5results about "Diarylmethane dyes" patented technology

The present invention relates to an indeno-naphthopyran compound represented by the following formula (I). In reference to formula (I), m, n, and R4-R7 are as described in the specification. Further referring to formula (I), R1 is an aryl group substituted by at least one perfluoroalkyl group, or a heteroaryl group substituted by at least one perfluoroalkyl group; r2 is an alkoxy group; and R3 is an alkoxy group, an amino group, or a substituted or unsubstituted nitrogen-containing heterocyclic ring, with the proviso that when R3 is not an alkoxy group, R3 is covalently bonded to position-7 via a nitrogen atom. The present invention also relates to a photochromic composition and a photochromic article comprising the indeno-naphthopyran compound represented by formula (I). (I)

A latent additive represented by general formula (1): wherein A is a 5- or 6-membered aromatic or heterocyclic ring; R1 and R2 are each hydrogen, halogen, cyano, hydroxyl, nitro, carboxyl, optionally substituted C1-C40 alkyl, C6-C20 aryl, C7-C20 arylalkyl, or C2-C20 heterocyclic ring-containing group; and R4 is C1-C20 alkyl, C2-C20 alkenyl, C6-C20 aryl, C7-C20 arylalkyl, C2-C20 heterocyclic ring-containing group, or trialkylsilyl.

The present invention relates to indenonaphthopyran compounds represented by the following Formula (I). With reference to Formula (I), m, n, and R4-R7 are as described in the specification. With further reference to Formula (I), R1 is aryl substituted with at least one perfluoroalkyl group, or heteroaryl substituted with at least one perfluoroalkyl group; R2 is alkoxy; and R3 is alkoxy, amino, or substituted or unsubstituted nitrogen-containing heterocycle, provided that when R3 is other than alkoxy, R3 is covalently bonded to position-7 by a nitrogen atom. The present invention also relates to photochromic compositions and photochromic articles that include indenonaphthopyran compounds represented by Formula (I).

Photochromic molecules denominated FC-YNAPHT or FC-RNAPHT usable as portions of a cosmetic ingredient, coloured cosmetic ingredients for cosmetic products changing colour when irradiated by ultraviolet light (UV, preferably UV-A). (Fomula AA & Formula BB) (AA) (BB) Method for the synthesis of said photochromic molecules. Monosubstituted and disubstituted transesterification product between FC-YNAPHT or FC-RNAPHT and a polymer or cosmetic oil having the aim to increase the molecular weight of the photochromic molecule. (Fomula CC & Formula DD) (CC) (DD) Method for the transesterification. Cosmetic compositions for make-up containing said photochromic transesterification products, capable of changing colour both per se and when applied to the skin when they are exposed to UV radiation.

The present invention relates to the following formula (I) This relates to the indenonaphthopyrane compound represented by JPEG2026517214000025.jpg60160. With respect to formula (I), m, n and R 4 ~R 7 This is as described herein. Furthermore, with respect to formula (I), R 1 is an aryl or heteroaryl substituted with at least one perfluoroalkyl group, and R 2 is an alkoxy, and R 3 R is an alkoxy, amino, or substituted or unsubstituted nitrogen-containing heterocycle, 3 If R is not an alkoxy, 3 This is conditional on the nitrogen atom being covalently bonded at position 7. The present invention also relates to photochromic compositions and photochromic articles comprising an indenonaphthopyrane compound represented by formula (I).