WO2010006852A1

WO2010006852A1 - Novel polymers

Info

Publication number: WO2010006852A1
Application number: PCT/EP2009/057126
Authority: WO
Inventors: Shin-Ichiro Kawano; Martin Baumgarten; Klaus MÜLLEN; Peter Murer; Thomas Schäfer; Moussa Saleh
Original assignee: Basf Se; Max-Planck-Gesellschaft Zur Foerderung Der Wissenschaften E.V.
Priority date: 2008-06-23
Filing date: 2009-06-10
Publication date: 2010-01-21
Also published as: JP2011526630A; US20110152491A1; EP2291469A1; JP5748660B2; CN102137902A; KR20110040857A; TW201008972A; US20140357898A1; CN102137902B; US8841411B2; TWI465478B

Abstract

The present invention relates to polymers comprising repeating unit(s) of the formula (I), and their use in electronic devices. The polymers according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In addition, high charge carrier mobilities and high temperature stability of the emission color are observed, if the polymers according to the invention are used in polymer light emitting diodes (PLEDs).

Description

Novel Polymers

The present invention relates to novel polymers comprising repeating unit(s) of the formula I and their use in electronic devices. The polymers according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In addition, high charge carrier mobilities and high temperature stability of the emission color can be observed, if the polymers according to the invention are used in polymer light emitting diodes (PLEDs).

WO2006043539 discloses among others light-emitting polymer compounds which emit blue light and contain pyrene.

EP0964045 describes polymeric fluorescent substances showing visible fluorescence in solid state, wherein the polymeric fluorescent substance comprises one or more repeating units represented by the following formula (1 ) and the amount of these repeating units is from 0.5 % by mole to 100 % by mole based on the total amount of repeating units: -Ar₁-CRi= C R₂- (1 ) wherein Ar₁ represents a condensed polycyclic aromatic group which may be substituted with a substituent selected from a cyano group, an alkyl group, alkoxy group or alkylthio group having 1 to 20 carbon atoms, an alkylsilyl group having 3 to 60 carbon atoms, an alkylamino group having 1 to 40 carbon atoms, an aryl group or aryloxy group having 6 to 20 carbon atoms, an arylalkenyl group or arylalkynyl group having 8 to 20 carbon atoms, an aralkyl group having 7 to 14 carbon atoms and a heterocyclic compound group having 4 to 14 carbon atoms, R₁ and R₂ each independently represents a group selected from a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, a heterocyclic compound having 4 to 20 carbon atoms and a cyano group.

Examples Of Ar₁ are among other groups of formula

wherein, R₅ to R₂o each independently represents a group selected from a hydrogen atom, a cyano group, an alkyl group, alkoxy group or alkylthio group having 1 to 20 carbon atoms; an alkylsilyl group having 3 to 60 carbon atoms; an alkylamino group having 1 to 40 carbon atoms; an aryl group or aryloxy group having 6 to 20 carbon atoms; an arylalkenyl group or arylalkynyl group having 8 to 20 carbon atoms; an aralkyl group having 7 to 14 carbon atoms; and a heterocyclic compound group having 4 to 14 carbon atoms.

There are a number of challenges faced with the introduction of organic EL displays when their performance is compared with existing technologies. Obtaining the exact color coordinates required by specific guidelines (i.e. NTSC) has been problematic. The operational lifetime of the EL device is still lower when contrasted to the existing inorganic technology for cathode ray tubes (CRTs) and liquid crystal displays (LCDs). In addition, producing a material with a pure blue color and a long lifetime is one of the greatest problems for this industry.

Accordingly, it is the object of the present invention to provide novel materials, which show significant advantages in color purity, device efficiency and/or operational lifetime, when incorporated in electro-optical devices.

Said object is solved by the polymers of the present invention comprising repeating units of formula I. Organic light emitting devices (OLEDs), comprising the polymers of the present invention, can show significant advantages in color purity, device efficiency and/or operational lifetime. In addition, the polymers can have good solubility characteristics and relatively high glass transition temperatures, which facilitates their fabrication into coatings and thin films, that are thermally and mechanically stable and relatively free of defects. If the polymers contain end groups which are capable of being crosslinked, the crosslinking of such groups after the films or coating is formed increases the solvent resistance thereof, which is beneficial in applications wherein one or more solvent-based layers of material are deposited thereon.

Hence, the present invention relates to polymers comprising repeating unit(s) of the formula

R¹, R², R³, R⁴, R⁵ and R ?⁶⁶ aarree iinnddeeppeenndd*ently of each other hydrogen, F, SiR¹⁰⁰R¹⁰¹R¹⁰², or an organic substituent, or R¹ and R², R³ and R⁴, and/or any of the substituents R¹, R², R³, R⁴, R⁵ and/or R⁶, which are adjacent to each other, together form an aromatic, or heteroaromatic ring, or ring system, which can optionally be substituted, m is 0, or an integer of 1 , or 2, n1 and n2 are 0, or an integer 1 , or 2,

R¹⁰⁰, R¹⁰¹ and R¹⁰² are independently of each other Ci-Cisalkyl, substituted or unsubstituted C₆-Ci₈aryl, and Ar¹ and Ar² are each independently of each other a substituted or unsubstituted arylene, or heteroarylene group. Examples of substituted or unsubstituted arylene, or heteroarylene groups are divalent groups selected from substituted or unsubstituted benzene group, a substituted or unsubstituted naphthalene group, a substituted or unsubstituted anthracene group, a substituted or unsubstituted diphenylanthracene group, a substituted or unsubstituted phenanthrene group, a substituted or unsubstituted acenaphthene group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted fluorene group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted thiophene group, a substituted or unsubstituted triazole group and a substituted or unsubstituted thiadiazole group.

The polymers of the present invention should have a glass transition temperature above 100⁰C, especially a glass transition temperature above 150⁰C.

R¹ and R² as well as R³ and R⁴ can be different from each other, but are preferably the same. Most preferred R¹, R², R³and R⁴ have the same meaning.

R¹, R², R³ and R⁴ are preferably selected from CrCi₈alkyl, d-Ci₈alkyl which is substituted by E and/or interrupted by D; d-Ci₈alkoxy, Ci-Ci₈alkoxy, which is substituted by E and/or interrupted by D; Ci-Ci₈perfluoroalkyl and are most preferred an optionally substituted C₆- C₂₄aryl, or C₂-C₂oheteroaryl group.

In a preferred embodiment of the present invention at least one, very especially at least two of R¹, R², R³ and R⁴ are different from H. Most preferred all of the substituents R¹, R², R³ and R⁴ are different from H. In another preferred embodiment of the present invention at least one, preferably two of the substituents R¹, R², R³ and R⁴ are an optionally substituted d- Ci₈alkoxy group. Most preferred all of the substituents R¹, R², R³ and R⁴ are an optionally substituted Ci-Ci₈alkoxy group.

Preferably, the polymer of the present invention comprises repeating unit(s) of formula I, wherein R¹, R², R³ and R⁴ are independently of each other H, F, Ci-Ci₈alkyl, Ci-Ci₈alkyl which is substituted by E and/or interrupted by D, Ci-Ci₈perfluoroalkyl, C₆-C₂₄aryl, C₆-C₂₄aryl which is substituted by G, C₂-C₂oheteroaryl, C₂-C₂oheteroaryl which is substituted by G; each group R⁵ and R⁶ is independently of each other in each occurrence H, halogen, especially F, Ci-Ci₈alkyl, d-Ci₈alkyl which is substituted by E and/or interrupted by D, d-

Ciβperfluoroalkyl, C₆-C₂₄aryl, C₆-C₂₄aryl which is substituted by G, C₂-C₂oheteroaryl, C₂-

C₂₀heteroaryl which is substituted by G, C₂-Ci₈alkenyl, C₂-Ci₈alkynyl, Ci-Ci₈alkoxy, d-

Ci₈alkoxy which is substituted by E and/or interrupted by D, C₇-C₂₅aralkyl, CN, or -CO-R²⁸, m is 0, or an integer 1 , or 2,

D is -CO-; -COO-; -S-; -SO-; -SO₂-; -0-; -NR²⁵-; -SiR³⁰R³¹-; -POR³²-; -CR²³=CR²⁴-; or -C≡C-; and

E is -OR²⁹; -SR²⁹; -NR²⁵R²⁶; -COR²⁸; -COOR²⁷; -CONR²⁵R²⁶; -CN; or halogen, especially F;

G is E, Ci-Ci₈alkyl, Ci-Ci₈alkyl which is interrupted by D, Ci-Ci₈perfluoroalkyl, Ci-Ci₈alkoxy, or Ci-Ci₈alkoxy which is substituted by E and/or interrupted by D,

R²³, R²⁴, R²⁵ and R²⁶ are independently of each other H; C₆-Ci₈aryl; C₆-Ci₈aryl which is substituted by Ci-Ci₈alkyl, or Ci-Ci₈alkoxy; Ci-Ci₈alkyl; or Ci-Ci₈alkyl which is interrupted by

-0-;

R²⁷ is H; C₆-Ci₈aryl; C₆-Ci₈aryl which is substituted by Ci-Ci₈alkyl, or Ci-Ci₈alkoxy; especially

Ci-Ci₈alkyl; or Ci-Ci₈alkyl which is interrupted by -O-,

R²⁸ is H; C₆-Ci₈aryl; C₆-Ci₈aryl which is substituted by Ci-Ci₈alkyl, or Ci-Ci₈alkoxy; d-

Ci₈alkyl; or Ci-Ci₈alkyl which is interrupted by -0-,

R²⁹ is H; C₆-Ci₈aryl; C₆-d₈aryl, which is substituted by Ci-Ci₈alkyl, or Ci-Ci₈alkoxy; d-

Ci₈alkyl; or Ci-Ci₈alkyl which is interrupted by -0-,

R³⁰ and R³¹ are independently of each other Ci-Ci₈alkyl, C₆-d₈aryl, or C₆-d₈aryl, which is substituted by Ci-Ci₈alkyl, and

R³² is Ci-Ci₈alkyl, C₆-Ci₈aryl, or C₆-d₈aryl, which is substituted by Ci-Ci₈alkyl.

Especially at least one, very especially at least two of R¹, R², R³ and R⁴ are different from H.

In an especially preferred embodiment the polymers contain repeating units of formula

(Ia), wherein R¹, R², R³ and R⁴ are independently of each other C₆-Ci₂aryl, or C₂-Cnheteroaryl, which may optionally be substituted by one or more groups G, wherein G is as defined above, or R¹, R², R³ and R⁴ are independently of each other Ci-Ci₈alkyl, d-Ci₈alkyl which is interrupted by -O-, Ci-Ci₈alkoxy; or d-Ci₈alkoxy which is interrupted by -O-. Preferably, R¹, R², R³and R⁴ have the same meaning. More preferred R³ and R⁴ have the same meaning and are Ci-Ci₈alkoxy; or Ci-Ci₈alkoxy, which is interrupted by -O-.

In another preferred embodiment of the present invention polymers of formula Ia are

preferred, wherein R¹, R², R³ and R⁴ are independently of each other ' , wherein n₃ is 0, or an integer 1 , 2, 3, 4, or 5, R¹¹ can be same, or different in each occurrence and is CrC₂₅alkyl, or CrC₂₅alkoxy, or R¹, R², R³ and R⁴ are independently of each other d- Ci₈alkyl, Ci-Ci₈alkyl which is interrupted by -O-, Ci-Ci₈alkoxy; or Ci-Ci₈alkoxy which is interrupted by -O-; especially Ci-Ci₈alkyl which is interrupted by -O-, Ci-Ci₈alkoxy; or d- d₈alkoxy which is interrupted by -O-. Preferably, R¹, R², R³ and R⁴ have the same meaning.

Preferably, R⁵ and R⁶ are independently of each other H, d-d₈alkyl, such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, sec-butyl, t-butyl, 2-methylbutyl, n-pentyl, isopentyl, n- hexyl, 2-ethylhexyl, or n-heptyl; d-d₈alkyl which is substituted by E and/or interrupted by D, such as -CH₂OCH₃, -CH₂OCH₂CH₃, -CH₂OCH₂CH₂OCH₃, Or -CH₂OCH₂CH₂OCH₂CH₃; d- Ci₈alkoxy, such as methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, isobutoxy, sec- butoxy, t-butoxy, 2-methylbutoxy, n-pentyloxy, isopentyloxy, n-hexyloxy, 2-ethylhexyloxy, or n-heptyloxy; C₆-Ci₄aryl, such as phenyl, naphthyl, or biphenylyl, C₅-Ci₂cycloalkyl, such as cyclohexyl, C₆-Ci₄aryl which is substituted by G, such as -C₆H₄OCH₃, -C₆H₄OCH₂CH₃, -C₆H₃(OCHs)₂, or -C₆H₃(OCH₂CH₃)₂, -C₆H₄CH₃, -C₆H₃(CHs)₂, -C₆H₂(CHs)₃, -C₆H₄OtBu, or -C₆H₄tBu. Most preferred R⁵ and R⁶ are H.

m is preferably O. If more than one group R⁵, or R⁶ is present within one molecule, they can have different meanings.

