Antiferroelectric orthoconic liquid crystalline material with long pitch and the method of its preparation
View Patent ↗The racemic and chiral compounds expressed by common formula 1 and formula 2: wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, bridge group Z represent independently the single bond or COO, CH 2 CH 2 , CH 2 O and OCH 2 group, substituent Y represents CH 3 , or CH 2 F, CHF 2 , CF 3 , C 2 H 5 group, symbols n, m, r and t are independently integers of 1 to 8; symbols p and s signify independently number of 0 to 1 and its orthoconic antiferroelectric long helical pitch mixtures prepared by the methods 1) to the racemic components selected from compounds 1 are added chiral components selected from the compound of formula 1 and/or chiral components selected from the compounds of formula 2 and/or another optically active compounds with high helical twisting power, 2) to chiral compound 1 which helical pitches increases with the temperature increase is added chiral compound 1 which helical pitch decreases with temperature increase. The mixture shows excellent optical contrast and is applied in displays and photonic devices.
1. The antiferroelectric mixture containing
at least one achiral compound of general formula 1,
wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or C 2 H 5 or CH 2 F or CHF 2 or CF 3 group; symbols n, m, r and t are independently integers of 1 to 8; symbols p and s are independently 0 to 1 and
at least one chiral compound (R or S enantiomer) of the said formula 1.
2. The antiferroelectric mixture containing
at least one racemic compound of general formula 1,
wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or C 2 H 5 or CH 2 F or CHF 2 or CF 3 group; symbols n, m, r and t are independently an integer of 1 to 8; symbols p and s are independently 0 to 1, and
a chiral compound (S or R enantiomer) of general formula 2,
wherein the lateral substituents X 1 , X 2 , X 3 , X 1 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or CH 2 F or CHF 2 or CF 3 group, symbols n, m, r and t are independently integers of 1 to 8; symbols p and s are independently 0 to 1 and/or another chiral component selected from the chiral compounds having strong helical twisting power.
3. The antiferroelectric mixture containing at least two of the same R or S enantiomeric chiral compounds of the general formula 1,
wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or C 2 H 5 or CH 2 F or CHF 2 or CF 3 group; symbols n, m, r and t are independently an integer of 1 to 8; symbols p and s are independently 0 to 1, wherein at least one of said compounds show long helical pitch at low temperature range which value decreases upon increase of the temperature.
4. The chiral compound of general formula 1,
wherein the lateral substituents X 1 , X 2 , X 3 , X4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or C 2 H 5 or CH 2 F or CHF 2 or CF 3 group, symbol n is equal 3 or 4, symbols m, r and t are independently integers of 1 to 8, symbols p and s are independently 0 to 1 and showing long helical pitch at room temperature which value decreases with the increase of temperature.
5. The chiral compound according to claim 4 , wherein symbols r=5 or 6 or 7, m=1, Z is the single bond or COO group, Y is CH 3 group.
6. The chiral compound according to claim 5 , wherein symbols r=7, m=1, t=6, Z is the single bond or COO group, Y=CH 3 group.
7. The chiral compound of general formula 2,
wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or CH 2 F or CHF 2 or CF 3 group, symbols n, m, r and t are independently integers of 1 to 8; symbols p and s are independently 0 to 1.
8. The chiral compound according to claim 7 , wherein Z signifies the single bond.
9. A preparation method of the antiferroelectric mixtures from smectic anticlinic compounds, which comprises the steps of adding to at least one achiral racemic compound of general formula 1,
wherein the lateral substituents X 1 , X 2 , X 3 , 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or C 2 H 5 or CH 2 F or CHF 2 or CF 3 group, symbol n is an integer 3 or 4, symbols m, r and t are independently integers of 1 to 8, symbols p and s are independently 0 to 1, at least one chiral compound (R or S enantiomer) of the said formula 1 in a weight ratio of an eutectic composition or in the less weight ratio.
10. A preparation method of the antiferroelectric mixtures from smectic anticlinic compounds, which comprise the steps of adding to at least one achiral racemic compound of general formula 1,
wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or C 2 H 5 or CH 2 F or CHF 2 or CF 3 group, symbols n, m, r and t are independently integers of 1 to 8; symbols p and s are independently 0 to 1, at least one chiral compound (R or S enantiomer) of general formula 2,
wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or CH 2 F or CHF 2 or CF 3 group, symbols n, m, r and t are independently integers of 1 to 8; symbols p and s are independently 0 to 1 and/or other chiral compounds with strong helical twisting power in the amount of 2 to 30 wt. %.
11. A preparation method of the antiferroelectric mixtures from smectic anticlinic compounds, which comprise the steps of adding to at least one compound selected from a chiral enantiomer R or S compound of general formula 1,
wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is the single bond or COO or CH 2 CH 2 or CH 2 O or OCH 2 group, the substituent Y in the chain is CH 3 or C 2 H 5 or CH 2 F or CHF 2 or CF 3 group; symbols n, m, r and t are independently an integer of 1 to 8; symbols p and s are independently 0 to 1, which helical pitch increases with temperature increase, and
at least one chiral compound of general formula 1 which helical pitch p decreases with temperature increase.
12. The antiferroelectric mixture of claim 1 , wherein n is 3 or 4.
13. The antiferroelectric mixture of claim 12 , wherein said chiral compound of formula 1 is present in an amount of 2 wt. % to 50 wt. % based on the total weight of the mixture.
14. A racemic compound of general formula 1,
wherein the lateral substituents X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , and X 8 in the benzene rings represent independently hydrogen and fluorine atoms, Z is a single bond or COO or CH 2 CH 2 or CH 2 O or OCH group, the substituent Y in the chain is CH 3 , C 2 H 5 , CH 2 F, CHF 2 or CF 3 group wherein n is 3 or 4, and m, r and t are independently integers of 1 to 8; p and s are independently 0 to 1.
15. The racemic mixture of general formula 1,
wherein X 1 -X 8 are independently hydrogen and fluorine atoms and at least one of X 1 -X 8 is fluorine, Z is a single bond, COO, CH 2 CH 2 , CH 2 O or OCH 2 group, Y is CH 3 , C 2 H 5 , CH 2 F, CHF 2 or CF 3 group, n, m, r and t are independently integers of 1 to 8; p and s are independently 0 to 1.
16. The racemic mixture of claim 15 , wherein n is 3 or 4.