IP Library Granted Patent US 10,190,226
Granted Patent B2
US 10,190,226 · App. 15/207,957 · Granted Jan 29, 2019

Reaction products of heterocyclic nitrogen compounds polyepoxides and polyhalogens

Inventors: Julia Kozhukh (Bear, DE); Zuhra I. Niazimbetova (Marlborough, MA)
Assignee: Rohm and Haas Electronic Materials LLC
C25D3/32C08G59/02C08G59/5046C25D3/30C25D3/38C25D3/58C25D3/60C25D7/00C25D7/123H05K3/18H05K3/188H05K3/42H05K3/421H05K3/465
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 10,190,226
App. No.
15/207,957
Granted
Jan 29, 2019
Kind
B2
Abstract

Reaction products of heterocyclic nitrogen compounds, polyepoxide compounds and polyhalogen compounds may be used as levelers in metal electroplating baths, such as copper electroplating baths, to provide good throwing power. Such reaction products may plate metal with good surface properties and good physical reliability.

Claims (21)

1. A compound comprising a reaction product of one or more heterocyclic nitrogen compounds comprising at least two reactive nitrogen atoms with the proviso that at least one of the reactive nitrogen atoms is in the ring of the one or more heterocyclic nitrogen compounds; one or more polyepoxide compounds and one or more polyhalogen compounds, wherein the one or more polyhalogen compounds have a formula:

X 1 —R 13 —X 2   (VII)

wherein X 1 and X 2 may be the same or different and are halogens chosen from chlorine, bromine, fluorine and iodine, R 13 is linear or branched, substituted or unsubstituted (C 1 -C 20 )alkyl, or is a moiety having formula:

—C(HR 14 )—R 15 —C(HR 14 )—  (VIII)

wherein each R 14 is independently selected from hydrogen, halogens chosen from chlorine, bromine, fluorine and iodine, linear or branched, substituted or unsubstituted (C 1 -C 18 )alkyl, substituted or unsubstituted (C 6 -C 12 )cycloalkyl, substituted or unsubstituted (C 6 -C 15 )aryl; R 15 is linear or branched, substituted or unsubstituted (C 1 -C 18 )alkyl, substituted or unsubstituted (C 6 -C 12 )cycloalkyl, substituted or unsubstituted (C 6 -C 15 )aryl, —CH 2 —O—(R 16 —O) d —CH 2 — where R 16 is a substituted or unsubstituted, linear or branched (C 2 -C 10 )alkyl and d is an integer of 1-10.

2. The compound of claim 1 , wherein the one or more heterocyclic nitrogen compounds are chosen from imidazoles, triazoles, tetrazoles, pyrazines, benzimidazoles, benzotriazoles, purines, piperazines, pyridazines, triazines, tetrazines and pyrimidines, pyrazoles, piperidines, benzoxazoles, oxazoles, pyridines, morpholines, pyrrolidines, pyrroles, quinolines, isoquinolines and benzothiazoles.

3. The compound of claim 1 , wherein the one or more heterocyclic nitrogen compounds have a formula:

wherein Q 1 -Q 4 may be nitrogen, oxygen, carbon, or sulfur with the proviso that at least one of the Q 1 -Q 4 is nitrogen, and that only one of the Q 1 -Q 4 may be oxygen or sulfur at any instance, the carbon atoms and nitrogen atoms may be substituted or unsubstituted and R 1 is hydrogen; hydroxyl; linear or branched alkoxy; linear or branched, substituted or unsubstituted (C 1 -C 10 )alkyl; linear or branched, substituted or unsubstituted hydroxy(C 1 -C 10 )alkyl; linear or branched, substituted or unsubstituted alkoxy(C 1 -C 10 )alkyl; linear or branched, substituted or unsubstituted carboxy(C 1 -C 10 )alkyl; linear or branched, substituted or unsubstituted amino(C 1 -C 10 )alkyl; substituted or unsubstituted aryl; linear or branched, substituted or unsubstituted aryl(C 1 -C 10 )alkyl; substituted or unsubstituted sulfonyl; and substituted or unsubstituted amine, with the proviso that when only one of Q 1 -Q 4 is an unsubstituted nitrogen atom, at least one substituent on the ring comprises a reactive nitrogen atom comprising one or more of a primary amino moiety; secondary amino moiety; an aromatic or non-aromatic heterocyclic nitrogen moiety comprising at least one unsubstituted nitrogen atom; an amide moiety; and a Schiff base moiety.

4. The compound of claim 1 , wherein the one or more heterocyclic nitrogen compounds have a formula:

wherein Q 9 -Q 14 is nitrogen, carbon or oxygen with the proviso that at least one of Q 9 -Q 14 is nitrogen and there are no more than four nitrogen atoms in the ring, the carbon atoms and nitrogen atoms in the ring may be substituted or unsubstituted, and when only one of Q 9 -Q 14 is an unsubstituted nitrogen atom, at least one substituent on the ring comprises a reactive nitrogen atom comprising one or more of a primary amino moiety; secondary amino moiety; an aromatic or non-aromatic heterocyclic nitrogen moiety comprising at least one unsubstituted nitrogen atom; an amide moiety; and a Schiff base moiety; and when oxygen is present in the ring, only one of Q 9 -Q 14 is oxygen.

5. The compound of claim 1 , wherein the one or more polyepoxide compounds 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 5 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 Rig 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, n=1-4, p=1-6, t=1-4 and y=0-6.

6. A composition comprising one or more sources of metal ions, an electrolyte and one or more compounds comprising a reaction product of one or more heterocyclic nitrogen compounds comprising at least two reactive nitrogen atoms with the proviso that at least one of the reactive nitrogen atoms is in the ring of the one or more heterocyclic nitrogen compounds; one or more polyepoxide compounds and one or more polyhalogen compounds, wherein the one or more polyhalogen compounds have a formula:

X 1 —R 13 —X 2   (VII)

wherein X 1 and X 2 may be the same or different and are halogens chosen from chlorine, bromine, fluorine and iodine, R 13 is linear or branched, substituted or unsubstituted (C 1 -C 20 )alkyl, or is a moiety having formula:

—C(HR 14 )—R 15 —C(HR 14 )—  (VIII)

wherein each R 14 is independently selected from hydrogen, halogens chosen from chlorine, bromine, fluorine and iodine, linear or branched, substituted or unsubstituted (C 1 -C 18 )alkyl, substituted or unsubstituted (C 6 -C 12 )cycloalkyl, substituted or unsubstituted (C 6 -C 15 )aryl; R 15 is linear or branched, substituted or unsubstituted (C 1 -C 18 )alkyl, substituted or unsubstituted (C 6 -C 12 )cycloalkyl, substituted or unsubstituted (C 6 -C 15 )aryl, —CH 2 —O—(R 16 —O) d —CH 2 — where R 16 is a substituted or unsubstituted, linear or branched (C 2 -C 10 )alkyl and d is an integer of 1-10.

7. The compound of claim 1 , wherein the one or more polyepoxide compounds 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 and poly(propyleneglycol) diglycidyl ether.

8. The compound of claim 1 , wherein the one or more polyepoxide compounds 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 compound of claim 1 , wherein the one or more polyepoxide compounds are chosen from dicyclopentadiene dioxide and 1,2,5,6-diepoxycyclooctane.

10. The compound of claim 1 , wherein the metal ions are copper ion, tin ions or mixtures thereof.

Assignments (3)
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 →
Continuity (2)
Division 14254792 · Apr 16, 2014
Related Publication 20160319447A1 · Nov 3, 2016