|Publication number||US3795436 A|
|Publication date||Mar 5, 1974|
|Filing date||Jul 11, 1972|
|Priority date||Jul 5, 1972|
|Publication number||US 3795436 A, US 3795436A, US-A-3795436, US3795436 A, US3795436A|
|Inventors||Boller A, Scherrer H|
|Original Assignee||Hoffmann La Roche|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (3), Non-Patent Citations (1), Referenced by (42), Classifications (11)|
|External Links: USPTO, USPTO Assignment, Espacenet|
Unite States atent OTHER PUBLICATIONS Usoltseva et al.; Chemical Characteristics, Structure, and Properties of Liquid Crystal, Russian Chemical Reviews, Vol. 32, pp. 49550'7, Sept. 1963.
Primary ExaminerEdward S. Bauer 7 Attorney, Agent, or FirmSamuel L. Welt; Bernard S.
Leon; William G. lsgro 4 Boiler et al. Mar. 5, 1974 NEMATOGENIC MATERIAL WHICH  ABSTRACT EXHIBIT THE KERR EFFECT AT An electro-optical light-modulation cell having a di- ISOTROPIC TEMPERATURES electric disposed between electrodes and being com-  Inventors: Arthur Boller, Binningen; Hanspeter prised of a nem1tgeI1iC fluid in the isotropic State, is
Sch rre Th il, b h f described. Said dielectric, upon application of a volts i l d age to the electrodes, becomes double refractihg. More particularly the nematogenic fluid comprises 173] Asslgnee: gf n' Roche Nutley compounds of the general formula  Filed: July 11, 1972 [2!] Appl. No.: 270,789 I  Foreign Application Priority Data June 21, 1972 Great Britain ..28987/72  US. Cl. 350/150, 252/408, 350/160 LC, wherein R is hyl, n-propyl, n-butyl, n-pentyl,
260/465 E, 260/465 D n-hexyl, isohexyl, n-heptyl or n-octyl  Int. Cl. G02f 1/16 or compounds of the general formula  Field of Search 350/150, 160 LC; 252/408  References Cited UNITED STATES PATENTS Q- Q H 3,687,515 8/1972 Haas et al 350/150 3,694,053 9/1972 Kahn 350/150 3,499,702 3/1970 Saldmacher et al. 350/150 wherein R is nbutyl, n-pentyl, n-hexyl,
n-heptyl or n-octyl, or mixtures thereof or mixtures of these compounds with other nematogenic substances.
17 Claims, 1 Drawing Figure NEMATOGENIC MATERIAL WHICH EXHIBIT THE KERR EFFECT AT ISOTROPIC TEMPERATURES The invention relates to an electro-optical lightmodulation cell, including a dielectric which is disposed between electrodes and which, being comprised of a nematogenic fluid in the isotropic state, upon application of a voltage to the electrodes, becomes doubly refracting as a result of the electro-optical Kerr effect. The negatogenic fluid used comprises compounds of formula I and/or 11 and/or mixtures with other nematogenic substances.
Detailed Description of the Invention Light modulation cells or Kerr cells are known and until now nitrobenzene, because of its high Kerr constant, has been the only substance used as the dielectric.
However, Kerr cells having a nitrobenzene dielectric have the disadvantage of requiring operating voltages of several kilovolts. Operation of such a cell places exacting requirements on the rise times and the highvoltage breakdown strength of an associated electronic control system. Consequently, when the cells are intensively modulated, it is impossible to make use of the theoretically very short response time of nitrobenzene. A further disadvantage of Kerr cells having a nitrobenzene dielectric comprises the fact that they need to be relatively thick in the direction of the light beam. For example, the thickness of the dielectric parallel to the light beam must be 5 cm. in order to produce a phase difference of 8 0.835 A (A 583 ,um, T 24 C.) at a field strength of 24 kV cm". Cells of this thickness are unsuitable for a number of practical applications.
