Substitution-type electroless gold plating solution containing purine or pyrimidine-based compound having carbonyl oxygen and substitution-type electroless gold plating method using the same

1. A substitution-type electroless gold plating solution comprising,

(A) a purine-based compound or a pyrimidine-based compound each having a carbonyl oxygen, as a localized corrosion inhibitor;

(B) a water-soluble gold compound;

(C) a complexing agent;

(D) a dicarboxylic acid as a conductivity improving agent;

(E-1) a nitrogen-containing heteroaryl carboxylic acid and (E-2) an α-hydroxycarboxylic acid as (E) a base metal elution and re-precipitation preventing agent, wherein the nitrogen in the heteroaryl carboxylic acid is located on a heteroaryl ring and are all shown as aromatic nitrogen; and

(F) a cyanide compound or a sulfite compound as a gold ion stabilizer,

wherein the carbonyl oxygen is contained in any one of the following chemical formulas a to c:

2. The solution of claim 1 , wherein the (A) purine-based compound or the pyrimidine-based compound each having carbonyl oxygen, as the localized corrosion inhibitor, is one or more selected from the group consisting of 2-amino-9H-purine-6(H)-one, 3,7-dihydro-purine-2,6-dione, 7,9-dihydro-1H-purine-2,6,8(3H)-trione, 5-methyl-pyrimidine-2,4(1H,3H)-dione, 2,4(1H,3H)-pyrimidine-dione, and 4-amino-1H-pyrimidine-2-one.

3. The solution of claim 1 , wherein the (B) water-soluble gold compound is one or more selected from the group consisting of, potassium gold (I) cyanide, potassium gold (III) cyanide, potassium gold (I) chloride, potassium gold (III) chloride, gold potassium sulfite, gold sodium sulfite, gold potassium thiosulfate, gold sodium thiosulfate, and a mixture thereof.

4. The solution of claim 1 , wherein the (C) complexing agent is one or more selected from the group consisting of, ethylene diamine tetraacetic acid (EDTA), diethylenetriamine pentaacetic acid (DTPA), triethylenetetramine hexaacetic acid, propane diamine tetraacetic acid, N-(2-hydroxyethyl)ethylene diamine triacetic acid, 1,3-diamino-2-hydroxypropane N, N, N′, N′-tetraacetic acid, bis-(hydroxyphenyl)-ethylenediamine diacetic acid, diaminocyclohexane tetraacetic acid, ethylene glycol-bis((β-aminoethyl ether)-N, N′-tetraacetic acid), N, N, N′, N′-tetrakis-(2-hydroxypropyl)-ethylenediamine, ethylenediamine, triethylenetetramine, diethylenetriamine, tetrakis(aminoethyl)ethylenediamine, a sodium, potassium or ammonium salt thereof, and a mixture thereof.

5. The solution of claim 1 , wherein the (D) dicarboxylic acid as the conductivity improving agent is one or more selected from the group consisting of oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, undecanoic acid, dodecanoic acid, 3,3-dimethylentanoic acid, cyclopentane dicarboxylic acid, cyclohexane dicarboxylic acid, and a mixture thereof.

6. The solution of claim 1 , wherein the (E-1) nitrogen-containing heteroaryl carboxylic acid is one or more selected from the group consisting of imidazole carboxylic acid, imidazole dicarboxylic acid, pyridine carboxylic acid, pyridine dicarboxylic acid, pyrimidine carboxylic acid, pyrimidine dicarboxylic acid, pyridazine carboxylic acid, pyridazine dicarboxylic acid, a pyrazine carboxylic acid, pyrazine dicarboxylic acid, and a mixture thereof.

7. The solution of claim 6 , wherein the (E-1) nitrogen-containing heteroaryl carboxylic acid is selected from the group consisting of imidazole-2-carboxylic acid, imidazole-4-carboxylic acid, imidazole-2,4-dicarboxylic acid, imidazole-4,5-dicarboxylic acid, pyridine-2-carboxylic acid (picolinic acid), pyridine-3-carboxylic acid (nicotinic acid), pyridine-4-carboxylic acid (isonicotinic acid), pyridine-2,3-dicarboxylic acid, pyridine-2,4-dicarboxylic acid, pyridine-2,5-dicarboxylic acid, pyridine-2,6-dicarboxylic acid, pyrimidine-3,4-dicarboxylic acid, pyrimidine-3,5-dicarboxylic acid, pyrimidine-2-carboxylic acid, pyrimidine-4-carboxylic acid, pyrimidine-5-carboxylic acid, pyrimidine-2,4-dicarboxylic acid, pyrimidine-2,5-dicarboxylic acid, pyrimidine-4,5-dicarboxylic acid, pyrimidine-4,6-dicarboxylic acid, pyridazine-3-carboxylic acid, pyridazine-4-carboxylic acid, pyridazine-3,4-dicarboxylic acid, pyridazine-3,5-dicarboxylic acid, pyridazine-4,5-dicarboxylic acid, pyrazine-2-carboxylic acid, pyrazine-2,3-dicarboxylic acid, pyrazine-2,5-dicarboxylic acid, pyrazine-2,6-dicarboxylic acid, and a mixture thereof.

8. The solution of claim 1 , wherein the (E-2) α-hydroxycarboxylic acid is one or more selected from the group consisting of glycolic acid, lactic acid, hydroxybutyric acid, hydroxyvaleric acid, hydroxypentanoic acid, hydroxycaproic acid, hydroxyheptanoic acid, malic acid, tartaric acid, citric acid, and a mixture thereof.

9. The solution of claim 1 , wherein the (F) gold ion stabilizer is a sulfite compound having a sulfite group (SO 3 2− ).

10. The solution of claim 1 , further comprising a (G) surface corrosion inhibitor and excluding the (A) localized corrosion inhibitor.

11. The solution of claim 10 , wherein the (G) surface corrosion inhibitor comprises an azole compound having one or more nitrogen atoms and two or more other elements in a 5-membered heterocycle.

12. The solution of claim 1 , further comprising (H) an other additive, wherein the other additive is one or more selected from the group consisting of, a surfactant, a crystallization modifier, a pH adjuster, and a buffer.

13. A substitution-type electroless gold plating method comprising,

preparing a substrate to be plated having a metal surface selected from copper or a copper alloy, and

bringing the substrate into contact with the substitution-type electroless gold plating solution according to claim 1 .