Production of 4,4'-di:halo-di:phenyl-sulphone

    公开(公告)号:DE19726805A1

    公开(公告)日:1999-01-07

    申请号:DE19726805

    申请日:1997-06-24

    Applicant: BASF AG

    Abstract: A process for the production of 4,4'-dihalo-diphenyl- sulphones (DHDPSO) comprises reacting chloro-, bromo- or fluoro- benzenes with 4-halophenylsulphonyl chlorides of formula (I); in which X = chlorine, bromine or fluorine. The reaction is carried out in the liquid phase at elevated temperature in presence of solid catalysts with acid centres, comprising (K1) layer silicates with negative layer charges neutralised by protons and essentially not doped with Lewis acids, (K2) zeolites in the acidic H-form, or (K3) mixed oxides with acid centres, consisting of a combination of (a) oxides of titanium, zirconium, hafnium, tin, iron or chromium(III) with (b) oxides of vanadium, chromium(VI), molybdenum, tungsten or scandium, or sulphated or phosphatised oxides of group (a), such mixed oxides having been calcined at 450-800 deg C after combination. Preferably type (K1) comprises aluminium silicate in which part of the silicon is replaced by aluminium and/or part of the Al is replaced by magnesium, especially a montmorillonite. Type (K2) comprises zeolites of structural types MFI, MEL, BOG, BEA, EMT, MOR, FAU, MTW, LTL, NES, CON or MCM 22, especially 12-ring zeolites of the BETA, Y, EMT or mordenite type, or 10-ring zeolites of the pentasil type. Type (K3) may be super-acid mixed oxides, preferably with group (a) oxides and group (b) oxides in a mol ratio of (70:30)-(98:2). The process comprises reacting chlorobenzene (PhCl) with 4-chlorophenyl-sulphonyl chloride (ClPhSOCl) in a mol ratio of 1-100, preferably using excess PhCl, at 100-250 deg C and 1-50 bar, preferably at boiling pt. under normal or autogenous pressure. The catalyst is in the form of a solid bed, and the reaction may be carried out as a continuous process in which excess PhCl is returned to the reactor.

    Stable electro-optical and photonic devices with small optical loss, resistant to relaxation after orientation

    公开(公告)号:DE19639447A1

    公开(公告)日:1998-03-26

    申请号:DE19639447

    申请日:1996-09-25

    Abstract: In electro-optical and photonic devices with a functional layer of oriented, cross-linked non-linear optical (NLO) polymer between 2 buffer layers, the polymer is a polyadduct (I) containing a NLO grouping, derived from (a) NLO active compound(s) (II) containing cyanate (NC-O-) group(s) and (b) organic di- or polycyanate(s) (III). Also claimed is a method of making the devices. (II) is a mono- or di-cyanatophenyl substituted thiophene or thiazole (IIA), where n = 1 or 2; X = nitrogen (N) or methine (CR ); Y = a chemical bond, sulphur (S), sulphinyl (SO), sulphonyl (SO2), oxygen (O) or imino (NR ); R = hydrogen (H), fluorine (F), chlorine (Cl), bromine (Br), cyano (CN), nitro (NO2), 1-10 carbon (C) alkyl, 3-6C cycloalkyl or 1-10C alkoxy; R = H, Cl, Br, CN, NO2, formyl (CHO), 2,2-dicyanovinyl (CH=C(CN)2) or a diazo group (N=N-D); R = N=N-G or amino (NQ Q ); R = H, CN, NO2 or 1-6C alkoxycarbonyl; R = H or 1-4C alkyl; D = the residue of a carbocyclic or heterocyclic diazo component; G = the residue of a coupling component; Q , Q = H, 1-10 C alkyl (optionally with ether O atom(s) in the chain and/or substituted by hydroxyl (OH), 1-4 C alkoxy or 1-8C alkoxycarbonyl), allyl, benzyl, phenylethyl or phenyl; or NQ Q = a heterocyclic group.

