Heteroaromatic compounds for organic electroluminescent devices
The invention relates to heteroaromatic compounds which are suitable for use in electronic devices, and to electronic devices, in particular organic electroluminescent devices, containing said compounds.
1 . A compound including at least one structure of the formula (IIb), (IIc) or (IId)
where the symbols used are as follows:
Z is the same or different at each instance and is N or B;
W 1 , W 2 , W 3 , W 4 is the same or different at each instance and is N or CR, where at least one W 1 , W 2 , W 3 , W 4 per ring is N;
X 1 is the same or different at each instance and is N, CR a or CAr, with the proviso that not more than two of the X 1 , X 2 groups in one cycle are N;
X 2 is the same or different at each instance and is N, CR b or CAr, with the proviso that not more than two of the X 1 , X 2 groups in one cycle are N;
X 3 is the same or different at each instance and is N, CR c or CAr, with the proviso that not more than two of the X 3 , X 4 groups in one cycle are N;
X 4 is the same or different at each instance and is N, CR d , CAr or C if a ring system is formed by a bond to an X 4 group, with the proviso that not more than two of the X 3 , X 4 groups in one cycle are N;
Ar is the same or different at each instance and is an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted by one or more R radicals; the Ar group here may form a ring system with at least one Ar, R group or a further group;
R, R a , R b , R c , R d is the same or different at each instance and is H, D, OH, F, Cl, Br, I, CN, NO 2 , N(Ar′) 2 , N(R 1 ) 2 , C(═O)Ar′, C(═O)R 1 , C(═O)OAr′, C(═O)OR 1 , C(═O)N(Ar′) 2 , C(═O)N(R 1 ) 2 , C(Ar′) 3 , C(R 1 ) 3 , Si(Ar′) 3 , Si(R 1 ) 3 , B(Ar′) 2 , B(R 1 ) 2 , P(═O)(Ar′) 2 , P(═O)(R 1 ) 2 , P(Ar′) 2 , P(R 1 ) 2 , S(═O)Ar′, S(═O)R 1 , S(═O) 2 Ar′, S(═O) 2 R 1 , OSO 2 Ar′, OSO 2 R 1 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms or an alkenyl or alkynyl group having 2 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 20 carbon atoms, where the alkyl, alkoxy, thioalkoxy, alkenyl or alkynyl group may in each case be substituted by one or more R 1 radicals, where one or more nonadjacent CH 2 groups may be replaced by R 1 C═CR 1 , C≡C, Si(R 1 ) 2 , C═O, C═S, C═Se, C═NR 1 , —C(═O)O—, —C(═O)NR 1 —, NR 1 , P(═O)(R 1 ), —O—, —Se—, —S—, SO or SO 2 , or an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted in each case by one or more R 1 radicals, or an aryloxy or heteroaryloxy group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 1 radicals; at the same time, two R, R a , R b , R d radicals may also form a ring system together or with a further group;
Ar′ is the same or different at each instance and is an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 1 radicals; at the same time, it is possible for two Ar′ radicals bonded to the same carbon atom, silicon atom, nitrogen atom, phosphorus atom or boron atom also to be joined together via a bridge by a single bond or a bridge selected from B(R 1 ), C(R 1 ) 2 , Si(R 1 ) 2 , C═O, C═NR 1 , C═C(R 1 ) 2 , O, S, S═O, SO 2 , N(R 1 ), P(R 1 ) and P(═O)R 1 ; R 1 is the same or different at each instance and is H, D, F, Cl, Br, I, CN, NO 2 , N(Ar″) 2 , N(R 2 ) 2 , C(═O)Ar″, C(═O)R 2 , C(═O)OAr″, C(═O)OR 2 , P(═O)(Ar″) 2 , P(Ar″) 2 , B(Ar″) 2 , B(R 2 ) 2 , C(Ar″) 3 , C(R 2 ) 3 , Si(Ar″) 3 , Si(R 2 ) 3 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 carbon atoms or an alkenyl group having 2 to 40 carbon atoms, each of which may be substituted by one or more R 2 radicals, where one or more nonadjacent CH 2 groups may be replaced by —R 2 C═CR 2 —, —C≡C—, Si(R 2 ) 2 , C═O, C═S, C═Se, C═NR 2 , —C(═O)O—, —C(═O)NR 2 —, NR 2 , P(═O)(R 2 ), —O—, —S—, SO or SO 2 and where one or more hydrogen atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms, each of which may be substituted by one or more R 2 radicals, or an aryloxy or heteroaryloxy group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 2 radicals, or an aralkyl or heteroaralkyl group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 2 radicals, or a combination of these systems; at the same time, two or more R 1 radicals together may form a ring system; at the same time, one or more R 1 radicals may form a ring system with a further part of the compound;
