CA2250867A1 - Compounds and methods for doping liquid crystal hosts - Google Patents

Abstract

This invention provides chiral thioindigo compounds for doping smectic liquid crystal hosts, wherein the compounds modulate a chiral bulk property of an induced chiral smectic liquid crystal phase upon irradiation at a wavelength in the visible range. Modulation of the chiral bulk property is effected by reversible trans-cis photoisomerization of the compound upon irradiation. The compounds maintain their rod-like shape in both isomeric forms, and hence do not destabilize the chiral smectic liquid crystal phase. Compounds according to the invention are useful in optical devices such as optical switches, displays, and memory.

Description

CA 022~0867 1998-10-02 WO 98~499~ PCT/CA98/00083 COMPOUNDS AND METHODS FOR DOPING LIQUID CRYSTAL HOSTS
~IELD OF THE INVENTION
This invention relates generally to dopants for liquid crystal hosts, and in particular to chiral thioindigo dopants for smectic liquid crystal hosts.

Ferroelectric liquid crystals (FLCs) are potentially useful as the active component in optoelectronic and photonic devices such as optical switches, displays, and spatial light modulators. To be useful in such applications, switching of an FLC, i.e., control of its light-llillhlg properties, must be possible. One approach is to dope the liquid crystal with a 10 photochromic compound that produces a reversible photomechanical effect, i.e., a structural change of the liquid crystal phase, in response to irradiation with light of a specific wavelength. The structural change of the liquid crystal phase changes the light-transmitting pl(pc.liesoftheliquidcrystal. Forexample,U.S.PatentNo.5,118,586toHattori etal., issued June 2, 1992, proposes the use of a photochromic dopant to achieve such switching in 15 a liquid crystal film, for photorecording of digital information. Irradiation of the aligned liquid crystal film in the ultra-violet (UV) range causes a change in the birefringence of the liquid crystal phase as shown by the rotation of plane-polarized light transmitted through the m~teri~l. The initial state can be restored by irr~ ting the film with visible light. As shown by Hattori et al., this principle can be applied to a FLC using a fulgide dopant, in which case 20 the irradiation merely modulates the birefringence of the liquid crystal phase in the absence of an electric field. However, the resulting rotation of plane-polarized light is very small, on the order of 0.2 degree, which is not enough to produce a sufficient contrast in some optoelectronic and photonic applications.
A different approach which may be useful for applications such as optical switches 25 and displays involves a system employing a photoactive chiral dopant in an achiral smectic C
(Sc) liquid crystal host (i.e., a liquid crystal phase which exhibits molecular ordering and a molecular tilt) to give an induced FLC. In principle, upon irradiation of the resulting chiral smectic C (Sc*) phase, switching can be achieved via modulation of the spontaneous polarization (Ps; a chiral bulk property of the FLC) above and below a switching threshold, to 30 change the light-transmitting properties of the FLC. Modulation ~f Ps is associated with a photo-in(lllce~ structural change in the dopant.
Recently it has been shown that Ps can be photomodulated in the near-W range via SUBSTITUTE StlEET (RULE 26) CA 022~0867 1998-10-02 WO 98l34995 PCT/CAs8/00083 the reversible trans-cis photoisomerization of chiral azobenzene dopants in Sc or Sc* liquid crystal hosts (Negishi et al., Chem. Lett., 319, 1996; Blinov et al., Jap. J. Appl. Phys., 35:5405, 1996; Sasaki et al., J. Phys. Chem., 99:13013, 1995; Walton et al., Liq. Cryst., 17:333, 1994; Sasaki et al., J. Am. Chem. Soc., 116:625, 1994; Lkeda et al., Nature, 361 :428, 5 1993) and of azobenzene side-chain-doped copolymer FLCs (Oge et al., Macromol. Chem.
Phys., 197: 1 ~05, 1996). In this system, the modulation Of Ps arises from a photomechanical effect associated with the change in shape of the azobenzene dopant from rod-like (trans) to bent (cis): the change to the bent cis-isomer destabilizes the Sc* phase of the liquid crystal ai~d decreases polar ordering, thus decreasing Ps~ The photomechanical effect results in 10 si~nific~nt decreases in the t~ lule of phase transition between chiral smectic A (SA*) (i.e., a smectic liquid crystal phase having the same molecular ordering as a Sc* phase, but without a molecular tilt) and Sc* phases or between chiral nematic (N*) (i.e. a liquid crystal phase having orientational ordering only) and Sc* phases, producing in some cases a complete loss of polarization due to an isothermal phase transition to the SA* or N* phase.
Thus, while the above system has demonstrated photomodulation ~f Ps, there are significant disadvantages to that approach: (i) the addressing wavelength causing trans-to-cis photoisomerization of the azobenzene dopant is in the near-ultraviolet range (365 nrn), which is undesirable for practical applications for which an inexpensive addressing light source is ~lef~ led; and (ii) the mechanical destabilization of the Sc* phase can produce a more fluid, less ordered nematic phase with lower structural integrity, which may be a severe impediment if the FLC film is to be used as a long-term digital information storage device.
OBJECT OF THE INVENTION
It is an object of the invention to provide chiral dopants for a smectic liquid crystal host, which dopants modulate chiral bulk properties of an inclllced chiral smectic phase upon irradiation in the visible range, without conco~ t destabilization of the chiral smectic liquid crystal phase.

SUMMARY OF THE INVENTION
According to a broad aspect, this invention provides chiral thioindigo compounds for doping smectic liquid crystal hosts, wherein the compounds modulate a chiral bulk property of an induced chiral smectic liquid crystal phase upon irradiation at a wavelength in the SUBSTITUTE SHEET (RULE 26) , .

visible range, without destabilizing the chiral smectic liquid crystal phase. According to the invention, the mo~ tion is effected by cis to trans photoisom~ i7.~tion of the chiral thioindigo compounds upon irr~ tio~, wherein the photoisomerization is reversible, the absol~tivily of the cis and trans isomers is at different wavelen~h~ so that the two isomers S can be addressed at dirrc~cml wavell n~h~ without overlap; and the absol~livily of the cis and trans i~ome~s in the visible range.
Chiral thioindigo comrollntl~ of the invention are l~ies."lled by general formula I, v~hcle.ll: R~ and R2 may be the same or dirrelclll from each other and may be, for example, hydrogen, fluoro, chloro, bromo, iodo, nitro, nitrile, alkyl, allcenyl alkoxy, hydroxy, 10 perfluoroalkyl, thioalkyl or the like; and R3 and R may be the same or different from each other and at least one of R3 and R4 is a chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-dipole inlcl~ctions, to the thioindigo core. In some embodim~nt~, one of R3 and R4 is an oli~osilo~c~ne side-chain, and the other of R3 and R4 is an a chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-15 dipole interactions, to the thioin~ o core.
R~ (I) According to a ~lcfcll~d embodiment, the compound is (R,R)-5,5'-dinitro-6,6'-bis(2-octyloxy)thioindigo, or a de.;vdlive or analogue thereof. According to a more ~rcÇ~,.Icd embodiment, the compound is (R,R)-5,5'-dichloro-6,6'-bis(2-octyloxy)thioindigo, or a derivative or analogue thereof.
According to another aspect of the invention, a chiral thioindigo compound as described above may be dispersed in a liquid c~ystal host such as an achiral smectic C (Sc) liquid crystal, a chiral smectic C (Sc*) liquid crystal, an achiral smectic A (SA) liquid crystal, a chiral smectic A (SA*) liquid crystal, or a polymeric smectic liquid crystal such as a smectic polysiloxane liquid crystal.
By a further aspect, the invention provides a method of synth~i7.in~ (R,R)-5,5'-dinitro-6,6'-bis(2-octyloxy)thioindigo, comprising the steps of: con~ ctin~ a Mitsunobu inversion reaction to produce a chiral methyl 2-chlorobenzoate plc~ OI, reacting the chiral methyl 2-chloroben7. ~te ple~ or with methyl thioglycolate to produce a chiral bicyclic enol SUBSTITUTE SHEET (RULE 26) , . ....

