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
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…
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.
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…
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…
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…
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.
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. …
ChemInform Abstract: Modular Approach to 9-Monosubstituted Fluorene Derivatives Using MoVReagents.
2016
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.