Ar″ is the same or different at each instance and is an aromatic or heteroaromatic ring system which has 5 to 30 aromatic ring atoms and may be substituted by one or more R 2 radicals; at the same time, it is possible for two Ar″ radicals bonded to the same carbon atom, silicon atom, nitrogen atom, phosphorus atom or boron atom also to be joined together via a bridge by a single bond or a bridge selected from B(R 2 ), C(R 2 ) 2 , Si(R 2 ) 2 , C═O, C═NR 2 , C═C(R 2 ) 2 , O, S, S═O, SO 2 , N(R 2 ), P(R 2 ) and P(═O)R 2 ;
R 2 is the same or different at each instance and is selected from the group consisting of H, D, F, CN, an aliphatic hydrocarbyl radical having 1 to 20 carbon atoms or an aromatic or heteroaromatic ring system which has 5 to 30 aromatic ring atoms and in which one or more hydrogen atoms may be replaced by D, F, Cl, Br, I or CN and which may be substituted by one or more alkyl groups each having 1 to 4 carbon atoms; at the same time, two or more substituents R 2 together may form a ring system;
Y 1 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R 1 ), P(Ar′) or P(R 1 ), —(O)C—C(O)—, —N(Ar′)—C(O)—, —(R 1 ) 2 C—C(R 1 ) 2 —, —(R 1 )C═C(R 1 )—, an aryl or heteroaryl group having 5 to 40 aromatic ring atoms, where the aryl or heteroaryl group binds to the further parts of the structure via two adjacent and mutually joined carbon atoms and may be substituted by one or more R 1 radicals;
j is 0, 1 or 2;
p is 1 for the compound of formula (IIb) and is 0 or 1 for the compound of formula (IId), where p=0 means that the Y 1 group is absent;
k is 0 or 1, where k=0 if p=1.
2 . The compound according to claim 1 , comprising at least one structure of the formula (IIIj) to (IIIv)
where Z, R, R a , R b , R c and R d have the definitions given in claim 1 ,
Y 1 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R′), P(Ar′) or P(R′), —(O)C—C(O)—, —N(Ar′)—C(O)—, —(R 1 ) 2 C—C(R 1 ) 2 —, —(R 1 )C═C(R 1 )—, an aryl or heteroaryl group having 5 to 40 aromatic ring atoms, where the aryl or heteroaryl group binds to the further parts of the structure via two adjacent and mutually joined carbon atoms and may be substituted by one or more R 1 radicals, where the symbols R 1 and Ar′ have the definition set out in claim 1 ;
j is 0, 1 or 2;
k is 0 or 1,
and the further symbols have the following definition:
Y 2 , Y 3 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R 1 ), P(Ar′) or P(R 1 ), where the symbols R 1 and Ar′ have the definition set out in claim 1 ; and
m is 0, 1, 2, 3 or 4.
3 . The compound according to claim 1 , wherein at least two R, R a , R b , R c , R d radicals together with the further groups to which the two R, R a , R b , R c , R d radicals bind form a fused ring, where the two R, R a , R b , R c , R d radicals form at least one structure of the formulae (RA-1) to (RA-12):
where R 1 has the definition set out above, the dotted bonds represent the sites of attachment via which the two R, R a , R b , R c , R d radicals bind, and the further symbols have the following definition:
Y 4 is the same or different at each instance and is C(R 1 ) 2 , (R 1 ) 2 C—C(R 1 ) 2 , (R 1 )C═C(R 1 ), NR 1 , NAr′, O or S;
R e is the same or different at each instance and is F, a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms or an alkyl or alkenyl group having 2 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 20 carbon atoms, where the alkyl, alkoxy, thioalkoxy, alkenyl or alkynyl group may be substituted in each case by one or more R 2 radicals, where one or more adjacent CH 2 groups may be replaced by R 2 C═CR 2 , C≡C, Si(R 2 ) 2 , C═O, C═S, C═Se, C═NR 2 , —C(═O)O—, —C(═O)NR 2 —, NR, P(═O)(R 1 ), —O—, —S—, SO or SO 2 , or an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted in each case by one or more R 2 radicals, or an aryloxy or heteroaryloxy group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 2 radicals; at the same time, it is also possible for two R radicals together or one R c radical together with an R 1 radical or together with a further group to form a ring system;
s is 0, 1, 2, 3, 4, 5 or 6;
t is 0, 1, 2, 3, 4, 5, 6, 7 or 8;
v is 0, 1, 2, 3, 4, 5, 6, 7, 8 or 9.
