The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jan. 24, 1995

Filed:

May. 20, 1993
Applicant:
Inventors:

Wolfgang Hemmerling, Sulzbach, DE;

Hans-Rolf Dubal, Konigstein, DE;

Claus Escher, Muhltal, DE;

Gerhard Illian, Frankfurt am Main, DE;

Yoshio Inoguchi, Tokyo, DE;

Ingrid Muller, Hofheim, DE;

Mikio Murakami, Konigstein, DE;

Dieter Ohlendorf, Liederbach, DE;

Rainer Wingen, Hattersheim am Main, DE;

Assignee:

Hoechst Aktiengesellschaft, Frankfurt am Main, DE;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C09K / ;
U.S. Cl.
CPC ...
25229961 ; 544318 ; 544298 ; 544335 ; 546268 ; 546275 ; 546276 ; 546277 ; 546290 ; 546296 ; 546301 ; 546339 ; 546342 ; 548128 ; 548129 ; 549357 ; 549473 ; 549499 ; 549502 ;
Abstract

The use of optically active tetrahydrofuran-2-carboxylic acid esters as dopants in liquid-crystal mixtures, liquid-crystal mixtures containing same and novel optically active tetrahydrofuran-2-carboxylic acid esters. Optically active tetrahydrofuran-2-carboxylic acid esters containing a mesogenic molecular building unit are suitable as dopants in liquid-crystal mixtures. They result in liquid-crystalline ferroelectric phases having short switching times and in electroclinic phases having large electroclinic coefficients. A further advantage is that they induce a helix having a very small pitch so that they are also suitable for helix compensation in LC mixtures. The compounds are symbolized by the general formula: ##STR1## in which the symbols and indices essentially denote: R.sup.1 =alkyl/alkenyl or tetrahydrofurancarbonyloxy or -thio; j, l, n=zero, 1 or 2; k, m=zero or 1; --A.sup.1, --A.sup.2, --A.sup.3 =phenylene, cycloalkylene or corresponding heterocyclates containing nitrogen, oxygen or sulfur; --M.sup.1, --M.sup.2 =bridges such as --CO--O, --OCH.sub.2 or --CH.dbd.CH; X=oxygen or sulfur.


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