Search results for "LIX"

showing 10 items of 891 documents

Rational Synthesis of Multicyclic Bis[2]catenanes

2004

Bis-loop tetraurea calix[4]arene 6 has been prepared by acylation of the wide-rim calix[4]arene tetraamine 1 with the activated bis(urethane) 8 under dilution conditions. Similarly the bis(Boc-protected) tetraamine 2 is converted into the mono-loop derivative 3 which after deprotection and acylation gives the bisalkenyl derivative 5. In apolar solvents this tetraurea calix[4]arene 5 forms regioselectively a single hydrogen-bonded homodimer, from which the bis[2]catenane 10 a is formed in 49 % by a metathesis reaction followed by hydrogenation. Bis-loop derivative 6 forms no homodimers for steric reasons, but a stoichiometric mixture with the open-chain tetraalkenyl derivative 7 a contains e…

Steric effectsStereochemistryChemistryOrganic ChemistryCatenaneGeneral ChemistryMetathesisMedicinal chemistryCatalysisAcylationchemistry.chemical_compoundCalixareneSalt metathesis reactionChirality (chemistry)Derivative (chemistry)Chemistry - A European Journal
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The in, out Asymmetric Pseudo-Triple Helical Form of a D3h Diaza-Macropentacycle

2007

A sterically encumbered [N(2)S(6)] macropentacycle (5) related to diazamacrobicycles and cryptands has been synthesized in 53% yield by the [1+1] condensation reaction between functionalized macrocyclic and macrotricyclic precursors. A macrononacycle (18) resulting from the corresponding [2+2] condensation was isolated in 7% yield from the reaction mixture. Both compounds showed broad features in their room-temperature (1)H NMR spectra, but their maximal average symmetry (D(3h) and D(2h), respectively) was achieved at high temperature (380 K). At low temperature (200 K, CD(2)Cl(2) solution), the macropentacycle is "frozen" to a single asymmetric (C1) conformation on the (1)H NMR time scale,…

Steric effects[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryStereochemistryOrganic ChemistryCryptandEnantioselective synthesisCrystal structure010402 general chemistryCondensation reaction01 natural sciences0104 chemical scienceschemistry.chemical_compoundTosylchemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryNitrogen inversionComputingMilieux_MISCELLANEOUSTriple helixThe Journal of Organic Chemistry
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A Self-Sorting Scheme Based on Tetra-Urea Calix[4]arenes

2009

Size and shape do matter: When dimerized in nonpolar solvents, an equimolar mixture of eleven tetra-urea calix[4]arenes with different wide-rim substituents self-sorts into only six out of 35 different homo- and heterodimers (see picture). Since the calixarene scaffold and the four urea units are the same in all cases, the self-sorting process is driven only by the cooperative action of steric requirements and stoichiometry.

Steric effectsbiologyHydrogen bondSupramolecular chemistryGeneral Chemistrybiology.organism_classificationCatalysischemistry.chemical_compoundchemistryCalixarenePolymer chemistryUreaTetraOrganic chemistrySelf-assemblyStoichiometryAngewandte Chemie International Edition
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Surface-immobilized DNAzyme-type biocatalysis

2014

The structure of the double helix of deoxyribonucleic acid (DNA, also called duplex-DNA) was elucidated sixty years ago by Watson, Crick, Wilkins and Franklin. Since then, DNA has continued to hold a fascination for researchers in diverse fields including medicine and nanobiotechnology. Nature has indeed excelled in diversifying the use of DNA: beyond its canonical role of repository of genetic information, DNA could also act as a nanofactory able to perform some complex catalytic tasks in an enzyme-mimicking manner. The catalytic capability of DNA was termed DNAzyme; in this context, a peculiar DNA structure, a quadruple helix also named quadruplex-DNA, has recently garnered considerable i…

StreptavidinSurface PropertiesImmobilized Nucleic AcidsDeoxyribozymeContext (language use)Nanotechnology010402 general chemistryG-quadruplex01 natural sciences[ CHIM ] Chemical Scienceschemistry.chemical_compoundNanobiotechnology[CHIM]Chemical Sciencesheterocyclic compoundsGeneral Materials ScienceComputingMilieux_MISCELLANEOUS010405 organic chemistryDNA Catalytic[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciencesG-QuadruplexesPeroxidaseschemistryBiotinylationHelixBiocatalysisOxidation-ReductionDNA
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Strontium complexes of calixarene amides in the solid state: structural dependence on the ligand size and on the counter ions

2000

For the first time, crystal structures of three strontium complexes of calixarene amides have been determined. A p-tert-butylcalix[6]arene hexaamide forms a 1∶1 complex with Sr(Pic)2 (Pic = picrate), whereas p-tert-butylcalix[8]arene and p-methoxycalix[8]arene octaamides encapsulate two strontium cations each. The binding geometries of the metal cations depend on the ligand size and on the counter anion used (chloride or picrate).

