PROCESS FOR THE PREPARATION OF TETRACARBOXYNAPHTHALENEDIIMIDE COMPOUNDS DISUBSTITUTED WITH HETEROARYL GROUPS

Description

[0001] The present invention relates to a process for the preparation of a tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups, comprising the reaction of at least one disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide with at least one heteroaryl compound.

[0002] Said tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups can be advantageously used as monomer in the synthesis of semiconductor polymers which can be advantageously used in the construction of organic field effect transistors (OFET) or of organic thin film transistors (OTFT). Furthermore, said tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups can be advantageously used as monomer in the synthesis of semiconductor polymers which can be advantageously used in the construction of photovoltaic devices such as, for example, photovoltaic cells, photovoltaic modules, solar cells, solar modules, on both rigid and flexible supports.

[0003] N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide compounds (NDIs) are at present of great interest for their physical and electronic properties.

[0004] In particular, (co)polymers comprising units deriving from said N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide compounds (NDIs) can be advantageously used in the construction of organic field effect transistors (OFET) or of organic thin film transistors (OTFT) and in the construction of photovoltaic devices such as, for example, photovoltaic cells, photovoltaic modules, solar cells, solar modules, on both rigid and flexible supports.

[0005] It is known that N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide compounds (NDIs) have very interesting characteristics such as, for example, a good thermal stability, good properties as electron-acceptor compounds, a good processability in organic solvents normally used in the construction of the above-mentioned transistors or of the above-mentioned photovoltaic devices.

[0006] It is also known that the substituents present on the imide nitrogen of said N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide compounds (NDIs) can considerably influence the molecular packing, the solubility in the above-reported organic solvents, the morphology of the thin films that comprise them.

[0007] Furthermore, said N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide compounds (NDIs) have good electronic properties such as, for example, a strong π-π interaction and consequently, when used in the construction of photovoltaic devices, for example photovoltaic cells, they have a short intermolecular distance and, in particular, optimum charge transport properties.

[0008] It is also known that said electronic properties can be modulated by introducing different substituents on the tetracaboxynaphthalenediimide nucleus.

[0009] It is known, for example, that (co)polymers comprising units deriving from tetracaboxynaphthalenediimide compounds disubstituted in position 2 and 6 with thienyl groups, have strong absorptions in the visible and near infrared (NIR), thus allowing the production of photovoltaic devices, for example photovoltaic cells, capable of more efficiently exploiting solar radiation.

[0010] Thanks to the above-reported characteristics, efforts of scientific community towards the development of both new tetracarboxynaphthalenediimide compounds and new processes for their preparation, are greatly encouraged.

[0011] N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide compounds (NDIs) disubstituted in position 2 and 6 with aryl or heteroaryl groups can generally be prepared by means of a Stille reaction or of a Suzuki reaction starting from 2,6-dihalogen-1,4,5,8-tetracarboxy-naphthalene-N,N'-dialkyldiimide which can be prepared through a two-step process starting from 1,4,5,8-tetracarboxynaphthalenedianhydride (NDA). In the first step, the halogenation of 1,4,5,8-tetracarboxynaphthalenedianhydride (NDA) is generally carried out to give 2,6-dihalogen-1,4,5,8-naphthalenedianhydride which, in the second step, by treatment with a primary amine, is transformed into the corresponding diimide.

[0012] The halogenation reaction of 1,4,5,8-tetracarboxynaphthalenedianhydride (NDA) can be carried out according to methods described in literature such as, for example:

• reaction of 1,4,5,8-tetracarboxynaphthalene-dianhydride (NDA) with dibromoisocyanuric acid in the presence of sulfuric acid, at 130°C, for 15 hours, as described by Chaignon F. at al. in the article: "Very large acceleration of the photoinduced electron transfer in a Ru(bpy)3-naphthalene bisimide dyad bridged on the naphthyl core", Chemical Communications (2007), pages 64-66) ;
• reaction of 1,4,5,8-tetracarboxynaphthalene-dianhydride (NDA) with dibromoisocyanuric acid, in the presence of oleum in a quantity higher than 20%, at room temperature, for 4 hours, as described in American patent application US 2008/0300405;
• reaction of 1,4,5,8-tetracarboxynaphthalene-dianhydride (NDA) with bromine and iodine, in the presence of oleum, at 95°C, for 24 hours, under a nitrogen stream, as described in international patent application WO 2007/146250;
• reaction of 1,4,5,8-tetracarboxynaphthalene-dianhydride (NDA) with bromine and iodine, in the presence of oleum, at room temperature, overnight, as described by Piyakulawat P. et al. in the article: "Synthesis and preliminary characterization of novel naphthalene bisimide based copolymers", Synthetic Metals (2009), Vol. 159, pages 467-472.

[0013] Subsequently, the 2,6-dihalogen-1,4,5,8-tetra-carboxynaphthalenedianhydride is transformed into the corresponding diimide following methods described in literature, such as, for example:

• reaction of 2,6-dibromo-1,4,5,8-tetra-carboxynaphthalenedianhydride with a primary amine (e.g., 2-ethyl-hexylamine), in the presence of acetic acid, at 120°C, as described by Guo X. et al. in the article: "Conjugated Polymers from Naphthalene Bisimide", Organic Letters, (2008), Vol. 10 (23), pages 5333-5336;
• reaction of 2,6-dibromo-1,4,5,8-tetra-carboxynaphthalenedianhydride with a primary amine (e.g., n-octylamine) in the presence of acetic acid and N-methyl pyrrolidone, at 85°C for 6 hours under a stream of nitrogen, as described in international patent application WO 2007/146250;
• reaction of 2,6-dibromo-1,4,5,8-tetracarboxy-naphthalenedianhydride with a primary amine (e.g., 2-octyl-dodecylamine) in the presence of a mixture of propionic acid and o-xylene, at 140°C, for 2 hours, as described by Chen Z. et al. in the article "Naphthalenedicarboximide- vs Perylene-dicarboximide-Based Copolymers. Synthesis and Semiconducting Properties in Bottom-Gate N-Channel Organic Transistors", Journal of the American Chemical Society (2009), Vol. 131, pages 8-9;
• reaction of 2,6-dichloro-1,4,5,8-tetra-carboxynaphthalenedianhydride with a primary amine (e.g., n-octylamine) in the presence of glacial acetic acid, at 140°C, for 2 hours, as described by Thalacker C. et al. in the article: "Synthesis and Optical and Redox Properties of Core-Substituted Naphthalene Diimide Dyes", Journal of Organic Chemistry, (2006), Vol. 71 (21), pages 8098-8105.

[0014] In the case of the Stille reaction, the N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide compounds (NDIs) disubstituted in position 2 and 6 with aryl or heteroaryl groups, can be prepared by the reaction of 2,6-dihalogen-1,4,5,8-tetracarboxy-naphthalene-N,N'-dialkyldiimide with a tributylstannyl-arene or with a tributylstannylheteroarene.

[0015] In the case of the Suzuki reaction, the N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalendiimide (NDIs) compounds disubstituted in position 2 and 6 with aryl or heteroaryl groups, can be prepared by reaction of 2,6-dihalogen-1,4,5,8-tetracarboxynaphthalene-N,N'-dialkyldiimide with the ester of 2-arylboronic acid or with the ester of 2-heteroarylboronic acid.

[0016] Both of the above Stille and Suzuki reactions are carried out in the presence of catalysts containing palladium, in the presence of solvents such as, for example, toluene, xylene, 1,2-dimethoxyethane, tetrahydrofuran, dimethylsulfoxide, N,N-dimethylformamide, 1,4-dioxane, at a temperature ranging from 80°C to 130°C, for a time ranging from 12 to 24 hours.

