GB2575579A - Light modulation element - Google Patents

Light modulation element Download PDF

Info

Publication number
GB2575579A
GB2575579A GB1915019.2A GB201915019A GB2575579A GB 2575579 A GB2575579 A GB 2575579A GB 201915019 A GB201915019 A GB 201915019A GB 2575579 A GB2575579 A GB 2575579A
Authority
GB
United Kingdom
Prior art keywords
light modulation
modulation element
element according
diyl
substrates
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB1915019.2A
Other versions
GB2575579B (en
GB201915019D0 (en
Inventor
Baker Phil
Holt Alex
Sargent Joseph
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Patent GmbH
Original Assignee
Merck Patent GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck Patent GmbH filed Critical Merck Patent GmbH
Publication of GB201915019D0 publication Critical patent/GB201915019D0/en
Publication of GB2575579A publication Critical patent/GB2575579A/en
Application granted granted Critical
Publication of GB2575579B publication Critical patent/GB2575579B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/02Liquid crystal materials characterised by optical, electrical or physical properties of the components, in general
    • C09K19/0225Ferroelectric
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/34Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
    • C09K19/3441Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
    • C09K19/3444Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom the heterocyclic ring being a six-membered aromatic ring containing one nitrogen atom, e.g. pyridine
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/34Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
    • C09K19/3441Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
    • C09K19/345Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom the heterocyclic ring being a six-membered aromatic ring containing two nitrogen atoms
    • C09K19/3458Uncondensed pyrimidines
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/34Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
    • C09K19/3491Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having sulfur as hetero atom
    • C09K19/3497Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having sulfur as hetero atom the heterocyclic ring containing sulfur and nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Liquid Crystal (AREA)

Abstract

The invention provides a defect-free light modulation element utilizing the vertically aligned deformed helix ferroelectric liquid crystal (VADHFLC) mode. Further, the present invention relates to a method of production of such light modulation element, to the use of such light modulation element in an electro-optical device, i.e. in a LC display device, and to an electro- optical device comprising the light modulation element according to the present invention.

Claims (7)

Patent Claims
1. Light modulation element comprising a pair of transparent substrates, a pair of polarizers, a liquid crystal medium capable of forming a chiral smectic C phase in homeotropic orientation that is located in between the pair of substrates, and an electrode structure which generates an electric field in directions parallel to the substrates main plane, characterized in that the electrode structure is formed by at least two electrodes protruding toward the interior of the formed cell.
The light modulation element according to claim 1 , wherein substrates are arranged with a separation from 1 Î1⁄4Î¹Ï Î¹ up to 20 Î1⁄4Î¹Ï Î¹ from another.
The light modulation element according to claim 1 or 2, wherein the gap between to electrodes is in a range of 500 nm to 150 Î1⁄4Î¹Ï Î¹.
The light modulation element according to one or more of claims 1 to 3, wherein at least one homeotropic alignment layer is provided on the inner side of at least one substrate.
The light modulation element according to one or more of claims 1 to 4, wherein the liquid crystalline media exhibit a spontaneous polarization (Ps) of 100 nC/cm2 or more.
The light modulation element according to one or more of claims 1 to 5, wherein the liquid-crystalline medium liquid crystalline medium is selected from liquid crystalline media wherein where nave is the effective average refractive index of the liquid crystalline media and P is the chiral pitch of the liquid crystalline media.
7. The light modulation element according to one or more of claims 1 to 6, wherein the liquid crystalline media for the light modulation element according to the present invention comprise one or more compounds selected from formulae I, II or III, R1 -(A 1-Z1 1 )a-A'-(Z12-A12)b-(-Z13-A13)c-R12 I R2 -(A21-Z2 )d-A"-(Z22-A22)e-R22 R31 _ A31 _Z31 )f_Alll_(Z32_A32)g_R32 wherein A1 denotes N-N 7 V A11 denotes X A11 denotes X denotes S or O, 31 denotes F or H, R11 to R32 are each independently a straight-chain or branched alkyl group with 1 to 25 C atoms which may be unsubstituted, mono- or polysubstituted by halogen or CN, it being also possible for one or more non-adjacent Ch groups to be replaced, in each occurrence independently from one another, by -O-, -S-, -NH-, -N(CH3)-, -CO-, -COO-, -OCO-, -O-CO-O-, -S-CO-, -CO-S-, -CH=CH-, -CH=CF-, -CF=CF- or -Câ ¡C- in such a manner that oxygen atoms are not linked directly to one another, Z11 to Z32 are each independently selected from -COO-, -OCO-, -O-CO-O-, -OCH2-, -CH2O-, -CH2CH2-, -(CH2)4-, -CF2CF2-, -CH=CH-,-CF=CF-, -CH=CH-COO-, -OCO-CH=CH-, -Câ ¡C- or a single bond, A11 to A32 are each independently in each occurrence 1 ,4- phenylene, wherein in addition one or more CH groups may be replaced by N, 1 ,4-cyclo-hexylene in which, in addition, one or two non-adjacent CH2 groups may be replaced by O and/or S, 1 ,4-cyclohexenylene, 1 ,4-bicyclo- (2,2,2)-octylene, piperidine-1 ,4-diyl, naphthalene-2,6-diyl, decahydro-naphthalene-2,6-diyl, 1 ,2,3,4-tetrahydro- naphthalene-2,6-diyl, cyclobutane-1 ,3-diyl, spiro[3.3]heptane-2,6-diyl or dispiro[3.1 .3.1 ] decane-2,8- diyl, it being possible for all these groups to be unsubstituted, mono-, di-, tri- or tetrasubstituted with F, CI, CN or alkyl, alkoxy, alkylcarbonyl or alkoxycarbonyl groups with 1 to 7 C atoms, wherein one or more H atoms may be substituted by F or CI, a, b and c are each and independently 0 or 1 , whereby a + b + c > 1 , d and e are each and independently 0 or 1 , whereby d + e > 1 , and f and g are each and independently 0 or 1 , whereby f + g > 1 . Process for the production of a light modulation element according to one or more of claims 1 to 7 comprising the following steps: cutting and cleaning the substrates, coating the substrates with an alignment layer agent, providing at least two trough cell electrodes on the substrates or the alignment layer assembling the cell using a UV curable adhesive, and filling the cell with the liquid-crystalline medium. Use of a light modulation element according to one or more of claims 1 to 7 in an electro-optical device. Electro-optical device comprising the light modulation element according to one or more of claims 1 to 7.
GB1915019.2A 2017-03-21 2018-03-19 Light modulation element Expired - Fee Related GB2575579B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP17162046 2017-03-21
PCT/EP2018/056785 WO2018172232A1 (en) 2017-03-21 2018-03-19 Light modulation element

