Naphthalene compound, and liquid crystal composition and liquid crystal element using the same

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a naphthalene compound, more specifically to a novel naphthalene compound and a naphthalene compound to be useful as an intermediate product for producing said compound and to a liquid crystal composition containing said novel naphthalene compound and a liquid crystal element using the liquid crystal composition.
2. Description of the Related Art
Liquid crystal display elements have so far widely been used for various display elements by making the best use of excellent characteristics thereof such as low voltage actuation, low power consumption, possibility of thin type display, and no fatigue of eyes because of light-receptive display element.
Among them, there have widely been used TN (twisted nematic) type liquid crystal display elements using nematic liquid crystal and STN (super twisted nematic) type liquid crystal display elements having a torsion angle adjusted from 180.degree. to 270.degree.. These display elements are nematic liquid crystal display elements using nematic liquid crystal. These nematic liquid crystal display elements have the defect that they have a long response time and therefore can provide only a response time falling on the order of some ten msec.
A recent progress in industrial techniques has been followed by strong requirement of high speed response to liquid crystal elements, and in order to meet such requirement, various attempts have been made by improving liquid crystal materials. For example, a display device making use of a photoswitching phenomenon of ferroelectric liquid crystal has been proposed �Appl. Phys. Lett., 36, 899 (1980)!. The liquid crystal elements are expected to be applied to not only displays for liquid crystal televisions, etc., but also to materials for optoelectronics-related elements such as optical printer heads, optical Fourier transform elements and light valves.
Ferroelectric liquid crystals belong to tilt series chiral smectic phases in terms of a liquid crystal phase, and among them, liquid crystal phase called a chiral smectic C phase having a low viscosity is preferred from a viewpoint of practical use. Various liquid crystal compounds showing chiral smectic C phases have so far been investigated, and a lot of compounds have already been found and produced. Conditions for using them for ferroelectric liquid crystal elements include:
showing a chiral smectic C phase in a wide temperature range including room temperature,
having a suitable phase series on a high temperature part of a chiral smectic C phase and large helical pitches thereof in order to obtain good orientation,
having a suitable tilt angle,
having a low viscosity,
having spontaneous polarization which is large to some extent, and the like.
No single ferroelectric liquid crystal which can satisfy these conditions has ever been known. Accordingly, ferroelectric liquid crystal compositions obtained by blending several liquid crystal compounds or non-liquid crystal compounds have to be used in practical uses.
A ferroelectric liquid crystal composition does not always comprise only ferroelectric liquid crystal compounds, and it is disclosed in, for example, Japanese Patent Application Laid-Open No. 61 195187 (1986) that compositions showing ferroelectric liquid crystal phases as a whole can be obtained by employing compounds or compositions showing non-chiral smectic C, F, G, H and I phases for fundamental materials and blending them with one or plural compounds showing ferroelectric liquid crystal phases. Further, it is reported that ferroelectric liquid crystal compositions can be obtained as a whole by employing compounds or compositions showing phases such as a non-chiral smectic C phase for fundamental materials and blending them with one or plural compounds which are optically active but do not show ferroelectric liquid crystal phases �Mol. Cryst. Liq. Cryst., 89, 327 (1982)!.
Phenylpyrimidine series liquid crystal compounds and phenylbenzoate series liquid crystal compounds as shown below have so far been known as typical compounds showing chiral smectic C phases: ##STR3## wherein R represents an alkyl group, and R* represents an optically active alkyl group.
Further, naphthalene series liquid crystal compounds as shown below are proposed in Japanese Patent Application Laid-open No. 63-246346 (1988), Japanese Patent Application Laid-open No. 1-193390 (1989), Japanese Patent Application Laid-open No. 3-68686 (1991) and Japanese Patent Application Laid-open No. 3-106850 (1991): ##STR4## wherein R represents an alkyl group, and R* represents an optically active alkyl group.
However, ferroelectric liquid crystal compositions using the phenylpyrimidine series liquid crystal compounds or phenylbenzoate series liquid crystal compounds described above have had the problems that they are liable to cause orientation unevenness so as to bring about defects when they are put into liquid crystal cells and that the good memory property can not be obtained and the contrast ratio is low. Meanwhile, ferroelectric liquid crystal compositions comprising the naphthalene series compounds described above show good orientation when liquid crystal cells are charged with them, and can provide a good memory property without having defects. However, it is not reasonable to say that they have sufficiently satisfactory characteristics in terms of high speed response and temperature dependency of a response time.
SUMMARY OF THE INVENTION
The present invention provides a liquid crystal compound suited to improve such various characteristics as high speed response, orientation and high contrast ratio when the liquid crystal compound is blended into a ferroelectric liquid crystal composition in order to put a ferroelectric liquid crystal element into practical use, a compound useful as a component for a liquid crystal composition, an intermediate product for producing the above compound and a liquid crystal composition containing the above compound, and a liquid crystal element using said liquid crystal composition.
First, the present invention relates to a naphthalene compound represented by the following Formula (1): ##STR5## wherein R.sub.1 and R.sub.2 each represent a linear or branched alkyl group having 1 to 20 carbon atoms, an alkoxyalkyl group having 2 to 20 carbon atoms or an alkenyl group having 2 to 20 carbon atoms which may be substituted with halogen atoms and have no asymmetric carbon atoms; A represents any of the groups represented by the following formulas: ##STR6## (wherein X.sub.1, X.sub.2, X.sub.3 and X.sub.4 each represent a hydrogen atom or a halogen atom, and 1,4-cyclohexylene ring is disposed in a trans position); and z represents 0 or 1.
Further, the present invention relates to a naphthalene compound represented by the following Formula (2) which is useful as an intermediate product when producing the naphthalene compound represented by Formula (1): ##STR7## wherein R.sub.3 represents a branched alkyl group having no asymmetric carbon atoms and having 3 to 20 carbon atoms, or a linear or branched alkyl group having 1 to 20 carbon atoms, an alkoxyalkyl group having 2 to 20 carbon atoms or an alkenyl group having 2 to 20 carbon atoms which are substituted with halogen atoms and have no asymmetric carbon atoms; and B.sub.1 represents a hydrogen atom or a benzyl group.
Furthermore, the present invention relates to a liquid crystal composition using the compound represented by Formula (1), and a liquid crystal element using said liquid crystal composition.
The liquid crystal composition using the naphthalene compound of the present invention is improved in various characteristics such as high speed response, temperature dependency of a response time, etc.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a schematic, cross-sectional view of one example of a liquid crystal element using a liquid crystal showing a chiral smectic phase.
FIG. 2 is a graph showing the temperature dependency of the response time of the liquid crystal compositions of Examples 115 and 116 and the comparative example.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The present invention will be explained below in detail.
The naphthalene compound of the present invention represented by Formula (1) is a novel compound. ##STR8##
In Formula (1), R.sub.1 and R.sub.2 each represent a linear or branched alkyl group having 1 to 20 carbon atoms, an alkoxyalkyl group having 2 to 20 carbon atoms or an alkenyl group having 2 to 20 carbon atoms which may be substituted with halogen atoms and have no asymmetric carbon atoms. More preferably, R.sub.1 and R.sub.2 each represent a linear or branched alkyl group represented by Formulas (I) and (II):
--C.sub.a H.sub.2a+1 (n) (I)
--(CH.sub.2).sub.b CH(C.sub.c H.sub.2c+1).sub.2 (II)
wherein a represents a natural number of 1 to 20; b represents a natural number of 0 to 17; and c represents a natural number of 1 to 9, provided that b+c.times.2.ltoreq.19, an alkoxyalkyl group represented by Formula (III):
--C.sub.d H.sub.2d O(C.sub.e H.sub.2e O).sub.f C.sub.g H.sub.2g+1(III)
wherein d represents a natural number of 1 to 10; e represents a natural number of 1 to 10; f represents a natural number of 0 to 5; and g represents a natural number of 1 to 12, provided that d+e.times.f+g.ltoreq.20, or a halogenated alkyl group represented by Formula (IV), (V) or (VI):
--(CH.sub.2).sub.h (CX.sub.2).sub.i H (IV)
--(CH.sub.2).sub.j (C.sub.k X.sub.2k).sub.l C.sub.m H.sub.2m+1(V)
--(CH.sub.2).sub.n (CX.sub.2).sub.p X (VI)
wherein X represents a halogen atom; h represents a natural number of 0 to 19; i represents a natural number of 1 to 20; j represents a natural number of 0 to 18; k represents a natural number of 1 to 10; 1 represents a natural number of 1 to 19; and m represents a natural number of 1 to 19; n represents a natural number of 0 to 19; p represents a natural number of 1 to 20, provided that h+i.ltoreq.20, j+k.times.l+m.ltoreq.20 and n+p.ltoreq.20.
More preferably, R.sub.1 and R.sub.2 each represent the group represented by Formula (I), (II), (III), (IV) or (VI).
Further preferably, R.sub.1 represents the group represented by Formula (I), (III), (IV) or (VI).
