Phenazine-Based Molecular and Polymeric Semiconductors
The present invention relates to new semiconducting compounds having at least one optionally substituted phenazine moiety. The compounds disclosed herein can exhibit high carrier mobility and/or efficient light absorption/emission characteristics, and can possess certain processing advantages such as solution-processability and/or good stability at ambient conditions.
1 . A semiconducting compound comprising one or more phenazine moieties represented by formula (I):
wherein:
R 1 , at each occurrence, independently is selected from the group consisting of a halogen, —CN, NO 2 , R 2 , -L-R 3 , OH, OR 2 , OR 3 , NH 2 , NHR 2 , N(R 2 ) 2 , NR 2 R 3 , N(R 3 ) 2 , SH, SR 2 , SR 3 , S(O) 2 OH, —S(O) 2 OR 2 , —S(O) 2 OR 3 , C(O)H, C(O)R 2 , C(O)R 3 , C(O)OH, C(O)OR 2 , C(O)OR 3 , C(O)NH 2 , C(O)NHR 2 , C(O)N(R 2 ) 2 , C(O)NR 2 R 3 , C(O)N(R 3 ) 2 , SiH 3 , SiH(R 2 ) 2 , SiH 2 (R 2 ), and Si(R 2 ) 3 , wherein L is selected from the group consisting of a divalent C 1-40 alkyl group, a divalent C 2-40 alkenyl group, a divalent C 1-40 haloalkyl group, and a covalent bond; R 2 is selected from the group consisting of a C 1-40 alkyl group, a C 2-40 alkenyl group, a C 2-40 alkynyl group, and a C 1-40 haloalkyl group; and R 3 is selected from the group consisting of a C 3-10 cycloalkyl group, a C 6-14 aryl group, a C 6-14 haloaryl group, a 3-12 membered cycloheteroalkyl group, and a 5-14 membered heteroaryl group, each of which optionally is substituted with 1-5 substituents selected from the group consisting of a halogen, —CN, NO 2 , R 2 , OR 2 , and SR 2 , and
q is 0 or an integer selected from the group consisting of 1, 2, 3, 4, 5, and 6; and
one or more linear and/or cyclic conjugated moieties other than the phenazine moieties represented by formula (I).
2 . The compound of claim 1 , wherein q is an integer selected from the group consisting of 1, 2, 3, 4, 5, and 6.
3 . The compound of claim 2 , wherein R 1 , at each occurrence, independently is selected from the group consisting of F, Cl, —CN, —NO 2 , a phenyl group, R 2 , OR 2 , and SR 2 , wherein R 2 is selected from the group consisting of a linear or branched C 1-40 alkyl group, a linear or branched C 2-40 alkenyl group, and a linear or branched C 1-40 haloalkyl group.
4 . The compound of claim 3 , wherein each R 1 is F.
5 . The compound of claim 1 , wherein the compound is a polymer having a first repeating unit M 1 comprising one or more divalent units represented by formula (I) and wherein said polymer has a degree of polymerization (n) ranging from 3 to 1,000.
6 . The compound of claim 5 , wherein M 1 is selected from the group consisting of:
wherein:
pi-2 is an optionally substituted conjugated polycyclic moiety selected from the group consisting of an optionally substituted C 8-26 aryl group and an optionally substituted 8-26 membered heteroaryl group;
Ar, at each occurrence, independently is an optionally substituted monocyclic moiety selected from the group consisting of an optionally substituted 5-membered aryl group, an optionally substituted 6-membered aryl group, an optionally substituted 5-membered heteroaryl group, and an optionally substituted 6-membered heteroaryl group;
Z is a conjugated noncyclic linker;
m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;
m″ is 1, 2, 3, 4, 5 or 6; and
p and p′ independently are 0 and 1, provided that at least one of p and p′ is 1.
7 . The compound of claim 6 , wherein pi-2 is selected from the group consisting of:
wherein:
R a is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, and —C(O)OR;
R b is selected from the group consisting of H, R, and -L′-R f ;
R c is H or R;
R d is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, —C(O)OR, and -L′-R f ;
R e is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, —C(O)OR, and R f ;
R f is a C 6-20 aryl group or a 5-20-membered heteroaryl group, each optionally substituted with 1-8 groups independently selected from the group consisting of F, Cl, —CN, R, —OR, and SR;
L′ is selected from the group consisting of —O—, —S—, —C(O)—, —OC(O)—, —C(O)O—, and a covalent bond; and
R is selected from the group consisting of a C 1-40 alkyl group, a C 1-40 haloalkyl group, a C 2-40 alkenyl group, and a C 2-40 alkynyl group.
