GB2280445A

GB2280445A - Liquid crystalline copolymer

Info

Publication number: GB2280445A
Application number: GB9413130A
Authority: GB
Inventors: Owain Llyr Parri; Ian Bonny; Ian Victor E Hassall; Mark John Goulding; Simon Greenfield; Emma Jane Brown; David Coates
Original assignee: Merck Patent GmbH
Current assignee: Merck Patent GmbH
Priority date: 1993-07-05
Filing date: 1994-06-30
Publication date: 1995-02-01
Anticipated expiration: 2014-06-30
Also published as: GB2280445B; GB9413130D0

Abstract

The invention relates to copolymers made from mono reactive liquid and/or di reactive liquid crystals which can be photopolymerised to form copolymers and to novel reactive liquid crystal compounds having a nematic phase. Preferably the reactive liquid crystal is polymerised while in the liquid crystal phase to produce an oriented birefringent polymer film. To do this the reactive liquid crystal, in its nematic or smectic phase is aligned (by well known techniques such as rubbed polyimide etc.) and the thin film containing a small amount of photoinitiator, is subjected to ultra-violet light whereupon it polymerises into a thin, aligned polymer film. Some of the monomers are claimed to be novel.

Description

LIQUID CRYSTALLINE COPOLYMER The invention relates to copolymers made from mono reactive liquid and/or di reactive liquid crystals which can be photopolymerised to form copolymers and to novel reactive liquid crystal compounds having a nematic phase. Preferentially the reactive liquid crystal is polymerised while in the liquid crystal phase to produce an oriented birefringent polymer film. To do this the reactive liquid crystal, in its nematic or smectic phase is aligned (by well known techniques such as mobbed polyimide etc.) and the thin film containing a small amount of photoinitiator, is subjected to ultra-violet light whereupon it polymerises into a thin, aligned polymer film.

Alternatively the mixture of reactive liquid crystal can be polymerised in a solution of for example dichloromethane or toluene or tetrahydrofuran, using AIBN as initiator and heated for 24 hours at 30-60 "C. This produces a non aligned polymer which is less easily manipulated than the polymer film but may have other applications.

Most reactive liquid crystals presently known exhibit a high melting point and a very short temperature range phase, also many are only smectic.

This severely limits the use of these materials. The authors have found new materials which exhibit a relatively low melting point and wide liquid crystal phase range particularly nematic. Advantageously, these can be mixed together to produce low melting, wide range nematic reactive liquid crystal mixtures. By changing the types of core group the optical properties of the film can be changed e.g. high birefringence core groups lead to films with a high birefringence. By changing the ratio of mono:di reactive groups the Tg of the system can be altered.

The incorporation of chiral groups into the reactive liquid crystal produces cholesteric phases. Typically this is done by the incorporation of a chiral alkyl chain but a chiral group between ring systems can also be used. By changing the amount of chiral reactive liquid crystal the pitch length of the cholesteric phase can be altered. Generally, when polymerised there is very little change in pitch length. It is also possible to add non reactive materials containing a chiral group to induce a cholesteric phase.

It was therefore necessary to develop a completely new material concept in order to fulfill the requirements outlined above resp. to fulfill them to a greater extent than is the case with conventional liquid crystal polymers.

Other objects of the present invention are evident for the expert from the following detailed description of the invention.

It was found that these objects could be achieved by the copolymers according to the present invention.

The invention thus relates to a liquid crystalline copolymer obtainable by copolymerization of at least one polymerizable reactive component A of formula R1-P-X-A1-z1-A2-R2 (I) wherein R1 is

HWN-, CH2=CH- or HS-CH2-(CH2)m-COO- with W being H, Cl or alkyl with 1-5 C atoms and m being 1-7 P is alkylene with up to 12 C atoms, it being also possible for one or more non adjacent CH2 groups to be replaced by 0-, X is -O-, -S-, -COO-, -OCO-, -CZC- or a single bond, R2 is a straight-chained, branched or chiral alkyl radical with up to 15 C atoms which is unsubstituted, mono- or polysubstituted by halogen, it being also possible for one or more CH2 groups in these radicals to be replaced, in each case independently of one another, by -O-, -S-, -CO-, -OCO-, -CO-O- or -O-CO-O- in such a manner that oxygen atoms are not linked directly to one another, or alternatively R2 has one of the meanings given for R1-P-X-, A1 is a 1 ,4-cyclohexylene, a 1 ,4-phenylene in which one or two CH groups may be replaced by N or a naphthalene-2,6 diyl radical which is unsubstituted or substituted by 1 to 4 halogen atoms, A2 is

it being possible for these rings to be substituted by CN or halogen and one of the 1 ,4-phenylene groups can also be replaced by a 1 ,4-phenylene radical in which one or two CH groups are replaced by N, and Z and Z are each independently -CO-O-, -O-CO-, -CH2CH2-, -C#C- or a single bond, n is Oor1, and at least one polymerizable component B of formula Il

