US3765936A - Electroless copper plate - Google Patents

Abstract

An electroless copper deposit from a plating solution comprising a source of cupric ions, hydroxyl radicals, formaldehyde or a formaldehyde precursor, preferably paraformaldehyde, and a complexing agent for copper which solution is characterized by the addition of at least two members selected from the group consisting of a formaldehyde addition agent, a solution soluble salt of a Group VIII metal of the Periodic Chart of the Elements, and an organic silicon compound. The copper plate deposited from the preferred solution is alloyed with the Group VIII metal cation and is distinguishable from prior art electroless copper deposits by substantially improved bending or tensile properties and a smoother, more highly reflecting surface appearance.

Description

United States Patent [191 Shipley, Jr. et al.

ELECTROLESS COPPER PLATE Inventors: Charles R. Shipley, Jr.; Lucia H.

Shipley; Michael Gulla, all of Newton; Oleh B. Dutkewych, Medfield, all of Mass.

Shipley Company, Inc., Newton, Mass.

Filed: Aug. 23, 1971 Appl. N0.: 174,198

Related US. Application Data Continuation-in-part of Ser. No. 752,250, Aug. 13, 1968, Pat. No. 3,615,735.

Assignee:

References Cited UNITED STATES PATENTS l0/l969 Dutkewych 106/1 Oct. 16, 1973 3,134,690 5/1964 Ericksson l l7/47 A 3,326,700 6/1967 Zeblisky 106/1 3,615,735 10/1971 Shipley et al, 106/1 Primary Examiner-Lorenzo B. Hayes Attorney-Sewall P. Bronstein et al.

[5 7] ABSTRACT An electroless copper deposit from a plating solution comprising a source of cupric ions, hydroxyl radicals, formaldehyde or a formaldehyde precursor, preferably paraformaldehyde, and a complexing agent for copper which solution is characterized by the addition of at least two members selected from the group consisting of a formaldehyde addition agent, a solution soluble salt of a Group VIII metal of the Periodic Chart of the Elements, and an organic silicon compound. The copper plate deposited from the preferred solution is alloyed with the Group VIII metal cation and is distinguishable from prior art electroless copper deposits by substantially improved bending or tensile properties and a smoother, more highly reflecting surface appearance.

7 Claims, No Drawings 1 ELECTROLESS COPPER PLATE CROSS REFERENCE .TO RELATED APPLICATIONS This application is a continuation-in-part of U.S. Pat. application Ser. No. 752,250 filed Aug. 13, 1968 now U.S. Pat. No. 3,615,735.

BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to electroless metal deposits of improved appearance and bending or tensile properties.

2. Description of the Prior Art Electroless copper deposition refers to the chemical plating of copper over clean catalytically active surfaces by chemical reduction in the absence of an external electric current. Such processes and compositions useful therefor are known and are in substantial commercial use. They are disclosed in a number of prior art patents, for example, U.S. Pat. Nos. 2,938,805; 3,011,920; 3,310,430; and 3,383,224.

Known electroless copper deposition solutions generally comprise four ingredients dissolved in water. They are (l) a source of cupric ions, usually a copper salt, such as copper sulphate (2) a reducing agent such as formaldehyde, or preferably, aformaldehyde precursor such as paraformaldehyde, (3) hydroxide, generally an alkali metal hydroxide and usually sodium hydroxide, sufficient to provide the required alkaline solution in which said compositions are effective, and (4) a complexing agent for copper sufficient to prevent its precipitation in alkaline solution. A large number of suitable complexing agents are known and'described in the above cited patents, and also in U. S. Pat. Nos. 2,874,072; 3,075,856; 3,119,709; 3,075,855 and 3,329,512 all incorporated hereinby reference. Known electroless plating solutions of the above type usually provide a plate which, if mechanically dense and strong, is somewhat brittle such that it can withstand only limited bending or thermal stress without fracture. This is not a substantial disadvantage where the electroless plate is of the order of millionths of an inch in thickness and-is over-plated with ductile electrolytic copper. However, where the entire desired thickness, typically 1 to 3 mils in an electrical application, is provided by electroless plating, limited ductility is a serious limitation.

