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Search for "liquid crystals" in Full Text gives 78 result(s) in Beilstein Journal of Organic Chemistry.

Themed series in organo- fluorine chemistry

  • David O'Hagan

Beilstein J. Org. Chem. 2008, 4, No. 11, doi:10.3762/bjoc.4.11

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  • ]. Organo-fluorine compounds have also found a significant role in soft materials chemistry such as liquid crystals, photoresist polymers and self assembling monolayers [3]. Allied to this breadth of activity is a steady development in the number and range of fluorination reagents and methodologies. DAST
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Editorial
Published 25 Apr 2008

Shape- persistent macrocycle with intraannular alkyl groups: some structural limits of discotic liquid crystals with an inverted structure

  • Sigurd Höger,
  • Jill Weber,
  • Andreas Leppert and
  • Volker Enkelmann

Beilstein J. Org. Chem. 2008, 4, No. 1, doi:10.1186/1860-5397-4-1

Graphical Abstract
  • defined surfaces [1][2][3][4][5][6][7][8]. Furthermore, shape-persistent macrocycles are interesting mesogens for discotic liquid crystalline materials [9][10][11][12]. The common design principle of conventional discotic liquid crystals (LCs) is a more or less rigid core (disk-like or macrocyclic) with
  • parameter to fine tune the thermal behavior of discotic liquid crystals with an inverted structure. This parameter is absent in conventional discotic liquid crystals. As expected, longer adaptable alkyl substituents (compared to 1) decrease the melting point of the macrocycles but at the same time also
  • /conts/retrieving.html, or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: (+44)1223-336033; or email: deposit@ccdc.cam.ac.uk. a) Design principle for common discotic liquid crystals; b) Design principle for discotic liquid crystals with an inverted structure
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Full Research Paper
Published 09 Jan 2008

A convenient catalyst system for microwave accelerated cross- coupling of a range of aryl boronic acids with aryl chlorides

  • Matthew L. Clarke,
  • Marcia B. France,
  • Jose A. Fuentes,
  • Edward J. Milton and
  • Geoffrey J. Roff

Beilstein J. Org. Chem. 2007, 3, No. 18, doi:10.1186/1860-5397-3-18

Graphical Abstract
  • biaryl products (see Supporting Information File 1 for experimental data). There has been some interest in the cross-coupling of fluorinated nucleophiles due to the application of fluoroaryl substituents in medicinal chemistry and in liquid crystals. [30][31][32][33][34] The Buchwald group recently
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Preliminary Communication
Published 30 May 2007
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