Compound, liquid crystal composition and photoelectric display device thereof

US2020255738A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2020255738-A1
Application numberUS-202016861320-A
CountryUS
Kind codeA1
Filing dateApr 29, 2020
Priority dateNov 23, 2017
Publication dateAug 13, 2020
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

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.

First claim

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,

Assignees

Inventors

Classifications

  • C07D319/06Primary

    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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What does patent US2020255738A1 cover?
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 ha…
Who is the assignee on this patent?
Jiangsu Hecheng Display Tech
What technology area does this patent fall under?
Primary CPC classification C07D319/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Aug 13 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).