IP Library Granted Patent US 9,783,905
Granted Patent B2
US 9,783,905 · App. 14/585,228 · Granted Oct 10, 2017

Reaction products of amino acids and epoxies

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Quick Facts
Patent No.
US 9,783,905
App. No.
14/585,228
Granted
Oct 10, 2017
Kind
B2
Abstract

Reaction products of one or more amino acids and one or more epoxies are included in copper and copper alloy electroplating baths to provide good throwing power. Such reaction products may plate copper and copper alloys with good surface properties and good physical reliability.

Claims (18)

1. An electroplating composition comprising one or more sources of copper ions, an electrolyte, and one or more compounds consisting of a reaction product of one or more amino acid monomers and one or more polyepoxide monomers and optionally one or more heterocyclic nitrogen compound monomers.

2. The electroplating composition of claim 1 , wherein the one or more amino acid monomers are chosen from α-amino acids, β-amino acids and γ-amino acids.

3. The electroplating composition of claim 2 , wherein the one or more α-amino acid monomers are chosen from arginine, alanine, glycine, tryptophan, asparagine, lysine, histidine, tyrosine, glutamine, proline and salts thereof.

4. The electroplating composition of claim 1 , wherein a molar ratio of a moiety from the amino acid monomer to a moiety from the polyepoxide monomer ranges from 0.5:2-2:0.5.

5. The electroplating composition of claim 1 , wherein the one or more polyepoxide monomers have a formula:

wherein R 2 and R 3 may be the same or different and are chosen from hydrogen and (C 1 -C 4 )alkyl, A=OR 4 or R 5 ; R 4 ═((CR 6 R 7 ) m O), (aryl-O) p , CR 6 R 7 —Z—CR 6 CR 7 , or OZ′ t O, R 5 ═(CH 2 ) y , B is (C 5 -C 12 )cycloalkyl, Z=a 5- or 6-membered ring, Z′ is R 8 OArOR 8 , (R 9 O) b Ar(OR 9 ), or (R 9 O) b , Cy(OR 9 ), Cy=(C 5 -C 12 )cycloalkyl, R 6 and R 7 are independently chosen from hydrogen, methyl, or hydroxyl, R 8 represents (C 1 -C 8 )alkyl, R 9 represents a (C 2 -C 6 )alkyleneoxy, R 10 is a hydrogen atom, a formyl group, or one or two glycidyl ether groups each optionally containing a carbonyl group constituted by C 4 -C 8 and C 2 -C 4 , R 11 is a hydrogen atom, a methyl group or an ethyl group, and R 12 is a hydrogen atom, a formyl group, or one or two glycidyl ether groups each optionally containing a carbonyl group constituted by C 4 -C 8 and C 2 -C 4 , b=1-10, m=1-6, p=1-6, t=1-4 and y=0-6.

6. The electroplating composition of claim 1 , wherein the one or more polyepoxide monomers are chosen from 1,4-butanediol diglycidyl ether, ethylene glycol diglycidyl ether, diethylene glycol diglycidyl ether, triethylene glycol diglycidyl ether, glycerol diglycidyl ether, neopentyl glycol diglycidyl ether, propylene glycol diglycidyl ether, dipropylene glycol diglycidyl ether, poly(ethyleneglycol) diglycidyl ether and poly(propyleneglycol) diglycidyl ether.

7. The electroplating composition of claim 1 , wherein the one or more polyepoxide monomers are chosen from dicyclopentadiene dioxide and 1,2,5,6-diepoxycyclooctane.

8. The electroplating composition of claim 1 , wherein the one or more polyepoxide monomers are chosen from glycerin triglycidyl ether, trimethylolpropanetriglycidyl ether, diglycerol tetraglycidyl ether, erythritol tetraglycidyl ether, arabinose tetraglycidyl ether, triglycerol pentaglycidyl ether, fructose pentaglycidyl ether, xylitol pentaglycidyl ether, tetraglycerol hexaglycidyl ether, and sorbitol hexaglycidyl ether.

9. The electroplating composition of claim 1 , wherein the one or more amino acid monomers are chosen from aromatic compounds having a general formula:

X′—COOH  (I)

wherein X′ is a substituted six membered aromatic ring or a substituted six membered heterocyclic ring wherein the hetero-atom is nitrogen, and substituent groups are —NH 2 and optionally —OH.

10. The electroplating composition of claim 9 , wherein the one or more amino acid monomers is chosen from 4-aminobenzoic acid, 3-aminobenzoic acid, 2-aminobenzoic acid, 3,5-diaminobenzoic acid, 4-aminosalicylic acid and 5-aminosalicylic acid.

11. The electroplating composition of claim 9 , wherein the one or more amino acid monomers are chosen from 3-aminoisonicotinic acid, 4-aminonicotinic acid, 5-aminonicotinic acid, 2-aminonicotinic acid, 6-aminonicotinic acid, 2-aminoisonicotinic acid and 6-aminopicolinic acid.

12. The electroplating composition of claim 1 , wherein the one or more heterocyclic nitrogen compound monomers are chosen from imidazoles, triazoles, tetrazoles, pyrazines, benzimidazoles, benzotriazoles, purines, piperazines, pyridazines, pyrazoles, triazines, tetrazines and pyrimidines.

13. The electroplating composition of claim 1 , further comprising one or more sources of tin ions.

14. The electroplating composition of claim 1 , wherein the electrolyte is acidic.

15. The electroplating composition of claim 14 , wherein a pH of the electrolyte is ≦2.

Assignments (4)
SECURITY INTEREST Recorded Nov 3, 2025
From: QNITY ELECTRONICS, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 073515/0243 →
SECURITY INTEREST Recorded Nov 3, 2025
From: QNITY ELECTRONICS, INC.
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 073517/0298 →
CHANGE OF NAME Recorded Oct 29, 2024
From: ROHM & HAAS ELECTRONIC MATERIALS LLC
To: DUPONT ELECTRONIC MATERIALS INTERNATIONAL, LLC
Reel/Frame 069272/0383 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2015
From: NIAZIMBETOVA, ZUHRA I; RZEZNIK, MARIA ANNA
To: ROHM AND HAAS ELECRONIC MATERIALS LLC
Reel/Frame 035370/0404 →