D is preferably -CO-, -COO-, -S-, -SO-, -SO₂-, -0-, -NR²⁵-, wherein R²⁵ is Ci-Ci₂alkyl, such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, or sec-butyl, or C₆-Ci₄aryl, such as phenyl, naphthyl, or biphenylyl.

E is preferably -OR²⁹; -SR²⁹; -NR²⁵R²⁵; -COR²⁸; -COOR²⁷; -CONR²⁵R²⁵; or -CN; wherein R²⁵, R²⁷, R²⁸ and R²⁹ are independently of each other Ci-Ci₂alkyl, such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, sec-butyl, hexyl, octyl, or 2-ethyl-hexyl, or C₆-Ci₄aryl, such as phenyl, naphthyl, or biphenylyl.

G has the same preferences as E, or is CrCi₈alkyl, especially d-C^alkyl, such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, sec-butyl, hexyl, octyl, 1-(2-hexyl)-decane, or 2- ethyl-hexyl.

Examples of especially preferred polymers, comprising repeating unit(s) of formula (Ia) are compounds A-1 to A-34 as described in claim 5.

The monomers for the preparation of the polymers of the present invention are new and form a further embodiment of the present invention. Accordingly, the present invention is also

directed to monomers of the formula

(Xl), wherein

Ar¹, Ar², n-i, n₂, R¹, R², R³, R⁴, R⁵, R⁶ and m are as defined above. X¹¹ is independently in each occurrence a halogen atom, especially I, Cl, or Br; -ZnX¹², -SnR²⁰⁷R²⁰⁸R²⁰⁹, wherein R²⁰⁷, R²⁰⁸ and R²⁰⁹ are identical or different and are H or d-C₆alkyl, wherein two radicals optionally form a common ring and these radicals are optionally branched or unbranched and X¹² is a halogen atom, very especially I, or Br; Or -OS(O)₂CF₃, -OS(O)₂-aryl, especially

, -BF₄Na, Or -BF₄K, wherein Y¹¹ is independently in each occurrence a Ci-Ci_Oalkyl group and Y¹² is independently in each occurrence a C₂-Ci₀alkylene group, such as -CY¹³Y¹⁴-CY¹⁵Y¹⁶-, or -

_Cγ17_γ18._cγ19γ20. γ₂₂ ^

independently of each other hydrogen, or a Ci-Ci_Oalkyl group, especially -C(CH₃)₂C(CH₃)₂-, or -C(CH₃)₂CH₂C(CH₃)₂-,

The compounds of formula

(XIV) are new and form a further embodiment of the present invention. Accordingly, the present invention is also directed compounds of the formula XIV, wherein X¹¹, Ar¹, Ar², n^ n₂, R⁵, R⁶ and m are as defined above.

2,7-Dibromo-pyrene-4,5,9,10-tetraones of formula XIVa (n-i = n₂ = O; X¹¹ = Br) can be produced by reacting 2,7-di-tert-butyl-pyrene-4,5,9,10-tetraones of formula XV or pyrene- 4,5,9,10-tetraones of formula XII with Br₂/Fe and NBS/H₂SO₄, respectively.

Pyrene-4,5,9,10-tetraones of formula XII can be produced by oxidizing pyrenes of formula XVI with sodium perchlorate or sodium periodate in the presence of ruthenium trichlorate in methylenechlorid according to the procedure described in J. Org. Chem. 2005, 70, 707-708.

Alternatively, 2,7-Dibromo-pyrene-4,5,9,10-tetraones of formula XIVa (n-i = n₂ = 0; X¹¹ = Br) can be prepared by oxidizing pyrenes of formula XVII with sodium perchlorate or sodium periodate in the presence of ruthenium trichlorate in methylenechlorid according to the procedure described in J. Org. Chem. 2005, 70, 707-708. The synthesis of 2,7- dibromopyrene is, for example, described in J. Org. Chem. 1986, 51 , 2847.

The monomers of formula XIa (In₁ = n₂ = 0) can be reacted by known procedures or in analogy to known procedures to monomers of formula XIb (ni = n₂ ≠ 0): - Example 22a of WO04039786:

- J. Org. Chem. 2007, 72, 2279:

2,7-Dibromo-pyrene-4,5,9,10-tetraones of formula XIVa (n-i = n₂ = 0; X¹¹ = Br) can be reacted to monomers of formula Xl (^ = n₂ = 0; X¹¹ = Br) by known procedures or in analogy to known procedures: - WO2005/104264 (R¹ = alkyl and aryl):

LiAIH

- Org. Lett. 10 (2008) 773:

Alternatively, monomers of formula Xl can be obtained by reacting compounds of formula XIII with bis(tricyclohexyltin)sulphide, or B₂S3. Reference is, for example, made to US20070191583 and Macromolecules 39 (2006) 5213-5221. The synthesis of compounds of formula XIII can be done according to, or in analogy to procedures described therein.

In one embodiment, the polymers according to the invention consist only of one or more type of repeating units of formula I. In a preferred embodiment, the polymers according to the invention consist of precisely one type of repeating unit of formula I (homopolymers).

According to the present invention the term "polymer" comprises polymers as well as oligomers, wherein a polymer is a molecule of high relative molecular mass, the structure of which essentially comprises the repetition of units derived, actually or conceptually, from molecules of low relative molecular mass and an oligomer is a molecule of intermediate molecular mass, the structure of which essentially comprises a small plurality of units derived, actually or conceptually, from molecules of lower relative molecular mass. A molecule is regarded as having a high relative molecular mass if it has properties which do not vary significantly with the removal of one or a few of the units. A molecule is regarded as having an intermediate molecular mass if it has properties which do vary significantly with the removal of one or a few of the units.

According to the present invention a homopolymer is a polymer derived from one species of (real, implicit, or hypothetical) monomer. Many polymers are made by the mutual reaction of complementary monomers. These monomers can readily be visualized as reacting to give an "implicit monomer", the homopolymerisation of which would give the actual product, which can be regarded as a homopolymer. Some polymers are obtained by chemical modification of other polymers, such that the structure of the macromolecules that constitute the resulting polymer can be thought of having been formed by the homopolymerisation of a hypothetical monomer.

Accordingly a copolymer is a polymer derived from more than one species of monomer, e.g. bipolymer, terpolymer, quaterpolymer, etc.

The oligomers of this invention have a weight average molecular weight of < 2,000 Daltons. The polymers of this invention preferably have a weight average molecular weight of 2,000 Daltons or greater, especially 2,000 to 2,000,000 Daltons, more preferably 10,000 to 1 ,000,000 and most preferably 20,000 to 500,000 Daltons. Molecular weights are determined according to gel permeation chromatography using polystyrene standards.

The present invention is illustrated in more detail on the basis of an especially preferred embodiment below, but should not be limited thereto. In said embodiment the polymer is a polymer of formula

(VII), wherein Ar¹, n-i, Ar², n₂, R¹, R², R³, R⁴, R⁵, R⁶ and m are as defined above, T and Ar³ are as defined in

WO06/097419, wherein Ar³ can also be a repeating unit of formula

as described in WO06/097419, and/or

. especially , as described in WO08/012250, wherein R^1", R² and R³ are independently of each other C₆-Ci₂aryl, or C₂-Cnheteroaryl, which may optionally be substituted by one or more groups G, wherein G is as defined above, and R⁴ has the meaning of R^{3 "}, or is Ci-Ci₈alkyl, especially C₄-Ci₈alkyl, R⁷ is an organic substituent, wherein two or more substituents R⁷ in the same molecule may have different meanings, or can form together an aromatic, or heteroaromatic ring, or ring system, and x' is 0, or an integer of 1 to 5.

A is a 5-, 6-, or 7-membered heteroaromatic ring, containing one heteroatom selected from nitrogen, oxygen and sulphur, which can be substituted and/or can be part of a fused aromatic or heteroaromatic ring system, R¹ and R⁴ are hydrogen,

R^2', R^3' R^5' and R⁶ are independently of each other H, d-Ci₈alkyl, C_rCi₈alkyl which is interrupted by D, Ci-Ci₈perfluoroalkyl, Ci-Ci₈alkoxy, Ci-Ci₈alkoxy which is interrupted by D, C₇-C₂₅aralkyl, or a group -X²-R^18',

R⁸ and R⁹ are independently of each other H, Ci-Ci₈alkyl, Ci-Ci₈alkyl which is interrupted by D, Ci-Ci₈perfluoroalkyl, Ci-Ci₈alkoxy, Ci-Ci₈alkoxy which is interrupted by D, or a group -X²- R¹⁸ , or two substituents R² and R³ and/or R⁵ and R'⁶, which are adjacent to each other, together form a group

or two substituents R⁵ and R³ , which are adjacent to

each other, together form a group

R⁸ and R⁹ together form a group

R²⁰⁹ and R²¹⁰ are independently of each other H, Ci-Cisalkyl, d-dsslkyl which is substituted by E and/or interrupted by D, Ci-Ci₈alkoxy, or d-Ci₈alkoxy which is substituted by E and/or interrupted by D, Ci-Ci₈perfluoroalkyl,

R¹⁰ is H, C₆-Ci8aryl, which can be substituted by G, C₂-Ci8heteroaryl, which can be substituted by G, Ci-Ci₈alkyl, d-Ci₈alkyl which is interrupted by D, Ci-Ci8perfluoroalkyl, d-

Ci₈alkoxy, Ci-Ci₈alkoxy which is substituted by E and/or interrupted by D, or a group -X²-

R¹⁸ , wherein X² is a spacer, such as C₆-Ci₂aryl, or C₆-Ci₂heteroaryl, especially phenyl, or naphthyl, which can be substituted one more, especially one to two times with CrCi₈alkyl,

Ci-Ci₈alkyl which is interrupted by D, Ci-Ci₈perfluoroalkyl, Ci-Ci₈alkoxy, or Ci-Ci₈alkoxy which is substituted by E and/or interrupted by D, and R¹⁸ is H, Ci-Ci₈alkyl, Ci-Ci₈alkyl which is interrupted by D, Ci-Ci₈perfluoroalkyl, Ci-Ci₈alkoxy, Ci-Ci₈alkoxy which is interrupted by

D, Or -NR²⁵ R^26'-;

X' is O, S, or NR^17',

R¹¹ and R¹⁴ are hydrogen,

R^12', R^13' _, R^15' and R^16' are hydrogen,

R¹⁷ is C₆-Ci₈aryl; C₆-Ci₈aryl which is substituted by Ci-Ci₈alkyl, Ci-Ci₈perfluoroalkyl, or d- d₈alkoxy; d-d₈alkyl; or Ci-Ci₈alkyl which is interrupted by -O-; or two substituents R^11' and R^12', and/or R^14' and R^16', R^12' and R^13', and/or R^15' and R^16', which are adjacent to each other, together form a group

, or two substituents R¹⁵ and R^{13 '},

which are adjacent to each other, together form a group

, wherein R¹⁰⁵ , R¹⁰⁶ , R¹⁰⁷ and R¹⁰⁸ are independently of each other H, or d-C₈alkyl, D, E and G are as defined above; a is 1 , b is 0, or 1 , c is 0.005 to 1 , d is 0, or 1 , e is 0, or 1 , wherein e is not 1 , if d is 0, f is 0.995 to 0, wherein the sum of c and f is 1 .