wherein R1, P, X and the meaning give for formula I, and Q has the meaning given for formula I, and Y is -H, -F or-CI, Q is -CF2, -OCF2, -C2F4, or -OC2F4, or a single bond, if Y is F or Cl AS and A4 are each independently (c) 1 ,4-phenylene radical in which one or two CH groups can be replaced by N, (d) a 1,4 cyclohexylene radical in which one or two non adjacent CH2 groups can be replaced by -O- or -S-, or (e) a naphthalene-2,6-diyl radical, a piperidine-1,4-diyl radical, a thiophene-2,5-diyl radical, a 1,3,4 thiadiazol-2,5 diyl radical, it being possible for radicals (c) and (d) to be substituted by CN or halogen, is, independently of one another, -CH2CH=, -COO-, -OCO-, C=C- or a single bond, Z4 is is -CH2CH2-, -C#C- or a single bond, L1 through L4 are each independently H, halogen, -CH3, -CF3 or -CN, preferably H or fluorine.

o is 0, 1 or 2, and the groups A3 being same or different in the case that o is 2.

The polymeric composite materials according to the present invention are being based on a liquid crystal copolymer. The liquid crystal copolymer can consist of one liquid crystal copolymer resp. oligomer or a mixture of two or more liquid crystal copolymers and/or oligomers of different chemical composition. Mixing can be effected by solving the different liquid crystal copolymers and/or oligomers in a suitable solvent like, for example, dichloromethane (DCM), with subsequent evaporation of the solvent or by other methods.

The liquid crystal copolymers used are side chain copolymers and/or oligomers of formula A

wherein Pm is a polymer main chain group SP is a bivalent spacer group, B is an organic rod-like radical containing at least two six membered groups, including the radicals of formula I' -A1-Z1-A2- R2(l') and of formula II'

< m > is the mean degree of polymerization.

Formula A is merely intended to symbolize side-chain copolymers in a relatively diagrammatic manner; thus, it is not necessary, for example, for each main-chain unit to carry a mesogenic unit, and it is also possible, for example, to use copolymers in which Pm represents various main-chain units. Furthermore, Pm or, in the case of copolymers, one or more groups Pm may be one or more mesogenic groups, so that formula I also covers combined main-chain/side-chain oligomers and polymers.

A good review on side-chain polymers and processes for their preparation is given by H. Finkelmann in Thermotropic Liquid Crystals, ed. by G.W.

Gray, Chichester 1987, p. 159 ff, which describe the preparation of side chain polymers by'solution polymerisation'.

If a mixture of 2 or more liquid-crystalline oligomers and/or polymers is used, < m > is the arithmetic mean of the mean degrees of the mean degrees of polymerization of the various components of the polymer phase.

Liquid-crystalline copolymers may be liquid-crystalline or not; in case they are liquid-crystalline they may have various phases, a correlation frequently being observed for side-chain polymers containing mesogenic groups B which are not too polar between the phase sequence of the corresponding low-molecularweight compounds B and that of the sidechain polymers (see Thermotropic Liquid Crystals, ed. by G.W. Gray, Chichester 1987, p. 164). Liquid-crystalline polymers and in particular side-chain polymers having a nematic and/or smectic phase and further particularly having a nematic phase are preferred, the terms nematic and smectic being broadly drawn and also covering cholesteric-nematic and cholesteric-smectic phases having a helical structure.

Suitable polymeric backbones -(-Pm-)- are in principal all polymers whose chains have a certain flexibility. These may be linear, branched or cyclic polymer chains. The degree of polymerization is normally at least 10 and in particular at least 15; however, oligomers containing 3 to 15 monomer units are also possible.

The polymers obtainable by solution polymerization show as a mle a degree of polymerization of 10-100. The polymers obtainable by in situ photopolymerization, which are a preferred embodiment of this invention exhibit as a rule a degree of polymerization which is higher than 100, preferably higher than 400, in particular higher than 500.

Preference is given to polymers containing C-C main chains, in particular polyacrylates, polymethacrylates, poly-a-halo-acrylates, poly-acyanoacrylates, polyacrylamides, polyacrylonitriles or polymethylene malonates. Further preference is also given to polyesters, polyamides, polyimides, polyphophazenes, polyurethanes, and, in particular, to polysiloxanes.

Suitable spacers are in particular linear or branched alkylene groups having 1-12 and, in particular, 1-8 carbon atoms, in which, in addition, one or more non-adjacent CH2 groups may be replaced by -O-, -S-, -O-CO-, CO-O-, -CH-, or-C-C-.

Examples of suitable spacers are the following groups: ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, nonylene, decyiene, undecylene, dodecylene, octadecylene, ethyleneoxyethylene, methyleneoxybutylene, ethylene-thioethylene, ethylene-N-methyliminoethylene and 1-methyl- alkylene.

The rod-like mesogenic groups are generally low-molecular-weight liquidcrystalline radicals which are bonded terminally or laterally to the polymer chain via sufficiently flexible spacers. In the case of terminal linking, which is generally preferred, these radicals are able to rotate about the molecular long axis and therefore have cylindrical symmetry.