The concrete examples of the groups represented by R.sub.1 and R.sub.2 include linear alkyl groups such as methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl, n-nonadecyl and n-eicocyl, branched alkyl groups such as 1-methylethyl, 2-methylpropyl, 3-methylbutyl, 4-methylpentyl, 5-methylhexyl, 6-methylheptyl, 7-methyloctyl, 8-methylnonyl, 9-methyldecyl, 11-methyldodecyl, 3-pentyl, 2-ethylbutyl, 3-ethylpentyl, 4-ethylhexyl, 5-ethylheptyl, 6-ethyloctyl, 4-heptyl, 2-n-propylpentyl, 3-n-propylhexyl, 4-n-propylheptyl, 5-n-propyloctyl, 6-n-propylnonyl, 7-n-propyldecyl, 8-n-propylundecyl, 9-n-propyldodecyl, 1-n-butylpentyl, 2-n-butylhexyl, 3-n-butylheptyl, 4-n-butyloctyl, 5-n-butylnonyl, 6-n-butyldecyl, 7-n-butylundecyl, 8-n-butyldodecyl, 2-n-pentylheptyl, 3-n-pentyloctyl, 5-n-pentyldecyl, 3-n-hexylnonyl, 4-n-hexyldecyl, 6-n-hexyldodecyl, 2,2-dimethylpropyl, 2,2-dimethylbutyl, 3,3-dimethylbutyl, 3,3-dimethylpentyl, 4,4-dimethylpentyl, 5,5-dimethylhexyl, 6,6-dimethylheptyl, 3,3-diethylpentyl and 2,2,4,4-tetramethylpentyl, halogenated alkyl groups such as fluoromethyl, difluoromethyl, 2-fluoroethyl, 3-fluoro-n-propyl, 4-fluoron-n-butyl, 5-fluoro-n-pentyl, 6-fluoro-n-hexyl, 2-chloroethyl, 3-chloro-n-propyl, 4-chloro-n-butyl, 5-chloro-n-pentyl, trifluoromethyl, perfluoroethyl, perfluoro-n-propyl, perfluoroisopropyl, perfluoro-n-butyl, perfluoroisobutyl, perfluoro-n-pentyl, perfluoroisopentyl, perfluoro-n-hexyl, perfluoro-n-heptyl, perfluoro-n-octyl, perfluoro-n-nonyl, perfluoro-n-decyl, perfluoro-n-undecyl, perfluoro-n-dodecyl, perfluoro-n-tetradecyl, 1-hydroperfluoroisopropyl, 1,1-dihydroperfluoroethyl, 1,1-dihydroperfluoro-n-propyl, 1,1-dihydroperfluoro-n-butyl, 1,1-dihydroperfluoroisobutyl, 1,1-dihydroperfluoro-n-pentyl, 1,1-dihydroperfluoro-n-hexyl, 1,1-dihydroperfluoro-n-heptyl, 1,1-dihydroperfluoron-n-octyl, 1,1-dihydroperfluoro-n-nonyl, 1,1-dihydroperfluoron-n-decyl, 1,1-dihydroperfluoro-n-undecyl, 1,1-dihydroperfluoro-n-dodecyl, 1,1-dihydroperfluoro-n-tetradecyl, 1,1-dihydroperfluoro-n-pentadecyl, 1,1-dihydroperfluoro-n-hexadecyl, 1,1,2-trihydroperfluoroethyl, 1,1,3-trihydroperfluoro-n-propyl, 1,1,4-trihydroperfluoro-n-butyl, 1,1,5-trihydroperfluoro-n-pentyl, 1,1,6-trihydroperfluoro-n-hexyl, 1,1,7-trihydroperfluoro-n-heptyl, 1,1,8-trihydroperfluoro-n-octyl, 1,1,9-trihydroperfluoro-n-nonyl, 1,1,11-trihydroperfluoro-n-undecyl, 2-(perfluoroethyl)ethyl, 2-(perfluoro-n-propyl)ethyl, 2-(perfluoro-n-butyl)ethyl, 2-(perfluoro-n-pentyl)ethyl, 2-(perfluoro-3-methylbutyl)ethyl, 2-(perfluoro-n-hexyl)ethyl, 2-(perfluoro-n-heptyl)ethyl, 2-(perfluoro-5-methylhexyl)ethyl, 2-(perfluoro-n-octyl)ethyl,2-(perfluoro-7-methyloctyl)ethyl, 2-(perfluoro-n-decyl)ethyl, 2-(perfluoro-n-nonyl)ethyl, 2-(perfluoro-9-methyldecyl)ethyl, 2-(perfluoro-n-dodecyl)ethyl, 2,2-bis(trifluoromethyl)propyl, 3-(perfluoro-n-propyl)-n-propyl, 3-(perfluoro-n-butyl)-n-propyl, 3-(perfluoro-n-hexyl)-n-propyl, 3-(perfluoro-n-heptyl)-n-propyl, 3-(perfluoro-n-octyl)-n-propyl, 3-(perfluoro-n-decyl)-n-propyl, 3-(perfluoro-n-dodecyl)-n-propyl, 4-(perfluoroethyl)-n-butyl, 4-(perfluoro-n-propyl)n-butyl, 4-(perfluoro-n-butyl)-n-butyl, 4-(perfluoro-n-pentyl)-n-butyl, 4-(perfluoro-n-hexyl)-n-butyl, 4-(perfluoro-n-heptyl)-n-butyl, 4-(perfluoro-n-octyl)-n-butyl, 4-(perfluoro-n-decyl)-n-butyl, 5-(perfluoro-n-propyl)-n-pentyl, 5-(perfluoro-n-butyl)-n-pentyl, 5-(perfluoro-npentyl)-n-pentyl, 5-(perfluoro-n-hexyl)-n-pentyl, 5-(perfluoro-n-heptyl)-n-pentyl, 5-(perfluoro-n-octyl)-n-pentyl, 6-(perfluoroethyl)-n-hexyl, 6-(perfluoro-n-propyl)-n-hexyl, 6-(perfluoro-1-methylethyl)-n-hexyl, 6-(perfluoro-n-butyl)-n-hexyl, 6-(perfluoro-n-hexyl)-n-hexyl, 6-(perfluoro-n-heptyl)-n-hexyl, 6-(perfluoro-5-methylhexyl)-nhexyl, 6-(perfluoro-n-octyl)-n-hexyl, 6-(perfluoro-7-methyloctyl)-n-hexyl, 7-(perfluoroethyl)-n-heptyl, 7-(perfluoro-n-propyl)-n-heptyl, 7-(perfluoro-n-butyl)-n-heptyl and 7-(perfluoro-n-pentyl)-n-heptyl, alkoxyalkyl groups such as methoxymethyl, 2-methoxyethyl, 3-methoxypropyl, 4-methoxybutyl, 5-methoxypentyl, 6-methoxyhexyl, 7-methoxyheptyl, 8-methoxyoctyl, 9-methoxynonyl, 10-methoxydecyl, ethoxymethyl, 2-ethoxyethyl, 3-ethoxypropyl, 4-ethoxybutyl, 5-ethoxypentyl, 6-ethoxyhexyl, 7-ethoxyheptyl, 8-ethoxyoctyl, 9-ethoxynonyl, 10-ethoxydecyl, n-propoxymethyl, 2-n-propoxyethyl, 3-n-propoxypropyl, 4-n-propoxybutyl, 5-n-propoxypentyl, 6-n-propoxyhexyl, 7-n-propoxyheptyl, 8-n-propoxyoctyl, 9-n-propoxynonyl, 10-n-propoxydecyl, n-butoxymethyl, 2-n-butoxyethyl, 3-n-butoxypropyl, 4-n-butoxybutyl, 5-n-butoxypentyl, 6-n-butoxyhexyl, 7-n-butoxyheptyl, 8-n-butoxyoctyl, 9-n-butoxynonyl, 10-n-butoxydecyl, n-pentyloxymethyl, 2-n-pentyloxyethyl, 3-n-pentyloxypropyl, 4-n-pentyloxybutyl, 5-n-pentyloxypentyl, 6-n-pentyloxyhexyl, 7-n-pentyloxyheptyl, 8-n-pentyloxyoctyl, 9-n-pentyloxynonyl, 10-n-pentyloxydecyl, n-hexyloxymethyl, 2-n-hexyloxyethyl, 3-n-hexyloxypropyl, 4-n-hexyloxybutyl, 5-n-hexyloxypentyl, 6-n-hexyloxyhexyl, 7-n-hexyloxyheptyl, 8-n-hexyloxyoctyl, 9-n-hexyloxynonyl, 10-n-hexyloxydecyl, n-heptyloxymethyl, 2-n-heptyloxyethyl, 3-n-heptyloxypropyl, 4-n-heptyloxybutyl, 5-n-heptyloxypentyl, 6-n-heptyloxyhexyl, 7-n-heptyloxyheptyl, 8-n-heptyloxyoctyl, 9-n-heptyloxynonyl, 10-n-heptyloxydecyl, n-octyloxymethyl, 2-n-octyloxyethyl, 3-n-octyloxypropyl, 4-n-octyloxybutyl, 5-n-octyloxypentyl, 6-n-octyloxyhexyl, 7-n-octyloxyheptyl, 8-n-octyloxyoctyl, 9-n-octyloxynonyl, 10-n-octyloxydecyl, n-nonyloxymethyl, 2-n-nonyloxyethyl, 3-n-nonyloxypropyl, 4-n-nonyloxybutyl, 5-n-nonyloxypentyl, 6-n-nonyloxyhexyl, 7-n-nonyloxyheptyl, 8-n-nonyloxyoctyl, 9-n-nonyloxynonyl, 10-n-nonyloxydecyl, n-decyloxymethyl, 2-n-decyloxyethyl, 3-n-decyloxypropyl, 4-n-decyloxybutyl, 5-n-decyloxypentyl, 6-n-decyloxyhexyl, 7-n-decyloxyheptyl, 8-n-decyloxyoctyl, 9-n-decyloxynonyl, 2-n-undecyloxyethyl, 4-n-undecyloxybutyl, 6-n-undecyloxyhexyl, 8-n-undecyloxyoctyl, 2-n-dodecyloxyethyl, 4-n-dodecyloxybutyl, 6-n-dodecyloxyhexyl, isopropoxymethyl, 2-isopropoxyethyl, 3-isopropoxypropyl, 4-isopropoxybutyl, 5-isopropoxypentyl, 6-isopropoxyhexyl, 7-isopropoxyheptyl, 8-isopropoxyoctyl, 9-isopropoxynonyl, 10-isopropoxydecyl, isobutoxymethyl, 2-isobutoxyethyl, 3-isobutoxypropyl, 4-isobutoxybutyl, 5-isobutoxypentyl, 6-isobuyoxyhexyl, 7-isobutoxyheptyl, 8-isobutoxyoctyl, 9-isobutoxynonyl, 10-isobutoxydecyl, tert-butoxymethyl, 2-tert-butoxyethyl, 3-tert-butoxypropyl, 4-tert-butoxybutyl, 5-tert-butoxypentyl, 6-tert-butoxyhexyl, 7-tert-butoxyheptyl, 