Ar³ is preferably selected from repeating units of formula:

, and wherein

R⁴⁴ and R⁴¹ are hydrogen, CrCi₈alkyl, or d-Ci₈alkoxy, and

R⁴⁵ is H, Ci-Ci₈alkyl, or Ci-Ci₈alkyl which is substituted by E and/or interrupted by D, especially Ci-Ci₈alkyl which is interrupted by -O-,

R¹¹⁶ and R¹¹⁷ are independently of each other H, halogen, -CN, Ci-Ci₈alkyl, Ci-Ci₈alkyl which is substituted by E and/or interrupted by D, C₆-C₂₄aryl, C₆-C₂₄aryl which is substituted by G,

C₂-C₂oheteroaryl, C₂-C₂oheteroaryl which is substituted by G, C₂-Ci₈alkenyl, C₂-Ci₈alkynyl, Ci-Ci8alkoxy, Ci-Ci₈alkoxy which is substituted by E and/or interrupted by D, C₇-C₂Sa ra Iky I, -

C(=O)-R¹²⁷, -C(=O)OR¹²⁷, or -C(=O)NR¹²⁷R¹²⁶,

R¹¹⁹ and R¹²⁰ are independently of each other H, Ci-C-i₈alkyl, Ci-C-i₈alkyl which is substituted by E and/or interrupted by D, C₆-C₂₄aryl, C₆-C₂₄aryl which is substituted by G, C₂-

C₂₀heteroaryl, C₂-C₂₀heteroaryl which is substituted by G, C₂-Ci₈alkenyl, C₂-Ci₈alkynyl, d-

Ci₈alkoxy, Ci-Ci₈alkoxy which is substituted by E and/or interrupted by D, or C₇-C₂₅aralkyl, or

R¹¹⁹ and R¹²⁰ together form a group of formula =CR¹²¹R¹²², wherein

R¹²¹ and R¹²² are independently of each other H, Ci-Ci₈alkyl, Ci-Ci₈alkyl which is substituted by E and/or interrupted by D, C6-C₂₄aryl, C₆-C₂₄aryl which is substituted by G, or C₂-

C₂₀heteroaryl, or C₂-C₂₀heteroaryl which is substituted by G, or

R¹¹⁹ and R¹²⁰ together form a five or six membered ring, which optionally can be substituted by Ci-Ci₈alkyl, Ci-Ci₈alkyl which is substituted by E and/or interrupted by D, C6-C₂₄aryl, C₆-

C₂₄aryl which is substituted by G, C₂-C₂₀heteroaryl, C₂-C₂₀heteroaryl which is substituted by

G, C₂-Ci₈alkenyl, C₂-Ci₈alkynyl, Ci-Ci₈alkoxy, Ci-Ci₈alkoxy which is substituted by E and/or interrupted by D, C₇-C₂₅aralkyl, or -C(=O)-R¹²⁷, and

R¹²⁶ and R¹²⁷ are independently of each other H; C₆-Ci₈aryl; C₆-Ci₈aryl which is substituted by Ci-Ci₈alkyl, or Ci-Ci₈alkoxy; Ci-Ci₈alkyl; or Ci-Ci₈alkyl which is interrupted by -O-, wherein G, D and E are as defined above.

The repeating units T are in particular selected from the following group Vl:

(VIf), wherein X¹ is a hydrogen atom, or a cyano group, R¹¹⁶ and R¹¹⁷ are as defined above,

R⁴¹ can be the same or different at each occurence and is Cl, F, CN, N(R⁴⁵)₂, a Ci-C₂₅alkyl group, a C₄-Ci₈cycloalkyl group, a Ci-C₂₅alkoxy group, in which one or more carbon atoms which are not in neighbourhood to each other could be replaced by -NR⁴⁵-, -O-, -S-, -C(=O)- O-, or -O-C(=O)-O-, and/or wherein one or more hydrogen atoms can be replaced by F, a C₆- C₂₄aryl group, or a C₆-C₂₄aryloxy group, wherein one or more carbon atoms can be replaced by O, S, or N, and/or which can be substituted by one or more non-aromatic groups R⁴¹, or two or more groups R⁴¹ form a ring system;

R⁴⁵ is H, a Ci-C₂₅alkyl group, a C₄-Ci₈cycloalkyl group, in which one or more carbon atoms which are not in neighbourhood to each other could be replaced by -NR⁴⁵-, -O-, -S-, -C(=O)- O-, or, -O-C(=O)-O-, and/or wherein one or more hydrogen atoms can be replaced by F, a C₆-C₂₄aryl group, or a C₆-C₂₄aryloxy group, wherein one or more carbon atoms can be replaced by O, S, or N, and/or which can be substituted by one or more non-aromatic groups

R⁴¹,

R⁴⁵ is H, a Ci-C₂₅alkyl group, or a C₄-Ci₈cycloalkyl group, n can be the same or different at each occurence and is 0, 1 , 2, or 3, especially 0,1 , or 2, very especially 0 or 1 , and u is 1 , 2, 3, or 4;

A⁴ is a C₆-C₂₄aryl group, a C₂-C₃oheteroaryl group, especially phenyl, naphthyl, anthryl, biphenylyl, 2-fluorenyl, phenanthryl, or perylenyl, which can be substituted by one or more non-aromatic groups R⁴¹, wherein T is preferably a repeating unit of formula Via, VIb or VIf. Homopolymers of formula VII, wherein a = 1 , b = 0, c = 1 , d = 0, e = 0, f = 0, are, for example, obtained by nickel coupling reactions, especially the Yamamoto reaction:

(I), wherein Ar¹, ni, Ar², n₂, R¹, R², R³, R⁴, R⁵, R⁶ and m are as defined above. In said aspect homopolymers consisting of repeating units of formula Ia are preferred.

Copolymers of formula VII, involving repeating units of formula I and -Ar³- (a = 1 , c = 0.995 to 0.005, b = 0, d = 1 , e = 0, f = 0.005 to 0.995), can be obtained by nickel coupling reactions:

(VlIb), wherein X is a repeating unit of formula I, especially Ia, c, f and Ar³ are as defined above.

Polymerization processes involving only dihalo-functional reactants may be carried out using nickel coupling reactions. One such coupling reaction was described by Colon et al. in J. Pol. ScL, Part A, Polymer Chemistry Edition 28 (1990) 367, and by Colon et al. in J. Org. Chem. 51 (1986) 2627. The reaction is typically conducted in a polar aprotic solvent (e.g., dimethylacetamide) with a catalytic amount of nickel salt, a substantial amount of triphenylphosphine and a large excess of zinc dust. A variant of this process is described by loyda et al. in Bull. Chem. Soc. Jpn, 63 (1990) 80 wherein an organo-soluble iodide was used as an accelerator.

Another nickel-coupling reaction was disclosed by Yamamoto in Progress in Polymer Science 17 (1992) 1153 wherein a mixture of dihaloaromatic compounds was treated with an excess amount of nickel (1 ,5-cyclooctadiene) complex in an inert solvent. All nickel-coupling reactions when applied to reactant mixtures of two or more aromatic dihalides yield essentially random copolymers. Such polymerization reactions may be terminated by the addition of small amounts of water to the polymerization reaction mixture, which will replace the terminal halogen groups with hydrogen groups. Alternatively, a monofunctional aryl halide may be used as a chain-terminator in such reactions, which will result in the formation of a terminal aryl group.

Nickel-coupling polymerizations yield essentially homopolymers or random copolymers comprising units of formula I and units derived from other co-monomers.

Homopolymers of formula VII, wherein a = 1 , c = 1 , b = 0, d = 1 , e = 0, f = 1 , can be obtained, for example, by the Suzuki reaction:

10

X -Ar-

(VIIc), wherein X¹⁰ and Ar³ are as defined above.

The condensation reaction of an aromatic boronate and a halogenide, especially a bromide, commonly referred to as the "Suzuki reaction", is tolerant of the presence of a variety of organic functional groups as reported by N. Miyaua and A. Suzuki in Chemical Reviews, Vol. 95, pp. 457-2483 (1995). This reaction can be applied to preparing high molecular weight polymers and copolymers. Preferred catalysts are 2-dicyclohexylphosphino-2',6'-di- alkoxybiphenyl/palladium(ll)acetates. An especially preferred catalyst is 2- dicyclohexylphosphino-2',6'-di-methoxybiphenyl (sPhos)/palladium(ll)acetate.

To prepare polymers corresponding to formula VIIc, a dihalogenide, such as a dibromide or dichloride, especially a dibromide corresponding to formula

is reacted with an X¹¹-^Ar³-}x¹¹ equimolar amount of a diboronic acid or diboronate corresponding to formula

wherein X¹¹ is independently in each occurrence -B(OH)₂, -B(OY¹¹)₂ or

, wherein

Y¹¹ is independently in each occurrence a Ci-Ci_Oalkyl group and Y¹² is independently in each occurrence a C₂-Ci₀alkylene group, such as -CY¹³Y¹⁴-CY¹⁵Y¹⁶-, or -

_Cγ17_γ18._cγ19γ20. _Cγ21γ22__{] wherein} Y^ ^ _γ1_{5] γ}1_{6] γ}1_{7] γ}1_{β] γ}1_9] ^ _γ21 _{and γ}22 ^ independently of each other hydrogen, or a Ci-Ci_Oalkyl group, especially -C(CH₃)₂C(CH₃)₂-, or -C(CH₃)₂CH₂C(CH₃)₂-, under the catalytic action of Pd and a phosphine ligand, especially triphenylphosphine. The reaction is typically conducted at about 70 ⁰C to 180 ⁰C in an aromatic hydrocarbon solvent such as toluene. Other solvents such as dimethylformamide and tetrahydrofuran can also be used alone, or in mixtures with an aromatic hydrocarbon. An aqueous base, preferably sodium carbonate, potassium carbonate, K₃PO₄, or bicarbonate, is used as the HBr scavenger. Depending on the reactivities of the reactants, a polymerization reaction may take 2 to 100 hours. Organic bases, such as, for example, tetraalkylammonium hydroxide, and phase transfer catalysts, such as, for example TBAB, can promote the activity of the boron (see, for example, Leadbeater & Marco; Angew. Chem. Int. Ed. Eng. 42 (2003) 1407 and references cited therein). Other variations of reaction conditions are given by T. I. Wallow and B. M. Novak in J. Org. Chem. 59 (1994) 5034-5037; and M. Remmers, M. Schulze, and G. Wegner in Macromol. Rapid Commun. 17 (1996) 239-252.

If desired, a monofunctional aryl halide or aryl boronate may be used as a chain-terminator in such reactions, which will result in the formation of a terminal aryl group.

It is possible to control the sequencing of the monomeric units in the resulting copolymer by controlling the order and composition of monomer feeds in the Suzuki reaction.

Homopolymers of formula VII, wherein a = 1 , c = 1 , b = 1 , d = 0, e = 0, f = 0, can be obtained, for example by the Heck reaction:

(VIId), wherein X¹⁰ and T are as defined above.

Polyphenylenethenylene derivatives and polyphenylenethynylene derivatives can be obtained by polymerization of divinyl or diethinyl compounds with dihalogen compounds by the Heck reaction (R. F. Heck, Palladium Reagents in Organic Synthesis, Academic Press, New York 1985, pp. 179; L. S. Hegedus, Organometalics in Synthesis, Ed. M. Schlosser, Wiley, Chichester, UK 1994, pp. 383; Z. Bao, Y. Chen, R. Cai, L. Yu, Macromolecules 26 (1993) pp. 5281 ; W.-K. Chan, L. Yu, Macromolecules 28 (1995) pp. 6410; A. Hilberer, H. -J. Brouwer, B. -J. van der Scheer, J. Wildeman, G. Hadziioannou, Macromolecules 1995, 28, 4525) and the Sonogaschira reaction (Dmitri Gelman and Stephen L. Buchwald, Angew. Chem. Int. Ed. 42 (2003) 5993 -5996; Rik R. Tykwinski, Angew. Chem. 115 (2003) 1604 - 1606; Jason M. Nolan and Daniel L. Comins, J. Org. Chem. 68 (2003) 3736-3738; Jiang Cheng et al., J. Org. Chem. 69 (2004) 5428-5432; Zolta^'n Nova^'k et al., Tetrahedron 59 (2003) 7509-7513):

