Liquid crystal compound, liquid crystal composition and liquid crystal display device
View Patent ↗The invention provides a liquid crystal compound having stability to heat, light and so forth, a wide temperature range of a nematic phase, a small viscosity, a suitable optical anisotropy, a suitable elastic constant K 33 , a suitable and negative dielectric anisotropy, and an excellent compatibility with other liquid crystal compounds. The invention provides a liquid crystal composition containing the compound described above and having stability to heat, light and so forth, a small viscosity, a suitable optical anisotropy, a suitable and negative dielectric anisotropy, a suitable elastic constant K 33 , a low threshold voltage, a high maximum temperature of a nematic phase, and a low minimum temperature of the nematic phase. The invention also provides a liquid crystal display device having a short response time, a small power consumption, a low driving voltage, and a large contrast, and containing the composition described above which can be used in a large temperature range. For example, a liquid crystal compound having four or more rings in which the central ring has 2,3-difluorophenoxy such as trans-4′-[2,3-difluoro-4-(trans-4-propylcyclohexyl)phenoxymethyl]-trans-4-pentylbicyclohexyl is provided. Further provided is a liquid crystal composition containing the compound, and a liquid crystal display device using this liquid crystal composition.
1. A compound represented by formula (a):
wherein
Ra and Rb are each independently hydrogen, alkyl having 1 to 12 carbons, alkenyl having 2 to 12 carbons, alkoxy having 1 to 11 carbons, alkoxyalkyl having 2 to 11 carbons, or alkenyloxy having 2 to 11 carbons, and in these alkyl, alkenyl, alkoxy, alkoxyalkyl, and alkenyloxy, arbitrary hydrogen may be replaced by fluorine;
ring A 1 , ring A 2 , ring A 3 , and ring A 4 are each independently 1,4-cyclohexylene, 1,4-cyclohexenylene, tetrahydropyran-2,5-diyl, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene, naphthalene-2,6-diyl, decahydronaphthalene-2,6-diyl, or 1,2,3,4-tetrahydronaphthalene-2,6-diyl;
Z 1 and Z 2 are each independently a single bond, —(CH 2 ) 2 —, —(CH 2 ) 4 —, —CH═CH—, —C≡C—, —CH 2 O—, —OCH 2 —, —COO—, —OCO—, —CF 2 O—, or —OCF 2 —;
W is —CH 2 —, —CO—, or —CF 2 —; and
m and n are each independently 0, 1, or 2, and the sum of m and n is 1 or 2,
provided that
when the sum of m and n is 1, W is —CH 2 — or —CO—;
when m=1 and n=0, ring A 3 is 1,4-cyclohexylene;
when ring A 2 is 3-fluoro-1,4-phenylene, W is —CH 2 —.
2. The compound according to claim 1 , wherein
Ra and Rb are each independently alkyl having 1 to 12 carbons, alkenyl having 2 to 12 carbons, alkoxy having 1 to 11 carbons, alkoxyalkyl having 2 to 11 carbons, or alkenyloxy having 2 to 11 carbons; and
ring A 1 , ring A 2 , ring A 3 , and ring A 4 are each independently 1,4-cyclohexylene, 1,4-cyclohexenylene, tetrahydropyran-2,5-diyl, 1,4-phenylene, 2-fluoro-1,4-phenylene, or 3-fluoro-1,4-phenylene.
3. A compound represented by any one of formula (a-1) and formula (a-2):
wherein
Ra 1 and Rb 1 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 11 carbons, or alkenyl having 2 to 12 carbons;
ring A 5 , ring A 6 , ring A 7 , and ring A 8 are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, or 3-fluoro-1,4-phenylene;
Z 3 and Z 4 are each independently a single bond or —(CH 2 ) 2 —; and
W is —CH 2 —, or —CO—;
provided that
when ring A 6 is 3-fluoro-1,4-phenylene, W is —CH 2 —.
4. A compound represented by any one of formulas (a-1-1) to (a-1-3) and formulas (a-2-1) to (a-2-6):
wherein Ra 1 and Rb 1 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 11 carbons, or alkenyl having 2 to 12 carbons; and W is —CH 2 —, or —CO—.
5. The compound according to claim 4 , wherein W is —CH 2 — in formulas (a-1-1) to (a-1-3) and formulas (a-2-1) to (a-2-6).
6. The compound according to claim 4 , wherein W is —CO— in formulas (a-1-1) to (a-1-3) and formulas (a-2-1) to (a-2-6).
7. A liquid crystal composition having a negative dielectric anisotropy that comprises a first component which is at least one compound selected from the group of compounds according to claim 1 and a second component which is at least one compound selected from the group of compounds represented by formulas (e-1) to (e-3):
wherein
Ra 11 and Rb 11 are each independently alkyl having 1 to 10 carbons, and in this alkyl, —CH 2 — may be nonadjacently replaced by —O—, —(CH 2 ) 2 — may be nonadjacently replaced by —CH═CH—, and hydrogen may be replaced by fluorine;
ring A 11 , ring A 12 , ring A 13 , and ring A 14 are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; and
Z 11 , Z 12 , and Z 13 are each independently a single bond, —(CH 2 ) 2 —, —CH═CH—, —C≡C—, —COO—, or —CH 2 O—.