8-tert-butoxyoctyl, 9-tert-butoxynonyl, 10-tert-butoxydecyl, (2-ethylbutoxy)methyl, 2-(2'-ethylbutoxy)ethyl, 3-(2'-ethylbutoxy)propyl, 4-(2'-ethylbutoxy)butyl, 5-(2'-ethylbutoxy)pentyl, 6-(2'-ethylbutoxy)hexyl, 7-(2'-ethylbutoxy)heptyl, 8-(2'-ethylbutoxy)octyl, 9-(2'-ethylbutoxy)nonyl, 10-(2'-ethylbutoxy)decyl, (3-ethylpentyloxy)methyl, 2-(3'-ethylpentyloxy)ethyl, 3-(3'-ethylpentyloxy)propyl, 4-(3'-ethylpentyloxy)butyl, 5-(3'-ethylpentyloxy)pentyl, 6-(3'-ethylpentyloxy)hexyl, 7-(3'-ethylpentyloxy)heptyl, 8-(3'-ethylpentyloxy)octyl, 9-(3'-ethylpentyloxy)nonyl, 10-(3'-ethylpentyloxy)decyl, 2-(2'-methoxyethoxy)ethyl, 2-(2'-ethoxyethoxy)ethyl, 2-(2'-n-propoxyethoxy)ethyl, 2-(2'-isopropoxyethoxy)ethyl, 2-(2'-n-butoxyethoxy)ethyl, 2-(2'-isobutoxyethoxy)ethyl, 2-(2'-tert-butoxyethoxy)ethyl, 2-(2'-n-pentyloxyethoxy)ethyl, 2-�2'-(2"-ethylbutoxy)ethoxy!ethyl, 2-(2'-n-hexyloxyethoxy)ethyl, 2-�2'-(3"-ethylpentyloxy)ethoxy!ethyl, 2-(2'-n-heptyloxyethoxy)ethyl, 2-(2'-n-octyloxyethoxy)ethyl, 2-(2'-n-nonyloxyethoxy)ethyl, 2-(2'-n-decyloxyethoxy)ethyl, 2-(2'-n-undecyloxyethoxy)ethyl, 2-(2'-n-dodecyloxyethoxy)ethyl, 2-�2'-(2"-methoxyethoxy)ethoxy!ethyl, 2-�2'-(2"-ethoxyethoxy)ethoxy!ethyl, 2-�2'(2"-n-propoxyethoxy)ethoxy!ethyl, 2-�2'-(2"-isopropoxyethoxy)ethoxy!ethyl, 2-�2'-(2"-n-butoxyethoxy)ethoxy!ethyl, 2-�2'-(2"-isobutoxyethoxy)ethoxy!ethyl, 2-�2'-(2"-tert-butoxyethoxy)ethoxy!ethyl, 2-{2'-�2"-(2"'-ethylbutoxy)ethoxy!ethoxy}ethyl, 2-�2'-(2"-n-pentyloxyethoxy)ethoxy!ethyl, 2-�2'-(2"-n-hexyloxyethoxy)ethoxy!ethyl,2-{2'-�2"-(3"'-ethylpentyloxy)ethoxy!ethoxy}ethyl, 2-�2'-(2"-n-heptyloxyethoxy)ethoxy!ethyl, 2-�2'-(2"-n-octyloxyethoxy)ethoxy!ethyl,2-�2'-(2"-n-nonyloxyethoxy)ethoxy!ethyl, 2-�2'-(2"-n-decyloxyethoxy)ethoxy!ethyl, 2-�2'-(2"-n-undecyloxyethoxy)ethoxy!ethyl, 2-{2'-�2"-(2"'-methoxyethoxy)ethoxy!ethoxy}ethyl, 2-{2'-{2"-�2"'-(2-methoxyethoxy)ethoxy!ethoxy}ethoxy}ethyl, 2-{2'-{2"-{2"'-�2-(2-methoxyethoxy)ethoxy!ethoxy}ethoxy}ethoxy}ethyl, (2-ethoxyethoxy)methyl, (2-n-butoxyethoxy)methyl, (2-n-hexyloxyethoxy)methyl, (3-ethoxypropoxy)methyl, (3-n-propoxypropoxy)methyl, (3-n-pentyloxypropoxy)methyl, (3-n-hexyloxypropoxy)methyl, (4-methoxybutoxy)methyl, (4-ethoxybutoxy)methyl, (4-n-butoxybutoxy)methyl, 2-(3'-methoxypropoxy)ethyl, 2-(3'-ethoxypropoxy)ethyl, 2-(4'-methoxybutoxy)ethyl, 2-(4'-ethoxybutoxy)ethyl, 2-�4'-(2"-ethylbutoxy)butoxy!ethyl, 2-�4'-(3"-ethylpentyloxy)butoxy!ethyl, 3-(2'-methoxyethoxy)propyl, 3-(2'-ethoxyethoxy)propyl, 3-(2'-n-pentyloxyethoxy)propyl, 3-(2'-n-hexyloxyethoxy)propyl, 3-(3'-ethoxypropoxy)propyl, 3-(3'-n-propoxypropoxy)propyl, 3-(3'-n-butoxypropoxy)propyl, 3-(4'-ethoxybutoxy)propyl, 3-(5'-ethoxypentyloxy)propyl, 4-(2'-methoxyethoxy)butyl, 4-(2'-ethoxyethoxy)butyl, 4-(2'-isopropoxyethoxy)butyl, 4-(2'-isobutoxyethoxy)butyl, 4-(2'-n-butoxyethoxy)butyl, 4-(2'-n-hexyloxyethoxy)butyl, 4-(3'-n-propoxypropoxy)butyl, 4-�2'-(2"-methoxyethoxy)ethoxy!butyl, 4-�2'-(2"-n-butoxyethoxy)ethoxy!butyl and 4-�2'-(2"-n-hexyloxyethoxy)ethoxy!butyl, halogenated alkoxyalkyl groups such as 2-(2'-fluoroethoxy)ethyl, 4-(2'-fluoroethoxy)butyl, 6-(2'-fluoroethoxy)hexyl, 8-(2'-fluoroethoxy)octyl, 2-(3'-fluoro-n-propoxy)ethyl, 4-(3'-fluoro-n-propoxy)butyl, 6-(3'-fluoro-n-propoxy)hexyl, 8-(3'-fluoro-n-propoxy)octyl, 2-(4'-fluoro-n-butoxy)ethyl, 4-(4'-fluoro-n-butoxy)butyl, 6-(4'-fluoro-n-butoxy)hexyl, 8-(4'-fluoro-n-butoxy)octyl, 2-(2'-chloroethoxy)ethyl, 4-(2'-chloroethoxy)butyl, 6-(2'-chloroethoxy)hexyl, 8-(2'-chloroethoxy)octyl, 2-(3'-chloro-n-propoxy)ethyl, 4-(3'-chloro-n-propoxy)butyl, 6-(3'-chloro-n-propoxy)hexyl, 8-(3'-chloro-n-propoxy)octyl, 2-(4'-chloro-n-butoxy)ethyl, 4-(4'-chloro-n-butoxy)butyl, 6-(4'-chloro-n-butoxy)hexyl and 8-(4'-chloro-n-butoxy)octyl, and alkenyl groups such as vinyl, propenyl, 2-butenyl, 3-butenyl, 3-hexenyl, 5-hexenyl, 2-octenyl, 3-octenyl, 7-octenyl, 2-nonenyl, 3-nonenyl, 6-nonenyl, 8-nonenyl, 2-decenyl, 3-decenyl, 9-decenyl, 2-undecenyl, 3-undecenyl, 10-undecenyl, 2-dodecenyl, 3-dodecenyl, and 11-dodecenyl.
In Formula (1) , A represents any of the groups represented by the following formulas: ##STR9## preferably any of the groups represented by the following formulas: ##STR10##
In A, X.sub.1, X.sub.2, X.sub.3 and X.sub.4 each represent a hydrogen atom or a halogen atom, preferably a hydrogen atom, a fluorine atom, a chlorine atom or a bromine atom, more preferably a hydrogen atom, a fluorine atom or a chlorine atom, and further preferably a hydrogen atom or a fluorine atom.
The substitution position of X.sub.1 or X.sub.2 is ortho positions or meta positions to the substituent R.sub.1 -- or R.sub.1 O--, preferably an ortho position. The substitution position of X.sub.3 is an ortho position or a meta position to a --COO-- group, preferably an ortho position.
The substitution position of X.sub.4 is an .alpha.-position or .beta.-position on the naphthalene ring, preferably an ortho position to the substituent R.sub.1 -- or R.sub.1 O-- and/or a --COO-- group, more preferably an ortho position to the substituent R.sub.1 -- or R.sub.1 O-- and/or a --COO-- group, and an .alpha.-position on the naphthalene ring.
In Formula (1) , z represents 0 or 1.
The naphthalene compounds represented by Formula (1) of the present invention are classified broadly into five kinds of the following structures (1-1) to (1-5): ##STR11##
The compounds having the structures shown below can be given as the concrete examples of the naphthalene compound represented by Formula (1): ##STR12##
The compound represented by Formula (1) can be produced typically by the following method.
That is, the above compound can be produced by carrying out esterification using a compound represented by Formula (3a) and a compound represented by Formula (4): ##STR13## wherein R.sub.1, R.sub.2, A and z are synonymous with those described above.
There can be applied as a method for carrying out the esterification, known methods, for example, (1) a method in which the compound represented by Formula (3a) is reacted with the compound represented by Formula (4) by the action of a condensing agent such as N,N'-dicyclohexylcarbodiimide (DCC) in the presence of a catalyst such as, for example, 4-pyrrolidinopyridine and 4-N,N-dimethylaminopyridine, or (2) a method in which the compound represented by Formula (4) is reacted with thionyl chloride or oxalyl chloride to prepare the halide, and then the compound represented by Formula (3a) is reacted therewith.