(Sonogashira) The Sonogashira reaction is done in the presence a copper (I) catalyst, and/or palladium(O), such as, for example, tetrakis (triphenyl-phosphine) palladium(O), optionally in a solvent, such as toluene, dimethyl formamide, or dimethyl sulfoxide, and optionally a base, such as sodium hydride, potassium carbonate, sodium carbonate, or an amine base, such as piperidine. With special palladium catalysts the copper catalyst is not required (Angew. Chem. 2007, 119, 850 - 888). The reaction time and temperature depends on the starting materials and reaction conditions. Usually the dibromo-compound is reacted with the alkine at a temperature of from 50 ⁰C to 100 ⁰C , especially 60 to 80 ⁰C for 1 h to 48 h hours. This reaction, referred to as an Sonogashira reaction (Pd/Cu-catalyzed cross-coupling of organohalides with terminal alkynes), Cadiot-Chodkiewicz coupling or Castro-Stephens reaction (the Castro-Stephens coupling uses stoichiometric copper, whereas the Sonogashira variant uses catalytic palladium and copper), is described by Sonogashira K.; Tohda, Y.; Hagihara, N. Tetrahedron Lett. 1975, 4467; Richard Heck (discovered the same transformation using palladium but without the use of copper) J. Organomet. Chem. 1975, 93, 259; McCrindle, R.; Ferguson, G.; Arsenaut, G. J.; McAlees, A. J.; Stephenson, D. K. J. Chem. Res. (S) 1984, 360; Sakamoto, T.; Nagano, T.; Kondo, Y.; Yamanaka, H. Chem. Pharm. Bull. 1988, 36, 2248; Rossi, R. Carpita, A.; Belina, F. Org. Prep. Proc. Int. 1995, 27, 129; Ernst, A.; Gobbi, L.; Vasella, A. Tetrahedron Lett. 1996, 37, 7959; Campbell, I. B. In Organocopper Reagents; Taylor, R. J. K. Ed.; IRL Press: Oxford, UK, 1994, 217. (Review); Hundermark, T.; Littke, A.; Buchwald, S. L.; Fu, G. C. Org. Lett. 2000, 2, 1729; Dai, W.-M.; Wu, A. Tetrahedron Lett. 2001 , 42, 81 ; Alami, M.; Crousse, B.; Ferri, F. J. Organomet. Chem. 2001 , 624, 1 14; Bates, R. W.; Boonsombat, J. J. Chem. Soc, Perkin Trans. 1 2001 , 654; Batey, R. A.; Shen, M.; Lough, A. J. Org. Lett. 2002, 4, 141 1 ; Balova, I. A.; Morozkina, S. N.; Knight, D. W.; Vasilevsky, S. F. Tetrahedron Lett. 2003, 44, 107; Garcia, D.; Cuadro, A. M.; Alvarez-Builla, J.; Vaquero, J. J. Org. Lett. 2004, 6, 4175; Li, P.; Wang, L.; Li, H. Tetrahedron 2005, 61, 8633, Lemhadri, M.; Doucet, H.; Santelli, M. Tetrahedron 2005, 61, 9839, Angew. Chem. 2007, 119, 8632 -8635, Angew. Chem. 2006, 118, 6335 -6339, J. Am. Chem. Soc. 2005, 127, 9332-9333, and Adv. Mater. 2007, 19, 1234-1238.

(Random) copolymers of formula VII, wherein a is 1 , b is 1 , c is 0.005 to 0.995, d is 1 , e is 1 , f is 0.995 to 0.005, wherein the sum of c and f is 1 , can also be obtained by the Heck reaction: Ir +^Arϊt " Ir (Vile), wherein a, b, c, d, e, f, X¹⁰, Ar³ and T are as defined above.

The polymers containing groups of formulas (I) may be prepared by any suitable process, but are preferably prepared by the processes described above.

The polymers of the present invention can optionally comprise end moieties E¹, wherein E¹ is an aryl moiety which may optionally be substituted with a reactive group capable of undergoing chain extension or crosslinking, or a tri(Ci-Ci₈)alkylsiloxy group. As used herein, a reactive group capable of undergoing chain extension or crosslinking refers to any group which is capable of reacting with another of the same group or another group so as to form a link to prepare polymers. Preferably, such reactive group is a hydroxy, glycidyl ether, acrylate ester, methacrylate ester, ethenyl, ethynyl, maleimide, naphthimide, oxetane, trifluorovinyl ether moiety or a cyclobutene moiety fused to the aromatic ring of E¹.

The polymers of the present invention, where E¹ are reactive groups as defined above, are capable of crosslinking to form solvent resistant, heat-resistant films at 100⁰C or more, more preferably at 150⁰C or more. Preferably, such crosslinking occurs at 350⁰C or less, more preferably 300°C or less and most preferably 250°C or less. The crosslinkable polymers of the invention are stable at 100⁰C or more and more preferably 150⁰C or more. "Stable" as used herein means that such polymers do not undergo crosslinking or polymerization reactions at or below the stated temperatures. If a crosslinkable material is desired, E¹ is preferably a vinylphenyl, an ethynylphenyl, or 4-(or 3-)benzocyclobutenyl radical. In another embodiment, E¹ is selected from a group of phenolic derivatives of the formula -CeH₄-O-Y, wherein Y is

desired, the cross-linkable groups can be present in other parts of the polymer chain. For example, one of the substituents of the co-monomer T may be a crosslinkable group E¹.

The end-capping agent E¹-X¹² (E¹ is as defined above and X¹² is either Cl or Br) is incorporated into the polymers of the present invention under the condition in which the resulting polymers are substantially capped by the reactive group E¹. The reactions useful for this purpose are the nickel-coupling, Heck reactions and Suzuki reactions described above. The average degree of polymerization is controlled by the mole ratio of monomers to end- capping agent.

The polymers according to the invention can be worked up by known methods which are familiar to the person skilled in the art, as described, for example, in D. Braun, H. Cherdron, H. Ritter, Praktikum der makromolekularen Stoffe, 1^st Edn., Wiley VCH, Weinheim 1999, p. 68-79 or R. J. Young, P. A. Lovell, Introduction to Polymers, Chapman & Hall, London 1991. For example, the reaction mixture can be filtered, diluted with aqueous acid, extracted and the crude product obtained after drying and stripping-off of the solvent can be further purified by reprecipitation from suitable solvents with addition of precipitants. Residual palladium can be removed by using activated carbon, chromatography etc. Advantageously, the residual palladium could be reduced to <3 ppm by washing the crude organic solvent layer containing the polymer with an aqueous solution of L-cysteine at room temperature to the boiling point of the organic solvent, especially by washing a toluene layer containing the polymer with an aqueous solution of L-cysteine at 85 to 90 ⁰C, optionally followed by washing with a solution of L-cysteine and sodium thiosulfate at 78 to 82 ⁰C (Mahavir Prashad, Yugang Liu, Oljan Repicoe, Adv. Synth. Catal. 2003, 345, 533 - 536; Christine E. Garrett, Kapa Prasad, Adv. Synth. Catal. 2004, 346, 889 - 900). Additionally the Pd can be removed by washing the polymer with an aqueous NaCN solution as described in US-B-6,956,095. Polymer- analogous reactions can subsequently be carried out for further functionalization of the polymer. Thus, for example, terminal halogen atoms can be removed reductively by reduction with, for example, LiAIH₄ (see, for example, J. March, Advanced Organic Chemistry, 3^rd Edn. McGraw-Hill, p. 510).

Another aspect of this invention is related to polymer blends containing 1 to 99 percent of at least one containing polymers comprising a unit of formula I. The remainder 1 to 99 percent of the blend is composed of one or more polymeric materials selected from among chain growth polymers such as polystyrene, polybutadiene, poly(methyl methacrylate), and poly(ethylene oxide); step-growth polymers such as phenoxy resins, polycarbonates, polyamides, polyesters, polyurethanes, and polyimides; and crosslinked polymers such as crosslinked epoxy resins, crosslinked phenolic resins, crosslinked acrylate resins, and crosslinked urethane resins. Examples of these polymers may be found in Preparative Methods of Polymer Chemistry, W. R. Sorenson and T. W. Campbell, Second Edition, lnterscience Publishers (1968). Also may be used in the blends are conjugated polymers such as poly(phenylene vinylene), substituted poly(phenylene vinylene)s, substituted polyphenylenes and polythiophenes. Examples of these conjugated polymers are given by Greenham and Friend in Solid State Physics, Vol. 49, pp. 1-149 (1995).

In an especially preferred embodiment the present invention is directed to polymers of formula

wherein R , R , R and R are independently of each other

, wherein n₃ is 0, or an integer 1 , 2, or 3, especially 0, or 1 ; and R¹¹ can be the same or different in each occurrence and is H, CrC₂₅alkyl, which can be optionally interrupted by O, or CrC₂5alkoxy, which can be optionally interrupted by O, and

Ar^3' i is

, wherein

R , R and R are independently of each other

, or , wherein n_r is 0, or an integer 1 ,

2, 3, or 4, especially 0, 1 , or 2; r\? is 0, or an integer 1 , 2, or 3, especially 0, 1 , or 2; n₃> is 0, or an integer 1 , 2, 3, 4, or 5, especially 0, 1 , 2, or 3; and R¹⁰ and R¹¹ are independently of each other CrC₂₅alkyl, or CrC₂₅alkoxy, and R⁴ has the meaning of R^3", or is CrCi₈alkyl, especially C₄-Ci₈alkyl, R⁴⁴, R¹¹⁶, R¹¹⁷, R¹¹⁹ and R¹²⁰ are as defined above,

R⁸ and R⁹ are independently of each other ' , wherein n₃ and R¹¹ are as defined above, R¹⁷ is CrC₂5alkyl, which can be optionally interrupted by O, and

R^ηu is R^b , or , wherein n₂ is 0, 1 , or 2.

R^1", R² and R³ are preferably independently of each other R :>4⁴" has the meaning of R^{3 "}, or is CrCi₈alkyl, especially C₄-Ci₈alkyl.

The following polymers are especially preferred:

The polymers of the present invention can show high photoluminescence and/or electroluminescence.

Halogen is fluorine, chlorine, bromine and iodine.

Ci-C₂5alkyl (d-Ci₈alkyl) is typically linear or branched, where possible. Examples are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec. -butyl, isobutyl, tert. -butyl, n-pentyl, 2-pentyl, 3-pentyl, 2,2-dimethylpropyl, 1 ,1 ,3,3-tetramethylpentyl, n-hexyl, 1-methylhexyl, 1 ,1 ,3,3,5,5- hexamethylhexyl, n-heptyl, isoheptyl, 1 ,1 ,3,3-tetramethylbutyl, 1-methylheptyl, 3-methylhep- tyl, n-octyl, 1 ,1 ,3,3-tetramethylbutyl and 2-ethylhexyl, n-nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, eicosyl, heneicosyl, docosyl, tetracosyl or pentacosyl. d-C₈alkyl is typically methyl, ethyl, n-propyl, isopropyl, n-butyl, sec. -butyl, isobutyl, tert. -butyl, n-pentyl, 2-pentyl, 3-pentyl, 2,2-dimethyl-propyl, n- hexyl, n-heptyl, n-octyl, 1 ,1 ,3,3-tetramethylbutyl and 2-ethylhexyl. Ci-C₄alkyl is typically methyl, ethyl, n-propyl, isopropyl, n-butyl, sec. -butyl, isobutyl, tert. -butyl. Ci-C₂5alkoxy (Ci-Ci₈alkoxy) groups are straight-chain or branched alkoxy groups, e.g. methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, amyloxy, isoamyloxy or tert-amyloxy, heptyloxy, octyloxy, isooctyloxy, nonyloxy, decyloxy, undecyloxy, dodecyloxy, tetradecyloxy, pentadecyloxy, hexadecyloxy, heptadecyloxy and octadecyloxy. Examples of Ci-C₈alkoxy are methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert.-butoxy, n-pentyloxy, 2-pentyloxy, 3-pentyloxy, 2,2-dimethylpropoxy, n- hexyloxy, n-heptyloxy, n-octyloxy, 1 ,1 ,3,3-tetramethylbutoxy and 2-ethylhexyloxy. Examples of Ci-C₄alkoxy are methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert.-butoxy. The term "alkylthio group" means the same groups as the alkoxy groups, except that the oxygen atom of the ether linkage is replaced by a sulfur atom.

C₂-C₂₅alkenyl (C₂-Ci₈alkenyl) groups are straight-chain or branched alkenyl groups, such as e.g. vinyl, allyl, methallyl, isopropenyl, 2-butenyl, 3-butenyl, isobutenyl, n-penta-2,4-dienyl, 3- methyl-but-2-enyl, n-oct-2-enyl, n-dodec-2-enyl, isododecenyl, n-dodec-2-enyl or n-octadec- 4-enyl.

