatacompositional heterogeneityNemerteaPhenacolepas pulchellaGadila tolmieiMolluscaMacrodasys sp.Crassostrea gigasPedicellina cernuaTaenia pisiformisDosidicus gigasCephalothrix linearisSpiralia
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Data from: Phylogenomics of Lophotrochozoa with consideration of systematic error

2016

Phylogenomic studies have improved understanding of deep metazoan phylogeny and show promise for resolving incongruences among analyses based on limited numbers of loci. One region of the animal tree that has been especially difficult to resolve, even with phylogenomic approaches, is relationships within Lophotrochozoa (the animal clade that includes molluscs, annelids, and flatworms among others). Lack of resolution in phylogenomic analyses could be due to insufficient phylogenetic signal, limitations in taxon and/or gene sampling, or systematic error. Here, we investigated why lophotrochozoan phylogeny has been such a difficult question to answer by identifying and reducing sources of sys…

Helobdella robustaGlycera dibranchiataMytilus edulisAnnelidaEntalina tetragonaLeptochiton asellusCerebratulus marginatusLoxosomella cf. viviparaGraptacme eboreaLineus longissimusmedicine and health careClymenella torquataRuditapes philippinarumNucella lapillusHaliotis rufescenslong branch attractionPlatyzoaBarentsia gracilisPriapulus caudatusLineus ruberAlitta virenssaturationProchaetoderma californicumPinctada fucataSchistosoma mansoniLife sciencesPolyzoaCephalothrix hongkongensisRhyssoplax olivaceusLoxosoma pectinaricolaPhascolosoma agassiziiAdineta vagaDrosophila melanogasterEntoproctaBugula neritinaPhoronis vancouverensisMedicineNovocrania anomalaVillosa lienosaDaphnia pulexSagitta sp.Pectinaria gouldiiSymbion americanusNuculana pernulaSepia esculentaEnucula tenuisSolemya velumLineus lacteusTubulanus polymorphus-StruckGnathostomula paradoxaBoccardia proboscideaMacellomenia schanderiLaevipilina hyalinaTubulanus polymorphus-HalanychBryozoaPomatoceros lamarckiiSepioteuthis lessonianaParanemertes peregrinaMalacobdella grossaHemithiris psittaceaLeptochiton rugatusTrochozoaBrachionus plicatilisSpathoderma clenchiLaqueus californicusPatella vulgataLottia giganteaCrepidula fornicataPhoronidaAplysia californicaGlottidia pyramidataPhoronis psammophilaSchmidtea mediterraneaAlexandromenia crassaBrachiopodaMegadasys sp.Octopus vulgarisCapitella teletaNeomenia carinatacompositional heterogeneityNemerteaPhenacolepas pulchellaGadila tolmieiMolluscaMacrodasys sp.Crassostrea gigasPedicellina cernuaTaenia pisiformisDosidicus gigasCephalothrix linearisSpiralia
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The preparation, IR spectrum and structure of the Di-μ3-hydroxo-μ-sulphatotetrakis-μ-(isonicotinato-N-oxide)tetraaqua-tetracopper(II)

1982

Abstract A very unusual new copper(II) complex with isonicotinate N-oxide (N-inicO), Cu4(N-inicO)4SO4(OH)2(H2O)4 has been prepared and its crystal and molecular structure determined from three dimensional X-ray diffraction data. The crystals belong to the monoclinic space group C2. The cell parameters are a = 19.089(8), b = 6.884(3), c = 19.533(12) A, β = 140.9(3)°, dobs = 1.99, dcalc = 2.01 and Z = 2. The structure was refined to a final R-value of 0.062. The monomeric tetranuclear complex resembles a space ship with the sulphate group at its top and pyridine rings as wings. Two copper atoms are very close to each other in the molecule; the Cu1Cu1′ distance is 2.885 A. The coordination ar…