The formula I' covers the bicyclic and tricyclic radicals of the sub-formulae 1'1 - 1'2:

The formula II' covers bicyclic, tricyclic and tetracyclic radicals of the subformulae II'1-II'3.

In the mesogenic radicals of the formula 1', R2 is preferably an alkyl or alkenyl radical which is unsubstituted or substituted by at least one halogen atom, it being possible for one or two non-adjacent CH2 groups of these radicals to be replaced by 0 atoms and/or by -O-CO-, -CO-O and/or-O-CO-Ogroups, Y1 is preferably For Cl.

Furthermore, the mesogenic radicals of the formula II' in which Q-Y is F or Cl are preferred.

If R2 is an alkyl radical or alkoxy radical, this may be straight-chain or branched. It is preferably straight-chain, has 2, 3, 4, 5, 6, 7 or 8 carbon atoms and accordingly is preferably ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, ethoxy, propoxy, butoxy, pentoxy, hexoxy, heptoxy or octoxy, furthmore methyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, methoxy, nonoxy, decoxy, undecocy, dodecocy, tridecoxy or tetradecoxy.

Oxaalkyl is preferably straight-chain 2-oxapropyl (= methoxymethyl), 2 (= ethoxymethyl) or 3-oxabutyl (= 2-methoxyethyl), 2-, 3- or 4-oxapentyl, 2-, 3-, 4- or 5-oxahexyl, 2-, 3-, 4-, 5- or 6-oxaheptyl, 2-, 3-, 4-, 5-, 6- or 7oxaoctyl, 2-, 3-, 4-, 5-, 6-, 7- or 8-oxanonyl, or 2-, 3-, 4-, 5-, 6-, 7-, 8- or 9-oxdecyl.

If R2 is an alkenyl radical, this may be straight-chain or branched. It is preferably straight-chain and has 2 to 20 carbon atoms. Accordingly, it is particularly vinyl, prop-1- or-2-enyl, but -1-, -2- or-3-enyl, pent-1-, -2-, -3or -4-enyl, hex-1 -2-, -3-, -4- or -5-enyl, hept-1 -2-, -3-, -4-, -5- or -6enyl, oct-i -2-, -3-, -4-, -5-, -6- or 7-enyl, non-i -2-, -3-, -4-, -5-, -6-, -7or -8-enyl, or dec-i -2-, -3-, -4-, -5-, -6-, -7-, -8- or -9-enyl.

Mesogenic radicals of the formula 1' containing a branched wing group RI may occasionally be of importance as comonomers, for example due to a reduction in the tendency towards crystallization. Branched groups of this type generally contain not more than one chain branch.Preferred branched radicals Rt are isopropyl, 2-butyl (= 1 -methylpropyl), isobutyl (= methylpropyl), 2-methylbutyl, isopentyl (= 3-methylbutyl), 2-methylpentyl, 3-methylpentyl, 2-ethylhexyl, 2-propylpentyl, 2-octyl, isoprpoxy, 2-methylpropoxy, 2-methylbutoxy, 3-methylbutoxy, 2-methylpentoxy, 3-methylpentoxy, 2-ethylhexoxy, 1-methylhexoxy, 2-octylloxy, 2-oxa-3methylbutyl, 3-cxa-4-methylpentyl, 4-methylhexyyl, 2-nonyl, 2-decyl, 2-dodecyl, 6-methoxyoctoxy, 6-methyloctanoyloxy, 5-methylheptyloxycarbonyl, 2-methylbutyryloxy, 3-methylvaleryloxy, 4-methylhexanoyloxy, 2-chloropropionyloxy, 2-chloro-3-methylvaleryloxy, 2-methyl3-oxapentyl and 2-methyl-3-oxahexyl.

Bicyclic, tricyclic and tetracyclic mesogenic radicals are preferred. Furthermore preferred are radicals which contain not more than one piperidine 1 ,4-diyl group or naphthalene-2,6-diyl group.

Of the mesogenic radicals of the formulae I' and II' which contain a heterocyclic groups, those containing a pyridine-2,5-diyl group, pyridazine2,5-diyl group, pyrimidine-2,5-diyl group or piperidine-1 ,4-diyl group are particularly preferred.

A smaller group of particularly preferred mesogenic radicals of the formulae 1', 1'2, 11'1 and 11'2 are listed below. For reasons of simplicity, Cyc denotes a 1 ,4-cyclohexylene group, Dio denotes a dioxane-2,5-diyl group, Cy denotes a 1 ,4-cyclohexylene group in which, in addition, one or two adjacent CH2 groups may be replaced by -O-, Phe denotes a 1,4phenylene group in which, in addition, one or more CH groups may be replaced by N, PheX denotes a 1 ,4-phenylene group which is monosubstituted or disubstituted by F, Cl and/or CH3, Pip denotes a piperidine-1,4diyl group and Nap denotes a naphtalene-2,6-diyl group.

