Liquid crystal compound having difluoromethyleneoxy, liquid crystal composition and liquid crystal display device
US-2015376502-A1 · Dec 31, 2015 · US
US2020255738A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2020255738-A1 |
| Application number | US-202016861320-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 29, 2020 |
| Priority date | Nov 23, 2017 |
| Publication date | Aug 13, 2020 |
| Grant date | — |
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A compound having the structure of general formula I is useful as a liquid crystal composition and as a photoelectric display device including the liquid crystal composition. The compound having the structure of general formula I is chemically and physically stable, and has higher clearing point, and both large dielectric anisotropy and large optical anisotropy at the same time. The compound having the structure of general formula I is well compatible with other liquid crystal compounds when applied in a liquid crystal composition, the composition has good stability especially in a low-temperature environment, the characteristic of fast response and a wide range of applicabilities, especially applicable to the IPS-type and TN-TFT-type liquid crystal display devices.
Opening claim text (preview).
We claim: 1 . A compound having the structure of general formula I: in which, R represents a C 1-18 alkyl or a C 2-18 alkenyl, one or more —CH 2 — in the alkyl or alkenyl can each be independently replaced by —O— or —CO— in a manner that oxygen atoms are not directly connected, one or more —H in the alkyl or alkenyl can be substituted by halogen or —CH 3 ; X represents —F, —OCF 3 or —CF 3 ; L 1 to L 6 each independently represents —H or —F; Z 1 , Z 2 and Z 3 each independently represents a single bond, —CH 2 CH 2 —, —CH 2 O—, —CF 2 O—, —COO—, —OCO—, —C≡C—, —OCH 2 —, —OCF 2 —, —CF 2 CF 2 — or —CH═CH—; ring and ring each independently represents one or more —CH 2 — in can be replaced by —O—, and one or more —H on can be substituted by —F; at least one of ring and ring represents 2 . The compound according to claim 1 , wherein X represents —F or —OCF 3 . 3 . The compound according to claim 2 , wherein Z 3 represents a single bond or —CF 2 O—. 4 . The compound according to claim 3 , wherein Z 1 and Z 2 each independently represents a single bond, —CH 2 CH 2 —, —CH 2 O— or —CF 2 O—. 5 . The compound according to claim 4 , wherein at least one of Z 1 , Z 2 and Z 3 is not a single bond. 6 . The compound according to claim 5 , wherein when ring represents on which —H is substituted by —F, Z 1 represents —CH 2 CH 2 — or Z 2 represents —CF 2 O—. 7 . The compound according to claim 1 , wherein at most four of L 1 to L 6 represents —F. 8 . The compound according to claim 7 , wherein L 3 and L 4 both represent —H. 9 . The compound according to claim 1 , wherein the compound is selected from a group consisting of the following compounds: in which, X represents —F or —OCF 3 ; ring represents and one or more —H on can be substituted by —F; L 7 and L 8 each independently represents H or F; Z 2 represents —CH 2 CH 2 — or —CH 2 O—. 10 . The compound according to claim 9 , wherein when L 5 represents —F, X represents —F. 11 . A liquid crystal composition, wherein the liquid crystal composition comprises: at least one compound of general formula I according to claim 1 ; at least one compound selected from a group consisting of the compounds of general formulas II-1 to II-4 at least one compound selected from a group consisting of the compounds of general formula III-1 and general formula III-2 in which, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 and R 10 each independently represents a C 1-7 alkyl or alkoxy, or a C 2-7 alkenyl or alkenoxy; R 8 represents —F, a C 1-7 alkyl or alkoxy, or a C 2-7 alkenyl or alkenoxy; L 9 to L 12 each independently represents —H or —F; X 1 represents —F, a C 1-18 alkyl or a C 2-18 alkenyl, one or more —CH 2 — in the alkyl or alkenyl can each be independently replaced by —O— in a manner that oxygen atoms are not directly connected, one or more —H in the alkyl or alkenyl can be substituted by halogen, and when X 2 represents alkyl or alkenyl, or, when one or more —CH 2 — in the alkyl or alkenyl each is independently replaced by —O— in a manner that oxygen atoms are not directly connected, at least one of L 10 to L 12 represents —F; ring represents one or more —CH 2 — in can be replaced by —O—, and one or more —H on can be substituted by —F; Z 4 and Z 5 each independently represents a single bond, —CH 2 CH 2 —, —CH 2 O—, —CF 2 O—, —OCH 2 — or —OCF 2 —; n represents 1 or 2, and when n represents 2, ring can be same or different, and Z 4 can be same or different. 12 . The liquid crystal composition according to claim 11 , wherein the compound of general formula I is selected from the group consisting of the compounds of general formulas I-1 to I-12 according to claim 9 . 13 . The liquid crystal composition according to claim 12 , wherein the compound of general formula I provides 1-50% of the total weight of the liquid crystal composition, the compound selected from the group consisting of the compounds of general formulas II-1 to II-4 provides 5-75% of the total weight of the liquid crystal composition, and the compound selected from the group consisting of the compounds of general formula III-1 and general formula III-2 provides 1-50% of the total weight of the liquid crystal composition. 14 . The liquid crystal composition according to claim 13 , wherein the liquid crystal composition comprises at least one compound selected from a group consisting of the compounds of general formula II-1-a and general formula II-1-b: 15 . The liquid crystal composition according to claim 14 , wherein the liquid crystal composition comprises at least one compound selected from a group consisting of the compounds of general formulas II-2 to II-4. 16 . The liquid crystal composition according to claim 15 , wherein in the compound selected from the group consisting of the compounds of general formula III-1 and general formula III-2,
not condensed with other rings · CPC title
the heterocyclic ring being a six-membered ring · CPC title
having oxygen as hetero atom (sugars C09K19/0422) · CPC title
containing compounds with benzene rings directly linked · CPC title
Cy-Cy-Ph · CPC title
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