[0017] Examples of the above Stille and Suzuki reactions are described in the art.

[0018] Piyakulawat P. et al., for example, in the article "Low band gap copolymers containing naphthalene-1,4,5,8-tetracarboxylic bisimide: Synthesis, properties and organic solar cell applications", Synthetic Metals (2011), Vol. 161, No. 18, pages 1238-1244, describe a process for the preparation of 2,6-di-(2,2'-thienyl)-N,N'-diethylhexyl-1,4,5,8-tetracarboxynaphthalenediimide [formula (Ia) wherein R = ethylhexyl] as reported in the following Scheme 1:

wherein 2,6-dibromo-N,N'-diethylhexyl-1,4,5,8-tetracarboxynaphthalenediimide [formula (IIa) wherein R = ethylhexyl] is reacted with 2-tri-n-butylstannylthiophene [formula (IIIa)], in the presence of anhydrous toluene, at reflux temperature, under a stream of argon, overnight. At the end of the reaction, after adding an aqueous solution of hydrochloric acid 2 N, extraction is carried out with chloroform. After washing the organic phase to neutrality with water and anhydrification on sodium sulfate, the solvent is removed by distillation at reduced pressure, obtaining, after purification by means of crystallization from ethanol, 2,6-di-(2,2'-thienyl)-N,N'-diethylhexyl-1,4,5,8-tetracarboxynaphthalenediimide with a yield of 92%.

[0019] In the article: "Synthesis and preliminary characterization of novel naphthalene bisimide based copolymers", Synthetic Metals (2009), Vol. 159, pages 467-472, reported above, Piyakulawat P. et al. describe a process for the preparation of 2,6-di-(2,2'-thienyl)-N,N'-dihexyl-1,4,5,8-tetracarboxynaphthalene-diimide [formula (Ib) wherein R₁ = hexyl] as reported in the following Scheme 2:

wherein 2,6-dibromo-1,4,5,8-tetracarboxynaphthalene dianhydride [formula (Va)] is reacted with 2-tri-n-butylstannyl thiophene [formula (IIIa)], in the presence of anhydrous toluene, at reflux temperature, for 15 hours, in the presence of bis(triphenylphosphine)palladium(II)chloride [PdCl₂(PPh₃)₂] as catalyst, in quantities equal to 3 moles per 100 moles of the starting 2,6-dibromo-1,4,5,8-tetracarboxynaphthalenedianhydride [formula (Va)]. At the end of the reaction, after adding an aqueous solution of hydrochloric acid 2 N, extraction is carried out with chloroform. After washing the organic phase to neutrality with water and after anhydrification with sodium sulfate, the solvent is removed by distillation at reduced pressure, obtaining, after purification by washing with hexane and crystallization from methanol, 2,6-di-(2,2'-thienyl)-1,4,5,8-tetracarboxynaphthalenedianhydride [formula (VIa)] with a yield equal to 41%. Subsequently, the 2,6-di-(2,2'-thienyl)-1,4,5,8-tetracarboxynaphthalene-dianhydride [formula (VIa)] is reacted with n-hexylamine [formula (VIIa) wherein R₁ = hexyl], at 150°C, under a stream of argon, for 5 hours. At the end of the reaction, after adding an aqueous solution of hydrochloric acid 2 N, extraction is carried out with chloroform. After washing the organic phase to neutrality with water and after anhydrification, the solvent is removed by distillation at reduced pressure, obtaining, after purification by means of elution on a chromatographic column of silica gel (eluent: chloroform), 2,6-di-(2,2'-thienyl)-N,N'-dihexyl-1,4,5,8-tetracarboxynaphthalenediimide [formula (Ib) wherein R₁ = hexyl] with a yield of 23%.

[0020] The 2-tri-n-butylstannylthiophene [formula (IIIa)] used in the above processes, is a commercial product, generally prepared starting from thiophene, n-butyllithium and tri-n-butylstannylchloride through a two-step process as reported in the following Scheme 3:

wherein thiophene [formula (VIIIa)] is reacted with n-butyl-lithium [formula (IXa)] to give 2-thienyl-lithium [formula (VIIIb)] which is reacted, in situ, with tributyl stannyl chloride [formula (Xa)] giving 2-tri-n-butyl stannyl thiophene [formula(IIIa)].

[0021] The above process has various drawbacks, such as, for example:

• use of organic derivatives of lithium, highly flammable substances which must be handled with care and with the absolute absence of oxygen and of humidity;
• use of the tin derivatives, highly toxic substances for human beings and harmful for the environment.

[0022] It is known that instead of 2-tri-n-butylstannylthiophene, the ester of 2-thienylboronic acid, also a commercial product, can be used, which is generally prepared starting from thiophene, with n-butyl-lithium and triester of boronic acid through a two-step process as reported in the following Scheme 4 :

wherein thiophene [formula (VIIIa)] is reacted with n-butyl-lithium [formula (IXa)] to give 2-thienyl-lithium [formula (VIIIb)] which is reacted in situ with a triester of boronic acid [formula (Xb)] wherein B = boron; R', equal to or different from each other, represent a hydrogen atom, or a linear or branched C₁-C₂₀ alkyl group; or the substituents R', together with the other atoms to which they are bound, can form a heterocyclic ring having formula (IV):

wherein B = boron; R', equal to or different from each other, represent a hydrogen atom, or a linear or branched C₁-C₂₀ alkyl group, obtaining the ester of 2-thienylboronic acid [formula (VIIIc)].

[0023] The above process however also has various drawbacks, such as, for example:

• use of organic derivatives of lithium, highly flammable substances which must be handled with care and with the complete absence of oxygen and of humidity;
• use of trialkyl esters of boronic acid which often have problems linked to their purification with low yields of the end-product.

[0024] It should also be noted that the above processes for the preparation of 2,6-di-(2,2'-thienyl)-N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide reported above, can have various drawbacks, such as, for example:

• use of derivatives of tin, toxic substances for human beings and harmful for the environment;
• use of organic derivatives of lithium, highly flammable substances which must be handled with care and with the complete absence of oxygen and of humidity;
• relatively long times, ranging from a few hours and a few tens of hours (normally from 3 hours to 24 hours);
• use of an excess of 2-tri-n-butylstannylthiophene (IIIa) in order to obtain high yields of end-product, with consequent higher production costs and wastewater disposal costs;
• use of 2-tri-n-tributylstannylthiophene (IIIa) which creates problems due to the fact that for each mole of 2,6-di-(2,2'-thienyl)-N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide obtained, two moles of tri-n-butyl-stannyl-bromide (IVa) are formed (as reported above in Scheme 1 and Scheme 2), which must be suitably disposed of with a consequent increase in the process costs;
• relatively high quantities of catalyst used, as normally a quantity of catalyst containing palladium not lower than 0.5 moles per 100 moles of 2,6-dibromo-1,4,5,8-tetracarboxy-naphthalene starting derivative, is used (these quantities, even if small in absolute terms, are in any case high considering the cost of palladium or its complexes, as it is not always possible to prepare the complexes in situ).

[0025] The development of new processes for the preparation of tetracarboxynaphthalenediimide compounds disubstituted with heteroaryl groups capable of overcoming the above drawbacks, is consequently of current interest.

[0026] Systems are described in literature, for example, for forming aryl-aryl (Ar-Ar) bonds without the use of tin or boron derivatives. Said reactions, known as direct arylation of aromatic systems, are normally carried out by reacting an aryl halide (Ib) with an aryl or heteroaryl compound (IIb), as reported in the following Scheme 5:

wherein X represents a chlorine, bromine or iodine atom in the presence of a catalyst containing palladium and, in some cases, in the presence of phosphines as ligands of the catalyst containing palladium.

