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    • 56. 发明授权
    • Photochromic pyrano-fused naphthopyrans
    • 光致变色吡喃并稠合萘并吡喃
    • US06106744A
    • 2000-08-22
    • US984387
    • 1997-12-03
    • Barry Van GemertChristopher D. Selvig
    • Barry Van GemertChristopher D. Selvig
    • G02C7/10C07D493/04C08K5/1545C08L101/00G02B5/23G02S5/23C07D311/78
    • C07D493/04C08K5/1545G02B5/23
    • Described are novel photochromic pyrano-fused naphthopyran compounds, examples of which are naphthopyran compounds having a substituted or unsubstituted "S" pyran ring, the 3,4 positions of which are fused to the f side of the naphtho portion of the naphthopyran, and certain substituents at the 2-position of the "T" pyran ring. Certain substituents may also be present at the number 5, 7, 8, 9, 10, 11 or 12 carbon atoms of the compounds. These compounds may be represented by the following graphic formula: ##STR1## Also described are polymeric organic host materials that contain or that are coated with such compounds or combinations thereof with complementary photochromic compounds, e.g., certain other naphthopyrans, benzopyrans, and spiro(indoline)type compounds.
    • 描述了新的光致变色吡喃并稠合萘并吡喃化合物,其实例是具有取代或未取代的“S”吡喃环的萘并吡喃化合物,其3,4位与萘并吡喃的萘酚部分的f​​侧稠合, “T”吡喃环2位的取代基。 某些取代基也可以存在于化合物的5,7,8,9,10,11或12个碳原子上。 这些化合物可以由以下图解表示:还描述了含有或被这些化合物或其组合与互补光致变色化合物(例如某些其它萘并吡喃,苯并吡喃和螺(二氢吲哚))化合物 。