One means of improving the bending or tensile characteristics of an electroless copper plate is described in U. S. Pat. No. 3,257,215 which discloses the addition of a cyanide or sulphur compound to a copper plating solution. An additional means is described in U.S. Pat. I

No. 3,310,430 which discloses the addition to a copper plating solution of a water soluble compound of cyanide, vanadium, molybdenum, niobium, tungsten, rhenium, arsenic, antimony, bismuth, rare earth of the actinium series and rare earths of the lanthanum series. Certain membersof the above groups, especially the vanadium compounds, provide significantly improved rapid deposition of copper with rapid evolution of hydrogen gas at the surface, the improved ductility or bending characteristics are frequently sacrificed or lost.

An alternative means for improving the tensile properties of an electroless copper deposit while simultaneously improving brightness and other appearance properties is described in U. S. Pat. No. 3,475,186 incorporated herein by reference. Improved properties are obtained by the addition of an organic silicon compound to an electroless copper solution where silicon is believed to be the active agent. A major advantage of this system is that the rate of copper desposition does not substantially affect tensile or bending properties. The manner in which silicon compound improves tensile properties is not fully understood but is believed to be due, at least in part, to a surface effect resulting in deposition of a smoother deposit having fewer structural defects as will be explained in greater detail below. 7

STATEMENT OF THE INVENTION The subject invention is an improvement over that described in the above noted patents and provides an electroless deposit of improved bending or tensile properties. The copper deposit is from a solution characterized by the addition of at least two members selected from the group consisting of a formaldehyde addition agent, a Group VIII metal salt of the Periodic Chart of the Elements, and a solution soluble organic silicon compound. The addition of either a formaldehyde addition agent or a Group VIII metalsalt provides some improvement in tensile properties. Combination of the two provides an additive improvement in tensile properties. Combination of the two with a silicon compound provides a synergism that results in a substantial improvement in tensile properties. In addition to the above noted improvement in tensile properties, electroless copper deposits from the solutions of this invention provide the advantages of excellent lay down properties, excellent solderability and improved smoothness, brightness, and over-all appearance.

DESCRIPTION OF THE PREFERRED EMBODIMENTS A typical electroless copper solution in accordance with the invention will have additives having the following concentration ranges:

Preferred Copper salt 0.002 moles to saturation 0.02 to 0.12 moles Formaldehyde 0.05 to 3.5 moles 0.1 to 1 moles Complexing minimum necessary to about 1 to 3 times agent maintain copper in the moles of cupric solution ion Free Hydroxide sufficient to provide 0.1 to 0.8 moles pH 10 or greater Silicon compound greater than 1 ppm 5 to 250 ppm Formaldehyde up to that amount that 0.01 to 1 times the addition agent restricts deposition moles of formaldehyde Group VIII metal 5 to 2500 ppm 30 to 1000 ppm salt Water to 1 liter of solution to 1 liter of solution It should be understood that the above concentration ranges are preferred, but not critical. Variations in the ranges are possible without departing from the scope of the invention. In most cases, additives may be added in an amount up to that amount that poisons the solution.

In the above formulations, any water soluble copper salt' heretofore used for preparing electroless copper deposition solutions may be used. For example, the halides, nitrate, acetate, sulfate and other organic and inorganic acid salts of copper are generally suitable as is known in the art. Copper sulphate is preferred.

Suitable complexing agents for the copper ions are well-known in the art and include Rochelle salts, the sodium salts (mono-,di-,tri-, and tetrasodium salts) of ethylene diaminetetraacetic acid, nitrilotriacetic acid and its alkali metal salts, triethanolamine, modified ethylene diaminetraacetic acids such as N-hydroxyethylenediaminetriacetate, hydroxyalkyl substituted dialkylene triamines such as pentahydroxypropyl diethylenetriamine, sodium salicylate, and sodium tartrate. Other complexing agents for copper ions are disclosed in U.S. Pat. Nos. 2,996,408; 3,075,855; 3,075,856; and 2,938,805.