Publications (3)

Publication Number Publication Date
GB201915019D0 GB201915019D0 (en) 2019-12-04
GB2575579A true GB2575579A (en) 2020-01-15
GB2575579B GB2575579B (en) 2022-08-10

Family

ID=58398090

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1915019.2A Expired - Fee Related GB2575579B (en) 2017-03-21 2018-03-19 Light modulation element

Country Status (2)

Country Link
GB (1) GB2575579B (en)
WO (1) WO2018172232A1 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080204608A1 (en) * 2006-03-01 2008-08-28 Yohei Takano Liquid Crystal Element, Optical Path Deflecting Element, and Image Displaying Apparatus

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6025897A (en) 1993-12-21 2000-02-15 3M Innovative Properties Co. Display with reflective polarizer and randomizing cavity
US6099758A (en) 1997-09-17 2000-08-08 Merck Patent Gesellschaft Mit Beschrankter Haftung Broadband reflective polarizer
DE10241301A1 (en) 2002-09-04 2004-03-18 Merck Patent Gmbh Electrooptic light control element and display and medium for television and computer screens has temperature driven control mechanism
US9771517B2 (en) 2012-06-06 2017-09-26 Dic Corporation Liquid-crystal optical modulation element

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080204608A1 (en) * 2006-03-01 2008-08-28 Yohei Takano Liquid Crystal Element, Optical Path Deflecting Element, and Image Displaying Apparatus

Also Published As

Publication number Publication date
GB2575579B (en) 2022-08-10
GB201915019D0 (en) 2019-12-04
WO2018172232A1 (en) 2018-09-27

Similar Documents

Publication Publication Date Title
EP2835410B1 (en) Nematic liquid crystal composition
US11788009B2 (en) Liquid-crystalline medium for use in a switching element
TWI586791B (en) Bimesogenic compounds and mesogenic media
KR101581889B1 (en) Nematic liquid crystal composition and liquid crystal display element using same
WO2016116254A1 (en) Light modulation element
JP7307064B2 (en) Liquid-crystalline media for use in switching elements
KR20150013698A (en) Liquid-crystal composition
TWI775724B (en) Reactive mesogens
KR20170104614A (en) Optical modulation element
KR20150027737A (en) Nematic liquid crystal composition and liquid crystal display element using same
CN114008176A (en) Liquid crystal based light valve
JP2019521372A (en) Light modulation element
WO2015096879A1 (en) Bimesogenic compounds and mesogenic media
JP2005206840A (en) Liquid crystal medium and liquid crystal display having high torsion
US20220220383A1 (en) Method for preparing a liquid crystal-based switching element
GB2575579A (en) Light modulation element
KR20210106495A (en) Switching layer for use in switching elements
WO2017001043A1 (en) Process of preparing a light modulation element
TW202206578A (en) Liquid-crystalline medium
KR20210102363A (en) Polymerizable Liquid Crystal Ink Formulations
WO2018104279A1 (en) Liquid crystal medium and liquid crystal device
TWI839426B (en) Switching layers for use in a switching element
TW201923043A (en) Liquid crystal medium and liquid crystal device
WO2019081389A1 (en) Liquid crystal medium and liquid crystal device
WO2019030150A1 (en) Liquid crystal medium and liquid crystal device

Legal Events

Date Code Title Description
PCNP Patent ceased through non-payment of renewal fee

Effective date: 20230319