[0027] Tamba S. et al., for example, in the article "Palladium-Catalyzed C-H Functionalization of Heteroarenes with Aryl Bromides and Chlorides", Journal of Organic Chemistry (2010), Vol. 75 (20), pages 6998-7001, describe an arylation reaction according to Scheme 5 reported above, wherein Ar' is a thiophene, in the presence of a catalyst containing palladium such as, for example, bis(tri-tert-butylphosphine) palladium(II) ([Pd(P-t-Bu₃)₂]), of a solvent such as, for example, dimethylformamide (DMF) and of a strong base such as, for example, lithium tert-butylate (LiO-t-Bu), at a temperature of 100°C, for 15 hours.

[0028] In the article "Ligand-less palladium-catalyzed direct 5-arylation of thiophenes at low catalyst loadings", Green Chemistry (2009), Vol. 11, pages 425-432, Roger J. et al. describe an arylation reaction according to Scheme 5 reported above, wherein Ar' is a thiophene substituted in position 2, in the presence of a catalyst containing palladium, such as, for example, palladium(II)acetate ([Pd(OAc)₂]), of a solvent such as, for example, dimethylacetamide (DMAc) and of a base such as, for example, potassium acetate (KOAc), at a temperature of 150°C, for 20 hours.

[0029] In the article "Palladium-catalyzed direct arylation of thiophenes tolerant silyl groups", Chemical Communication (2011), Vol. 47, pages 1872-1874, Chen L. et al. describe an arylation reaction according to Scheme 5 reported above, wherein Ar' is a thiophene substituted in position 2 with a (R)₃Si group wherein R can be an alkyl group (e.g., a methyl group), in the presence of a catalyst containing palladium such as, for example, palladium(II)acetate ([Pd(OAc)₂]) associated with diphenylphosphinebutane (dppb) as ligand, of a solvent such as, for example, dimethylacetamide (DMAc) and of a base such as, for example, potassium acetate (KOAc), at a temperature of 120°C, for a time ranging from 1 hour to 48 hours.

[0030] In the article: "Mechanistic Analysis of Azine N-Oxide Direct Arylation: Evidence for a Critical Role of Acetate in the Pd(OAc)2 Precatalyst", Journal of Organic Chemistry (2010), Vol. 75 (23), pages 8180-8189, Sun H. Y. et al. describe various reaction mechanisms for direct mono-arylation, basically distinguishing three types of direct arylation on the basis of the nature of the arene under examination, which can be: a) electron-rich, b) electron-neutral and c) electron-poor. In all cases the presence of palladium (II) acetate ([Pd(OAc)₂]) is of crucial importance.

[0031] Sheshanath V. Bhosale et al. disclose a process for the preparation of a 2,6-diaryl-naphthalenediiimide through a "cross-coupling" Suzuki reaction.

[0032] Phimwipha Piyakulawat et al. disclose an alternating donor-acceptor copolymer containing fluorene, as the donor segment and naphthalene bisimide, dithienylbenzothiazole, as the acceptor segment. Said copolymer being synthesized for the use of photovoltaic cells.

[0033] The processes reported above, however, can have various critical aspects, such as, for example:

• use of aryl or heteroaryl compounds, in particular thiophene, substituted in position 2 and, consequently, the necessity of subjecting the end-product to further treatment (e.g., deprotection) in order to obtain the desired product, and the impossibility of using the product obtained as precursor of monomeric units in the preparation of semiconductor polymers;
• use of strong bases (e.g., lithium tert-butylate (LiO-t-Bu) and, consequently, difficulty in handling said bases, an increase in the possibility of damage with respect to both the health of the operators and to the environment, and higher disposal costs;
• relatively high temperatures and long reaction times and, consequently, higher energy costs and longer process times which can cause degradation of the product obtained.

[0034] The Applicant has therefore considered the problem of finding a process for the preparation of a tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups, capable of overcoming the drawbacks reported above. In particular, the Applicant has considered the problem of finding a process for the preparation of a tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups, through direct arylation, more specifically through a double direct arylation, of a tetracarboxynaphthalenediimide compound.

[0035] The Applicant has now found that the preparation of a tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups, can be carried out through a process comprising a double direct arylation of a disubstituted tetracarboxynaphthalenediimide compound, more specifically through a process comprising the reaction of at least one disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimmide with at least one heteroaryl compound.

[0036] There are numerous advantages in operating according to the above process, such as, for example:

• reduction in the process steps with a consequent reduction in the process times and lower production costs;
• non-use of substances toxic for human beings and harmful for the environment such as tin derivatives and highly flammable substances such as lithium alkyls;
• possibility of functionalizing the product obtained to allow it to be used, for example, in (co)polymerizations;
• relatively low temperatures and low reaction times with lower energy costs and lower process times in order to avoid the possible degradation of the product obtained;
• greater safety conditions (e.g., absence of strong bases), with respect to both the health of the operators and the environment.

[0037] Said tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups can be advantageously used as monomer in the synthesis of semiconductor polymers which can be advantageously used in the construction of organic field effect transistors (OFET) or of organic thin film transistors (OTFT)]. Furthermore, said tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups can be advantageously used as monomer in the synthesis of semiconductor polymers which can be advantageously used in the construction of photovoltaic devices such as, for example photovoltaic cells, photovoltaic modules, solar cells, solar modules, on both rigid and flexible supports. In addition, said tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups has a good thermal stability, good properties as electron-acceptor compound, a good processability in organic solvents normally used in the construction of the above-mentioned transistors or of the above-mentioned photovoltaic devices.

[0038] An object of the present invention therefore relates to a process according to appended claim 1.

[0039] For the purposes of the present description and of the following claims, the definitions of the numerical ranges always comprise the extremes unless otherwise specified.

[0040] The term "C₁-C₃₀ alkyl group" or "C₁-C₂₀ alkyl group" refers to a linear or branched alkyl group having from 1 to 30 carbon atoms or from 1 to 20 carbon atoms, respectively. Specific examples of a C₁-C₃₀ or C₁-C₂₀ alkyl group are: methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, pentyl, ethyl-hexyl, hexyl, n-heptyl, octyl, nonyl, decyl, dodecyl, dodecyloctyl.

[0041] The term "C₁-C₂₀ alkylene group" refers to a linear or branched alkylene group having from 1 to 20 carbon atoms. Specific examples of a C₁-C₂₀ alkylene group are: methylene, ethylene, n-propylene, iso-propylene, n-butylene, iso-butylene, tert-butylene, pentylene, ethyl-hexylene, hexylene, heptylene, octylene, nonylene, decylene, dodecylene.

[0042] The term "cycloalkyl group" means a cycloalkyl group having from 3 to 10 carbon atoms. Said cycloalkyl group can be optionally substituted by one or more groups, equal to or different from each other, selected from: halogen atoms; hydroxyl groups; C₁-C₂₀ alkyl groups; C₁-C₂₀ alkoxyl groups; cyano groups; amino groups; nitro groups. Specific examples of a cycloalkyl group are: cyclopropyl, 2,2-difluorocyclopropyl, ciclobutyl, ciclopentyl, ciclohexyl, methylcyclohexyl, methoxycyclohexyl, fluorocyclohexyl, phenylcyclohexyl.