C_2-24alkynyl (C_2-i₈alkynyl) is straight-chain or branched and preferably C_2-8alkynyl, which may be unsubstituted or substituted, such as, for example, ethynyl, 1-propyn-3-yl, 1-butyn-4-yl, 1-pentyn-5-yl, 2-methyl-3-butyn-2-yl, 1 ,4-pentadiyn-3-yl, 1 ,3-pentadiyn-5-yl, 1-hexyn-6-yl, cis-3-methyl-2-penten-4-yn-1 -yl, trans-3-methyl-2-penten-4-yn-1 -yl, 1 ,3-hexadiyn-5-yl, 1-octyn-8-yl, 1-nonyn-9-yl, 1-decyn-10-yl, or 1-tetracosyn-24-yl.

d-Ciβperfluoroalkyl, especially Ci-C₄perfluoroalkyl, is a branched or unbranched radical such as for example -CF₃, -CF₂CF₃, -CF₂CF₂CF₃, -CF(CF₃)₂, -(CF₂)₃CF₃, and -C(CF₃)₃.

The terms "haloalkyl, haloalkenyl and haloalkynyl" mean groups given by partially or wholly substituting the above-mentioned alkyl group, alkenyl group and alkynyl group with halogen, such as trifluoromethyl etc. The "aldehyde group, ketone group, ester group, carbamoyl group and amino group" include those substituted by an alkyl group, a cycloalkyl group, an aryl group, an aralkyl group or a heterocyclic group, wherein the alkyl group, the cycloalkyl group, the aryl group, the aralkyl group and the heterocyclic group may be unsubstituted or substituted. The term "silyl group" means a group of formula -SiR⁶²R⁶³R⁶⁴, wherein R⁶², R⁶³ and R⁶⁴ are independently of each other a Ci-C₈alkyl group, in particular a CrC₄ alkyl group, a C₆-C₂₄aryl group or a C₇-Ci₂aralkylgroup, such as a trimethylsilyl group. The term "cycloalkyl group" is typically C₄-Ci₈cycloalkyl, especially C₅-Ci₂cycloalkyl, such as cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, cycloundecyl, cyclododecyl, preferably cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl, which may be unsubstituted or substituted. The term "cycloalkenyl group" means an unsaturated alicyclic hydrocarbon group containing one or more double bonds, such as cyclopentenyl, cyclopentadienyl, cyclohexenyl and the like, which may be unsubstituted or substituted. The cycloalkyl group, in particular a cyclohexyl group, can be condensed one or two times by phenyl which can be substituted one to three times with d-C₄-alkyl, halogen and cyano.

Examples of such condensed cyclohexyl groups are:

, wherein R , R , R , R⁰⁴, R^bb and

R⁵⁶ are independently of each other CrC₈-alkyl, Ci-Cβ-alkoxy, halogen and cyano, in particular hydrogen.

Aryl is usually C₆-C₃oaryl, preferably C₆-C₂₄aryl (C₆-Ci₈aryl), which optionally can be substituted, such as, for example, phenyl, 4-methylphenyl, 4-methoxyphenyl, naphthyl, especially 1-naphthyl, or 2-naphthyl, biphenylyl, terphenylyl, pyrenyl, 2- or 9-fluorenyl, phenanthryl, anthryl, tetracyl, pentacyl, hexacyl, or quaderphenylyl, which may be unsubstituted or substituted.

The term "aralkyl group" is typically C₇-C₂Sa ra Iky I, such as benzyl, 2-benzyl-2-propyl, β- phenyl-ethyl, α,α-dimethylbenzyl, ω-phenyl-butyl, ω,ω-dimethyl-ω-phenyl-butyl, ω-phenyl- dodecyl, ω-phenyl-octadecyl, ω-phenyl-eicosyl or ω-phenyl-docosyl, preferably C₇-Ci₈aralkyl such as benzyl, 2-benzyl-2-propyl, β-phenyl-ethyl, α,α-dimethylbenzyl, ω-phenyl-butyl, ω,ω-dimethyl-ω-phenyl-butyl, ω-phenyl-dodecyl or ω-phenyl-octadecyl, and particularly preferred C₇-Ci₂aralkyl such as benzyl, 2-benzyl-2-propyl, β-phenyl-ethyl, α,α-dimethylbenzyl, ω-phenyl-butyl, or ω,ω-dimethyl-ω-phenyl-butyl, in which both the aliphatic hydrocarbon group and aromatic hydrocarbon group may be unsubstituted or substituted.

The term "aryl ether group" is typically a C_6-24aryloxy group, that is to say O-C_6-24aryl, such as, for example, phenoxy or 4-methoxyphenyl. The term "aryl thioether group" is typically a C₆-₂₄arylthio group, that is to say S-C₆-₂₄aryl, such as, for example, phenylthio or 4-methoxyphenylthio. The term "carbamoyl group" is typically a Ci-i₈carbamoyl radical, preferably Ci_-8carbamoyl radical, which may be unsubstituted or substituted, such as, for example, carbamoyl, methylcarbamoyl, ethylcarbamoyl, n-butylcarbamoyl, tert- butylcarbamoyl, dimethylcarbamoyloxy, morpholinocarbamoyl or pyrrolidinocarbamoyl.

The terms "aryl" and "alkyl" in alkylamino groups, dialkylamino groups, alkylarylamino groups, arylamino groups and diarylgroups are typically Ci-C₂5alkyl and C₆-C₂₄aryl, respectively.

Alkylaryl refers to alkyl-substituted aryl radicals, especially C₇-Ci₂alkylaryl. Examples are tolyl, such as 3-methyl-, or 4-methylphenyl, or xylyl, such as 3,4-dimethylphenyl, or 3,5- dimethylphenyl.

Heteroaryl is typically C₂-C₂6heteroaryl (C₂-C₂oheteroaryl), i.e. a ring with five to seven ring atoms or a condensed ring system, wherein nitrogen, oxygen or sulfur are the possible hetero atoms, and is typically an unsaturated heterocyclic group with five to 30 atoms having at least six conjugated π-electrons such as thienyl, benzo[b]thienyl, dibenzo[b,d]thienyl, thianthrenyl, furyl, furfuryl, 2H-pyranyl, benzofuranyl, isobenzofuranyl, dibenzofuranyl, phenoxythienyl, pyrrolyl, imidazolyl, pyrazolyl, pyridyl, bipyridyl, triazinyl, pyrimidinyl, pyrazinyl, pyridazinyl, indolizinyl, isoindolyl, indolyl, indazolyl, purinyl, quinolizinyl, chinolyl, isochinolyl, phthalazinyl, naphthyridinyl, chinoxalinyl, chinazolinyl, cinnolinyl, pteridinyl, carbazolyl, carbolinyl, benzotriazolyl, benzoxazolyl, phenanthridinyl, acridinyl, pyrimidinyl, phenanthrolinyl, phenazinyl, isothiazolyl, phenothiazinyl, isoxazolyl, furazanyl or phenoxazinyl, which can be unsubstituted or substituted.

Possible substituents of the above-mentioned groups are Ci-C₈alkyl, a hydroxyl group, a mercapto group, Ci-C₈alkoxy, Ci-C₈alkylthio, halogen, halo-Ci-C₈alkyl, a cyano group, an aldehyde group, a ketone group, a carboxyl group, an ester group, a carbamoyl group, an amino group, a nitro group or a silyl group, especially Ci-C₈alkyl, d-C₈alkoxy, Ci-C₈alkylthio, halo-CrC₈alkyl, or a cyano group.

If a substituent, such as, for example R⁶ occurs more than one time in a group, it can be different in each occurrence.

The wording "substituted by G" means that one, or more, especially one to three substituents G might be present.

As described above, the aforementioned groups may be substituted by E and/or, if desired, interrupted by D. Interruptions are of course possible only in the case of groups containing at least 2 carbon atoms connected to one another by single bonds; C₆-Ci₈aryl is not interrupted; interrupted arylalkyl or alkylaryl contains the unit D in the alkyl moiety. Ci-Ci₈alkyl substituted by one or more E and/or interrupted by one or more units D is, for example, (CH₂CH₂O)i-9-R^x, where R^x is H or C_rCi_Oalkyl or C₂-Ci₀alkanoyl (e.g. CO-CH(C₂H₅)C₄H₉), CH₂-CH(OR^y')-CH₂- O-R^y, where R^y is Ci-Ci₈alkyl, C₅-Ci₂cycloalkyl, phenyl, C₇-Ci₅phenylalkyl, and R^y' embraces the same definitions as R^y or is H;

Ci-C₈alkylene-COO-R^z, e.g. CH₂COOR² CH(CH₃)COOR², C(CH₃)₂COOR^Z, where R^z is H, Ci-Ci₈alkyl, (CH₂CH₂O)i_-9-R^x, and R^x embraces the definitions indicated above; CH₂CH₂-O-CO-CH=CH₂; CH₂CH(OH)CH₂-O-CO-C(CH_S)=CH₂.

Preferred arylene radicals are 1 ,4-phenylene, 2,5-tolylene, 1 ,4-naphthylene, 1 ,9 antracylene, 2,7-phenantrylene and 2,7-dihydrophenantrylene.

Preferred heteroarylene radicals are 2,5-pyrazinylene, 3,6-pyridazinylene, 2,5-pyridinylene, 2,5-pyrimidinylene, 1 ,3,4-thiadiazol-2,5-ylene, 1 ,3-thiazol-2,4-ylene, 1 ,3-thiazol-2,5-ylene, 2,4-thiophenylene, 2,5-thiophenylene, 1 ,3-oxazol-2,4-ylene, 1 ,3-oxazol-2,5-ylene and 1 ,3,4- oxadiazol-2,5-ylene, 2,5-indenylene and 2,6-indenylene.

Another aspect of the invention is the films formed from the polymers of the invention. Such films can be used in polymeric light-emitting diodes (PLEDs). Preferably, such films are used as emitting layers. These films may also be used as protective coatings for electronic devices and as fluorescent coatings. The thickness of the coating or film is dependent upon the ultimate use. Generally, such thickness can be from 0.01 to 200 microns. In that embodiment wherein the coating is used as a fluorescent coating, the coating or film thickness is from 10 to 200 microns. In that embodiment where the coatings are used as electronic protective layers, the thickness of the coating can be from 5 to 20 microns. In that embodiment where the coatings are used in a polymeric light-emitting diode, the thickness of the layer formed is 0.01 to 0.5 microns. The polymers of the invention form good pinhole- and defect-free films. Such films can be prepared by means well known in the art including spin-coating, spray- coating, dip-coating and roller-coating. Such coatings are prepared by a process comprising applying a composition to a substrate and exposing the applied composition to conditions such that a film is formed. The conditions which form a film depend upon the application technique. Preferably, the solution contains from 0.1 to 10 weight percent of the polymers. This composition is applied to the appropriate substrate by the desired method and the solvent is allowed to evaporate. Residual solvent may be removed by vacuum and/or by heat-drying. The films are preferably substantially uniform in thickness and substantially free of pinholes. In another embodiment, the polymers may be partially cured. This is known as B-staging.

A further embodiment of the present invention is directed to an electronic device or a component therefore, comprising a substrate and a polymer according to the present invention.

In such a device the polymers according to the present invention are used as electroluminescent material. For the purposes of the present invention, the term "electroluminescent material" is taken to mean materials which can be used as or in an active layer in an electroluminescent device. The term "active layer" means that the layer is capable of emitting light (light-emitting layer) on application of an electric field and/or that it improves the injection and/or transport of the positive and/or negative charges (charge injection or charge transport layer). The invention therefore also relates to the use of the polymers according to the invention as electroluminescent material. The invention furthermore relates to an electroluminescent material which comprises the polymers according to the invention. Electroluminescent devices are used, for example, as self-illuminating display elements, such as control lamps, alphanumeric displays, signs and in opto-electronic couplers.

A device according to the present invention may be prepared in accordance with the disclosure of WO99/48160, the contents of which are incorporated by reference. Polymers according to the present invention may be present in the device as the sole light emitting polymer or as a component in a blend further comprising hole and/or electron transporting polymers. Alternatively, the device may comprise distinct layers of a polymer of the present invention, a hole transporting polymer and/or an electron transporting polymer. In one embodiment the electronic device comprises an electroluminescent device, which comprises

(a) a charge injecting layer for injecting positive charge carriers,

(b) a charge injecting layer for injecting negative charge carriers,

(c) a light-emissive layer located between the layers (a) and (b) comprising a polymer according to the present invention.

The layer (a) may be a positive charge carrier transport layer which is located between the light emissive layer (c) and an anode electrode layer, or may be an anode electrode layer. The layer (b) may be a negative charge carrier transport layer which is located between the light emissive layer (c) and an cathode electrode layer, or may be an cathode electrode layer. Optionally, an organic charge transport layer can be located between the light emissive layer (c) and one of the charge carrier injecting layers (a) and (b).

