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  • Y10S428/917—Electroluminescent

Definitions

• the present invention relates to a process for the preparation of a conjugated polymer, in particular conjugated polymers suitable for use as an active material in organic semiconductor devices including optical devices such as electroluminescent or photovoltaic devices.
• Conjugated polyarylenes are widely used as the active material.
• examples of such materials include polyfluorenes as disclosed in, for example, WO 99/54385, spirofluorenes as disclosed in, for example, EP 0707020, polyphenylenes as disclosed in, for example, G.Grem, G. Leditzky, B. Ullrich, G. Leising, Adv. Mater. (1992), 4, 36 and phenylene-thienylene copolymers as disclosed in, for example, K.Kaeriyama et al, Synth. Met. (2000), 111-112, 519-522.
• Polyarylenes may suitably be prepared by Suzuki or Yamamoto polymerisation. Of these two techniques, Suzuki polymerisation is the only technique that enables exertion of control over the regioregularity of the copolymer. Thus Suzuki polymerisation may be used to generate AB, block or random copolymers depending on the relative quantities of boron and halo monomers used.
• polyarylenes for use in the aforementioned optical devices it is desirable for polyarylenes for use in the aforementioned optical devices to be of high molecular weight as this improves their processability. High viscosity is also advantageous for certain applications.
• a known drawback of Suzuki polymerisation is the difficulty in reproducibly generating high molecular weight polymers. This has been attributed to the problem of side reactions competing with the polymerisation, e.g. reductive elimination and deboronation of the monomers, which limit. the molecular weight of the polymer. These side reactions are initially relatively insignificant but become prevalent at longer reaction times. A fast reaction rate is therefore desirable from the point of view of obtaining high molecular weight material.
• US 5777070 discloses the use of the phase transfer catalyst tricaprylylmethyl ammonium chloride in Suzuki polymerisation reactions to facilitate the movement of the reactive boronate species between the organic and aqueous phases of the reaction mixture.
• GB 2360291 describes the use of tetraalkyl ammonium boronate salts soluble in the organic phase such that the polymerisation reaction takes place in a single phase.
• the invention provides a process for preparing a conjugated polymer, which comprises polymerising in a reaction mixture (a) an aromatic monomer having at least two boron derivative functional groups selected from a boronic acid group, a boronic ester group and a borane group, and an aromatic monomer having at least two reactive halide functional groups; or (b) an aromatic monomer having one reactive halide functional group and one boron derivative functional group selected from a boronic acid group, a boronic ester group and a borane group; an amount of a catalyst suitable for catalysing the polymerisation of the aromatic monomers; and a base in an amount sufficient to convert the boron derivative functional groups into boron anionic groups, characterised in that said reaction mixture further comprises a first solvent and a second solvent with which said first solvent is substantially immiscible and a emulsifier in an amount sufficient to form an emulsion of said reaction mixture.
• conjugated polymer refers to either a fully conjugated polymer i. e. a polymer which is conjugated along the full length of its chain, or a partially conjugated polymer i.e. a polymer which contains conjugated segments together with non-conjugated segments.
• emulsion refers to a colloidal suspension comprising a first solvent dispersed within a second solvent, or vice-versa, wherein each of said first and second solvents contain reactive species dissolved therein during at least part of the reaction.
• emulsifier refers to a substance that coats the particles of the dispersed solvent and prevents coagulation of colloidal particles.
• the boron anionic group is of formula -B(OR) 3 - wherein each R is independently selected from hydrogen or optionally substituted alkyl or aryl and two R groups may be linked.
• the emulsifier is used in an amount ranging from 1-20% w/v, more preferably in an amount ranging from 1-10% w/v.
• the first solvent is selected from the group comprising alkylated aromatics.
• the first solvent is toluene.
• the second solvent is preferably water.
• the ratio of first solvent to second solvent may range from 0.1:1 up to 10:1 by volume. Preferably, the ratio is in the range 1:1 up to 10:1.
• the monomers are selected from the group consisting of optionally substituted arylenes, heteroaromatics and fused aromatic systems.
• at least one of the monomers comprises a triarylamine, a phenylene, a thiophene, a benzothiadiazole or a fluorene wherein each of said monomers is optionally substituted by an alkyl or alkoxy group.
• Particularly preferred types of monomers include dialkylphenylenes, dialkoxy phenylenes, substituted and non-substituted thiophenes and benzothiadiazoles, and dialkylfluorenes such as 9,9-di-n-octylfluorenes.