[0043] The term "aryl group" means an aromatic carbocyclic group. Said aromatic carbocyclic group can be optionally substituted with one or more groups, equal to or different from each other, selected from: halogen atoms such as, for example, fluorine, chlorine, bromine, preferably fluorine; hydroxyl groups; C₁-C₂₀ alkyl groups; C₁-C₂₀ alkoxyl groups, cyano groups; amino groups; nitro groups. Specific examples of an aryl group are: phenyl, methylphenyl, trimethylphenyl, methoxyphenyl, hydroxyphenyl, phenyloxyphenyl, fluorophenyl, pentafluorophenyl, nitrophenyl, dimethylaminophenyl, naphthyl, phenylnaphthyl, phenanthrene, anthracene.

[0044] The term "C₁-C₂₀ alkoxyl group" means a linear or branched alkoxyl group having from 1 to 20 carbon atoms. Specific examples of a C₁-C₂₀ alkoxyl group are: methoxyl, ethoxyl, n-propoxyl, iso-propoxyl, n-butoxyl, iso-butoxyl, tert-butoxyl, pentoxyl, hexyloxyl, heptyloxyl, octyloxyl, nonyloxyl, decyloxyl, dodecyloxyl.

[0045] The term "polyethyleneoxyl group" means a group having oxyethylene units in the molecule. Specific examples of a polyethyleneoxyl group are: methyloxy-ethyleneoxyl, methyloxy-diethyleneoxyl, 3-oxatetraoxyl, 3,6-dioxaheptyloxyl, 3,6,9-trioxadecyloxyl, 3,6,9,12-tetraoxahexadecyloxyl.

[0046] The term "heteroaryl group" means an aromatic heterocyclic group, penta- or hexa-atomic, also benzocondensed or heterobicyclic, containing from 1 to 4 heteroatoms selected from nitrogen, oxygen, sulfur, silicon, selenium, phosphorus. Specific examples of a heteroaryl group are: pyridine, methylpyridine, methoxypyridine, phenylpyridine, fluoropyridine, pyrimidine, pyridazine, pyrazine, triazine, tetrazine, quinoline, quinazoline, furan, thiophene, hexylthiophene, pyrrole, oxazole, thiazole, isooxazole, isothiazole, oxadiazole, thiadiazole, pyrazole, imidazole, triazole, tetrazole, indole, benzofuran, benzothiophene, benzooxazole, benzothiazole, triazolepyridine, triazolepyrimidine, coumarin.

[0047] The term "cycle or polycyclic system" means a system containing one or more rings containing from 3 to 14 carbon atoms, optionally containing heteroatoms selected from nitrogen, oxygen, sulfur, silicon, selenium, phosphorus. Specific examples of a cycle or polycyclic system are: thiadiazole, benzothiophene, quinoxaline, pyridine.

[0048] The above process can be carried out according to the following scheme:

wherein X, Y, Z, R¹, R³ and R⁴, have the same meanings described above.

[0049] According to a particularly preferred embodiment of the present invention, said process relates to the preparation of 2,6-di-(2,2'-thienyl)-N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide corresponding to a tetracarboxynaphthalenediimide compound disubstituted, in positions 2 and 6, with heteroaryl groups having general formula (I) wherein R¹ represents an ethyl-hexyl group or a n-heptyl group, Y represents a sulfur atom, Z represents a group CR² wherein R² represents a hydrogen atom, and R³ and R⁴, represent a hydrogen atom.

[0050] According to a preferred embodiment of the present invention, said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said heteroaryl compound having general formula (III) can be used in molar ratios ranging from 1:2 to 1:20, preferably ranging from 1:4 to 1:12.

[0051] Said process is carried out in the presence of at least one weak organic base.

[0052] Said weak organic base is selected from: carbonates of alkaline metals (e.g., lithium, sodium, potassium, caesium) or of alkaline-earth metals (e.g., magnesium, calcium) such as, for example, lithium carbonate, potassium carbonate, sodium carbonate, caesium carbonate, magnesium carbonate, calcium carbonate, or mixtures thereof. Said weak organic base is preferably potassium carbonate.

[0053] According to a preferred embodiment of the present invention, said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said weak organic base can be used in molar ratios ranging from 1:2.2 to 1:20, preferably ranging from 1:2.5 to 1:4.

[0054] Said process is carried out in the presence of at least one weak organic acid.

[0055] Said weak organic acid is selected from: acetic acid, propionic acid, pivalic acid, isobutyl acid, or mixtures thereof. Said weak organic acid is preferably pivalic acid.

[0056] According to a preferred embodiment of the present invention, said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said weak organic acid can be used in molar ratios ranging from 100:10 to 100:50, preferably ranging from 100:15 to 100:40.

[0057] Said process is carried out in the presence of at least one catalyst containing palladium, selected from: palladium(II) chloride [PdCl₂], palladium(II) acetate [Pd(OAc)₂], palladium(0) bis(dibenzylidene) [Pd(dba)₂ wherein dba = C₆H₅CH=CHCOCH=CHC₆H₅], palladium(II) bis(acetonitrile) chloride [Pd(CH₃CN)₂Cl₂], or mixtures thereof . Said catalyst containing palladium is preferably palladium(II) acetate [Pd(OAc)₂].

[0058] According to a preferred embodiment of the present invention, said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said catalyst containing palladium can be used in molar ratios ranging from 100:0.1 to 100:3, preferably ranging from 100:0.4 to 100:2.

[0059] According to a preferred embodiment of the present invention, said process can be carried out in the presence of at least one ligand of the catalyst containing palladium.

[0060] According to a preferred embodiment of the present invention, said ligand can be selected, for example, from: triphenylphosphine, tricyclohexylphosphonium tetrafluoroborate, 2-dicyclo-hexylphosphine-2'-(N,N-dimethylamino)-biphenyl (DavePhos), di-tert-butyl(methyl)phosphonium tetrafluoroborate, tri-tert-butyl(methyl)phosphonium tetrafluoroborate, or mixtures thereof. Said ligand is preferably di-tert-butyl(methyl)phosphonium tetrafluoroborate.

[0061] According to a preferred embodiment of the present invention, said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said ligand can be used in molar ratios ranging from 100:1 to 100:10, preferably ranging from 100:3 to 100:6.

[0062] According to a preferred embodiment of the present invention, said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) can be used in a molar concentration ranging from 0.05 mmoles to 2 mmoles, preferably ranging from 0.1 mmoles to 1.5 mmoles.

[0063] Said process can be carried out in the presence of at least one non-polar organic solvent.

[0064] Said non-polar organic solvent is selected from: toluene, xylene, chlorobenzene, or mixtures thereof. Said non-polar organic solvent is preferably toluene.

[0065] According to a preferred embodiment of the present invention, said process can be carried out at a temperature ranging from 80°C to 170°C, preferably ranging from 100°C to 150°C.

[0066] According to a preferred embodiment of the present invention, said process can be carried out for a time ranging from 30 minutes to 24 hours, preferably ranging from 1 hour to 20 hours.

[0067] The disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) can be obtained according to processes known in the art, for example, by halogenation of the corresponding N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenedianhydride and subsequent diamidation reaction. Greater details relating to these processes can be found, for example, in international patent application WO 2007/146250; or in the article of Chaignon F. et al.: "Very large acceleration of the photoinduced electron transfer in a Ru(bpy)3-naphthalene bisimide dyad bridged on the naphthyl core", Chemical Communications (2007), pages 64-66; or in the article of Thalacker C. et al.: "Synthesis and Optical and Redox Properties of Core-Substituted Naphthalene Diimide Dyes", Journal of Organic Chemistry, (2006), Vol. 71 (21), pages 8098-8105.

[0068] The heteroaryl compound having general formula (III) can be easily found on the market.

[0069] The analysis and characterization methods reported hereunder were used.