Particularly preferred mesogenic radicals of the sub-formula 1'1 are those of the sub-formulae I' 1-1 to 1' 1-8: R-Cyc-Z-Cyc- I' 1-1 R-Phe-Z-Phe- I' 1-2 R2-Phe-Zl-PheX- I' 1-3 R-Phe-Z-Cyc- I' 1-4 R2-Cyc-Z1-Phe- I' 1-5 R-Cyc-Z-PheX- I' 1-6 R-Cyc-Z-PheX- I' 1-7 RPheX-ZI-Phe- I' 1-8 In the compounds of the sub-formulae I' 1-1 to 1' 1-8, R2 is very particularly preferably an aikyl or alkenyl group, furthermore alkoxy or alkanoyloxy, in each case having 1-13 carbon atoms. Furthermore, Z2 in these compounds is very particularly preferably an ester group (-CO-O- or -O- CO-), -CH2CH2- or a single bond.

Particularly preferred mesogenic radicals of the sub-formula 1'2 are those of the sub-formulae 1' 2-1 to 1' 2-16: R2-Phe-Z2-Phe-Z2-Phe 1' 2-1 R2-PheX-Z2-Phe-Z2-Phe- 1' 2-2 R2-Phe-Z2-Phe-Z2-PheX- I' 2-3 R-Cyc-Z-Cyc-Z-Cyc- I' 2-4 R-Cyc-Z-Phe-Z-Phe- I' 2-5 R2-Cyc-Z2-Cyc-Z2-Phe- It 2-6 R-Cyc-Z-Cyc-Z-Dio- I' 2-7 R2-Cyc-Z2-Phe-Z2-PheX- I' 2-8 R2-Cyc-Z2-Cyc-Z2-PheX- I' 2-9 R-Nap-Z-Cyc-Z-Phe- I' 2-10 R-Cy-Z-Phe-Z-Phe- I' 2-11 R-Nap-Z-Cyc-Z-Cyc I' 2-12 R-Phe-Z-Cyc-Z-Cyc- I' 2-13 R-Cyc-Z-Phe-Z-Cyc- I' 2-14 R-Cyc-Z-PheX-Z-Cyc- I' 2-15 Of the compounds of the sub-formulae 1' 2-1 to 1' 2-16 which contain a 1 ,4phenylene group in which one or two CH2 groups have been replaced by N, those containing a pyridine-2,5-diyl group or pyrimidine-2,5-diyl group are very particularly preferred.

Particularly preferred mesogenic radicals of the sub-formula Ilti are those of the sub-formulae II' 1-1 to II' 1-6 (PheL denotes a group of formula

YI-Q-PheL-Z4Phe- II' 1-1 Z-Q-PheL-Z4-Cyc- II' 1-2 YI-Q-PheL-Z4PheX- Il' 1-3 Y1-Q-PheL-Z6Dio- II' 1-4 Y-Q-PheL-Z4-Pip- II' 1-5 Y-Q-PheL-Z4-Nap- II' 1-6 Particular preferred mesogenic radicals of sub-formula II' 2 are those of the sub-formulae II' 2-1 to II' 2-9:: Y-Q-PheL-Z4-Phe-Z -Phe- II' 2-1 Y-Q-PheL-Z4-Phe-Z -Cyc- II' 2-2 Y-Q-PheL-Z4-Cyc-Z -Cyc- II' 2-3 Y-Q-PheL-Z4-PheX-Z -Phe- II' 2-4 Y-Q-PheL-Z4-PheX-Z -Cyc- II' 2-5 Y-Q-PheL-Z4-PheX-Z -PheX- II' 2-6 Y1-Q-PheL-ZPhe-Z=PheX- II' 2-7 Y1-Q-PheL-Z6Phe-Z=Nap- Il' 2-8 Y-Q-PheL-Z4-PheX-Z -Nap- II' 2-9 In the compounds of the sub-formulae 11' 2-1 to 11' 2-9, at least one of the two groups Z4 and Z3 is very particularly preferably a single bond or CH2CH2 and the other is preferably also a single bond or -CO-O- or -O- C.

Liquid-crystalline side-chain polymers are prepared by polymerization processes which are known per se and are described in the literature (for example in the standard works such as Ocian, Principles of Polymerization, McGraw-Hill, New York), to be precise under reaction conditions which are known and suitable for the reactions. Use may also be made here of variants which are known per se, but are not described here in greater detail.

Obtaining a liquid crystal copolymer with a sufficiently high glass transition temperature is routine work for the expert, and does not require any inventive effort, in particular in case the liquid crystal copolymer is being based on side chain polymers and/or oligomers according to formulae I and II. It is, for example, well known among experts that the glass transition temperature of liquid crystalline polymers and/or oligomers can be increased if the length of the spacer is chosen to be rather short, for example, as 02-06 and, in particular, C2-C4, and/or if a rather "stiff" polymer backbone like, for example, a polymethacry- late, or a poly-ahaloacrylate is used. The glass transition temperature of the liquid crystal polymer component can also be increased by adding a high-TG liquid crystal polymer to a given base mixture.

