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    • 48. 发明申请
    • Photochromic 2H-naphthopyrans
    • 光致变色2H-萘并吡喃
    • US20070145337A1
    • 2007-06-28
    • US11317577
    • 2005-12-23
    • Anu Chopra
    • Anu Chopra
    • G02B5/23F21V9/00
    • C07D311/92C09K9/02C09K2211/1011C09K2211/1088G02B1/10G02B1/11G02B5/23G03C1/73
    • Described are photochromic 2H-naphtho[1,2-b]pyrans characterized by two adjacent moderate to strong electron donor substituents at the 7 and 8 positions, a moderate to strong electron withdrawing substituent at the 5 position, and at the 2 position, one substituent that is a weak electron donor and another substituent that is a weak to moderate electron donor. An optional substituent is located at the 6 position and each of the positions may have reactive substituents that enable the photochromic material to be more compatible with the host polymer. The selection and placement of the aforementioned substituents being done on the naphthopyran to demonstrate a lambda max of less than 490 nanometers in the Photochromic Performance Test. The selection and placement of substituents also enables the balancing of photochromic properties, such as the intensity, as measured in the Photochromic Performance Test. Also described are polymeric organic host materials that contain or that are coated with such naphthopyrans or combinations thereof with complementary photochromic compounds to produce photochromic articles such as ophthalmic lenses.
    • 描述的是光致变色的2H-萘并[1,2-b]吡喃,其特征在于在7和8位有两个相邻的中等到强电子给体取代基,在5位是中等到强的吸电子取代基,在2位是1个 取代基是弱电子给体,另一个取代基是弱至中等电子给体。 任选的取代基位于6位,并且每个位置可以具有使得光致变色材料能够与主体聚合物更相容的反应性取代基。 上述取代基的选择和放置在萘并吡喃上进行,以证明在光致变色性能测试中λmax小于490纳米。 取代基的选择和置换还使得能够平衡光致变色性质,例如在光致变色性能测试中测量的强度。 还描述了含有或被这些萘并吡喃或其组合与互补的光致变色化合物一起涂覆以产生光致变色制品如眼镜的聚合物有机主体材料。