The preferred class of complexing agents are those described in U.S. Pat. No. 3,329,512 noted above. They include hydroxyalkyl substituted tertiary amines, corresponding to one of the following structures:

ROH and ROH where R is an alkyl group having from two to four carbon atoms, R is a lower alkylene radical and n is a positive integer. Examples of these complexing agents include tetrahydroxpropyl ethylene diamine, pentahydroxypropyl diethylene triamine, trihydroxypropylamine (tripropanolamine), trihydroxpropyl hydroxyethyl ethylene diamine, etc. As disclosed in said patent, the aforesaid amines are preferably used in small amounts in combination with other complexing agents and with certain polymers dispersed in solution such as cellulose ethers, hydroxyethyl starch, polyvinyl alcohol, polyvinylpyrrolidone, peptone, gelatin, polyamides and polyacrylamides.

The rate of copper deposition is, to some extent, dependent upon the selection of the complexing agent. Complexing agents such as pentahydroxypropyl diethylene triamine provide a fast rate of copper deposition,

usually in excess of 1.0 mil per hour. Though the cop per solutions of this invention provide copper deposits from solutions containing any of the known complexing agents for copper ions, they are particularly well adapted for copper solutions having complexing agents that provide a rapid rate of copper deposition.

The silicon additive is one that is soluble in the copper solutions and comprises the organic silicon com-' pounds disclosed in the above-noted U.S. Pat. No. 3,475,186. It should be noted that many silicon compounds are not fully soluble in aqueous alkaline solutions and many are considered insoluble. However, the solicon, for purposes of the present invention, is required in solution in parts per million and silicon compounds termed insoluble in aqueous solution usually are soluble to the extent of a few parts per million parts of solution and suitable for purposes of the present invention. For those silicon compounds considered insolpound will be required to provide the necessary concentration of silicon compound in solution.

Exemplary of the silicon compounds within the scope of the invention are the silanes, such as silane itself, disilane, tetramethylsilane, trimethylethylsilane, tetraethylsilane, tetraphenylsilane, dimethyldichlorosilane, etc., and low to intermediate molecular weight polysiloxanes, such as silicone fluids, gums, and resins substituted with methyl-, ethyl-, vinyl-, phenyl-, chloro-, bromo-, methoxy-, hydroxy-, etc. Other suitable organic silicon compounds are disclosed in the above noted U.S. Pat. No. 3,475,186.

The polysiloxanes are the least soluble silicon compounds in basic copper solutions, but are preferred because they provide the greatest increase in ductility and also enhance appearance by yielding a finer grained, more highly reflecting copper deposit. Of the polysiloxanes, the silicone fluids are most preferred. The solid polysiloxanes are preferably dissolved in a solvent such as alcohol and added to the copper solution.

Silicon codeposits with the copper in minor quantity, typically in amounts varying from as little as 1 part per million parts of the deposit to about 500 parts per million parts. The amount of codeposited silicon, though small, is believed to be significant in providing the improved deposits of this invention.

The formaldehyde addition agent for purposes of this invention is one that may be added to solution in amounts sufficient to undergo reaction with formaldehyde to form a relatively unstable formaldehyde adduct without poisoning the solution. Reactions of this nature and formaldehyde addition agents are well-known in the art and described in various publications, such as Formaldehyde" by J. Frederick Walker, Reinhold Publishing Company, Third Edition 1964, pages 219 to 221, included herein by reference.'Preferred formaldelyde addition agents are sulfites, bisulfites, and phosphites of a metal cation that does not codeposit with copper and preferably, an alkali metal cation. Preferred formaldehyde addition agents are sodium sulfite, potassium bisulfite, and sodium phosphite.

The formaldehyde addition agent and formaldehyde or preferably, paraformaldehyde are reacted with each other to form the adduct prior to addition to the remaining components of the copper solution.

The Group VIII metal salts are preferably water soluble inorganic salts of iron, cobalt, nickel, ruthenium, rhodium, palladium, osmium, iridium, and platinum; salts of iron, nickel, and platinum being most preferred and salts of palladium being least preferred due to solution stability problems caused by palladium. Suitable salts include phosphates, nitrates, halides, and acetates of the above metals. Iron, nickel and platinum to a greater extent and the remaining Group VIII metals to a lesser extent codeposit with copper to form a copper alloy. The Group VIII metal codeposits in a proportionally lesser amount relative to copper present in the A wetting agent may be added to solution in accordance with art recognized procedure.