4 . The compound as claimed in claim 3 , wherein the compounds have at least two additional fused rings, wherein at least one fused ring comprises structures of the formulae (RA-1) to (RA-12) and a further ring comprises structures of the formulae (RA-1) to (RA-12) or (RB),
where the dotted bonds represent the sites of attachment to the atoms of the groups to which the two R, R a , R b , R c , R d radicals bind, the index m is 0, 1, 2, 3 or 4 and Y 5 is C(R 1 ) 2 , NR 1 , NAr′, BR 1 , BAr′, O or S;
comprising at least one structure of the formulae (VI-12) to (VI-22):
where
Z is the same or different at each instance and is N or B;
R, R a , R c , R d is the same or different at each instance and is H, D, OH, F, Cl, Br, I, CN, NO 2 , N(Ar′) 2 , N(R 1 ) 2 , C(═O)Ar′, C(═O)R 1 , C(═O)OAr, C(═O)OR 1 , C(═O)N(Ar′) 2 , C(═O)N(R 1 ) 2 , C(Ar′) 3 , C(R 1 ) 3 , Si(Ar′) 3 , Si(R 1 ) 3 , B(Ar′) 2 , B(R 1 ) 2 , P(═O)(Ar′) 2 , P(═O)(R 1 ) 2 , P(Ar′) 2 , P(R 1 ) 2 , S(═O)Ar′, S(═O)R 1 , S(═O) 2 Ar′, S(═O) 2 R 1 , OSO 2 Ar′, OSO 2 R 1 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms or an alkenyl or alkynyl group having 2 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 20 carbon atoms, where the alkyl, alkoxy, thioalkoxy, alkenyl or alkynyl group may in each case be substituted by one or more R 1 radicals, where one or more nonadjacent CH 2 groups may be replaced by R 1 C═CR 1 , C≡C, Si(R 1 ) 2 , C═O, C═S, C═Se, C═NR 1 , —C(═O)O—, —C(═O)NR 1 —, NR 1 , P(═O)(R 1 ), —O—, —Se—, —S—, SO or SO 2 , or an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted in each case by one or more R 1 radicals, or an aryloxy or heteroaryloxy group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 1 radicals; at the same time, two R, R a , R b , R c , R d radicals may also form a ring system together or with a further group;
Ar′ is the same or different at each instance and is an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 1 radicals; at the same time, it is possible for two Ar′ radicals bonded to the same carbon atom, silicon atom, nitrogen atom, phosphorus atom or boron atom also to be joined together via a bridge by a single bond or a bridge selected from B(R 1 ), C(R 1 ) 2 , Si(R 1 ) 2 , C═O, C═NR 1 , C═C(R 1 ) 2 , O, S, S═O, SO 2 , N(R 1 ), P(R 1 ) and P(═O)R 1 ;
R 1 is the same or different at each instance and is H, D, F, Cl, Br, I, CN, NO 2 , N(Ar″) 2 , N(R 2 ) 2 , C(═O)Ar″, C(═O)R 2 , C(═O)OAr″, C(═O)OR 2 , P(═O)(Ar″) 2 , P(Ar″) 2 , B(Ar″) 2 , B(R 2 ) 2 , C(Ar″) 3 , C(R 2 ) 3 , Si(Ar″) 3 , Si(R 2 ) 3 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 carbon atoms or an alkenyl group having 2 to 40 carbon atoms, each of which may be substituted by one or more R 2 radicals, where one or more nonadjacent CH 2 groups may be replaced by —R 2 C═CR 2 —, —C≡C—, Si(R 2 ) 2 , C═O, C═S, C═Se, C═NR 2 , —C(═O)O—, —C(═O)NR 2 —, NR 2 , P(═O)(R 2 ), —O—, —S—, SO or SO 2 and where one or more hydrogen atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms, each of which may be substituted by one or more R 2 radicals, or an aryloxy or heteroaryloxy group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 2 radicals, or an aralkyl or heteroaralkyl group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 2 radicals, or a combination of these systems; at the same time, two or more R 1 radicals together may form a ring system; at the same time, one or more R 1 radicals may form a ring system with a further part of the compound;
