Abstract:
An object of the present invention is to provide a polymerizable liquid crystal compound having excellent solubility, which is used for the formation of an optically anisotropic film having excellent durability, a method for producing the same, a polymerizable liquid crystal composition, an optically anisotropic film, an optical film, a polarizing plate, and an image display device. The polymerizable liquid crystal compound of the embodiment of the present invention is a polymerizable liquid crystal compound represented by Formula (1), L1-SP1-A1-D3-G1-D1-Ar-D2-G2-D4-A2-SP2-L2 . . . (1) in Formula (1), the ClogP value of the group represented by L1-SP1-A1-D3-G1-D1 and the ClogP value of the group represented by L2-SP2-A2-D4-G2-D2 are different from each other, and at least one of the ClogP values is 3.3 or more.
Abstract:
A compound represented by a formula [1D] as shown below (wherein R1A, R1B, R2A, R2B, R3A and R3B represent a hydrogen atom, an optionally substituted C1-6 alkyl group, and the like) is useful as an intermediate for producing a thionucleoside, and the production method of the present invention is useful as a method for producing a thionucleoside.
Abstract:
A compound which has a benzoxazinone ring and an aromatic ring that directly bonds to the benzoxazinone ring, and has a mesogenic core substituted by a substituent having a polymerizable functional group is excellent in terms of durability, colorless, and exhibits a high Δn while having an azomethine bond.
Abstract:
A polymerizable liquid crystal composition having excellent solubility, used for formation of an optically anisotropic film having excellent durability. The polymerizable liquid crystal composition contains a polymerizable liquid crystal compound P1 represented by Formula (1): A-Ar-A ⋅ ⋅ ⋅ , a polymerizable liquid crystal compound P2 represented by Formula (2): A-Ar-B ⋅ ⋅ ⋅ , and a polymerizable liquid crystal compound P3 represented by Formula (3): B—Ar-B ⋅ ⋅ ⋅ .In Formulae (1) and (2), A's represent predetermined side chains, all of which exhibit the same C log P value, and in Formulae (2) and (3), B's represent predetermined side chains, all of which exhibit the same C log P value. It should be noted that A and B represent side chains having C log P values different from each other, in which the C log P value of A is larger than the C log P value of B and the C log P value of at least one of A or B is 3.3 or more.
Abstract:
A compound represented by a formula [1D] as shown below (wherein R1A, R1B, R2A, R2B, R3A and R3B represent a hydrogen atom, an optionally substituted C1-6 alkyl group, and the like) is useful as an intermediate for producing a thionucleoside, and the production method of the present invention is useful as a method for producing a thionucleoside.
Abstract:
A compound represented by a formula [1D] as shown below (wherein R1A, R1B, R2A, R2B, R3A and R3B represent a hydrogen atom, an optionally substituted C1-6 alkyl group, and the like) is useful as an intermediate for producing a thionucleoside, and the production method of the present invention is useful as a method for producing a thionucleoside.
Abstract:
A compound represented by a formula [1D] as shown below (wherein R1A, R1B, R2A, R2B, R3A and R3B represent a hydrogen atom, an optionally substituted C1-6 alkyl group, and the like) is useful as an intermediate for producing a thionucleoside, and the production method of the present invention is useful as a method for producing a thionucleoside.