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    • 1. 发明申请
    • 2, 2', 6, 6'- TETRASUBSTITUTED AMINOPHOSPHINE LIGAND AND ITS SYNTHESIS METHOD
    • 2,2',6,6'-四唑基氨基磷酰胺配体及其合成方法
    • US20100217040A1
    • 2010-08-26
    • US12377000
    • 2007-08-10
    • Wanbin ZhangFang XieFang Fang
    • Wanbin ZhangFang XieFang Fang
    • C07F9/50
    • C07F9/46
    • The present invention relates to a 2,2′,6,6′-tetrasubstituted aminophosphine ligand and its synthesis method. The structure of the ligand is shown as below. Its synthesis method comprises: Step (1) coupling 2,6-dinitrochlorobenzene as the starting material to obtain 2,2′,6,6′-tetranitrobiphenyl; Step (2): hydrogenating the 2,2′,6,6′-tetranitrobiphenyl with Pd/C to obtain 2,2′,6,6′-tetraminobiphenyl; Step (3): reacting the 2,2′,6,6′-tetraminobiphenyl with a phosphine halide to obtain the 2,2′,6,6′-tetrasubstituted aminophosphine ligand. The ligand of the present invention is an achiral compound, and its preparation method is simple. The ligand can be converted to a chiral bimetallic catalyst with single configuration eventually through introduction of external chirality. Moreover, the ligand can be used in various asymmetric reaction catalyzed by metals with high reactivity and stereoselectivity.
    • 本发明涉及2,2',6,6'-四取代氨基膦配体及其合成方法。 配体的结构如下所示。 其合成方法包括:步骤(1)以2,6-二硝基氯苯为原料,得到2,2',6,6'-四硝基联苯; 步骤(2):用Pd / C氢化2,2',6,6'-四硝基二苯并得到2,2',6,6'-四氨基联苯; 步骤(3):使2,2',6,6'-四磺酰联苯与卤化膦反应,得到2,2',6,6'-四取代氨基膦配体。 本发明的配体是非手性化合物,其制备方法简单。 最终可以通过引入外部手性将配体转化为具有单一配置的手性双金属催化剂。 此外,配体可用于由具有高反应性和立体选择性的金属催化的各种不对称反应中。
    • 2. 发明授权
    • 2,2′,6,6′-tetrasubstituted aminophosphine ligand and its synthesis method
    • 2,2',6,6'-四取代氨基膦配体及其合成方法
    • US08729303B2
    • 2014-05-20
    • US12377000
    • 2007-08-10
    • Wanbin ZhangFang XieFang Fang
    • Wanbin ZhangFang XieFang Fang
    • C07F9/02
    • C07F9/46
    • The present invention relates to a 2,2′,6,6′-tetrasubstituted aminophosphine ligand and its synthesis method. The structure of the ligand is shown as below. Its synthesis method comprises: Step (1) coupling 2,6-dinitrochlorobenzene as the starting material to obtain 2,2′,6,6′-tetranitrobiphenyl; Step (2): hydrogenating the 2,2′,6,6′-tetranitrobiphenyl with Pd/C to obtain 2,2′,6,6′-tetraminobiphenyl; Step (3): reacting the 2,2′,6,6′-tetraminobiphenyl with a phosphine halide to obtain the 2,2′,6,6′-tetrasubstituted aminophosphine ligand. The ligand of the present invention is an achiral compound, and its preparation method is simple. The ligand can be converted to a chiral bimetallic catalyst with single configuration eventually through introduction of external chirality. Moreover, the ligand can be used in various asymmetric reaction catalyzed by metals with high reactivity and stereoselectivity.
