Photochromic spiro(indoline)naphthoxazines

Organic compounds -- part of the class 532-570 series – Organic compounds – Chalcogen in the nitrogen containing substituent

Reexamination Certificate

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C252S586000

Reexamination Certificate

active

06891038

ABSTRACT:
A photochromic compound for incorporation into plastic articles, particularly into a plastic lens, is selected from a spiro(indoline)naphtho(2,1-b)(1,4)oxazine and a spiro(indoline)naphtho(1,2-b)(1,4)oxazine containing a group selected from: (a) —CH2—CnF2n+1 at the nitrogen atom in the 1-position on the indoline part of the molecule, wherein n is an integer of 1 to 6; (b) —COOR at the 3-position on the indoline part of the molecule, wherein R is (i) C1-C6 alkyl optionally substituted by fluoro, C1-C4 alkoxy or fluoroalkoxy, C1-C4 alkylcarbonyloxy, C2-C4 alkenylcarbonyloxy, C3-C6 cycloalkyl or aryl; (ii) C2-C6 alkenyl with a terminal double bond; (iii) C3-C6 cycloalkyl optionally substituted by fluoro; or (iv) aryl; (c) an —OCF3 group on the benzene ring of the indoline part of the molecule; (d) an aryl(dialkyl)methyl group of the formula —C(aryl)(CnH2n+1)(CmH2m+1), wherein n and m are integers from 1 to 5, linked to one of the benzene rings of the naphthoxazine part of the molecule; and (e) any combination of (a), (b), (c) and/or (d).

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Patent Abstract of Japan,Photochromic Material,Suga Atsuo, application No. 02075535, application date Mar. 27, 1990; publication No. 03275789, publication date 03275789.
Crano et al., “Spiroxazines and their use in photochromic lenses”,Applied Photochromic Polymer Systems,(C.B. McArdle, Ed) Blackie & Sons, Glasgow, London, (1992), pp. 31-76.

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