A″ is the same or different at each instance and is an aromatic or heteroaromatic ring system which has 5 to 30 aromatic ring atoms and may be substituted by one or more R 2 radicals; at the same time, it is possible for two Ar″ radicals bonded to the same carbon atom, silicon atom, nitrogen atom, phosphorus atom or boron atom also to be joined together via a bridge by a single bond or a bridge selected from B(R 2 ), C(R 2 ) 2 , Si(R 2 ) 2 , C═O, C═NR 2 , C═C(R 2 ) 2 , O, S, S═O, SO 2 , N(R 2 ), P(R 2 ) and P(═O)R 2 ;
R 2 is the same or different at each instance and is selected from the group consisting of H, D, F, CN, an aliphatic hydrocarbyl radical having 1 to 20 carbon atoms or an aromatic or heteroaromatic ring system which has 5 to 30 aromatic ring atoms and in which one or more hydrogen atoms may be replaced by D, F, Cl, Br, I or CN and which may be substituted by one or more alkyl groups each having 1 to 4 carbon atoms; at the same time, two or more substituents R 2 together may form a ring system,
Y 1 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R′), P(Ar′) or P(R′), —(O)C—C(O)—, —N(Ar′)—C(O)—, —(R 1 ) 2 C—C(R 1 ) 2 —, —(R 1 )C═C(R 1 )—, an aryl or heteroaryl group having 5 to 40 aromatic ring atoms, where the aryl or heteroaryl group binds to the further parts of the structure via two adjacent and mutually joined carbon atoms and may be substituted by one or more R radicals, where the symbols R 1 and Ar′ have the definition set out in claim 1 ;
j is 0, 1 or 2;
k is 0 or 1,
Y 2 , Y 3 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R 1 ), P(Ar′) or P(R 1 );
and the symbol o represents the attachment sites to the at least one fused ring.
5 . The compound as claimed in claim 1 , wherein at least two R, R a , R b , R c , R d radicals together with the further groups to which the two R, R a , R b , R c , R d radicals bind form a fused ring, where the two R, R a , R b , R c , R d radicals form structures of the formulae (RA-1a) to (RA-4f):
where the dotted bons represent the sites of attachment via which the two R, R a , R b , R c , R d radicals bind, the index m is 0, 1, 2, 3 or 4 and the symbols R 1 , R 2 , R c and the indices s and t have the definition detailed above.
6 . The compound as claimed in claim 1 , wherein at least two R, R a , R b , R c , R d radicals together with the further groups to which the two R, R a , R b , R c , R d radicals bind form a fused ring, where the two R, R a , R b , R c , R d radicals form structures of the formula (RB):
where R 1 has the definition set out in claim 1 , the dotted bonds represent the sites of attachment to the atoms of the groups to which the two R, R a , R b , R c , R d radicals bind, the index m is 0, 1, 2, 3 or 4 and Y5 is C(R 1 ) 2 , NR 1 , NAr′, BR 1 , BAr′, O or S.
7 . The compound as claimed in claim 1 , comprising at least one structure of the formulae (IV-15) to (IV-36), where the compounds have at least one additional fused ring,
where Z, R, R a , R c and R d have the definitions given in claim 1 ,
Y 1 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R′), P(Ar′) or P(R′), —(O)C—C(O)—, —N(Ar′)—C(O)—, —(R 1 ) 2 C—C(R 1 ) 2 —, —(R 1 )C═C(R 1 )—, an aryl or heteroaryl group having 5 to 40 aromatic ring atoms, where the aryl or heteroaryl group binds to the further parts of the structure via two adjacent and mutually joined carbon atoms and may be substituted by one or more R 1 radicals, where the symbols R 1 and Ar′ have the definition set out in claim 1 ;
j is 0, 1 or 2;
k is 0 or 1,
Y 2 , Y 3 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R 1 ), P(Ar′) or P(R 1 ), where the symbols R 1 and Ar′ have the definition set out in claim 1 ; and
the symbol o represents the attachment sites, and the index m is 0, 1, 2, 3 or 4.