CA 022~0867 1998-10-02 W 098~4g95 rCT/CA98/~W~3 ester; pelro,~ g base-catalyzed hydrolysis and decarboxylation of the chiral bicyc}ic enol ester to produce a chiral benzothiophenone; and oxi~i7ing the chiral bel~olhiophenone to obtain (R,R)-5,5'-dinitro-6,6'-bis(2-octyloxy)thioindigo. Preferably the oxidizing step is p~lrulllled without prior isolation of the chiral bellzotl~iophenone.
S By a further aspect, the invention provides to a method of synthesi7ing (R,R)-5,5'-dichloro-6,6'-bis(2-octyloxy)thioindigo, comprising the steps of: conducting a Mitsunobu inversion reaction to produce a chiral methyl 2-fluorobenzoate precursor; reacting the chiral methyl 2-chloroben7:0~te ~,r~ or with methyl thioglycolate to produce a chiral bicyclic enol ester; con-lnsting a base-catalyzed hydrolysis and decarboxylation of the chiral bicyclic enol ester to produce chiral benzothiophenone; and oxidizing the chiral benzothiophenone to obtain (R,R)-5,5'-dichloro-6,6'-bis(2-octyloxy)thioindigo. Preferably the oxidizing step is performed without prior isolation of the chiral benzothiophenone.
The invention also provides an optical device for operation with a direct current ffeld, compri.~ing a liquid crystal host selected from the group con.ci~ting of an achiral smectic C
(Sc) liquid crystal host and a chiral smectic C (Sc*) liquid crystal host; and a chiral thioindigo compound dispersed in the liquid crystal host to produce a chiral smectic C (Sc*) liquid crystal phase across which the field is applied, the chiral compound, upon irradiation in the visible range, mocl~ ting a spontaneous polarization of the liquid crystal phase without destabilization of the liquid crystal phase.
According to another embodiment, the invention provides an optical device for operation with a direct current field, compricing a liquid crystal host selected from the group con~ictin~ of an achiral smectic C (SA) liquid crystal host and a chiral smectic C (SA*) liquid crystal host; and a chiral thioindigo compound dispersed in the liquid crystal host to produce a chiral smectic C (SA*) liquid crystal phase across which the field is applied, the chiral compound, upon irradiation in the visible range, mo~illl~tin~ an electroclinic coefficient of the liquid crystal phase without destabilization of the liquid crystal phase.
In acculd~lce with the invention such optical devices can be, for example, optical switches.
By another aspect, the invention provides a FLC optical switch for operation under an applied direct current field, comprising: a smectic C liquid crystal host; a chiral photochromic compound dispersed in the liquid crystal host, the chiral compound inducing in the liquid crystal host polarization in a first polarity, and being capable of undergoing ~rans-cis SUBSTITUTE SHEET (RULE 26) . .

CA 022~0867 1998-10-02 isomerization upon irradiation in the visible range without destabilizing the liquid crystal;
and a photochemically inert compound dispersed in the liquid crystal host, the inert compound inducing in the liquid crystal polarization in a second polarity; wherein the proportions of the chiral compound and the inert compound are such that the polarization induced by the inert compound is greater than that induced by a first isoform of the photochromic dopant, such that the total polarization of the liquid crystal is in the second polarit,v; and wherein, upon irradiation in the visible range, the polarization induced by the inert compound is less than that in(lllce(l by the photochromic dopant in a second isoform, such that the total polarization of the liquid crystal is in the first polarity, resulting in a change in light tr~n~mi~ion through the liquid crystal.

BRIEF DESCRIPTION OF T~IE DRAWINGS
Embodiments of the invention will now be described, by way of example, with reference to the accompanying drawings, wherein:
Figure 1 is a diagrammatic ~ csellt~lion of spontaneous polarization of an FLC;
Figure 2 is a diagrarnmatic representation of switching in a SA* liquid crystal phase via an electroclinic effect;
Figure 3 is a diagram of a synthetic process for a nitro-substituted chiral thioindigo dopant according to the invention;
Figure 4 is a diagram of a synthetic process for a chloro-substituted thioindigo dopant according to the invention;
Figure 5 is a diagram of a synthetic process for a chloro-substituted unsymmetrical chiral thioindigo dopant according to the invention;
Figure 6 is a plot of spontaneous polarization as a function of temperature for a FLC
doped with the chloro-substituted chiral thioindigo compound of the invention;
Figure 7 is a dia~ atic rc~res~"t~tion of a Sc~ liquid crystal optical switch wherein ~witchil~g is via photoinduced polarization inversion;
Figure 8 is a diagram of an a~pa~atu~ used to demonstrate a FLC optical switch according to the invention;
Figure 9 shows a change in tran~mi~ion of a light beam through a FLC optical switch under a DC field, upon irradiation by an addressing wavelength at 532 nm, indicated by a change in voltage as a function of time; and SU.,~ 11 l UTE SHEET (RULE 26) CA 022~0867 1998-10-02 wo 98/34995 PCT/CAg8/00083 Figure 10 shows changes in tr~n.~mi.e.~ion of a light beam through a FLC opticalswitch under a square wave AC field, upon irradiation by an addressing wavelength at 532 nm, indicated by changes in voltage as a function of time.

