会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 57. 发明专利
    • DE1643063B1
    • 1972-03-16
    • DE1643063
    • 1967-04-08
    • STUDIENGESELLSCHAFT KOHLE MBH
    • WILKE GUENTHER PROF DIPL-CHEMHEIMBACH PAUL DIPL-CHEM DRBRENNER WOLF-BERND DIPL-CHEM D
    • C07C2/44B01J31/00C07C1/00C07C2/46C07C13/06C07C67/00C07C3/10
    • 1,214,513. Dimerizing dienes; cyclobulane derivatives. STUDIENGESELLSCHAFT KOHLE m.b.H. 27 March, 1968 [8 April, 1967], No. 14628/68. Heading C5E. 1,3 - Dienes are cylodimerized by contact with a catalyst prepared by either (1) mixing a reducible nickel compound with an electron donor and a metal, metal hydride or halogenfree organometallic compound, having in each case a reducing action on the nickel compound, or (2) mixing a nickel complex compound containing zero-valent nickel with an electron donor. The cyclodimerization is conducted under conditions resulting in incomplete conversion of the diene. Suitable catalysts are formed from these components: nickel acetylacetonate / diethyl aluminium ethoxyl / tri- (o - phenyl - phenyl) phosphite (i.e. type 1), and bis (cyclooctadienyl) nickel / tri - (o - phenylphenyl) phosphite (i.e. type 2). In examples: (1-5, 8, 11 - 12) butadiene yields mainly cis-divinylcyclobutane and cyclooctadiene; (6 and 7) butadiene yields the same plus 4-vinylcyclohexene; (9) piperylene yields mainly dimethylcyclooctadiene and a mixture of the novel compounds 1,2 - cis - divinyl - 3,4 - dimethylcyclobutane and 1 - propenyl - 2 - vinyl- 3 - methyl - cyclobutane; and (10) a butadiene/ 2-butyne mixture yields mainly cis-divinylcyclobutane, cyclooctadiene, and dimethylcyclodecatriene.
    • 58. 发明专利
    • PROCESS FOR THE CATALYTIC DIMERISATION OF 1,3-DIOLEFINS
    • GB1214513A
    • 1970-12-02
    • GB1462868
    • 1968-03-27
    • STUDIENGESELLSCHAFT KOHLE MBH
    • C07C2/44B01J31/00C07C1/00C07C2/46C07C13/06C07C67/00
    • 1,214,513. Dimerizing dienes; cyclobulane derivatives. STUDIENGESELLSCHAFT KOHLE m.b.H. 27 March, 1968 [8 April, 1967], No. 14628/68. Heading C5E. 1,3 - Dienes are cylodimerized by contact with a catalyst prepared by either (1) mixing a reducible nickel compound with an electron donor and a metal, metal hydride or halogenfree organometallic compound, having in each case a reducing action on the nickel compound, or (2) mixing a nickel complex compound containing zero-valent nickel with an electron donor. The cyclodimerization is conducted under conditions resulting in incomplete conversion of the diene. Suitable catalysts are formed from these components: nickel acetylacetonate / diethyl aluminium ethoxyl / tri- (o - phenyl - phenyl) phosphite (i.e. type 1), and bis (cyclooctadienyl) nickel / tri - (o - phenylphenyl) phosphite (i.e. type 2). In examples: (1-5, 8, 11 - 12) butadiene yields mainly cis-divinylcyclobutane and cyclooctadiene; (6 and 7) butadiene yields the same plus 4-vinylcyclohexene; (9) piperylene yields mainly dimethylcyclooctadiene and a mixture of the novel compounds 1,2 - cis - divinyl - 3,4 - dimethylcyclobutane and 1 - propenyl - 2 - vinyl- 3 - methyl - cyclobutane; and (10) a butadiene/ 2-butyne mixture yields mainly cis-divinylcyclobutane, cyclooctadiene, and dimethylcyclodecatriene.
    • 59. 发明专利
    • BE713167A
    • 1968-08-16
    • BE713167D
    • 1968-04-03
    • C07C2/44B01J31/00C07C1/00C07C2/46C07C13/06C07C67/00
    • 1,214,513. Dimerizing dienes; cyclobulane derivatives. STUDIENGESELLSCHAFT KOHLE m.b.H. 27 March, 1968 [8 April, 1967], No. 14628/68. Heading C5E. 1,3 - Dienes are cylodimerized by contact with a catalyst prepared by either (1) mixing a reducible nickel compound with an electron donor and a metal, metal hydride or halogenfree organometallic compound, having in each case a reducing action on the nickel compound, or (2) mixing a nickel complex compound containing zero-valent nickel with an electron donor. The cyclodimerization is conducted under conditions resulting in incomplete conversion of the diene. Suitable catalysts are formed from these components: nickel acetylacetonate / diethyl aluminium ethoxyl / tri- (o - phenyl - phenyl) phosphite (i.e. type 1), and bis (cyclooctadienyl) nickel / tri - (o - phenylphenyl) phosphite (i.e. type 2). In examples: (1-5, 8, 11 - 12) butadiene yields mainly cis-divinylcyclobutane and cyclooctadiene; (6 and 7) butadiene yields the same plus 4-vinylcyclohexene; (9) piperylene yields mainly dimethylcyclooctadiene and a mixture of the novel compounds 1,2 - cis - divinyl - 3,4 - dimethylcyclobutane and 1 - propenyl - 2 - vinyl- 3 - methyl - cyclobutane; and (10) a butadiene/ 2-butyne mixture yields mainly cis-divinylcyclobutane, cyclooctadiene, and dimethylcyclodecatriene.