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Curable mixtures based on diglycidyl compounds and metal complex compounds

  • US 4,716,185 A
  • Filed: 01/16/1987
  • Issued: 12/29/1987
  • Est. Priority Date: 01/17/1986
  • Status: Expired due to Fees
First Claim
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1. A curable mixture, containing(a) at least one bisphenol diglycidyl ether based on bisphenol a, hydrogenated bisphenol A or bisphenol F,(b) as a curing catalyst, a colorless or slightly yellow solution of a metal complex compound of the formula I


  • space="preserve" listing-type="equation">[Me(H.sub.2 O).sub.x (Lm).sub.y ].sup.2+ (A.sup.⊖

    ).sub.2 (I),
in whichMe is a divalent metal from the group consisting of Zn, Cd, Sn, Pb, Ca or Mg,Lm is a saturated cyclic ether having 5 to 7 ring atoms, a linear or cyclic saturated aliphatic ether compound or a mixture of the ether and the ether compound, the ether and the ether compound having a boiling point of at least 60°

C., andA is an anion of the formula BF4.sup.⊖

, PF6.sup.⊖

, AsF6.sup.⊖

or SbF6.sup.⊖

,x is the number 4, 5 or 6 and y is zero or the number 1 or 2, the sum of x and y always being 6, the complex being dissolved in an excess of the corresponding ether or the corresponding ether compound,(c) a sterically hindered mononuclear or polynuclear phenol, a phosphite of the formula II or III ##STR3## in which R1, R2 and R3 independently of one another are each phenyl, alkyl-substituted phenyl having 1-12 carbon atoms in the alkyl radical or alkyl having 1 to 20 carbon atoms, or a mixture of a sterically hindered mononuclear or polynuclear phenol and a phosphite of the formula II or III and, optionally,(d) as a reactive diluent, up to 25 parts by weight, relative to 100 parts by weight of (a), of at least one diglycidyl ether of 1,4-butanediol, 1,6-hexanediol or neopentyl glycol or a cresol glycidyl ether and, optionally,(e) as an adhesion promoter, an organic silane, titanate or zirconate.

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