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    • 1. 发明申请
    • SUBSTITUTED BIPYRIDINES FOR USE IN ORGANIC LIGHT-EMITTING DEVICES
    • 用于有机发光装置的替代双嘧啶
    • US20120179089A1
    • 2012-07-12
    • US13232837
    • 2011-09-14
    • David T. SiskSazzadur Rahman KhanAmane Mochizuki
    • David T. SiskSazzadur Rahman KhanAmane Mochizuki
    • A61M37/00C07D401/14A61N5/06C07D413/14C09K11/06H01L51/54C07D401/04C07D417/14
    • C07D401/04C07D401/14C07D413/14C07D417/14H01L51/0061H01L51/0072H01L51/0077H01L51/0085H01L51/5012H01L51/5048H01L51/5092
    • Optionally substituted bipyridine compounds, optionally substituted phenylbipyridine compounds, or optionally substituted bis-phenylbipyridine compounds may be useful in light-emitting devices. Some examples include, but are not limited to, optionally substituted 4-(5-(6-(4-(diphenylamino)phenyl)pyridin-3-yl)pyridin-2-yl)-N,N-diphenylbenzenamine, optionally substituted 9-(4-(5-(6-(4-(9H-carbazol-9-yl)phenyl)pyridin-3-yl)pyridin-2-yl)phenyl)-9H-carbazole, optionally substituted 4-(5-(6-(benzo[d]thiazol-2-yl)pyridin-3-yl)pyridin-2-yl)-N,N-diphenylbenzenamine, optionally substituted 4-(5-(6-(benzo[d]oxazol-2-yl)pyridin-3-yl)pyridin-2-yl)-N,N-diphenylbenzenamine, optionally substituted N,N-diphenyl-4-(5-(6-(1-phenyl-1H-benzo[d]imidazol-2-yl)pyridin-3-yl)pyridin-2-yl)benzenamine, optionally substituted 4-(5-(6-(4-(9H-carbazol-9-yl)phenyl)pyridin-3-yl)pyridin-2-yl)-N,N-diphenylbenzenamine, optionally substituted 2-(5-(6-(benzo[d]thiazol-2-yl)pyridin-3-yl)pyridin-2-yl)benzo[d]thiazole, optionally substituted 2-(5-(6-(benzo[d]thiazol-2-yl)pyridin-3-yl)pyridin-2-yl)benzo[d]oxazole, optionally substituted 9-(4-(5-(6-(benzo[d]thiazol-2-yl)pyridin-3-yl)pyridin-2-yl)phenyl)-9H-carbazole, optionally substituted 9-(4-(5-(6-(benzo[d]oxazol-2-yl)pyridin-3-yl)pyridin-2-yl)phenyl)-9H-carbazole, optionally substituted 9-(4-(6′-(1-phenyl-1H-benzo[d]imidazol-2-yl)-3,3′-bipyridin-6-yl)phenyl)-9H-carbazole, and 6,6′-bis(9-phenyl-9H-carbazol-3-yl)-3,3′-bipyridine.
    • 任选取代的联吡啶化合物,任选取代的苯基联吡啶化合物或任选取代的双苯基联吡啶化合物可用于发光器件中。 一些实例包括但不限于任选取代的4-(5-(6-(4-(二苯基氨基)苯基)吡啶-3-基)吡啶-2-基)-N,N-二苯基苯胺,任选取代的9 - (4-(5-(6-(4-(9H-咔唑-9-基)苯基)吡啶-3-基)吡啶-2-基)苯基)-9H-咔唑,任选取代的4- (6-(苯并[d]噻唑-2-基)吡啶-3-基)吡啶-2-基)-N,N-二苯基苯胺,任选取代的4-(5-(6-(苯并[d] 吡啶-2-基)吡啶-2-基)-N,N-二苯基苯胺,任选取代的N,N-二苯基-4-(5-(6-(1-苯基-1H-苯并[d] 咪唑-2-基)吡啶-3-基)吡啶-2-基)苯胺,任选取代的4-(5-(6-(4-(9H-咔唑-9-基)苯基)吡啶-3-基) 吡啶-2-基)-N,N-二苯基苯胺,任选取代的2-(5-(6-(苯并[d]噻唑-2-基)吡啶-3-基)吡啶-2-基)苯并[d] 噻唑,任选取代的2-(5-(6-(苯并[d]噻唑-2-基)吡啶-3-基)吡啶-2-基)苯并[d]恶唑,任选取代的9-(4-(5 - (6-(苯并[d]噻唑-2-基)吡啶-3-基)吡啶-2-基)苯基)-9H-咔唑, (4-(5-(6-(苯并[d]恶唑-2-基)吡啶-3-基)吡啶-2-基)苯基)-9H-咔唑,任选取代的9- (6' - (1-苯基-1H-苯并[d]咪唑-2-基)-3,3'-联吡啶-6-基)苯基)-9H-咔唑和6,6'-双(9- 苯基-9H-咔唑-3-基)-3,3'-联吡啶。
    • 7. 发明授权
    • Ambipolar host in organic light emitting diode
    • 双极主机在有机发光二极管
    • US08062773B2
    • 2011-11-22
    • US12694994
    • 2010-01-27
    • David T. SiskSheng LiAmane Mochizuki
    • David T. SiskSheng LiAmane Mochizuki
    • H01L51/54C07D401/14
    • C07D401/14C07D213/38C09K11/06C09K2211/1022C09K2211/1029H01L51/0037H01L51/0067H01L51/0072H01L51/0085H01L51/5016H01L51/5036H05B33/20Y10S428/917
    • Some embodiments provide a compound represented by Formula 1: wherein R1, R2, R3, R6, R7, and R8 are independently selected from the group consisting of H, optionally substituted C1-12 alkyl, optionally substituted phenyl, optionally substituted carbazolyl, optionally substituted diphenylamine and optionally substituted diphenylaminophenyl; provided that: at least one of R1, R2, and R3 is selected from optionally substituted carbazolyl, optionally substituted diphenylamine and optionally substituted diphenylaminophenyl and at least one of R6, R7, and R8 is selected from optionally substituted carbazolyl, optionally substituted diphenylamine and optionally substituted diphenylaminophenyl; and R4 and R5 are independently selected from the group consisting of H, optionally substituted C1-12 alkyl, optionally substituted phenyl, optionally substituted diphenylamine and optionally substituted diphenylaminophenyl. Other embodiments provide an organic light-emitting diode device comprising a compound of Formula I.
    • 一些实施方案提供由式1表示的化合物:其中R 1,R 2,R 3,R 6,R 7和R 8独立地选自H,任选取代的C 1-12烷基,任选取代的苯基,任选取代的咔唑基, 二苯胺和任选取代的二苯基氨基苯基; 条件是:R 1,R 2和R 3中的至少一个选自任选取代的咔唑基,任选取代的二苯胺和任选取代的二苯基氨基苯基,并且R 6,R 7和R 8中的至少一个选自任选取代的咔唑基,任选取代的二苯胺和任选的 取代的二苯基氨基苯基; 并且R 4和R 5独立地选自H,任选取代的C 1-12烷基,任选取代的苯基,任选取代的二苯胺和任选取代的二苯基氨基苯基。 其它实施方案提供了包含式I化合物的有机发光二极管器件。