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  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K19/00—Liquid crystal materials
  • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
  • C09K19/06—Non-steroidal liquid crystal compounds
  • C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
  • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
  • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
  • C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
  • C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
  • C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
  • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
  • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
  • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
  • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
  • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
  • C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
  • C07D333/78—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems condensed with rings other than six-membered or with ring systems containing such rings
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K19/00—Liquid crystal materials
  • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
  • C09K19/0403—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit the structure containing one or more specific, optionally substituted ring or ring systems
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K19/00—Liquid crystal materials
  • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
  • C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K19/00—Liquid crystal materials
  • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
  • C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
  • C09K19/46—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing esters

Definitions

• the invention relates to supertwist nematic liquid-crystal displays (STN- LCDs) having short switching times and good steepnesses and angle dependencies, and to the novel nematic liquid-crystal mixtures used therein.
• STN- LCDs supertwist nematic liquid-crystal displays
• STN-LCDs as in the heading are known, for example from EP 0,131 ,216 B1 ; DE 3,423,993 A1 ; EP 0,098,070 A2; M. Schadt and F. Leenhouts, 17th Koch conference on liquid crystals (8-10.04.87); K. Kawasaki et al., SID 87 Digest 391 (20.6); M. Schadt and F. Leenhouts, SID 87 Digest 372 (20.1); K. Katoh et al., Japanese Journal of Applied Physics, Vol. 26, No. 11 , L 1784-L1786 (1987)rF. Leenhouts et al., Appl. Phys. Lett.
• STN-LCD here includes any relatively highly twisted display element having a twist angle with a value between 160 ° and 720 °, such as, for example, the display elements of Waters et al. (CM. Waters et al., Proc. Soc. Inf. Disp. (New York) (1985) (3rd Intern. Display Conference, Kobe, Japan), the STN-LCDs (DE OS 3,503,259), SBE-LCDs (T.J. Scheffer and J. Nehring, Appl. Phys. Lett. 45 (1984) 1021), OMI- LCDs (M. Schadt andF. Leenhouts, Appl. Phys. Lett. 50 (1987), 236, DST- LCDs (EP OS 0,246,842) or BW-STN-LCDs (K. Kawasaki et al., SID 87 Digest 391 (20.6)).
• CM Waters et al.
• STN-LCDs of this type are distinguished by significantly better steepnesses of the electrooptical characteristic curve (in the following simply called 'steepness') and, associated therewith, better contrast values, and by a significantly lower angle dependence of the contrast.
• STN-LCDs with extremely short switching times in particular also at relatively low temperatures.
• the rotational viscosities, in particular of the liquid crystal mixtures have hitherto been optimized using usually optimized combinations of liquid crystal components and optionally also monotropic additives of relatively high vapour pressure.
• Shorter switching times can also be achieved by reducing the thickness of LC layer of the STN-LCD and using liquid-crystal mixtures with a higher birefringence ⁇ n.
• the liquid crystal mixtures should exhibit comparatively high values of the ratio of the elastic constants K 33 /K- ⁇ and comparatively low values of ⁇ / ⁇ ⁇ , wherein ⁇ is the dielectric anisotropy and ⁇ x is the dielectric constant in vertical direction to the long molecular axis.
• liquid crystal mixtures should fulfill further important requirements such as:
• a broad d/p window of cell gap d and pitch p which is defined as the range between the lower and upper limit of the d/p values.
• the invention has the object of providing STN-LCDs which only have the above mentioned disadvantages to a small extent, or not at all, and at the same time have very useful overall properties, especially short switching times at low temperatures, a high steepness and an improved temperature dependence of the operating voltage.
• R J is an alkenyl group with 2 to 7 C atoms
• Q is CF 2 , OCF 2 , CFH, OCFH or a single bond
• Y is F or CI
• L 1 and L 2 are each independently H or F
• n 0 or 1 , -
• Y 1 and Y 2 are each independently H or F
• R 5 is alkenyl or alkynyl having 2 to 10 C atoms
• R 6 is alkyl or alkoxy having 1 to 10 C atoms, alkenyl, aikenyloxy, alkynyl or alkynyloxy having 2 to 10 C atoms and
• R 7 is alkynyl or alkynyloxy having 2 to 10 C atoms.
• Y 1 and Y 2 are F, most preferably both are F.
