IP Library Granted Patent US 11,739,270
Granted Patent B2
US 11,739,270 · App. 16/968,961 · Granted Aug 29, 2023

Polymerizable compound as well as liquid crystal composition and liquid crystal display device each including polymerizable compound

Inventors: Masanao Hayashi (Kita-adachi-gun, JP); Ayaki Hosono (Kita-adachi-gun, JP); Shota Kosaka (Kita-adachi-gun, JP)
Assignee: DIC CORPORATION
C09K19/56C07C69/54C07C69/653C09K19/3066C09K19/3402C09K2019/3425
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Quick Facts
Patent No.
US 11,739,270
App. No.
16/968,961
Granted
Aug 29, 2023
Kind
B2
Abstract

The present invention provides a compound represented by the general formula (i), which has a partial structure K i1 represented by one of the general formulae (K-1) to (K-6) and has a ring B with at least one P-Sp- group and with at least one R i2 (R i2 denotes a linear or branched alkyl group having 2 to 10 carbon atoms or a linear or branched halogenated alkyl group having 2 to 10 carbon atoms, —CH 2 — in the alkyl or halogenated alkyl group is optionally substituted with —CH═CH—, —O—, —COO—, or —OCO—, but —O— is not adjacent to another —O—). Thus, the compound in a liquid crystal composition adsorbs to substrates between which the liquid crystal composition (a liquid crystal layer) exists. The compound can hold vertically aligned liquid crystal molecules, can improve alignment stability, and can ensure low-temperature storage stability.

Claims (38)

1. A compound represented by a general formula (i):

wherein

R i1 denotes a hydrogen atom, an alkyl group having 1 to 30 carbon atoms, or a halogenated alkyl group having 1 to 30 carbon atoms, —CH 2 — in the alkyl or halogenated alkyl group is optionally replaced with —CH═CH—, —C≡—, —O—, —NH—, —COO—, —OCO—, or —OCOO—, but —O— is not adjacent to another —O—,

R i2 denotes a linear alkyl group having 2 to 10 carbon atoms, a branched alkyl group having 3 to 10 carbon atoms, a linear halogenated alkyl group having 2 to 10 carbon atoms, or a branched halogenated alkyl group having 3 to 10 carbon atoms, wherein —CH 2 — in the alkyl or halogenated alkyl group is optionally replaced with —CH═CH—, —O—, —COO—, or —OCO—, but —O— is not adjacent to another —O—,

a ring A denotes a divalent aromatic group, a divalent alicyclic group, a divalent heterocyclic compound group, a divalent fused ring, or a divalent fused polycyclic ring, a hydrogen atom in these ring structures is optionally replaced with L i1 , L i1 denotes a halogen atom, a cyano group, a nitro group, P-Sp-, a monovalent organic group having a group represented by a general formula K i1 , a linear alkyl group having 1 to 10 carbon atoms, a branched alkyl group having 3 to 10 carbon atoms, a linear halogenated alkyl group having 1 to 10 carbon atoms, or a branched halogenated alkyl group having 3 to 10 carbon atoms, wherein —CH 2 — in the alkyl or halogenated alkyl group is optionally replaced with —CH═CH—, —C≡C—, —O—, —NH—, —COO—, —OCO—, or —OCOO—, but —O— is not adjacent to another —O—,

a ring B denotes a formula (B-1),

wherein a hydrogen atom in the ring B is optionally replaced with L i2 , L i2 denotes a halogen atom, a monovalent organic group having a group represented by the general formula K i1 , a linear alkyl group having 1 to 10 carbon atoms, wherein—CH 2 — in the alkyl or halogenated alkyl group is optionally replaced with —CH═CH—, —C≡—, —O—, —COO—, or —OCO—, but —O— is not adjacent to another —O—,

Z i1 denotes a single bond, —O—, —CH═CH—, —CF═CF—, —C≡C—, —COO—, —OCO—, —OCOO—, —CF 2 O—, —OCF 2 —, —CH═CHCOO—, —OCOCH═CH—, —CH═C(CH 3 )COO—, —OCOC(CH 3 )═CH—, —CH 2 —CH(CH 3 )COO—, —OCOCH(CH 3 )—CH 2 —, —OCH 2 CH 2 O—, or an alkylene group having 2 to 10 carbon atoms, and one —CH 2 — or two or more nonadjacent —CH 2 — groups in the alkylene group are optionally replaced with —O—, —COO—, or —OCO—,

