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    • 5. 发明授权
    • Optically active compounds, and a liquid-crystalline phase
    • 光学活性化合物和液晶相
    • US5393459A
    • 1995-02-28
    • US956938
    • 1992-10-05
    • Andreas WachtlerThomas GeelhaarReinhard HittichEkkehard BartmannJoachim KrauseEike Poetsch
    • Andreas WachtlerThomas GeelhaarReinhard HittichEkkehard BartmannJoachim KrauseEike Poetsch
    • C07C43/225C07C255/46C07D213/30C07D213/50C07D239/26C07D239/34C07D285/12C09K19/30C09K19/34C09K19/58C09K19/12G09F1/13
    • C07D213/30C07C255/46C07C43/225C07D213/50C07D239/26C07D239/34C07D285/12C09K19/3001C09K19/3444C09K19/3463C09K19/3497C09K19/588C07C2101/14
    • The invention relates to optically active compounds of the formula I ##STR1## in which R is an alkyl or alkenyl radical having up to 15 carbon atoms which is unsubstituted, monosubstituted by --CN or at least monosubstituted by fluorine or chlorine, it also being possible for a CH.sub.2 group in these radicals to be replaced by --O--, --CO--, --O--CO--, --CO--O-- or --O--CO--O--,A.sup.1 and A.sup.2 are each, independently of one another, a 1,4-phenylene radical, pyridine-2,5-diyl radical, pyrimidine-2,5-diyl radical, pyrazine-2,5-diyl radical, pyridazine-3,6-diyl radical, 1,3,4-thiadiazole-2,5-diyl radical, 1,2,4-thiadiazole-3,5-diyl radical or trans-1,4-cyclohexylene radical, each of which is unsubstituted or substituted by one or two fluorine atoms, and in which, in addition, one or two non-adjacent CH.sub.2 groups may be replaced by --O-- and/or --S--, and/or a CH group,Z.sup.1, Z.sup.2 and Z.sup.3 are each, independently of one another, --CO--O--, --O--CO--, --CH.sub.2 O--, --OCH.sub.2 --, --CH.sub.2 CH.sub.2 --, --CH.dbd.CH--, --C.tbd.C-- or a single bond,Q.sup.1 is --CH.sub.2 CH.sub.2 --, --CH.sub.2 CH.sub.2 CH.sub.2 --, --OCH.sub.2 --, --CH.sub.2 OCH.sub.2 --, --OCH.sub.2 CH.sub.2 --, --O--CO-- or --CO--OCH.sub.2 --,Q.sup.2 is --O--, --O--CO--, --(CH.sub.2).sub.3 --)-- or a single bond,m is 0, 1, 2 or 3,n is 0 or 1, ando is 1 to 9, and the use thereof as components of liquid-crystalline phases.
    • 本发明涉及式I的旋光活性化合物,其中R是具有至多15个碳原子的烷基或烯基,其未被取代,被-CN单取代或至少被氟或氯单取代,也可能是 对于这些基团中的CH 2基团被-O-,-CO-,-O-CO-,-CO-O-或-O-CO-O-,A1和A2各自彼此独立地取代, 吡啶-2,5-二基,嘧啶-2,5-二基,吡嗪-2,5-二基,哒嗪-3,6-二基,1,3,4-三基, 噻二唑-2,5-二基,1,2,4-噻二唑-3,5-二基或反-1,4-亚环己基,其各自为未取代的或被一个或两个氟原子取代,其中 另外,一个或两个不相邻的CH 2基团可以被-O-和/或-S-代替,和/或CH基,Z 1,Z 2和Z 3彼此独立地是-CO-O - , - O - CO - , - CH 2 O - , - OCH 2 - , - CH 2 CH 2 - , - CH = CH - , - C 3BOND C-或单键,Q 1是-CH 2 CH 2 - CH 2 CH 2 CH 2 - , - OCH 2 - , - CH 2 OCH 2 - , - OCH 2 CH 2 - , - O-CO-或-CO-OCH 2 - ,Q 2是-O - , - O - CO - , - (CH 2)3 - ) - 键,m为0,1,2或3,n为0或1,o为1至9,并且其用作液晶相的组分。