• Y 1 and Y 2 are F and most preferably both are F
• liquid crystal mixtures according to the present invention show the following advantageous properties
• the invention thus relates to an STN-LCD having two plane-parallel outer plates which, together with a frame, form a cell, a nematic liquid-crystal mixture of positive dielectric anisotropy which is present in the cell, electrode layers with superposed alignment layers on the insides of the outer plates, a pre-tilt angle between the longitudinal axis of the molecules at the surface of the outer plates and the outer plates of from about 1 degree to 30 degrees, and a twist angle of the liquid-crystal mixture in the cell from alignment layer to alignment layer with a value of between 22.5 and 600°,
• nematic liquid-crystal mixture essentially consists of
• a liquid-crystalline component A comprising one or more compounds having a dielectric anisotropy of more than +1.5;
• a liquid-crystalline component B comprising one or more compounds having a dielectric anisotropy from -1.5 to +1.5;
• a liquid-crystalline component D comprising one or more compounds having a dielectric anisotropy of less than -1.5 and
• R is an alkenyl group with 2 to 7 C atoms
• Q is CF 2 , OCF 2 , CFH, OCFH or a single bond
• Y is F or CI
• L 1 and L 2 are each independently H or F
• n 0 or 1 —
• Y 1 and Y 2 are each independently H or F, preferably at least one is F, most preferably both are F,
• R 5 is alkenyl or alkynyl having 2 to 10 C atoms
• R 6 is alkyl or alkoxy having 1 to 10 C atoms, alkenyl, aikenyloxy, alkynyl or alkynyloxy having 2 to 10 C atoms and
• R 7 is alkynyl or alkynyloxy having 2 to 10 C atoms.
• Another object of the invention are inventive liquid crystal mixtures as described above and below for use in STN-LCDs.
• the formula IA comprises the following subformulae
• R 3 , L 1 , L 2 , Q and Y have the meanings of formula IA and
• R 3 is especially preferably 1 E-alkenyl oder 3 E-alkenyl with 2 to 7 C-atoms.
• R 4 is alkenyl with 2 to 7 C atoms, in particular those of the following formulae
• R 3a and R 4a are each independently H, CH 3 , C 2 H 5 or n-C 3 H and alkyl is an alkyl group with 1 to 7 C atoms.
• liquid crystal mixture comprises at least one compound selected of formulae IA-1 a and IA-1 c, wherein R 3a and R 4a respectively have the same meaning.
• R 4 is alkyl with 1 to 8, in particular 1 , 2 or 3 C-atoms
• R 3 is 1 E-alkenyl or 3E- alkenyl with 2 to 7, in particular 2, 3 or 4 C-atoms.
• the compounds of formulae IA-1 and IA-2 having a dielectric anisotropy from - 1.5 to + 1.5 belong to component B as defined above, whereas polar compounds of formula IA-2 and in particular of formula IA-3 having a dielectric anisotropy of more than + 1.5 belong to component A as defined above.
• the formula IB comprises the following preferred subformulae:
• R a is alkenyl having 2 to 5 C atoms, preferably vinyl or 3-butenyl
• R b is alkyl having 1 to 7 C atoms or alkenyl having 2 to 7 C atoms, preferably n-alkyl having 1 to 5 C atoms
• R c is alkynyl having 2 to 7 C atoms, preferably 1-pentynyl, 1-butynyl or 1-propynyl.
• L 5 and L 6 are each independently H or F
• n 0, 1 or 2.
• R is as defined in formula II.
• R in these formulae is particularly preferably alkyl or alkoxy with 1 to 8 C atoms.
• component A further comprises one or more compounds of formula
• R 8 is alkyl or alkoxy having 1 to 7 C atoms
• Z 2 and n have each independently one of the meanings given for formula II
• L 1 , L 2 , L 5 and L 6 are each independently H or F.
• the compounds of formula III are preferably selected from the following formulae
• R, L 1 and L 2 have each independently one of the meanings of formula III.
• R 8 is as defined above.
• liquid crystal mixtures according to the present invention comprise one or more compounds of formula V
• R has one of the meanings of formula II and Y 2 is F or Cl, in particular wherein R is alkyl or alkoxy with 1 to 8 C-atoms and/or Y 2 is F.
