Method for manufacturing probe structure
    1.
    发明授权
    Method for manufacturing probe structure 有权
    探针结构的制造方法

    公开(公告)号:US07824561B2

    公开(公告)日:2010-11-02

    申请号:US11782949

    申请日:2007-07-25

    CPC classification number: G01R3/00 G01R1/06727

    Abstract: A method for manufacturing a probe structure is disclosed. In accordance with the method, two semiconductor substrates having different crystal directions are bonded and selectively etched utilizing an etch selectivity due to the different crystal directions to form a probe tip region and a probe beam region. A cantilever structure for a probe card is formed by filling the probe tip region and the probe beam region with a conductive material.

    Abstract translation: 公开了一种用于制造探针结构的方法。 根据该方法,由于不同的晶体方向,使用具有不同晶体方向的两个半导体衬底被结合并选择性蚀刻,以形成探针尖端区域和探针光束区域。 通过用导电材料填充探针尖端区域和探针束区域来形成用于探针卡的悬臂结构。

    Quinolone carboxylic acid derivatives
    2.
    发明授权
    Quinolone carboxylic acid derivatives 有权
    喹诺酮羧酸衍生物

    公开(公告)号:US06313299B1

    公开(公告)日:2001-11-06

    申请号:US09446697

    申请日:1999-12-23

    CPC classification number: C07D487/10

    Abstract: The present invention relates to quinolonecarboxylic acid derivatives having more excellent and broad antibacterial activities than the existing quinolone-series antibiotics. More specifically, it pertains to novel quinolonecarboxylic acid derivatives represented by following formula 1, which have a derivative of 7-[8-(alkoxyimino)-2,6-diazaspiro[3.4]oct-6-yl] as a substituent, and pharmaceutically acceptable salts and isomers thereof: Wherein, A is C—H, C—F, C—Cl, C—O—CH3 or N; Y is H or amino; R1 is cyclopropyl or 2,4-difluorophenyl; R2 is C1-4 alkyl; and R3 is H or C1-4 alkyl.

    Abstract translation: 本发明涉及具有比现有的喹诺酮系列抗生素更优异和更广泛的抗菌活性的喹诺酮羧酸衍生物。 更具体地说,涉及具有7- [8-(烷氧基亚氨基)-2,6-二氮杂螺[3.4]辛-6-基]作为取代基的衍生物的下式1所示的新型喹诺酮羧酸衍生物, 其中A为CH,CF,C-Cl,CO-CH 3或N; Y是H或氨基; R1是环丙基或2,4-二氟苯基; R2是C1-4烷基; 且R 3为H或C 1-4烷基。

    USER INTERFACE APPARATUS AND METHOD FOR USER INTERFACE IN TOUCH DEVICE
    6.
    发明申请
    USER INTERFACE APPARATUS AND METHOD FOR USER INTERFACE IN TOUCH DEVICE 有权
    用户界面设备和用于接口设备的用户界面的方法

    公开(公告)号:US20100306650A1

    公开(公告)日:2010-12-02

    申请号:US12612303

    申请日:2009-11-04

    CPC classification number: G06F3/0482 G06F3/04883 G06F3/04886

    Abstract: A user interface apparatus includes a position identification unit to identify a first position where a first touch is generated on a display screen; a priority assignment unit to respectively assign priorities to menu items displayed on the display screen; and a menu item movement unit to move the menu items to the first position as a destination according to the assigned priorities and in response to the first touch. A user interface method in a touch device includes identifying a first position where a first touch is generated on a display screen, respectively assigning priorities to menu items displayed on the display screen, and moving the menu items to the first position according to the assigned priorities in response to receiving the first touch.

    Abstract translation: 用户界面装置包括位置识别单元,用于识别在显示屏上产生第一触摸的第一位置; 优先级分配单元,分别对显示在显示画面上的菜单项赋予优先权; 以及菜单项移动单元,用于根据分配的优先级和响应于第一次触摸将菜单项移动到作为目的地的第一位置。 触摸装置中的用户界面方法包括:识别在显示屏幕上产生第一触摸的第一位置,分别对显示在显示屏幕上的菜单项分配优先级,并根据分配的优先级将菜单项移动到第一位置 响应于接收到第一触摸。

    Quinolone carboxylic acid derivatives
    7.
    发明授权
    Quinolone carboxylic acid derivatives 有权
    喹诺酮羧酸衍生物

    公开(公告)号:US06552196B2

    公开(公告)日:2003-04-22

    申请号:US09946541

    申请日:2001-09-06

    CPC classification number: C07D487/10

    Abstract: The present invention relates to quinolonecarboxylic acid derivatives having more excellent and broad antibacterial activities than the existing quinolone-series antibiotic. More specifically, it pertains to novel quinolonecarboxylic acid derivative represented by following formula 1, which have a derivative of 7-[8-(alkoxyimino)-2,6-diazaspiro[3.4]oct-6-yl] as a substituent, and pharmaceutically acceptable salts and isomers thereof: Wherein A is C—H, C—F, C—Cl, C—O—CH3 or N; Y is H or amino; R1 is cyclopropyl or 2,4-difluorsophenyl R2 is C1-4 alkyl; and R3 is H or C1-4 alkyl.

    Abstract translation: 本发明涉及具有比现有的喹诺酮系列抗生素更优异和更广泛的抗菌活性的喹诺酮羧酸衍生物。 更具体地说,涉及具有7- [8-(烷氧基亚氨基)-2,6-二氮杂螺[3.4]辛-6-基]作为取代基的衍生物的下式1所示的新型喹诺酮羧酸衍生物, 其可接受的盐和异构体:其中A是CH,CF,C-Cl,CO-CH 3或N; Y是H或氨基; R1是环丙基或2,4-二氟苯基R2是C1-4烷基; 且R 3为H或C 1-4烷基。

    METHOD OF FORMING CIGS THIN FILM
    9.
    发明申请
    METHOD OF FORMING CIGS THIN FILM 审中-公开
    形成薄膜薄膜的方法

    公开(公告)号:US20120006687A1

    公开(公告)日:2012-01-12

    申请号:US12985654

    申请日:2011-01-06

    Abstract: Disclosed herein is a method of forming a CIGS thin film, comprising the steps of: immersing a substrate comprising an electrode into an electrolyte solution comprising Na2SO4, a water-soluble copper (Cu) precursor, a water-soluble indium (In) precursor, a water-soluble gallium (Ga) precursor, and a water-soluble selenium (Se) precursor; performing electrodeposition in such a way as to apply a direct current (DC) voltage of −0.95V˜−0.85V to the electrolyte solution at room temperature and normal pressure for 10˜120 minutes to form a preliminary CIGS thin film; and heat-treating the preliminary CIGS thin film at 230˜270° C. to form a CIGS thin film.

    Abstract translation: 本文公开了一种形成CIGS薄膜的方法,包括以下步骤:将包含电极的基底浸入包含Na 2 SO 4,水溶性铜(Cu)前体,水溶性铟(In)前体的电解质溶液中, 水溶性镓(Ga)前体和水溶性硒(Se)前体; 以在室温和常压下向电解液施加-0.95V〜0.85V的直流(DC)电压10〜120分钟进行电沉积,形成预备的CIGS薄膜; 并在230〜270℃下对预备的CIGS薄膜进行热处理以形成CIGS薄膜。

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