BENZOXAZOLE AND BENZOTHIAZOLE COMPOUNDS AND METHODS THEREFOR
A compound of Formula (I): wherein R 1 is selected from the group consisting of an aliphatic functionality having 2 to 12 carbons, an aromatic functionality having 3 to 20 carbons, and a cycloaliphatic functionality having 3 to 20 carbons; with the proviso that R 1 is not —C 6 H 5 or —NH—C 10 H 7 ; R 2 and R 3 are independently selected from the group consisting of a hydroxyl group, a halogen atom, an aliphatic functionality having 2 to 12 carbons, an aromatic functionality having 3 to 20 carbons, and a cycloaliphatic functionality having 3 to 20 carbons; X is either an oxygen atom or a sulfur atom; “n” has a value of 0 to 4; and “m” has a value of 0 to 3.
1 . A compound of Formula (I):
wherein R 1 is selected from the group consisting of an aliphatic functionality having 2 to 12 carbons, an aromatic functionality having 3 to 20 carbons, and a cycloaliphatic functionality having 3 to 20 carbons; with the proviso that R 1 is not —C 6 H 5 or —NH—C 10 H 7 ; R 2 and R 3 are independently selected from the group consisting of a hydroxyl group, a halogen atom, an aliphatic functionality having 2 to 12 carbons, an aromatic functionality having 3 to 20 carbons, and a cycloaliphatic functionality having 3 to 20 carbons; X is either an oxygen atom or a sulfur atom; “n” has a value of 0 to 4; and “m” has a value of 0 to 3.
2 . The compound of claim 1 , wherein R 1 is selected from the group consisting of an aliphatic functionality having 2 to 6 carbons, an aromatic functionality having 6 to 10 carbons, and a cycloaliphatic functionality having 4 to 8 carbons; with the proviso that R 1 is not —C 6 H 5 or a —NH—C 10 H 7 ; R 2 and R 3 are independently selected from the group consisting of a hydroxyl group, a halogen atom, an aliphatic functionality having 2 to 6 carbons, an aromatic functionality having 6 to 10 carbons, and a cycloaliphatic functionality having 4 to 8 carbons; X is either an oxygen atom or a sulfur atom; “n” has a value of 0 to 4; and “m” has a value of 0 to 3.
3 . The compound of claim 1 , wherein R 1 is selected from the group consisting of an aliphatic functionality having 2 to 4 carbons, an aromatic functionality having 6 to 10 carbons, and a cycloaliphatic functionality having 6 to 7 carbons; with the proviso that R 1 is not —C 6 H 5 or a —NH—C 10 H 7 ; R 2 and R 3 are independently selected from the group consisting of a hydroxyl group, a halogen atom, an aliphatic functionality having 2 to 6 carbons, an aromatic functionality having 6 to 10 carbons, and a cycloaliphatic functionality having 6 to 7 carbons; X is an oxygen atom; “n” has a value of 0 to 4; and “m” has a value of 0 to 3.
4 . The compound of claim 1 , wherein R 1 is selected from the group consisting of an aliphatic functionality having 2 to 4 carbons, an aromatic functionality having 6 to 10 carbons, and a cycloaliphatic functionality having 6 to 7 carbons; with the proviso that R 1 is not —C 6 H 5 or a —NH—C 10 H 7 ; R 2 and R are independently selected from the group consisting of a hydroxyl group, a halogen atom, an aliphatic functionality having 2 to 4 carbons, an aromatic functionality having 6 to 10 carbons, and a cycloaliphatic functionality having 6 to 8 carbons; X is a sulfur atom; “n” has a value of 0 to 4; and “m” has a value of 0 to 3.
5 . The compound of claim 1 , having a Formula (II):
6 . The compound of claim 1 , having a Formula (III):
7 . The compound of claim 1 , having a Formula (IV):
8 . The compound of claim 1 , having a Formula (V):
9 . The compound of claim 1 , having a Stokes shift of greater than or equal to about 150 nanometers.
10 . The compound of claim 1 , having a T d of greater than or equal to about 300° C.