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    • 1. 发明授权
    • Indeno-fused photochromic naphthopyrans
    • 印度融合的光致变色萘并吡喃
    • US06296785B1
    • 2001-10-02
    • US09656510
    • 2000-09-06
    • Clara M. NelsonAnu ChopraOlga G. PetrovskaiaDavid B. KnowlesBarry Van GemertAnil Kumar
    • Clara M. NelsonAnu ChopraOlga G. PetrovskaiaDavid B. KnowlesBarry Van GemertAnil Kumar
    • C07D31178
    • C07D311/94C07D311/96G02B5/23
    • Described are novel photochromic indeno-fused naphthopyran compounds, examples of which include naphthopyran compounds having a substituted or unsubstituted indeno group, the 2,1 positions of which are fused to the naphtho portion of the naphthopyran as shown below. Also present on the naphthopyran are moderate to strong electron donor substituents at the number 6- and 7-positions and optionally at the 8-position of the pyran ring or a cyclic group fused to the h side of the naphtho portion and weak to moderate electron donor substiuents at the 3-position of the pyran ring. Certain substituents may also be present at the number 5, 8, 9, 10, 11, 12, or 13 carbon atoms of the compounds. These compounds have a rating of at least 80 in the Relative &Dgr;OD at Saturation Test and may be represented by the following graphic formula: Also described are polymeric organic host materials that contain or that are coated with such compounds. Optically clear articles such as ophthalmic lenses or other plastic transparencies that incorporate the novel naphthopyran compounds or combinations thereof with complementary photochromic compounds, e.g., certain other naphthopyrans, benzopyrans, and spiro(indoline)type compounds, are also described.
    • 描述了新的光致变色茚并稠合萘并吡喃化合物,其实例包括具有取代或未取代的茚并基团的萘并吡喃化合物,其2,1个位置与萘并吡喃的萘酚部分稠合,如下所示。 还存在于萘并吡喃上的是中子至强电子给体取代基,位于吡喃环的6-位和7-位,任选在8-位或稠合于萘酚部分的h侧的环状基团,弱至中等电子 在吡喃环3位的供体位。 某些取代基也可以存在于化合物的5,8,9,10,11,12或13个碳原子上。 这些化合物在饱和度测试中的相对DELTAOD中的等级至少为80,并且可以由以下图形表示:还描述了含有或涂覆有这些化合物的聚合物有机主体材料。 还描述了光学透明的物品,例如将眼用透镜或其它塑料透明胶片掺入新的萘并吡喃化合物或其组合与互补的光致变色化合物,例如某些其它萘并吡喃,苯并吡喃和螺(二氢吲哚)型化合物。
    • 2. 发明申请
    • PHOTOCHROMIC MATERIALS COMPRISING HALOALKYL GROUPS
    • 包含HALOALKYL组的光致变色材料
    • US20070278461A1
    • 2007-12-06
    • US11695126
    • 2007-04-02
    • Olga G. PetrovskaiaAnu ChopraPatrick M. Brown
    • Olga G. PetrovskaiaAnu ChopraPatrick M. Brown
    • C08L73/00C07D309/00C07D413/02
    • G03C1/73C07D309/32C07F7/1804C09B57/00C09K9/02
    • Various non-limiting embodiments of the present invention relate to photochromic materials which include a haloalkyl group. More particularly, various non-limiting embodiments disclosed herein provide photochromic materials including an indeno-fused naphthopyran, such as, an indeno[2′,3′:3,4]naphtho[1,2-b] pyran, and a haloalkyl group bonded at the 13-position thereof, wherein the haloalkyl group is a perhalogenated group or a group represented by —O(CH2)a(CX2)bCT3, wherein T is a halogen, each X is independently hydrogen or halogen, a is an integer ranging from 1 to 10, and b is an integer ranging from 1 to 10. Other non-limiting embodiments disclosed herein provide photochromic composition and photochromic articles, such as, but not limited to ophthalmic lens, which include the disclosed photochromic materials and methods of making the same.
    • 本发明的各种非限制性实施方案涉及包含卤代烷基的光致变色材料。 更具体地,本文公开的各种非限制性实施方案提供光致变色材料,包括茚并稠合的萘并吡喃,例如茚并[2',3':3,4]萘并[1,2-b]吡喃和卤代烷基 在其13位上键合,其中卤代烷基是全卤代基或由-O(CH 2 CH 2)a表示的基团(CX 2) 其中T是卤素,每个X独立地是氢或卤素,a是1到10的整数,并且b是一个整数。 本文公开的其它非限制性实施方案提供光致变色组合物和光致变色制品,例如但不限于眼科镜片,其包括所公开的光致变色材料及其制备方法。
    • 3. 发明授权
    • Indeno-fused photochromic naphthopyrans
    • 印度融合的光致变色萘并吡喃
    • US06736998B2
    • 2004-05-18
    • US10039984
    • 2001-10-29
    • Olga G. PetrovskaiaAnil Kumar
    • Olga G. PetrovskaiaAnil Kumar
    • G02B523
    • C07D311/94C08K5/1545G03C1/73
    • Described are novel reversible photochromic indenonaphthopyran compounds, examples of which are 2H-naphtho[1,2-b]pyrans characterized by having a substituted or unsubstituted indeno group fused at the 2,3 positions of the group to the 1 side of the 2H-naphthopyran. The compounds also have substituents at the 3 position of the pyran ring. Substituents may also be present at the number 5, 6, 7, 8, 9, 10, 11, 12, or 13 carbon atoms of the compounds. These compounds may be represented by the following graphic formulae: Also described are various substrates, e.g., paper, glass, organic polymeric materials, etc., that contain or that are coated with such compounds. Optically clear articles such as ophthalmic lenses or other plastic transparencies that incorporate the novel indenonaphthopyran compounds or combinations thereof with complementary photochromic compounds, e.g., indenonaphthopyrans, naphthopyrans, benzopyrans, oxazine-type compounds, etc., are also described.
    • 描述的是新颖的可逆光致变色茚并萘并吡喃化合物,其实例是2H-萘并[1,2-b]吡喃,其特征在于在该基团的2,3个位上稠合了取代或未取代的茚并基团, 萘并吡喃 该化合物在吡喃环的3位也具有取代基。 取代基也可以存在于化合物的5,6,7,8,9,10,11,12或13个碳原子上。 这些化合物可以由以下图解表示:还描述了含有或涂覆有这些化合物的各种基材,例如纸,玻璃,有机聚合材料等。 还描述了光学透明的物品,例如将眼用镜片或其它塑料透明胶片结合到新的茚并萘并吡喃化合物或其组合与互补的光致变色化合物,例如茚并萘并吡喃,萘并吡喃,苯并吡喃,恶嗪型化合物等。