    • 本发明涉及2,2',6,6'-四取代氨基膦配体及其合成方法。 配体的结构如下所示。 其合成方法包括:步骤(1)以2,6-二硝基氯苯为原料,得到2,2',6,6'-四硝基联苯; 步骤(2):用Pd / C氢化2,2',6,6'-四硝基二苯并得到2,2',6,6'-四氨基联苯; 步骤(3):使2,2',6,6'-四磺酰联苯与卤化膦反应,得到2,2',6,6'-四取代氨基膦配体。 本发明的配体是非手性化合物,其制备方法简单。 最终可以通过引入外部手性将配体转化为具有单一配置的手性双金属催化剂。 此外,配体可用于由具有高反应性和立体选择性的金属催化的各种不对称反应中。
    • 3. 发明申请
    • C2-SYMMETRICAL RUTHENOCENE DIPHOSPHINE LIGANDS ONLY WITH SURFACE CHIRALITY AND THEIR MANUFACTURE
    • C2-对称二硫代磷酸酯配体仅具有表面光洁度及其制造
    • US20110160474A1
    • 2011-06-30
    • US12303767
    • 2007-06-08
    • Wanbin ZhangFang XieDelong LiuLi LuoGenghong HuaJian Shang
    • Wanbin ZhangFang XieDelong LiuLi LuoGenghong HuaJian Shang
    • C07F17/02
    • C07F17/02B01J31/2295B01J31/24B01J31/2409B01J2531/0205B01J2531/0263B01J2531/821
    • The invention affords C2-symmetrical ruthenocene diphosphine ligands with surface chirality and their manufacture. The present invention uses (S)—(S)-1,1′-2(diphenylphosphino)-2,2′-2[(S)-4-isopropyloxazolinyl]ruthenocene as raw material and the product is prepared through two or three steps of reaction. At the action of trifluoroacetic acid, (S)—(S)-1,1′-2(diphenylphosphino)-2,2′-2[(S)-4-isopropyloxazolinyl]ruthenocene first removes oxazoline and gets ester amides compound which then carries out ester exchange or reduction alkylation and gets the product of ruthenocene diphosphine ligand with surface chirality. The ligands prepared with the structure as follows from the invention can be used in all kinds of metallic catalysis asymmetric reaction and has good reaction activity and stereoselectivity, wherein R is methyl or ethyl, R1 is linear or branched alkyl, cycloalkyl, alkoxy, aryl, aralkyl and alkyl amino.
    • 本发明提供具有表面手性及其制造的C2对称的二茂铁二膦配体。 本发明使用(S) - (S)-1,1'-2(二苯基膦基)-2,2'-2 [(S)-4-异丙唑恶唑啉基] rut烯为原料,通过2或3 反应步骤。 在三氟乙酸的作用下,(S) - (S)-1,1'-2(二苯基膦基)-2,2'-2 [(S)-4-异丙基恶唑啉基] rut hen ene首先除去恶唑啉并得到酯酰胺化合物, 然后进行酯交换或还原烷基化,得到具有表面手性的钌基二膦配体的产物。 由本发明制备的具有如下结构的配位体可用于各种金属催化不对称反应,具有良好的反应活性和立体选择性,其中R为甲基或乙基,R 1为直链或支链烷基,环烷基,烷氧基,芳基, 芳烷基和烷基氨基。
    • 4. 发明授权
    • C2-symmetrical ruthenocene diphosphine ligands only with surface chirality and their manufacture
    • C2对称的二茂铁二膦配体仅具有表面手性及其制造
    • US08507705B2
    • 2013-08-13
    • US12303767
    • 2007-06-08
    • Wanbin ZhangFang XieDelong LiuLi LuoGenghong HuaJian Shang
    • Wanbin ZhangFang XieDelong LiuLi LuoGenghong HuaJian Shang
    • C07F15/00
    • C07F17/02B01J31/2295B01J31/24B01J31/2409B01J2531/0205B01J2531/0263B01J2531/821
    • The invention affords C2-symmetrical ruthenocene diphosphine ligands with surface chirality and their manufacture. The present invention uses (S)-(S)-1,1′-2(diphenylphosphino)-2,2′-2[(S)-4-isopropyloxazolinyl] ruthenocene as raw material and the product is prepared through two or three steps of reaction. At the action of trifluoroacetic acid, (S)-(S)-1,1′-2(diphenylphosphino)-2,2′-2[(S)-4-isopropyloxazolinyl] ruthenocene first removes oxazoline and gets ester amides compound which then carries out ester exchange or reduction alkylation and gets the product of ruthenocene diphosphine ligand with surface chirality. The ligands prepared with the structure as follows from the invention can be used in all kinds of metallic catalysis asymmetric reaction and has good reaction activity and stereoselectivity, wherein R is methyl or ethyl, R1 is linear or branched alkyl, cycloalkyl, alkoxy, aryl, aralkyl and alkyl amino.
