IP Library Granted Patent US 11,174,217
Granted Patent B2
US 11,174,217 · App. 16/615,503 · Granted Nov 16, 2021

Polymerizable compound and liquid crystal composition

Inventors: Ayaki Hosono (Kitaadachi-gun, JP); Masanao Hayashi (Kitaadachi-gun, JP)
Assignee: DIC CORPORATION
C07C69/54C07D319/06C09K19/56B32B2457/20B32B2457/202C07C2601/16C09K2323/00
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Quick Facts
Patent No.
US 11,174,217
App. No.
16/615,503
Granted
Nov 16, 2021
Kind
B2
Abstract

A compound represented by formula (i) has, as K i1 in the formula (i), a structure represented by any one of formula (K-1) to formula (K-3). When used in a liquid crystal composition, it adheres to substrates which hold the liquid crystal composition (liquid crystal layer) therebetween, thereby permitting liquid crystal molecules to be maintained in the state of being aligned in the vertical direction. The liquid crystal composition using the compound enables liquid crystal molecules to be aligned even when the PI layer is not provided (vertical alignment of liquid crystal molecules is induced without the voltage applied and horizontal alignment of liquid crystal molecules is realized with the voltage applied). It is possible to provide a polymerizable compound being excellent in storability and capable of uniform vertical alignment of liquid crystal molecules with no PI layer provided.

Claims (33)

1. A compound represented by general formula (i),

(in the formula, R i1 represents a hydrogen atom, a linear or branched alkyl group having 1 to 40 carbon atoms, an alkyl halide group, or P i1 -Sp i1 -, in which —CH 2 — in the alkyl group in the linear or branched alkyl group or the alkyl halide group may be substituted by —CH═CH—,—C≡C—, —O—, —NH—, —COO—, or —OCO— so that oxygen atoms are not directly adjacent to each other; A i1 represents a divalent 6-membered aromatic cyclic group, a divalent 6-membered aromatic heterocyclic group, a divalent 6-membered aliphatic cyclic group, or a divalent 6-membered aliphatic heterocyclic group, in which a hydrogen atom in a cyclic structure of A i1 may be substituted by a halogen atom, P i1 -Sp i1 -, a monovalent organic group having a substituent represented by K i1 , or R i1 ; Z i1 represents a single bond, —CH═CH—, —CF═CF—, —C≡C—, —COO—, —OCO—, —OCOO—, —OOCO—, —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 20 carbon atoms, in which one or two or more nonadjacent —CH 2 — may be substituted by —O—, —COO—, or —OCO—; K i1 represents a group represented by general formulae (K-1) to (K-3); X K1 and Y K1 each independently represent —CH 2 —, an oxygen atom, or a sulfur atom; Z K1 represents an oxygen atom or a sulfur atom; S 1 , S 3 , S 4 , and S 5 each represent an alkylene group having 1 to 6 carbon atoms or a single bond; S 2 represents C, or Si; X 1 and X 2 each represent OH, —NH 2 , —NHR i1 , —CHO, —COOH, or —SH; P and P i1 each represent a polymerizable group; Sp i1 represents a spacer group or a single bond; m i1 represents an integer of 2 to 4; n represents 1; when a plurality of each of R i1 , A i1 , Z i1 , K i1 , X K1 , Y K1 , Z K1 , S 1 , S 2 , S 3 , S 4 , S 5 , p i1 , Sp i1 , and n are present in the general formula (i), they may be the same or different)

2. The compound according to claim 1 , wherein in the general formula (i), A i1 represents a group having a cyclic 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 indane-2,5-diyl group, a 1,2,3,4-tetrahydronaphthalene-2,6-diyl group, and a 1,3-dioxane-2,5-diyl group, in which the cyclic structure may be unsubstituted or substituted by an alkyl group having 1 to 12 carbon atoms, an alkyl halide group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, an alkoxy halide group having 1 to 12 carbon atoms, a halogen atom, or P i1 -Sp i1 -.

