31.
    发明专利
    未知

    公开(公告)号:DE50102568D1

    公开(公告)日:2004-07-22

    申请号:DE50102568

    申请日:2001-03-08

    Applicant: BASF AG

    Abstract: Chiral 2,4,5-tri-substituted 1,3-dioxane compounds (I), with different substituents containing a mesogenic group, and their diastereomers are new. Chiral 2,4,5-tri-substituted 1,3-dioxane compounds of formula (I), with different substituents containing a mesogenic group, and their diastereomers are new: [Image] R1>[P-Y1>-(A1>)m-Y2>-]qM-Y3>-(A2>)n-Y4>- group; R2>, R3>[P-Y1>-(A1>)m-Y2>-]qM-Y3>-(A2>)n-Y4>'-; A1>, A2>spacers with 1-30 carbon atoms; M : a mesogenic group; Y1>, Y2>, Y3>, Y4>a single bond, -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-N(R)-, -(R)N-CO-, -O-CO-O-, -O-CO-N(R)-, -(R)N-CO-O- or -(R)N-CO-N(R)-; Y4>' : -O-, -O-CO-, -O-CO-O- or -O-CO-N(R)-, with the O atom attaching R2>, R3> to the 1,3-dioxane ring; R : hydrogen or 1-4C alkyl; P : H, 1-12C alkyl, a polymerizable group or a group containing a polymerizable group; m, n : 0 or 1; q : 1, 2 or 3. Independent claims are also included for: (a) liquid crystal (LC) compositions containing chiral compound(s) (I); (b) polymerizable LC compositions containing chiral compound(s) (I); (c) optical devices produced using these compositions; (d) printed or coated substrates, dispersions and emulsions, films or pigments prepared using the polymerizable LC compositions.

    CHIRAL 3,4-DIHYDRO-2H-PYRAN COMPOUNDS

    公开(公告)号:AU2003250860A1

    公开(公告)日:2004-01-19

    申请号:AU2003250860

    申请日:2003-06-30

    Applicant: BASF AG

    Abstract: The invention relates to chiral 3,4-dihydro-2H-pyran compounds and diastereomers thereof, and to the use of these compounds as chiral dopants for liquid-crystalline systems. The invention furthermore relates to non-polymerizable or polymerizable liquid-crystalline compositions which comprise at least one chiral 3,4-dihydro-2H-pyran compound according to the invention, to the use of these non-polymerizable or polymerizable liquid-crystalline compositions for the production of optical components, to the use of the polymerizable liquid-crystalline compositions for printing or coating substrates, for the preparation or production of dispersions and emulsions, films or pigments and optical components of this type, printed or coated substrates, dispersions and emulsions, films and pigments.

    METHOD FOR PRODUCING ORGANIC ALKYNE COMPOUNDS

    公开(公告)号:AU2003222836A1

    公开(公告)日:2003-11-17

    申请号:AU2003222836

    申请日:2003-04-25

    Applicant: BASF AG

    Abstract: The invention relates to a method for producing organic alkyne compounds of formula (I), X-C-C-Y According to said method, organic halogen compounds of formula (Ia), X-Hal, are reacted with organic terminal alkyne compounds of formula (Ib), H-C-C-Y, X and Y representing the same or different organic radicals and Hal representing chlorine or bromine, in inert solvents under the action of microwave radiation, in the presence of at least one metallic compound and at least one base.

    35.
    发明专利
    未知

    公开(公告)号:DE10061625A1

    公开(公告)日:2002-06-13

    申请号:DE10061625

    申请日:2000-12-11

    Applicant: BASF AG

    Abstract: The use of chiral, uncharged metal compounds containing two tridentate ligands with mesogenic groups, spacer groups and other groups as dopants for liquid crystalline materials. The use of chiral, uncharged compounds of formula (Ia) or (Ib) as dopants for liquid crystalline (LC) materials. ((P -Y -A -Y M -Y -)nL)2Me (Ia) ((P -Y -A -Y -M -Y -)nL)Me(L'(-Y -M -Y -A -Y -P )n')m (Ib) P , P = H, 1-12C alkyl, polymerizable groups, groups suitable for polymerization, or residues bearing such polymerizable groups; Y -Y = single bonds, -O-, -S-, -CO-, -COO-, -OCO-, -CONR-, -NRCO-, -OCOO-, -OCONR-, -NRCOO- or -NRCONR-; R = H or 1-4C alkyl; A , A = 1-30C spacer groups; M , M = mesogenic groups; n, n' = 0 or 1; m = 1, 2 or 3; Me = a transition metal of Period 4, 5 or 6 (other than technetium, silver, cadmium, gold, mercury or lanthanides) or a Main Group 14 element (other than carbon or lead); L = a tridentate ligand of formula (II); U, V, W = nitrogen-, phosphorus- or sulfur-containing groups with N, O, P or S atoms with free electron pair(s) for coordination with the central metal atom (Me); b1, b2 = 2-3C alkylene bridges attached to U and V or V and W, optionally substituted with up to two 1-12C organic residues in the case of 2C bridges and up to 4 such residues in other cases, and in which 2 adjacent carbon atoms may form part of an optionally substituted, optionally anellated benzene ring; L' = a 1-12C organic group. The groups L'(Y -M -Y -A -Y -P )n' in formula (Ib) may be different. Independent claims are also included for the following: (1) New compounds of formula (IIIa) and (IIIb). (2) LC materials containing compound(s) (Ia) and/or (Ib) or (IIIa) and/or (IIIb). ((P -Y -A -Y M -Y -)L)2Me (IIIa) ((P -Y -A -Y -M -Y -)L)Me(L'(-Y -M -Y -A -Y -P )n')m (IIIb) n' = 0 or 1.