According to a broad aspect of the invention, chiral thioindigo compounds are provided which are useful as dopants in a smectic liquid crystal host. Chiral thioindigo compounds of the invention undergo reversible trans-cis photoisomerization, which isomerization modulates a chiral bulk property of the host liquid crystal to trigger switching.
10 The compounds of the invention m~int~in their rod-like shape in both isomeric forms, and hence do not destabilize the liquid crystal phase.
Chiral thioindigo dopants of the invention are therefore different from prior art chiral dopants such as azobenzene dopants, also used in smectic C liquid crystal hosts (Negishi et al., Chem. Lett., 319, 1996; Blinov et al., Jap. J. Appl. Phys., 35:5405, 1996; Sasaki et al., J.
Phys. Chem., 99:13013, 1995; Walton et al., Lig. Cryst., 17:333, 1994; Sasaki et al., J. Am.
Chem. Soc., 116:625, 1994;Ikeda etal.,Nature, 361:428, 1993). Suchchiralazobenzene dopants also undergo trans-czs photoisomerization upon irradiation; however, thephotoisomers change between a rod-like shape and a bent shape, which change in shape destabilizes the liquid crystal phase. Moreover, the prior art dopants undergo isomerization 20 in the near-W range, whereas the compounds of the invention undergo isomerization in the visible range. As W light sources are substantially more expensive than visible light sources, the use of visible wavelengths with the inventive compounds is an advantage.
In accordance with a broad aspect of the invention, chiral thioindigo compounds are provided which are useful as dopants in a smectic C liquid crystal host. Chiral thioindigo 25 dopants of the invention induce a ferroelectric chiral (*) smectic C (Sc*) phase, and a spontaneous polarization (Ps; a chiral bulk property of the liquid crystal host) in the resulting ferroelectric phase. Upon irradiation in the visible range of wavelengths, of a Sc* liquid crystal phase doped with a compound of the invention, Ps is modulated via a photo-induced isomerization of the dopant. Switching of the FLC between opposite tilt orientations (i.e.
30 Goldstone-mode switching) is achieved via modulation of Ps above or below a switching threshold, c?l-~ing a polarization reversal of Ps . The polarization reversal results in a rotation of plane-polarized light transmitted through the FLC, and hence in a change in the light-Sl,~S 111 ~JTE SHEET (RULE 26) CA 022~0867 1998-10-02 transmitting properties of the liquid crystal. The switching threshold is set by, for example, a direct current field applied across the FLC, and can therefore be adjusted to suit specific applications. Moreover, an FLC according to the invention is bistable, as switching of the FLC only occurs while the DC field is applied, and the FLC retains its state in the absence of any applied field.
Spontaneous polarization is intrinsic to the FLC. It is a perrnanent macroscopicdipole moment oriented along the axis perpendicular to the tilt plane (polar axis), which is defined by the orientation of the molecular long axis _ (director) and the layer norrnal z, as shown in Figure 1. The spontaneous polarization is a macroscopic manifestation of molecular chirality and is a function of the molecular structure of the chiral dopant in the indllce(l Sc* phase. In order for a polar functional group in the chiral dopant to contribute to Ps~ it must (i) have a component of its dipole moment vector oriented along the polar axis, and (ii) be coupled to the chiral center(s) via steric and/or dipole-dipole interactions.
In accordance with another broad aspect of the invention, chiral thioindigo compounds are provided which are useful as dopants in a smectic A liquid crystal host. In such a host, the chiral thioindigo dopants of the invention induce a chiral smectic (SA*) phase exhibiting an electroclinic effect (i.e., an inrlllced molecular tilt orientation) with an electroclinic coefficient (ec; a chiral bulk ~lopel Iy of the liquid crystal host). Upon irradiation in the visible range of wavelengths, of a SA* liquid crystal phase doped with a compound of the invention, switching is triggered via modulation of ec. The modulation of ec is associated with a photo-in~lllced isomerization of the dopant. When a direct current field is applied across the liquid crystal, the isomerization triggers a change in the induced molecular tilt orientation of the SA* phase. This results in a change in the light-transmitting properties of the liquid crystal, caused by a rotation of plane-polarized light transmitted through the liquid crystal.
SA* liquid crystals exhibit an electroclinic effect wherein application of an electric field across the liquid crystal induces a molecular tilt ~ that is a linear function of the applied field E, as shown in Figure 2 (Garoff et al., Phys. Rev. A, 19:338, 1979). The electroclinic coefficient ec is defined by the following equation:
ec= tl [a (T - Tc)]-wherein a is the first constant in the Landau free-energy expansion, T - Tc is the reduced phase transition temperature, and 11 is a structural coefficient characteristic of the chiral SUBSTITUTE SHEET (RULE 26) CA 022~0867 1998-10-02 WO 98/34995 PC'r/CA98/00083 component of the SA* phase (Andersson et al., Ferroelectrics, 84:285, 1988). Spatial light modulators based on the electroclinic effect are capable of continuous intensity modulation with a response time about 100 times faster than a FLC switch, although they }ack bistability.
The invention contemplates mo~ tinE the electroclinic coefficient ec of a SA* liquid crystal phase by transverse dipole modulation of a chiral photochromic dopant of the invention such as, for example, III. At a constant field E, photomodulation of ec would result in a change in in~ c.ed tilt angle ~ that can be detected as a change in light tr~n.~mi.c~ion between crossed polarizers.
As used herein, the term "switching" means a polarization reversal ~f Ps in the case of Sc* liquid crystal phases, and a change in the field-induced molecular tilt angle in the case of SA* liquid crystal phases, whereby the switching effects a change in the light-transmitting properties of the liquid crystal. In the case of Sc* liquid crystal phases, modulation ~f Ps triggers the switching, whereas in the case of SA* liquid crystal phasesl modulation of ec triggers the switching. In both cases, the modulation is achieved by photoisomerization of a chiral thioindigo compound of the invention dispersed in the liquid crystal phase.
In principle, in a SA* liquid crystal phase, a photoinduced change in tilt angle (~) can be tuned (i.e., adjusted) by controlling the cis:trans ratio of the chiral thioindigo dopant present in the liquid crystal at the photostationary state by, for example, irradiating the liquid crystal with a writing beam of variable wavelength.
In general, an electroclinic liquid crystal optical switch according to the invention is tunable, has sub-microsecond response time, and is not bistable. In contrast, a FLC optical switch is substantially untunable, has a response time that is about 100 times slower, and is bistable. The two devices therefore lend themselves to distinctly different applications as will be apparent to one skilled in the art. Typical examples of applications of a FLC optical switch according to the invention are discussed below. An electroclinic optical switch according to the invention is particularly useful in applications such as, for example, a holographic interconnect for optical col~ ication n~lwolh~.
In general, chiral thioindigo dopants according to the invention can be effective photoactive components of electro-optical devices such as, for example, FLC and electroclinic optical switches, as the dopants undergo trans-cis photoisomerization in SA and Sc phases, and they are highly miscible in a liquid crystal host. In addition, chiral side-chains of the compounds of the invention are strongly coupled to the thioindigo core, such that the SUBSTITUTE SHEET ~RULE 26) _, photoin~hlced change in l~ svel~e dipole mornent is as high as possible.
By one aspect, this invention provides chiral thioindigo compounds represented by the general formula I. In a pl~r~lled embodiment corresponding to (R,R)-5,5'-dinitro-6,6'-bis(2-octyloxy)thioindigo, shown in formula II, Rl and R2 are NO2 and R3 and R4 are (R)-2-5 octyloxy. In a more plerelled embodiment corresponding to (R,R)-5,5'-dichloro-6,6'-bis(2-octyloxy)thioindigo, shown in formula III, Rl and R2 are Cl, and R3 and R4 are 2-octyloxy.

R1~RR2 (I) o o Cl~ 4 S ~~~~ (III) ~ oJ~s)=~c~ I

In the case of compound II of the invention, trans-to-cis photoisomerization is triggered by irradiation with light in the range of wavelengths from about 480 to about 550 nm, and an Ar laser at 514 nm may conveniently be used. Isomerization back to the trans-isomer is triggered by irradiation in the range of about 400 to 480 nm. In the case of compound III of the invention, irradiation in the range of wavelengths from about 500 to 575 nm triggers trans-to-cis photoi~om~.ri7~tion, and a Nd:YAG laser at 532 nm may co"v~i~iently be used. Isomerization back to the trans-isomer is triggered by irradiation in the range of about 400 to 500 nm. Of course, other wavelengths will be a~plopl;ate for other 30 compounds acco~ lg to the invention, but such other wavelengths will be within the range of about 400 to about 800 nm.
An increase in Ps upon trans-cis photoisomerization of the dopants of the invention SUBSTITUTE SHEET (RULE 26) WO 98134g95 PCT/CA98/00083 has been demonstrated up to 85% in the case of II, and up to 250% in the case of III. This effect results from a change in transverse dipole moment of the thioindigo core, which is strongly coupled to each chiral side-chain through the R3 and R4 substituents at the ort~lo position. The coupling function provided by the R3 and R4 sllbsti1llents is critical in 5 achieving the effect. This has been shown through previous work where, in the absence of ortho subsl~ Pnt~, the chiral side-chains are decoupled from the core and trans-cis photoisomeri7.~tion has virtually no effect on Ps (Dinescu et al., Liq. C~yst., 20:741-749, 1996). Mea~ulcment of the ferroelectric ~ lies and Ps photomodulation of the preferred embodiments are described in Example 1.
Compounds ofthe invention are not limited to the above pler~,.. ed embo~inlent~ and in other embodiments Rl and R2 may independPntly be, but are not limited to, hydrogen, fluoro, chloro, bromo, iodo, nitro, nitrile, alkyl, alkenyl, alkoxy, hydroxy, perfluoroalkyl, or thioalkyl. R3 and R4 may independently be any chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-dipole interactions, to the thioindigo core. For 15 example, R3 and R4 can be, but are not limited to, any of the chiral side-chains shown in formula IV; that is, filnr.ti~n~lities included in the chiral side-chain may be: alkyl, alkenyl, ether, epoxide, ester, carbonyl, amide, aromatic, heterocyclic, halide, nitrile or the like.
a,R3,R4= ~ ~ ~ t,R3,R4=

b,R3,R4= ~ ~ ~ RS R4= ~ ~

CF3 Me Me c,R3,R4= ~ ~ ~ Si- O ~ Me h,R3,R4= ~ ~ ~ (IV) d,R3,R4= ~ ~ I,R3,R4_ ~ O ~ O ~ O

e,R3,R4= ~ O ~ I,R3,R4 _ /o~".. ~ o~ " A~"~

The invention contemplates ~d-lition~l compounds in which groups other than those listed above may be substituted for Rl and R2, and R3 and R4 . For exarnple, compounds of the invention include those having only a single chiral side chain at either of the R3 and R4 SUBSTITUTE S~EET (RULE 26) . ~ , . .

CA 022~0867 1998-10-02 positions. Any such compound is considered to be within the scope of the invention, so long as the substitution of additional groups does not materially alter the photophysical properties of the thioindigo chromophore relative to those properties of the compounds of the pl~r~lled embodiments. The photophysical plol,ellies of chiral thioindigo compounds of the invention 5 comprise: reversible photoisomerization; sufficiently different wavelengths of absorptivity of the cis and trans isomers so that the two isomers can be addressed at different wavelengths without overlap; and absol~tivily of the cis and trans isomers in the visible range.
By another aspect, this invention pertains to use of chiral thioindigo compounds of the invention as dopants in achiral smectic C (Sc) hosts and in achiral smectic A (SA) hosts. In 10 these hosts, a chiral bulk property is in~ .ed by a chiral thioindigo compound of the invention. Chiral thioindigo compounds of the invention may also be used as dopants in chiral smectic C (Sc*) and chiral smectic A (SA*) hosts, wherein the dopants alter a chiral bulk property in the host.
The SA and Sc liquid crystals systems described above are monomeric and thus may15 be considered low molecular weight systems. However, the invention is not limited to such systems, and also encomp~.c~es use of chiral thioindigo compounds of the invention as dopants in polymeric SA and Sc liquid crystal phases, which may be considered high molecular weight systems. According to this aspect of the invention, the compounds undergo Ps or ec photomodulation via the same transverse dipole modulation mechanism as that 20 described in the above monomeric systems. Thioindigo-doped polymeric liquid crystals are suitable for applications such as, for example, FLC and electroclinic optical switches. As high molecular weight systems, they have certain advantages over the above monomeric systems, such as: (i) higher mechanical stability and shock resistance; (ii) ability to be processed into flexible films; and (iii) good bistability in the absence of an applied field, thus 25 making it unnecessary to ~ an electric field across the liquid crystal to m~int~in a particular state. The last point is particularly advantageous in applications such as optical storage of digital information, also encompassed by the invention.
In accordance with the invention, an example of a thioindigo dopant suitable fordoping into a side-chain polysiloxane Sc or SA liquid crystal is shown in formula V. The 30 oligosiloxane side-chain of the compound in formula V increases the compatibility of the chiral thioindigo dopant with a side-chain polysiloxane Sc or SA host.