The baths may be used at widely varying temperatures, c.g., at least room temperature and preferably up to about 140F. As temperature is increased, it is customary to find an increase in the rate of plating. Temperature is not highly critical, and within the usual operating range, excellent,- bright deposits of electroless copper having excellent tensile properties are obtained. Preferably, the bath is used without agitation.

In using the electroless copper solutions to plate metal, the surface to be plated should becatalytically active and free of grease and contaminating material. Where a non-metallic surface is to be plated, the surface area to receive the deposit must first be sensitized to render it catalytically active as by the well-known treatment with an acidic aqueous solution of stannous chloride followed by treatment with a dilute aqueous acidic solution of palladium chloride. Alternatively, extremely good sensitization of non-metallic surfaces is achieved by contact with an acidic colloidal formulation formed by the admixture of stannous chloride and a precious metal chloride, preferably palladium chloride, the stannous chloride being present in stoichiometric excess based upon the amount of precious metal chloride.

The invention will be better understood by reference to the following examples where all parts were plated using the following procedure:

a. Cut a phenolic substrate to a size of 2 X 2 inches.

b. Scrub part clean using an abrasive cleaner.

c. Rinse in cold water.

d. Immerse in a solution of a wetting agent identified as Shipley conditioner 1159 at room temperature for 1 to 3 minutes.

e. Rinse in cold water.

f. Immerse in a colloidal stannic acid-palladium catalyst (identified as Cuposit Catalyst 6F) maintained at room temperature for 1 to 5 minutes.

g. Rinse in cold water.

h. Immerse in Cuposit Accelerator 19 or a mild perchloric acid solution maintained at room temperature for 3 to minutes.

i. Rinse in cold water j. Immerse in electroless copper solution maintained at between 110 and 130F for a period sufficient to provide a deposit of desired thickness not to exceed 3 hours.

k. Dry parts and examine deposit for appearance and ductility. Ductility is determined by peeling a copper deposit from the substrate and bending it through 180 in one direction, creasing at the fold, then returning it to its original position with pressing along the crease to flatten it. This cycle constitutes one bend. The procedure is repeated-until the sample breaks at the crease. A sample unable to withstand at least one-half bend is considered brittle.

Water to 1 liter of solution The above formulation, with various additives, is used to deposit electroless copper. Additive composition and deposit properties are set forth in the following table.

Duc- Ex. Additives Additive Deposit Deposit tility No. concentraappearthickness (Bends) tion ance in. X10 1 control poor 0.50 brittle 2 M 300 ppm poor 0.37 brittle 3 Fe (SO 300 ppm poor 0.25 brittle 4 H PtCl 150 ppm poor 0.10 brittle 5 080 ppm fair 0.14 brittle 6 C080 300 ppm poor 0.36 brittle 7 Na SO; 8 g/ 1 poor 0.46 brittle 8 NaHSO 20 g/ 1 poor 0.43 brittle 9 ua n o -srno 20 g/l fair 0.45 brittle l0 F-l-3514 200 ppm fair 0.34 A 1 l methylvinyl- 250 ppm fair 0.87 v.

silane 12 SF-l 138" 200 ppm fair 0.46 h 13 F-1-3514 200 ppm fair 0.41 l

NaHSO 20 g/l I 14 methylvinylsilane 250 ppm fair 0.42 1 NaHSO 20 g]! 15 F-1-3514" 200 ppm unstable I-bPtCl ppm 0.38 1 l6 methylvinylsilane 250 ppm good 0.22 k H PtCl 150 ppm 17 F-1-3514' 200 ppm good 0.18

H PtCl 150 ppm NaHSO 20 g/l 18 methylvinylsilane 250 ppm good 0.39 5 H PtCl 150 ppm NaI-ISO 20 g/l 19 SF-l 138 200 ppm good 0.41 2

050 100 ppm NaHSO 20 g/l 20 SF-l138 200 ppm good 0.35 3

M80, 300 ppm NaHPO -5 H 0 20 g/l F-1-35l4 A sinicone fluid believed to be a dimethylpoly-siloxaneethylene glycol copolymer available from the General Electric Co. SF-1138 A silicone fluid believed to be a dimethylpoly-siloxanepolyalkylene oxide copolymer available from the General Electric Company.