The present invention provides an electro-optical light-modulation cell which is very quickly responsive and one requiring a control voltage in a range which only necessitates the utilization of relatively inexpensive circuitry, using transistors where possible.
In particular, the present invention relates to an electrooptical light-modulation cell having a dielectric disposed between electrodes which becomes doubly refracting upon an application of a voltage to the electrodes, in which the general formula 1 and/or 11, and/or mixtures with other nematogenic substances.
Preferably, the nematogenic fluid compound of the above mentioned compounds is at a temperature near the temperature T,. of the phase change between the isotropic and the anisotropic state.
In order that the invention may be readily understood, an embodiment thereof will now be described in more detail, by way of example, with reference to the accompanying drawing. The drawing shows a lightmodulation arrangement including a light-modulation cell embodying the invention.
As shown in the drawing, a light-modulation cell 10 comprises two parallel rectangular electrodes 16 and 17 between which is disposed of a dielectric 13 composed of a nematogenic substance. The electrodes are made of stainless steel, but can be made of any other metal, which does not react with nematogenic substances, for example, gold or the like.
The distance between the electrodes depends on the diameter of a light beam which is to be modulated. In the example, this distance is so small that the nematogenic substance is held between the electrodes by capillary forces. In such a case, no additional walls are needed for laterally binding the space between the electrodes. If the distance between the electrodes is greater, the space for the dielectric must be sealed on all sides, using plates of suitable size and made of electrically insulating material. At least two opposite insulating plates must be transparent to the light beam, i.e., they should advantageously be made of glass, acrylic glass or the like.
The dielectric is made of a nematogenic substance, i.e., a substance having a nematic liquid-crystal phase over a certain temperature range. Specially good results are obtained with nematogenic substances which are dielectrically and optically strongly anisotropic and which have a pronounced electric dipole moment extending parallel to the direction of maximum polarizability of the molecules. The substances must also have a marked tendency for parallel orientation over a number of molecular spacings, i.e., the tendency to form clusters. Since the tendency to form clusters is particularly marked in the immediate neighborhood of the temperature T, at which there is a change from the isotropic to the nematic state, the cell is desirably operated in the temperature range T t s T +l C.
Particularly preferred are mixtures of p-[(p-nhexylbenzylidene)aminolbenzonitrile and p-[(p-nbutylbenzylidene)amino]-benzonitrile in a molar ratio Of 22 l l to 1:2;
a mixture of p-[(p-n-propylbenzylidene)amino]benzonitrile and p-[(p-n-hexylbenzylidene)amino1- benzonitrile in a molar ratio of 1:2;
a mixture of p[(p-n-heptylbenzylidene)amino]ben zonitrile and of p-[(p-n-butylbenzy1idene)amino]- benzonitrile in a molar ratio of 2:1;
a mixture of p-[(p-n-octylbenzylidene)amino]benzonitrile and p-[(p-n-pentylbenzylidene)amino]- benzonitrile in a molar ratio of 2:1;
a mixture of p-n-heptyl benzoic acid-p'-cyanophenyl ester and p-n-butylbenzoic acid-p-cyanophenyl ester or p-n-pentylbenzoic acid-pcyanophenylester in a molar ratio of 2:];
a mixture of p-n-octylbenzoic acid-p'-cyanophenyl ester and p-n-butylbenzoic acid-p'-cyanophenyl ester or p-n-hexylbenzoic acid-p'-cyanophenyl ester in a molar ratio of 2:1; or
a mixture of p-n-hexylbenzoic acid-p'-cyanophenyl ester and p-n-butylbenzoic acid-p-cyanophenyl ester in a molar ratio of 2: 1.