The EL device emits light in the visible electro-magnetic spectrum between 400 nm and 780 nm, preferably between 430 nm and 470 nm for a blue color, preferably between 520 nm and 560 nm for a green color, preferably between 600 nm and 650 nm for a red color. By incorporating specific repeating units in the backbone of the polymer the emission can be even shifted to the near infrared (NIR, > 780 nm).

It will be appreciated that the light emissive layer may be formed from a blend or mixture of materials including one or more polymers according to the present invention, and optionally further different polymers. The further different polymers may be so-called hole transport polymers (i.e. to improve the efficiency of hole transport to the light-emissive material) or electron-transport polymers (i.e. to improve the efficiency of electron transport to the light- emissive material). Preferably, the blend or mixture would comprise at least 0.1 % by weight of a polymer according to the present invention, preferably at least 0.5 % by weight, more preferably at least 1 % by weight.

An organic EL device typically consists of an organic film sandwiched between an anode and a cathode such that when a positive bias is applied to the device, holes are injected into the organic film from the anode, and electrons are injected into the organic film from the cathode. The combination of a hole and an electron may give rise to an exciton, which may undergo radiative decay to the ground state by liberating a photon. In practice the anode is commonly an mixed oxide of tin and indium for its conductivity and transparency. The mixed oxide (ITO) is deposited on a transparent substrate such as glass or plastic so that the light emitted by the organic film may be observed. The organic film may be the composite of several individual layers each designed for a distinct function. Since holes are injected from the anode, the layer next to the anode needs to have the functionality of transporting holes. Similarly, the layer next to the cathode needs to have the functionality of transporting electrons. In many instances, the hole-(electron) transporting layer also acts as the emitting layer. In some instances one layer can perform the combined functions of hole and electron transport and light emission. The individual layers of the organic film may be all polymeric in nature or combinations of films of polymers and films of small molecules deposited by thermal evaporation. The total thickness of the organic film be less than 1000 nanometers (nm), especially less than 500 nm. It is preferred that the total thickness be less than 300 nm, while it is more preferred that the thickness of the active layer is in the range from 40 - 160 nm.

The ITO-glass, which serves as the substrate and the anode, may be used for coating after the usual cleaning with detergent, organic solvents and UV-ozone treatment. It may also be first coated with a thin layer of a conducting substance to facilitate hole injection. Such substances include copper phthalocyanine, polyaniline (PANI) and poly(3,4-ethylenedioxy- thiophene) (PEDOT); the last two in their (doped) conductive forms, doped, for example, with FeCI₃ or Na₂S₂O₈. They contain poly(styrenesulfonic acid) (PSS) as counter-ion to ensure water solubility. It is preferred that the thickness of this layer be 200 nm or less; it is more preferred that the thickness be 100 nm or less.

In the cases where a hole-transporting layer is used, the polymeric arylamines described in U.S. Pat. No. 5,728,801 , may be used. Other known hole-conducting polymers, such as polyvinylcarbazole, may also be used. The resistance of this layer to erosion by the solution of the copolymer film which is to be applied next is obviously critical to the successful fabrication of multi-layer devices. The thickness of this layer may be 500 nm or less, preferably 300 nm or less, most preferably 150 nm or less.

In the case where an electron-transporting layer is used, it may be applied either by thermal evaporation of low molecular weight materials or by solution coating of a polymer with a solvent that would not cause significant damage to the underlying film.

Examples of low molecular weight materials include the metal complexes of 8- hydroxyquinoline (as described by Burrows et al. in Appl. Phys. Lett. 64 (1994) 2718-2720), metallic complexes of 10-hydroxybenzoquinoline (as described by Hamada et al. in Chem. Lett. (1993) 906-906), 1 ,3,4-oxadiazoles (as described by Hamada et al. in Optoelectronics- Devices and Technologies 7 (1992) 83-93), 1 ,3,4-triazoles (as described by Kido et al. in Chem. Lett. (1996) 47-48), and dicarboximides of perylene (as described by Yoshida et al. in Appl. Phys. Lett. 69 (1996) 734-736).

Polymeric electron-transporting materials are exemplified by 1 ,3,4-oxadiazole-containing polymers (as described by Li et al. in J. Chem. Soc. (1995) 221 1-2212, by Yang and Pei in J. Appl. Phys. 77 (1995) 4807-4809), 1 ,3,4-triazole-containing polymers (as described by Strukelj et al. in Science 267 (1995) 1969-1972), quinoxaline-containing polymers (as described by Yamamoto et al. in Jpn. J. Appl. Phys. 33 (1994) L250-L253, O'Brien et al. in Synth. Met. 76 (1996) 105-108), and cyano-PPV (as described by Weaver et al. in Thin Solid Films 273 (1996) 39-47). The thickness of this layer may be 500 nm or less, preferably 300 nm or less, most preferably 150 nm or less.

The cathode material may be deposited either by thermal evaporation or by sputtering. The thickness of the cathode may be from 1 nm to 10,000 nm, preferably 5 nm to 500 nm.

OLEDs made according to the present invention may include phosphorescent dopants dispersed in the device's emissive layer, capable of achieving internal quantum efficiencies approaching 100%. As used herein, the term "phosphorescence refers to emission from a triplet excited state of an organic or metal-organic molecule. High efficiency organic light emitting devices using phosphorescent dopants have been demonstrated using several different conducting host materials (M. A. Baldo et al., Nature,Vol 395, 151 (1998), C. Adachi et al., Appl. Phys. Lett., Vol. 77, 904 (2000)).

In a preferred embodiment, the electroluminescent device comprises at least one hole- transporting polymer film and a light-emitting polymer film comprised of the polymer of the invention, arranged between an anode material and a cathode material such that under an applied voltage, holes are injected from the anode material into the hole-transporting polymer film and electrons are injected from the cathode material into the light-emitting polymer films when the device is forward biased, resulting in light emission from the light-emitting layer.

In another preferred embodiment, layers of hole-transporting polymers are arranged so that the layer closest to the anode has the lower oxidation potential, with the adjacent layers having progressively higher oxidation potentials. By these methods, electroluminescent devices having relatively high light output per unit voltage may be prepared.

The term "hole-transporting polymer film" as used herein refers to a layer of a film of a polymer which when disposed between two electrodes to which a field is applied and holes are injected from the anode, permits adequate transport of holes into the emitting polymer. Hole-transporting polymers typically are comprised of triarylamine moieties. The term "light- emitting polymer film" as used herein refers to a layer of a film of a polymer whose excited states can relax to the ground state by emitting photons, preferably corresponding to wavelengths in the visible range. The term "anode material" as used herein refers to a semi- transparent, or transparent, conducting film with a work function between 4.5 electron volts (eV) and 5.5 eV. Examples are gold, silver, copper, aluminum, indium, iron, zinc, tin, chromium, titanium, vanadium, cobalt, nickel, lead, manganese, tungsten and the like, metallic alloys such as magnesium/copper, magnesium/silver, magnesium/aluminum, aluminum/indium and the like, semiconductors such as Si, Ge, GaAs and the like, metallic oxides such as indium-tin-oxide ("ITO"), ZnO and the like, metallic compounds such as CuI and the like, and furthermore, electroconducting polymers such polyacetylene, polyaniline, polythiophene, polypyrrole, polyparaphenylene and the like. Oxides and mixed oxides of indium and tin, and gold are preferred. Most preferred is ITO, especially ITO on glass, or on a plastics material, such as polyester, for example polyethylene terephthalate (PET), as substrate.

The term "cathode material" as used herein refers to a conducting film with a work function between 2.0 eV and 4.5 eV. Examples are alkali metals, earth alkaline metals, group 13 elements, silver, and copper as well as alloys or mixtures thereof such as sodium, lithium, potassium, calcium, lithium fluoride (LiF), sodium-potassium alloy, magnesium, barium, magnesium-silver alloy, magnesium-copper alloy, magnesium-aluminum alloy, magnesium- indium alloy, aluminum, aluminum-aluminum oxide alloy, aluminum-lithium alloy, indium, calcium, and materials exemplified in EP-A 499,011 , such as electroconducting polymers e.g. polypyrrole, polythiophene, polyaniline, polyacetylene etc. Preferably lithium, barium, calcium, magnesium, indium, silver, aluminum, or blends and alloys of the above are used. In the case of using a metal or a metallic alloy as a material for an electrode, the electrode can be formed also by the vacuum deposition method. In the case of using a metal or a metallic alloy as a material forming an electrode, the electrode can be formed, furthermore, by the chemical plating method (see for example, Handbook of Electrochemistry, pp 383-387, Mazuren, 1985). In the case of using an electroconducting polymer, an electrode can be made by forming it into a film by means of anodic oxidation polymerization method onto a substrate, which is previously provided with an electroconducting coating.

As methods for forming said thin films, there are, for example, the vacuum deposition method, the spin-coating method, the casting method, the Langmuir-Blodgett ("LB") method, the ink jet printing method and the like. Among these methods, the vacuum deposition method, the spin-coating method, the ink jet printing method and the casting method are particularly preferred in view of ease of operation and cost.

In the case of forming the layers by using the spin-coating method, the casting method and ink jet printing method, the coating can be carried out using a solution prepared by dissolving the composition in a concentration of from 0.0001 to 90% by weight in an appropriate organic solvent such as benzene, toluene, xylene, tetrahydrofurane, methyltetrahydrofurane, N, N- dimethylformamide, acetone, acetonitrile, anisole, dichloromethane, dimethylsulfoxide and mixtures thereof.

Patterning of active matrix OLED (AMOLED) materials for large format, high resolution displays can be done using Laser Induced Thermal Imaging (LITI; Organic Light-Emitting Materials and Devices VII, edited by Zakya H. Kafafi, Paul A. Lane, Proceedings of SPIE Vol. 5519, 12-23).

The organic EL device of the present invention is seen as a future replacement technology for a flat panel display of an on-wall television set, a flat light-emitting device, such as a wall paper, a light source for a copying machine or a printer, a light source for a liquid crystal display or counter, a display signboard and a signal light and perhaps even to replace incandescent and fluorescent lamps. The polymers and compositions of the present invention can be used in the fields of an organic EL device, a photovoltaic device, an electrophotographic photoreceptor, a photoelectric converter, a solar cell, an image sensor, and the like.

Accordingly, the present invention relates also to PLEDs, organic integrated circuits (0-ICs), organic field effect transistors (OFETs), organic thin film transistors (OTFTs), organic solar cells (0-SCs), thermoelectric devices, or organic laser diodes comprising one or more of the polymers according to the present invention. The following examples are included for illustrative purposes only and do not limit the scope of the claims. Unless otherwise stated, all parts and percentages are by weight. Weight-average molecular weight (M_w) and polydispersity (M_w/M_n = PD) are determined by Gel Permeation Chromatography (GPC) [Apparatus: GPC_max + TDA 302 from Viscotek (Houston, TX, USA) yielding the responses form refractive index (Rl), low angle light scattering (LALS), right angle light scattering (RALS) and differential viscosity (DP) measurements. Chromatographic conditions: Column: PL_geι mixed C (300 x 7.5 mm, 5 μm particles) covering the molecular weight range from about 1 x 10³to about 2.5 x 10⁶ Da from Polymer Laboratories (Church Stretton, UK); Mobile phase: tetrahydrofuran containing 5 g/l of sodium trifluoroacetate; Mobile phase flow: either 0.5 or 0.7 ml/min; Solute concentration: about 1-2 mg/ml; Injection volume: 100 μl; Detection: Rl, LALS, RALS, DP. Procedure of molecular weight calibration: Relative calibration is done by use of a set of 10 polystyrene calibration standards obtained from Polymer Laboratories (Church Stretton, UK) spanning the molecular weight range from 1 '930OOO Da - 5O50 Da, i. e., PS 1 '930OOO, PS 1 '460'000, PS 1 O75O00, PS 560O00, PS 330O00, PS 96O00, PS 52O00, PS 30'300, PS 10'100, PS 5'05O Da. Absolute calibration is done on the base of the responses of LALS, RALS and DP. As experienced in a large number of investigations this combination provides optimum calculation of molecular weight data. Usually PS 96'00O is used as the molecular weight calibration standard, but in general every other PS standard lying in the molecular weight range to be determined can be chosen for this purpose.

All polymer structures given in the examples below are idealized representations of the polymer products obtained via the polymerization procedures described. If more than two components are copolymerized with each other sequences in the polymers can be either alternating or random depending on the polymerisation conditions.