¹H-NMR Spectroscopy

[0070] The ¹H-NMR spectra of the tetracarboxynaphthalenediimide compounds disubstituted with heteroaryl groups object of the present invention, were registered by means of a nuclear magnetic resonance spectrometer Bruker Avance 400, at a temperature of 25°C, using deuterated chloroform (CDCl₃). The signal of the solvent used [i.e. deuterated chloroform (CDCl₃)] set at 7.26 ppm was used as reference for the chemical shifts.

[0071] Solutions of the tetracarboxynaphthalenediimide compounds disubstituted with heteroaryl groups object of the present invention, having concentrations equal to 5 mg - 10 mg of tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups to be analyzed in 0.75 ml of solvent, were used for the purpose.

Mass spectra

[0072] The mass spectra of the tetracarboxynaphthalenediimide compounds disubstituted with heteroaryl groups were carried out with an inverse geometry double-focusing spectrometer AT 95S in DCI ("Desorption Chemical Ionization") with iso-butane as reagent gas in positive ion modality. The emission current of the filament was calibrated at 0,1 mA with an electron beam energy equal to 100 eV and with a temperature of the ion source maintained at 90°C.

[0073] Some illustrative and non-limiting examples are provided hereunder for a better understanding of the present invention and for its embodiment.

EXAMPLE 1

Preparation of 2,6-di-(2,2'-thienyl)-N,N'-di-(2-ethyl-hexyl)-1,4,5,8-tetracarboxynaphthalenediimmide having formula (a)

[0074] 

[0075] 2,6-dibromonaphthalene-1,4,5,8-tetracarboxy-N,N'-di(2-ethyl-hexyl)imide (0.324 g, 0.5 mmoles), potassium carbonate (0.207 g, 1.5 mmoles), pivalic acid (15 mg, 0.15 mmoles), anhydrous toluene (5 ml), thiophene (0.421 g, 5 mmoles) and palladium (II) acetate [Pd(OAc)₂] (1.2 mg, 0.005 mmoles), were charged into a 10 ml Pyrex glass reactor equipped with a screw stopper.

[0076] The reactor was placed in an oil bath preheated to 120°C and left under vigorous stirring for 18 hours. After cooling to room temperature (25°C), the reaction mixture was put in a saturated solution of sodium chloride (25 ml) and extracted with ethyl acetate (3 x 25 ml). The organic phase obtained was dried on anhydrous sodium sulfate and evaporated. The residue obtained (brown solid) was purified by flash chromatography on silica gel using toluene as eluent, obtaining 262 mg of pure 2,6-di-(2,2'-thienyl)-N,N'-di-(2-ethyl-hexyl)-1,4,5,8-tetracarboxynaphthalenediimmide as a red solid (yield 80%).

[0077] Said 2,6-di-(2,2'-thienyl)-N,N'-di-(2-ethyl-hexyl)-1,4,5,8-tetracarboxynaphthalenediimmide was characterized by means of ¹H-NMR (400 MHz, CDCl₃) obtaining the following spectrum: δ = 8.76 (s, 2H), 7.56 (dd, J = 5.2, 1.2 Hz, 2H), 7.29 (dd, J = 3.2, 1.2 Hz, 2H), 7.19 (dd, J = 5.2, 3.2 Hz, 2H), 4.13-4.10 (m, 4H), 1.94-1.88 (m, 2H), 1.38-1.25 (m, 16 H), 0.95-0.89 (m, 12H) .

[0078] Said 2,6-di-(2,2'-thienyl)-N,N'-di-(2-ethyl-hexyl)-1,4,5,8-tetracarboxynaphthalenediimmide was also characterized by means of mass spectrum MS obtaining the following value: m/z: 654.9 (M⁺).

EXAMPLE 2

Preparation of 2,6-di-(2,2'-thienyl)-N,N'-di-(n-heptyl)-1,4,5,8-tetracarboxynaphthalenediimmide having formula (b)

[0079] 

[0080] 2,6-dibromonaphthalene-1,4,5,8-tetracarboxy-N,N'-di(n-heptyl)imide (0.310 g, 0.5 mmoles), potassium carbonate (0.207 g, 1.5 mmoles), pivalic acid (15 mg, 0.15 mmoles), anhydrous toluene (5 ml), thiophene (0.421 g, 5 mmoles) and palladium (II) acetate [Pd(OAc)₂] (1.2 mg, 0.005 mmoles), were charged into a 10 ml Pyrex glass reactor equipped with a screw stopper.

[0081] The reactor was placed in an oil bath preheated to 120°C and left under vigorous stirring for 18 hours. After cooling to room temperature (25°C), the reaction mixture was put in a saturated solution of sodium chloride (25 ml) and extracted with ethyl acetate (3 x 25 ml). The organic phase obtained was dried on anhydrous sodium sulfate and evaporated. The residue obtained (brown solid) was purified by flash chromatography on silica gel using toluene as eluent, obtaining 266 mg of pure 2,6-di-(2,2'-thienyl)-N,N'-di-(n-heptyl)-1,4,5,8-tetracarboxynaphthalenediimmide as a red solid (yield 85%).

[0082] Said 2,6-di-(2,2'-thienyl)-N,N'-di-(n-heptyl)-1,4,5,8-tetracarboxynaphthalenediimmide was characterized by means of ¹H-NMR (400 MHz, CDCl₃) obtaining the following spectrum: : δ = 8.72 (s, 2H), 7.59 (dd, J = 5.2, 1.2 Hz, 2H), 7.29 (dd, J = 3.6, 1.2 Hz, 2H), 7.21 (dd, J = 5.2, 3.6 Hz, 2H), 4.10-4.07 (m, 4H), 1.69-1.64 (m, 4H), 1.37-1.27 (m, 16H), 0.90-0.86 (m, 6H).

[0083] Said 2,6-di-(2,2'-thienyl)-N,N'-di-(n-heptyl)-1,4,5,8-tetracarboxynaphthalenediimmide was also characterized by means of mass spectrum MS obtaining the following value: m/z: 627.2 (M⁺).

Claims

1. A process for the preparation of a tetracarboxynaphthalenediimide compound disubstituted with heteroaryl groups having general formula (I)

wherein:

- R¹ represents a C₁-C₃₀ alkyl group;

- Y represents an oxygen atom; a sulfur atom; a group NR⁵ wherein R⁵ represents a hydrogen atom, or a C₁-C₂₀ alkyl group;

- Z represents a nitrogen atom; or a group CR² wherein R² has the meanings below reported;

- R³ represents a hydrogen atom; a linear or branched C₁-C₂₀ alkyl group; a cycloalkyl group optionally substituted; an aryl group optionally substituted; a linear or branched C₁-C₂₀ alkoxyl group; a polyethyleneoxyl group R¹-O-[-CH₂-CH₂-O]_n- wherein R¹ has the same meaning above reported and n is an integer ranging from 1 to 4; a group -R⁶-OH wherein R⁶ represents a linear or branched C₁-C₂₀ alkylene group; a group -R⁶-OR⁷ wherein R⁶ has the same meanings above reported and R⁷ represents a linear or branched C₁-C₂₀ alkyl group, or a polyethyleneoxyl group R¹-O-[-CH₂-CH₂-O]_n- wherein R¹ has the same meaning above reported and n is an integer ranging from 1 to 4; a group -COR¹ wherein R¹ has the same meanings above reported; a group -COOR¹ wherein R¹ has the same meanings above reported; a -CHO group; a cyano group (-CN);

- R² represents a hydrogen atom; a linear or branched C₁-C₂₀ alkyl group; or, when R³ is different from hydrogen or when R³ = R², it represents a linear or branched C₁-C₂₀ alkoxyl group;