• One or more of the monomers could also be a pre-formed oligomeric or polymeric chain comprising several smaller units with the necessary functional groups provided at the desired positions on the chain.
• this invention could also be extended to the use of monomers in which some or all of the functional groups are not directly substituted on an aromatic ring, in particular to other kinds of unsaturated monomers.
• the catalyst used in the method of the present invention is preferably a palladium catalyst.
• the palladium catalyst may be a Pd (0) or Pd (II) species.
• Particularly preferred catalysts include Pd(Ph 3 P) and PdCI 2 (Ph 3 P) 2 .
• the amount of palladium catalyst in the reaction mixture is 0.01 to 1 mol. %, preferably about 0.15 mol. %, based on the total number of moles of monomers used.
• the base may be an inorganic base such as a hydroxide, carbonate or hydrogencarbonate of an alkali or alkali earth metal.
• the base is an organic base, for example a tetraalkylammonium hydroxide, tetraalkylammonium carbonate or tetraalkylammonium hydrogencarbonate.
• the quantity of base used is up to 2 equivalents per monomer with a boron derivative functional group or groups
• the polymer produced is a semiconductive conjugated polymer, in particular a semiconductive conjugated luminescent polymer.
• the invention provides a process for the production of an optical device or acomponent for an optical device, which comprises providing a substrate and producing a polymer in accordance with the process of any one of the preceding claims, whereby the polymer is supported by the substrate.
• the optical device comprises an electroluminescent device or photovoltaic device.
• the present invention provides a method for the reproducible production of high molecular weight polymer in a short time. This is achieved by means of the emulsion which greatly increases the surface contact area between the two phases of the reaction mixture as compared with prior art systems.
• Figure 1 shows the reaction of Example 1.
• the process of the present invention applies to the polymerisation of monomers by Suzuki polymerisation. Accordingly, known methodology for Suzuki polymerisation as disclosed in, for example, WO 00/53656 or the aforementioned prior art, is applicable to the present invention.
• the process of the invention may be applied to a wide range of aromatic monomers such as fluorenes, phenylenes, heteroaromatics and triarylamines.
• triarylamine repeat units derived from triarylamine monomers include units of formulae 1-6:
• X and Y may be the same or different and are substituent groups.
• A, B, C and D may be the same or different and are substituent groups. It is preferred that one or more of X, Y, A, B, C and D is independently selected from the group consisting of alkyl, aryl, perfluoroalkyl, thioalkyl, cyano, alkoxy, heteroaryl, alkylaryl and arylalkyl groups.
• One or more of X, Y, A, B, C and D also may be hydrogen.
• one or more of X, Y, A, B, C and D is independently an unsubstituted, isobutyl group, an n-alkyl, an n-alkoxy or a trifluoromethyl group because they are suitable for helping to select the HOMO level and/or for improving solubility of the polymer.
• heteroaryl repeat units include units of formulae 7-21:
• R 6 and R 7 are the same or different and are each independently hydrogen or a substituent group, preferably alkyl, aryl, perfluoroalkyl, thioalkyl, cyano, alkoxy, heteroaryl, alkylaryl or arylalkyl.
• R 6 and R 7 are preferably the same. More preferably, they are the same and are each a phenyl group.
• the first and second solvents may each independently comprise a single solvent or may comprise a blend of miscible solvents.
• emulsifiers include the following, available from either Aldrich Chemicals or Raschig GmbH: poly(ethylene glycol)-block-polypropylene glycol)-block-poly(ethyleneglycol) Mn 4400, Mn 1100, Mn 1900, Mn 8400, Mn 5800, Mn 2800, or Mn 2000; polyethylene glycol) 4-nonylphenyl ether acrylate Mn 450, poly(ethylene glycol) 4-nonylphenyl 3-sulfopropyl ether, potassium salt 9 EO/Mole, 20 EO/Mole, polyethylene glycol) methyl ether Mn 350, Mn 550, Mn 750, Mn 2000, or Mn 5000; poly(ethylene glycol) n-alkyl 3-sulfopropyl ether, potassium salt 7 EO/mole or 11 EO/mole; poly(ethylene glycol) Mn 10000, Mn 8000, Mn 4600, Mn 3400, Mn
• Cocoamidopropylbetaine Polyethyleneglycol octyl-(3-sulfopropyl)-diether potassium salt; Octaethylene glycol octyl ether; Polyethyleneglycol alkyl-3-sulfopropyl diether, potassium salt; Polyethyleneglycol alkyl-3sulfopropyl diether, potassium salt; Polyethyleneglycol alkyl-3-sulfopropyl diether, potassium salt or N,N-Dimethyl-N-hydrogenated-tallow alkyl-N-(3-sulfopropyl) ammonium betaine.