8 . The compound of claim 6 , wherein Ar in (Ar) m , (Ar) m′ , and (Ar) m″ is represented by:
wherein each W independently is selected from the group consisting of N, CH, and CR 4 , wherein R 4 is selected from the group consisting of F, Cl, —CN, R 2 , OR 2 , SR 2 , C(O)R 2 , OC(O)R 2 , and C(O)OR 2 , and wherein R 2 is selected from the group consisting of a C 1-40 alkyl group, a C 2-40 alkenyl group, a C 2-40 alkynyl group, and a C 1-40 haloalkyl group.
9 . The compound of claim 8 , wherein (Ar) m , (Ar) m′ , and (Ar) m″ independently are selected from the group consisting of:
10 . The compound of claim 6 , wherein Z is selected from the group consisting of:
wherein R 4 is selected from the group consisting of F, Cl, —CN, R 2 , OR 2 , SR 2 , C(O)R 2 , OC(O)R 2 , and C(O)OR 2 , and wherein R 2 is selected from the group consisting of a C 1-40 alkyl group, a C 2-40 alkenyl group, a C 2-40 alkynyl group, and a C 1-40 haloalkyl group.
11 . The compound of claim 5 , further comprising one or more repeating units other than M 1 , the one or more other repeating units (M 2 ) being selected from the group consisting of:
wherein:
pi-2 is an optionally substituted conjugated polycyclic moiety selected from the group consisting of an optionally substituted C 8-26 aryl group and an optionally substituted 8-26 membered heteroaryl group;
Ar, at each occurrence, independently is an optionally substituted monocyclic moiety selected from the group consisting of an optionally substituted 5-membered aryl group, an optionally substituted 6-membered aryl group, an optionally substituted 5-membered heteroaryl group, and an optionally substituted 6-membered heteroaryl group;
Z is a conjugated noncyclic linker;
m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;
m″ is 1, 2, 3, 4, 5 or 6; and
p and p′ independently are 0 and 1, provided that at least one of p and p′ is 1.
12 . The compound of claim 11 , wherein:
Z is selected from the group consisting of:
(Ar) m , (Ar) m′ , and (Ar) m″ independently are selected from the group consisting of:
wherein R 4 is selected from the group consisting of F, Cl, —CN, R 2 , OR 2 , SR 2 , C(O)R 2 , OC(O)R 2 , and C(O)OR 2 , and wherein R 2 is selected from the group consisting of a C 1-40 alkyl group, a C 2-40 alkenyl group, a C 2-40 alkynyl group, and a C 1-40 haloalkyl group; and
pi-2 is selected from the group consisting of:
wherein:
R a is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, and —C(O)OR;
R b is selected from the group consisting of H, R, and -L′-R f ;
R c is H or R;
R d is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, —C(O)OR, and -L′-R f ; and
R e is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, —C(O)OR, and R f ; wherein
R f is a C 6-20 aryl group or a 5-20-membered heteroaryl group, each optionally substituted with 1-8 groups independently selected from the group consisting of F, Cl, —CN, R, —OR, and —SR;
L′ is selected from the group consisting of —O—, —S—, —C(O)—, —OC(O)—, —C(O)O—, and a covalent bond; and R is selected from the group consisting of a C 1-40 alkyl group, a C 1-40 haloalkyl group, a C 2-40 alkenyl group, and a C 2-40 alkynyl group; and
R is selected from the group consisting of a C 1-40 alkyl group, a C 1-40 haloalkyl group, a C 2-40 alkenyl group, and a C 2-40 alkynyl group.