SUBSTITUTESHEET(RULE26) CA 022~0867 1998-10-02 W 0 98/34995 PCT/CAg8/00083 a ~o H3C~ CH3 (V) O n=7 HgC- i--CH3 Cl ~0 ~0 S Cl CF9 It should be noted that any chiral thioindigo compound of the invention may be used as a dopant in any of the smectic liquid crystal hosts described above. Chiral side-chains of the compounds of the invention impart various degrees of mesogenicity and miscibility of the 10 thioindigo compound in smectic hosts, and can affect the free volume for trans-cis photoi~om.ori7~tion. Accordingly, it is contemplated that chiral side-chains used in the compounds of the invention will be selected for compatibility with specific hosts and specific applications. A dete~ ion of a suitable chiral side-chain for a given host can be made without undue eXperim~ont~tion~ by employing the procedures generally set forth herein.
15 Compounds arising through such routine experiment~tion are considered to be within the scope of the present invention. Compound III of the invention is a p~ ed dopant because it exhibits very high solubility in a smectic liquid crystal host. For example, III has been dissolved in a phenyl benzoate (PhBz; (~)-4-(4-methylhexyloxy)phenyl 4-decyloxybenzoate) host at a concentration of 10 mol% with minim~l destabilization of the Sc liquid crystal 20 phase. Compound II of the invention has been dissolved in PhBz at a concentration of 3 mol% with minim~l destabilization of the Sc liquid crystal phase. Of course, in each case, lower doping levels are also possible.
According to a further aspect of the invention, methods for synthesis of the compounds of the invention are provided. These methods are described in detail for the 25 plcfelled embo-iimpnt~ II and III, re~e.;lively, in Examples 2 and 3, below. A method for syn~h~i7inP. II may be ~ ;7.e~1 as colll~.lisillg the steps of: con~ cting a Mitsunobu inversion reaction to produce a chiral methyl 2-chlorobenzoate precursor; reacting the chiral methyl 2-chloroben7.o~te ~ iUl~iOl with methyl thioglycolate to produce a chiral bicyclic enol ester; pe~ ~u. ~l l; llg base-catalyzed hydrolysis and decarboxylation of the chiral bicyclic enol 30 ester to produce a chiral benz l}~iophenone; and oxi~ii7.in~ the chiral benzothiophenone to obtain (R,R)-5,5'-dinitro-6,6'-bis(2-octyloxy)thioindigo. Preferably the oxidizing step is pelîolllled without prior isolation of the chiral benzothiophenone.

SUBSTITUTE SHEET (RULE 26) CA 022~0867 1998-10-02 W O 98/34g95 PCT/CA98/00083 A method for synthesizing III may be sllmm~ ed as comprising the steps of:
conducting a Mitsunobu inversion reaction to produce a chiral methyl 2-fluorobenzoate precursor, reacting the chiral methyl 2-fluorobenzoate precursor with methyl thioglycolate to - produce a chiral bicyclic enol ester; conducting a base-catalyzed hydrolysis and 5 decarboxylation of the chiral bicyclic enol ester to produce chiral benzothiophenone; and oxidizing the chiral benzothiophenone to obtain (R,R)-5,5'-dichloro-6,6'-bis(2-octyloxy)thioindigo. Preferably the o~i~li7.ing step is perforrned without prior isolation of the chiral benzothiophenone.
It should be noted that the chiral bicyclic enol ester, shown as S5 in Figure 3 or S10 in 10 Figure 4, which is a precursor to II and III as well as to analogues and derivatives of II and III, is a very stable compound and hence may advantageously be prepared in advance of the actual synthesis of the chiral thioindigo dopants, and stored and/or shipped.
Example 3 also describes a process for preparing chiral thioindigo compounds with Rl different from R2 and/or R3 different from R4 (see formula I). Such "unsyrnmetrical"
15 compounds are precursors in the synthesis of chiral thioindigo dopants with oligosiloxane side-chains such as V, described above. Methods for preparing chiral thioindigo-doped polymeric liquid crystals according to the invention are generally described in Example 4.
Those skilled in the art will recognize that it is possible to make various modifications to the synthetic procedures of Examples 2 to 4 and still arrive at the desired compounds, or 20 analogues and derivatives thereof. Such modifications are intended to be within the scope of the invention.
By a further aspect, the invention pertains to a FLC optical switch. The operation of a FLC optical switch according to the invention is based on a photoinduced sign reversal of the spontaneous polarization vector Ps~ i.e., a polarization inversion mech~ni~m. As shown in 25 Figure 7, this can be achieved by mixing, in a smectic C liquid crystal host (e.g., PhBz), a photochromic dopant such as, for exarnple, compound III of the invention, which induces a positive polarization, and a photochemically inert dopant (e.g., (S,S)-4,4'-bis[(2-chloro-3-methylbutanoyl)oxy]biphenyl), which induces a negative polarization. When mixed in the right proportions (e.g., a 2.3:1 ratio), the polarization induced by the inert dopant is greater 30 than that induced by the photochromic dopant in the trans-form (i.e., Pjnd(inert dopant) >
Pjnd(photochromic dopant)), and the total spontaneous polarization of the FLC optical switch is negative. Upon irradiation at an ~ iate wavelength (e.g., 532 nrn using a Nd:YAG

SUBSTITUTE SHEET (RULE 26) WO 9fV34~S PCT/C~98100083 laser for III), the polarization in~luced by the photochromic dopant increases to a level where Pjnd~inert dopant) c Pjnd(photochromic dopant), resulting in a reversal of the total spontaneous pol~ tion from negative to positive. If this sign reversal occurs while the FLC
cell is subjected to a static DC field (E), it results in a ~wilcl~illg of the molecular tilt 5 orientation (Goldstone-mode switching) that can be readily ~letected between crossed polarizers by virtue of a change in light tr~n~mic.sion through the FLC cell. Moreover, because switching of the FLC will only occur while the DC field is applied, the FLC switch is inherently bistable. An FLC optical switch according to the invention thererole retains its state in the ~bs~nce of any applied field, m~1ring it particularly advantageous in applications 10 such as long-term optical storage devices. The principle of such a light switch accol.ling to the invention is described in detail in Example 5.
In accordance with the invention, an optical switch may be prepared using any of the chiral thioindigo dopants of the invention. For example, chiral thioindigo oligosiloxane compounds of the invention, such as V, may also be used, and the invention contemplates at 15 least two different a~)ploaclles for achieving Ps photoinversion. A first approach is by int~rmolecular Ps subtraction using a combination of chiral thioindigo dopants and non-photoactive chiral dopants which respectively induce polarizations in opposite directions. An example of this a~proach is represented by a compound according to formula VI.

/=\
~ ~~~~~
H3C- ''i-CH3 O n = 7 ~ Ps (VI) H3C-''i--CH3 Cl~S=~S_~O~

~O S ~cl CF3 ~ I~PS I

A second approach colllen~lated by the invention is by intramolecular Ps subtraction using a thioindigo dopant with chiral side-chains inducing polarizations in opposite directions, such as, for example, a compound according to general formula VII. An unsymmetrical thioindigo system such as this includes a chiral side-chain A with -Ps that is decoupled from the thioindigo core, and a chiral side-chain B with +Ps that is coupled to the Sl,~S ~ JTE SHEET tRULE 26) thioindigo core through an ortho sl1b~ Pr,t The side chains are selected so that the polarization in~luced by A is predominant with the thioindigo core in the trans form. Upon photoi~omeri7~tion to the cis form, the polarization in~uced by side-chain A remains consl~
due to the lack of steric coupling to the core, whereas the polarization in-luce~l by the coupled 5 side-chain B increases due to the added contribution of the thioindigo core. By selecting a suitable combination of chiral side-chains, this effect causes the polarization inflllced by B to predominate, resllltin~ in Ps inversion.