• component A can also comprise one or more compounds with terminal fluoro or fluohnated groups selected of formula II *
• R, A, B, Z 1 , Z 2 and n have each independently one of the meanings of formula II,
• L 3 and L 4 are each independently H or F
• Y 1 is F or Cl
• Q 1 is CF 2 , OCF 2 , CFH, OCFH or a single bond
• R is not an alkenyl group with 2 to 7 C atoms.
• R is as defined in formula II, and L 3 and L 4 are each independently H or F.
• R in these formulae is particularly preferably alkyl or n c alkoxy with 1 to 8 C atoms.
• DCC Dicyclohexylcarbodiim.de
• DMAP 4-N,N-Dimethylaminopyhdine
• BuLi n-Butyllithium 5
• the compounds of the formulae IA have low viscosities, in particular low rotational viscosities, low values of the ratio of the elastic constants (K 3 /K 1 ) and lead therefore to short switching times, whereas the compounds of formula II with a high dielectric anisotropy, especially when being present in high amounts like in the inventive displays, lead to a reduced threshold voltage.
• Preferred liquid-crystal mixtures which can be used according to the invention contain one or more compounds from component A preferably in a proportion of 30 % to 90 %, preferably 45 % to 75 %. These compounds or this compound have a dielectric anisotropy of more than +3 (preferably of more than +8, in particular more than +12).
• compositions comprise • one or more, in particular two to five compounds of formula IA,
• Preferred liquid-crystal mixtures contain one or more compounds from group B, preferably in a proportion of 10 to 45 %. These compounds or this compound from group B have in particular low values of the rotational viscosity y . .
• component B comprises one or more compounds selected from the group comprising IV1 to IV9 with two rings
• R 1 and R 2 have each independently one of the meanings given for R in formula II, and the 1 ,4-phenyl groups in IV10 to IV19 and IV23 to IV31 can also independently of each other be mono- or polysubstituted by F.
• R 1 and R 2 in the compounds of formulae IV1 to IV30 is particularly preferably straight chain alkyl or alkoxy with 1 to 12 C-atoms.
• the LC mixtures optionally also comprise an optically active component C, in an amount such that the ratio between the layer thickness (separation of the plane-parallel carrier plates) and the natural pitch of the chiral nematic liquid crystal mixture is.more than 0.2 suitable to the desired twist angle.
• Suitable dopants can be selected from a wide variety of known chiral materials and commercially available dopants such as cholesteryl nonanoate, S 811 (Merck KGaA, Darmstadt, FRG) and CB 15 (Merck Ltd., former, BDH, Poole, UK). The choice thereof is not crucial per se.
• the amount of compounds of component C is preferably 0 to 10 %, in particular 0 to 5 %, very preferably 0 to 3 %.
• the LC mixtures comprise 2 to 65 %, preferably 5 to 35 % by weight of liquid crystalline tolane compounds.
• the tolane compounds are preferably selected from group T comprising T1 a, T1 b and T2a to T2h
• R 1 has one of the meanings of R in formula II
• L 1 to L 6 are each independently H or F
• Q and Y have one of the meanings given in formula I.
• Particularly preferred compounds of formula T2e are those wherein one, two or three of the groups L 1 to L 6 are F and the others are H, with both of L 1 and L 2 , L 3 and L 4 , L 5 and L 6 not being at the same time F.
• the proportion of component(s) from group T is preferably 2 % to 65 %, in particular 5 % to 35 %.
• the liquid crystal mixtures may ⁇ also comprise 0 to 10 % of one or more compounds having a dielectric anisotropy of -2 or less (component D).
• the component D preferably comprises one or more compounds containing the structural element 2,3-difluoro-1 ,4-phenylene, such as described e.g. in DE-OS 38 07 801 , 38 07 861 , 38 07 863, -38 07 864 and 38 07 908.
• Especially preferred are tolane compounds with this structural element according to the PCT/DE 88/00133, in particular those of formulae T2f and T2g.
• component D is e.g. 2,3-Dicyano- hydroquinone or cyclohexane derivatives containing the structural element
• the proportion of compounds of the component D comprising one or more compounds having a dielectric anisotropy ⁇ -1.5 is preferably about 0 % to 10 %, in particular about 0 % to 5 %. Those skilled in the art can easily adjust this proportion to produce the threshold voltage desired, it being possible to use, in principle, all customary liquid-crystal compounds where ⁇ ⁇ -1.5.
• inventive displays contain no compounds of component D.
