Results 261 to 270 of about 25,797 (319)
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Fluorene-1-carboxylic Acid

Acta Crystallographica Section C Crystal Structure Communications, 1996
In fluorene-1-carboxylic acid, C14H10O2, the sole hydrogen bond is of the cyclic dimer type about a center of symmetry. The carboxyl H atom is ordered. Distances in the fluorene core are very similar to those in fluorene itself; the fluorene core dihedral angle is, however, larger than in fluorene.
A C, Blackburn, A J, Dobson, R E, Gerkin
openaire   +2 more sources

Catalytic Asymmetric Synthesis of Chiral Fluorenes: Recent Developments and Future Perspectives

Annalen der Pharmacie
The chiral fluorene fragment constitutes one of the most important scaffolds frequently found in numerous bioactive molecules, ligands, and advanced functional materials due to its unique physical properties.
Tianyuan Ou   +5 more
semanticscholar   +1 more source

Straightforward Synthesis and Properties of Highly Fluorescent [5]- and [7]-Helical Dispiroindeno[2,1-c]fluorenes.

Angewandte Chemie, 2019
This work presents a general approach for synthesis of substituted [5]-helical dispiroindeno[2,1-c]fluorenes based on Rh-catalyzed intramolecular cyclotrimerization of triynes.
R. Kaiser   +7 more
semanticscholar   +1 more source

Dispiro(fluorene-9,4'-[1,3]dithiolane-5',9''-fluorene)

Acta Crystallographica Section C Crystal Structure Communications, 1995
The crystal structure of dispiro(fluorene-9,4'-[1,3]dithiolane-5',9-fluorene), C 27 H 18 S 2 , is reported. The C4-C5 bond connecting the two fluorenyl groups is 1.580 (4) A which is slightly longer than the C-C bond lengths [1.36-1.49 A] in other 1,3-dithiolanes.
R. P. Leino   +4 more
openaire   +1 more source

ChemInform Abstract: THIOPHENANALOGE DES FLUORENS 5. MITT. KONKURRIERENDE METALLIERUNG VON TETRAMETHYLCYCLOPENTADITHIOPHENEN, FLUOREN UND 3‐METHYL‐FLUOREN

Chemischer Informationsdienst. Organische Chemie, 1971
AbstractDie Metallierung des Cyclopentadithiophens (I) mit Äthyllithium/ Äther und anschließender Carboxylierung führt zur Carbonsäure (II) (Ausbeute 58%).
ALLERT K. WIERSEMA, SALO GRONOWITZ
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Direct access to benzo[b]fluorenes via a gold-catalysed A3-coupling strategy

Organic Chemistry Frontiers, 2019
A one-pot combination of gold catalysis and thermal cyclization provides a fast convergent route to benzo[b]fluorenes.
D. Lustosa   +6 more
semanticscholar   +1 more source

Enynone-enabled migratory insertion and Schmittel cyclization cascade for the synthesis of furan-fused fluorenes

Organic Chemistry Frontiers, 2019
A new method for the synthesis of furan-/benzo-fused fluorenes through copper(i)-catalyzed coupling of conjugated enynones or α-diazocarbonyl compounds with dialkynylbenzenes has been developed.
He Zhang   +4 more
semanticscholar   +1 more source

Vapor pressure measurements on fluorene and methyl-fluorenes

Fluid Phase Equilibria, 2004
Vapor pressures, molar enthalpies of sublimation, and molar enthalpies of vaporization of fluorene, 9-methyl-fluorene, and 1-methyl-fluorene have been determined by the transpiration method. Results were tested for internal consistency and compared with available literature data.
openaire   +1 more source

Anisotropic electron mobility in fluorene-PPV and fluorene-MEH-PPV

Molecular Physics, 2016
ABSTRACTPolyfluorene copolymers are attractive semiconductor materials, in particular for applications in the organic electronics field. They are versatile to be chemically modified and allow a tuning of the emission to cover the entire visible spectrum.
Carlos E. T. Magalhães   +3 more
openaire   +1 more source

Novel Soluble Fluorene–Thienothiadiazole and Fluorene–Carbazole Copolymers for Optoelectronics

Macromolecular Symposia, 2010
AbstractSummary: Optical, photophysical, electrochemical and photoelectrical properties of novel soluble low‐bandgap fluorene – thienothiadiazole based copolymers (CHTF and CDTF) and luminescent fluorene – carbazole copolymers, (CFCzE and CFCZA) were studied.
Věra Cimrová   +2 more
openaire   +1 more source

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