8. A liquid crystal composition having a negative dielectric anisotropy that comprises a first component which is at least one compound selected from the group of compounds represented by formulas (a-1-1) to (a-1-3) and formulas (a-2-1) to (a-2-6) according to claim 4 , and a second component selected from the group of compounds represented by formulas (e-1) to (e-3)
wherein Ra 11 and Rb 11 are each independently alkyl having 1 to 10 carbons, and in this alkyl, —CH 2 — may be nonadjacently replaced by —O—, —(CH 2 ) 2 — may be nonadjacently replaced by —CH═CH—, and hydrogen may be replaced by fluorine; ring A 11 , ring A 12 , ring A 13 , and ring A 14 are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; and Z 11 , Z 12 , and Z 13 are each independently a single bond, —(CH 2 ) 2 —, —CH═CH—, —CC—, —COO—, or —CH 2 O—.
9. The liquid crystal composition according to claim 8 , wherein the content ratio of the first component is in the range of 5% to 60% by weight, and the content ratio of the second component is in the range of 40% to 95% by weight, based on the total weight of the liquid crystal composition.
10. The liquid crystal composition according to claim 9 that further comprises a third component which is at least one compound selected from the group of compounds represented by formulas (g-1) to (g-6), in addition to the first and second components:
wherein
Ra 21 and Rb 21 are each independently hydrogen or alkyl having 1 to 10 carbons, and in this alkyl, —CH 2 — may be nonadjacently replaced by —O—, —(CH 2 ) 2 — may be nonadjacently replaced by —CH═CH—, and hydrogen may be replaced by fluorine;
ring A 21 , ring A 22 , and ring A 23 are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3 -dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl;
Z 21 , Z 22 , and Z 23 are each independently a single bond, —(CH 2 ) 2 —, —CH═CH—, —C≡C—, —OCF 2 —, —CF 2 O—, —OCF 2 CH 2 CH 2 —, —CH 2 CH 2 CF 2 O—, —COO—, —OCO—, —OCH 2 —, or —CH 2 O—;
Y 1 , Y 2 , and Y 4 are each independently fluorine or chlorine;
q, r, and s are each independently 0, 1, or 2, and q+r+s is 1, 2, or 3; and
t is 0, 1, or 2.
11. The liquid crystal composition according to claim 10 , wherein the third component is at least one compound selected from the group of compounds represented by formulas (h-1) to (h-7):
wherein
Ra 22 and Rb 22 are a straight-chain alkyl having 1 to 8 carbons, a straight-chain alkenyl having 2 to 8 carbons, or alkoxy having 1 to 7 carbons;
Z 24 , Z 25 , and Z 26 are a single bond, —(CH 2 ) 2 —, —COO—, —OCO—, —CH 2 O—, or —OCH 2 —; and
Y 1 and Y 2 are simultaneously fluorine or one of Y 1 and Y 2 is fluorine and the other is chlorine.
12. A liquid crystal composition having a negative dielectric anisotropy that comprises a first component which is at least one compound selected from the group of compounds represented by formulas (a-1-1) to (a-1-3) and formulas (a-2-1)to (a-2-6) according to claim 4 , a second component which is at least one compound selected from the group of compounds represented by formulas (e-1) to (e-3)
wherein Ra 11 and Rb 11 are each independently alkyl having 1 to 10 carbons, and in this alkyl, —CH 2 — may be nonadjacently replaced by —O—, —(CH 2 ) 2 — may be nonadjacently replaced by —CH═CH—, and hydrogen may be replaced by fluorine; ring A 11 , ring A 12 , ring A 13 , and ring A 14 are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; and Z 11 , Z 12 , and Z 13 are each independently a single bond, —(CH 2 ) 2 —, —CH═CH—, —CC—, —COO—, or —CH 2 O—; and a third component which is at least one compound selected from the group of compounds represented by formulas (h-1) to (h-7) according to claim 13
wherein Ra 22 and Rb 22 are a straight-chain alkyl having 1 to 8 carbons, a straight-chain alkenyl having 2 to 8 carbons, or alkoxy having 1 to 7 carbons; Z 24 , Z 25 , and Z 26 are a single bond, —(CH 2 ) 2 —, —COO—, —OCO—, —CH 2 O—, or —OCH 2 —; and Y 1 and Y 2 are simultaneously fluorine or one of Y 1 and Y 2 is fluorine and the other is chlorine.
13. The liquid crystal composition according to claim 12 , wherein the content ratio of the first component is in the range of 5% to 60% by weight, the content ratio of the second component is in the range of 20% to 75% by weight, and the content ratio of the third component is in the range of 20% to 75% by weight, based on the total weight of the liquid crystal composition.
14. A liquid crystal display device that comprises the liquid crystal composition according to claim 7 .
15. The liquid crystal display device according to claim 14 , wherein the operation mode thereof is a VA mode or an IPS mode, and the driving mode thereof is an active matrix mode.
16. A liquid crystal composition having a negative dielectric anisotropy that comprises a first component which is at least one compound selected from the group of compounds represented by formulas (a-1) and (a-2) according to claim 3 and a second component which is at least one compound selected from the group of compounds represented by formulas (e-1) to (e-3)
wherein Ra 11 and Rb 11 are each independently alkyl having 1 to 10 carbons, and in this alkyl, —CH 2 — may be nonadjacently replaced by —O—, —(CH 2 ) 2 — may be nonadjacently replaced by —CH═CH—, and hydrogen may be replaced by fluorine; ring A 11 , ring A 12 , ring A 13 , and ring A 14 are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; and Z 11 , Z 12 , and Z 13 are each independently a single bond, —(CH 2 ) 2 —, —CH═CH—, —CC—, —COO—, or —CH 2 O—.
17. A liquid crystal display device that comprises the liquid crystal composition according to claim 11 .
18. The liquid crystal display device according to claim 17 , wherein the operation mode thereof is a VA mode or an IPS mode, and the driving mode thereof is an active matrix mode.