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・ Fluopicolide
・ FluoProbes
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・ Fluor Field at the West End
・ Fluor-buergerite
・ Fluor-liddicoatite
・ Fluor-uvite
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・ Fluorellestadite
・ Fluoren-9-ol dehydrogenase
Fluorene
・ Fluorenol
・ Fluorenone
・ Fluorenylidene
・ Fluorenylmethyloxycarbonyl chloride
・ Fluorescamine
・ Fluorescein
・ Fluorescein amidite
・ Fluorescein angiography
・ Fluorescein diacetate hydrolysis
・ Fluorescein isothiocyanate
・ Fluorescein-labeled proaerolysin
・ Fluorescence
・ Fluorescence (album)
・ Fluorescence anisotropy


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Fluorene : ウィキペディア英語版
Fluorene

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Fluorene , or 9''H''-fluorene, is a polycyclic aromatic hydrocarbon. It forms white crystals that exhibit a characteristic, aromatic odor similar to that of naphthalene. It is combustible. It has a violet fluorescence, hence its name. For commercial purposes it is obtained from coal tar.〔 It is insoluble in water and soluble in many organic solvents.
==Synthesis, structure, and reactivity==
Although fluorene is obtained from coal tar, it can also be prepared by dehydrogenation of diphenylmethane.〔Karl Griesbaum, Arno Behr, Dieter Biedenkapp, Heinz-Werner Voges, Dorothea Garbe, Christian Paetz, Gerd Collin, Dieter Mayer, Hartmut Höke "Hydrocarbons" in Ullmann's Encyclopedia of Industrial Chemistry 2002 Wiley-VCH, Weinheim. 〕 Alternatively, it can be prepared by the reduction of fluorenone with zinc.〔Fittig, Rud. (1873), "Ueber einen neuen Kohlenwasserstoff aus dem Diphenylenketon" Ber. Dtsch. Chem. Ges. volume 6, p. 187.〕 The fluorene molecule is nearly planar,〔
D. M. Burns, John Iball (1954), ''Molecular Structure of Fluorene'' Nature volume 173, p. 635. 〕 although each of the two benzene rings is coplanar with the central carbon 9.〔R. E. Gerkin, A. P. Lundstedt and W. J. Reppart (1984) ''Structure of fluorene, C13H10, at 159 K'' Acta Crystallographica, volume C40, pp. 1892–1894 〕

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