The copolymer preferably exhibits a nematic, cholesteric or smectic phase; the clearing point is preferably somewhat higher than the glass temperature, in particular, 5-25 C, in order to have a sufficient temperature range of processing. Outside the temperature range of processing, the mixture can be liquid-crystalline or not liquid-crystalline.

It is usually sufficient if one of the liquid crystal copolymer components exhibits one or more liquid crystal states, in particular in the temperature range of processing since it was frequently observed that the reactive liquid crystalline component induces a liquid crystalline phase in the resulting mixture. Mixtures wherein both the liquid crystal copolymer components exhibit one or more liquid crystalline states are particularly preferred while mixtures wherein none of these components is liquidcrystalline, are usually less preferred.

In the case where the copolymer is formed in solution, it could be used by dissolving in a suitable solvent e.g. toluene and coating onto a substrate (with no alignment layer). Upon evaporation of the solvent and subsequent heating to the isotropic phase of the copolymer, followed by slow cooling, a scattering texture is produced. For this to occur the copolymer must have a clearing point > 10 C above Tg which ideally should be above ambient temperature. If a suitable dye is incorporated into the copolymer film the film can be locally heated into the isotropic liquid (wrilten on) using a laser beam. On fast c;ooling the written areas remain 'clear' and the clear state is locked in by cooling by Tg. Such devices exhibit permanent storage etc.

The copolymers obtained are especially useful for permanent data storage. Verbal information, symbols, diagrams etc. can be written in by heating the desired parts of the composite material with a finely focussed laser beam or other heat sources to temperatures above the glass transition resp. clearing temperature thus rendering the composite material transparent. The transparent state can be maintained by rapidly cooling the composite material below the glass transition temperature of the composite material, and the information is depicted in form of transparent characters, symbols etc. on a scattering background.

Heating should be effected rather rapidly in order to avoid dissipation of the thermal energy; heating with laser energy therefore is usually especially preferred. The composite materials according to the present invention sometimes exhibits no precise clearing temperature but the become progressively clearer in a temperature range of, for example, 1020 "C, and the maximum temperature is preferably adjusted in such a way that a high transparency and thus a high contrast is obtained.

Subsequently, the material is cooled below the glass transition temperature with a high cooling rate in order to avoid restoration of the scattering state; the cooling rate preferably is not less than 20 K/min and, in particular, more than 40 Klmin; these values are, however, thought to be only illustrative and by no means limitative.

The copolymer can preferably be used, for example, as master-fiche in card-indices, as permanent overhead sheet etc. and is thus of enormous economic importance.

The polymerizable reactive components A and B are partly known and partly novel. thus the invention relates to novel polymerizable, reactive liquid crystal compound of formulae I or Il in particular, wherein X is -C C .

Furthermore the invention relates to polymerizable, reactive liquid crystal compound of formula la

wherein RI, R2, P, - B - and X have the meaning given, and Z2 is -CH2CH2- or a single bond, preferably -CH2CH2

in particular compounds of formula lal and la2:

and of formula Ib

wherein R1, R2, P,

and X have the meaning given, and Z2 is -CH2-CH2- or a single bond, or in the case that Lo is Cl Z2 denotes also -O-CO

denotes a 4,4'-biphenyidiyl group being optionally substituted by p fluorine or chlorine atoms, and p is 0 or an integer between 1 and 4 in particular of formulae lb1 and lb2

Preferred embodiments of the invention are: a) polymerizable reactive liquid crystal compounds wherein R2 is achiral; b) polymerizable reactive liquid crystal compound of formula II, wherein Q-Y is F, Cl, -OCF3, -OCF2H, -CF3 or OC2F5, in particular F or Cl; c) polymerizable reactive liquid crystal compounds of formulae Ila or lib

wherein R1, P, X, Q, Y and p have the meaning given, is iS -CH2CH2 of a single bond, and q and r are each independently 0 or an integer selected from 0 to 4; d) polymerizable reactive liquid crystal compounds of formula I, wherein X iS-CiC-, or of formulae la and lb, of formula II, wherein Q-Y1 is F, Cl, OCF3, -OCF2H, -CF3, -OC2F5, of formula llb wherein R1 is CHTCW-COO- with W being H, Cl or CHs.

A further aspect of the invention are liquid crystalline polymers obtainable by polymerization of at least one of the inventive polymerizable reactive liquid crystal compounds.

A further aspect of the invention are liquid crystalline polymers obtainable by substance photo-polymerization of at least one polymerizable reactive liquid crystal compound of formulae I or II, in the presence of a photoinitiator, at least one of said reactive liquid crystal compounds being oriented in its liquid crystalline phase, preferably in its nematic phase.

Liquid crystalline (co-)polymers obtainable by polymerization in the presence of a plastificiser, in particular a dialkylphtalate, or a chiral dopant, in particular a chiral cyanobiphenyl or phenyl benzoate, a menthol or lactic acid derivative, are preferred.

The invention relates to the use of a liquid crystalline (co)polymer according to the invention in the field of integrated optics, opto-electronic and/or information storage.

