Search results for "cages"

showing 10 items of 15 documents

Size-selective incorporation of DNA nanocages into nanoporous antimony-doped tin oxide materials.

2011

A conductive nanoporous antimony-doped tin oxide (ATO) powder has been prepared using the sol-gel method that contains three-dimensionally interconnected pores within the metal oxide and highly tunable pore sizes on the nanoscale. It is demonstrated that these porous materials possess the capability of hosting a tetrahedral-shaped DNA nanostructure of defined dimensions with high affinity. The tunability of pore size enables the porous substrate to selectively absorb the DNA nanostructures into the metal oxide cavities or exclude them from entering the surface layer. Both confocal fluorescence microscopy and solution FRET experiments revealed that the DNA nanostructures maintained their int…

AntimonyModels MolecularMaterials scienceNanoporousDopingGeneral EngineeringOxideElectric ConductivityGeneral Physics and AstronomyTin CompoundsNanotechnologyDNACarbocyaninesTin oxidechemistry.chemical_compoundNanoporesNanocageschemistryDNA nanotechnologyNucleic Acid ConformationGeneral Materials SciencePorous mediumNanoscopic scaleACS nano
researchProduct

Tetrameric and Dimeric [N∙∙∙I+∙∙∙N] Halogen-Bonded Supramolecular Cages

2017

Tripodal N-donor ligands are used to form halogen-bonded assemblies via structurally analogous Ag+-complexes. Selective formation of discrete tetrameric I6L4 and dimeric I3L2 halonium cages, wherein multiple [N∙∙∙I+∙∙∙N] halogen bonds are used in concert, can be achieved by using sterically rigidified cationic tris(1-methyl-1-azonia-4-azabicyclo[2.2.2]octane)-mesitylene ligand, L1(PF6)3, and flexible ligand 1,3,5-tris(imidazole-1-ylmethyl)-2,4,6-trimethylbenzene, L2, respectively. The iodonium cages, I6L14(PF6)18 and I3L22(PF6)3, were obtained through the [N∙∙∙Ag+∙∙∙N] → [N∙∙∙I+∙∙∙N] cation exchange reaction between the corresponding Ag6L14(PF6)18 and Ag3L22(PF6)3 coordination cages, prepar…

Steric effectssupramolecular cagesHalogen bond010405 organic chemistryStereochemistryLigandOrganic Chemistryhalogen bondsCationic polymerizationSupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryHalogenHalonium ionta116OctaneChemistry: A European Journal
researchProduct

1,2-Bis(methylsulfanyl)-1,2-dicarba-closo-dodecaborane(12)

2004

3 pages, 1 figure, 2 tables

Crystal-structures010405 organic chemistryStereochemistryHETEROBORANESBoranesGeneral MedicineCrystal structureBoraneDihedral angle010402 general chemistry01 natural sciencesGeneral Biochemistry Genetics and Molecular Biology3. Good health0104 chemical scienceschemistry.chemical_compoundCAGESchemistryCarboraneMoleculeCageMOLECULAR-STRUCTURECarborane
researchProduct

Retrospective Data Analysis of Anterior Cervical Discectomies and Fusion Without Plate and Screws

2019

Abstract Surgical intervention in cervical disease can relieve neurological symptoms and improve life quality. This study aimed to analyse retrospective data of microscope-assisted anterior cervical discectomy and fusion (ACDF) surgeries. The retrospective study was carried out at the ORTO clinic, Rīga, Latvia, from 2013 to 2017. Data from 198 patients were extracted retrospectively. Data on patient gender, age, diagnosis, extent of operation, type of cage and the overall height of the implants were used. Comparative analysis was carried out with the SPSS 22 software. P < 0.05 represented statistical significance. During the study period, 198 elective ACDF were carried out with increasin…

Orthodontics030222 orthopedics03 medical and health sciences0302 clinical medicineMultidisciplinaryGeneral interestScienceanterior cervical discectomyQcervical cages030217 neurology & neurosurgeryRetrospective dataProceedings of the Latvian Academy of Sciences. Section B, Natural Sciences
researchProduct

Self-assembly of catalytically-active supramolecular coordination compounds within metal-organic frameworks

2019

[EN] Supramolecular coordination compounds (SCCs) represent the power of coordination chemistry methodologies to self-assemble discrete architectures with targeted properties. SCCs are generally synthesized in solution, with isolated fully coordinated metal atoms as structural nodes, thus severely limited as metal-based catalysts. Metal-organic frameworks (MOFs) show unique features to act as chemical nanoreactors for the in situ synthesis and stabilization of otherwise not accessible functional species. Here, we present the self-assembly of Pd-II SCCs within the confined space of a pre-formed MOF (SCCs@MOF) and its post-assembly metalation to give a Pd-II-Au-III supra molecular assembly, c…

Mechanistic characterizationMetalationCavitySupramolecular chemistryQuímica organometàl·licaNanoreactor010402 general chemistry7. Clean energy01 natural sciencesBiochemistryCatalysisCoordination complexSupramolecular assemblyClustersQUIMICA ORGANICAColloid and Surface ChemistryOxidationPolyhedraConstructionchemistry.chemical_classificationChemistryCagesGeneral ChemistryCombinatorial chemistry0104 chemical sciencesEfficientAlkynesMetal-organic frameworkCatalystSelf-assemblySupramolecular catalysis
researchProduct

Polyoxometalate Metal–Organic Frameworks: Keggin Clusters Encapsulated into Silver-Triazole Nanocages and Open Frameworks with Supercapacitor Perform…

2019

To investigate the relationship between the structures of polyoxometalate host–guest materials and their energy-storage performance, three novel polyoxometalate-based metal–organic compounds, [Ag10...

