IP Library Granted Patent US 7,153,449
Granted Patent B2
US 7,153,449 · App. 10/311,395 · Granted Dec 26, 2006

Acidic treatment liquid and method of treating copper surfaces

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,153,449
App. No.
10/311,395
Granted
Dec 26, 2006
Kind
B2
Abstract

The present invention relates to a solution and to a method of treating copper surfaces, the copper surfaces being brought into contact with an acidic treatment liquid which contains hydrogen peroxide and at least one five-membered heterocyclic compound as well as additionally at least one microstructure modifying agent selected from the group comprising thioles A, disulfides B, sulfides C and thioamides D having the following respective general formulae: wherein R 1 and R 2 =alkyl, alkenyl, aryl, aralkyl, especially benzyl, cycloalkyl and the derivatives thereof and R 3 =R 1 , R 1 —O, R 1 —S, amino or substituted amino, wherein R 1 and R 2 may especially be phenyl or substituted phenyl.

Claims (29)

1. Acid treatment liquid for the treatment of copper surfaces comprising:

a. hydrogen peroxide and

b. at least one five-membered heterocyclic compound

wherein

c. additionally at least one microstructure modifying agent is contained, selected from the group consisting of organic thiols, organic disulfides and organic sulfides, wherein the organic sulfides have the general formula

 wherein

R 1 and R 2 =alkyl, alkenyl, aryl, aralkyl, cycloalkyl and the derivatives thereof.

2. Treatment liquid according claim 1 , wherein the organic thiols have the general formula

the organic disulfides have the general formula

wherein

R 1 and R 2 =alkyl, alkenyl, aryl, aralkyl, cycloalkyl and the derivatives thereof.

3. Treatment liquid according to any one of the preceding claims 1 – 2 , wherein R 1 and R 2 contain a group mediating the solubility of the microstructure modifying agent in an aqueous solution.

4. Treatment liquid according to claim 3 , wherein the functional group mediating the solubility of the microstructure modifying agent in an aqueous solution is selected from the group consisting of amino, carboxy and sulfo.

5. Treatment liquid according to any one of the preceding claims 1 – 2 , wherein the at least one five-membered heterocyclic compound is selected from the group consisting of tetrazole and the derivatives thereof.

6. Treatment liquid according to claim 5 , wherein the at least one five-membered heterocyclic compound is selected from the group consisting of 5-aminotetrazole and 5-phenyltetrazole.

7. Treatment liquid according to any one of the preceding claims 1 – 2 , wherein the at least one microstructure modifying agent is selected from the group consisting of L-cysteine, DL-cysteine, 2-aminoethanethiol, mercaptoacetic acid, 3-mercapto-propionic acid, 2-mercaptoethanesulfonic acid, 3-mercaptopropanesulfonic acid, L-cystine, DL-cystine, D-cystine, bis-(2-aminoethyl) disulfide, dithiodiacetic acid, 3,3′-dithiodipropionic acid, 4,4′-dithiodibutyric acid, 3,3′-dithio-bis-(propanesulfonic acid), thiodiacetic acid, 3,3′-thiodipropionic acid, 3,3′-thio-bis-(propanesulfonic acid), thiobenzamide as well as the salts thereof.

8. Treatment liquid according to any one of the preceding claims 1 – 2 , wherein at least one inorganic acid is contained.

9. Use of the acidic treatment liquid according to any one of the claims 1 to 2 for forming copper surfaces on printed circuit boards, the copper surfaces being suitable for the subsequent coating with plating resists, etch resists, solder masks and other dielectric films.

10. Method of treating copper surfaces comprising bringing into contact the copper surfaces with an acidic treatment liquid comprising

a. hydrogen peroxide and

b. at least one five-membered heterocyclic compound

wherein

c. additionally at least one microstructure modifying agent is contained, selected from the group consisting of organic thiols, organic disulfides and organic sulfides, wherein the organic sulfides have the formula

 wherein

R 1 and R 2 =alkyl, alkenyl, aryl, aralkyl, cycloalkyl and the derivatives thereof.

11. Method according to claim 10 , wherein the organic thiols have the general formula

the organic disulfides have the general formula

wherein

R 1 and R 2 =alkyl, alkenyl, aryl, aralkyl, cycloalkyl and the derivatives thereof.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Aug 18, 2022
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: ATOTECH DEUTSCHLAND GMBH & CO. KG (F/K/A ATOTECH DEUTSCHLAND GMBH); ATOTECH USA, LLC
Reel/Frame 061521/0103 →
SECURITY INTEREST Recorded Mar 18, 2021
From: ATOTECH DEUTSCHLAND GMBH; ATOTECH USA, LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 055650/0093 →
RELEASE OF SECURITY INTEREST Recorded Mar 18, 2021
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: ATOTECH DEUTSCHLAND GMBH; ATOTECH USA, LLC
Reel/Frame 055653/0714 →
SECURITY INTEREST Recorded Feb 1, 2017
From: ATOTECH DEUTSCHLAND GMBH; ATOTECH USA INC
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 041590/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 13, 2002
From: HAUF, UWE; FUERHAUPTER, HARRY; STIOP, ALEXEY; GRIESER, UDO
To: ATOTECH DEUTSCHLAND GMBH
Reel/Frame 013921/0697 →