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  <abstract>A cholesteric liquid crystal composition includes a) a cholesteric liquid crystal compound or a cholesteric liquid crystal precursor; and b) a compound of formula (I), formula (II) or formula (III): where, n is 1, 2, 3, or 4; m is 1, 2, or 3; R is an acrylate, methacrylate, acrylamide, isocyanate, epoxy, or silane; R1 is a (C3-C8) alkylene, (C3-C8) alkenylene, or (C3-C8) alkylyne; R2 is a bond, -O-, -C(O)O-, -O(O)C-, -OC(O)O-, -C(O)N-, -CH=N-, -N=CH-, or -NC(O)-; R3 is a cycloalkylene, cycloalkenylene, heterocyclylene, arylene, or hetroarylene; R4 is a bond, (C1-C8) alkylene, (C2-C8) alkenylene, (C2-C8) alkylyne, carbonyl, -O-, -C(O)O-, -O(O)C-, -OC(O)O-, -C(O)N-, -CH=N-, -N=CH-, or -NC(O)-; R5 is a bond, cycloalkylene, cycloalkenylene, hetrocyclylene, arylene, or hetroarylene; R6 is hydrogen, cyano, halo, (C1-C8) alkoxy, (C1-C8) alkyl, nitro, amino, carboxy, mercapto, (C1-C4)thioalkyl, COCH3, CF3, OCF3, or SCF3; R7 is a (C1-C2) alkylene, (C2) alkenylene, or (C2) alkylyne; R8 is is hydrogen, halo, (C1-C8) alkoxy, (C1-C8) alkyl, nitro, amino, carboxy, mercapto, (C1-C4)thioalkyl, COCH3, CF3, OCF3, or SCF3, R9 is a cycloalkylene, cycloalkenylene, heterocyclylene, arylene, or hetroarylene; and R10 is a (C1-C8) alkylene, (C2-C8) alkenylene, or (C2-C8) alkylyne.</abstract>
  <anum-serial type="integer" nil="true"></anum-serial>
  <applicant-address>3M Center, Post Office Box 33427, Saint Paul, MN 55133-3427, USA U.S.A.</applicant-address>
  <applicant-name>3M INNOVATIVE PROPERTIES COMPANY</applicant-name>
  <application-num>709/CHENP/2006 A</application-num>
  <clean-application-num>709/CHENP/2006</clean-application-num>
  <country>INDIA</country>
  <created-at type="datetime">2009-03-20T08:08:15Z</created-at>
  <document-date type="date">2007-06-22</document-date>
  <filing-date type="date">2006-02-27</filing-date>
  <id type="integer">303679</id>
  <international-application-date type="date">2004-07-06</international-application-date>
  <international-application-num>PCT/US04/21610</international-application-num>
  <international-class>C09K 19/40, 19/42</international-class>
  <international-publication-num>WO 2005/023964 A3</international-publication-num>
  <inventor-name>RADCLIFFE, Marc, D.;, POKORNY, Richard, J.;, SPAWN, Terence, D.;, SOLOMONSON, Steven, D.;</inventor-name>
  <journal-page-number type="integer">20572</journal-page-number>
  <number-of-claims type="integer" nil="true"></number-of-claims>
  <number-of-pages type="integer" nil="true"></number-of-pages>
  <origin type="integer">0</origin>
  <pdf-page-number type="integer">805</pdf-page-number>
  <priority-document-country>U.S.A.</priority-document-country>
  <priority-document-date type="date">2003-08-29</priority-document-date>
  <priority-document-num>10/652,700</priority-document-num>
  <publication-date type="date">2007-06-22</publication-date>
  <questionable-score type="integer">0</questionable-score>
  <title>CHOLESTERIC LIQUID CRYSTAL COPOLYMERS AND ADDITIVES</title>
  <token>3Oxdaznm</token>
  <updated-at type="datetime">2009-04-30T18:38:05Z</updated-at>
  <names type="array">
    <name>
      <id type="integer">70172</id>
      <name>RADCLIFFE, MARC, D.;, POKORNY, RICHARD, J.;, SPAWN, TERENCE, D.;, SOLOMONSON, STEVEN, D</name>
    </name>
    <name>
      <id type="integer">448</id>
      <name>3M INNOVATIVE PROPERTIES COMPANY</name>
    </name>
  </names>
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