In the above examples, a deposit was considered poor if it was dark in color and powdery in appearance. A fair deposit was one lighter in color though powdery in appearance. A good deposit was one having a fine grained metallic copper appearance.

The improvements in tensile properties using the preferred electroless copper solutions of the present invention are readily apparent by reference to the above examples. Examples 2 to 6 illustrate copper containing only a Group VIII metal salt. Examples 7 to 9 illustrate copper solutions containing only a formaldehyde addition agent. No recordable improvement in properties is apparent using either of these additives in the above copper solution. Examples 10 to 12 illustrate the use of a silicon compound and show some improvement in both appearance and tensile properties. The combination of a silicon compound with either a Group VIII metal salt or a formaldehyde addition agent (Examples 13 to 16) provides a somewhat greater improvement. Combination of the silicon compound with both a formaldehyde addition agent and a Group VIII metal salt (Examples 17 to 20) provides substantial improvement in tensile properties as evidenced by the ductility in all cases in excess of 2 bends and in some cases, as high as 5 bends.

EXAMPLES 21-28 pentahydroxypropyldiethylenetriamine 20.0 gm water to 1 liter of solution The above formulation, with various additives, is

EXAMPLE 29 a. CuSO -H,O 8.0 gm b. Paraformaldehyde 7.5 gm c. NaOH (25% solution by weight) 50.0 ml

d. trihydroxypropylhydroxyethyl ethylene diamine 20.0 gm

e. SF-1138 200 ppm f. M80, 300 ppm g. NaHSO, '20 gm h. Water to 1 liter of solution Electroless copper deposited from the above solution was bright and withstood 3 1/2 bends. Copper deposited from a control solution free of additives e,f and g had a poor appearance and was brittle.

EXAMPLE 30 a. CuSOrSl-LO 8.0 gm 0. Paraformaldehyde 7.5 gm c. NaOl-l(25% solution by weight) 50.0 ml d. Tetrahydroxypropylethylene diamine 15.0 gm e. SF-1138' 200 ppm f. NiSO 300 ppm g. NaHSO, 20 gm h. Water to 1 liter of solution Copper deposited from the above solution was bright in color and capable of withstanding in excess of five bends. Copper deposited from a solution free of additive e,f and g was found to be brittle.

EXAMPLES 31-38 CuSO;-5H,O 8.0 gm Paraformaldehyde 7.5 gm

NaOH (25% solution by weight) 50.0 ml Ethylenediaminetetraacetic acid 25.0 gm Tetrahydroxypropylethylene diamine 6.0 gm

Water to 1 liter of solution The above formulation, with various additives was used to deposit electroless copper. Additive composiused to deposit electroless copper. Additive composi- 5 tion and deposit properties is set forth in the following table:

Duc- EX. Additive Additive Deposit Deposit tibility No. Concentra- Appear- Thickness Bends tion ance in. X" 10 21 control poor 0.30 brittle 22 SF-1138 200 ppm good 0.34 n 23 NiSO 300 ppm poor 0.46 A 24 NaHSO, 20 g/l fair 0.43 v= 2s SF-1138 200 ppm fair 0.15 as NiSO 300 ppm 26 81 -1138 200 ppm good 0.30 A

Natuso gll 27 Niso, 300 ppm fair 0.41 v.