Some of the compounds represented by Formula (4) are commercially available. Further, they can be produced by known methods �for example, J. Chem. Soc., 1874 (1935), J. Chem. Soc., 2556 (1954), J. Chem. Soc., 1412 (1955), J. Chem. Soc., 393 (1957) and J. Chem. Soc., 1545 (1959)!.
That is, a 4-alkoxybenzoic acid derivative can be produced by reacting, for example, a 4-hydroxybenzoic acid derivative with an alkylating agent such as an alkyl halide and an alkyl tosylate in the presence of a base.
Further, a 4-alkoxybiphenyl-4'-carboxylic acid derivative can be produced by reacting a 4-hydroxybiphenyl-4'-carboxylic acid derivative with an alkylating agent such as an alkyl halide and an alkyl tosylate in the presence of a base.
The compounds represented by Formulas (3a) or (3b) can be produced typically through the following steps: ##STR14## wherein R.sub.2 is synonymous with that described above; Y represents a halogen atom; and Bz represents a benzyl group.
That is, 2-benzyloxy-6-naphthoic acid represented by Formula (5) produced by benzylation of 2-hydroxy-6-naphthoic acid with a benzyl halide is reacted with thionyl chloride or oxalyl chloride to produce an acid halide represented by Formula (6). Then, the acid halide represented by Formula (6) is reacted with an alcoholic compound represented by Formula (7):
R.sub.2 --OH (7)
wherein R.sub.2 is synonymous with that described above, whereby the compound represented by Formula (3b) can be produced.
Further, the compound represented by Formula (3b) can be produced as well by reacting 2-benzyloxy-6-naphthoic acid represented by Formula (5) with the alcoholic compound represented by Formula (7) by the action of a condensing agent such as N,N'-dicyclohexylcarbodiimide (DCC) in the presence of a catalyst such as, for example, 4-pyrrolidinopyridine and 4-N,N-dimethylaminopyridine.
Further, the compound represented by Formula (3b) can be produced as well by reacting 2-benzyloxy-6-naphthoic acid represented by Formula (5) with an alkylating agent represented by Formula (8) in the presence of an aprotic polar solvent and an alkaline metal salt:
R.sub.2 --W (8)
wherein R.sub.2 is synonymous with that described above, and W represents a halogen atom or an leaving group such as an arylsulfonyloxy group.
Then, the compound represented by Formula (3a) can be produced by hydrogenation (debenzylation) of the compound represented by Formula (3b).
The hydrogenation can be carried out by known methods. That is, the hydrogenation can be done by carrying out hydrogenation in an organic solvent (for example, alcoholic solvents and ester solvents) at a pressure of atmospheric pressure to about 50 kg/cm.sup.2 in the presence of a catalyst prepared by carrying metals such as, for example, Pd, Pt, Rh, Co and Ni on activated carbon, alumina, barium sulfate, or the like. In general, the hydrogenation is carried out at 0.degree. to 200.degree. C., preferably 10.degree. to 150.degree. C.
Further, the compound represented by Formula (3a) can be produced as well by reacting 2-hydroxy-6-naphthoic acid with an alkylating agent represented by Formula (8) in the presence of an aprotic polar solvent and an alkaline metal salt.
2-Hydroxy-6-naphthoic acid can be produced by known methods �for example, a method described in J. Chem. Soc., 678 (1954)!.
Among the naphthalene compounds represented by (3a) and (3b), the naphthalene compounds represented by Formula (2), that is, the compounds represented by Formula (2a) and (2b) are novel compounds, and the present invention provides these compounds. ##STR15##
In Formula (2), B.sub.1 represents a hydrogen atom or a benzyl group, and in formula (2b), Bz represents a benzyl group.
In Formulas (2a) and (2b), R.sub.3 represents a branched alkyl group having no asymmetric carbon atoms and having 3 to 20 carbon atoms which have no asymmetric carbon atoms, or a linear or branched halogenated alkyl group having 1 to 20 carbon atoms, or an alkoxyalkyl group having 2 to 20 carbon atoms or an alkenyl group having 2 to 20 carbon atoms which may be substituted with halogen atoms and have no asymmetric carbon atoms, preferably the branched alkyl group represented by Formula (II), the alkoxyalkyl group represented by Formula (III), or the halogenated alkyl group represented by Formula (IV), (V) or (VI), each described above.
There can be given as the concrete examples of R.sub.3, the branched alkyl groups, halogenated alkyl groups, alkoxyalkyl groups, halogenated alkoxyalkyl groups, and alkenyl groups, each given as the concrete examples of R.sub.1 and R.sub.2 in Formula (1).
Many of the compounds thus prepared and represented by Formula (1) has intrinsically liquid crystallinity and is useful for constituting a liquid crystal composition and a liquid crystal element using said liquid crystal composition.
The naphthalene compounds of the present invention include compounds showing liquid crystallinity in itself and compounds showing no liquid crystallinity in itself. Further, the naphthalene compounds showing liquid crystallinity include compounds showing a smectic C phase and compounds showing liquid crystallinity but no smectic C phase. These compounds each can effectively be used as components for liquid crystal compositions.
Next, the liquid crystal composition of the present invention will be explained.
In general, a liquid crystal composition comprises two or more kinds of components. The liquid crystal composition of the present invention contains at least one naphthalene compound of the present invention as an essential component.
The naphthalene compound of the present invention used for the liquid crystal composition of the present invention includes naphthalene compounds showing no liquid crystallinity, compounds showing a smectic C phase, and naphthalene compounds showing liquid crystallinity but no smectic C phase.
The liquid crystal composition of the present invention shall not specifically be restricted and includes, for example, liquid crystal compositions showing a smectic phase and liquid crystal compositions showing a chiral smectic phase, preferably liquid crystal compositions showing smectic C, F, G, H and I phases, and liquid crystal compositions showing chiral smectic C, F, G, H and I phases, more preferably liquid crystal compositions showing a chiral smectic C phase.
The liquid crystal composition showing a smectic C phase contains at least one compound represented by Formula (1) and can contain, as an optional component, compounds showing a smectic C phase other than the compound represented by Formula (1), for example, liquid crystal compounds such as phenylbenzoate series liquid crystal compounds, biphenylbenzoate series liquid crystal compounds, naphthalene series liquid crystal compounds, phenylnaphthalene series liquid crystal compounds, phenylpyrimidine series liquid crystal compounds, naphthylpyrimidine series liquid crystal compounds and tolan series liquid crystal compounds. Further, a compound showing no smectic C phase in itself may be contained, if desired.
The content of at least one compound represented by Formula (1) in the compositions showing smectic C phases shall not specifically be restricted and is usually 1 to 100 weight %, preferably 2 to 80 weight %, and more preferably 2 to 50 weight %.
The liquid crystal composition of the present invention showing a chiral smectic C phase comprises at least one compound represented by Formula (1) and further contains as an optically active compound, at least one of known optically active liquid crystal compounds such as optically active phenylbenzoate series liquid crystal compounds, optically active biphenylbenzoate series liquid crystal compounds, optically active naphthalene series liquid crystal compounds, optically active phenylnaphthalene series liquid crystal compounds, optically active phenylpyrimidine series liquid crystal compounds, optically active naphthylpyrimidine series liquid crystal compounds and optically active tolan series liquid crystal compounds.
The content of at least one compound represented by Formula (1) in the compositions showing chiral smectic C phases shall not specifically be restricted and is usually 1 to 99 weight %, preferably 2 to 80 weight %, and more preferably 2 to 50 weight %.
Further, in addition to the essential components described above, the liquid crystal composition of the present invention may contain, as an optional component, a compound showing no liquid crystallinity other than the naphthalene compound of the present invention (for example, dichromatic pigments such as anthraquinone pigments and azo pigments, electroconductivity-providing agents, and life improving agents).
The use of the liquid crystal composition of the present invention can provide a liquid crystal element improved in characteristics such as high speed response, temperature dependency of a response time, orientation, a memory property, and contrast ratio.
The liquid crystal element of the present invention means a liquid crystal element using a liquid crystal composition containing at least one naphthalene compound represented by Formula (1). The liquid crystal element shall not specifically be restricted and relates preferably to a smectic liquid crystal element, more preferably to a ferroelectric liquid crystal element.
The liquid crystal compositions showing ferroelectricity cause a switching phenomenon by applying voltage, and liquid crystal elements having a shorter response time can be prepared by making use of the phenomenon �for example, Japanese Patent Application Laid-Open No. 56-107216 (1981), Japanese Patent Application Laid-Open No. 59-118744 (1984), and Appl. Phys. Lett., 36 899 (1980)!.
Next, the liquid crystal element of the present invention shall be explained.
The liquid crystal element of the present invention comprises the liquid crystal composition of the present invention disposed between a pair of electrode substrates to form a liquid crystal layer. In general, the liquid crystal layer can be formed by heating the liquid crystal composition under vacuum until it becomes an isotropic solution, injecting it into a liquid crystal cell, then cooling it to form a liquid crystal layer, and restoring pressure in the system to atmospheric pressure.
Shown in FIG. 1 is a schematic, cross-sectional view showing one example of the liquid crystal elements having a chiral smectic phase for explaining the structure of the liquid crystal element making use of ferroelectricity.
The liquid crystal element shown in FIG. 1 is a transmitting type liquid crystal element. As a matter of course, the form of the liquid crystal element of the present invention shall not specifically be restricted and includes not only a transmitting type liquid crystal element but also, for example, a reflecting type liquid crystal element.
In FIG. 1, 1 represents a liquid crystal (chiral smectic) layer; 2 represents a substrate; 3 represents a transparent electrode; 4 represents an insulating orientation controlling layer; 5 represents a spacer; 6 represents a lead wire; 7 represents a power source; 8 represents a polarizing plate; 9 represents a light source; I.sub.o represents incident light; and I represents transmitted light.