    • 9. 发明授权
    • 2,3-difluorohydroquinone derivatives
    • 2,3-二氟氢醌衍生物
    • US5248447A
    • 1993-09-28
    • US871620
    • 1992-04-21
    • Volker ReiffenrathJoachim KrauseAndreas WachtlerGeorg WeberThomas GeelhaarDavid CoatesIan C. SageSimon Greenfield
    • Volker ReiffenrathJoachim KrauseAndreas WachtlerGeorg WeberThomas GeelhaarDavid CoatesIan C. SageSimon Greenfield
    • C07C43/225C07D239/26C09K19/20C09K19/30C09K19/34
    • C07D239/26C07C43/225C09K19/2007C09K19/2021C09K19/3066C09K19/3068C09K19/3441C09K19/3458C07C2101/14C09K2019/0407
    • 2,3-difluorohydroquinone compounds of the formula I ##STR1## in which R.sup.1 and R.sup.2, in each case independently of one another, are alkyl having 1 to 15 C atoms or alkenyl having 3 to 15 C atoms which are unsubstituted, monosubstituted by cyano or at least monosubstituted by fluorine or chlorine, it also being possible for one CH.sub.2 group in these radicals to be replaced by --O--, --CO--, --CO--O--, --O--CO-- or --O--CO--O--,A.sup.1, A.sup.2 and A.sup.3, in each case independently of one another, are(a) trans-1,4-cyclohexylene, in which, in addition, one or two non-adjacent CH.sub.2 groups may be replaced by --O-- and/or --S--,(b) 1,4-phenylene, in which, in addition, one or two CH groups may be replaced by N, or(c) a radical from the group comprising piperidine-1,4-diyl, 1,4-bicylo (2,2,2)-octylene (sic), 1,3,4-thiadiazole-2,5-diyl, napththalene-2,6-diyl, decahydronaphthalene-2,6-diyl and 1,2,3,4-tetrahydronaphthalene-2,6-diyl, it being possible for the radicals (a) and (b) to be monosubstituted or polysubstituted by F, Cl, CH.sub.3 or CN,Z.sup.1 is --CO--O--, --O--CO--, --CH.sub.2 CH.sub.2 --, --OCH.sub.2 --, --CH.sub.2 O--, --C.tbd.C-- or a single bond,Q.sup.1 and Q.sup.2, in each case independently of one another, are --CO-- or --CH.sub.2 --,m and n are each 0, 1 or 2, and(m+n) is 0, 1 or 2,are suitable as components of liquid-crystalline phases.
    • PCT No.PCT / EP89 / 00179 371日期:1989年5月15日 102(e)日期1989年5月15日PCT提交1989年2月27日PCT公布。 出版物WO89 / 08637 日本1989年9月21日。式I的1,3-二氟氢醌化合物其中R 1和R 2各自独立地为具有1至15个碳原子的烷基或具有3至15个C原子的烯基, 是未取代的,被氰基单取代或至少被氟或氯单取代,这些基团中的一个CH 2基团也可被-O - , - CO - , - CO-O-,-O-CO-或 -O-CO-O-,A1,A2和A3各自独立地是(a)反式-1,4-亚环己基,此外,一个或两个不相邻的CH 2基可以是 被-O-和/或-S-取代,(b)1,4-亚苯基,其中另外一个或两个CH基团可被N取代,或(c)包含哌啶 - 1,4-二酰基,1,4-双酰(2,2,2) - 辛烯(sic),1,3,4-噻二唑-2,5-二基,萘-2,2二基,十氢萘-2, 6-二基和1,2,3,4-四氢化萘-2,6-二基,基团(a)和(b)可以是单取代的或聚合的 被F,Cl,CH 3或CN取代,Z 1是-CO-O - , - O - CO - , - CH 2 CH 2 - , - OCH 2 - , - CH 2 O-,-C 在每种情况下彼此独立地是-CO-或-CH2-,m和n各自为0,1或2,并且(m + n)为0,1或2,适合作为液晶相的组分 。