O
Cl~ S~O
~ lo~s ~ CF3 (VII) o ~PS

The COI1tel1~7 of all patent and scientific publications cited in this application are inc~ led herein by lcrere'lce.

Example 1 M~urclllent of ferroelectric ~)roptl lies and Ps photomodulation of II is described in 20 Dinescu et al., Proceedings of the SPIE-International Society for Optical Engineeffng, 3015:16, 1997.
Mea~u~cnlent of ferroelectric properties and Ps photomodulation of III was carried out as follows: Mixtures of III in PhBz were prepared over the mole fraction range 0.015 > xd >
0.07, and Ps and tilt angle (~) values were measured at a temperature 10 ~C below the Sc~ -25 SA~ phase transition temperature (T-TAC = -10 C). A plot of Ps/sin~ vs xd gave a polarization power (~p) value for III of +20.7 nC/cm2. The spont~n~.ous polarization of a 2.9 mol%
llli~lule of III in PhBz at T-TAC = -~0 C was measured in the dark and upon irradiation with a Nd:YAG laser at 532 rlm: Ps (dark) = +0.92 nC/cm2 and Ps (532 nm) = +2.28 nC/cm2.
- To demonstrate that the above photomodulation takes place in the absence of any 30 destabilization of the liquid crystal phase, Ps was measured as a function of temperature with the sample in the dark and under constant irradiation at 532 nm. As shown in Figure 6, the two curves can be extrapolated to the same Sc~ - SA~ phase transition temperature, thus SUBSTITUTE SltEET (RULE 26) CA 022~0867 1998-10-02 wo 98/34995 PCT/CA98/00083 suggesting that the photomodulation takes place without a photomechanical effect.
The photostability of II was verified as no decomposition of the dopant was a~)pa~
after 80 hours of continuous irradiation of a 2.6 mol% mixture in PhBz at a wavelength of 514 nm with an argon laser. Similarly, no decomposition of III was observed after 24 hours of continuous irradiation of the 2.9 mol% mixture in PhBz at 532 nm with a Nd:YAG laser.

Example 2 Compound II of the invention was synthesized according to the procedure shown inFigure 3, using intermediates having reference numerals S1 to S5. Intermediates S2 to S5 were synthesized as set forth below.
General. 'H and 13C NMR spectra were recorded on a Bruker ACF-200 NMR
spectrometer in deuterated chloroform or deuterated acetone. The chemical shifts are reported in ~ (ppm) relative to tetramethylsilane as internal standard. Low-resolution EI and CI mass spectra were recorded on a Fisons VG Quattro triple quadrupole mass spectrometer;
peaks are reported as m/e (% intensity relative to the base peak). High-resolutiori EI mass spectra were performed by the University of Ottawa Regional Mass Spectrometry Center.
W-visible spectra were recorded on a Varian Cary 3 spectrophotometer in benzene. Melting points were measured on a Mel-Temp II melting point apparatus and are uncorrected.
Materials. All reagents were obtained from commercial sources and used without further purification unless otherwise noted. Dimethylformamide (DMF) was distilled from BaO under reduced ples~ule and stored over molecular sieves. Methylene chloride (CH2CI2) was distilled from P2Os under N2. 2-Chloro-4-hydroxybenzoic acid (S1, Figure 3) was prepared according to the procedure of Molnar et al. (Helv. Chim. Acta, 52:401, 1969), and shown to have the expected physical and spectral properties.
Methyl 2-chloro 1 ~l~dr~xy-5-nitrobenzoate (S3). A solution of S1 (1.55 g, 9.0 mmol) in acetic anhydride (5 ml) was heated on a steam bath for 30 min, then poured over ice and filtered in a Buchner furmel. The solid residue was washed with water and air dried to give 1.76 g of the acetoxy derivative S2. Without further purification, compound S2 was dissolved in a mixture of 95% HN~l (15 ml) and glacial acetic acid (15 ml) and stirred at room temperature for 24 h. The mixture was then concentrated, and the yellow residue was dissolved in a mixture of methanol (20 ml) and concentrated H2SO4 (0.5 ml) and refluxed overnight. After cooling, the mixture was poured into H2O and extracted with ether. The SUBSTlTUTE SHEET (RULE 26) .

CA 022~0867 1998-10-02 extracts were washed with H20, brine, then dried (MgSO4) and concentrated. Purification by flash chromatography on silica gel (30% e~yl acetate/toluene) gave 0.64 g (31 %) of S3 as a yellow solid: mp 94-95 ~C; 'H NMR ~200 MHz, acetone-d6) ~ 3.91 (s, 3H), 7.36 (s, lH), 8.64 (s, lH), 10.8 (s, OH); 13C NMR (50 MHz, acetone-d6) ~ 52.9, 122.3, 122.9, 130.0, 134.0, 142.3, 157.0, 164.1; MS (EI) m/e 233 (M+2, 6), 231 (M+, 18), 202 (35), 200 (100), 170 (5), 156 (15), 154 (38), 142 (8), 126 (13), 113 (6), 97 (12); HRMS (EI) calculated for C8H6NO537Cl: 232.9905. Found: 232.9888.
Methyl (R)-2-~hloro-4-(2-octyloxy)-S-nitrob~7.~t~ (S4). Under a N~ atmosphere, diisopropylazodicarboxylate (DIAD, 202 mg, 0.99 mrnol) was added dropwise to a stirred solution of S3 (153 mg, 0.66 mmol), triphenyl phosphine (260 mg, 0.99 mmol) and (S)-2-octanol (90 mg, 0.69 mmol) in dry CH2Cl2 (10 ml). After stirring at room temperature for 2 h, the solvent was removed in vacuo, and the oily residue was purified by flash chromatography on silica gel (30% ethyl acetate/toluene) to give 195 mg (86%) of S4 as a yellow oil: 'H
NMR (200 MHz, CDCl3) ~ 0.87 (t, J= 6.6 Hz, 3H), 1.20-1.80 (m, 10H), 1.38 (d, J= 6.0 Hz, 3H), 3.92 (s, 3H), 4.56 (m, J= 6.0 Hz, IH), 7.10 (s, lH), 8.45 (s, lH); '3C NMR (50 MHz, CDCl3) ~ 14.0, 19.3, 22.5, 25.0, 29.0, 31.6, 36.0, 52.6, 77.6, 117.6, 120.5, 129.5, 138.0, 140.3, 154.0, 163.6; MS (CI) m/e 346 (M+3, 32), 344 (M+1, 100), 316 (22), 314 (67), 301 (13), 299 (36), 279 (17), 262 (35), 260 (96), 234 (25), 232 (69), 201 (6), 149 (4), 91 (16);
HRMS (EI) calculated for C~5H~gNO435Cl (M-OCH3): 312.1001. Found: 312.1004.
Methyl (R)-3-hydroxy-6-(2-octyloxy)-5-nitrobenzo[blthiophene-2-carboxylate (S5). Under a N2 atmosphere, a ~ Lu~e of S4 (197 mg, 0.57 mmol), anhydrous LiOH (48 mg, 2 mmol) and methyl thioglycolate (91 mg, 0.86 mmol) in dry DMF (10 ml) was stirred oveInight at room temperature. The mixture was poured into H20 (40 ml), acidified with 3M
HCl and extracted with ethyl acetate. The combined extracts were washed with lM HCl, brine, dried (MgSO4) and concentrated to give a yellow oil. Purification by flash chromatography on silica gel (30% ethyl acetate/toluene) gave 135 mg (62%) of S5 as a yellow waxy solid: mp 54-55 ~C; lH NMR (200 MHz, CDC13) ~ 0.87 (t, J= 6.7 Hz, 3H), 1.24-1.80 (m, 10H), 1.39 (d, J= 6.2 Hz, 3H), 3.95 (s, 3H), 4.54 (m, J= 6.0 Hz, lH), 7.26 (s, lH), 8.31 (s, lH), 10.1 (s, lH); '3C NMR (50 MHz, CDCl3) ~ 14.0, 19.2, 22.6, 25.2, 29.1, 31.7, 36.1, 52.3, 77.0, 101.5, 107.8, 120.1, 122.3, 140.0, 143.5, 151.7, 159.2, 166.8; MS (CI) mle 382 (M+1, 3), 270 (100), 232 (98), 212 (18), 202 (48), 149 (12), 113 (19); HRMS (EI) calculated for C~8H23NO6S: 381.1246. Found: 381.1252.

