Ketopyrroles useful as ligands in organic iridium compositions
View Patent ↗The present invention provides novel ketopyrroles having structure XXIV wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cyclcoaliphatic radical; “a” is an integer from 0 to 3; and X 1 and X 2 are independently at each occurrence a bromine atom, a hydroxy group, or the group OR 10 , and wherein the group R 10 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cyclcoaliphatic radical. Ketopyrroles XXIV are useful ligands for the preparation of Type (1) and Type (2) organic iridium compositions. In one aspect, the present invention provides deuterated analogs of XXIV. Organic iridium compositions are useful in the preparation optoelectronic devices, such as OLED devices and photovoltaic devices exhibiting enhanced performance characteristics.
1. A composition comprising a ketopyrrole having structure XXIV
wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 2 -C 50 aliphatic radical, or a C 3 -C 40 cyclcoaliphatic radical;
“a” is an integer from 0 to 3; and
X 1 and X 2 are independently at each occurrence a bromine atom, a hydroxy group, or the group OR 10 ,
and wherein the group R 10 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cyclcoaliphatic radical.
2. The composition according to claim 1 , wherein the group R 10 is a C 1 -C 50 aliphatic radical.
3. The composition according to claim 2 , wherein the group R 10 is deuterated.
4. The composition according to claim 3 , wherein the group R 10 is at least 50 percent deuterated.
5. The composition according to claim 4 , wherein R 2 is deuterium and “a” is 3.
6. The composition according to claim 1 , wherein X 1 and X 2 are selected from the group consisting of trimethylsilyloxy and t-butyldimethylsilyloxy.
7. The composition according to claim 1 , wherein X 1 and X 2 are identical.
8. The composition according to claim 7 , wherein X 1 and X 2 are bromine atoms.
9. The composition according to claim 7 , wherein X 1 and X 2 are hydroxy groups.
10. The composition according to claim 7 , wherein X 1 and X 2 are methoxy groups.
11. The composition according to claim 7 , wherein X 1 and X 2 are methacryloyloxy groups.
12. A composition comprising a ketopyrrole having structure XXV
wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cyclcoaliphatic radical;
“a” is an integer from 0 to 3; and
X 1 and X 2 are independently at each occurrence a bromine atom, a hydroxy group, or the group OR 10 ,
and wherein the group R 10 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cyclcoaliphatic radical.
13. The composition according to claim 12 , wherein the group R 10 is a C 1 -C 50 aliphatic radical.
14. The composition according to claim 13 , wherein the group R 10 is deuterated.
15. The composition according to claim 14 , wherein the group R 10 is at least 50 percent deuterated.
16. The composition according to claim 12 , wherein R 2 is deuterium and “a” is 3.
17. The composition according to claim 12 , wherein X 1 and X 2 are selected from the group consisting of trimethylsilyloxy and t-butyldimethylsilyloxy.
18. The composition according to claim 12 , wherein X 1 and X 2 are identical.
19. The composition according to claim 18 , wherein X 1 and X 2 are bromine atoms.
20. The composition according to claim 18 , wherein X 1 and X 2 are hydroxy groups.
21. The composition according to claim 18 , wherein X 1 and X 2 are methoxy groups.
22. The composition according to claim 18 wherein X 1 and X 2 are methacryloyloxy groups.
23. A composition comprising (bis(trimethylsilyloxy)-2,4,6-trideuterio benzoyl)-3,4,5-trideuteriopyrrole.