NaHSO 20 g/l 28 SF-1l38 200 ppm good 0.025 3 Manse, 20 g/l NiSO, 300 ppm tion and deposit properties are set forth in the following table:

' Duc- Ex. Additive Additive Deposit Deposit tility No. concentraappearthickness (Bends) tion ance in. X10" 3 1 control poor 0.35 brittle 32 SF-1l38 200 ppm fair 0.15 l y: 33 M80, 300 ppm poor 0.32 l 34 Nal-ISO, 20 g/l poor 0.33 1 35 SF-1138 200 ppm fair 0.18 3

M80, 300 ppm 36 SF-1138 200 ppm fair 0.24 1 37 NiSO, 300 ppm poor 0.27 brittle NaHSO 20 g/l 38 SF-1138 ppm fair 0.19 4 54 NiSO, 100 ppm Nal-lSO; 20 g/l Each additive, alone or in combinations of two, increased ductility substantially. However, the combination of the three additives (Example 38) provided a substantially greater increase in ductility.

EXAMPLE 39 a. CuSOySl-LO 8.0 gm b. Paraformaldehyde 7.5 gm c. NaOH (25% solution by weight) 50.0 ml d. Sodium/potassium tartrate 25.0 gm e. Pentahydroxypropyldiethylene 6.0 gm triamine f. SF-1138 200 ppm g NiS04 300 ppm h NaHSO 20 g/l 1 Water to 1 liter of solution Copper deposited from the above solution was bright and withstood in excess of five bends. Copper deposited from the same solution free of additives f, g and h was found to be brittle.

EXAMPLES 40-47 CuSOySlfiO 8.0 gm Paraformaldehyde 7.5 gm NaOl-l (25% solution by weight) 50.0 ml Sodium/potassium tartrate 40.0 gm Water to 1 liter of solution The above formulation, containing various additives,

was used to deposit electroless copper. Additive composition and deposit properties are set forth in the following table:

Duc- Ex. Additive Additive Deposit Deposit tibility No. Concentra- Appearthickness (Bends) tion ance in. X10 40 control fair 0.06 1/2 41 F-1-3514 200 ppm fair 0.10 5 42 M80, 300 ppm fair 0.09 3 43 Nal-lSO, 20 g/l fair 0.09 l 44 F-l-3514 200 ppm good 0.13 3

NiSO 300 ppm 1 45 F-1-3514' 200 ppm good 0.09 5

Nal-lSO, 20 g/l 46 NiSO, 300 ppm good 0.34 1 H2 Nal-lSO 20 g/l 47 F-l-3514 200 ppm good 0.24 5

NiSO 300 ppm NaHSO, 20 g/l In the particular copper solution used, the addition of any additive alone was effective. However, use of the silicon compound in combination with the nickel sulfate and the sodium hyposulfite produced a substantial improvement in ductility. In Example 47, there was no indication of fracture of the copper deposit following the fifth bend.

EXAMPLES 48-54 CuSO;I-l,0 8.0 gm Paraformaldehyde 7.5 gm NaOl-I (25% solution by weight) 50.0 ml Tetrahydroxypropylethylene diamine 12.0 gm Triisopropanolamine 2.0 gm

Water to 1 liter of solution The above formulation containing various additives was used to deposit electroless copper. Additive compositions and deposit properties are set forth in the following table:

Duc- Ex. Additive Additive Deposit tibility No. Concentraappear- (Bends) tion ance 48 control poor brittle 49 F-68" 350 ppm fair H2 50 R68 350 ppm good l/2 SF-l I38 200 ppm 5l F 68 350 ppm good 5 SF-l 138 200 ppm NaHSO 20 g/l' M80, 300 ppm 52 F-68 350 ppm good 5 SF-l 1318 200 ppm NaHSO 20 g/l H PtCl 150 ppm 53 R68 350 ppm good 4 SF-1133 200 ppm NaHSO 20 g/l CoSO 300 ppm 54 R68 350 ppm good 3 SF-l 138 200 ppm NaI-ISO; 20 g/l FE: (S0,), 300 ppm I -68. A wetting agent EXAMPLE 55 CuSO '5l-I,O 8.0 gm Formaldehyde 7.5 gm NaOl-I (25% solution by weight) 50.0 ml Tetrahydroxypropylethylene diamine 12.0 gm Triisopropanolamine 2.0 gm SF-l 138 200 ppm NiSO 300 ppm I-I,PtCl 150 ppm Natl-ISO, 20 g/l Water to 1 liter of solution The electroless copper deposited from the above formulation was capable of withstanding in excess of five bends.