Z i3 denotes a single bond, —O—, —CH═CH—, —COO—, —OCO—, —OCOO—, —CH═CHCOO—, —OCOCH═CH—, —CH═C(CH 3 )COO—, —OCOC(CH 3 )═CH—, —CH 2 —CH(CH 3 )COO—, —OCOCH(CH 3 )—CH 2 —, or a linear alkylene group having 2 to 20 carbon atoms, a branched alkylene group having 3 to 20 carbon atoms, one —CH 2 — or two or more nonadjacent —CH 2 — groups in the alkylene group are optionally replaced with —O—, —COO—, or —OCO—,

K i1 denotes a group represented by one of general formulae (K-1) to (K-6),

R K1 denotes a hydrogen atom, a linear alkyl group having 1 to 6 carbon atoms, or a alkyl group having 3 to 6 carbon atoms, and T K1 independently denotes a group represented by one of general formulae (T-1) to (T-6),

S T1 denotes a single bond, a linear alkylene group having 1 to 15 carbon atoms, a branched alkylene group having 3 to 15 carbon atoms, a linear alkenylene group having 2 to 18 carbon atoms, or a branched alkenylene group having 3 to 18 carbon atoms, wherein —CH 2 — in the alkylene or alkelene group is optionally replaced with —O—, —COO—, —C(═O)—, —C(═CH 2 )—, or —OCO— such that oxygen atoms are not directly adjacent to each other, R T1 denotes an alkyl group having 1 to 5 carbon atoms, —CH 2 — in the alkyl group is optionally replaced with —O—, —COO—, —C(═O)—, —C(═CH 2 )—, or —OCO— such that oxygen atoms are not directly adjacent to each other, and R T2 and R T3 independently denote a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, and

P denotes a polymerizable group, Sp denotes a spacer group or a single bond, m denotes an integer in the range of 1 to 4, a plurality of As, if present, may be the same or different, a plurality of Z i1 s, if present, may be the same or different, a plurality of Ps, if present, may be the same or different, and a plurality of Sps, if present, may be the same or different.

2. The compound according to claim 1 , wherein A in the general formula (i) denotes a ring structure selected from a 1,4-phenylene group, a 1,4-cyclohexylene group, an anthracene-2,6-diyl group, a phenanthrene-2,7-diyl group, a pyridine-2,5-diyl group, a pyrimidine-2,5-diyl group, a naphthalene-2,6-diyl group, an indan-2,5-diyl group, a 1,2,3,4-tetrahydronaphthalene-2,6-diyl group, and a 1,3-dioxane-2,5-diyl group, and the ring structure is unsubstituted or denotes a group optionally substituted with an alkyl group having 1 to 12 carbon atoms, a halogenated alkyl group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogenated alkoxy group having 1 to 12 carbon atoms, a halogen atom, a cyano group, a nitro group, or P-Sp-.

3. The compound according to claim 1 , wherein P in the general formula (i) denotes a substituent selected from a group represented by the following general formulae (P-1) to (P-14).

4. The compound according to claim 1 , wherein K i1 in the general formula (i) is represented by the general formula (K-1) or (K-2).

5. A liquid crystal composition comprising: a compound represented by the general formula (i) according to claim 1 ; a polymerizable compound different from the compound represented by the general formula (i); and a nonpolymerizable liquid crystal compound.

6. The liquid crystal composition according to claim 5 , wherein the polymerizable compound is one or two or more compounds represented by a general formula (P):

wherein

Z p1 denotes a fluorine atom, a cyano group, a hydrogen atom, an alkyl group having 1 to 15 carbon atoms in which a hydrogen atom is optionally replaced with a halogen atom, an alkoxy group having 1 to 15 carbon atoms in which a hydrogen atom is optionally replaced with a halogen atom, an alkenyl group having 2 to 15 carbon atoms in which a hydrogen atom is optionally replaced with a halogen atom, an alkenyloxy group having 2 to 15 carbon atoms in which a hydrogen atom is optionally replaced with a halogen atom, or -Sp p2 -R p2 ,

