Passivation of metal in metal/polyimide structures

Claim 2

A process for forming a polyimide layer on a substrate comprising a metal surface, comprising the steps of: applying to said substrate an organic solution, prepared by reacting an aminoalkoxysilane monomer and water in a solvent; heating said substrate under such conditions as to form a layer of cured silsesquioxane polymer, containing reactive amino groups which coordinate to said metal, so as to passivate said metal and inhibit interaction between said metal and a polyimide precursor material to be applied; applying to said cured layer a solution comprising a polyimide precursor material; and heating said substrate under such conditions as to imidize said polyimide precursor material.

Claim 3

The process of claim 1, wherein said aminoalkoxysilane monomer is reacted with water by employing a mole ratio of water/monomer in the range from about 1:1 to about 1.7:1.

Claim 4

The process of claim 2, wherein said reaction is carried out by employing a mole ratio of water/monomer in the range from about 1.2:1 to about 1.4:1.

Claim 5

The process of claim 2, wherein said aminoalkoxysilane monomer is an aminotrialkoxysilane represented by the formula: ##STR2## wherein: R 1 is a hydrogen atom; a saturated hydrocarbon residue or an amino-substituted, saturated hydrocarbon residue, having 1 to 5 carbon atoms a phenyl group or an alkyl-substituted phenyl group or derivatives thereof, the alkyl group having 1 to 5 carbon atoms; R 2 is a saturated hydrocarbon residue having 2 to 6 carbon atoms; and R 3 is a saturated hydrocarbon residue having 1 to 5 carbon atoms; or a mixture thereof.

Claim 6

The process of claim 1, wherein said aminoalkoxysilane monomer is an aminotrialkoxysilane represented by the formula: ##STR3## wherein: R 1 is a hydrogen atom or a saturated hydrocarbon residue or an amino-substituted, saturated hydrocarbon residue, having 2 or 3 carbon atoms; R 2 is a saturated hydrocarbon residue having 3 to 6 carbon atoms; and R 3 is a saturated hydrocarbon residue having 1 to 4 carbon atoms; or a mixture thereof; and said aminotrialkoxysilane monomer is reacted with water by employing a mole ratio of water/monomer in the range from about 1.2:1 to about 1.4:1.

Claim 7

The process of claim 5, wherein said aminotrialkoxysilane monomer is selected from the group consisting of γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-β-(aminoethyl)-γ-minopropyltrimethoxysilane and N-.sup.β -(aminoethyl)-.sup.γ -aminopropyltriethoxysilane.

Claim 8

The process of claim 1, wherein said organic solution is prepared by reacting an aminoalkoxysilane monomer, an arylalkoxysilane or arylsilazane monomer and water in a solvent.

Claim 9

The process of claim 7, wherein: said aminoalkoxysilane monomer is an aminotrialkoxysilane represented by the formula: ##STR4## wherein R 1 is a hydrogen atom; a saturated hydrocarbon residue or an amino-substituted, saturated hydrocarbon residue, having 1 to 5 carbon atoms; or an alkyl-substituted phenyl group or derivatives thereof, the alkyl group having 1 to 5 carbon atoms; R 2 is a saturated hydrocarbon residue having 2 to 6 carbon atoms or an alkyl-substituted phenyl group, each alkyl group having 1 to 5 carbon atoms; and R 3 is a saturated hydrocarbon residue having 1 to 8 carbon atoms; or a mixture thereof; and said arylalkoxysilane or arylsilazane monomer is represented by the formula, R 4 --Si--(Y) 3 , wherein R 4 is an unsubstituted or substituted aromatic residue and Y is (OR 6 ) or N(R 7 ) 2 , wherein R 6 is a saturated hydrocarbon residue having 1 to 5 carbon atoms and R 7 is a hydrogen atom or a saturated hydrocarbon residue having 1 to 5 carbon atoms.

Claim 10

The process of claim 8, wherein said reaction is carried out by employing a mole ratio of arylalkoxysilane or arylsilazane monomer to aminoalkoxysilane monomer in the range from about 1:3 to about 4:1, and a mole ratio of water/total monomer in the range from about 0.5:1 to about 2:1.