- or R³ and R² can be optionally bound to each other so as to form, together with the carbon atoms to which they are bound, a cycle or polycyclic system containing from 3 to 14 carbon atoms, saturated, unsaturated, or aromatic, optionally containing one or more heteroatoms such as oxygen, sulfur, nitrogen, silicon, phosphorous, selenium;

- R⁴ represents a hydrogen atom; a linear or branched C₁-C₂₀ alkyl group; a cycloalkyl group optionally substituted; an aryl group optionally substituted; a heteroaryl group optionally substituted; a -CHO group; a group -COR¹ wherein R¹ has the same meanings above reported; a group -COOR¹ wherein R¹ has the same meanings above reported; a group -CONR² wherein R² has the same meanings above reported; a cyano group (-CN);

- or R² and R⁴ can be optionally bound to each other so as to form, together with the carbon atoms to which they are bound, a cycle or polycyclic system containing from 3 to 14 carbon atoms, saturated, unsaturated, or aromatic, optionally containing one or more heteroatoms such as oxygen, sulfur, nitrogen, silicon, phosphorous, selenium;

said process comprising reacting at least one disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II):

wherein X represents a halogen atom selected from chlorine, bromine, iodine; R¹ has the same meanings above reported;
with at least one heteroaryl compound having general formula (III):

wherein Y, Z, R³ e R⁴, have the same meanings above reported; characterized in that said process is carried out:

in the presence of at least one weak organic base selected from: carbonates of alkaline or of alkaline-earth metals; or in the presence of at least one weak organic acid selected from: acetic acid, propionic acid, pivalic acid, isobutyl acid, or mixtures thereof; and

in the presence of at least one catalyst containing palladium selected from: palladium(II) chloride [PdCl₂], palladium(II) acetate Pd(OAc)₂], palladium(0) bis(dibenzylidene) [Pd(dba)₂ wherein dba = C₆H₅CH=CHCOCH=CHC₆H₅], palladium(II) bis(acetonitrile) chloride [Pd(CH₃CN)₂Cl₂], or mixtures thereof; and

in the presence of at least one non-polar organic solvent selected from: toluene, xylene, chlorobenzene, or mixtures thereof.

2. The process according to claim 1, wherein said process relates to the preparation of 2,6-di-(2,2'-thienyl)-N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide corresponding to a tetracarboxynaphthalenediimide compound disubstituted, in positions 2 and 6, with heteroaryl groups having general formula (I) wherein R¹ represents an ethyl-hexyl group or a n-heptyl group, Y represents a sulfur atom, Z represents a group CR² wherein R² represents a hydrogen atom, and R³ and R⁴, represent a hydrogen atom.

3. The process according to claim 1 or 2, wherein said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxy-naphthalenediimide having general formula (II) and said heteroaryl compound having general formula (III) are used in molar ratios ranging from 1:2 to 1:20.

4. The process according to any of the previous claims, wherein said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said weak organic base are used in molar ratios ranging from 1:2.2 to 1:20.

5. The process according to any of the previous claims, wherein said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said weak organic acid are used in molar ratios ranging from 100:10 to 100:50.

6. The process according to any of the previous claims, wherein said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said catalyst containing palladium are used in molar ratios ranging from 100:0.1 to 100:3.

7. The process according to any of the previous claims, wherein said process is carried out in the presence of at least one ligand of the catalyst containing palladium.

8. The process according to claim 7, wherein said ligand is selected from: triphenylphosphine, tricyclohexylphosphonium tetrafluoroborate, 2-di-cyclohexylphosphine-2'-(N,N-dimethyl-amino)-biphenyl (DavePhos), di-tert-butyl(methyl)-phosphonium tetrafluoroborate, tri-tert-butyl(methyl)phosphonium tetrafluoroborate, or mixtures thereof.

9. The process according to any of the previous claims, wherein said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) and said ligand are used in molar ratios ranging from 100:1 to 100:10.

10. The process according to any of the previous claims, wherein said disubstituted N,N'-dialkyl-1,4,5,8-tetracarboxynaphthalenediimide having general formula (II) is used in a molar concentration ranging from 0.05 mmoles to 2 mmoles.

11. The process according to any of the previous claims, wherein said process is carried out at a temperature ranging from 80°C to 170°C.

12. The process according to any of the previous claims, wherein said process is carried out for a time ranging from 30 minutes to 24 hours.

Ansprüche

1. Ein Verfahren zur Herstellung einer Tetracarboxynaphthalindiimidverbindung, disubstituiert mit Heteroarylgruppen, mit der allgemeinen Formel (I)

worin:

- R¹ steht für eine C₁-C₃₀-Alkylgruppe;

- Y steht für ein Sauerstoffatom, ein Schwefelatom, eine Gruppe NR⁵, worin R⁵ für ein Wasserstoffatom oder eine C₁-C₂₀-Alkylgruppe steht;

- Z steht für ein Stickstoffatom, oder eine Gruppe CR² worin R² die unten angegebene Bedeutungen hat;

- R³ steht für ein Wasserstoffatom, eine lineare oder verzweigte C₁-C₂₀-Alkylgruppe, eine Cycloalkylgruppe gegebenenfalls substituiert, eine Arylgruppe gegebenenfalls substituiert, eine lineare oder verzweigte C₁-C₂₀-Alkoxylgruppe, eine Polyethylenoxyl-gruppe R¹-O-[-CH₂-CH₂-O]_n-, worin R¹ die gleiche Bedeutung hat wie oben angegeben und n ist eine ganze Zahl im Bereich von 1 bis 4, eine Gruppe -R⁶-OH, worin R⁶ für eine lineare oder verzweigte C₁-C₂₀-Alkylengruppe steht; eine Gruppe -R⁶-OR⁷, worin R⁶ die gleichen Bedeutungen hat wie oben angegeben, und R⁷ steht für eine lineare oder verzweigte C₁-C₂₀-Alkylgruppe, oder eine Polyethylenoxyl-gruppe R¹-O-[-CH₂-CH₂-O]_n-, worin R¹ die gleiche Bedeutung hat wie oben angegeben, und n ist eine ganze Zahl in einem Bereich von 1 bis 4; eine Gruppe -COR¹, worin R¹ die gleichen Bedeutungen hat wie oben angegeben; eine Gruppe -COOR¹, worin R¹ die gleichen Bedeutungen hat wie oben angegeben; eine -CHO Gruppe; eine Cyanogruppe (-CN);

- R² steht für ein Wasserstoffatom; eine lineare oder verzweigte C₁-C₂₀-Alkylgruppe; oder, wenn R³ anders ist als Wasserstoff oder wenn R³ = R², steht es für eine lineare oder verzweigte C₁-C₂₀-Alkoxylgruppe;

- oder R³ und R² können gegebenenfalls miteinander verbunden sein, sodass sie, zusammen mit dem Kohlenstoffatom, an das sie binden, einen Zyklus, oder einen polyzyklisches System bilden, enthaltend von 3 bis 14 Kohlenstoffatomen, gesättigt, oder ungesättigt oder aromatisch, gegebenenfalls enthaltend ein oder mehrere Heteroatome wie beispielsweise Sauerstoff, Schwefel, Stickstoff, Silicium, Phosphor, Selen;

- R⁴ steht für ein Wasserstoffatom, eine lineare oder verzweigte C₁-C₂₀-Alkylgruppe, eine Cycloalkylgruppe gegebenenfalls substituiert; eine Arylgruppe gegebenenfalls substituiert; eine Heteroarylgruppe gegebenenfalls substituiert; eine -CHO Gruppe; eine Gruppe -COR¹, worin R¹ die gleichen Bedeutungen hat wie oben angegeben; eine Gruppe -COOR¹, worin R¹ die gleichen Bedeutungen hat wie oben angegeben; eine Gruppe -CONR², worin R² die gleichen Bedeutungen hat wie oben angegeben, eine Cyanogruppe (-CN);