8 . The compound as claimed in claim 7 , wherein the compound comprises exactly two or exactly three structures of formula (IIb) to (IId), or (IV-15) to (IV-36).
9 . A compound as claimed in claim 1 , comprising at least one structure of the formulae (V-12) to (V-22), where the compounds have at least one additional fused ring,
where Z, R, R a , R c and R d have the definitions given in claim 1 ,
Y 1 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R 1 ), P(Ar′) or P(R 1 ), —(O)C—C(O)—, —N(Ar′)—C(O)—, —(R 1 ) 2 C—C(R 1 ) 2 —, —(R 1 )C═C(R 1 )—, an aryl or heteroaryl group having 5 to 40 aromatic ring atoms, where the aryl or heteroaryl group binds to the further parts of the structure via two adjacent and mutually joined carbon atoms and may be substituted by one or more R 1 radicals, where the symbols R 1 and Ar′ have the definition set out in claim 1 ;
j is 0, 1 or 2;
k is 0 or 1,
Y 2 , Y 3 is the same or different at each instance and is a bond, N(Ar′), N(R 1 ), B(Ar′), B(R 1 ), P(═O)(Ar′), P(═O)(R 1 ), C(═O), C(Ar′) 2 , C(R 1 ) 2 , Si(Ar′) 2 , Si(R 1 ) 2 , O, S, Se, S═O, SO 2 , C(═O)N(Ar′), C(═O)N(R 1 ), P(Ar′) or P(R 1 ), where the symbols R 1 and Ar′ have the definition set out in claim 1 ;
the symbol o represents the attachment sites, and the index m is 0, 1, 2, 3 or 4.
10 . An oligomer, polymer or dendrimer containing one or more compounds as claimed in claim 1 , wherein, in place of a hydrogen atom or a substituent, there are one or more bonds of the compounds to the polymer, oligomer or dendrimer.
11 . A formulation comprising at least one compound as claimed in claim 1 and at least one further compound.
12 . A composition comprising at least one compound as claimed in claim 1 and at least one further compound selected from the group consisting of fluorescent emitters, phosphorescent emitters, emitters that exhibit TADF, host materials, electron transport materials, electron injection materials, hole conductor materials, hole injection materials, electron blocker materials and hole blocker materials.
13 . A process for preparing the compound as claimed in claim 1 , wherein a base skeleton having at least one of the W 1 , W 2 , W 3 , W 4 groups or a precursor of one of the W 1 , W 2 , W 3 , W 4 groups is synthesized, and the Z group is introduced by means of a metalation reaction, a nucleophilic aromatic substitution reaction or a coupling reaction.
14 . A method comprising providing the compound as claimed in claim 1 and incorporating the compound in an electronic device.
15 . An electronic device comprising at least one compound as claimed in claim 1 .
16 . A compound, selected from compounds of the formula (D-1) and (D-2):
where the L 1 group represents a connecting group,
Z is the same or different at each instance and is N or B;
W 1 , W 2 , W 3 , W 4 is the same or different at each instance and is N or CR, where at least one W 1 , W 2 , W 3 , W 4 per ring is N;
X 1 is the same or different at each instance and is N, CR a or CAr, with the proviso that not more than two of the X 1 , X 2 groups in one cycle are N;
X 2 is the same or different at each instance and is N, CR b or CAr, with the proviso that not more than two of the X 1 , X 2 groups in one cycle are N;
X 3 is the same or different at each instance and is N, CR c or CAr, with the proviso that not more than two of the X 3 , X 4 groups in one cycle are N;
X 4 is the same or different at each instance and is N, CR d , CAr or C if a ring system is formed by a bond to an X 4 group, with the proviso that not more than two of the X 3 , X 4 groups in one cycle are N;
Ar is the same or different at each instance and is an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted by one or more R radicals; the Ar group here may form a ring system with at least one Ar, R group or a further group;
