Search results for "Fluorene"

showing 10 items of 82 documents

CCDC 1551855: Experimental Crystal Structure Determination

2017

Related Article: Isabella Pyka, Joachim Nikl, Dieter Schollmeyer and Siegfried R. Waldvogel|2017|Eur.J.Org.Chem.|2017|3501|doi:10.1002/ejoc.201700758

Space GroupCrystallographytetrakis(dibenzobicyclo[2.2.2]octano)[56:5'6':5''6'':5'''6''']-tetrapyrazino[23-b:2'3'-h:2''3''-b':2'''3'''-h']-99'-spirobifluorene toluene solvate monohydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Regioselective substitution of 6,7-dichloroquinoline-5,8-dione: synthesis and X-ray crystal structure of 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dion…

2003

6,7-Dichloroquinoline-5,8-dione (1) was reacted with a number of 2-aminopyridine derivatives. Of the several possible products of this reaction, 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dione (6), produced by condensation and rearrangement, was obtained as the major product, and its structure was subsequently unambigously determined by X-ray crystallographic study. Ortho-quinones were produced via nucleophilic substitution at position C7, which was unexpected, considering that para-quinones were produced via C6 substitution in the reaction between compound 1 and ethyl acetoacetate in our previous work. Such unexpected nucleophilic substitution at C7 provides an effective, yet simple route, t…

StereochemistryClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsCrystallography X-RayBiochemistryMedicinal chemistryChemical synthesisInhibitory Concentration 50chemistry.chemical_compoundNucleophilic aromatic substitutionDrug DiscoveryTumor Cells CulturedNucleophilic substitutionHumansMolecular BiologySubstitution reactionFluorenesMolecular StructureOrganic ChemistryQuinonesRegioselectivityStereoisomerismQuinonechemistryDoxorubicinEthyl acetoacetateQuinolinesMolecular MedicineAcid hydrolysisDrug Screening Assays AntitumorBioorganic & Medicinal Chemistry
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Synthesis of Polyfused Heterocycle Derivatives Containing the Dipyridoimidazole Core by Friedländer’s Reaction: Access to Analogs of Ellipticine

2005

Reaction of 3-amino-2-formylimidazo[l,2-a]pyridine with various aldehydes and ketones by Friedlander's methodology afforded an entry to dipyridoimidazole, tri(tetra)azacyclopenta[b]fluorene, tri(tetra)azabenzo[b]-fluorene and triazaindeno[2,1-b]phenanthrene derivatives. Intercalation with a synthetic oligodeoxynucleotide was examined.

StereochemistryIntercalation (chemistry)[CHIM.THER]Chemical Sciences/Medicinal ChemistryFluorene010402 general chemistry01 natural sciencesAnalytical ChemistryEllipticinechemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPyridine[CHIM.COOR]Chemical Sciences/Coordination chemistryComputingMilieux_MISCELLANEOUSPharmacologybiology[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.THER ] Chemical Sciences/Medicinal ChemistryPhenanthrenebiology.organism_classification0104 chemical scienceschemistryTetra[ CHIM.RADIO ] Chemical Sciences/Radiochemistry[CHIM.RADIO]Chemical Sciences/RadiochemistryHETEROCYCLES
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Self-assembly of metallosupramolecular rhombi from chiral concave 9,9'-spirobifluorene-derived bis(pyridine) ligands.

2014

Two new 9,9’-spirobifluorene-based bis(4-pyridines) were synthesised in enantiopure and one also in racemic form. These ligands act as concave templates and form metallosupramolecular [(dppp)2M2L2] rhombi with cis-protected [(dppp)Pd]2+ and [(dppp)Pt]2+ ions. The self-assembly process of the racemic ligand preferably occurs in a narcissistic self-recognising manner. Hence, a mixture of all three possible stereoisomers [(dppp)2M2{(R)-L}2](OTf)4, [(dppp)2M2{(S)-L}2](OTf)4, and [(dppp)2M2{(R)-L}{(S)-L}](OTf)4 was obtained in an approximate 1.5:1.5:1 ratio which corresponds to an amplification of the homochiral assemblies by a factor of approximately three as evidenced by NMR spectroscopy and m…

Stereochemistryconcave templatesSupramolecular chemistrymetal complexesFull Research Paperself-sortingsupramolecular chemistrylcsh:QD241-441lcsh:Organic chemistrysupramolekulaarinen kemialcsh:Scienceta1169LigandChemistryOrganic ChemistryNuclear magnetic resonance spectroscopyself-assemblyPyridine ligandCrystallographyChemistrySelf sortingEnantiopure drug99’-spirobifluorenelcsh:QSelf-assembly9’-spirobifluoreneSingle crystalBeilstein journal of organic chemistry
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Synthesis and photophysical properties of hyperbranhced polyfluorenes containing 2,4,6-tris(tiophen-2-yl)-1,3,5-triazine as the core