SUBSTITUTE Sl-IEET (RULE 26) .

W O 98/34ggS PCT/CA98/00083 (R,~)-5,5'-dinitro-6,6'-bis(2-octyloxy)thioindigo. A suspension of S5 (153 mg, 0.36 mmol) in a 15% solution of KOH in 1:1 ethanol/H2O (15 ml) was heated to reflux for 5h.
After cooling to room temperature, the mixture was treated with 300 mg of K3[Fe(CN)6]
dissolved in H2O (2 ml) and stirred for 1 h. After removing the alcohol in vacuo, the ~ lu~e 5 was extracted with CHCl3, and the extracts were washed with H2O, dried (MgS04) and concentrated to a red solid. Purification by flash chromatography on silica gel (benzene) gave 40 mg (35%) of II as a red solid. The compound was further purified for doping experiments by recryst~lli7~tion from 15% CHClJhexanes: mp 189-190 ~C; 'H NMR (200 MHz, CDCl~) ~ 0.88 (t, J= 6.6 Hz, 6H), 1.15-1.85 (m, 20H), 1.44 (d, J= 6.1 Hz, 6H), 4.66 (m, J= 6.0 Hz, 2H), 7.12 (s, 2H), 8.37 (s, 2H); '3C NMR (50 MHz, CDCl3) ~ 14.0, 19.3, 22.5, 25.1, 29.0, 31.6, 36.0, 78.1, 109.0, 120.3, 124.4, 133.1, 139.6, 154.6, 157.6, 186.8; MS (EI) m/e 642 (M+, 1), 418 (100), 388 (4), 372 (5), 359 (2), 326 (2), 253 (2), 208 (4), 165 (16), 111 (26), 83 (59); HRMS (EI) calculated for C32H38N2O8S2: 642.2070. Found: 642.2044.
F,l~mrle 3 With reference to Figure 4, the following method was employed for the synthesis of III. Steps Sl to S10 refer to the steps of the synthesis and correspond to the intermediate compounds employed therein, as indicated in Figure 4 and in the description below.
GeneYal. 'H and l3C NMR spectra were recorded on a Bruker ACF-200 NMR
spectrometer in deuterated chloroform or deuterated acetone. The chemical shifts are reported in ~ (ppm) relative to tetramethylsilane as internal standard. Low-resolution EI and CI mass spectra were recorded on a Fisons VG Quattro triple quadrupole mass spectrometer;
peaks are reported as m/e (% intensity relative to the base peak). High-resolution EI mass spectra were performed by the University of Ottawa Regional Mass Spectrometry Center.
UV-visi~le spectra were recorded on a Varian Cary 3 spectrophotometer in benzene. Melting points were measured on a Mel-Temp II melting point apparatus and are uncorrected.
Materials. All reagents were obtained from commercial sources and used without further purification unless otherwise noted. Dimethylformamide (DMF) was distilled from BaO under reduced pressure and stored over molecular sieves. Methylene chloride (CH2C12) was distilled from P2O5 under N2. 4-Methyl-2-nitroanisole was obtained from Aldrich and used without further purification.

2-acetylamino-4-methylanisole (Sl). A solution of 4-methyl-2-nitroanisole SIJC~S 111 ~JTE SHEET (RULE 26) CA 022~0867 1998-10-02 WO 98/34gg5 PCT/CA98/00083 (Aldrich) (10 g, 0.06 mol) in 100 ml of absolute ethanol was hydrogenated in the presence of 0.25 g of Pd/C ( 10%) at room temperature. The catalyst was removed by filtration and the clear solution was concentrated to give 2-amino-4-methylanisole as a white solid. To this solid was added 70 ml of acetic anhydride and a few drops of concentrated sulfuric acid.
5 After stirring for 1 h, the ~ lule was poured into ice/water and the ~ cipilated product was filtered and dried to give 9.48g (88%) of Sl as a white solid.
2-acetylamino-4-methyl-5-nitroanisole (S2). Compound S1 (7 g, 39 rnmol) was added in portions to a stirred solution of 24 ml of fuming nitric acid and 100 ml of glacial acetic acid cooled at -18 ~C using a salt-ice bath. After stirring for 2 h, the mixture was 10 poured into ice/water and the ~ cipil~ted product was filtered and dried to give 7.~ g (89%) of S2 as a light yellow powder.
2-amino-4-methyl-5-nitroanisole (S3). A ~ ure of S2 (3 g, 13.4 mmol) and 20 mlof 10% aq HCl was refluxed for 1 h. The resulting solution was neutralized and then cooled in an ice/water bath. The resulting yellow precipitate was filtered and dried to give 2.1 g (86%)ofS3.
2-chloro-4-methyl-5-nitroanisole (S4). To a solution of S3 (0.5 g, 2.75 mmol) in 5 ml of water and 5 ml of concentrated HCl cooled at 5 ~C was added dropwise a solution of 200 mg of NaNO2 in 3 ml of water. The mixture was stirred at 5 ~C for 1 h, then poured slowly into a stirred solution of 0.35 g of CuCl in 5 ml of concentrated HCl. After N~
20 evolution ceased, the precipitate formed was filtered, washed three times with cold water and dried to give 0.45 g (81 %) of S4 as a grey-yellow solid.
5-amino-2-chloro-4-methyl~ni~ole (S5). Compound S4 (5.0 g, 24.8 mmol) in 50 ml of methanol was hydrogenated in the presence of 0.25 g of Pd/C (10%) at room temperature.
The catalyst was removed by filtration and the clear solution concentrated to give 4.1 g (96%) 25 of S5.
2-chloro-5-fluoro 4 ~Pthyl~ lc (S6). To a solution of S5 (7.5 g, 43.7 mmol) in10 ml of water and 10 ml of 45% aq ~IBF4 was added dropwise a solution of 3 .5 g of NaNO.
in 30 ml of water. The precipitated tetrafluoroborate salt was filtered and washed successively with cold water, cold methanol and cold diethyl ether. After drying, the salt was 30 decomposed by heating in 100 ml of toluene under reflux. When the evolution of BF3 ceased, the solution was concentrated to give S6 as a dark viscous oil that was used in the next step without further purification.