Compounds of formula I can be manufactured in analogy to the following example:
150 mg p-toluenesulfonic acid were added to 5,9 g (0,05 Mol) p-aminobenzonitrile and 6,7 g (0,05 Mol) p-ethylbenzaldehyde in ml benzene. The resulting mixture was heated in a nitrogen atmosphere during 1 hour under reflux (temperature of the bath The water formed was removed in a water separator. The benzene condensed in the reflux condenser was passed through a layer of 50 g aluminiumoxide and returned into the reaction flask. After cooling, 2 g potassiumcarbonate were added, the mixture was filtered and the filtrate separated from the solvent under vacuum (bath temperature 50 C). 1 1,5 g yellow oil which crystallized after cooling, were obtained. The resulting product was recrystallized several times in iso-propanol until the melting point remains constant and the 'gaschromatography shows no impurities. The pure p-[(p-ethylbenzylidene)amino]-benzonitri1e melted at 76,277,0 and forms liquid crystals after cooling to 63,0-59,7. UV
(ETOH); E211 25, 800 (shoulder at 316 nm) NMR, MS, Ir and microanalyse correspond to the structure attributed to the substance.
Compounds of formula II can be manufactured in analogy to the following example.
5,6g (28,5 mMol) p-n-butylbenzoyl chloride in 12 ml dry benzene were added to 3,1 g (26 mMol) p-hydroxybenzonitrile in 25 ml dry pyridine. The resulting mixture was stirred overnight at room-temperature and then 2 hours at 60 C. After cooling the mixture was extracted with ether and the extract washed with diluted hydrochloric acid and water. 9 g crude p-nbutylbenzoic acid-p'-cyanophenyl ester were obtained. This product was dissolved in toluene and was submitted to chromatography using 250 g silica gel. From the resulting pure fractions, 4 g of product were obtained after recrystallization from hexane. Melting point 67 C. Liquid crystals are formed at 41 ,5 C. NMR and IR correspond to the structure attributed to the substance.
The light modulating arrangement shown in the drawing comprises, in addition to cell 10, a polarizer 12 disposed upstream of the cell and an analyzer 14 disposed downstream of the cell. A beam of light from a source 11 travels through polarizer 12 and cell parallel to the electrodes and strikes analyzer 14. If the polarizer 12 and analyzer 114 are rotated 90 relative to one another as shown by the arrow in FIG. 1 and if the dielectric of cell 10 is isotropic, the light beam does not reach the eye of an observer downsteam of the analyzer 14.
Ifa d.c. (direct current) voltage is applied to the electrodes of cell 10, the dielectric 12 becomes doubly refracting, so that the linearly polarized light from polarizer 12 is converted to elliptically polarized light, some of which can travel through the analyzer 14. The observer therefore notices a brightening of his field of view through the analyzer.
Maximum brightening occurs at an optical phase difference of8 =(2i+ I))\/2, with i= 0, l, 2 The optical phase difference is directly proportional to the Wavelength. the thickness of the cell or dielectric parallel to the light beam, the Kerr constant and the square of the electric field strength.
An important criterion of the capacity of electrooptical light-modulation cells is the attainable contrast between the light intensity when no voltage is applied to the electrodes and the light intensity at maximum drive. The contrast obtainable in a cell embodying the invention is of the order of 1:1,000, and varies with the fourth power of the field strength.
Electro-optical light-modulation cells embodying the invention are suitable for a number of applications. In general, they can be used for controlling and modulating light far beyond the acoustic frequency range. An important application is to electronic shutters. particularly in cases in which large aperatures are required. In very specific applications the double refraction may be optically induced. e.g. by the field of high-powered light sources.
1. In an electro-optical light-modulation cell having a dielectric which is disposed between electrodes and which becomes doubly refracting on application of a voltage to the electrodes, the improvement which comprises a dielectric in the isotropic state comprised of a compound characterized by the formula wherein R is ethyl, n-propy], n butyl, n-pentyl,
n-hexyl, isohexyl, n-heptyl or n-octyl, mixtures thereof and/or mixtures with other nematogenie substances.
2. A cell in HCCOI'CBIUC with claim 1, wherein the nematogenic fluid is at a temperature near the temperature T,. of the phase change between the isotropic and the anisotropic state.