R p1 and R p2 denote one of the following formulae (R-I) to (R-VIII),

wherein

* is bonded to Sp p1 ,

R 2 to R 6 independently denote a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or a halogenated alkyl group having 1 to 5 carbon atoms,

W denotes a single bond, —O—, or a methylene group,

T denotes a single bond or —COO—, and

p, t, and q independently denote 0, 1, or 2,

Sp p1 and Sp p2 denote a spacer group,

L p1 and L p2 independently denote a single bond, —O—, —S—, —CH 2 —, —OCH 2 —, —CH 2 O—, —CO—, —C 2 H 4 —, —COO—, —OCO—, —OCOOCH 2 —, —CH 2 OCOO—, —OCH 2 CH 2 O—, —CO—NR a —, —NR a —CO—, —SCH 2 —, —CH 2 S—, —CH═CR a —COO—, —CH═CR a —OCO—, —COO—CR a ═CH—, —OCO—CR a ═CH—, —COO—CR a ═CH—COO—, —COO—CR a ═CH—OCO—, —OCO—CR a ═CH—COO—, —OCO—CR a ═CH—OCO—, —(CH 2 ) z —C(═O)—O—, —(CH 2 ) z —O—(C═O)—, —O—(C═O)—(CH 2 ) z —, —(C═O)—O—(CH 2 ) z —, —CH 2 (CH 3 )C—C(═O)—O—, —CH 2 (CH 3 )C—O—(C═O)—, —O—(C═O)—C(CH 3 )CH 2 , —(C═O)—O—C(CH 3 )—CH 2 , —CH═CH—, —CF═CF—, —CF═CH—, —CH═CF—, —CF 2 —, —CF 2 O—, —OCF 2 —, —CF 2 CH 2 —, —CH 2 CF 2 —, —CF 2 CF 2 —, or —C≡C— (wherein R a independently denotes a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, and z denotes an integer in the range of 1 to 4,

M p2 denotes a 1,4-phenylene group, a 1,4-cyclohexylene group, an anthracene-2,6-diyl group, a phenanthrene-2,7-diyl group, a pyridine-2,5-diyl group, a pyrimidine-2,5-diyl group, a naphthalene-2,6-diyl group, an indan-2,5-diyl group, a 1,2,3,4-tetrahydronaphthalene-2,6-diyl group, a 1,3-dioxane-2,5-diyl group, or a single bond, M p2 is unsubstituted or optionally substituted with an alkyl group having 1 to 12 carbon atoms, a halogenated alkyl group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogenated alkoxy group having 1 to 12 carbon atoms, a halogen atom, a cyano group, a nitro group, or —R p1 ,

M p1 denotes one of the following formulae (i-11) to (ix-11),

wherein * is bonded to Sp p1 , and ** is bonded to L p1 , L p2 , or Z p1 ,

M p3 denotes one of the following formulae (i-13) to (ix-13),

wherein * is bonded to Z p1 , and ** is bonded to L p2 ,

m p2 to m p4 independently denote 0, 1, 2, or 3,

m p1 and m p5 independently denote 1, 2, or 3, and

a plurality of Z p1 s, if present, may be the same or different, a plurality of R p1 s, if present, may be the same or different, a plurality of R p2 s, if present, may be the same or different, a plurality of Sp p1 s, if present, may be the same or different, a plurality of Sp p2 s, if present, may be the same or different, a plurality of L p1 s, if present, may be the same or different, and a plurality of M p2 s, if present, may be the same or different.

7. A liquid crystal display device in which at least one of two substrates with the liquid crystal compositions according to claim 5 has no alignment film.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2024
From: DIC CORPORATION
To: SHIJIAZHUANG CHENGZHI YONGHUA DISPLAY MATERIAL CO., LTD.
Reel/Frame 067528/0688 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2020
From: HAYASHI, MASANAO; HOSONO, AYAKI; KOSAKA, SHOTA
To: DIC CORPORATION
Reel/Frame 053455/0988 →
Priority Claims (1)
JP 2018-036499 · Mar 1, 2018 · national
Continuity (1)
Related Publication 20200399539A1 · Dec 24, 2020