0000000000313176

AUTHOR

Yudong Cao

showing 6 related works from this author

Synthesis of huge macrocycles using two calix[4]arenes as templates.

2005

Macrocycles with up to 100 atoms have been synthesised using two calix[4]arenes as templates: first, (3,5-dialkenyloxy)phenyl groups are attached to the wide rim of a calix[4]arene via urea links, then the alkenyl groups are connected via a metathesis reaction using a tetratosylurea calix[4]arene for their correct prearrangement and finally the urea functions are cleaved to detach the newly formed macrocycles.

Metals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundTemplatechemistryPolymer chemistryMaterials ChemistryCeramics and CompositesSalt metathesis reactionUreaOrganic chemistryChemical communications (Cambridge, England)
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Stepwise synthesis and selective dimerisation of bis- and trisloop tetra-urea calix[4]arenes.

2008

Tetra-urea calix[4]arenes substituted with four mono- or bisalkenyl residues have been converted into bis- or tetraloop compounds by intramolecular olefin metathesis, with use of a tetratosylurea calix[4]arene as template. The same strategy has now been used to synthesise trisloop compounds and bisloop compounds with adjacent loops, completing the series of the loop-containing tetra-urea derivatives. A tetra-urea calix[4]arene of the AABB type, where A stands for a bisalkenyl- and B for a monoalkenyl-substituted urea unit, was used as precursor for the three loops. It was easily synthesised from a tetraamino calix[4]arene in which two adjacent amino groups were Boc-protected. The ABCB-type …

Spectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyOlefin metathesisbiologyStereochemistryOrganic ChemistryGeneral ChemistryMetathesisbiology.organism_classificationMedicinal chemistryTetraloopCatalysischemistry.chemical_compoundchemistryPhenolsIntramolecular forceCalixareneUreaTetraUreaSelf-assemblyCalixarenesDimerizationChemistry (Weinheim an der Bergstrasse, Germany)
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Vierfache [2]Rotaxane von Calix[4]arenen durch Ringschluss

2006

ChemistryGeneral MedicineAngewandte Chemie
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Fourfold [2]rotaxanes of calix[4]arenes by ring closure.

2006

Models MolecularRotaxanesChemistryStereochemistryClosure (topology)Hydrogen BondingGeneral ChemistryRing (chemistry)MetathesisCatalysisCyclizationPolymer chemistryCalixareneCalixarenesAngewandte Chemie (International ed. in English)
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Wide Rim Urethanes Derived from Calix[4]arenes:  Synthesis and Self-Assembly

2006

[reaction: see text] Calix[4]arenes 4, substituted at the wide rim by four N-tolyl-urethane groups, were synthesized, as well as derivatives 10a,b bearing two or three tolyl-urea groups beside of one or two urethane group(s). In contrast to tetra-tolyl urea 11, the urethane derivatives do not form hydrogen-bonded, dimeric capsules in CDCl3 or benzene-d6, but the dimerization can be induced for the triurea 10b by tetraethylammonium cations as guests. The quantitative formation of heterodimers is observed for all urethanes 4 and 10a,bin benzene-d6 in mixtures with a "tetra-loop" tetraurea 14, while "bisloop" tetraureas 13 require di- or triurea derivatives 10a,b for a clean heterodimerization.

chemistry.chemical_compoundTetraethylammoniumStereochemistryChemistryHydrogen bondDimerOrganic ChemistryPolymer chemistryCalixareneUreaSelf-assemblyChemical synthesisInclusion compoundThe Journal of Organic Chemistry
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CCDC 265476: Experimental Crystal Structure Determination

2005

Related Article: Yudong Cao, Leyong Wang, M.Bolte, M.O.Vysotsky, V.Bohmer|2005|Chem.Commun.||3132|doi:10.1039/b505223h

Space GroupCrystallographyCrystal System6177101105-Tetramethoxy-415213238498697-octaoxa-55578183102104106108-octaazatridecacyclo(50.33.12.31872.33566.1384.11620.1333715054.15862.16078.16468.17074.17680) dodecahecta-13(98)16(112)171933(111)343650(110)515358(109)596164 (105)656770(101)717376(99)777984-tetracosaene-5682103107-tetraone methanol solvate sesquihydrateCrystal StructureCell ParametersExperimental 3D Coordinates
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