Claim 11

The process of claim 9, wherein said reaction is carried out by employing a mole ratio of arylalkoxysilane or arylsilazane monomer to aminoalkoxysilane monomer in the range from about 2:3 to about 2.5:1, and a mole ratio of water/total monomer in the range from about 0.9:1 to about 1.7:1.

Claim 12

The process of claim 8, wherein said organic solution is prepared by reacting an aminoalkoxysilane monomer, an arylalkoxysilane or arylsilazane monomer, a tetraalkoxysilane monomer and water in a solvent.

Claim 13

The process of claim 8 wherein: said aminotrialkoxysilane monomer is represented by the formula: ##STR5## wherein: R 1 is a hydrogen atom or a saturated hydrocarbon residue or an amino-substituted, saturated hydrocarbon residue, having 2 or 3 carbon atoms; R 2 is a saturated hydrocarbon residue having 3 to 6 carbon atoms; and R 3 is a saturated hydrocarbon residue having 1 to 4 carbon atoms; or a mixture thereof; and said arylalkoxysilane or arylsilazane monomer is represented by the formula, R 4 --Si--(Y) 3 , wherein R 4 is an unsubstituted or substituted phenyl group and Y is OR 6 or N(R 7 ) 2 , wherein R 6 is a saturated hydrocarbon residue having 1 to 4 carbon atoms, and R 7 is a hydrogen atom or a saturated hydrocarbon residue having 1 to 4 carbon atoms.

Claim 14

The process of claim 12, wherein said aminotrialkoxysilane monomer is selected from the group consisting of γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane and N-β-(aminoethyl)-γ-aminopropyltriethoxysilane, and said arylalkoxysilane monomer is phenyltriethoxysilane.

Claim 15

The process of claim 1, wherein said substrate is heated at a temperature in excess of about 200° C. for a period from about 15 to about 60 minutes to form said cured layer.

Claim 16

The process of claim 14, wherein said substrate is heated at a temperature in excess of about 350° C. to form said cured layer.

Claim 17

The process of claim 1, wherein a solution comprising pyromellitic dianhydride-oxydianiline polyamic acid is applied to said cured layer.

Claim 18

The process of claim 1, wherein said imidization step is carried out at a temperature in excess of about 200° C. for a period from about 15 to about 60 minutes.

Claim 19

The process of claim 17, wherein said imidization step is carried out at a temperature in excess of about 350° C.

Claim 20

The process of claim 1, wherein said metal is selected from the group consisting of copper, aluminum, silver, chromium, lead, tin, gold, titanium, zirconium, hafnium, vanadium, tantalum and tungsten.

Claim 21

The process of claim 1, wherein said metal is copper or an alloy of copper.

Claim 22

The process of claim 1, wherein said metal is a composite which includes a lower layer selected from the group consisting of titanium, zirconium and hafnium and an upper layer selected from the group consisting of copper, gold, silver and aluminum.

Claim 23

The process of claim 21, wherein said lower layer is about 100-1,000 Å of titanium or zirconium and said upper layer is about 500-10,000 Å of copper.

Claim 24

The process of claim 1, wherein said metal is a composite which includes lower and upper layers independently selected from the group consisting of titanium, zirconium, hafnium, chromium, vanadium and tantalum and an. intermediate layer selected from the group consisting of copper, gold, silver or aluminum therebetween.