2011

A series of new hyperbranched polymers containing a 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine core unit and polyfluorene chain arms have been synthesized via Suzuki coupling, and characterized by NMR, IR and GPC. All the polymers exhibit good thermal stability with a high decomposition temperature. By changing the 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine/fluorene ratio the UV-vis absorption and emission spectra can be partially tuned. It has been found that the polymers containing a low ratio of 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine units (P1-P3) have an absorption maximum around 385 nm, localized in the polyfluorene chain, and a shoulder around 425 nm ascribable to a charge transfer stat…

chemistry.chemical_classificationFluorenesMolecular StructureAbsorption spectroscopyPolymersTriazinesGeneral Physics and AstronomyThiophenesPolymerFluorenePhotochemical ProcessesPhotochemistryTwo-photon absorptionchemistry.chemical_compoundPolyfluorenechemistryOrganic chemistryPhysical and Theoretical ChemistryAbsorption (chemistry)HOMO/LUMOta116TriazinePhysical Chemistry Chemical Physics
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Novel dithieno[3,2-b:2′,3′-d]pyrrole-based organic dyes with high molar extinction coefficient for dye-sensitized solar cells

2013

Abstract Three new metal-free organic dyes FD1 – 3 with a planar dithieno[3,2- b :2′,3′- d ]pyrrole unit as linker were synthesized and used for dye-sensitized solar cells with high molar extinction coefficients. In this work, dithieno[3,2- b :2′,3′- d ]pyrrole was employed as π-conjugated bridge to construct A–π– d –π–A organic dyes, where 9,9-dihexyl-9 H -fluorene was used as a donor, and cyanoacrylic acid as an electron acceptor. For a typical device, a solar energy conversion efficiency ( η ) of 6.36% based on FD2 was achieved under simulated AM 1.5 solar irradiation (100 mW cm −2 ) with a short-circuit photocurrent density ( J sc ) of 13.76 mA cm −2 , an open-circuit voltage ( V oc ) o…

chemistry.chemical_classificationPhotocurrentMaterials scienceGeneral ChemistryElectron acceptorMolar absorptivityFluoreneCondensed Matter PhysicsPhotochemistryElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundDye-sensitized solar cellchemistryExtinction (optical mineralogy)Materials ChemistryIrradiationElectrical and Electronic EngineeringPyrroleOrganic Electronics
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ChemInform Abstract: Modular Access to 9,9-Spirobifluorenes by Oxidative Coupling Using Molybdenum Pentachloride.

2013

The reactions of diarylfluorenes and substrates (III) or (V) result in formation of spirobifluorenes and fluorene derivatives.

chemistry.chemical_compoundchemistryOrganic chemistryOxidative coupling of methaneGeneral MedicineMolybdenum pentachlorideFluoreneChemInform
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Synthese von methyl- und methylenosubstituierten p-Oligophenylenen durch cokondensierende ULLMANN-Reaktion. 12. Mitt.

1963

Es wird ein Syntheseverfahren fur p-Oligophenylene beschrieben, das eine Variante der ULLMANNschen Biarylverknupfungsreaktion darstellt. Dabei wird eine bifunktionelle Jodverbindung mit einem groseren Uberschus an einer monofunktionellen Komponente umgesetzt. Dieses als cokondensierende ULLMANN-Reaktion bezeichnete Syntheseprinzip, das Ausbeuten von 40–50% d. Th. ergibt, wird eingehend erlautert und die Leistungsfahigkeit an zahlreichen Beispielen belegt. Neben einer Reihe von methylsubstituierten p-Oligophenylenen, welche Derivate vom p-Terphenyl bis zum p-Septiphenyl einschliest, werden auch Oligophenylene mit endstandigem oder mittelstandigem Fluorenrest als Strukturelement hergestellt. …

chemistry.chemical_compoundchemistryStereochemistryPolymer chemistryFluoreneBifunctionalCoupling reactionUllmann reactionDie Makromolekulare Chemie
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ChemInform Abstract: Modular Approach to 9-Monosubstituted Fluorene Derivatives Using MoVReagents.

2016

chemistry.chemical_compoundchemistrybusiness.industryReagentGeneral MedicineFluoreneModular designbusinessCombinatorial chemistryChemInform
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Modular Approach to 9-Monosubstituted Fluorene Derivatives Using Mo(V) Reagents.

2016

Oxidative coupling using molybdenum(V) reagents provides fast access to highly functionalized 9-monosubstituted fluorenes. This synthetic approach is highly modular, is high yielding, and tolerates a variety of labile moieties, e.g. amides or iodo groups. The established protocol leads to promising precursors for pharmacologically important analogues of melatonin.

chemistry.chemical_elementFluorene010402 general chemistry01 natural sciencesBiochemistryHigh yieldingchemistry.chemical_compoundMoleculeOrganic chemistryCombinatorial Chemistry TechniquesPhysical and Theoretical ChemistryMelatoninMolybdenumFluorenesMolecular StructureOxidative Coupling010405 organic chemistrybusiness.industryOrganic ChemistryModular design0104 chemical scienceschemistryMolybdenumReagentOxidative coupling of methaneIndicators and ReagentsbusinessOrganic letters
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