Deposits from representative examples were analyzed for the codeposition of the Group VIII metal cation with results as set forth in the following table:

Ex. No. Cu Cone. (96) Ni Conc. (96) Pt. Conc. (36) 17 97.85 1.83 47 98.65 0.l70 5l 99.35 0.056 55 97.07 0.036 2.48

From the above table, it can be seen that the Group VIII metal codeposits with copper to form an alloy.

Copper solutions of this invention find utility for all purposes for which electroless copper solutions have heretofore been used including both decorative and industrial applications. They are especially useful for the formation of printed circuit boards where the deposits act as ductile conductors and as ductile connectors plated onto the walls of through-holes. The formation of a printed circuit board having conductive throughholesis illustrated in the following example.

EXAMPLE 56 a. Sandblast one side of a phenolic substrate leaving the second surface smooth.

b. Drill through-holes at desired locations.

c. Silk screen a reverse image of a printed circuit pattern onto the roughened surface of the phenolic substrate using an epoxy resin.

d. Immerse in a colloidal palladium sensitizing solution maintained at room temperature for a period of five minutes.

e. Immerse in a stripping solution comprising 10 grams of copper chloride, grams of 37 percent hydrochloric acid and water to one liter maintained at room temperature for 6 minutes.

f. Deposit electroless copper of Example 18 with copper deposition taking place on the walls of the throughholes and on the roughened surfaces in the image pattern. No copper deposition takes place on the epoxy resist or on the smooth sides of the plastic laminate.

It should be understood that various changes may be made in the embodiments described above without departing from the spirit and scope of the invention as defined by the following claims.

We claim:

1. An article of manufacture comprising a catalytic substrate plated with ductile copper produced by contacting said substrate with an electroless copper plating solution comprising a source of cupric ions, hydroxyl radicals, formaldehyde, sufficient complexing agent to render said cupric ions soluble in alkaline solution and a combination of at least two members of the group consisting of an organic silicon compound, a formaldehyde addition agent and a Group VIII metal salt of the Periodic Chart of the Elements, said organic silicon compound being present in solution in an amount such that the codeposited silicon varies between I and 500 parts per million parts of the deposit, said Group VIII metal being present in solution in an amount such that the codeposited Group VIII metal varies between 0.1 and 5 percent by weight of the deposit and said formaldehyde addition agent being present in an amount of from 0.01 moles per mole of formaldehyde to that amount that restricts deposition from said solution.

2. The article of manufacture of claim 1 where said combination comprises the organic silicon compound, the formaldehyde addition agent and the solution soluble salt of the Group VIII metal of the Periodic Chart of the Elements.

3. The article of manufacture of claim 1 where said combination comprises the organic silicon compound and the solution soluble salt of the Group VIII metal of the Periodic Chart of the Elements.

4. The article of manufacture of claim 2 where the organic silicon compound is selected from the group consisting of silanes and polysiloxanes. 1

5. The article of manufacture of claim 2 where the Group VIII metal salt is selected from the group of nickel, iron and platinum.

6. The article of manufacture of claim 1 in the form of a printed circuit board having ductile copper conductors.

7. The printed circuit board of claim 6 having copper plated through-holes.

Claims (6)

1. 2. The article of manufacture of claim 1 where said combination comprises the organic silicon compound, the formaldehyde addition agent and the solution soluble salt of the Group VIII metal of the Periodic Chart of the Elements.
2. 3. The article of manufacture of claim 1 where said combination comprises the organic silicon compound and the solution soluble salt of the Group VIII metal of the Periodic Chart of the Elements.
3. 4. The article of manufacture of claim 2 where the organic silicon compound is selected from the group consisting of silanes and polysiloxanes.
4. 5. The article of manufacture of claim 2 where the Group VIII metal salt is selected from the group of nickel, iron and platinum.
5. 6. The article of manuFacture of claim 1 in the form of a printed circuit board having ductile copper conductors.
6. 7. The printed circuit board of claim 6 having copper plated through-holes.