Claim 25

A process for forming a polyimide layer on a semiconductor substrate containing a pattern of mettalization, comprising the steps of: applying to said substrate an organic solution, prepared by reacting; an aminoalkoxysilane monomer and water in a solvent, wherein said aminoalkoxysilane monomer is represented by the formula: ##STR6## wherein: R 1 is a hydrogen atom or a saturated hydrocarbon residue or an amino-substituted, saturated hydrocarbon residue, having 2 or 3 carbon atoms; R 2 is a saturated hydrocarbon residue having 3 to 6 carbon atoms; and R 3 is a saturated hydrocarbon residue having 1 to 4 carbon atoms; or a mixture thereof; and said reaction is carried out by employing a mole ratio of water/monomer in the range from about 1.2:1 to about 1.4:1; or by reacting: an aminoalkoxysilane monomer, an arylalkoxysilane or arylsilazane monomer and water in a solvent, wherein said aminoalkoxysilane monomer is represented by the formula above; said arylalkoxysilane or arylsilazane monomer is represented by the formula, R 4 --Si--(Y) 3 , wherein R 4 is an unsubstituted or substituted phenyl group and Y is OR 6 or N(R 7 ) 2 , wherein R 6 is a saturated hydrocarbon residue having 1 to 4 carbon atoms, and R 7 is a hydrogen atom or a saturated hydrocarbon residue having 1 to 4 carbon atoms; and said reaction is carried out by employing a mole ratio of arylalkoxysilane monomer to aminoalkoxysilane or arylsilazane monomer in the range from about 2:3 to about 2.5:1, and a mole ratio of water/total monomer in the range from about 0.9:1 to about 1.7:1; heating said substrate at a temperature in excess of about 200° C. for a period from about 15 to about 60 minutes to form a layer of cured silsesquioxane polymer, containing reactive amino groups which coordinate to said metal, so as to passivate said metal and inhibit interaction between said metal and a polyimide precursor material to be applied; applying to said cured layer a solution comprising a polyimide precursor material; and heating said substrate at a temperature in excess of about 200° C. for a period from about 15 to about 60 minutes ti imidize said polyimide precursor material.

Claim 26

A process for forming a polyimide layer on a semiconductor substrate containing a pattern of mettalization, comprising the steps of: applying to said substrate an organic solution, prepared by reacting; an aminoalkoxysilane monomer and water in a solvent, wherein said aminoalkoxysilane monomer is represented by the formula: ##STR6## wherein: R 1 is a hydrogen atom or a saturated hydrocarbon residue or an amino-substituted, saturated hydrocarbon residue, having 2 or 3 carbon atoms; R 2 is a saturated hydrocarbon residue having 3 to 6 carbon atoms; and R 3 is a saturated hydrocarbon residue having 1 to 4 carbon atoms; or a mixture thereof; and said reaction is carried out by employing a mole ratio of water/monomer in the range from about 1.2:1 to about 1.4:1; or by reacting: an aminoalkoxysilane monomer, an arylalkoxysilane or arylsilazane monomer and water in a solvent, wherein said aminoalkoxysilane monomer is represented by the formula above; said arylalkoxysilane or arylsilazane monomer is represented by the formula, R 4 --Si--(Y) 3 , wherein R 4 is an unsubstituted or substituted phenyl group and Y is OR 6 or N(R 7 ) 2 , wherein R 6 is a saturated hydrocarbon residue having 1 to 4 carbon atoms, and R 7 is a hydrogen atom or a saturated hydrocarbon residue having 1 to 4 carbon atoms; and said reaction is carried out by employing a mole ratio of arylalkoxysilane monomer to aminoalkoxysilane or arylsilazane monomer in the range from about 2:3 to about 2.5:1, and a mole ratio of water/total monomer in the range from about 0.9:1 to about 1.7:1; heating said substrate at a temperature in excess of about 200° C. for a period from about 15 to about 60 minutes to form a layer of cured silsesquioxane polymer, containing reactive amino groups which coordinate to said metal, so as to passivate said metal and inhibit interaction between said metal and a polyimide precursor material to be applied; applying to said cured layer a solution comprising a polyimide precursor material; and heating said substrate at a temperature in excess of about 200° C. for a period from about 15 to about 60 minutes ti imidize said polyimide precursor material.

Claim 27

The process of claim 24, wherein said aminotrialkoxysilane monomer is selected from the group consisting of γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane and N-β-(aminoethyl)-γ-aminopropyltriethoxysilane, and said arylalkoxysilane monomer is phenyltriethoxysilane.

Claim 28

The process of claim 25, wherein said substrate is heated at a temperature in excess of about 350° C. to form said cured layer; and said imidization step is carried out at a temperature in excess of about 350° C.

Claim 29

The process of claim 26, wherein a solution comprising biphenylenedianhydride-p-phenylenediamine polyamic acid or pyromellitic dianhydride-oxydianiline polyamic acid is applied to said cured layer; and said metal is copper or an alloy of copper.

Claim 30

The process of claim 27, wherein said organic solution is prepared by reacting an aminoalkoxysilane monomer, an arylalkoxysilane or arylsilazane monomer, a tetraalkoxysilane monomer and water in a solvent.