SU~ JTE SHEET (RULE 26) W O 9~34995 PCT/CA98/00083 S-chloro-2-fluoro-4-methoxybenzoic acid (S7). Crude S6 (540 mg, 3.1 mmol) was mixed in a solution of 1.3 g of potassium penn~ng~ te in 100 ml of water. The mixture was refluxed for 2 h, then filtered hot. The filtrate was cooled in an ice bath and acidified with 2M aq HCI to produce a white ~r~ ,iL~le, which was filtered and dried to give 200 mg (35%) S of S7 as a white solid.
Methyl 5-chloro-2-fluoro-4-hydroxybenzoate (S8). A Illixlure of S7 (627 mg, 3.0 mmol) and 30 mg of the phase transfer catalyst Ct(Me)3N+Br- in 25 ml of 40% aq HBr was refluxed for 8 hours with vigorous stirring After cooling, the mixture was concentrated to a solid residue, which was mixed with 70 ml of dry methanol and 10-20 drops of concentrated H2SO4. The mixture was refluxed overnight, then cooled and concentrated. The solid residue was dissolved in ethyl acetate, and the solution was washed with water, then with brine. The organic layer was dried (MgSO4) and the solvent removed in vacuo to give 514 mg (82%) of S8.
Methyl (R)-5-chloro-2-fluoro~-(2-octyloxy)b~n7.o~te (S9). Under a N2 atmosphere,diisopropylazodicarboxylate (DIAD, 146 mg, 0.72 mmol) was added dropwise to a stirred solution of S8 (98 mg, 0.47 mmol), triphenyl phosphine (189 mg, 0.72 mmol) and (5)-2-octanol (95 mg, 0.72 mmol) in dry CH2Cl2 (10 ml). After stirring at 25 ~C for 2 h, the solvent was removed in vacuo, and the oily residue was purified by flash chromatography on silica gel (30% ethyl acetate/toluene) to give 158 mg (95%) of S9 as an oil.
Methyl (R)-5-chloro-3-hydroxy-6-(2-octyloxy)benzolblthio phene-2-carboxylate (S10). Under a N2 atmosphere, a mixture of S9 (168 mg, 0.53 mmol), anhydrous LiOH (70 mg, 2.9 mmol) and methylthioglycolate (150 mg, 1.4 mmol) in dry DMF (10 ml) was stirred overnight at 25 ~C. After cooling, the mixture was poured into water (40 ml), acidified with 3M aq HCl and extracted twice with ethyl acetate. The combined extracts were washed with lM aq HCl, brine, dried and concentrated to give an oily residue. Purification by flash chromatography on silica gel (30~/O ethyl acetate/toluene) gave 129 mg (66%) of S10 as a clear oil.
(R,R)-5,5'-Dichloro-6,6'-bis(2-octyloxy)thioindigo. A suspension of S10 (110 mg,0.3 mmol) in a 15% solution of KOH in 1:1 ethanol/H,O (20 ml~ was heated to reflux for 5 h.
After cooling, the mixture was treated with 250 mg of K3[Fe(CN)6], dissolved in water (3 ml) and stirred for 1 h. After removing the alcohol in vacuo, the llliX~ule was extracted twice with ethyl acetate, and the combined extracts were washed with water, dried and concentrated SUBSTITUTE SHEET (RULE 26) CA 022~0867 1998-10-02 wo 98/34995 PCT/CA98/00083 to give a dark red solid. Purification by flash chlo~ lography on silica gel (30% ethyl acetate/toluene) gave 40 mg (40%) of III as a red solid. The compound was further purified by recry~t~ tion from 95% ethanol in water: mp 103-105 ~C, IH NMR (200 MHz, CDCl3) d 0.87 (t, 6H), 1.23-1.83 (m, 20 H), 1.40 (d, 6H), 4.49-4.58 (m, 2H), 6.93 (s, 2H), 7.86 (s, 2H); '3C NMR (50 MHz, CDCl3) d 14.3, 19.7, 22.8, 25.4, 29.3, 31.9, 36.3, 77.0, 108.1, 122.1, 123.3, 128.4, 133.3, 149.8, 160.4, 187.5; MS (EI) m/e 624 (M+4, 1.4), 622 (M+2, 4.8), 620 (M+, 6.3), 400 (20), 398 (76), 396 (100), 258 (12), 226 (47), 213 (10), 171 (23), 149 (88).
High-resolutionMScalculatedforC32H38Cl2S2O4:620.1593. Found: 620.1591.
It should be noted that in the above synthetic procedure, the conversion from intermediate S9 to intermediate S10, i.e., the conversion from a monocyclic to a bicyclic system, must be done under basic conditions. This is because the secondary alkoxy side chain is very acid-sensitive. If acid conditions were employed, the optically active center would r~r,e~ e. Thus, both the conversion from S9 to S10 and from S10 to III areperformed under basic conditions. Similar procedures are employed for analogues or derivatives of III according to the invention.
Unsymmetrical chiral thioindigo dopants and components of general formula I can be synthesized according to the cross-coupling reaction shown in Figure 5. This reaction is a key step in the synthesis of chiral thioindigo oligosiloxane side-chain dopants such as V
according to the invention. The synthesis shown in Figure 5 is based on the procedure described by Wakemoto et al. in European Patent Application No. 86103922.0, published on October 10, 1986, which procedure was used to synthesize achiral unsymmetrical thioindigo compounds. Figure 5 shows a specific example of a chloro-substituted unsymmetrical chiral thioindigo compound.

Example 4 In accordance with the invention, there is provided an approach for preparing thioindigo-doped polyrneric liquid crystals that undergo Ps or ec photomodulation. The approach involves synthesizing a chiral thioindigo compound of general formula I but having an oligosiloxane side-chain, as shown in formula V, and introducing such compound as a dopant into a side-chain polysiloxane or oligosiloxane Sc or SA host.
Appending an oligosiloxane side-chain onto a thioindigo dopant, as in general formula V, requires that one of the chiral side-chains of the thioindigo be a t~nnin~l alkene SUBSTITUTE S~lErT (RULE 26) , .. . .

CA 022~0867 1998-10-02 Wo 98/34995 PCT/CA98/00083 such as, for exa~nple, that shown in formula IVf. The chiral side-chain can be appended to the oligosiloxane structure via, for example, standard hydrosilation chemistry.

Example 5 A light switch according to the invention was demonstrated using the following procedure:
In a 0.4 ml Reacti-Vial were mixed 0.524 mg of III, 0.152 mg of (S,S)-4,4'-bis[(2-chloro-3-methylbutanoyl)oxy]biphenyl and 13.46 mg of PhBz to give a homogeneous material. A cell consisting of two polyimide-coated glass slides with an indium/tin oxide-coated addressed area of 0.25 cm2 and a spacing of 3.5 ,um was filled by capillary action with the above liquid crystal mixture at a temperature of 120 ~C (cell purchased from Displaytech, Inc., Longmont, CO). The cell cont~3ining the above mixture (hereinafter FLC cell) was then placed in a Instec HS 1 -i microscope hot stage with the addressed area fully exposed through the aperture and heated to 80 ~C, which is above the clearing point of the liquid crystal phase.
The sample was then cooled to 71 ~C, which is just above the Sc~ - SA~ transition temperature, at a rate of 1 ~C/min. The sample was held at that temperature for 3 hours in order to align the liquid crystal material, and then cooled to 60 DC at a rate of 2 ~C/min, which is 10 ~C below the Sc~ - SA~ transition temperature (T-TAC = -10 ~C). The sample was then annealed at 60 ~C overnight. Throughout this entire operation, a triangular AC voltage was m~int~ined across the cell (100 Hz, 20V).
With reference to Figure 8, the FLC cell/hot stage assembly 1 was positioned vertically between two crossed polarizers 2, 3, and a constant DC voltage of 17 V was m~int~ined across the cell throughout the experiment. The temperature of the sample was m~int~ined at T-TAC =-10~C. A circularly polarized reading beam 4 at 665 nm was generated from a 5 mW diode laser 5 using a Fresnel rhomb 6, and the beam 4 was aligned in such a way as to pass through the addressed area of the FLC cell 1. The FLC sample does not absorb 665 nm light. The crossed polarizers 2, 3 were aligned in such a way as to minimi7e the tr~n.~mi~ion of the reading beam 4 through the FLC cell/polarizers assembly. A
photodiode detector 7 interfaced to a computer 10 via an analogue-to-digital converter 8 was used to measure the intensity of the reading beam 4 through the FLC cell/polarizers assembly. A writing beam 11 at 532 nm was generated from a 50 mW Nd:YAG laser 12, and the beam 11 was aligned through a lens 13 to irradiate the FLC cell 1 as shown in Figure 7.

SUBSTITUTE SHEET (RULE 26) CA 022~0867 1998-10-02 The writing beam 11 was turned ON and OFF by a shutter 1 4 controlled by the computer 1 0 via a digital-to-analogue converter 9.
In a typical experiment, the writing beam 11 was turned ON for 2.5 seconds and the tr~n~mi.c~ion of the reading beam 4 through the FLC cell/polarizers assembly was measured 5 as a function of time, as shown in Figure 9. The results show an increase in tr:~n~mis~ion upon irradiation of the FLC cell at 532 nm. The tr:~n~mi~sion level of the reading beam 4 retumed to its original value about 150 seconds after the writing beam 1 1 was turned OFF, as a result of thermal relaxation of the thioindigo dopant from the cis form back to the trans form.
To show that the observed change in tran~mi~ion of the reading beam is caused byphotoinduced Goldstone-mode switching of the FLC cell, the above experiment was repeated using a square wave AC voltage (17 V, 0.01 Hz). Under these conditions, Goldstone-mode switching is field-induced instead of photoinduced. As shown in Figure 10, when the FLC
cell is in the dark, electric field reversal causes an increase in tr~n.~mi.~ion that is about 20%
15 less than that shown in Figure 9. When the FLC cell is under constant irradiation at 532 nm, electric field reversal causes the same net change in tr~n~mi.~ion, but with an upward baseline shift. The overall change in tr~n~mi~.sion from the low tr~3n~mi~ion level in the dark to the high tr~n~mi~sion level under constant irradiation is approximately equal to that shown in Figure 9, thus confirming the occurrence of photoinduced Goldstone-mode FLC switching.
- 20 The response time corresponding to a 90% change in tr~n~mi~sion is 0.5 seconds at T - TAC =
-10~C in this experiment.
Those skilled in the art will recognize, or be able to ascertain through routineexperimentation, equivalents to the specific embodiments described herein. Such equivalents are considered to be within the scope of the invention and are covered by the appended 25 claims.

