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Search for "crystal design" in Full Text gives 4 result(s) in Beilstein Journal of Organic Chemistry.

Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes

  • Zeguo Fang,
  • Nawaf Al-Maharik,
  • Peer Kirsch,
  • Matthias Bremer,
  • Alexandra M. Z. Slawin and
  • David O’Hagan

Beilstein J. Org. Chem. 2020, 16, 674–680, doi:10.3762/bjoc.16.65

Graphical Abstract
  • compromised by conformational flexibility. Although none of the compounds prepared here met all of the criteria for commercial development, the study gives an insight into the potential for this novel difluorocyclopropane motif in liquid crystal design and development. Examples of liquid crystal candidates
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Published 14 Apr 2020

The use of isoxazoline and isoxazole scaffolding in the design of novel thiourea and amide liquid-crystalline compounds

  • Itamar L. Gonçalves,
  • Rafaela R. da Rosa,
  • Vera L. Eifler-Lima and
  • Aloir A. Merlo

Beilstein J. Org. Chem. 2020, 16, 175–184, doi:10.3762/bjoc.16.20

Graphical Abstract
  • liquid crystal design [10][11]. N,N′-Bis(3,4,5-trialkoxylphenyl)ureas were identified as columnar liquid crystalline compounds presenting ferroelectric properties [12]. Another study reported cyclic disubstituted ureas with liquid crystalline ferroelectric and antiferroelectric phases [13]. Relating to
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Published 06 Feb 2020

1,2,3,4-Tetrahydro-1,4,5,8-tetraazaanthracene revisited: properties and structural evidence of aromaticity loss

  • Arnault Heynderickx,
  • Sébastien Nénon,
  • Olivier Siri,
  • Vladimir Lokshin and
  • Vladimir Khodorkovsky

Beilstein J. Org. Chem. 2019, 15, 2059–2068, doi:10.3762/bjoc.15.203

Graphical Abstract
  • atoms. This molecule can be easily modified at either ethylenediamino or ethylenediimino moiety and can thus serve as an attractive precursor for crystal design and creation of supramolecular assemblies. Of special interest is that the quinoxaline moiety of THTAA (3) and its derivatives are losing their
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Published 28 Aug 2019

Crystal design using multipolar electrostatic interactions: A concept study for organic electronics

  • Peer Kirsch,
  • Qiong Tong and
  • Harald Untenecker

Beilstein J. Org. Chem. 2013, 9, 2367–2373, doi:10.3762/bjoc.9.272

Graphical Abstract
  • isotropic charge transport compared to the “herring bone” stacking observed for other acenes. Keywords: aromatic stacking; charge carrier transport; crystal design; electrostatic control; organic semiconductor; organo-fluorine; Introduction Within a very few years the first organic semiconductors have
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Published 05 Nov 2013
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