Hydrogen bondInorganic chemistrychemistry.chemical_elementBridging ligandCopperSquare pyramidal molecular geometryInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryPyridineMaterials ChemistryMoleculeCarboxylatePhysical and Theoretical ChemistryMonoclinic crystal systemInorganica Chimica Acta
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The key role of hydrogen bonding in the nuclearity of three copper(II) complexes with hydrazone-derived ligands and nitrogen donor heterocycles

2011

International audience; Three new Cu(II) complexes of formula [Cu(L1)(pyz)(CH3OH)]ClO4 (1), [Cu(L1)(4,4′-bpy)(ClO4)]·0.5H2O (2) and [{Cu(L2)(ClO4)}2(μ-4,4′-bpy)] (3) have been synthesised by using pyrazine (pyz) and 4,4′-bipyridine (4,4′-bpy) and tridentate O,N,O-donor hydrazone ligands, L1H and L2H, obtained by the condensation of 1,1,1-trifluoro-2,4-pentanedione with salicyloylhydrazide and benzhydrazide, respectively. The ligands and their complexes have been characterized by elemental analyses, FT-IR, and UV–Vis spectroscopies. Single crystal X-ray structure analysis evidences the metal ion in a slightly deformed square pyramidal geometry in all the complexes. However complexes 1 and 2 …

Hydrogen bondingDenticityPyrazineStereochemistryHydrazonechemistry.chemical_elementAntiferromagnetic couplingCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical SciencesMonodentate pyz and 4Physical and Theoretical ChemistryCu(II) hydrazone complexescopper complexhydrazone ligandchemistry.chemical_classificationhydrogen bondHydrogen bondSelf assemblyCopperSquare pyramidal molecular geometry0104 chemical sciencesCrystallographychemistryCrystal structures4′-bpySingle crystalhydrogen bond; copper complex; hydrazone ligand
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Synthesis and characterization of triorganotin(IV) complexes of 5-[(E)-2-(aryl)-1-diazenyl]-2-hydroxybenzoic acids.

2001

Abstract The triphenyltin and tri-n-butyltin complexes of some 5-[(E)-2-(aryl)-1-diazenyl]-2-hydroxybenzoic acids have been synthesized and characterized by 1H-, 13C-, 119Sn-NMR, IR and 119mSn Mossbauer spectroscopic techniques in combination with elemental analysis. The crystal structures of triphenyltin 5-[(E)-2-(aryl)-1-diazenyl]-2-hydroxybenzoates (aryl=phenyl, 2-methylphenyl, 3-methylphenyl and 4-methoxyphenyl) are reported. Both X-ray and 119Sn Mossbauer data indicate that the triphenyltin complexes adopt a monomeric distorted tetrahedral configuration with the carboxylate ligand coordinating in a monodentate mode. By contrast, 119Sn Mossbauer spectroscopy shows that each tributyltin …

Hydroxybenzoic acidDenticityLigandStereochemistryChemistryArylOrganic ChemistryCrystal structureBiochemistryMedicinal chemistryInorganic ChemistryBipyramidchemistry.chemical_compoundMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryHydroxybenzoatesJournal of Organometallic Chemistry
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Automatic image enhancement by picture fusion

2005

This paper describes an automatic technique able to fuse different images of the same scene, acquired with different camera settings, in order to obtain an enhanced single representation of the interested. This allows to extend the functionalities (depth of field, dynamic range) of medium and low cost digital cameras. When Multi-Scale Decomposition (MSD) is used on differently focused images, magnification and blurring effects of lens focusing systems often compromise the final image with unpleasant artifacts. In our approach new techniques able to reduce these artifacts are introduced. Even if the algorithm has been essentially designed to extend depth of field it can be also used on multi…

