Etching metal using N-heterocyclic carbenes

US11840766B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11840766-B2
Application numberUS-201716305915-A
CountryUS
Kind codeB2
Filing dateJun 1, 2017
Priority dateJun 1, 2016
Publication dateDec 12, 2023
Grant dateDec 12, 2023

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

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An etchant is described that includes an N-heterocyclic carbene and optionally an appropriate solvent. The etchant was effective at etching a metallic surface having, for example, a metal oxide and/or metal, in both solution phase and vapour-phase. The etchant has been shown to effectively etch oxidized copper and tungsten.

First claim

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We claim: 1. A method of etching metal oxide from a metallic surface, comprising contacting the metal oxide with an etchant comprising: a compound of general formula (II), (IIa), (III), (IIIa), (IV), (IVa) or (VI) wherein: n is an integer from 1 to 8; m is an integer from 0 to 4; A is absent, an aliphatic cycle, a heterocycle, an aromatic ring, a fused aromatic ring system, a heteroaromatic ring, and/or a fused heteroaromatic ring system, each of which is optionally substituted; B is a counter ion that optionally acts as a base; G is a perhalogenated alkyl, perhalogenated alkenyl, perhalogenated alkynyl, a perhalogenated aryl, or OR′, wherein R′ is an aliphatic group; Y, Y′, Y 2 and Y 3 are independently C or a heteroatom, and the dashed line is an optional double bond; each R o is independently H, halogen, the substituent X-L-Z as defined above, C 1 -C 10 alkyl, C 10 -C 20 alkyl, C 1 -C 10 alkenyl, C 10 -C 20 alkenyl, C 1 -C 10 alkynyl, C 10 -C 20 alkynyl, C 1 -C 10 alkoxyl, C 10 -C 20 alkoxyl, C 3 -C 20 cyclic aliphatic moiety, aryl, heteroaryl, ether, thioether, amine, polyamine, polyether, or polythioether, each of which is optionally substituted; or, two of R o , together with the atoms to which they are attached, are connected to form a cycle, heterocycle, or an N-heterocyclic carbene precursor, each of which is optionally substituted; R 1 and R 2 are independently absent, at least one lone pair of electrons, H, C 1 -C 10 alkyl, C 10 -C 20 alkyl, branched C 3 -C 10 alkyl, C 10 -C 20 alkenyl, C 1 -C 10 alkynyl, or C 10 -C 20 alkynyl), C 3 -C 20 cyclic aliphatic moiety, aryl, heteroaryl, ether, thiol, thioether, amine, polyamine, polyether, polythioether, or polythiol, each of which is optionally substituted; or, one of R 1 or R 2 , with one of R o , together with the atoms to which they are attached, are connected to form a cycle, or heterocycle, each of which is optionally substituted; R 3 and R 4 are independently H, halogen, the substituent X-L-Z as defined for Formula II, C 1 -C 10 alkyl, C 10 -C 20 alkyl, C 1 -C 10 alkenyl, C 10 -C 20 alkenyl, C 1 -C 10 alkynyl, C 10 -C 20 alkynyl, C 1 -C 10 alkoxyl, C 10 -C 20 alkoxyl, C 3 -C 20 cyclic aliphatic, aryl, heteroaryl, ether, thioether, amine, polyamine, polyether, or polythioether, each of which is optionally substituted; or, any one of R 3 or R 4 , with any one of R 1 or R 2 , together with the atoms to which they are attached, are connected to form a cycle, or heterocycle, each of which is optionally substituted; X-L-Z is absent, or X is C or a heteroatom; L is a divalent moiety, C 1 -C 10 alkylene, C 10 -C 20 alkylene, C 1 -C 10 alkenylene, C 10 -C 20 alkenylene, C 1 -C 10 alkynylene, C 10 -C 20 alkynylene, or dextran, a simple sugar, complex sugar, carbohydrate, ether, thioether, amine, polyamine, polyether, and/or polythioether, each of which is optionally substituted; Z is H, an aliphatic cycle, a heterocycle, an aromatic ring, a fused aromatic ring system, a heteroaromatic ring, a fused heteroaromatic ring system, an organometallic complex, a transition-metal catalyst, a metal-oxide catalyst, a simple sugar, a complex sugar, a carbohydrate, or a chemically derivatizable group, OH, azide, carboxylic acid, carbonyl chloride, anhydride, ester, aldehyde, alcohol, amine, halogen, epoxide, thiirane, aziridine, amino acid, nucleic acid, alkene, alkyne, conjugated diene, thiol, or thioester, each of which is optionally substituted; and a solvent that solvates the compound of general formula (II), (IIa), (III), (IIIa), (IV), (IVa) or (VI), wherein the metallic surface comprises metal oxide; metal oxide and metal; metal oxide and metal alloy; or metal oxide, metal, and metal alloy, and wherein, when in contact with the metallic surface, the etchant etches metal oxide. 2. The method of claim 1 , wherein the metallic surface comprises copper, tungsten, and/or silver. 3. The method of claim 1 , wherein the etchant is a solid. 4. The method of claim 1 , wherein the contacting the metal oxide is a solution phase process. 5. The method of claim 1 , wherein the contacting the metallic surface is a vapour phase process. 6. The method of claim 1 , wherein the compound of general formulas (II), (IIa), or (IVa) is:

Assignees

Inventors

Classifications

  • C23F1/10Primary

    Etching compositions (C23F1/44 takes precedence) · CPC title

  • Gaseous compositions · CPC title

  • Brightening metals by chemical means · CPC title

  • Cleaning or pickling metallic material with solutions or molten salts (with organic solvents C23G5/02) · CPC title

  • Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents · CPC title

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What does patent US11840766B2 cover?
An etchant is described that includes an N-heterocyclic carbene and optionally an appropriate solvent. The etchant was effective at etching a metallic surface having, for example, a metal oxide and/or metal, in both solution phase and vapour-phase. The etchant has been shown to effectively etch oxidized copper and tungsten.
Who is the assignee on this patent?
Univ Kingston, Univ Court Univ St Andrews
What technology area does this patent fall under?
Primary CPC classification C23F1/10. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).