Luminescent materials
View Patent ↗The invention provides photoluminescent compounds, reactive intermediates used to synthesize photoluminescent compounds, and methods of synthesizing and using photoluminescent compounds, among others. The compounds comprise phenanthrene and dipyridylamine moieties. The compounds are colored and fluoresce upon excitation. Methods are included for using the compounds to detect metal ions by spectral changes of wavelength shift or a change in fluorescence intensity. Compositions in polymers and solvents are provided for use as a film, paint, reflective surfaces, and electroluminescent devices are provided.
1. A luminescent compound of formula I,
A is hydrogen or -L A -R 1 ;
B is hydrogen or -L B -R 1 ;
C is hydrogen or -L C -R 1 ;
wherein R 1 is
E is a hydrogen, halogen, -G, —O-G, or NG 2 ;
G is an aryl, substituted aryl, heteroaryl, substituted heteroaryl, or alkyl;
wherein -L A -, -L B -, and -L C - are independently a bond or ethynyl;
at least one of A, B and C is -L A -R 1 , -L B -R 1 , or -L C -R 1 ;
if B is -L B -R 1 and -L B - is a bond, then E is hydrogen, G, or —O-G;
and salts thereof.
2. The compound of claim 1 , wherein G is phenyl, substituted phenyl, biphenyl, substituted biphenyl, pyridyl, substituted pyridyl, naphthyl, substituted naphthyl, quinolyl, substituted quinolyl, isoquinolyl, substituted isoquinolyl, fluorenyl, substituted fluorenyl, terphenyl, substituted terphenyl, methyl, ethyl, propyl, isopropyl, or t-butyl.
3. The compound of claim 1 , wherein G is phenyl, biphenyl, pyridyl, naphthyl, quinolyl, isoquinolyl, fluorenyl or terphenyl.
4. The compound of claim 1 , wherein G is phenyl.
5. The compound of claim 1 , wherein G is 2-pyridyl.
6. The compound of claim 1 , wherein G is methyl, ethyl, propyl, isopropyl, or t-butyl.
7. The compound of claim 1 , wherein A is -L A -R 1 and -L A - is a bond; B is hydrogen; and C is hydrogen.
8. The compound of claim 1 , wherein B is -L B -R 1 and -L B - is a bond; A is hydrogen; and C is hydrogen.
9. The compound of claim 1 , wherein A is -L A -R 1 and -L A - is ethynyl; B is hydrogen; and C is hydrogen.
10. The compound of claim 1 , wherein substitution on G is one or more of alkyl, aryl, alkoxy, alkylamino, halogen, aryloxy, arylamino, alkylsilyl, or arylsilyl.
11. The compound of claim 1 , wherein substitution on G is t-butylphenyl, dimethylaminophenyl, methoxyphenyl, or cyanophenyl.
12. The compound of claim 1 , wherein G is a para substituted phenyl.
13. The compound of claim 1 , wherein G is p-t-butylphenyl, p-dimethylaminophenyl, p-methoxyphenyl, or p-cyanophenyl.
14. The compound of claim 1 , wherein E is hydrogen.
15. The compound of claim 1 , wherein E is G.
16. The compound of claim 1 , wherein E is —O-G.
17. The compound of claim 1 , wherein E is —N(G) 2 .
18. The compound of claim 1 , wherein A is -L A -R 1 , B is hydrogen, C is hydrogen.
19. The compound of claim 1 , wherein A is -L A -R 1 , B is hydrogen, and C is -L C -R 1 and -L A - and -L C - are bonds.
20. The compound of claim 1 , wherein A is -L A -R 1 , B is hydrogen, C is -L C -R 1 , and -L A - and -L C - are ethynyl.
21. The compound of claim 1 , wherein the compound is a salt.
22. The compound of claim 1 , wherein E is halogen.
23. The compound of claim 1 , wherein E is bromo.
24. The compound of claim 1 , wherein the compound is:
6-(anthracen-9-yl)-N-(pyridin-2-yl)pyridin-2-amine;
4-(10-((6-(pyridin-2-ylamino)pyridin-2-yl)ethynyl)anthracen-9-yl)benzonitrile;
N-(anthracen-9-yl)-N-(pyridin-2-yl)pyridin-2-amine;
6-(anthracen-9-ylethynyl)-N-(pyridin-2-yl)pyridin-2-amine;
6-((10-(4-methoxyphenyl)anthracen-9-yl)ethynyl)-N-(pyridin-2-yl)pyridin-2-amine;
6-((10-(4-(dimethylamino)phenyl)anthracen-9-yl)ethynyl)-N-(pyridin-2-yl)pyridin-2-amine;
bis(6-(anthracen-9-ylethynyl)pyridin-2-yl)amine;
6-((10-(bis(4-tert-butylphenyl)amino)anthracen-9-yl)ethynyl)-N-(pyridin-2-yl)pyridin-2-amine;
6-((10-(bis(4-methoxyphenyl)amino)anthracen-9-yl)ethynyl)-N-(pyridin-2-yl)pyridin-2-amine; and
6-((10-bromoanthracen-9-yl)ethynyl)-N-(pyridin-2-yl)pyridin-2-amine;
or salts thereof.