IP Library Granted Patent US 6,930,136
Granted Patent B2
US 6,930,136 · App. 09/966,453 · Granted Aug 16, 2005

Adhesion promoters containing benzotriazoles

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Quick Facts
Patent No.
US 6,930,136
App. No.
09/966,453
Granted
Aug 16, 2005
Kind
B2
Abstract

Benzotriazole adducts contain a benzotriazole segment and a segment with a curable and polymerizable functionality, or an adhesion promoting functionality, particularly suitable for use on metal substrates or in adhesive, sealant or coating compositions for use in proximity to metal substrates.

Claims (39)

1. A benzotriazole adduct having the structure:

in which

n is 0, 1, 2, or 3;

E and E′ independently are an organic moiety containing vinyl, ether, vinyl silane, carbon to carbon double bond attached to an aromatic ring and conjugated with the unsaturation in the aromatic ring, epoxy, acetyl acetonate, fumarate, maleate, or maleimide functionality;

Z is hydrogen, hydrocarbyl, or an organic moiety containing electron donor, epoxy, acetyl acetonate, or electron acceptor excluding acrylate, functionality;

Z′ is hydrogen, hydrocarbyl, an electron donating group, or an electron withdrawing group,

L and L′ independently are a hydrocarbyl group, or a functionality selected from the group consisting of:

in which R is a hydrocarbyl group attached to the benzotriazole segment; and R′ is hydrogen, an aromatic, or an alkyl group of 1 to 6 carbon atoms, and

provided that if n is 0 for each of (E-L), (L-E), or (L′-E′), then Z is not hydrogen or alkyl; and

provided that if L or L′ is alkyl and E is a maleimide or a styrene group, then for (L-E) or (L′-E′), n must be more than 1, or for (E-L), n must be at least one.

2. The benzotriazole adduct according to claim 1 in which n is 0 for (E-L), (L′-E′) and for (OH), Z is hydrogen, Z′ is hydrogen; n is 1for (L-E), and L is not alkyl.

3. The benzotriazole adduct according to claim 1 in which n is 0 for (E-L), (L′-E′), and for (OH), n is 1 for (L-E), L is not alkyl, Z is an organic moiety containing electron donor, epoxy, vinyl, acetyl acetonate, or electron acceptor excluding acrylate, functionality; and Z′ is hydrogen.

4. The benzotriazole adduct according to claim 1 in which n is 0 for (E-L) and (L′-E′), n is 2 for (L-E), Z is hydrogen ; and Z′ is hydrogen.

5. The benzotriazole adduct according to claim 1 having the structure:

6. The benzotriazole adduct according to claim 1 having the structure:

7. A benzotriazole adduct having the structure:

in which

n is 0, 1, 2, or 3;

E and E′ independently are an organic moiety containing vinyl, ether, vinyl silane, carbon to carbon double bond attached to an aromatic ring and conjugated with the unsaturation in the aromatic ring, epoxy, acetyl acetonate, fumarate, maleate, or maleimide functionality;

Z is hydrogen, hydrocarbyl, or an organic moiety containing electron donor, epoxy, acetyl acetonate, or electron acceptor excluding acrylate, functionality;

Z′ is hydrogen, hydrocarbyl, an electron donating group, or an electron withdrawing group,

at least one of Z and Z′ cannot be hydrogen or alkyl;

L and L′ independently are a hydrocarbyl group, or a functionality selected from the group consisting of:

in which in which R is a hydrocarbyl group attached to the benzotriazole segment; and R′ is hydrogen, an aromatic, or an alkyl group of 1 to 6 carbon atoms.

8. A curable composition comprising a benzotriazole adduct, optionally a curing agent, and optionally a filler, the benzotriazole adduct having the structure

in which

n is 0, 1, 2, or 3;

E and E′ independently are an organic moiety containing vinyl ether, vinyl silane, carbon to carbon double bond attached to an aromatic ring and conjugated with the unsaturation in the aromatic ring, fumarate, maleate, maleimide, epoxy, vinyl, acetyl acetonate, (meth)acrylate, (meth)acryl amino, glycidyl, or siloxane functionality;

Z is hydrogen, hydrocarbyl, or an organic moiety containing electron donor, epoxy, vinyl, acetyl acetonate, (meth)acrylate, (meth)acryl amino, glycidyl, or siloxane functionality;

Z′ is hydrogen, hydrocarbyl, an electron donating group, or an electron withdrawing group,

L and L′ independently are a hydrocarbyl group, or a functionality selected from the group consisting of:

in which R is a hydrocarbyl group attached to the benzotriazole segment; and R′ is hydrogen, an aromatic, or an alkyl group of 1 to 6 carbon atoms.

9. A curable composition comprising a benzotriazole adduct, optionally a curing agent, and optionally a filler, the benzotriazole adduct having the structure

in which

E and E′ independently are an organic moiety containing vinyl ether, vinyl silane, carbon to carbon double bond attached to an aromatic ring and conjugated with the unsaturation in the aromatic ring, fumarate, maleate, maleimide, epoxy, vinyl, acetyl acetonate, (meth)acrylate, (meth)acryl amino, glycidyl, or siloxane functionality;

Z is hydrogen, hydrocarbyl, or an organic moiety containing electron donor, electron acceptor, epoxy, vinyl, acetyl acetonate, (meth)acrylate, (meth)acryl amino, glycidyl, or siloxane functionality;

Z′ is hydrogen, hydrocarbyl, an electron donating group, or an electron withdrawing group,

L and L′ independently are a hydrocarbyl group, or a functionality selected from the group consisting of:

in which R is a hydrocarbyl group attached to the benzotriazole segment; and R′ is hydrogen, an aromatic, or an alkyl group of 1 to 6 carbon atoms.

Assignments (3)
CHANGE OF NAME Recorded Dec 3, 2008
From: HENKEL KGAA
To: HENKEL AG & CO. KGAA
Reel/Frame 022309/0718 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 19, 2008
From: NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CORPORATION; INDOPCO, INC.
To: HENKEL KGAA
Reel/Frame 021912/0634 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2002
From: MUSA, OSAMA M.; KUDER, HARRY RICHARD
To: NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CORPORATION
Reel/Frame 012462/0054 →