SUBSTITUTE SHEET (RULE 26)

Claims (29)

1. A chiral thioindigo compound for doping a smectic liquid crystal host, wherein the compound modulates a chiral bulk property of an induced chiral smectic liquid crystal phase upon irradiation at a wavelength in the visible range, without destabilizing the chiral smectic liquid crystal phase.

2. A chiral thioindigo compound according to claim 1, wherein the modulation is effected by trans-cis photoisomerization of the compound upon irradiation.

3. A chiral thioindigo compound according to claim 2, wherein the compound exhibits: reversible photoisomerization; absorptivity of the cis and trans isomers at different wavelengths so that the two isomers can be addressed at different wavelengths without overlap; and absorptivity of the cis and trans isomers in the visible range.

4. A chiral thioindigo compound according to claim 1, wherein the wavelength is within the range of about 400 nm to about 800 nm.

5. A chiral thioindigo compound according to claim 1, wherein the compound is of the general formula I:

wherein R1 and R2 may be the same or different from each other and are selected from the group consisting of hydrogen, fluoro, chloro, bromo, iodo, nitro, nitrile, alkyl, alkenyl, alkoxy, hydroxy, perfluoroalkyl, and thioalkyl; and R3 and R4 may be the same or different from each other and at least one of R3 and R4 is a chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-dipole interactions, to the thioindigo core.

6. A chiral compound according to claim 1, wherein the compound is dinitro-6,6'-bis(2-octyloxy)thioindigo, or a derivative or analogue thereof.

7. A chiral compound according to claim 1, wherein the compound is (R,R)-5,5'-dichloro-6, 6'-bis(2-octyloxy)thioindigo, or a derivative or analogue thereof.

8. A chiral compound according to claim 5, wherein one of R3 and R4 is an oligosiloxane side-chain, and the other of R3 and R4 is a chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-dipole interactions, to the thioindigo core.

9. A chiral thioindigo compound according to claim 1, wherein the liquid crystalhost is selected from the group consisting of an achiral smectic C (S c) liquid crystal host, and a chiral smectic C (S c*) liquid crystal host.

10. A chiral thioindigo compound according to claim 9, wherein the compound modulates a spontaneous polarization of the liquid crystal phase upon irradiation in the visible range.

11. A chiral compound according to claim 1, wherein the liquid crystal host is selected from the group consisting of an achiral smectic A (S A) liquid crystal host and a chiral smectic A (S A*) liquid crystal host.

12. A chiral thioindigo compound according to claim 11, wherein the compound modulates an electroclinic coefficient of the liquid crystal phase upon irradiation in the visible range.

13. A chiral compound according to claim 1, wherein the liquid crystal host is selected from the group consisting of a polymeric smectic C (S c) liquid crystal host and a polymeric smectic A (S A) liquid crystal host.

14. A chiral compound according to claim 13, wherein the liquid crystal host is selected from the group consisting of a polysiloxane smectic C (S c) liquid crystal host and a polysiloxane smectic A (S A) liquid crystal host.

15. A method for synthesizing (R,R)-5,5'-dinitro-6,6'-bis(2-octyloxy)thioindigo,comprising the steps of:
conducting a Mitsunobu inversion reaction to produce a chiral methyl 2-chlorobenzoate precursor;
reacting the chiral methyl 2-chlorobenzoate precursor with methyl thioglycolate to produce a chiral bicyclic enol ester;
performing base-catalyzed hydrolysis and decarboxylation of the chiral bicyclic enol ester to produce a chiral benzothiophenone; and, oxidizing the chiral benzothiophenone to produce (R,R)-S,S'-dinitro-6,6'-bis(2-octyloxy) thioindigo.

16. A method according to claim 15, wherein the oxidizing step is performed without prior isolation of the chiral benzothiophenone.

17. A method for synthesizing (R,R)-5,5'-dichloro-6,6'-bis(2-octyloxy)thioindigo, comprising the steps of:
conducting a Mitsunobu inversion reaction to produce a chiral methyl 2-fluorobenzoate precursor;
reacting the chiral methyl 2-fluorobenzoate precursor with methyl thioglycolate to produce a chiral bicyclic enol ester;
conducting a base-catalyzed hydrolysis and decarboxylation of the chiral bicyclic enol ester to produce chiral benzothiophenone; and oxidizing the chiral benzothiophenone to produce (R,R)-5,5'-dichloro-6,6'-bis (2-octyloxy)thioindigo .

18. A method according to claim 17, wherein the oxidizing step is performed without prior isolation of the chiral benzothiophenone.

19. A chiral bicyclic enol ester selected from the group consisting of:

and,

20. A method for synthesizing the chiral bicyclic enol ester of claim 19, comprising the steps of:
comprising a Mitsunobu inversion reaction to produce a chiral methyl 2-fluorobenzoate precursor;
reacting the chiral methyl 2-fluorobenzoate precursor with methyl thioglycolate to produce the chiral bicyclic enol ester.

21. An optical device for operation with a direct current field, comprising:
a liquid crystal host selected from the group consisting of an achiral smectic C (S c) liquid crystal host and a chiral smectic C (S c*) liquid crystal host; and a chiral thioindigo compound dispersed in the liquid crystal host to produce a chiral smectic C (S c*) liquid crystal phase across which the field is applied, the chiral compound, upon irradiation in the visible range, modulating a spontaneous polarization of the liquid crystal phase without destabilization of the liquid crystal phase.

22. An optical device according to claim 21, wherein the chiral thioindigo compound is of the general formula I, wherein R1 and R2 may be the same or different from each other and are selected from the group consisting of hydrogen, fluoro, chloro, bromo, iodo, nitro, nitrile, alkyl, alkenyl, alkoxy, hydroxy, perfluoroalkyl, and thioalkyl; and R3 and R4 may be the same or different from each other and at least one of R3 and R4 is a chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-dipole interactions, to the thioindigo core.

23. An optical device according to claim 22, wherein one of R3 and R4 is an oligosiloxane side-chain, and the other of R3 and R4 is an a chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-dipole interactions, to the thioindigo core.

24. An optical device for operation with a direct current field, comprising:
a liquid crystal host selected from the group consisting of an achiral smectic C (S A) liquid crystal host and a chiral smectic C (S A*) liquid crystal host; and a chiral thioindigo compound dispersed in the liquid crystal host to produce a chiral smectic C (S A*) liquid crystal phase across which the field is applied, the chiral compound, upon irradiation in the visible range, modulating an electroclinic coefficient of the liquid crystal phase without destabilization of the liquid crystal phase.

25. An optical device according to claim 24, wherein the chiral thioindigo compound is of the general formula I:

wherein R1 and R2 may be the same or different from each other and are selected from the group consisting of hydrogen, fluoro, chloro, bromo, iodo, nitro, nitrile, alkyl, alkenyl, alkoxy, hydroxy, perfluoroalkyl, and thioalkyl; and R3 and R4 may be the same or different from each other and at least one of R3 and R4 is a chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-dipole interactions, to the thioindigo core.

26. An optical device according to claim 25, wherein one of R3 and R4 is an oligosiloxane side-chain, and the other of R3 and R4 is an a chiral side-chain with at least one chiral center that is coupled, via steric and/or dipole-dipole interactions, to the thioindigo core.

27. An optical device according to claim 21, wherein the device is an optical switch.

28. An optical device according to claim 24, wherein the device is an optical switch.

29. An optical switch for operation under a direct current field, comprising:
a smectic C liquid crystal host;
a chiral photochromic compound dispersed in the liquid crystal host, the chiral compound inducing in the liquid crystal host polarization in a first polarity, and being capable of undergoing trans-cis isomerization upon irradiation in the visible range without destabilizing the liquid crystal; and a photochemically inert compound dispersed in the liquid crystal host, the inertcompound inducing in the liquid crystal polarization in a second polarity;
wherein the proportions of the chiral compound and the inert compound are such that the polarization induced by the inert compound is greater than that induced by a first isoform of the photochromic dopant, such that the total polarization of the liquid crystal is in the second polarity; and wherein upon irradiation in the visible range the polarization induced by the inert compound is less than that induced by the photochromic dopant in a second isoform, such that the total polarization of the liquid crystal is in the first polarity, resulting in a change in light transmission through the liquid crystal.