StrontiumLigandPicrateInorganic chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureChlorideIonMetalchemistry.chemical_compoundCrystallographychemistryvisual_artCalixarenevisual_art.visual_art_mediummedicinemedicine.drugJournal of the Chemical Society, Dalton Transactions
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Binding abilities of a chiral calix[4]resorcinarene: a polarimetric investigation on a complex case of study

2017

Polarimetry was used to investigate the binding abilities of a chiral calix[4]resorcinarene derivative, bearing L-proline subunits, towards a set of suitably selected organic guests. The simultaneous formation of 1:1 and 2:1 host–guest inclusion complexes was observed in several cases, depending on both the charge status of the host and the structure of the guest. Thus, the use of the polarimetric method was thoroughly revisited, in order to keep into account the occurrence of multiple equilibria. Our data indicate that the stability of the host–guest complexes is affected by an interplay between Coulomb interactions, π–π interactions, desolvation effects and entropy-unfavorable conformatio…

Supramolecular chemistryPolarimetryhost–guest complexes010402 general chemistry01 natural scienceshost-guest complexesFull Research Papersupramolecular chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryComputational chemistryp-nitroanilinesDesolvationlcsh:Sciencepolarimetrycalix[4]resorcinarene010405 organic chemistryChemistryOrganic ChemistryHost-guest complexeSettore CHIM/06 - Chimica OrganicaResorcinarene0104 chemical sciencesChemistrylcsh:QP-nitroanilineDerivative (chemistry)Beilstein Journal of Organic Chemistry
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Analysis of the Impact of the Triple Helix on Sustainable Innovation Targets in Spanish Technology Companies

2020

The establishment of broad-based networks, such as the Triple Helix, for innovation and sustainability is sufficiently corroborated. In this work we suggest that the information received from the Triple Helix has a significant and different impact on the objectives of sustainable innovation, depending on whether companies cooperate or not. To this end, an empirical analysis of a stratified sample of more than 5000 Spanish medium and high technology companies in 2010-2014-2015 was carried out. The results confirm that companies that do not cooperate place more importance on the information received from the Triple Helix to establish their sustainable innovation targets.

Sustainable developmentsustainable developmentgenetic structuresEnvironmental effects of industries and plantsRenewable Energy Sustainability and the EnvironmentSpanish technology companiesGeography Planning and DevelopmentSustainable innovationTJ807-830Management Monitoring Policy and LawEconomiaTD194-195Renewable energy sourcesStratified samplingEnvironmental sciencesWork (electrical)Sustainabilitycollaboration networksGE1-350BusinessTriple HelixIndustrial organizationTriple helixSustainability
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Novel triplet of flexor muscles in the posterior tentacles of the snail, Helix pomatia.

2012

The anatomy of three novel flexor muscles in the posterior tentacles of Helix pomatia is described. The muscles originate from the ventral side of the sensory pad and are anchored at different sites in the base of the tentacle stem. The muscles span the tentacle and always take the length of the stem which depends on the rate of tentacle protrusion indicating that the muscles are both contractile and extremely stretchable. The three anchoring points at the base of the stem determine three space axes along which the contraction of a muscle or the synchronous contraction of the muscles can move the tentacle in space.

TentaclebiologyHelix SnailsMovementMusclesVentral sideSnailHelix pomatiaAnatomyFlexor musclesbiology.organism_classificationGeneral Biochemistry Genetics and Molecular BiologyEyestalkNeurologybiology.animalAnimalsGeneral Environmental ScienceActa biologica Hungarica
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Dimeric Capsules Formed by Tetra-CMPO Derivatives of (Thia)Calix[4]arenes

2010

Thiacalix[4]arene 2, calix[4]arene 3 a and its tetraether fixed in the cone conformation 3 b form homo- and heterodimeric capsules in apolar solvents, which are held together by a seam of NH⋅⋅⋅O=P hydrogen bonds between carbamoylmethyl phospine oxide functions attached to their wide rim. Their internal volume of ∼370 A3 requires the inclusion of a suitable guest. Although neutral molecules such as adamantane (derivatives) or tetraethylammonium cations form kinetically stable complexes (1H- and 31P-time scale), the included solvent is rapidly exchanged. The internal mobility of the included tetraethylammonium cation is distinctly higher (ΔG=42.5 and 49.7 kJ mol−1 for 3 a and 3 b) than that f…

TetraethylammoniumbiologyHydrogen bondAdamantaneOrganic ChemistryCationic polymerizationGeneral Chemistrybiology.organism_classificationBiochemistrySolventchemistry.chemical_compoundchemistryCalixarenePolymer chemistryMoleculeTetraChemistry - An Asian Journal
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CCDC 218498: Experimental Crystal Structure Determination

2003

Related Article: M.Makinen, P.Vainiotalo, M.Nissinen, K.Rissanen|2003|J.Am.Soc.Mass.Spectrom.|14|143|doi:10.1016/S1044-0305(02)00863-2

Tetramethylammonium (46101216182224-octahydroxy-281420-tetraethylcalix(4)arene) bromide dihydrate clathrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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