- oder R² und R⁴ können gegebenenfalls miteinander verbunden sein, sodass sie zusammen mit dem Kohlenstoffatom, an das sie binden, einen Zyklus oder ein polyzyklisches System bilden, enthaltend von 3 bis 14 Kohlenstoffatomen, gesättigt, ungesättigt, oder aromatisch, gegebenenfalls enthaltend ein oder mehrere Heteroatome wie beispielsweise Sauerstoff, Schwefel, Stickstoff, Silicium, Phosphor, Selen;

wobei das Verfahren die Umsetzung mindestens eines disubstituierten N, N'-Dialkyl-1,4,5,8-tetracarboxy-naphthalindimids mit der allgemeinen Formel (II) umfasst:

worin X für ein Halogenatom steht, ausgewählt aus Chlor, Brom, Iod; R¹ hat die gleichen Bedeutungen wie oben angegeben;
mit mindestens einer Heteroarylverbindung der allgemeinen Formel (III):

worin Y, Z, R³ und R⁴ die gleichen Bedeutungen haben wie oben angegeben; dadurch gekennzeichnet, dass das Verfahren ausgeführt wird:

in Gegenwart mindestens einer schwachen organischen Base ausgewählt aus: Carbonaten der Alkali- oder Erdalkali-Metalle; oder in Gegenwart mindestens einer schwachen, organischen Säure ausgewählt aus Essigsäure, Propionsäure, Pivalinsäure, Isobutylsäure, oder Mischungen davon; und

in Gegenwart mindestens eines Katalysatoren, enthaltend Palladium, ausgewählt aus: Palladium(II)-chlorid [PdCl₂], Palladium(II)-acetat [Pd(OAc)₂], Palladium (0)-bis(dibenzyliden) [Pd(dba)₂, worin dba = C₆H₅CH=CHCOCH=CHC₆H₅], Palladium(II)-bis(acetonitril)-chlorid [Pd(CH₃CN)₂Cl₂] oder Mischungen davon; und

in Gegenwart mindestens eines nicht polaren organischen Lösungsmittels ausgewählt aus: Toluen, Xylen, Chlorbenzen, oder Mischungen davon.

2. Verfahren nach Anspruch 1, worin sich das Verfahren auf die Herstellung von 2,6-Di-(2,2'-thienyl)-N, N'-dialkyl-1,4,5,8-tetracarboxynaphthalindiimid bezieht, entsprechend einer Tetracarboxynaphtalindiimid-Verbindung, disubstituiert in den Positionen 2 und 6 mit Heteroarylgruppen, mit der allgemeinen Formel (I), worin R¹ für eine Ethyl-hexyl-Gruppe oder eine n-Heptylgruppe steht, Y steht für ein Schwefelatom, Z steht für eine Gruppe CR², worin R² für ein Wasserstoffatom steht, und R³ und R⁴ stehen für ein Wasserstoffatom.

3. Verfahren nach Anspruch 1 oder 2, worin das disubstituierte N, N'-Dialkyl-1,4,5,8-tetracarboxy-naphthalindiimid mit der allgemeinen Formel (II) und die Heteroarylverbindung mit der allgemeinen Formel (III) in molaren Verhältnissen in einem Bereich von 1:2 bis 1:20 verwendet werden.

4. Verfahren nach irgendeinem der vorhergehenden Ansprüche, worin das disubstituierte N, N'-Dialkyl-1,4,5,8-tetracarboxy-naphthalindiimid mit der allgemeinen Formel (II) und die schwache, organische Base in molaren Verhältnissen in einem Bereich von 1:2,2 bis 1:20 verwendet werden.

5. Verfahren nach irgendeinem der vorhergehenden Ansprüche, worin das disubstituierte N, N'-Dialkyl-1,4,5,8-tetracarboxy-naphthalindiimid mit der allgemeinen Formel (II) und die schwache, organische Säure in molaren Verhältnissen in einem Bereich von 100:10 bis 100:50 verwendet werden.

6. Verfahren nach irgendeinem der vorherigen Ansprüche, worin das disubstituierte N, N'-Dialkyl-1,4,5,8-tetracarboxy-naphthalindiimid mit der allgemeinen Formel (II) und der Palladium enthaltende Katalysator in molaren Verhältnissen in einem Bereich von 100:0,1 bis 100:3 verwendet werden.

7. Verfahren nach irgendeinem der vorhergehenden Ansprüche, worin das Verfahren mindestens in Gegenwart eines Liganden des Palladium enthaltenden Katalysatoren durchgeführt wird.

8. Verfahren nach Anspruch 7 worin der Ligand ausgewählt ist aus: Triphenylphosphin, Tricyclohexylphosphonium-tetrafluorborat, 2-Di-cyclohexylphosphin-2'-(N, N'-dimethyl-amino)-biphenyl (DavePhos), Di-tert-butyl(methyl)-phosphonium-tetrafluoroborat, Tri-tert-butyl(methyl)-phosphonium-tetrafluorborat, oder Mischungen davon.

9. Verfahren nach irgendeinem der vorhergehenden Ansprüche, worin das disubstituierte N, N'-Dialkyl-1,4,5,8-tetracarboxy-naphthalindiimid mit der allgemeinen Formel (II) und der Ligand in Molverhältnissen in einem Bereich von 100:1 bis 100:10 verwendet werden.

10. Verfahren nach irgendeinem der vorhergehenden Ansprüche, worin das disubstituierte N, N'-Dialkyl-1,4,5,8-tetracarboxy-naphthalindiimid mit der allgemeinen Formel (II) in einer molaren Konzentration in einem Bereich von 0,05 mmol bis 2 mmol verwendet wird.

11. Verfahren nach irgendeinem der vorhergehenden Ansprüche, worin das Verfahren bei einer Temperatur in einem Bereich von 80°C bis 170°C durchgeführt wird.

12. Verfahren nach irgendeinem der vorhergehenden Ansprüche, worin das Verfahren über einen Zeitraum in einem Bereich von 30 Minuten bis 24 Stunden durchgeführt wird.

Revendications

1. Procédé de préparation d'un composé de type diimide d'acide naphtalène-tétracarboxylique, porteur de deux groupes substituants hétéroaryle, de formule générale (I) :

dans laquelle

- R¹ représente un groupe alkyle en C₁-C₃₀,

- Y représente un atome d'oxygène ou de soufre ou un groupe de formule NR⁵ où R⁵ représente un atome d'hydrogène ou un groupe alkyle en C₁-C₂₀,

- Z représente un atome d'azote ou un groupe de formule CR² où R² a l'une des significations données ci-dessous,

- R³ représente :

- un atome d'hydrogène,

- un groupe alkyle en C₁-C₂₀, à chaîne linéaire ou ramifiée,

- un groupe cycloalkyle, en option porteur de substituant(s),

- un groupe aryle, en option porteur de substituant(s),

- un groupe alcoxy en C₁-C₂₀, à chaîne linéaire ou ramifiée,

- un groupe poly(éthylène-oxy), de formule R¹-O-[CH₂-CH₂-O-]_n- où R¹ a la même signification que celle donnée ci-dessus et l'indice n est un nombre entier valant de 1 à 4,

- un groupe de formule -R⁶-OH où R⁶ représente un groupe alcane-diyle en C₁-C₂₀, à chaîne linéaire ou ramifiée,