3. The compound according to claim 1 , wherein P i1 -Sp i1 -represents a substituent selected from the group represented by general formula (P-1) to general formula (P-14) below,

(in the formulae, a black spot at the right end represents a bond).

4. The compound according to claim 1 , wherein in the general formula (i), K i1 represents (K-1),

5. The compound according to claim 4 , wherein S 4 and S 5 each represent the alkylene group having 1 to 6 carbon atoms, and X i and X 2 each represent —OH.

6. The compound according to claim 1 , wherein in the general formula (i), K i1 represents (K-2):

7. The compound according to claim 1 , wherein in the general formula (i), K i1 represents (K-1),

wherein a hydrogen atom in a cyclic structure of at least one A i1 is substituted by P i1 -Sp i1 -.

8. A liquid crystal composition comprising the compound according to claim 1 , a polymerizable compound, and a nonpolymerizable liquid crystal composition.

9. The liquid crystal composition according to claim 8 , comprising, as the polymerizable compound, one or two or more compounds represented by general formula (P),

(in the formula,

Z p1 represents a fluorine atom, a cyano group, a hydrogen atom, an alkyl group having 1 to 15 carbon atoms, in which a hydrogen atom may be substituted by a halogen atom, an alkoxy group having 1 to 15 carbon atoms, in which a hydrogen atom may be substituted by a halogen atom, an alkenyl group having 1 to 15 carbon atoms, in which a hydrogen atom may be substituted by a halogen atom, an alkenyloxy group having 1 to 15 carbon atoms, in which a hydrogen atom may be substituted by a halogen atom, or -Sp p2 —R p2

R p1 and R p2 each represent any one of the following formula (R-I) to formula (R-VIII):

(in the formulae,

* represents a bond to Sp p1 or Sp p2

R 2 to R 6 each independently represent a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or an alkyl halide group having 1 to 5 carbon atoms;

W represents a single bond, —O—, or a methylene group;

T represents a single bond or —COO—; and

p, t, and q each independently represent 0, 1, or 2);

Sp p1 and Sp p2 each represent a spacer group;

L p1 and L p2 each independently represent 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 each independently represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, and z represents an integer of 1 to 4);

Mp 2 represents 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 indane-2,5-diyl group, a 1,2,3,4-tetrehydronaphthalene-2,6-diyl group, a 1,3-dioxane-2,5-diyl group, or a single bond, and Mp 2 is may be unsubstituted or substituted by an alkyl group having 1 to 12 carbon atoms, an alkyl halide group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, an alkoxy halide group having 1 to 12 carbon atoms, a halogen atom, a cyano group, a nitro group, or —R p1 ;

M p1 represents any one of the following formulae (i-11) to (ix-11):

(in the formulae, * represents a bond to Sp p1 , and ** represents a bond to L P1 , L p2 , or Z p1 );

MP 3 represents any one of the following formulae (i-13) to (ix-13):

(in the formulae, * represents a bond to Z p1 , and ** represents a bond to L p2 );

m p2 to m p4 each independently represent 0, 1, 2, or 3;

m p1 and m p5 each independently represent 1, 2, or 3;

when a plurality of Z p1 are present, they may be the same or different; when a plurality of R P1 are present, they may be the same or different; when a plurality of RP 2 are present, they may be the same or different; when a plurality of Sp p i are present, they may be the same or different; when a plurality of Sp p2 are present, they may be the same or different; when a plurality of L P1 are present, they may be the same or different; and when a plurality of MP P2 are present, they may be the same or different).

10. A liquid crystal display device comprising the liquid crystal composition according to claim and two substrates at least one of which does not have an 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 Nov 21, 2019
From: HOSONO, AYAKI; HAYASHI, MASANAO
To: DIC CORPORATION
Reel/Frame 051076/0647 →
Priority Claims (1)
JP JP2017-115118 · Jun 12, 2017 · national
Continuity (1)
Related Publication 20200087240A1 · Mar 19, 2020