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Title: US5658502: Photochromic articles
[ Derwent Title ]
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Country: US United States of America

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17 pages

 
Inventor: Hughes, Frank J.; Edina, MN

Assignee: Vision-Ease Lens, Inc., Brooklyn Center, MN
other patents from VISION-EASE LENS, INC. (730114) (approx. 29)
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Published / Filed: 1997-08-19 / 1995-10-30

Application Number: US1995000550161

IPC Code: Advanced: G02B 5/23;
Core: G02B 5/22;
IPC-7: G02B 5/23;

ECLA Code: G02B5/23;

U.S. Class: Current: 252/586;
Original: 252/586;

Field of Search: 252/586

Priority Number:
1995-10-30  US1995000550161

Abstract: A photochromic article comprising a host material and a photochromic amount of a photochromic compound or a structural isomer of the photochromic compound, the photochromic compound represented by the formula: [Figure] wherein R1, R2, R4, R5, R6, R8, A, B, C, and D are each selected from the group consisting essentially of hydrogen, a stable organic radical, a heterocyclic group, halogen, a nitrogen-substituted radical, and a nitrogen-substituted ring radical.

Attorney, Agent or Firm: Kinney & Lange, P.A. ;

Primary / Asst. Examiners: Kelly, C. H.;

Maintenance Status: E3 Expired  Check current status
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Family: None

First Claim:
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What is claimed is:     1. A photochromic article comprising a host material and a photochromic amount of a photochromic compound or a structural isomer of the photochromic compound, the photochromic compound represented by the formula: [Figure] wherein R1, R2, R4, R5, R6, and R8, are each selected from the group consisting essentially of hydrogen, alkyl, alkoxy, phenyl, naphthyl, cycloalkyl, furyl, alkoyl, alkoyloxy, aroyl, aroyloxy, halogen, amino, nitro, morpholino, piperidino, and piperazino; and wherein A, B, C, and D are each selected from the group consisting essentially of alkyl, alkoxy, phenyl, naphthyl, cycloalkyl, furyl, alkoyl, alkoyloxy, aroyl, aroyloxy, hydrogen, an unsubstituted monovalent aromatic radical, a substituted monovalent aromatic radical, halogen, amino, nitro, morpholino, piperidino, and piperazino.

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Forward References: Show 20 U.S. patent(s) that reference this one

       
U.S. References: Go to Result Set: All U.S. references   |  Forward references (20)   |   Backward references (14)   |   Citation Link

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Patent  Pub.Date  Inventor Assignee   Title
Get PDF - 4pp US3567605  1971-03 Becker   PHOTOCHEMICAL PROCESS
Get PDF - 21pp US4685783  1987-08 Heller et al.  The Plessey Company P.L.C. Polychromic tetracyclo-spiro-adamatylidene derivatives, and polychromic lens incorporating said compounds
Get PDF - 22pp US4818096  1989-04 Heller et al.  The Plessey Company plc Photoreactive lenses with adamantane spiro compounds
Get PDF - 27pp US4826977  1989-05 Heller et al.  The Plessey Company plc Photochromic spiropyran compounds
Get PDF - 53pp US4882438  1989-11 Tanaka et al.  Tokuyama Soda Kabushiki Kaisha Photochromatic compounds
Get PDF - 15pp US4931221  1990-06 Heller  PPG Industries, Inc. Photochromic spiropyran compounds
Get PDF - 7pp US4990287  1991-02 Bennion et al.  The Plessey Company PLC Optical devices utilizing photochromic compounds
Get PDF - 11pp US4994208  1991-02 McBain et al.  PPG Industries, Inc. Photochromic polymeric article
Get PDF - 5pp US5055576  1991-10 Castaldi et al.  Enichem Synthesis, S.p.A. Photochromatic and thermochromatic spiro-oxazepin-oxazine compounds and the process for their preparation
Get PDF - 48pp US5106998  1992-04 Tanaka et al.  Tokuyama Soda Kabushiki Kaisha Photochromic compound, composition and use thereof
Get PDF - 16pp US5238981  1993-08 Knowles  Transitions Optical, Inc. Photochromic naphthopyrans
Get PDF - 11pp US5242624  1993-09 Malatesta et al.  Enichem Synthesis S.p.A. Stabilizing mixture for compounds having a photochromatic activity
Get PDF - 18pp US5244602  1993-09 Van Gemert  PPG Industries, Inc. Photochromic naphthopyrans
Get PDF - 9pp US5274132  1993-12 Van Gemert  Transitions Optical, Inc. Photochromic naphthopyran compounds
       
Foreign References: None

Other References:
  • Besace, Yvon, Israel Marszak, and Jocelyne Maisse; Synthesis and Applications of Monoaryl Ethers of Butynediol; Bull. Soc. Chim. Fr. ; No. 6, pp. 2275-2279; (1971). Cited by 2 patents
  • Dean, Francis M., Steven N. France and Ulku Oyman; Cation Radicals in the Bromination of Benzodipyran Derivatives; Tetrahedron; vol. 44, No. 15; pp. 4857-4862; (1988). (6 pages) Cited by 2 patents
  • Liska, Kenneth J.; Preparation and Antitumor Properties of Analogs of Acronycine; Journal of Medicinal Chemistry, vol. 15, No. 11; pp. 1177-1179; (1972). Cited by 13 patents
  • Sadykov, T., K.B. Erzhanov, M.B. Basymbekov, and S.D. Praliev; Hydration of o-, m-, and p-bis (Propynyloxy) Benzenes and Their Glycols; Ivz. Akad. Nauk Kaz. SSR, Ser. Khim; No. 1; pp. 63-67; (1988).
  • Venugopalan, Bindumadhavan and Kalpattu Kuppuswamy Balasubramanian; Studies on Claisen Rearrangement of Bis-Propargyl Ethers--Synthesis of Naphthodipyrans, Naphthodifurans and Naphthofuropyrans; Heterocycles; vol. 23, No. 1; pp. 81-92; (1985). (12 pages) Cited by 2 patents


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