3. A cell in accordance with claim 2, wherein the temperature I of the nematogenic fluid is in the range T,. 2 l,.+1,..
4. A cell in accordance with claim 3, wherein the dielectric comprises a mixture of p[(p-n-hexylbenzylidene )amino]-benzonitrile and p-[ p-nbutylbenzylidene)-amino]benzonitrile in a molar ratio of 2:1 to 1:2.
5. A cell in accordance with claim 3, wherein the dielectric comprises a mixture of p-[(p-npropylbenzylidene)-amino]-benzonitrile and p'[(p-nhexylbenzylidene)amino]benzonitrile in a molar ratio of 1:2.
6. A cell in accordance with claim 3, wherein the dielectric comprises a mixture of p-[(p-nheptylbenzylidene)-amino]-benzonitrile and p-[(p-n butylbenzylidene)aminolbenzonitrile in a molar ratio of 2:1.
7. A cell in accordance with claim 3, wherein the dielectric comprises a mixture of p-[(p-n-octylbenzylidene)amino]-benzonitrile and p-[(p-n-pentylbenzylidene)amino]-benzonitrile in a molar ratio of 2:1.
8. A cell in accordance with claim 3, which comprises polarizers for continuously modulating light transmitted through the cell, one polarizer being disposed upstream of the cell and the other being disposed downstream of the cell in the direction oflight traveling through the cell.
9. A cell in accordance with claim 8 wherein the two polarizers are crossed.
110. In an electrooptical light-modulation cell having a dielectric which is disposed between electrodes and which becomes doubly refracting on application of a voltage to the electrodes, the improvement which comprises a dielectric in the isotropic state comprised of a compound characterized by the formula:
p'-cyanophenyl ester in a molar ratio of 2: 1.
16. A cell in accordance with claim 12, which comprises polarizers for continuously modulating light transmitted through the cell, one polarizer being disposed upstream of the cell and the other being disposed downstream of the cell in the direction of light traveling through the cell.
17. A cell in accordance with claim 16 wherein the two polarizers are crossed.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3499702 *||Dec 5, 1967||Mar 10, 1970||Rca Corp||Nematic liquid crystal mixtures for use in a light valve|
|US3687515 *||Jan 6, 1971||Aug 29, 1972||Xerox Corp||Electro-optic liquid crystal system with polyamide resin additive|
|US3694053 *||Jun 22, 1971||Sep 26, 1972||Bell Telephone Labor Inc||Nematic liquid crystal device|
|1||*||Usol tseva et al.; Chemical Characteristics, Structure, and Properties of Liquid Crystal, Russian Chemical Reviews, Vol. 32, pp. 495 507, Sept. 1963.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
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|US3925238 *||Jun 28, 1974||Dec 9, 1975||Rca Corp||Novel liquid crystal electro-optic devices|
|US3925444 *||Feb 22, 1974||Dec 9, 1975||Hoffmann La Roche||Liquid crystalline isonitriles|
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|US3947375 *||Nov 6, 1973||Mar 30, 1976||Secretary Of State For Defence In Her Britannic Majesty's Govt. Of U.K. Of Gt. Britain And Northern Ireland||Liquid crystal materials and devices|
|US3951846 *||Jun 28, 1974||Apr 20, 1976||Rca Corporation||Novel liquid crystal electro-optic devices|
|US3954653 *||Jul 3, 1974||May 4, 1976||Kabushiki Kaisha Suwa Seikosha||Liquid crystal composition having high dielectric anisotropy and display device incorporating same|
|US3960749 *||Jan 23, 1974||Jun 1, 1976||International Liquid Xtal Company||Liquid-crystal mixtures for use in liquid-crystal displays|