The liquid crystal element comprises a liquid crystal layer 1 showing a chiral smectic phase disposed between a pair of substrates 2 each of which is provided with a transparent electrode 3 and an insulating orientation controlling layer 4, wherein the layer thickness thereof is controlled by spacers 5, and a power source 7 is connected to a pair of the transparent electrodes 3 via lead wires 6 so that voltage can be applied between the transparent electrodes 3.
Further, a pair of the substrates 2 are interposed between a pair of polarizing plates 8 disposed in a cross-nicol state, and a light source 9 is disposed on one outside thereof.
In general, a glass substrate or a plastic substrate is used for the substrate 2.
The transparent electrodes 3 disposed on two sheets of the substrates 2 include, for example, transparent electrodes comprising thin films of In.sub.2 O.sub.3, SnO.sub.2 and ITO (indium tin oxide).
The insulating orientation controlling layers 4, which are prepared by rubbing a thin films of polymers such as polyimide with gauze or acetate cloth, are for orienting liquid crystal. The materials for the insulating orientation controlling layer 4 include, for example, inorganic materials such as silicon nitride, silicon nitride containing hydrogen, silicon carbide, silicon carbide containing hydrogen, silicon oxide, boron nitride, boron nitride containing hydrogen, cerium oxide, aluminum oxide, zirconium oxide, titanium oxide and magnesium fluoride, and organic materials such as, for example, polyvinyl alcohol, polyimide, polyamideimide, polyesterimide, polyparaxylene, polyester, polycarbonate, polyvinylacetal, polyvinyl chloride, polyvinyl acetate, polyamide, polystyrene, cellulose resins, melamine resins, urea resins, acrylic resins and photoresist resins. Further, the insulating orientation controlling layer 4 may be of a dual layer structure in which an organic insulating layer is formed on an inorganic insulating layer, or a structure comprising only the inorganic insulating layer or the organic insulating layer.
When the insulating orientation controlling layer comprises an inorganic insulating layer, it can be formed by deposition. When it comprises an organic insulating layer, it can be formed by applying a solution dissolving a precursor thereof by spinner coating, dip coating, screen printing, spray coating or roll coating and then curing a resulting film on prescribed curing conditions (for example, heating).
The layer thickness of the insulating orientation controlling layer 4 shall not specifically be restricted and is usually about 1 nm to 10 .mu.m, preferably 1 to 300 nm, more preferably 1 to 100 nm.
Two sheets of the substrates 2 are maintained at an optional space with the spacer 5. The substrates can be maintained at an optional space by interposing, for example, silica beads or alumina beads each having a prescribed diameter as the spacer between the substrates 2 and sealing the circumference thereof with sealant (for example, epoxy adhesives). Further, polymer films and glass fibers may be used as the spacers.
Liquid crystal showing a chiral smectic phase is charged between two sheets of the substrates. The liquid crystal layer 1 is controlled usually to a thickness of 0.5 to 20 .mu.m, preferably 1 to 5 .mu.m.
A display system of the liquid crystal element using the liquid crystal composition of the present invention shall not specifically be restricted, and there can be used, for example, display systems of (a) helical distortion type, (b) SSFLC (surface stabilized ferroelectric liquid crystal) type, (c) TSM (transient scattering mode) type and (d) G-H (guest-host) type.
The naphthalene compound of the present invention and the liquid crystal composition containing said compound are applicable as well to fields other than liquid crystal elements for display (for example, (1) non-linear photofunctional element, (2) electronics materials such as a condenser material, (3) electronics elements such as a limiter, a memory, an amplifier and a modulator, (4) voltage sensing elements and sensors for heat, light, pressure and mechanical deformation, and (5) power generating elements such as thermoelectric generating element).
EXAMPLES
The present invention shall be explained in further detail with reference to examples, but the present invention shall not be restricted to them. The determination of the phase transition temperatures and the identification of the liquid crystal phases in the examples were carried out by observation under a polarizing microscope equipped with a temperature controller.
Symbols shown in the examples and tables mean the following:
I: isotropic liquid
N: nematic phase
SA: smectic A phase
Sc: smectic C phase
Sc*: chiral smectic C phase
C: crystal phase
In Table 2, the mark ".multidot." means the presence of the liquid crystal phase, and the mark "-" means the absence of the liquid crystal phase. Numerals in parentheses in Table 2 mean temperatures in a step of lowering temperature.
Production Example 1
Production of n-butyl 2-hydroxy-6-naphthoate
The mixture of 2-hydroxy-6-naphthoic acid of 18.8 g, N,N-dimethylformamide of 150 g and anhydrous sodium carbonate of 13.3 g was heated to 70.degree. C., and n-butyl bromide of 16.4 g was dropwise added thereto in one hour. After finishing dropwise adding, the suspension was further stirred at 70.degree. to 80.degree. C. for 6 hours. The reaction mixture was cooled down to room temperature and filtrated off the inorganic salt. Then the filtrate was discharged into water of 1000 g. The deposited solid was separated, and sludging was carried out in n-hexane, whereby n-butyl 2-hydroxy-6-naphthoate of 22.0 g was obtained in the form of brown crystal.
Melting point: 107.0.degree. to 112.0.degree. C.
Production Example 2
Production of n-pentyl 2-hydroxy-6-naphthoate
The same procedure as described in Production Example 1 was repeated, except that n-pentyl bromide of 18.1 g was substituted for n-butyl bromide in Production Example 1, whereby n-pentyl 2-hydroxy-6-naphthoate of 23.7 g was obtained in the form of brown crystal.
Melting point: 89.0.degree. to 93.0.degree. C.
Production Example 3
Production of n-hexyl 2-hydroxy-6-naphthoate
The same procedure as described in Production Example 1 was repeated, except that n-hexyl bromide of 19.8 g was substituted for n-butyl bromide in Production Example 1, whereby n-hexyl 2-hydroxy-6-naphthoate of 23.9 g was obtained in the form of brown crystal.
Melting point: 93.0.degree. to 98.0.degree. C.
Production Example 4
Production of n-octyl 2-hydroxy-6-naphthoate
The same procedure as described in Production Example 1 was repeated, except that n-octyl bromide 23.2 g was substituted for n-butyl bromide in Production Example 1, whereby n-octyl 2-hydroxy-6-naphthoate of 27.0 g was obtained in the form of brown crystal.
Melting point: 82.0.degree. to 86.0.degree. C.
Production Example 5
Production of n-decyl 2-hydroxy-6-naphthoate
The same procedure as described in Production Example 1 was repeated, except that n-decyl bromide 26.5 g was substituted for n-butyl bromide in Production Example 1, whereby n-decyl 2-hydroxy-6-naphthoate of 30.2 g was obtained in the form of brown crystal.
Melting point: 92.0.degree. to 96.0.degree. C.
Example 1
Production of 1'-methylethyl 2-benzyloxy-6-naphthoate
Heated for refluxing were 2-benzyloxy-6-naphthoic acid of 27.8 g and oxalyl chloride of 15.2 g in toluene of 200 g for 3 hours, and then excess oxalyl chloride and toluene were distilled off under reduced pressure to obtain 2-benzyloxy-6-naphthoyl chloride. This acid chloride was dissolved in toluene of 120 g, and pyridine of 9.5 g and 2-propanol of 6.6 g were added thereto, followed by stirring the solution at 80.degree. C. for 3 hours. Then, after filtering off deposited pyridine hydrochloride, an organic layer was washed with 1N-hydrochloric acid and further washed with water to neutral. The organic layer was separated, and toluene was distilled off under reduced pressure to obtain a crude product. The product was recrystallized from ethanol, whereby 1'-methylethyl 2-benzyloxy-6-naphthoate of 27.2 g was obtained in the form of colorless crystal.
Melting point: 89.0 to 96.0 g.
Example 2
Production of 2'-methylpropyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 2-methyl1-propanol of 8.1 g was substituted for 2-propanol in Example 1, whereby 2'-methylpropyl 2-benzyloxy-6-naphthoate of 30.1 g was obtained in the form of colorless crystal.
Melting point: 114.0.degree. to 115.5.degree. C.
Example 3
Production of 3'-methylbutyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 3-methyl-1-butanol of 9.7 g was substituted for 2-propanol in Example 1, whereby 3'-methylbutyl 2-benzyloxy-6-naphthoate of 31.0 g was obtained in the form of colorless crystal.
Melting point: 89.5.degree. to 91.0.degree. C.
Example 4
Production of 4'-methylpentyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 4-methyl-1-pentanol of 11.2 g was substituted for 2-propanol in Example 1, whereby 4'-methylpentyl 2-benzyloxy-6-naphthoate of 29.0 g was obtained in the form of colorless crystal.
Melting point: 64.0.degree. to 67.0.degree. C.
Example 5
Production of 1'-ethylpropyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 3-pentanol of 9.7 g was substituted for 2-propanol in Example 1, whereby 1'-ethylpropyl 2-benzyloxy-6-naphthoate of 26.1 g was obtained in the form of colorless crystal.
Melting point: 65.0.degree. to 70.0.degree. C.
Example 6
Production of 2'-ethylbutyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 2-ethyl-1-butanol of 11.2 g was substituted for 2-propanol in Example 1, whereby 2'-ethylbutyl 2-benzyloxy-6-naphthoate of 31.7 g was obtained in the form of colorless crystal.
Melting point: 84.0.degree. to 86.0.degree. C.
Example 7
Production of 1',1',5'-trihydroperfluoro-n-pentyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 1,1,5-trihydroperfluoro-n-pentyl alcohol of 25.5 g was substituted for 2-propanol in Example 1, whereby 1',1',5'-trihydroperfluoro-n-pentyl 2-benzyloxy-6-naphthoate of 38.4 g was obtained in the form of colorless crystal.
Melting point: 98.0.degree. to 100.0.degree. C.