Supercapacitor010405 organic chemistryTriazole010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundNanocageschemistryPolyoxometalateMetal-organic frameworkPhysical and Theoretical ChemistryInorganic Chemistry
researchProduct

Cyclotriveratrylene-Containing Porphyrins

2016

International audience; The C-3-symmetric cyclotriveratrylene (CTV) was covalently bonded via click chemistry to 1, 2, 3, and 6 zinc(II) porphyrin units to various host for C-60. The binding constants, Ka, were measured from the quenching of the porphyrin fluorescence by C-60. These constants vary between 400 and 4000 M-1 and are considered weak. Computer modeling demonstrated that the zinc(II) porphyrin units, [Zn], exhibit a strong tendency to occupy the CTV cavity, hence blocking the access for C-60 to land on this site. Instead, the pincer of the type [Zn]-[Zn] and in one case [Zn]-CTV, were found to be the most probable geometry to promote host-guest associations in these systems.

cagesStereochemistrychemistry.chemical_elementCyclotriveratryleneZinc010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencessupramolecular chemistrydendrimersInorganic Chemistrychemistry.chemical_compoundc-60[CHIM]Chemical SciencesmoleculesctvPhysical and Theoretical Chemistryinclusion complexesQuenching (fluorescence)010405 organic chemistryfullereneFluorescencePorphyrin0104 chemical sciencesPincer movementCrystallographychemistryCovalent bondClick chemistryderivativeshosts
researchProduct

Encapsulation of Xenon by a Self-Assembled Fe4L6 Metallosupramolecular Cage

2015

We report (129)Xe NMR experiments showing that a Fe4L6 metallosupramolecular cage can encapsulate xenon in water with a binding constant of 16 M(-1). The observations pave the way for exploiting metallosupramolecular cages as economical means to extract rare gases as well as (129)Xe NMR-based bio-, pH, and temperature sensors. Xe in the Fe4L6 cage has an unusual chemical shift downfield from free Xe in water. The exchange rate between the encapsulated and free Xe was determined to be about 10 Hz, potentially allowing signal amplification via chemical exchange saturation transfer. Computational treatment showed that dynamical effects of Xe motion as well as relativistic effects have signific…

Xenon010405 organic chemistryChemistryChemical exchangechemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryBinding constantCatalysis0104 chemical sciencesSelf assembledColloid and Surface ChemistryXenon13. Climate actionComputational chemistrySaturation transferChemical physicsmetallosupramolecular cagesmolecular encapsulationCageRelativistic quantum chemistrySignal amplificationta116Journal of the American Chemical Society
researchProduct

A cyanide and hydroxo-bridged nanocage: a new generation of coordination clusters.

2013

International audience; Combining serendipitously-formed hydroxo-clusters, [CoII3(OH)(piv)4(L)]+ (where L = MeCN or Hpiv), with assembling cyanide building block, [FeIII(Tp)(CN)3]−, has led to an unprecedented architecture where polymetallic cobalt clusters and blocked tris-cyanide iron complexes define the apexes of a unique magnetic cubic nanocage.

010405 organic chemistryCyanideInorganic chemistryMetals and Alloyschemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographyNanocageschemistryBlock (telecommunications)Materials ChemistryCeramics and Composites[CHIM.COOR]Chemical Sciences/Coordination chemistryCobaltChemical communications (Cambridge, England)
researchProduct

Spin state switching in iron coordination compounds

2013

The article deals with coordination compounds of iron(II) that may exhibit thermally induced spin transition, known as spin crossover, depending on the nature of the coordinating ligand sphere. Spin transition in such compounds also occurs under pressure and irradiation with light. The spin states involved have different magnetic and optical properties suitable for their detection and characterization. Spin crossover compounds, though known for more than eight decades, have become most attractive in recent years and are extensively studied by chemists and physicists. The switching properties make such materials potential candidates for practical applications in thermal and pressure sensors …

chemistry.chemical_classificationLigand field theorycagespolyfunctional materialsSpin statesOrganic Chemistryphysical techniquesSpin transitionNanotechnologySpin engineeringiron(II) coordination compoundsReviewLIESSTCoordination complexCharacterization (materials science)lcsh:QD241-441Chemistrychemistryspin crossoverlcsh:Organic chemistryChemical physicsSpin crossoverCondensed Matter::Strongly Correlated Electronslcsh:Qlcsh:ScienceBeilstein Journal of Organic Chemistry
researchProduct