|US3960752 *||Nov 12, 1973||Jun 1, 1976||Eastman Kodak Company||Liquid crystal compositions|
|US3963311 *||Aug 20, 1975||Jun 15, 1976||Hoffmann-La Roche Inc.||Liquid crystal esters|
|US3963313 *||Sep 9, 1975||Jun 15, 1976||Hoffmann-La Roche Inc.||Liquid crystal Schiffs bases|
|US3981817 *||Mar 27, 1974||Sep 21, 1976||Hoffmann-La Roche Inc.||Mixtures of liquid crystals|
|US3983049 *||May 2, 1974||Sep 28, 1976||General Electric Company||Liquid crystal compositions with positive dielectric anisotropy|
|US3988054 *||Apr 23, 1974||Oct 26, 1976||Dai Nippon Toryo Kabushiki Kaisha||Nematic liquid crystal compositions|
|US3997242 *||Aug 18, 1975||Dec 14, 1976||Hoffmann-La Roche Inc.||Electro-optical cell containing dielectric isonitriles|
|US4000084 *||Dec 17, 1973||Dec 28, 1976||Hughes Aircraft Company||Liquid crystal mixtures for electro-optical display devices|
|US4004848 *||Mar 13, 1974||Jan 25, 1977||Kabushiki Kaisha Suwa Seikosha||Liquid crystal display device|
|US4009938 *||Dec 6, 1973||Mar 1, 1977||Kabushiki Kaisha Suwa Seikosha||Liquid crystal display device|
|US4011173 *||Apr 17, 1974||Mar 8, 1977||Merck Patent Gesellschaft Mit Beschrankter Haftung||Modified nematic mixtures with positive dielectric anisotropy|
|US4018507 *||Sep 5, 1974||Apr 19, 1977||American Micro-Systems, Inc.||Liquid crystal device, composition therefor, and method for preparing the composition|
|US4020002 *||Feb 28, 1974||Apr 26, 1977||Beckman Instruments, Inc.||Non-schiff base field effect liquid crystal composition|
|US4027950 *||Aug 16, 1974||Jun 7, 1977||Matsushita Electric Industrial Co., Ltd.||Electro-optical display device|
|US4043935 *||Jul 3, 1974||Aug 23, 1977||Kabushiki Kaisha Suwa Seikosha||Liquid crystal composition having high dielectric anisotropy and display device incorporating same|
|US4058476 *||Aug 18, 1975||Nov 15, 1977||Hoffmann-La Roche Inc.||Liquid crystalline isonitriles|
|US4058477 *||Sep 8, 1975||Nov 15, 1977||Hoffmann-La Roche Inc.||Liquid crystal Schiffs bases|
|US4058478 *||Aug 20, 1975||Nov 15, 1977||Hoffmann-La Roche Inc.||Liquid crystal esters|
|US4061587 *||Jul 8, 1976||Dec 6, 1977||Hoffmann-La Roche Inc.||Liquid crystalline cinnamic acid esters|
|US4086002 *||Nov 20, 1973||Apr 25, 1978||Haffmann-La Roche Inc.||Field effect light shutter employing low temperature nematic liquid crystals|
|US4190343 *||Aug 27, 1975||Feb 26, 1980||Agfa-Gevaert Ag||Photographic camera with exposure control utilizing a phase controllable crystal|
|US4232951 *||Aug 4, 1978||Nov 11, 1980||Allied Chemical Corporation||Mesomorphic isocyanate extended rigid polymers|
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|US20040150633 *||Apr 18, 2002||Aug 5, 2004||Michael Heckmeier||Electro-optic light control element, display and medium|
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|CN100487545C *||Nov 12, 2003||May 13, 2009||默克专利股份有限公司||Electrooptical light modulating element, electrooptical display and modulating medium|
|WO2002093244A2 *||Apr 18, 2002||Nov 21, 2002||Merck Patent Gmbh||Electro-optic light control element, display and medium|
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|WO2004046805A1 *||Nov 12, 2003||Jun 3, 2004||Merck Patent Gmbh||Electrooptical light modulating element, electrooptical display and modulating medium|
|U.S. Classification||359/253, 558/418, 359/258, 359/322, 252/299.68, 558/416, 252/299.67|
|International Classification||G02F1/07, G02F1/01|