    2-Di:cyano-methylene-thiazole methine dyes, esp. useful in nonlinear optics

    公开(公告)号:DE4434990A1

    公开(公告)日:1996-04-04

    申请号:DE4434990

    申请日:1994-09-30

    Applicant: BASF AG

    Abstract: 2-Dicyanomethylene-thiazole methine dyes of formula (I) are new. In formula (I), R = H or an opt. substd. 1-10 C alkyl or phenyl gp.; X = N, CQ , CH-CQ -CH, CH=CH-CH=CH-CH or a gp. of formula (IIA) or (IIB), where Q = H, 1-4C alkyl, Cl or Br; Q = H or 1-4 C alkyl; and Y = the residue of the aniline, aminonaphthalene, indole, aminoquinoline, aminothiazole or aminothiophene series; with the proviso that x does not = CH if R = phenyl and Y = a residue of the aniline series. Also claimed are certain 2-dicyanomethylene-4-phenyl-thiazoles used as starting materials for (I). Pref. in (I), Y = the residue of the aminonaphthalene, aminoquinoline or esp. the aniline series; R = 1-6 C alkyl or phenyl, opt. substd. by OH or (meth)acryloyloxy; X = N, CH, CH-CH-CH or CH-CH-CH=CH-CH. (I) can be prepd. by well-known methods.(I) (where L = CQ , CH-CQ -CH, CH=CH-CH=CH or a (IIA) or (IIB) gp.) can be prepd. by reacting an aldehyde Y-L=O with a 2-dicyanomethylene-4-R-substd.-thiazole (III). (I) (where L = N) can be prepd. by condensation of nitroso cpds. of the formula Y-NO or oxidative coupling of amino cpds. of the formula Y-NH2 with (III). (III), including (IIIA), are prepd. by reacting ketones of the formula Hal-CH2-CO-R (hal = halogen) with NH4CNS and malodinitrile. (I) and (III) (R = hydroxyphenyl), including (IIIA; W = H can be prepd. by aq. alkaline hydrolysis of the substd. cpds. (R = alkanoyl-oxyphenyl), including (IIIA; W = 1-6 C alkanoyl).

    Hyper-polarisable fluorescent di:oxa:borin(s) with good polymer compatibility

    公开(公告)号:DE19532828A1

    公开(公告)日:1996-03-21

    申请号:DE19532828

    申请日:1995-09-06

    Applicant: BASF AG

    Abstract: Dioxaborins (I) of formula (A) are new. R = CH=(CH-CH=)qCH-D (q = o, 1, 2, 3 or 4); p = 1, 2 or 3; L , L = halogen or 1-6C alkoxy, or L L = a gp. of formula (IIA), (IIB) or (IIC): n = 0, 1 or 2; Y , Y = H, Me, -CH2OH or -CH(OH)-CH2OH; Y , Y = H or -CH2OH; Z , Z = H or 1-6C alkyl; D = a gp. of formula (IIIA), (IIIB), (IIIC) or (IIID): R , R = H, opt. substd. 1-8C alkyl, opt. with 1 or 2 ether O atoms in the chain, 3-4 C alkenyl, 5-7 C cycloalkyl, phenol or tolyl; or NR R = a 5-6 membered satd. heterocyclic gp., opt. contg. other heteroatoms; R = 1-8 C alkyl; A = a mono- to tri-valent gp. derived from a benzene of formula (IV): ring K may be benzoannelated; X = 1-6 C alkyl, 1-6 C alkoxy, 1-6 C alkoxythio, CN, CHO, NO2, halogen or N(R )3An ; An = the equiv. of an anion; if p = 1, A may also = 5-halothien-2-yl; and if p = 2 or 3, X may also = H.

    40.
    发明专利
    未知

    公开(公告)号:DE4416476A1

    公开(公告)日:1995-11-16

    申请号:DE4416476

    申请日:1994-05-10

    Applicant: BASF AG

    Abstract: The invention pertains to thiophenes of the formula (I), where n is 2 to 6; L and L are hydrogen, optionally substituted C1-C10 alkyl, C3-C7 cycloalkyl or phenyl, or L and L together with the connecting nitrogen atom represent a heterocyclic radical; X and Y are hydrogen, optionally substituted C1-C10 alkyl, C3-C7 cycloalkyl or phenyl; and Z is cyano, hydroxysulfonyl, C1-C10 alkoxycarbonyl, optionally substituted C1-C4 alkylsulfonyl, optionally substituted phenylsulfonyl or a radical of the formula (a), where R is hydrogen or cyano and R and R are cyano, nitro, C1-C10 alkoxycarbonyl, optionally substituted C1-C4 alkylsulfonyl or optionally substituted phenylsulfonyl. The invention also relates to the use of said thiophenes in nonlinear optics, a method for the preparation of bithiophenes, and stannylthiophenes as their intermediates.

Patent Agency Ranking