Example 8
Production of 1',1',7'-trihydroperfluoro-n-heptyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 1,1,7-trihydroperfluoro-n-heptyl alcohol of 36.5 g was substituted for 2-propanol in Example 1, whereby 1',1',7'-trihydroperfluoro-n-heptyl 2-benzyloxy-6-naphthoate of 39.4 g was obtained in the form of colorless crystal.
Melting point: 108.0.degree. to 112.0.degree. C.
Example 9
Production of 2'-(perfluoro-n-butyl)ethyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 2-(perfluoro-n-butyl)ethanol of 51.6 g was substituted for 2-propanol in Example 1, whereby 2'-(perfluoro-n-butyl)ethyl 2-benzyloxy-6-naphthoate of 63.4 g was obtained in the form of colorless crystal.
Melting point: 108.0.degree. to 109.0.degree. C.
Example 10
Production of 2'-(perfluoro-n-hexyl)ethyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 1 was repeated, except that 2-(perfluoro-n-hexyl)ethanol of 40.0 g was substituted for 2-propanol in Example 1, whereby 2'-(perfluoro-n-hexyl)ethyl 2-benzyloxy-6-naphthoate of 52.4 g was obtained in the form of colorless crystal.
Melting point: 115.0.degree. to 117.0.degree. C.
Example 11
Production of 2'-n-butoxyethyl 2-benzyloxy-6-naphthoate
The mixture of 2-benzyloxy-6-naphthoic acid of 27.8 g, N,N-dimethylformamide of 150 g and anhydrous potassium carbonate of 13.8 g was heated to 80.degree. C., and 2-n-butoxyethyl p-toluenesulfonate of 40.8 g was dropwise added thereto in one hour. After finishing dropwise adding, the suspension was further stirred at 70.degree.-80.degree. C. for 8 hours. After the reaction mixture was cooled down to room temperature, and the inorganic salt was filtered off. Then the filtrate was neutralized with hydrochloric acid and extracted with toluene. A toluene layer was washed with water, and then toluene was distilled off under reduced pressure, whereby 2-n-butoxyethyl 2-benzyloxy-6-naphthoate of 24.6 g was obtained in the form of colorless crystal.
Melting point: 57.0.degree. to 58.0.degree. C.
Example 12
Production of 2'-n-hexyloxyethyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 11 was repeated, except that 2-n-hexyloxyethyl p-toluenesulfonate of 45.0 g was substituted for 2-n-butoxyethyl p-toluenesulfonate in Example 11, whereby 2'-n-hexyloxyethyl 2-benzyloxy-6-naphthoate of 28.4 g was obtained in the form of colorless oily substance.
Example 13
Production of 2'-(2"-n-hexyloxyethoxy)ethyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 11 was repeated, except that 2-(2'-n-hexyloxyethoxy)ethyl p-toluenesulfonate of 51.6 g was substituted for 2-n-butoxyethyl p-toluenesulfonate in Example 11, whereby 2'-(2"-n-hexyloxyethoxy)ethyl 2-benzyloxy-6-naphthoate of 29.3 g was obtained in the form of colorless oily substance.
Example 14
Production of 2'-�2"-(2"'-n-butoxyethoxy)-ethoxy!ethyl 2-benzyloxy-6-naphthoate
The same procedure as described in Example 11 was repeated, except that 2-�2'-(2"-n-butoxyethoxy)ethoxy!ethyl p-toluenesulfonate of 54.0 g was substituted for 2-n-butoxyethyl p-toluenesulfonate in Example 11, whereby 2'-�2"-(2"'-n-butoxyethoxy)ethoxy!ethyl 2-benzyloxy-6-naphthoate of 35.6 g was obtained in the form of colorless oily substance.
Example 15
Production of 1'-methylethyl 2-hydroxy-6-naphthoate
1'-methylethyl 2-benzyloxy-6-naphthoate of 16.0 g was dissolved in 2-propanol of 100 g and hydrogenated at 40.degree. C. in a hydrogen atmosphere at atmospheric pressure in the presence of 5 weight % Pd/C of 1 g. Pd/C was filtered off, and then 2-propanol was distilled off under reduced pressure, whereby 1'-methylethyl 2-hydroxy-6-naphthoate of 10.2 g was obtained in the form of colorless crystal.
Melting point: 110.0.degree. to 114.0.degree. C.
Example 16
Production of 2'-methylpropyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 2'-methylpropyl 2-benzyloxy-6-naphthoate of 16.7 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 2'-methylpropyl 2-hydroxy-6-naphthoate of 10.7 g was obtained in the form of colorless crystal.
Melting point: 112.5.degree. to 123.5.degree. C.
Example 17
Production of 3'-methylbutyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 3'-methylbutyl 2-benzyloxy-6-naphthoate of 17.4 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 3'-methylbutyl 2-hydroxy-6-naphthoate of 12.3 g was obtained in the form of colorless crystal.
Melting point: 119.5.degree. to 121.5.degree. C.
Example 18
Production of 4'-methylpentyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 4'-methylpentyl 2-benzyloxy-6-naphthoate of 18.1 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 4'-methylpentyl 2-hydroxy-6-naphthoate of 11.6 g was obtained in the form of colorless crystal.
Melting point: 73.0.degree. to 74.5.degree. C.
Example 19
Production of 1'-ethylpropyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 1'-ethylpropyl 2-benzyloxy-6-naphthoate of 17.4 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 1'-ethylpropyl 2-hydroxy-6-naphthoate of 11.6 g was obtained in the form of colorless crystal.
Melting point: 89.0.degree. to 92.0.degree. C.
Example 20
Production of 2'-ethylbutyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 2'-ethylbutyl 2-benzyloxy-6-naphthoate of 18.1 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 2'-ethylbutyl 2-hydroxy-6-naphthoate of 12.8 g was obtained in the form of colorless crystal.
Melting point: 96.5.degree. to 97.5.degree. C.
Example 21
Production of 1',1',5'-trihydroperfluoro-n-pentyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 1',1',5'-trihydroperfluoro-n-pentyl 2-benzyloxy-6-naphthoate of 24.6 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 1',1',5'-trihydroperfluoro-n-pentyl 2-hydroxy-6-naphthoate of 17.5 g was obtained in the form of colorless crystal.
Melting point: 105.0.degree. to 113.0.degree. C.
Example 22
Production of 1',1',7'-trihydroperfluoro-n-heptyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 1',1',7'-trihydroperfluoro-n-heptyl 2-benzyloxy-6-naphthoate of 29.6 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 1',1',7'-trihydroperfluoro-n-heptyl 2-hydroxy-6-naphthoate of 20.1 g was obtained in the form of colorless crystal.
Melting point: 123.0.degree. to 132.0.degree. C.
Example 23
Production of 2'-(perfluoro-n-butyl)ethyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 2'-(perfluoro-n-butyl)ethyl 2-benzyloxy-6-naphthoate of 26.2 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 2'-(perfluoro-n-butyl)ethyl 2-hydroxy-6-naphthoate of 18.6 g was obtained in the form of colorless crystal.
Melting point: 101.0.degree. to 103.0.degree. C.
Example 24
Production of 2'-(perfluoro-n-hexyl)ethyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 2'-(perfluoro-n-hexyl)ethyl 2-benzyloxy-6-naphthoate of 31.2 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 2'-(perfluoro-n-hexyl)ethyl 2-hydroxy-6-naphthoate of 21.4 g was obtained in the form of colorless crystal.
Melting point: 124.0.degree. to 127.0.degree. C.
Example 25
Production of 2'-n-butoxyethyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 2'-n-butoxyethyl 2-benzyloxy-6-naphthoate of 18.9 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 2'-n-butoxyethyl 2-hydroxy-6-naphthoate of 13.7 g was obtained in the form of colorless crystal.
Melting point: 54.0.degree. to 56.0.degree. C.
Example 26
Production of 2'-n-hexyloxyethyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 2'-n-hexyloxyethyl 2-benzyloxy-6-naphthoate of 20.3 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 2'-nhexyloxyethyl 2-hydroxy-6-naphthoate of 15.0 g was obtained in the form of colorless crystal.
Melting point: 67.0.degree. to 68.0.degree. C.
Example 27
Production of 2'-(2"-n-hexyloxyethoxy)ethyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 2'-(2"-n-hexyloxyethoxy)ethyl 2-benzyloxy-6-naphthoate of 22.5 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 2'-(2"-n-hexyloxyethoxy)ethyl 2-hydroxy-6-naphthoate of 15.3 g was obtained in the form of colorless crystal.
Melting point: 59.0.degree. to 62.0.degree. C.
Example 28
Production of 2'-�2"-(2"'-n-butoxyethoxy)ethoxy!ethyl 2-hydroxy-6-naphthoate
The same procedure as described in Example 15 was repeated, except that 2'-�2"-(2"'-n-butoxyethoxy)ethoxy!ethyl 2-benzyloxy-6-naphthoate of 23.3 g was substituted for 1'-methylethyl 2-benzyloxy-6-naphthoate in Example 15, whereby 2'-�2"-(2"'-n-butoxyethoxy)ethoxy!ethyl 2-hydroxy-6-naphthoate of 14.2 g was obtained in the form of colorless oily substance.
Example 29
Production of Exemplified Compound 15
Dissolved in chloroform of 5 g were 1'-methylethyl 2-hydroxy-6-naphthoate of 230 mg, 4-n-decyloxybenzoic acid of 278 mg, N,N'-dicyclohexylcarbodiimide of 247 mg and 4-pyrrolidinopyridine of 7 mg, and the solution was stirred at room temperature for 24 hours. By-produced N,N'-dicyclohexylurea was filtered off, and then chloroform was distilled off under reduced pressure to obtain a crude product. The crude product was refined with silica gel column chromatography (eluent: toluene) and further recrystallized twice from ethanol/ethyl acetate, whereby the intended product of 392 mg was obtained in the form of colorless crystal.
The phase transition temperatures of this compound are shown in Table 2.
