Stock material or miscellaneous articles – Liquid crystal optical display having layer of specified...
Reexamination Certificate
2000-10-06
2004-04-13
Wu, Shean C. (Department: 1756)
Stock material or miscellaneous articles
Liquid crystal optical display having layer of specified...
C252S299300, C252S299620, C252S501100, C560S056000, C560S100000, C585S410000, C257S059000, C430S056000, C430S058050, C349S069000
Reexamination Certificate
active
06720039
ABSTRACT:
BACKGROUND OF THE INVENTION
The present invention relates to liquid crystalline compounds and more particularly to novel crystalline compounds, which exhibit liquid crystallinity and, in addition, charge transport capability, and a process for producing the same.
Liquid crystalline compounds having various structures are known in the art and are widely used mainly as materials for information display devices using an electro-optic effect based on the alignment effect of liquid crystal molecules attained by application of voltage. Further, application of liquid crystalline compounds to optical shutters, optical stops, modulating devices, lenses, light beam deflection/optical switches, phase diffraction gratings, optical logic devices, memory devices and the like are under study. External simulation by heat, electric field, magnetic field, pressure or the like results in transition of the alignment of liquid crystal molecules which enables optical properties and electric capacity to be easily changed. Sensors and measuring instruments, utilizing this property, for temperature, electric field/voltage, infrared radiation, ultrasonic wave, flow rate/acceleration, gas or pressure have been studied in the art.
DISCLOSURE OF THE INVENTION
An object of the present invention is to provide liquid crystalline compounds having a novel structure and a process for producing the same.
The above object can be attained by the following present invention. Specifically, according to one aspect of the present invention, there is provided a liquid crystalline compound represented by the following general formula (I):
wherein R
1
and R
2
each independently represent a straight-chain, branched or cyclic, saturated or unsaturated hydrocarbon group having 1 to 22 carbon atoms and may be attached directly to the aromatic ring without through X
1
or X
2
; R
3
represents a hydrogen atom, a cyano group, a nitro group, a fluorine atom, or a methyl group; and X
1
and X
2
each independently represent an oxygen atom, a sulfur atom, or a —CO—, —OCO—, —COO—, —N═CH—, —CONH—, —NH—, —NHCO—, or —CH
2
— group.
According to another aspect of the present invention, there is provided a liquid crystalline compound represented by the following general formula (II):
wherein R
1
and R
2
each independently represent a straight-chain, branched or cyclic, saturated or unsaturated hydrocarbon group having 1 to 22 carbon atoms and may be attached directly to the aromatic ring without through X
1
or X
2
; R
3
represents a hydrogen atom, a cyano group, a nitro group, a fluorine atom, or a methyl group; X
1
and X
2
each independently represent an oxygen atom, a sulfur atom, or a —CO—, —OCO—, —COO—, —N═CH—, —CONH—, —NH—, —NHCO—, or —CH
2
— group; and Z represents a —COO—, —OCO—, —N═N—, —CH═N—, —CH
2
S—, —CH═CH—, or —C≡C— group.
According to still another aspect of the present invention, there is provided a process for producing the liquid crystalline compound represented by the general formula (I), comprising the step of reacting a compound represented by the following general formula (1) with a compound represented by the following general formula (2):
wherein R
1
, R
2
, R
3
, X
1
, and X
2
are as defined above.
According to a further aspect of the present invention, there is provided a process for producing the liquid crystalline compound represented by the general formula (II), comprising the step of reacting a compound represented by the following general formula (3) with a compound represented by the following general formula (4):
wherein R
1
, R
2
, R
3
, X
1
, and X
2
are as defined above; and Y
1
and Y
2
are respectively groups which are reacted with each other to form a —COO—, —OCO—, —N═N—, —CH═N—, —CH
2
S—, —CH═CH—, or —C≡C— group.
The present invention can provide novel liquid crystalline compounds having not only liquid crystallinity but also charge transport capability. The novel liquid crystalline compounds can be used in applications, where the conventional liquid crystalline compounds are used, and, in addition, are useful as materials for optical sensors, electroluminescence devices, photoconductors, space light modulating devices, thin film transistors, other sensors and the like, utilizing the charge transfer capability. In particular, some of the liquid crystalline compounds of the present invention have both electron transport capability and hole transport capability and, when mixed with a fluorescent material in order to use them as a material for an electroluminescence device, can provide luminescence.
REFERENCES:
patent: 4386007 (1983-05-01), Krause et al.
patent: 5072021 (1991-12-01), Nakatsuka et al.
patent: 5143644 (1992-09-01), Yamaoka et al.
patent: 5252253 (1993-10-01), Gray et al.
patent: 5589103 (1996-12-01), Yamada et al.
patent: 5698740 (1997-12-01), Enokida et al.
patent: 5766510 (1998-06-01), Hanna et al.
patent: 6174455 (2001-01-01), Hanna et al.
patent: 6224787 (2001-05-01), Hanna et al.
patent: 38 37 208 (1989-05-01), None
patent: 41 16 158 (1992-11-01), None
patent: 341922 (1989-11-01), None
patent: 517498 (1992-12-01), None
patent: 517 498 (1992-12-01), None
patent: 518 636 (1992-12-01), None
patent: 757 032 (1997-02-01), None
patent: 2 551 561 (1985-03-01), None
patent: 1 603 075 (1981-11-01), None
patent: 8-109145 (1996-04-01), None
patent: WO 87/06577 (1987-11-01), None
patent: WO 90/08119 (1990-07-01), None
patent: 90/08119 (1990-07-01), None
patent: WO 95/04306 (1995-02-01), None
Hird et al., “Palladium-catalysed cross-coupling reactions in the synthesis of some high polarizability materials”, Liquid Crystals, 1993, vol. 14, No. 3, pp. 741-761.*
Kato, T. et al. “Solid-state CP/MAS carbon-13 NMR studies of naphthalene-based thermotropic polyesters and model compounds”, J. Polym. Sci. Part A: Polym. Chem, 1989, vol. 27 pp. 1447-1465 XP002103112.
Chemical Abstracts, vol. 120, No. 26, Jun. 27, 1994, Columbus, Ohio Abstract No. 335199, Sato et al., “Liquid Crystal Naphthalene Compound and its Composition for Display” XP002103115 Abstract & JP 06 025061.
Gaetano Aloisi et al. “Triplet and radical ion properties of styrylnaphthalenes and their aza-derivatives: a laser flash photolytic study”, J. Chem. Soc., Faraday Trans. 1992, vol. 88 pp. 2139-2145 XP002103113 pp. 2139-2145.
Wong et al. “Novel approach in molecular design for quadratic nonlinear optics (NLO): Design, syntheses and characterizations of new classes of dipolar and multi-dipolar molecules” MCLC S&T, Sect. B: Nonlinear Opt, 1995, vol. 9 pp. 181-186, XP002103114.
Funahashi et al. “Fast ambipolar carrier transport in smectic phases of phenylnaphthalene liquid crystal” Applied Physics Letters, vol. 71, No. 5, Aug. 4, 1997, pp. 602-604, XP000699625.
Funahashi Masahiro
Hanna Jun-ichi
Kafuku Komei
Kogo Kyoko
Dai Nippon Printing Co. Ltd.
Wu Shean C.
LandOfFree
Liquid crystalline compounds and process for producing the same does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Liquid crystalline compounds and process for producing the same, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Liquid crystalline compounds and process for producing the same will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3204144