Chiral esters of α-substituted phenylalkanoic acids and mesogenic hydroxy compounds, and their use as a doping substance in liquid crystal phases

Abstract

Abstract The novel compounds are chiral esters of α-substituted phenylalkanoic acids and mesogenic hydroxy compounds, the symbols in the general formula (I) ##STR1## being defined as follows: MO=molecular radical of a mesogenic hydroxy compound MOH after removal of one H, the radical MO being expressed by the general formula (II) R.sup.2 --(A.sup.1).sub.n1 --(B--).sub.n2 (A.sup.2).sub.n3 --O (II) where R 2 =straight-chain or branched (C 1 -C 12 )-alkyl, it being possible for one or two non-adjacent CH 2 groups to be replaced by O and/or S atoms, or, if n1=1, also F, Cl, Br, CN or CF 3 , A 1 , A 2 =independently of one another 1,4-phenylene, diazine-2,5-diyl, diazine-3,6-diyl, 1,4-cyclohexylene, 1,3-dioxane-2,5-diyl, 1,3-dithiane-2,5-diyl or 1,4-bicyclo(2,2,2)octylene, it being possible for these groups also to be at least monosubstituted by F, Cl, Br, CN, CF 3 and/or (C 1 -C 12 )-alkyl (one or two non-adjacent CH 2 groups may be replaced by O and/or S atoms), B=CO--O, O--CO, CH 2 --CH 2 , OCH 2 , CH 2 O, CH═N, N═CH, N═N, N(O)═N, n1, n2, n3=independently of one another 0, 1 or 2, n1 and n3 not being 0 simultaneously, Y=an electron-attracting substituent, Z=H or an electron-attracting substituent, but not identical with Y, and R 1 =benzyl or phenyl, it being possible for these groups to be substituted in the aromatic moiety in the same way as A 1 and A 2 , with the exception of the compounds with Z=H, Y=F, Cl or Br, R 2 =(C 1 -C 11 )-alkoxy, A 1 and A 2 =phenyl, n 1 , and n 3 =1 and n 2 =0. The compounds are preferably used in tilted smectic liquid crystal phases, which are converted into ferroelectric liquid crystal phases by these compounds; they show high values of spontaneous polarization.

Inventors

• 👤 Gerd Heppke
• 👤 Gunter Scherowsky
• 👤 Christian Bahr
• 👤 Lutz Lehmann

Bibliographic Details