R, R a , R b , R c , R d is the same or different at each instance and is H, D, OH, F, Cl, Br, I, CN, NO 2 , N(Ar′) 2 , N(R 1 ) 2 , C(═O)Ar′, C(═O)R 1 , C(═O)OAr′, C(═O)OR 1 , C(═O)N(Ar′) 2 , C(═O)N(R 1 ) 2 , C(Ar′) 3 , C(R 1 ) 3 , Si(Ar′) 3 , Si(R 1 ) 3 , B(Ar′) 2 , B(R 1 ) 2 , P(═O)(Ar′) 2 , P(═O)(R 1 ) 2 , P(Ar′) 2 , P(R 1 ) 2 , S(═O)Ar′, S(═O)R 1 , S(═O) 2 Ar′, S(═O) 2 R 1 , OSO 2 Ar′, OSO 2 R 1 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms or an alkenyl or alkynyl group having 2 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 20 carbon atoms, where the alkyl, alkoxy, thioalkoxy, alkenyl or alkynyl group may in each case be substituted by one or more R 1 radicals, where one or more nonadjacent CH 2 groups may be replaced by R 1 C═CR 1 , C≡C, Si(R 1 ) 2 , C═O, C═S, C═Se, C═NR 1 , —C(═O)O—, —C(═O)NR 1 —, NR 1 , P(═O)(R′), —O—, —Se—, —S—, SO or SO 2 , or an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted in each case by one or more R 1 radicals, or an aryloxy or heteroaryloxy group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 1 radicals; at the same time, two R, R a , R b , R d radicals may also form a ring system together or with a further group;
Ar′ is the same or different at each instance and is an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 1 radicals; at the same time, it is possible for two Ar′ radicals bonded to the same carbon atom, silicon atom, nitrogen atom, phosphorus atom or boron atom also to be joined together via a bridge by a single bond or a bridge selected from B(R 1 ), C(R 1 ) 2 , Si(R 1 ) 2 , C═O, C═NR 1 , C═C(R 1 ) 2 , O, S, S═O, SO 2 , N(R 1 ), P(R 1 ) and P(═O)R 1 ;
R 1 is the same or different at each instance and is H, D, F, Cl, Br, I, CN, NO 2 , N(Ar″) 2 , N(R 2 ) 2 , C(═O)Ar″, C(═O)R 2 , C(═O)OAr″, C(═O)OR 2 , P(═O)(Ar″) 2 , P(Ar″) 2 , B(Ar″) 2 , B(R 2 ) 2 , C(Ar″) 3 , C(R 2 ) 3 , Si(Ar″) 3 , Si(R 2 ) 3 , a straight-chain alkyl, alkoxy or thioalkoxy group having 1 to 40 carbon atoms or a branched or cyclic alkyl, alkoxy or thioalkoxy group having 3 to 40 carbon atoms or an alkenyl group having 2 to 40 carbon atoms, each of which may be substituted by one or more R 2 radicals, where one or more nonadjacent CH 2 groups may be replaced by —R 2 C═CR 2 —, —C≡C—, Si(R 2 ) 2 , C═O, C═S, C═Se, C═NR 2 , —C(═O)O—, —C(═O)NR 2 —, NR 2 , P(═O)(R 2 ), —O—, —S—, SO or SO 2 and where one or more hydrogen atoms may be replaced by D, F, Cl, Br, I, CN or NO 2 , or an aromatic or heteroaromatic ring system which has 5 to 60 aromatic ring atoms, each of which may be substituted by one or more R 2 radicals, or an aryloxy or heteroaryloxy group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 2 radicals, or an aralkyl or heteroaralkyl group which has 5 to 60 aromatic ring atoms and may be substituted by one or more R 2 radicals, or a combination of these systems; at the same time, two or more R 1 radicals together may form a ring system; at the same time, one or more R 1 radicals may form a ring system with a further part of the compound;
Ar″ is the same or different at each instance and is an aromatic or heteroaromatic ring system which has 5 to 30 aromatic ring atoms and may be substituted by one or more R 2 radicals; at the same time, it is possible for two Ar″ radicals bonded to the same carbon atom, silicon atom, nitrogen atom, phosphorus atom or boron atom also to be joined together via a bridge by a single bond or a bridge selected from B(R 2 ), C(R 2 ) 2 , Si(R 2 ) 2 , C═O, C═NR 2 , C═C(R 2 ) 2 , O, S, S═O, SO 2 , N(R 2 ), P(R 2 ) and P(═O)R 2 ;
R 2 is the same or different at each instance and is selected from the group consisting of H, D, F, CN, an aliphatic hydrocarbyl radical having 1 to 20 carbon atoms or an aromatic or heteroaromatic ring system which has 5 to 30 aromatic ring atoms and in which one or more hydrogen atoms may be replaced by D, F, Cl, Br, I or CN and which may be substituted by one or more alkyl groups each having 1 to 4 carbon atoms; at the same time, two or more substituents R 2 together may form a ring system.