Examples

a) 4-Chloro-2,6-dimethyliodobenzene (9.6 g, 36 mmol) is dissolved in pyrene (60 mL). To this solution, a hot solution of KMnO₄ (28 g, 0.18 mol) is poured and the mixture is stirred at 1 15 ⁰C for 8 hours. After additional heating for 5 hours, a 1 M HCI solution is added. The precipitate is filtered off and washed with THF. The resultant filtrate is washed with THF and dried over Na₂SO₄. After the evaporation, the dicarboxylic acid derivative is obtained as a solid. Yield 9.1 g (78%). FD-MS (8kV): m/z = 326.7. ¹H NMR (250 MHz, DMSOd₆) δ ppm 7.24 (s, Ar): ¹³C NMR (62.5 MHz, CD₃OD-d₄): δ ppm 126.7, 128.1 , 134.5, 150.1 , 174.6.

b) The δ-chloro^-iodo-isophthalic acid (product Example 1a, 3.8 g, 12 mmol) is added to SOCI₂ (30 ml_, excess) and the mixture is refluxed under nitrogen for 2 days. The excess SOCI₂ is evaporated under reduced pressure, then the resultant oil containing the 5-chloro-2- iodo-isophthaloyl dichloride (4.2 g, 12 mmol) is dissolved in dichloromethane (50 ml_). To this solution, 1-phenyldodecane (10 g, 47 mmol) and AICI₃ (4.7 g, 35 mmol) are added at 0 ⁰C. The mixture is stirred from 0 ⁰C to room temperature overnight. After quenching with 1 M HCI solution, the residue is extracted by dichloromethane. The mixture is dried over MgSO₄ and purified by column chromatography (silica gel, hexane/ethyl acetate = 80:1 ) to afford the chloro-iododibenzoylbenzene as a colorless oil. Yield 2.3 g (27%). FD-MS (8kV): m/z = 727.7. ¹H NMR (250 MHz, CDCI₃-d) δ ppm 0.88-0.90 (m, 6 H, CH₃), 1.26-1.30 (m, 32 H, CH₂), 2.69 (t, J = 7.3, 4 H, CH₂), 7.27-7.41 (m, 6 H, Ar), 7.75 (t, J = 7.9, 4 H, Ar); ¹³C NMR (62.5 MHz, CD₂CI₂-d₂): ¹³C NMR (250 MHz, CD₂CI₂-d₂): δ ppm 14.3, 23.1 , 29.7, 29,8, 29.9, 30.0, 31.4, 32.3, 36.5, 128.8, 129.4, 130.9, 132.9, 135.3, 148.2, 151.1 , 195.4.

c) Under argon the dibenzoyl derivative (product of example 1 b , 0.57 g, 0.22 mmol) and copper powder (0.11 g, 1.8 mmol) are added to DMF (10 ml_). The mixture is stirred at 1 10 ⁰C for 2 days. After cooling, the residue is filtered and ethyl acetate and brine are added to the filtrate. The organic phase is washed with brine three times and dried over MgSO₄. The residue is purified by column chromatography (silica gel, hexane/ethyl acetate = 20:1 ) to afford the biphenylderivative as a colorless oil. Yield 0.52 g (42%). FD-MS (8kV): m/z = 1202.3. ¹H NMR (250 MHz, CDCI₃-d) δ ppm 0.81 (m, 12 H, CH₃), 1.10-1.20 (m, 64 H, CH₂), 2.51 (t, J = 7.6, 8 H, CH₂), 7.02 (d, J = 7.9, 8 H, Ar), 7.42 (s, 4 H, Ar), 7.55 (d, J = 7.9, 8 H, Ar); ¹³C NMR (62.5 MHz, CD₂CI₂-Cl₂): δ ppm 14.3, 21.9, 23.1 , 29.7, 29,8, 29.9, 30.0, 31.6, 32.3, 36.4, 128.4, 131.2, 131.8, 131.9, 134.9, 136.8, 140.9, 149.2, 194.4.

d) Under argon the biphenyldrivative (product of example 1c (0.26 g, 0.22 mmol) and bis(tricyclohexyltin)sulfide (0.70 g, 0.91 mmol) are dissolved in toluene (50 ml_). To the solution, 1 M BCI₃ in dichloromethane (0.91 ml_, 0.91 mmol) is added. The mixture is stirred at room temperature for 10 minutes and refluxed at 125 ⁰C for 3 days. After cooling the solvent is evaporated and ethyl acetate and brine are added to the filtrate. The organic phase is washed with brine three times and dried over MgSO₄. The residue is purified by column chromatography (silica gel, hexane) to afford the new 2,7-dichloropyrene derivative as a powder. Yield 80 mg (33%). FD-MS (8kV): m/z = 1 135.9. ¹H NMR (250 MHz, CD₂CI₂-d₂) δ ppm 0.89 (t, J = 6.6, 12 H, CH₃), 1.20-1.30 (m, 56 H, CH₂), 1.50-1.60 (m, 8 H, CH₂), 2.62 (t, J = 7.3, 8 H, CH₂), 7.15 (m, 16 H, Ar), 7.80 (s, 4 H, Ar); ¹³C NMR (175 MHz, CD₂CI₂-d₂): δ ppm 14.3, 23.1 , 29.7, 29.8, 29.9, 31.7, 32.4, 36.0, 122.2, 125.1 , 128.2, 131.2, 132.6, 133.3, 136.3, 138.8, 142.2.

a) Synthesis of oligo (2,7-pyrenylene):

A Schlenk tube containing DMF (3.5 ml.) and dry toluene (3.5 ml_), (1 ,5- cyclooctadiene)nickel (0) (64 mg, 0.23 mmol), 2,2'-bipyridyl (36 mg, 0.23 mmol), and 1 ,5- cyclooctadiene (28 μl_, 0.23 mmol) is heated under argon at 80 ⁰C for 30 minutes. The 2,7- dichloro-(4,5,9,10-tetraphenyl)-pyrene derivative (product of example 1d, 0.1 1 g, 97 μmol) is dissolved in dry toluene (5 mL) and added under argon to the solution. The reaction mixture is maintained at 80 ⁰C for 3 days in the dark. Bomobenzene (0.1 mL) is added to reaction mixture. The mixture is allowed to react for another day. The reaction mixture is then poured into concentrated hydrochloric acid / methanol 1 :1 (300 mL). The isolated polymer is dissolved in dichloromethane and reprecipitated in methanol. The residue is purified with a Soxhlet extractor to wash off the small molecules for 2 days in acetone. The residue is dissolved in THF and precipitated from methanol and dried. Yield 0.056 g (54%). ¹H NMR (250 MHz, C₂D₂Cl₄-d₂) δ ppm 0.86-0.89 (m, CH₃), 1.20-1.40 (m, CH₂), 1.50-1.60 (m, CH₂), 2.59 (t, J = 7.3, CH₂), 7.00-7.15 (m, Ar), 7.86-7.91 (m, Ar), 8.10 (s, Ar); ¹³C NMR (175 MHz, C₂D₂CI₄-d₂): δ ppm 13.7, 22.2, 28.6, 28.9, 29.0, 29.2, 30.8, 31.4, 35.1 , 121.2, 124.3, 127.1 , 127.3, 130.2, 131.7, 132.1 , 132.4, 135.0, 135.3, 138. 0, 140.3, 140.7, 140.9. M_n = 2600 g/mol; Mw = 3100 g/mol; PD = 1.2 (PPP standard).

b) Synthesis of poly (2,7-pyrenylene):

A sample tube for microwave containing DMF (3 mL) and dry toluene (2 mL), (1 ,5- cyclooctadiene)nickel (0) (58 mg, 0.21 mmol), 2,2'-bipyridyl (33 mg, 0.21 mmol), and 1 ,5- cyclooctadiene (26 μL, 0.21 mmol) is heated under argon at 80 ⁰C for 30 minutes. The 2,7- dichloropyrene derivative (product of example 1d, 0.1 g, 88 μmol) is dissolved in dry toluene (3 mL) and added under argon to the solution. The reaction mixture is maintained and reacted in a microwave at 80 ⁰C (80 W , 60 min). Bromobenzene (0.2 mL) is added to the reaction mixture and the mixture is allowed to react in the microwave (80 W, 30 min). The reaction mixture is then poured into concentrated hydrochloric acid / methanol 1 :1 (300 mL). The precipitated polymer is filtered and dissolved in dichloromethane and reprecipitated in methanol. The residue is purified with a Soxhlet extractor to wash off the small molecules for 2 days in acetone. The residue is dissolved in THF and precipitated from methanol and dried. Yield 66 mg (66%). ¹H NMR (250 MHz, C₂D₂CI₄-d₂) δ ppm 0.86-0.89 (m, CH₃), 1.20-1.40 (m, CH₂), 1.50-1.70 (m, CH₂), 2.80-2.83 (m, CH₂), 6.90-7.25 (m, Ar), 8.00-8.25 (m, Ar); ¹³C NMR (175 MHz, C₂D₂CI₄-d₂): δ ppm 14.4, 19.9, 21.1 , 24.6, 25.0, 25.7, 27.2, 30.3, 32.9, 33.3, 34.3, 35.9, 37.2, 37.6, 125.0, 126.5, 127.4, 127.7, 129.1 , 129.9, 131.1 , 131.8, 136.3, 136.3, 136.4, 138. 6, 140.6, 149.8.

M_n = 21800 g/mol; Mw = 39000g/mol PD = 1.7 (PPP standard) The absorption maximum in 1 ,2-dichlorobenzene is observed at 376 nm, while the fluorescence maximum occurs at 429 nm.

Example 3 - Poly[2,7-(4,5,9,10-tetraalkoxy)pyrenylene]

A sample tube for microwave containing DMF (2 ml.) and dry toluene (2 ml_), (1 ,5- cyclooctadiene)nickel (0) (0.13 g, 0.48 mmol), 2,2'-bipyridyl (76 μg, 0.48 mmol), and 1 ,5- cyclooctadiene (60 μl_, 0.48 mmol) is heated under argon at 80 ⁰C for 30 minutes. The 2,7- dibromo-(4,5,9,10-tetraalkoxy)-pyrene (0.2 g, 0.20 mmol) is dissolved in dry toluene (3 ml.) and added under argon to the solution. The reaction mixture is maintained and reacted in a microwave at 80 ⁰C (80 W, 60 min). Bomobenzene (0.2 ml.) is added to the reaction mixture and the mixture is allowed to react in the microwave (80 W, 30 min). The reaction mixture is then poured into concentrated hydrochloric acid / methanol 1 :1 (300 ml_). The precipitated polymer is filtered and dissolved in dichloromethane and reprecipitated in methanol. The residue is purified with a Soxhlet extractor to wash off the small molecules for 2 days in acetone. The residue is dissolved in THF and precipitated from methanol and dried. Yield 0.1 g (50%).

¹H NMR (250 MHz, C₂D₂CI₄) δ ppm 0.75-0.78 (24 H, CH₃), 1.05-2.0 (m, CH₃, CH₂), 2.19 (4 H, m, CH), 4.59 (m, 8 H, OCH₂), 9.05 (m, 4 H, Ar).

The GPC analysis yielded molecular weights Mn = 29700 g/mol Mw = 58800 g/mol and polydispersity PD = 2.0 (PPP standard).

The optical properties were measured in THF solution and in thin films showing a maximum of absorption λmax at 371 and 375 nm, respectively. The emission maximum is in the blue range with 441 and 451 nm for the solution and the film, respectively.

Example 4 a) 2,7-Dibromopyrene-4,5,9,10-tetraone

a) The 4,5,9, 10-pyrenetetraone is obtained in one step starting from pyrene according to J.

Org. Chem. 2005, 70, 707-708.

3 g of pyrene-4,5,9,10-tetraone are dissolved in 80 ml of cone. H₂SO₄. At room temperature an excess of 2.2 equivalents N-bromosuccinimide (NBS) is added slowly. The reaction mixture is stirred for another hour and finally put in ice water. After precipitation the product is filtered and washed with water. The crude product is stirred in methanol, dried and boiled again in ethyl ether and finally in methylenchloride. 2,7-Dibromopyrene-4,5,9,10-tetraone is obtained in a yield of 78%.

FD-MS (8 KV): m/z 420.1 (100%), calculated 420.0.

¹H-NMR (C₂D₂CI₄, 250 MHz, 140 ⁰C): d = 8.61 (s, 4 H).