13 . The compound of claim 12 , wherein each divalent phenazine moiety
is more specifically
wherein R 1a and R 1b are identical or different, independently being selected from the group consisting of a halogen, —CN, NO 2 , R 2 , -L-R 3 , OH, OR 2 , OR 3 , NH 2 , NHR 2 , N(R 2 ) 2 , NHR 3 , NR 2 R 3 , N(R 3 ) 2 , SH, SR 2 , SR 3 , S(O) 2 OH, —S(O) 2 OR 2 , —S(O) 2 OR 3 , C(O)H, C(O)R 2 , C(O)R 3 , C(O)OH, C(O)OR 2 , C(O)OR 3 , C(O)NH 2 , C(O)NHR 2 , C(O)N(R 2 ) 2 , C(O)NHR 3 , C(O)NR 2 R 3 , C(O)N(R 3 ) 2 , SiH 3 , SiH(R 2 ) 2 , SiH 2 (R 2 ), and Si(R 2 ) 3 , wherein L is selected from the group consisting of a divalent C 1-40 alkyl group, a divalent C 2-40 alkenyl group, a divalent C 1-40 haloalkyl group, and a covalent bond; R 2 is selected from the group consisting of a C 1-40 alkyl group, a C 2-40 alkenyl group, a C 2-40 alkynyl group, and a C 1-40 haloalkyl group; and R 3 is selected from the group consisting of a C 3-10 cycloalkyl group, a C 6-14 aryl group, a C 6-14 haloaryl group, a 3-12 membered cycloheteroalkyl group, and a 5-14 membered heteroaryl group, each of which optionally is substituted with 1-5 substituents selected from the group consisting of a halogen, —CN, NO 2 , R 2 , OR 2 , and SR 2 ; and
q′, at each occurrence, independently, is 0 or an integer selected from the group consisting of 1, 2, and 3, provided that at least one of q′ is not 0.
14 . The compound of claim 13 , wherein
is selected from the group consisting of:
15 . The compound of claim 11 , wherein M 1 is selected from the group consisting of:
wherein R 4 , at each occurrence, independently is selected from the group consisting of R 2 , OR 2 , and SR 2 , where R 2 is a linear or branched C 1-40 alkyl or haloalkyl group; and
M 2 is selected from the group consisting of:
wherein (Ar), and (Ar) m′ are selected from the group consisting of:
16 . The compound of claim 15 , wherein the compound is a copolymer having a formula selected from the group consisting of:
wherein M 1A and M 1B represent different repeating units M 1 , and M 2A and M 2B represent different repeating units M 2 , x and y are real numbers representing molar ratios, and n is the degree of polymerization.
17 . The compound of claim 1 , wherein the compound is a small molecule represented by a formula selected from the group consisting of:
wherein:
Q 1 and Q 2 independently are selected from the group consisting of H, R 2 , and C(O)R 2 , wherein R 2 is a C 1-40 alkyl or haloalkyl group;
pi-2 is an optionally substituted conjugated polycyclic moiety selected from the group consisting of an optionally substituted C 8-26 aryl group and an optionally substituted 8-26 membered heteroaryl group;
Ar, at each occurrence, independently is an optionally substituted monocyclic moiety selected from the group consisting of an optionally substituted 5-membered aryl group, an optionally substituted 6-membered aryl group, an optionally substituted 5-membered heteroaryl group, and an optionally substituted 6-membered heteroaryl group;
Z is a conjugated noncyclic linker;
m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;
m″ is 1, 2, 3, 4, 5 or 6; and
p and p′ independently are 0 and 1, provided that at least one of p and p′ is 1.
18 . The compound of claim 17 , wherein the compound is represented by a formula selected from the group consisting of:
19 . The compound of claim 17 selected from the group consisting of:
20 . An electronic, optical or optoelectronic device comprising a semiconductor component, the semiconductor component comprising a compound of claim 1 , wherein the electronic, optical or optoelectronic device optionally is selected from (a) an organic photovoltaic device comprising an anode, a cathode, optionally one or more anode interlayers, optionally one or more cathode interlayers, and in between the anode and the cathode a semiconductor component comprising a blend material, the blend material comprising an electron-acceptor compound and an electron-donor compound, wherein either the electron-acceptor compound or the electron-donor compound is a compound of claim 1 ; and (b) an organic thin film transistor comprising a substrate, a thin film semiconductor, a dielectric layer, a gate electrode, and source and drain electrodes, wherein the thin film semiconductor comprises a compound of claim 1 .