These reactive liquid crystals (RLC) can be used for either of two main uses: 1) Conversion into side chain liquid crystallinepolymers (SCLCP) in solution.

2) In-situ photopolymerisation of the RLC when oriented in their liquid crystalline phase.

Conversion Into SCLCP The RLC may be dissolved in a suitable solvent and the polymerisation initiated. This may be done with various initiator depending on the nature of the reactive group.

For example, when the reactive group is an acrylate, radical polymerisation initiated thermally may be used to obtain the polymer.

Reference: C.B. McArdle in "Side chain liquid crystalline polymers" (1989) Blackie & Son Ltd ISBN 0-216-92503-7 In-situ photopolymensation In this instance, the monomers are heated to their LC phase, aligned on a substrate and subsequently photopolymerised whilst still in the aligned LC phase. This gives an anisotropic polymer film.

RM U.V. light +

Polymer film Photoinitiator D.J. Broer, "In-Situ Photopolymerisation of Oriented Liquid Crystalline Acrylates" (1990) D.J. Broer, Die Angewandte Makromolekulare Chemie (1990), 183 45.

These oriented polymers may be used for several passive and active optical components: (EP 0 397 263), (EP 0 428 213) or (EP 0 451 905).

The inventive reactive compounds can be made according to the following reaction schemes: Scheme 1 R-P-X-A-COOH

HO.A2.R2 Trifluoroacetic and ride Dichloromethane (TFAA) room temperature 20 hrs (yield 80-98 %) R-P-X-A-COO-A-R Scheme 2

F AlOl3 F R2CH2COCI + OCH3 e R2)CHZr0OCH, H2 F F n2 29 CH2CH240CH3 H R2w-CH2CH2tFOH F H 2 22 2CF3 + (HO)2BOCH2 Pd[P(Ph)4 l Na2CO3/toluene R2 02H4 4)m OBz R2 C2H4 $mo OH H R2c2)ThOO(cH2)nOH - R2 C2H4 ẏ O(CH2)QCCH=CH2 Scheme 3

F F Pd[P(Ph)314 OCHO ()0B(OH)2 + Br-OY' -------+ (o) Na,cotoruene F (+C20 F H2 CH2O H2 F F HO-( Q Q-Y' F F r HO-(CH,),O-(--Q-Y' F F cH?CWCQ(CH2)nO( O-Yi F F Pd[P(Ph)314 CH,oBr + (HO)2BOOOY Na2C03/toluene F F < +CH20 < > -Qy H2 FF HO HO < QY' 000 QYi CH2=CW-CO2(CH2)nO < QY Scheme 4

[X = halogen, CN, etc.]

R is alkyl with up to 18 C-atoms, Bz is benzyl, (F) denotes an optional fluorine substitution Scheme 5

Scheme 6

The following examples are intended to be illustrative but by no means limitative.

Example 1 Preparation of

Quantities

230.5 C5H.l+CliCOCI 100 g a 3.0368 m F 126 XOCH3 374g - 2.961 m 133.5 AlOl3 426g 3.188m DCM 3.5 L The AICI3, o-fluoroamide and DCM (2 1) were charged into a 10 1 flask fitted with stirrer, dropping funnel and thermometer which was vented to a scrubber. This mixture was then cooled to 10 C and the acid chloride in DCM (1-5 l) was added maintaining the temperature below 15 "C. On addition the mixture was allowed to achieve room temperature, with stirring, overnight. Checked by TLC.Slight amount of anesole remaining, insignificant. Reaction mixture poured onto ice, 1-5 kg and ice allowed to melt Aqueous removed and extracted with DCM (3 x 500 ml). Organics combined and washed to neutral with water before drying over Na2SO4, filtering and evaporating to dryness. Crude, hot liquid then diluted with MS (21) and mixture heated, hot filtered and left to crystallize.

Yield = 655 9

650 g E 2.03 moles Potassium hydroxide 162.5 g = 1/4 wts Hydrazine hydrate 715 mls - 1.1 v Digol 3.757 # 5.5 v The starting materials were charged into a 20 1 flange top flask sited on a mantle and fitted with an air stirred and reflux condenser. The mixture was then heated to -138 C and refluxed for two hours. The condenser was then rearranged and the mixture heated to 190 C, collecting the distillate. The condenser was then changed back and the mixture stirred and refluxed for 20 hours.

Sample taken out and checked by AC, reaction complete. Mixture poured onto ice (2 kg), acidified and extracted with DCM (3 x 1 I).

Organics combined and washed to neutral with water. Dried, fiitered and evaporated to dryness.

Analysis by GC showed that not only had the starting material been reduced by it had been totally demethylated as well.

Yield crude = 640 g (14 % by GC) Distilled yield = 360 g Quantities 71 9

(C.J. Broer et al., Makromol.

