NAPHTHOPYRAN-CONTAINING COMPOUND, POLYMER, MIXTURE, COMPOSITION AND USE THEREOF IN WATER-SOLUBLE PHOTOCHROMIC MATERIALS

1 . A water-soluble photochromic naphthopyran compound having a general structural formula represented by Formula (1):

wherein G1 is selected from the group consisting of an aromatic containing 5 to 20 ring atoms, a heteroaromatic containing 5 to 20 ring atoms, or a non-aromatic ring system containing 5 to 20 ring atoms; G1 has a substituent R 1 and the R 1 is the same or different in multiple occurrences;

wherein G2 is selected from the group consisting of an aromatic containing 5 to 20 ring atoms, a heteroaromatic containing 5 to 20 ring atoms, or a non-aromatic ring system containing 5 to 20 ring atoms; G2 has a substituent R 2 , and the R 2 is the same or different in multiple occurrences;

wherein “*” represent possible bonding locations of Formula (1) with following chemical formula:

wherein X 1 is selected from CR 5 CR 6 , O, S, NR 7 , Se, S(═O) 2 , C═O, S═O, PR 8 ;

wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 are independently selected from the group consisting of hydrogen, deuterium, a halogen atom, water-solubilizing group, —OCH 3 , —NO 2 , —C≡N, —N≡C, a linear alkyl group containing 1 to 20 carbon atoms, a branched alkyl group containing 1 to 20 carbon atoms, and a linear alkenyl group containing 1 to 20 carbon atoms, a branched alkenyl group containing 1 to 20 carbon atoms, an alkane ether group containing 1 to 20 carbon atoms, an aromatic containing 1 to 20 carbon atoms, a heteroaromatic containing 1 to 20 carbon atoms or a non-aromatic ring system containing 1 to 20 carbon atoms; and

wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 independently contain at least one water-solubilizing group selected from —SO 3 H, —COOH, —OH, —NH 2 , —NC n H 2n+1 H + , —N(C n H 2n+1 ) 3 + , —SO 3 Na, —OSO 3 H, —SO 2 NH 2 , —PO 3 H 2 , —PO 3 Na 2 , —SH, —SeH, —CONH 2 , —(OC n H 2n ) m OH, —OC n H 2n SO 3 H, —NH(C n H 2n+1 )SO 3 H, —O-morpholinylethyl, —O-glucoside, —O-crown ether, —O-cyclodextrin.

2 . The photochromic naphthopyran compound according to claim 1 , wherein G1 and G2 in Formula (1) is selected from the following formulae:

wherein # represents the bonding location in Formula (1);

wherein Z 1 -Z 9 are independently or jointly selected from the group consisting of carbon, nitrogen, oxygen, silicon, boron, sulfur or phosphorus atom;

wherein R 9 are independently or jointly selected from the group consisting of hydrogen, deuterium, a halogen atom, —OCH 3 , —NO 2 ,—C≡N, —N≡C, —NPh 2 , N-carbazole, dibenzofuran, dibenzothiophene, —SO 3 H, —OH, —NC n H 2n+1 H + , —N(C n H 2n+1 ) 3 + , —SO 3 Na, —OSO 3 H , —SO 2 NH 2 , —PO 3 H 2 , —PO 3 Na 2 , —SH, —SeH, —CONH 2 , —(OC n H 2n+1 ) m OH, —OC n H 2n SO 3 H, —NH(C n H 2n+1 )SO 3 H, —O-morpholinylethyl, —O-glucoside, —O-crown ether, —O-cyclodextrin or a linear alkyl group containing 1 to 20 carbon atoms, a branched alkyl group containing 1 to 20 carbon atoms, and a linear alkenyl group containing 1 to 20 carbon atoms, a branched alkenyl group containing 1 to 20 carbon atoms, an alkane ether group containing 1 to 20 carbon atoms, an aromatic containing 1 to 20 carbon atoms, a heteroaromatic containing 1 to 20 carbon atoms or a non-aromatic ring system containing 1 to 20 carbon atoms.

3 . The photochromic naphthopyran compound according to claim 1 , containing a structure represented by one of general formulas (A-1) to (A-15):

wherein R 10 , R 11 , R 12 , R 13 are independently or jointly selected from the group consisting of hydrogen, deuterium, a halogen atom, —OCH 3 , —NO 2 , —C≡N, —N≡C, —NPh 2 , N-carbazole, dibenzofuran, dibenzothiophene, —SO 3 H, —OH, —NC n H 2n+1 H + , —N(C n H 2n+1 ) 3 + , —SO 3 Na, —OSO 3 H , —SO 2 NH 2 , —PO 3 H 2 , —PO 3 Na 2 , —SH, —SeH, —CONH 2 , —(OC n H 2n ) m OH, —OC n H 2n SO 3 H, —NH(C n H 2n+1 )SO 3 H, —O-morpholinylethyl, —O-glucoside, —O-crown ether, —O-cyclodextrin or a linear alkyl group containing 1 to 20 carbon atoms, a branched alkyl group containing 1 to 20 carbon atoms, and a linear alkenyl group containing 1 to 20 carbon atoms, a branched alkenyl group containing 1 to 20 carbon atoms, an alkane ether group containing 1 to 20 carbon atoms, an aromatic containing 1 to 20 carbon atoms, a heteroaromatic containing 1 to 20 carbon atoms or a non-aromatic ring system containing 1 to 20 carbon atoms;

wherein X 2 is selected from CR 5 CR 6 , O, S, NR 7 , Se, S(═O) 2 , C═O, S═O, PR 8 .

4 . The photochromic naphthopyran compound according to claim 3 , at least one R 10 or R 11 or R 12 or R 13 is selected from —SO 3 H, —OH, —NC n H 2n+1 H + , —N(C n H 2n+1 ) 3 + , —SO 3 Na, —OSO 3 H, —SO 2 NH 2 , —PO 3 H 2 , —PO 3 Na 2 , —SH, —SeH, —CONH 2 , —(OC n H 2n ) m OH, —OC n H 2n SO 3 H, —NH(C n H 2n+1 )SO 3 H, —O-morpholinylethyl, —O-glucoside, —O-crown ether, —O-cyclodextrin.

5 . The photochromic naphthopyran compound according to claim 1 , wherein the naphthopyran compound is selected from the following chemical structures:

6 . The photochromic naphthopyran compound according to claim 1 , wherein the conformation of the molecule can be changed to ring-open form upon UV or visible light irradiation, and can be thermodynamically changed backward to the ring-close form:

7 . The photochromic naphthopyran compound according to claim 1 , wherein the water solubility of the compound is greater than or equal to 10 mg L −1 .

8 . A photochromic mixture comprising at least one photochromic naphthopyran compound according to claim 1 , wherein the weight percent of the photochromic naphthopyran compound in the mixture is greater than 0.01%.

9 . The photochromic mixture according to claim 8 , comprising the water solubility greater than or equal to 10 mg L −1 .

10 . The photochromic mixture according to claim 8 , wherein the mixture displays photochromic property upon UV or visible light irradiation, and wherein the photochromism is thermodynamically reversible.

11 . The photochromic naphthopyran compound according to claim 1 , wherein an absorption peak in UV/v is absorption spectrum ranges from 100 nm to 1500 nm.