    • 本发明提供具有表面手性及其制造的C2对称的二茂铁二膦配体。 本发明使用(S) - (S)-1,1'-2(二苯基膦基)-2,2'-2 [(S)-4-异丙唑恶唑啉基] rut烯为原料,通过2或3 反应步骤。 在三氟乙酸的作用下,(S) - (S)-1,1'-2(二苯基膦基)-2,2'-2 [(S)-4-异丙基恶唑啉基] rut hen ene首先除去恶唑啉并得到酯酰胺化合物, 然后进行酯交换或还原烷基化,得到具有表面手性的钌基二膦配体的产物。 由本发明制备的具有如下结构的配位体可用于各种金属催化不对称反应,具有良好的反应活性和立体选择性,其中R为甲基或乙基,R 1为直链或支链烷基,环烷基,烷氧基,芳基, 芳烷基和烷基氨基。
    • 9. 发明授权
    • Infrared inductive light switch using triac trigger-control and early-charging-peak current limiter with adjustable power consumption
    • 红外感应灯开关采用三端双向可控硅触发控制和早期充电峰值电流限制器,功耗可调
    • US06369517B2
    • 2002-04-09
    • US09681273
    • 2001-03-12
    • Qun SongJian LiFang Xie
    • Qun SongJian LiFang Xie
    • G05F100
    • H05B39/08H05B37/0209H05B37/0227Y02B20/44Y10T307/766
    • An electronic switch can replace a standard mechanical light switch for 110-240 volt alternating-current (A.C.) devices. A triac switches the A.C. current to an A.C. device such as a light. A rectifier bridge generates a direct-current (D.C.) voltage that is applied to a special current limiter. The special current limiter generates a large current peak at low voltages, but limits current at high voltages. The large current peak from the special current limiter charges a capacitor when voltage is low at the beginning of each A.C. half-cycle, before the triac turns on. The capacitor has enough charge to supply D.C. current to an Infrared detector and trigger control logic for the rest of the A.C. half-cycle. When the detector detects a person nearby, it signals the trigger control logic. The D.C. voltage from the rectifier bridge is filtered to generate a sync pulse to the trigger control logic when adds a phase delay to the sync pulse which triggers the triac.
    • 电子开关可以替代110-240伏交流(交流)装置的标准机械灯开关。 三端双向可控硅开关将交流电流切换到交直流设备,如灯。 整流桥产生施加到特殊限流器的直流(直流)电压。 特殊电流限制器在低电压下产生大电流峰值,但限制高电压下的电流。 在三端双向可控硅开关导通之前,每个交流电半周期的电压低电平时,特殊电流限制器的大电流峰值将对电容器充电。 电容器具有足够的电荷,以将红外线检测器的电流提供给红外检测器,并触发交流半周期的其余部分的触发控制逻辑。 当检测器检测到附近的人时,它会发出触发控制逻辑信号。 当对触发三端双向可控硅开关元件的同步脉冲添加相位延迟时,来自整流桥的直流电压被滤波以产生到触发控制逻辑的同步脉冲。
    • 10. 发明申请
    • SHORT MESSAGE SENDING METHOD, SHORT MESSAGE SERVICE CENTER AND GATEWAY
    • 短信息发送方式,短消息服务中心和网关
    • US20150304825A1
    • 2015-10-22
    • US14233858
    • 2012-05-23
    • Hao WuFang Xie
    • Hao WuFang Xie
    • H04W4/14H04L12/58H04L12/741H04M1/725
    • H04W4/14H04L45/74H04L51/06H04M1/72552H04W40/02H04W88/02H04W88/16H04W88/184
    • A short message sending method, a short message service center (SMS-SC) and a gateway are provided. The short message service center constructs a message body for bearing short message, includes routing information of the short message in this message body, and sends the message body to a short message mobile switching center gateway; after receiving the message body and determining that the message body includes the routing information of the short message, the short message mobile switching center gateway sends the short message to a core network service node according to the routing information. The SMS-SC sends the obtained routing information together with the short message to an SMS-GMSC, so that the SMS-GMSC does not need to request the routing information from an HSS or an HLR, which can reduce the interactive signaling, save the network resources, and optimize the system performance.
    • 提供短消息发送方法,短消息服务中心(SMS-SC)和网关。 短消息服务中心构建用于承载短消息的消息体,包括短消息在该消息体中的路由信息​​,并将消息体发送到短消息移动交换中心网关; 在接收到消息体并确定消息体包括短消息的路由信息​​之后,短消息移动交换中心网关根据路由信息将短消息发送到核心网业务节点。 SMS-SC将获取的路由信息​​与短消息一起发送到SMS-GMSC,使得SMS-GMSC不需要从HSS或HLR请求路由信息,这可以减少交互信令,保存 网络资源,优化系统性能。