Chem. (1989) 190. 2255) 0.1 ml dimethylformamide (DMF) 40 ml diethyl ether 2.7 ml SOC12 40 ml water 20 ml brine 0.022 mol Phenol W 40 ml DCM 4.6 ml triethylamine To a mixture of 71 g hydroxyhexoxybenzoic acid (methacrylate ester) dimethylformamide and 40 ml of diethyl ether, through wich a stream of nitrogen was bubbled, was added, over a period of 20 minutes 27 ml of SOCI2. After addition of the SOCI2 stirring was contained for one hour until the mixture had become clear. The mixture was then poured onto 40 ml of water in a separating funnel. After separation the ethereal layer was extracted with 20 ml of brine and dried over MgSO4. The ether was then evaporated at 90 "C using a rotor evaporator.The yield of acyl chloride was 8.17g.

To 8.17 g of the acyl chloride was added 5.82 g of the phenol (0.022 mol) (b) 40 ml DCM and 46 ml triethylamine the reaction was left to mix initially in a cold bath for a period of 3 days.

The reaction was worked up by pouring into 1 ml HCI in 20 ml water. The aqueous layer was extracted with DCM. The DCM layers were then combined and washed with water and dried over an hydros sodium suiphate.

The acide product was then columned on a silica column (60.7 g) and eluted with 5 % ethyl acetate in petrol 40-60 C. The product being first preabsorbed onto 2 weights of silica.

Results: Yield = 10.60 g (81.0 %) Purity = 95.58 % by HPLC The product was then recrystallized from 4 volumes, yield 9.19, HPLO 99.7 %, of ethanol and dried ovemight in the vacuum oven.

The product exhibits: K51.1 N125.8l Analogously the following reactive compounds are obtained: L CH2=CH-COO-(CH2)m-#-COO-#-C2H4-#-R

m L + R2 4 F < C5Hll 6 F < 03H7 K 54.9 N 124.51 4 F < 03H7 6 H < 03H7 K 47.0 4 H < 05H7 K 54.9 N 124.51 6 H o ClThol CI K 85.8SA104.6N119.8 4 H Thol 6 H Th 03H7 K 96.3 N 106.5 1 4 H Th 03H7 Example 2 Preparation of

A solution of n-butyllithium (10.0 M in hexane, 3.30 ml) is added dropwise to a stirred solution of 3-fluoro-4-benzyl-bromobenzene (9.0 g) in THF (70 ml). The stirred solution is maintained under these conditions for 2.5 hrs and then a cooled solution of triisopropylborate (11.28 g) in dry THF (50 ml) is added.

After usual work-up the solvent is removed in vacuo to afford the product 2a.

A solution of ) in ethanol is added to a stirred mixture of pfluorobromobenzene and tetratros (triphenyl(phosphine)) palladium (0) in benzene and 2M-Na2CO3 at room temperature.

The stirred mixture is heated under reflux (90-95 "C) for 23 hrs.

After usual work-up the solvent is removed in vacua and the residue is used in the following steps without further purification.

5 % Palladium-on-charcoal (4.0 g) is added to the benzylether Zk in toluene. The stirred mixture is hydrogenated at atmospheric pressure for 4 hrs and the mixture is filtered. After usual work-up the solvent is removed to afford L.

(d) The esterification with

is carried out in analogy to example lc and yields

K84.0 N 113.51 Analogously the following reactive compounds are obtained:

m L L2 R2 4 F H F 6 H F F K 86.8 N 110.8 1 4 H F F 6 H F Cl K 67.7 SA 90.7 N 131.7 I 4 H F Cl 6 H F C3H7 K74.2 SA 82.7 N 128.2 I 4 H F 03H7 6 H F 05H11 4 H F C5H11

K 41.7 Sc 69.4 SA 76.7 N 77.2 1 Example 3 Preparation of

4'-Benzyl-2-fluorobiphenyl-4-ylboronic acid is obtained analogously to example 2a from 4'-benzyl-2-fluoro-4-bromobiphenyl and is reacted with 4chloro-2-fluorobromobenzene as described in Example 2b.

is is hydrogenated analogously to the method described in Example X

is is reacted with oxirane in the presence of pyridine and esterified with acrylic acid in the presence of trifluoroacetic anhydride and dichloromethane 20 hrs at room temperature.

The resulting product shows K1 73 K2 83 1.

After polymerization the side-chain polymer of formula

exhibits the following mesophases: Tg 53.8 N 1811.

