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    • 2. 发明专利
    • DE19631864A1
    • 1998-02-12
    • DE19631864
    • 1996-08-07
    • BAYER AG
    • BERNETH HORST DRCLAUSSEN UWE DRKOSTROMINE SERGUEI DRNEIGL RALF DRRUEBNER JOACHIM DRRUHMANN RALF DR
    • C09K3/00C07C245/08C07C255/50C07C255/54C07C255/65C07C311/37C08F20/10C08F20/52C08F246/00C09K19/38G11B7/24G11B7/25C08L101/12C08L33/08C08L33/10
    • Photoaddressable polymers have a main chain as backbone and covalently attached lateral groups of formula -S -T -Q -A (I) and -S -T -Q -M (II), in which S , S = O, S or NR ; R = H or 1-4C alkyl; T , T = (CH2)n, optionally with in-chain -O-, -NR - or -OSi(R )2O- and/or optionally substituted with methyl or ethyl; Q , Q = direct single bond, O, COO, OCO, CONR , NR CO or NR ; or in which S T Q or S T Q = a piperazine-1,4-diyl group; A = a unit which is able to absorb electromagnetic radiation; M = a mesogenic, dimensionally anisotropic unit; n = 2-12. A has a linear absorption coefficient DELTA DELTA E of more than 0.2, measured on a compound of formula A-Q H or A-Q T S H from 6 separate measurements, in which two measurements are made in each case at the long-wave edge of the absorption curve with (A) the compound at the lowest possible concentration in a solvent of the lowest possible polarity, (B) the standard at the highest possible concentration in the same solvent and (C) compound and standard at concentrations as above in the same solvent. One measurement is taken at the wavelength (L) at which the absorption value of curve (C) is 0.8, and one at L + 50 nm; this gives the three absorption differences DELTA E = EL - EL+50 for the constituents (A)-(C) and hence the three values DELTA EA, DELTA EB and DELTA EC, from which is obtained the required difference DELTA DELTA E = DELTA EC - ( DELTA EB + DELTA EA). Also claimed are 6 compounds of formula A-Q -T -S -R, in which R = H, -OC-CH=CH2, -OC-CMe=CH2, -(CH2)n-OH, -CH2-CHOH-CH3 or -CHMe-CH2OH, and (meth)acrylates of the last three of these compounds.
    • 3. 发明专利
    • DE4434966A1
    • 1996-04-04
    • DE4434966
    • 1994-09-30
    • BAYER AG
    • BIERINGER THOMASGESNER UWEHAARER DIETRICH PROF DRRUEBNER JOACHIM DRWUTTKE ROLAND DRCLAUSSEN UWE DR
    • G03C1/73C08F20/22C08F20/30C08F20/34C08F20/38C08F220/34C08F220/36C08F220/38C09K19/38G02B1/04G11B7/244G11B7/246G11B7/2467G11B7/253C08F220/10C08F220/26
    • Polymers with a poly(meth)acrylate main chain and side chains of formula (I) and (II) are claimed. In the formulae: S and S = O, S or NR1 (with R1 = H, 1-6C alkyl or Ph); T and T = -(CR1R12)n-, opt. with in-chain -O-, -S-, -NR1- or -OSi(R1)2O- (with n = 2-12); Q and Q = -O-, -COO-, -OCO-, -CONR1-, -NR1CO-, -NR1-, -O-Phe-COO- or -O-Phe-CONR1- (with Phe = C6H4); or the combinations S T Q and/or S T Q may also represent a ring of formula (a); R2-R6 = H, halogen, 1-4C alkyl or alkoxy, CF3, nitro, -SO2Me, -SO2NH2 or CN; at least one of these gps. must not be H; R7-R9 = H, 1-6C alkyl, alkoxy, alkylthio, alkylsulphonyl or alkylaminocarbonyl, OH, -OPh, -SPh, halogen, CF3, CCl3, CBr3, nitro, CN, phenylsulphonyl, -COOR1, aminosulphonyl, phenylaminosulphonl, aminocarbonyl or phenylaminocarbonyl; R10 = H, halogen, 1-6C alkyl or alkoxy, OH, OPh, or 1-4C alkylamino or alkylsulphonylamino; R11 = H, halogen, 1-6C alkyl or alkoxy, OH or OPh; Y = direct bond, -COO-, -OCO-, -CONH-, -NHCO-, -O-, -NH-, -NMe- or -N=N-; X and X = H, OH, SH, CF3, CCl3, CBr3, halogen, CN, nitro, COOR1, 1-6C alkyl, alkylsulphonyl, alkylaminosulphonyl or alkylaminocarbonyl, 5-12C cycloalkyl, 1-12C alkoxy or alkylthio, 6-12C aryl, aryloxy, arylthio or arylsulphonyl, aminosulphonyl, phenylaminosulphonyl, aminocarbonyl, phenylaminocarbonyl, -NR12R13, -NHCOR12, -NHSO2R12, -NHCONR1R2, -NHCOOR12 or -SO2CF3; R12 and R13 = H, 1-4C alkyl or Ph; if R7-R11 = H and ring B is substd. with 1-4C alkyl or alkoxy, nitro or CN, at least one second substit. is present in the system (ring A)-Y-(ring B).