• Polymers preparable according to the invention include, but are not limited to,, straight chain, branched and dendrimeric polymers.
• These polymers may have hole transporting, electron transporting and / or emissive properties.
• the polymer may have one or more of these properties. Where the polymer has more than one of these properties, different properties may be provided by different segments of the polymer, in particular segments of the polymer backbone as described in WO 00/55927 or pendant groups as described in WO 02/26859. Alternatively, if the polymer of the invention has only one or two of the properties of hole transport, electron transport and emission, it may be blended with one or more further polymers having the remaining required property or properties.
• the monomers must each have the appropriate functional groups for the Suzuki reaction.
• a first reactive dihalide monomer is polymerised with a second monomer having two boron derivative functional groups.
• the first and the second monomers may be the same or different.
• a monomer having a boron derivative functional group and a reactive halide functional group is polymerised to form a homopolymer. It is also possible to form copolymers from this second arrangement simply by polymerising together two or more different types of monomers each containing both functionalities.
• the reactive halide functional group on the reactive dihalide monomer or the monomer having the reactive halide functional group is Br or I although it is possible to use instead groups such as chlorine, triflate (CF 3 SO 3 -), tosylate and mesylate.
• the boronic acid group is represented by -B(OH) 2 ;
• the boronic ester group is preferably -B(OR 1 )(OR 2 ) or -B(OR 5 0) and the borane group is preferably -BR 3 R 4 , wherein R 1 is a substituted or non-substituted C C 6 alkyl group and R 2 is H or a substituted or non-substituted C C 6 alkyl group;
• R 3 and R are each independently substituted or nonsubstituted C C 6 alkyl groups, and R 5 is a substituted or non-substituted divalent hydrocarbon radical resulting in a 5 or 6 membered ester ring.
• suitable groups as R 5 include substituted or non-substituted C2 or C3 alkylene groups, or substituted or non-substituted ortho-or meta- phenylene groups.
• Suitable boronic ester groups include, for example, the products of esterification of the corresponding boronic acid group with monovalent C
• a suitable heater/chiller unit e.g. Julabo F25 HP programmable, connected to the reactor via M16 fittings and with 2m hoses.
• a suitable stirrer motor for the reactor e.g. an IKA Eurostar power control visk or any appropriate overhead mechanical stirrer motor.
• 9,9-dioctylfluorene-2,7di(ethylenylboronate) 50.56 g; 95.33 mmol; 1.0 eq.
• 2,7-dibromo-9,9 , -dioctylfluorene 41.83 g; 76.26 mmol; 0.8 eq.
• N,N-bis(4-bromophenyl)-N-(4-sec-butylphenyl)amine (8.76 g; 19.07 mmol; 0.2 eq.), toluene and emulsifier.
• the mixture was stirred for 5 minutes at room temperature and then degassed for 1 hour with a nitrogen sparge.
• Dichloro-bis(triphenylphosphine) palladium (0.21 g; 0.3 mmol; 0.003 eq.) was then added and followed by addition of 20% w/w aqueous tetraethylammonium hydroxide (available from Fluka Chemicals) (320 mL) at which point formation of an emulsion was observed.
• the stirring mixture was heated to arid maintained at reflux until the torque or viscosity no longer increased, or the reaction mixture gelled. In the event of gellation, additional toluene was added.
• the mixture was allowed to cool to room temperature and poured slowly into methanol to precipitate the polymer.
• the crude polymer was recovered by filtration, washed with fresh methanol polymer and then redissolved in toluene.
• the toluene solution is warmed to 65°C and washed with diethyldithiocarbamic acid sodium salt solution, dilute hydrochloric acid, aqueous sodium acetate and deionised water.
• the toluene phase was separated and filtered through Celite 545 (available from Aldrich Chemicals) and eluted with toluene.
• the toluene eluant was then concentrated in vacuo, the polymer was precipitated from it with methanol, isolated by filtration and dried in vacuo.
• the reaction was performed with varying emulsifiers, quantitites of emulsifiers, and quantities of solvents as illustrated in the table below wherein percentage weight of emulsifier per unit volume is calculated by multiplying the weight of emulsifier in grammes by the combined volume of toluene and aqueous base in millilitres.

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