Examples 30 to 114
The naphthalene compounds were produced in the same manner as described in Example 29, except that 2-hydroxy-6-naphthoic acid esters represented by Formula (3a) and various carboxylic acids represented by Formula (4), each shown in Table 1, were used.
The phase transition temperatures of these compounds are shown in Table 2.
TABLE 1__________________________________________________________________________Example No. Compound (4) R.sub.1 -(O).sub.z -A-COOH ##STR16##29 ##STR17## ##STR18##30 ##STR19## ##STR20##31 ##STR21## ##STR22##32 ##STR23## ##STR24##33 ##STR25## ##STR26##34 ##STR27## ##STR28##35 ##STR29## ##STR30##36 ##STR31## ##STR32##37 ##STR33## ##STR34##38 ##STR35## ##STR36##39 ##STR37## ##STR38##40 ##STR39## ##STR40##41 ##STR41## ##STR42##42 ##STR43## ##STR44##43 ##STR45## ##STR46##44 ##STR47## ##STR48##45 ##STR49## ##STR50##46 ##STR51## ##STR52##47 ##STR53## ##STR54##48 ##STR55## ##STR56##49 ##STR57## ##STR58##50 ##STR59## ##STR60##51 ##STR61## ##STR62##52 ##STR63## ##STR64##53 ##STR65## ##STR66##54 ##STR67## ##STR68##55 ##STR69## ##STR70##56 ##STR71## ##STR72##57 ##STR73## ##STR74##58 ##STR75## ##STR76##59 ##STR77## ##STR78##60 ##STR79## ##STR80##61 ##STR81## ##STR82##62 ##STR83## ##STR84##63 ##STR85## ##STR86##64 ##STR87## ##STR88##65 ##STR89## ##STR90##66 ##STR91## ##STR92##67 ##STR93## ##STR94##68 ##STR95## ##STR96##69 ##STR97## ##STR98##70 ##STR99## ##STR100##71 ##STR101## ##STR102##72 ##STR103## ##STR104##73 ##STR105## ##STR106##74 ##STR107## ##STR108##75 ##STR109## ##STR110##76 ##STR111## ##STR112##77 ##STR113## ##STR114##78 ##STR115## ##STR116##79 ##STR117## ##STR118##80 ##STR119## ##STR120##81 ##STR121## ##STR122##82 ##STR123## ##STR124##83 ##STR125## ##STR126##84 ##STR127## ##STR128##85 ##STR129## ##STR130##86 ##STR131## ##STR132##87 ##STR133## ##STR134##88 ##STR135## ##STR136##89 ##STR137## ##STR138##90 ##STR139## ##STR140##91 ##STR141## ##STR142##92 ##STR143## ##STR144##93 ##STR145## ##STR146##94 ##STR147## ##STR148##95 ##STR149## ##STR150##96 ##STR151## ##STR152##97 ##STR153## ##STR154##98 ##STR155## ##STR156##99 ##STR157## ##STR158##100 ##STR159## ##STR160##101 ##STR161## ##STR162##102 ##STR163## ##STR164##103 ##STR165## ##STR166##104 ##STR167## ##STR168##105 ##STR169## ##STR170##106 ##STR171## ##STR172##107 ##STR173## ##STR174##108 ##STR175## ##STR176##109 ##STR177## ##STR178##110 ##STR179## ##STR180##111 ##STR181## ##STR182##112 ##STR183## ##STR184##113 ##STR185## ##STR186##114 ##STR187## ##STR188##
TABLE 2 - Example Exemplified compound Phase transition temperature (.degree.C.) No. No. C S.sub.C S.sub.A N I 29 15 ##STR189## .multidot. 65 .multidot. (60) .multidot. 98 -- .multidot. 30 16 ##STR190## .multidot. 73 .multidot. (62) .multidot. 97 -- .multidot. 31 19 ##STR191## .multidot. 57 .multidot. (43) .multidot. 113 -- .multidot. 32 27 ##STR192## .multidot. 61 .multidot. (48) .multidot. 113 .multidot. 118 .multidot. 33 28 ##STR193## .multidot. 66 .multidot. (62) .multidot. 114 .multidot. 116 .multidot. 34 29 ##STR194## .multidot. 67 .multidot. (64) .multidot. 116 -- .multidot. 35 30 ##STR195## .multidot. 79 .multidot. (68) .multidot. 115 -- .multidot. 36 31 ##STR196## .multidot. 57 .multidot. (51) .multidot. 115 -- .multidot. 37 33 ##STR197## .multidot. 64 .multidot. (54) .multidot. 77 -- .multidot. 38 35 ##STR198## .multidot. 83 .multidot. (71) .multidot. 106 -- .multidot. 39 41 ##STR199## .multidot. 64 -- .multidot. (57) .multidot. 65 .multidot. 40 44 ##STR200## .multidot. 76 -- .multidot. 107 -- .multidot. 41 45 ##STR201## .multidot. 68 .multidot. (52) .multidot. 103 -- .multidot. 42 46 ##STR202## .multidot. 79 .multidot. (66) .multidot. 105 -- .multidot. 43 47 ##STR203## .multidot. 77 .multidot. (74) .multidot. 104 -- .multidot. 44 48 ##STR204## .multidot. 75 .multidot. (74) .multidot. 104 -- .multidot. 45 49 ##STR205## .multidot. 83 .multidot. (58) .multidot. 96 -- .multidot. 46 50 ##STR206## .multidot. 65 .multidot. (38) .multidot. (52) -- .multidot. 47 51 ##STR207## .multidot. 60 .multidot. (41) .multidot. (58) -- .multidot. 48 52 ##STR208## .multidot. 64 .multidot. (38) .multidot. (58) -- .multidot. 49 55 ##STR209## .multidot. 73 .multidot. 74 .multidot. 109 -- .multidot. 50 56 ##STR210## .multidot. 76 .multidot. 77 .multidot. 110 -- .multidot. 51 57 ##STR211## .multidot. 67 .multidot. (64) .multidot. 110 -- .multidot. 52 60 ##STR212## .multidot. 87 .multidot. (66) .multidot. 99 -- .multidot. 53 62 ##STR213## .multidot. 64 .multidot. 67 .multidot. 105 -- .multidot. 54 63 ##STR214## .multidot. 71 .multidot. 79 .multidot. 104 -- .multidot. 55 65 ##STR215## .multidot. 69 .multidot. .multidot. (53) .multidot. (55) .multidot. 56 66 ##STR216## .multidot. 75 .multidot. (72) .multidot. 94 -- .multidot. 57 67 ##STR217## .multidot. 68 .multidot. (55) .multidot. 78 -- .multidot. 58 68 ##STR218## .multidot. 83 .multidot. (56) .multidot. (78) -- .multidot. 59 72 ##STR219## .multidot. 56 .multidot. (48) .multidot. 67 -- .multidot. 60 86 ##STR220## .multidot. 75 .multidot. (58) .multidot. 108 -- .multidot. 61 106 ##STR221## .multidot. 79 .multidot. (72) .multidot. 105 -- .multidot. 62 107 ##STR222## .multidot. 86 .multidot. (77) .multidot. 107 -- .multidot. 63 148 ##STR223## .multidot. 103 -- .multidot. 127 -- .multidot. 64 149 ##STR224## .multidot. 96 .multidot. (88) .multidot. 148 -- .multidot. 65 150 ##STR225## .multidot. 103 -- .multidot. 170 -- .multidot. 66 152 ##STR226## .multidot. 112 .multidot. (111) .multidot. 228 -- .multidot. 67 161 ##STR227## .multidot. 80 .multidot. (76) .multidot. 99 -- .multidot. 68 162 ##STR228## .multidot. 81 .multidot. (78) .multidot. 115 -- .multidot. 69 163 ##STR229## .multidot. 102 .multidot. (77) .multidot. 138 -- .multidot. 70 164 ##STR230## .multidot. 120 .multidot. 140 .multidot. 206 -- .multidot. 71 185 ##STR231## .multidot. 91 .multidot. (88) .multidot. 108 -- .multidot. 72 187 ##STR232## .multidot. 79 .multidot. 88 .multidot. 110 -- .multidot. 73 188 ##STR233## .multidot. 72 .multidot. 87 .multidot. 104 -- .multidot. 74 189 ##STR234## .multidot. 93 .multidot. 103 .multidot. 133 -- .multidot. 75 190 ##STR235## .multidot. 82 .multidot. 110 .multidot. 124 -- .multidot. 76 191 ##STR236## .multidot. 93 .multidot. 110 .multidot. 116 -- .multidot. 77 193 ##STR237## .multidot. 84 .multidot. 136 .multidot. 157 -- .multidot. 78 194 ##STR238## .multidot. 89 .multidot. 138 .multidot. 150 -- .multidot. 79 195 ##STR239## .multidot. 83 .multidot. 137 .multidot. 146 -- .multidot. 80 196 ##STR240## .multidot. 89 .multidot. 134 .multidot. 141 -- .multidot. 81 197 ##STR241## .multidot. 87 .multidot. 130 .multidot. 136 -- .multidot. 82 202 ##STR242## .multidot. 102 .multidot. 150 .multidot. 176 -- .multidot. 83 203 ##STR243## .multidot. 96 .multidot. 151 .multidot. 164 -- .multidot. 84 204 ##STR244## .multidot. 101 .multidot. 146 .multidot. 152 -- .multidot. 85 207 ##STR245## .multidot. 116 .multidot. (92) .multidot. 123 -- .multidot. 86 216 ##STR246## .multidot. 116 .multidot. 132 .multidot. 134 -- .multidot. 87 220 ##STR247## .multidot. 52 .multidot. (35) .multidot. 57 -- .multidot. 88 221 ##STR248## .multidot. 66 -- .multidot. (59) -- .multidot. 89 224 ##STR249## .multidot. 48 -- .multidot. (36) -- .multidot. 90 232 ##STR250## .multidot. 83 .multidot. (72) .multidot. 95 -- .multidot. 91 233 ##STR251## .multidot. 74 .multidot. 89 .multidot. 126 -- .multidot. 92 236 ##STR252## .multidot. 57 .multidot. 87 .multidot. 115 -- .multidot. 93 244 ##STR253## .multidot. 71 .multidot. (50) .multidot. 88 -- .multidot. 94 245 ##STR254## .multidot. 71 -- .multidot. 90 -- .multidot. 95 248 ##STR255## .multidot. 72 -- .multidot. 86 -- .multidot. 96 249 ##STR256## .multidot. 74 -- .multidot. 87 -- .multidot. 97 257 ##STR257## .multidot. 60 -- .multidot. (57) -- .multidot. 98 258 ##STR258## .multidot. 65 -- .multidot. (60) -- .multidot. 99 306 ##STR259## .multidot. 112 .multidot. 164 .multidot. 243 -- .multidot. 100 308 ##STR260## .multidot. 105 .multidot. 143 .multidot. 225 -- .multidot. 101 309 ##STR261## .multidot. 117 .multidot. 186 .multidot. 231 -- .multidot. 102 310 ##STR262## .multidot. 102 .multidot. 151 .multidot. 218 -- .multidot. 103 316 ##STR263## .multidot. 117 .multidot. 186 .multidot. 227 -- .multidot. 104 318 ##STR264## .multidot. 76 .multidot. 162 .multidot. 204 -- .multidot. 105 323 ##STR265## .multidot. 134 .multidot. 181 .multidot. 212 -- .multidot. 106 335 ##STR266## .multidot. 111 .multidot. 139 .multidot. 204 -- .multidot. 107 340 ##STR267## .multidot. 71 .multidot. 132 .multidot. 180 -- .multidot. 108 345 ##STR268## .multidot. 74 .multidot. 135 .multidot. 178 -- .multidot. 109 346 ##STR269## .multidot. 32 .multidot. 111 .multidot. 152 -- .multidot. 110 363 ##STR270## .multidot. 109 .multidot. 119 .multidot. 170 -- .multidot. 111 364 ##STR271## .multidot. 91 .multidot. 120 .multidot. 156 -- .multidot. 112 403 ##STR272## .multidot. 90 .multidot. 116 .multidot. 148 -- .multidot. 113 460 ##STR273## .multidot. 111 -- -- -- .multidot. 114 521 ##STR274## .multidot. 88 -- -- -- .multidot.
