676545-61-2Relevant academic research and scientific papers
Facile synthesis of 1,7,8-trifluoro-2-naphthol via DMAP catalyzed cycloaromatization
Araki, Keisuke,Katagiri, Tomohiro,Inoue, Munenori
, p. 41 - 47 (2014)
A facile synthesis of 1,7,8-trifluoro-2-naphthol, an important synthetic intermediate for liquid crystal compounds with a 1,7,8-trifluoronaphthalene structure, was developed starting from 4-bromo-1,2-difluorobenzene via DMAP catalyzed intramolecular cycloaromatization in 51% overall yield for the 6 steps.
Unilaterally Fluorinated Acenes: Synthesis and Solid-State Properties
Bischof, Daniel,Breuer, Tobias,Grell, Yvonne,Hofmann, Philipp E.,Ivlev, Sergei I.,Koert, Ulrich,Schiller, Anna L. C.,Tripp, Matthias W.,Witte, Gregor
, p. 16501 - 16505 (2020/07/20)
The rapid development of organic electronics is closely related to the availability of molecular materials with specific electronic properties. Here, we introduce a novel synthetic route enabling a unilateral functionalization of acenes along their long side, which is demonstrated by the synthesis of 1,2,10,11,12,14-hexafluoropentacene (1) and the related 1,2,9,10,11-pentafluorotetracene (2). Quantum chemical DFT calculations in combination with optical and X-ray absorption spectroscopy data indicate that the single-molecule properties of 1 are a connecting link between the organic semiconductor model systems pentacene (PEN) and perfluoropentacene (PFP). In contrast, the crystal structure analysis reveals a different packing motif than for the parent molecules. This can be related to distinct F???H interactions identified in the corresponding Hirshfeld surface analysis and also affects solid-state properties such as the exciton binding energy and the sublimation enthalpy.
1,7,8-TRIFLUORONAPHTHALENE-2-NAPHTHOL, AND METHOD FOR PRODUCING LIQUID CRYSTAL COMPOUND USING SAME
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Page/Page column 10, (2010/02/12)
The present invention provides 1,7,8-trifluoro-2-naphthol and a derivative thereof as intermediates for efficiently producing a trifluoronaphthalene liquid crystal material. A method for efficiently producing a trifluoronaphthalene liquid crystal material