Image fusionDynamic rangeComputer sciencebusiness.industryComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONDepth of Field (DOF) Image Fusion Color Filter Array (CFA) Multi-Scale Decomposition (MSD) Pyramidal Decomposition Dynamic Rangelaw.inventionLens (optics)lawColor gelColor filter arrayComputer visionDepth of fieldArtificial intelligencebusinessSPIE Proceedings
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The first authenticated example of triorganotin(IV) perchlorate complexes of some heterocyclic bases

1993

Abstract A convenient method is reported for the synthesis of some novel complexes of composition (R 3 SnL 2 ) ClO 4 where L represents pyridine, γ-picoline, 2,2′-bipyridine and 1,10-phenanthroline; and R  n Bu or Ph. All of the new ionic complexes have been characterized by elemental analysis, molar conductance, infrared, multinuclear nuclear magnetic resonance ( 1 H, 13 C and 119 Sn) and 119 Sn Mossbauer spectroscopies. The complexes of composition (R 3 SnL 2 )ClO 4 exist both in solution and in the solid state with trans -trigonal bipyramidal structure where the R-groups occupy the equatorial positions while the ligands are in the axial position.

InfraredChemistryStereochemistryOrganic ChemistryIonic bondingNuclear magnetic resonance spectroscopyBiochemistryInorganic ChemistryTrigonal bipyramidal molecular geometryPerchloratechemistry.chemical_compoundCrystallographyElemental analysisMössbauer spectroscopyPyridineMaterials ChemistryPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Complexes of organometallic compounds

1974

Abstract Novel complexes RClSntrid, where R is Me, Ph, n-Oct, and trid 2− are dianions of tridentate “planar” ligands with ONO and SNO donor atoms, were synthesized and investigated in the solid state by infrared and Mossbauer spectroscopy. Possible configurations are discussed; polymeric trigonal bipyramidal structures seem to occur, although five-coordinated monomers as well as octahedral dimers (via oxygen or sulfur bridges) are not excluded.

InfraredStereochemistryOrganic Chemistrychemistry.chemical_elementBiochemistryOxygenSulfurInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographyMonomerOctahedronchemistryMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryGroup 2 organometallic chemistryJournal of Organometallic Chemistry
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2-(1-Aryliminoethyl)-9-arylimino-5,6,7,8- tetrahydrocycloheptapyridyl iron(II) dichloride: synthesis, characterization, and the highly active and tun…

2014

A series of 2-(1-arylimino)ethyl-9-arylimino-5,6,7,8-tetrahydrocycloheptapyridine derivatives was synthesized and fully characterized, and thereafter reacted with iron dichloride to form their corresponding iron(II) complexes. The single crystals of representative organic and iron complex compounds were obtained and analyzed by the X-ray diffraction analysis, indicating the distorted bipyramidal geometry around the iron core. Moreover, DFT calculations were performed on selected species to determine their structural features. On treatment with either MAO or MMAO, all iron complex pre-catalysts showed high activities (up to 1.56 × 10(7) gPE mol(-1)(Fe) h(-1)) toward ethylene polymerization. …

Inorganic ChemistryBipyramidEthylene polymerizationChemistryInorganic chemistryDispersityPolymer chemistryIron complexCatalysisRing strainCharacterization (materials science)Dalton Transactions
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Complexes of organometallic compounds

1971

Abstract A number of novel compounds of dimethyllead(IV) and diphenyllead(IV) moieties with ligands having a rigid geometry when coordinating, have been prepared and characterized. The goal of the work was the building of model molecules for five-coordinated R 2 Pb IV , with known configuration of the CPbC skeleton. From spectroscopic data it is inferred that the complexes under investigation have a distorted bipyramidal trigonal structure, with the CPbC moiety allocated in the trigonal plane.

Inorganic ChemistryBipyramidStereochemistryChemistryOrganic ChemistryMaterials ChemistryMoleculeMoietyTrigonal crystal systemTrigonal structurePhysical and Theoretical ChemistryBiochemistryGroup 2 organometallic chemistryJournal of Organometallic Chemistry
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