Example 115
Preparation of Liquid Crystal Composition
The following compounds were blended in the ratio shown below and heated at 100.degree. C. to be dissolved, whereby a liquid crystal composition A (ferroelectric liquid crystal composition) was prepared. In the formulas, the mark "*" shows optically active carbon.
Phase transition temperatures (.degree.C.):
I.fwdarw.SA.fwdarw.Sc*.fwdarw.C
84 54 0.degree. C. or lower
Composition A
__________________________________________________________________________ ##STR275## 30% ##STR276## 30% ##STR277## 40%__________________________________________________________________________
Preparation of Liquid Crystal Element
Transparent electrodes and insulating orientation controlling layers made of polyimide were provided on two glass plates having a thickness of 0.7 mm, and alumina beads having an average particle diameter of 2 .mu.m were dispersed on one of the glass plates. Then, the glass plates were stuck together with sealant to prepare a cell shown in FIG. 1. This cell was charged with the liquid crystal composition prepared above after heating it to be in an isotropic phase, and the liquid crystal composition was gradually cooled down to be in a ferroelectric liquid crystal phase at a rate of 1.degree. C./minute, whereby a liquid crystal element was prepared. This liquid crystal element was interposed between two polarizing plates disposed in a cross-nicol state, and was applied a voltage of 20 V to detect an optical response (change in a transmitted light quantity: 10 to 90%), whereby the response time was determined. The measured results are shown in FIG. 2.
Example 116
Preparation of Liquid Crystal Composition
The following compounds were blended in the ratio shown below and heated at 100.degree. C. to be dissolved, whereby a liquid crystal composition B (ferroelectric liquid crystal composition) was prepared. In the formulas, the mark "*" shows optically active carbon.
Phase transition temperatures (.degree.C.):
I.fwdarw.SA.fwdarw.Sc*.fwdarw.C
88 60 0.degree. C. or lower
Composition B
__________________________________________________________________________ ##STR278## 30% ##STR279## 30% ##STR280## 40%__________________________________________________________________________
Preparation of Liquid Crystal Element
Transparent electrodes and insulating orientation controlling layers made of polyimide were provided on two glass plates having a thickness of 0.7 mm, and alumina beads having an average particle diameter of 2 .mu.m were dispersed on one of the glass plates. Then, the glass plates were stuck together with sealant to prepare a cell shown in FIG. 1. This cell was charged with the liquid crystal composition prepared above after heating it to be in an isotropic phase, and the liquid crystal composition was gradually cooled down to be in a ferroelectric liquid crystal phase at a rate of 1.degree. C./minute, whereby a liquid crystal element was prepared. This liquid crystal element was interposed between two polarizing plates disposed in a cross-nicol state, and was applied a voltage of 20 V to detect an optical response (change in a transmitted light quantity: 10 to 90%), whereby the response time was determined. The measured results are shown in FIG. 2.
Comparative Example
Preparation of Liquid Crystal Composition
The following compounds were blended in the ratio shown below and heated at 100.degree. C. to be dissolved, whereby a liquid crystal composition C (ferroelectric liquid crystal composition) was prepared. In the formulas, the mark "*" shows optically active carbon.
Phase transition temperatures (.degree.C.):
I.fwdarw.SA.fwdarw.Sc*.fwdarw.C
80 52 0.degree. C. or lower
Composition C
__________________________________________________________________________ ##STR281## 30% ##STR282## 30% ##STR283## 40%__________________________________________________________________________
Preparation of Liquid Crystal Element
Transparent electrodes and insulating orientation controlling layers made of polyimide were provided on two glass plates having a thickness of 0.7 mm, and alumina beads having an average particle diameter of 2 .mu.m were dispersed on one of the glass plates. Then, the glass plates were stuck together with sealant to prepare a cell shown in FIG. 1. This cell was charged with the liquid crystal composition prepared above after heating it to be in an isotropic phase, and the liquid crystal composition was gradually cooled down to be in a ferroelectric liquid crystal phase at a rate of 1.degree. C./minute, whereby a liquid crystal element was prepared. This liquid crystal element was interposed between two polarizing plates disposed in a cross-nicol state, and was applied a voltage of 20 V to detect an optical response (change in a transmitted light quantity: 10 to 90%), whereby the response time was determined. The measured results are shown in FIG. 2.
It has been found from the comparison of the examples of the present invention with the comparative example each shown in FIG. 2 that while the response time is 55 .mu.sec at 25.degree. C. in the liquid crystal composition C, it is 40 .mu.sec in the liquid crystal compositions A and B and therefore the response time is shortened. With respect to a variation in the response time at 20.degree.-40.degree. C., while the response time at 20.degree. C. is about five times as long as the response time at 40.degree. C. in the liquid crystal composition C, a variation in the response time is about four times in the liquid crystal compositions A and B. Accordingly, it can be found that the liquid crystal compositions of the present invention have less temperature dependency on the response time.

Number	Date	Country	Kind
7-171665	Jul 1995	JPX
7-331383	Dec 1995	JPX

Number	Name	Date
4680137	Isoyama et al.	Jul 1987
4696759	Isoyama et al.	Sep 1987
5082587	Janulis	Jan 1992
5190688	Sage et al.	Mar 1993
5194177	Nohira et al.	Mar 1993
5196140	Poetsch et al.	Mar 1993
5246622	Shimizu et al.	Sep 1993
5254747	Janulis	Oct 1993
5262082	Janulis et al.	Nov 1993
5310500	Aihara et al.	May 1994
5495037	Hsu et al.	Feb 1996

Number	Date	Country
0458320	Nov 1991	EPX
0518636	Dec 1992	EPX
56-107216	Aug 1981	JPX
59-118744	Jul 1984	JPX
61-195187	Aug 1986	JPX
63-246346	Oct 1988	JPX
1-193390	Aug 1989	JPX
3031392	Feb 1991	JPX
3-68686	Mar 1991	JPX
3-106850	May 1991	JPX

Naphthalene compound, and liquid crystal composition and liquid crystal element using the same

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US Referenced Citations (11)

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Non-Patent Literature Citations (10)

Entry
Patent Abstracts of Japan, vol. 015, No. 154, (C-0825), Apr. 18, 1991 & JP 03031392 A, (Mitsui Toatsu Chemicals, Inc.), Feb. 12, 1991 Abstract.
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Gray et al, "The Preparation of 4-and 5-n-Alkoxy-1-Naphthoic and 6-and 7-n-Alkoxy-2-Naphthoic Acids", J. Chem. Soc., 1954, pp. 678-683.
Gray et al, "Mesomorphism and Chemical Constitution. Part III, The Effect of Halogen Substitutes on the Mesomorphism of the 4-Alkoxybenzoic Acids", J. Chem. Soc., 1954, pp. 2556-2562.
Gray et al, "Mesomorphism and Chemical Constitution, Part V, the Mesomorphic Properties of the 4'-n-Alkoxydiphenyl-4-Carboxylic Acids and Their Simple Alkyl Esters",J. Chem. Soc., 1955, pp. 1412-1420.
Gray et al, "Mesomorphism and Chemical Constitution. Part VIII, The Effect of 3'-Substituents on the Mesomorphism of the 4'-n-Alkoxydiphenyl-4-Carboxylic Acids and Their Simple Alkyl Esters",J. Chem. Soc., 1957, pp. 393-394.
Gray et al, "The Mesomorphic Transition Temperatures of 3'-Substituted 4'-n-Octyloxydiphenyl-4-Carboxylic Acids", J. Chem. Soc., 1959, pp. 1545-1550.