    36.
    发明专利
    未知

    公开(公告)号:DE19949284A1

    公开(公告)日:2001-04-19

    申请号:DE19949284

    申请日:1999-10-12

    Applicant: BASF AG

    Abstract: Chiral glucosides of the type 2,4,7-trioxa-bicyclo(4.4.0)decane compounds are new. Chiral glucosides of the type 2,4,7-trioxa-bicyclo(4.4.0)decane compounds of formula (I) are new (when R = R = H). An Independent claim is also included for cholesteric liquid crystal compositions comprising a wider range of compounds of formula (I) (when R = R = as below), optionally in admixture with achiral liquid crystal polymerizable monomers of formula (II). R = Z -Y -(A )m-Y -M -Y -(A )n-Y -; R = H, 1-12C alkyl, 1-12C alkylcarbonyl, aryl, arylcarbonyl or Z -Y -(A )o-Y -M -Y -(A )p-Y -; R = H, 1-12C alkyl, aryl or OR ; R = H, 1-12C alkyl, aryl or OR ; R , R = H, 1-12C alkyl, 1-12C alkylcarbonyl, aryl, arylcarbonyl or Z -Y -(A )q-Y -M -Y -(A )r-Y -; A -A = 1-30C spacer group; M -M = mesogenic group; Y -Y and Y -Y = bond, -O-, -S-, -C(=O)-, -C(=O)-O-, -O-C(=O)-, -CH=CH-C(=O)-O-, -O-C(=O)-O-, -C(=O)-N(R)-, -(R)N-C(=O)-, -CH2-O-, -O-CH2-, -CH=N-, -N=CH- or -N=N-; Y , Y = bond, -C(=O)-, -O-C(=O)-, -CH=CH-C(=O)-, -(R)N-C(=O)-, -CH2- or -O-CH2-; R = H or 1-4C alkyl; Z -Z = H, 1-12C alkyl, polymerizable group or a residue containing a polymerizable group; and m-t = 0 or 1.

    38.
    发明专利
    未知

    公开(公告)号:DE50102665D1

    公开(公告)日:2004-07-29

    申请号:DE50102665

    申请日:2001-12-01

    Applicant: BASF AG

    Abstract: The use of chiral, uncharged metal compounds containing two tridentate ligands with mesogenic groups, spacer groups and other groups as dopants for liquid crystalline materials. The use of chiral, uncharged compounds of formula (Ia) or (Ib) as dopants for liquid crystalline (LC) materials. ((P -Y -A -Y M -Y -)nL)2Me (Ia) ((P -Y -A -Y -M -Y -)nL)Me(L'(-Y -M -Y -A -Y -P )n')m (Ib) P , P = H, 1-12C alkyl, polymerizable groups, groups suitable for polymerization, or residues bearing such polymerizable groups; Y -Y = single bonds, -O-, -S-, -CO-, -COO-, -OCO-, -CONR-, -NRCO-, -OCOO-, -OCONR-, -NRCOO- or -NRCONR-; R = H or 1-4C alkyl; A , A = 1-30C spacer groups; M , M = mesogenic groups; n, n' = 0 or 1; m = 1, 2 or 3; Me = a transition metal of Period 4, 5 or 6 (other than technetium, silver, cadmium, gold, mercury or lanthanides) or a Main Group 14 element (other than carbon or lead); L = a tridentate ligand of formula (II); U, V, W = nitrogen-, phosphorus- or sulfur-containing groups with N, O, P or S atoms with free electron pair(s) for coordination with the central metal atom (Me); b1, b2 = 2-3C alkylene bridges attached to U and V or V and W, optionally substituted with up to two 1-12C organic residues in the case of 2C bridges and up to 4 such residues in other cases, and in which 2 adjacent carbon atoms may form part of an optionally substituted, optionally anellated benzene ring; L' = a 1-12C organic group. The groups L'(Y -M -Y -A -Y -P )n' in formula (Ib) may be different. Independent claims are also included for the following: (1) New compounds of formula (IIIa) and (IIIb). (2) LC materials containing compound(s) (Ia) and/or (Ib) or (IIIa) and/or (IIIb). ((P -Y -A -Y M -Y -)L)2Me (IIIa) ((P -Y -A -Y -M -Y -)L)Me(L'(-Y -M -Y -A -Y -P )n')m (IIIb) n' = 0 or 1.

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