• alkenyl in the meanings of R and R 1 to R 4 is comprising straight chain and branched alkenyl groups, in case of R with 2 to 7 C atoms, in case of R, R 2 , R 3 and R 4 with 2 to 12 C atoms.
• Straight chain alkenyl groups are preferred.
• Further preferred alkenyl groups are C 2 -C 4 -1 E-alkenyl, C 4 -C 7 -3E- alkenyl, C 5 -C 7 -4-alkenyl, C 6 -C 7 -5-alkenyl and C 7 -6-alkenyl, in particular C 2 -
• alkenyl groups examples are vinyl, 1 E-propenyl, 1 E-butenyl, 1 E-pentenyl, 1 E-hexenyl, 1 E-heptenyl, 3-bute ⁇ yl, 3E-pehtenyl, 3E-hexenyl, 3E-heptenyl, 4-pentenyl, 4Z-hexenyl, 4E-hexenyl, 4Z-heptenyl, 5-hexenyl and 6-heptenyl.
• Alkenyl groups with up to 5 C atoms are particularly preferred. Very particularly preferred are vinyl, 1 E-propenyl, 1 E-butenyl, 3E- butenyl and 3E-pentenyl, in particular vinyl and 3E-butenyl.
• liquid crystal mixtures according to the present invention contain
• alkenyl and alkenyl* are each independently an alkenyl group with 2 to 7 C atoms, and alkyl * is an alkyl group with 1 , 2 or 3 C atoms,
• R a and R b have the meaning given above.
• Low switching times are an especially important requirement for STN- LCDs e.g. when used in laptops, to allow better displaying of the cursor movements.
• displays having switching times of 300 msec or less, in particular 250 msec or less.
• the inventive STN-LCDs are characterized by a low threshold voltage.
• the threshold voltage is 1.3 V or less, in particular 1.25 V or less.
• the liquid crystal mixtures in the inventive STN-LCDs are dielectrically positive with ⁇ > 1.5. Particularly preferred are mixtures with ⁇ 3, very particularly preferred mixtures with ⁇ > 5.
• inventive liquid crystal mixtures exhibit advantageous values of the threshold voltage V 10 o /2 o and of the rotational viscosity ⁇ -
• the liquid crystal mixtures according to the present invention are further characterized by their advantageous values of the steepness, and, in particular at temperatures above 20 °C, can be driven at high multiplex rates. Furthermore, the mixtures exhibit a high stability, a high electrical resistance and a low frequency dependency of the threshold voltage.
• the liquid crystal displays according to the present invention show a broad working temperature range and a good viewing angle dependency of the contrast.
• the construction of the liquid-crystal display elements according to the present invention from polarizers, electrode base plates and electrodes having a surface treatment such that the preferential orientation (director) of the liquid-crystal molecules in each case adjacent thereto is usually mutually twisted from one electrode to the other by a value of 160 ° to 720 °, corresponds to the customary construction for display elements of this type.
• customary construction here is used in broad terms and also includes all derivatives and modifications of supertwist cells, in particular also matrix display elements.
• the surface tilt angle at the two support plates may be identical or different. Identical tilt angles are preferred.
• the tilt angle between the long axes of the molecules at the surface of the base plates and the base plate is preferably in the range from 0° to 7°, in particular from 0,01 ° to 5°, very preferably from 0,1 to 2°.
• the tilt angle is preferably in the range from 1 ° to 30°, in particular from 1° to 12°, very preferably from 3° to 10°.
• the twist angle of the liquid crystal mixture between the alignment layers on the two base plates of the cell is in case of inventive TN-displays in the range from 22,5° to 170°, in particular from 45° to 130°, very preferably from 80° to 115°.
• the twist angle is in the range from 100° to 600°, in particular from 170° to 300°, very preferably from 180° to 270°.
• liquid-crystal mixtures which can be used according to the invention are prepared in a manner customary per se.
• the desired amount of the components used in a relatively small amount is dissolved in the components making up the principal constituent, expediently at elevated temperature.
• the dielectrics may also contain further additives known to those skilled in the art and described in the literature. For example, 0-15 % of pleochroic dyes may be added.
• T ave average switching time 0.5 (T on + T off )
• the STN-LCD is addressed in multiplex operation (multiplex ratio 1 :240, bias 1 :15).
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:
• a STN display contains a liquid crystalline medium with the following properties:

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  • 2000-12-14 EP EP00987402A patent/EP1261679A1/de not_active Withdrawn
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