¹³C-NMR (THF-d8, 175 MHz): d = 125.9, 133.4, 134.8, 137.6, 176.3.

2-hexyldec-1-yl

b) 2,7-Dibromopyrene-4,5,9,10-tetraalkoxypyrene

A mixture of 2,7-dibromopyrene-4,5,9,10-tetraone (0.50 g, 1.2 mmol), H-Bu₄NBr (0.50 g, 1.5 mmol), Na₂S₂O₄ (2.5 g, 14 mmol), THF (8 ml_), and H₂O (4m L) is stirred at 25 ⁰C for 10 minutes 1-Bromo-2-hexyldecane (1.7 g, 7.9 mmol) and aqueous potassium hydroxide (4 mL, 36 mmol) are added to the solution and the mixture is stirred at 70 ⁰C for 5 h. Then, THF and brine are added and the organic phase is washed with brine (3 times) and dried over MgSO₄ and concentrated in vaccum. The residue is purified by column chromatography (SiO₂, hexane : CH₂CI₂ = 10 : 1 ) to give a colorless oil (0.62 g) in 53% yield. FD-MS (8 KV): m/z 986.3 (100%), calculated 985.1.

¹H-NMR (CD₂CI₂, 250 MHz): δ = 0.84-0.86 (m, 24H), 0.98-1.00 (m, 12H), 1.47-2.00 (m, 40H), 4.23-4.36 (m, 8H), 8.50 (s, 4H).

a) The synthesis of the 2,7-dibromopyrene is described in J. Org. Chem. 1986, 51 , 2848. 5.3 g (25 mmol) NaIO₄, 25 ml. H₂O, and 0.14 g RuCI₃XH₂O are added to a solution of 1 g (2.8 mmol) 2,7-dibromopyrene in 20 mL CH₂CI₂ and 20 mL CH₃CN. The dark brown suspension is heated to 50 ⁰C overnight. The reaction mixture is poured into 100 mL of H₂O, and extracted with 100 mL of THF. The organic phase is separated and concentrated. The crude product 2,7-dibromopyrene-4,5,9,10-tetraone is obtained as red orange substance (yield < 15 %, m/z 420.0).

Example 6

a) 6,11-dibromo-1 ,2,3,4-tetraphenyltriphenylene (1.1 g, 1.6 mmol), bis(pinacolato)diboron (0.9 g, 3.5 mmol), AcOK (0.5 g, 4.7 mmol), are charged in Schlenck flask and dissolved in 17 ml dioxane. The whole mixture is degassed and the catalyst [PdCI₂(dppf)]CH₂CI₂ (0.065 g, 0.08 mmol) is added and the whole reaction mixture is heated up to 9O⁰C for 20 h. The solvent is removed under reduced pressure and the product is finally purified by chromatography on silica gel with hexane : dichloromethane (1 :3), to afford the desired product (0.309 g, 25 %).

R = 3,7-dιmethyl-1-octyl

b) A suspension of 2,7-di-4,4,5,5-tetramethyl(9,10,11 ,12-tetraphenyl-triphenylen-2-yl)- [1 ,3,2]dioxaborolane (0.309 g, 0.39 mmol), 2,7-dibromo-4,5,9,10-tetrakis-(3,7-dimethyl- octyloxy)-pyrene (0.388 g, 0.39 mmol), aqueous K₂CO₃ (3 ml / 2M), Aliquat® 336 (0.04 g, 0.1 mmol), and Pd(PPh₃)₄ (0.023 g, 0.02 mmol) in toluene (4.5 mL) is charged in a microwave tube equipped with a magnetic stirrer bar, which has been purged with argon and sealed. The mixture is vigorously stirred in a CEM Discover microwave at 50 W and activated cooling; keeping the temperature at 100⁰C for 5 h. Sequentially bromobenzene (0.56 g, 3.6 mmol), and benzene boronic acid (0.28 g, 2.3 mmol) in degassed toluene (3 ml) are added to the reaction mixture and stirred at 100⁰C for Vi h each. At room temperature the organic layer is extracted and washed with aqueous sodium cyanide (1 %, 2 x 50 ml). The organic layer is extracted again with toluene and the solution is concentrated in vacuo until a high viscous solution is obtained. The polymer is precipitated by slow addition to 300 ml methanol. The polymer is filtered off and sequentially washed with methanol, water, acetone, and methanol. The polymer is dissolved again in toluene and vigorously stirred in aqueous sodium cyanide (1 %, 100 ml) at 90⁰C for 2 h. The organic phase is extracted, concentrated, and finally poured into an excess of methanol. The polymer is filtered off, and the oligomeric fractions are removed by extraction (1 day/Soxhlet apparatus/ethyl acetate). Yield of polymer: 0.28 g (52 %). GPC analysis: M_w = 12.4 x 1 θ3 g mol^"1, PDI = 1.4 (PPP standard).

Claims

1. A polymer comprising repeating unit(s) of the following formula

R¹, R², R³, R⁴, R⁵ and R⁶ are independently of each other hydrogen, F₁ SiR¹⁰⁰R¹⁰¹R¹⁰², or an organic substituent, or

R¹ and R², R³ and R⁴, and/or any of the substituents R¹, R², R³, R⁴, R⁵ and/or R⁶, which are adjacent to each other, together form an aromatic, or heteroaromatic ring, or ring system, which can optionally be substituted, m is 0, or an integer of 1 , or 2, n1 and n2 are 0, or an integer 1 , or 2,

R¹⁰⁰, R¹⁰¹ and R¹⁰² are independently of each other d-Ci₈alkyl, substituted or unsubstituted C₆-C₁₈aryl, and

Ar¹ and Ar² are each independently of each other a substituted or unsubstituted arylene, or heteroarylene group.

2. The polymer according to claim 1 comprising repeating units of formula I, wherein

R¹, R², R³ and R⁴ are independently of each other H, F, d-C₁₈alkyl, d-C₁₈alkyl which is substituted by E and/or interrupted by D, d-C₁₈alkoxy, d-d₈alkoxy which is substituted by E and/or interrupted by D, d-C₁₈perfluoroalkyl, C₆-d₄aryl, C₆-C₂₄aryl which is substituted by G, d-doheteroaryl, d-doheteroaryl which is substituted by G; each group R⁵ and R⁶ is independently of each other in each occurrence H, halogen, especially F, d-d₈alkyl, d-d₈alkyl which is substituted by E and/or interrupted by D, C₁- dsperfluoroalkyl, C₆-d4aryl, C₆-d4aryl which is substituted by G, d-doheteroaryl, C₂- doheteroaryl which is substituted by G, C₂-Ci₈alkenyl, C₂-Ci₈alkynyl, Ci-Ci₈alkoxy, C₁- Ci₈alkoxy which is substituted by E and/or interrupted by D, C₇-C₂₅aralkyl, CN, or -CO-R²⁸, m is 0, or an integer 1 , or 2,

D is -CO-; -COO-; -S-; -SO-; -SO₂-; -O-; -NR²⁵-; -SiR³⁰R³¹-; -POR³²-; -CR²³=CR²⁴-; or -C≡C- ; and E is -OR²⁹; -SR²⁹; -NR²⁵R²⁶; -COR²⁸; -COOR²⁷; -CONR²⁵R²⁶; -CN; or halogen, especially F, G is E, d-C₁₈alkyl, d-C₁₈alkyl which is interrupted by D, d-C₁₈perfluoroalkyl, C₁-

C₁₈alkoxy, or C₁-C₁SaIkOXy which is substituted by E and/or interrupted by D, R²³, R²⁴, R²⁵ and R²⁶ are independently of each other H; C₆-C₁₈aryl; C₆-C₁₈aryl which is substituted by C^C^alkyl, or C₁-C₁SaIkOXy; C^C^alkyl; or C^C^alkyl which is interrupted by -O-;

R²⁷ is H; C₆-C₁₈aryl; C₆-C₁₈aryl which is substituted by CrC₁₈alkyl, or CrC₁₈alkoxy; especially CrC₁₈alkyl; or CrC₁₈alkyl which is interrupted by -O-,

R²⁸ is H; C₆-C₁₈aryl; C₆-C₁₈aryl which is substituted by CrC₁₈alkyl, or CrC₁₈alkoxy; C₁-

C₁₈alkyl; or C^C^alkyl which is interrupted by -O-,

R²⁹ is H; C₆-C₁₈aryl; C₆-C₁₈aryl, which is substituted by CrC₁₈alkyl, or CrC₁₈alkoxy; C₁-

C₁₈alkyl; or C^C^alkyl which is interrupted by -O-,

R³⁰ and R³¹ are independently of each other C^C^alkyl, C₆-C₁₈aryl, or C₆-C₁₈aryl, which is substituted by C^C^alkyl, and

R³² is C^C^alkyl, C₆-C₁₈aryl, or C₆-C₁₈aryl, which is substituted by C^C^alkyl.

3. The polymer according to claim 1 , or 2, wherein the polymer contains repeating unit(s) of formula

wherein R¹, R², R³ and R⁴ are independently of each other

or C₂-C₁₁heteroaryl, which may optionally be substituted by one or more groups G, wherein G is as defined in claim 2, or R¹, R², R³ and R⁴ are independently of each other C^C^alkyl, CrC₁₈alkyl which is interrupted by -O-, C₁-C₁SaIkOXy; or C^C^alkoxy which is interrupted by -O-.

4. The polymer according to claim 3, wherein R¹, R², R³ and R⁴ are independently of each

other ^' , wherein n₃ is 0, or an integer 1 , 2, 3, 4, or 5, R¹¹ can be same, or different in each occurrence and is C₁-C₂5alkyl, or C₁-C₂SaIkOXy, or R¹, R², R³ and R⁴ are independently of each other CrC₁₈alkyl, C^C^alkyl which is interrupted by -O-, C₁- C₁₈alkoxy; or C₁-C₁SaIkOXy which is interrupted by -O-.

5. The polymer according to claim 4, comprising repeating unit(s) of formula

(Ia), wherein

6. The polymer of claim 1 :

7. An electronic device or a component therefore, comprising the polymer according to any of claims 1 to 6.

8. Use of the polymers according to any of claims 1 to 6 in polymer light emitting diodes (PLEDs), especially as electroluminescent material.

9. PLEDs, organic integrated circuits (0-ICs), organic field effect transistors (OFETs), organic thin film transistors (OTFTs), organic solar cells (0-SCs), thermoelectric decices, electrochromic devices, or organic laser diodes comprising one or more of the polymers according to any of claims 1 to 6.

10. A compound of the formula

(Xl), wherein Ar¹, Ar², rv, , n₂, R¹, R², R³, R⁴, R⁵

R⁶ and m are as defined in claim 1 ;

X¹¹ is independently in each occurrence a halogen atom, especially I, Cl, or Br; -ZnX¹², - SnR²⁰⁷R²⁰⁸R²⁰⁹, wherein R²⁰⁷, R²⁰⁸ and R²⁰⁹ are identical or different and are H or C,- C₆alkyl, wherein two radicals optionally form a common ring and these radicals are optionally branched or unbranched and X¹² is a halogen atom, very especially I, or Br; or -

OS(O)₂CF₃, -OS(O)₂-aryl, especially

, -OS(O)₂CH₃, -B(OH)₂, -B(OY¹¹)₂,

, -BF₄Na, or -BF₄K, wherein Y¹¹ is independently in each occurrence a Ci- C₁₀alkyl group and Y¹² is independently in each occurrence a C₂-C₁₀alkylene group, such as -CY¹³Y¹⁴-CY¹⁵Y¹⁶-, or -CY¹⁷Y¹⁸-C Y¹⁹Y²⁰- CY²¹Y²²-, wherein Y¹³, Y¹⁴, Y¹⁵, Y¹⁶, Y¹⁷, Y¹⁸, γⁱ⁹ γ²o γ²ⁱ _anc| γ²² _gre independently of each other hydrogen, or a Ci-Ci_Oalkyl group, especially -C(CH₃)2C(CH₃)2-, or -C(CH₃)2CH₂C(CH3)2-.

11. A compound of the formula

(XIV), wherein X¹¹, Ar¹, Ar², rv,, n₂, R⁵, R⁶ and m are as defined in claim 10.

12. A process for preparing a compound of the formula

(XIV), comprising reacting a compound of formula

(XII) with a brominating agent, such as N-bromosuccinimide (NBS), or 1 ,3-bromo-5,5-dimethyldantoin, wherein X¹¹ is Br, n-i and n₂ are 0, Ar¹, Ar², R⁵, R⁶ and m are as defined in claim 10.