- un groupe de formule -R⁶-OR⁷ où R⁶ a la même signification que celle donnée ci-dessus et R⁷ représente un groupe alkyle en C₁-C₂₀, à chaîne linéaire ou ramifiée, ou un groupe poly(éthylène-oxy), de formule R¹-O-[CH₂-CH₂-O-]_n- où R¹ a la même signification que celle donnée ci-dessus et l'indice n est un nombre entier valant de 1 à 4,

- un groupe de formule -COR¹ où R¹ a la même signification que celle donnée ci-dessus,

- un groupe de formule -COOR¹ où R¹ a la même signification que celle donnée ci-dessus,

- un groupe formyle (-CHO),

- ou un groupe cyano (-CN),

- R² représente un atome d'hydrogène ou un groupe alkyle en C₁-C₂₀, à chaîne linéaire ou ramifiée, ou bien, si R³ représente une autre entité qu'un atome d'hydrogène ou si R³ représente la même entité que R², il représente un groupe alcoxy en C₁-C₂₀, à chaîne linéaire ou ramifiée,

- ou bien R³ et R² peuvent, en option, représenter des entités liées l'une à l'autre pour former, conjointement avec les atomes de carbone auxquels elles sont liées, un cycle ou un système polycyclique comportant de 3 à 14 atomes de carbone, saturé, insaturé ou aromatique, et comportant, en option, un ou plusieurs hétéroatome(s), tel(s) un ou des atome(s) d'oxygène, de soufre, d'azote, de silicium, de phosphore et/ou de sélénium,

- et R⁴ représente :

- un atome d'hydrogène,

- un groupe alkyle en C₁-C₂₀, à chaîne linéaire ou ramifiée,

- un groupe cycloalkyle, en option porteur de substituant(s),

- un groupe aryle, en option porteur de substituant(s),

- un groupe hétéroaryle, en option porteur de substituant(s),

- un groupe formyle (-CHO),

- un groupe de formule -COR¹ où R¹ a la même signification que celle donnée ci-dessus,

- un groupe de formule -COOR¹ où R¹ a la même signification que celle donnée ci-dessus,

- un groupe de formule -CONR² où R² a la même signification que celle donnée ci-dessus,

- ou un groupe cyano (-CN),

- ou bien R² et R⁴ peuvent, en option, représenter des entités liées l'une à l'autre pour former, conjointement avec les atomes de carbone auxquels elles sont liées, un cycle ou un système polycyclique comportant de 3 à 14 atomes de carbone, saturé, insaturé ou aromatique, et comportant, en option, un ou plusieurs hétéroatome(s), tel(s) un ou des atome(s) d'oxygène, de soufre, d'azote, de silicium, de phosphore et/ou de sélénium ;

lequel procédé comporte le fait de faire réagir au moins un N,N'-di-alkyl-diimide d'acide naphtalène-1,4,5,8-tétracarboxylique porteur de deux substituants, de formule générale (II) :

dans laquelle X représente un atome d'halogène choisi parmi les atomes de chlore, de brome et d'iode, et R¹ a la même signification que celle donnée plus haut,
avec au moins un composé hétéroaromatique de formule générale (III) :

dans laquelle Y, Z, R³ et R⁴ ont les mêmes significations que celles données plus haut ;
et lequel procédé est caractérisé en ce qu'il est mis en oeuvre

- en présence d'au moins une base organique faible choisie parmi les carbonates de métal alcalin ou alcalino-terreux, ou en présence d'au moins un acide organique faible choisi parmi les acides acétique, propionique, pivalique et isobutyrique et leurs mélanges,

- et en présence d'au moins un catalyseur au palladium, choisi parmi les suivants : chlorure de palladium-(II) [PdCl₂], acétate de palladium-(II) [Pd(OAc)₂], palladium-(0)-bis(dibenzylidène-acétone) [Pd(dba)₂ où dba représente C₆H₅CH=CHCOCH=C₆H₅], chlorure de palladium-(II)-bis(acétonitrile) [Pd(CH₃CN)₂Cl₂], et leurs mélanges,

- et en présence d'au moins un solvant organique non-polaire choisi parmi les toluène, xylène et chlorobenzène et leurs mélanges.

2. Procédé conforme à la revendication 1, lequel procédé concerne la préparation d'un N,N'-dialkyl-diimide d'acide 2,6-di(thién-2-yl)-naphtalène-1,4,5,8-tétracarboxylique, c'est-à-dire d'un composé de type diimide d'acide naphtalène-tétracarboxylique porteur, en positions 2 et 6, de deux groupes substituants hétéroaryle, de formule générale (I) dans laquelle R¹ représente un groupe éthyl-hexyle ou un groupe n-heptyle, Y représente un atome de soufre, Z représente un groupe de formule CR² où R² représente un atome d'hydrogène, et R³ et R⁴ représentent des atomes d'hydrogène.

3. Procédé conforme à la revendication 1 ou 2, dans lequel ledit N,N'-dialkyl-diimide d'acide naphtalène-1,4,5,8-tétracarboxylique porteur de deux substituants, de formule générale (II), et ledit composé hétéroaromatique de formule générale (III) sont utilisés en un rapport molaire valant de 1/2 à 1/20.

4. Procédé conforme à l'une des revendications précédentes, dans lequel ledit N,N'-dialkyl-diimide d'acide naphtalène-1,4,5,8-tétracarboxylique porteur de deux substituants, de formule générale (II), et ladite base organique faible sont utilisés en un rapport molaire valant de 1/2,2 à 1/20.

5. Procédé conforme à l'une des revendications précédentes, dans lequel ledit N,N'-dialkyl-diimide d'acide naphtalène-1,4,5,8-tétracarboxylique porteur de deux substituants, de formule générale (II), et ledit acide organique faible sont utilisés en un rapport molaire valant de 100/10 à 100/50.

6. Procédé conforme à l'une des revendications précédentes, dans lequel ledit N,N'-dialkyl-diimide d'acide naphtalène-1,4,5,8-tétracarboxylique porteur de deux substituants, de formule générale (II), et ledit catalyseur au palladium sont utilisés en un rapport molaire valant de 100/0,1 à 100/3.

7. Procédé conforme à l'une des revendications précédentes, lequel procédé est mis en oeuvre en présence d'au moins un ligand pour le catalyseur au palladium.

8. Procédé conforme à la revendication 7, dans lequel ledit ligand est choisi parmi les suivants : triphényl-phosphine, borofluorure de tricyclohexyl-phosphonium, 2-(dicyclohexyl-phosphino)-2'-(N,N-di-méthyl-amino)-biphényle (Davephos), borofluorure de ditertiobutyl-méthyl-phosphonium, borofluorure de tritertiobutyl-méthyl-phosphonium, et leurs mélanges.

9. Procédé conforme à l'une des revendications précédentes, dans lequel ledit N,N'-dialkyl-diimide d'acide naphtalène-1,4,5,8-tétracarboxylique porteur de deux substituants, de formule générale (II), et ledit ligand sont utilisés en un rapport molaire valant de 100/1 à 100/10.

10. Procédé conforme à l'une des revendications précédentes, dans lequel ledit N,N'-dialkyl-diimide d'acide naphtalène-1,4,5,8-tétracarboxylique porteur de deux substituants, de formule générale (II), est utilisé en une concentration molaire valant de 0,05 à 2 millimoles.

11. Procédé conforme à l'une des revendications précédentes, lequel procédé est mis en oeuvre à une température de 80 à 170 °C.

12. Procédé conforme à l'une des revendications précédentes, lequel procédé est mis en oeuvre durant 30 minutes à 24 heures.