Example 4 The following compounds are obtained in analogy to Example 2d by esterification of the corresponding phenols with the corresponding benzoic acids:

K74.4S089.1 N 100.6 1

K 38.5 1

K 75.5 (S 65.4) N 170.2 1

K 83.3 (Sc 84.6) N 158 1

K 53.5 Sc 84.5 SA 133.4 N 140 1

K 77 S 131 N 162 I

K 62.4 (N 32) I

Claims

PATENT CLAIMS 1. Liquid crystalline copolymer obtainable by copolymerization of at least one polymerizable reactive component A of formula I Rl.P-X-Al-Z1-A2-R2 (1) wherein R1 is CH2=CW-COO-,

HWN-, CH2=CH- or HS-CH2-(CH2)m-COO- with W being H, Cl or alkyl with 1-5 C atoms and m being 1-7 P is alkylene with up to 12 C atoms, it being also possible for one or more non adjacent CH2 groups to be replaced by 0-, X is -O-, -S-, -COO-, -OCO-, -C#C- or a single bond, R2 is a straight-chained, branched or chiral alkyl radical with up to 15 C atoms which is unsubstituted, mono- or polysubstituted by halogen, it being also possible for one or more CH2 groups in these radicals to be replaced, in each case independently of one another,-by -0-, -S-, -CO-, -OCO-, -CO-O- or -O-CO-O- in such a manner that oxygen atoms are not linked directly to one another, or alternatively R2 has one of the meanings given for R1-P-X-, A1 is a 1,4-cyclohexylene, a 1 ,4-phenylene in which one or two CH groups may be replaced by N or a naphthalene-2,6 diyl radical which is unsubstituted or substituted by 1 to 4 halogen atoms, A2 is

with the and the being Tho or it being possible for these rings to be substituted by CN or halogen and one of the 1 ,4-phenylene groups can also be replaced by a 1 ,4-phenylene radical in which one or two CH groups are replaced by N, and Z and Z are each independently -CO-O-, -O-CO, -CH2CH2-, -C#C- or a single bond, n is Core, and at least one polymerizable component B of formula ll

wherein R1, P, X and the meaning give for formula I, and Q has the meaning given for formula I, and Y1 is -H, -F or-Cl, Q is -CF2, -OCF2, -C2F4, or -OC2F4, or a single bond, if Y1 is F or Cl A3 and A4 are each independently (c) 1 ,4-phenylene radical in which one or two CH groups can be replaced by N, (d) a 1,4 cyclohexylene radical in which one or two non adjacent CH2 groups can be replaced by -O- or -S-, or (e) a naphthalene-2,6-diyl radical, a piperidine-1,4-diyl radical, a thiophene-2,5-diyl radical, a 1,3,4 thiadiazol-2,5 diyl radical, it being possible for radicals (c) and (d) to be substituted by CN or halogen, is, independently of one another, -CH2CH2-, -COO-, -OCO-, CiC- or a single bond, Z4 is -CH2CH2-, -C#C- or a single bond, L1 through L4 are each independently H, halogen, -CH3, -CF3 or -CN, preferably H or fluorine.

o is 0, 1 or 2, and the groups A3 being same or different in the case that o is 2.
2. Polymerizabel, reactive liquid crystal compound of formulae I or II, wherein X is -C#C-
3. Polymerizable, reactive liquid crystal compound of formula la

wherein R1, R2, P,

and X have the meaning given, and Z2 is -CH2CH2- or a single bond, preferably -CH2CH2

denotes
4. Polymerizable, reactive liquid crystal compound of formula Ib

wherein R, R2, P,

and X have the meaning given, and Z2 is -CH2-CH2- or a single bond, or in the case that Lo is Cl Z2 denotes also -O-CO-.

denotes a 4,4'-biphenyidiyl group being optionally substituted by p fluorine or chlorine atoms1 and p is O or an integer between 1 and 4.
5. Polymerizable reactive liquid crystal compound according to one of the claims 2 to 4 wherein R2 is achiral.
6. Polymerizable reactive liquid crystal compound of formula II, wherein O y1 is F, Cl, -OCF3, -OCF2H, -CF3 or OC2Fs
7. Polymerizable reactive liquid crystal compound of formula Ila

wherein R1, P, X, Q, y1 and p have the meaning given and Z4 is -CH2CH2 of a single bond.
8. Polymerizable reactive liquid crystal compound of formula lib

wherein R1, P, X, Q, Y1 and p have the meaning given and q and r are each independently 0 or an integer selected from 1 to 4.
9. Polymerizable reactive liquid crystal compound according to one of the claims 2 to 8, wherein R1 is CH2=CW-COOwith W being H, Cl or OH3.
10. Liquid crystalline polymer obtainable by polymerization of at least one polymerizable reactive liquid crystal compound according to the Claims 2 to 9.
11. Liquid crystalline polymer obtainable by substance photo polymerization of at least one polymerizable reactive liquid crystal compound of formulae I or II, in the presence of a photoinitiator, at least one of said reactive liquid crystal compounds being oriented in its liquid crystalline phase.
12. Liquid crystalline polymer according to claim 11, characterized in that the reactive liquid crystal compound is oriented in its nematic phase.
13. Liquid crystalline (co-)polymer according to one of the claims 9 to 12, obtainable by polymerization in the presence of a plasticizer, preferably a dialkylphthalate, and/or a chiral dopant, preferably a chiral cyanobiphenyl, phenyl benzoate, menthol or lactic acid derivative.
14. Use Of a liquid crystalline copolymer according to Claim 1 in the field of integrated optics, opto-electronic and/or information storage.
15. Use of a liquid crystalline polymer according to one of the claims

9-13 in the field of integrated optics and/or opto-electronic.