IP Library › Granted Patent US 12,338,260
Granted Patent B2
US 12,338,260 · App. 18/404,081 · Granted Jun 24, 2025

Monoalkyl tin compounds with low polyalkyl contamination, their compositions and methods

Inventors: Joseph B. Edson (Corvallis, OR); Thomas J. Lamkin (Corvallis, OR); William Earley (Corvallis, OR); Truman Wambach (Portland, OR); Jeremy T. Anderson (Corvallis, OR)
Assignee: Inpria Corporation
C07F7/2284C07F7/2224
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Quick Facts
Patent No.
US 12,338,260
App. No.
18/404,081
Granted
Jun 24, 2025
Kind
B2
Abstract

A pure composition comprises a monoalkyltin trialkoxide compound represented by the chemical formula RSn(OR′) 3 or a monoalkyl tin triamide compound represented by the chemical formula RSn(NR′ 2 ) 3 and no more than 4 mole % dialkyltin compounds relative to the total tin amount, where R is a hydrocarbyl group with 1-31 carbon atoms, and wherein R′ is a hydrocarbyl group with 1-10 carbon atoms. Methods are described for the formation of the pure compositions. A solid composition comprises a monoalkyl triamido tin compound represented by the chemical formula RSn-(NR′COR″) 3 , where R is a hydrocarbyl group with 1-31 carbon atoms, and where R′ and R″ are independently a hydrocarbyl group with 1-10 carbon atoms. The compositions are 10 suitable for the formation of resist compositions suitable for EUV patterning in which the compositions have a high EUV absorption.

Claims (12)

1. A high purity liquid composition comprising a mixture of a compound represented by the formula (CH 2 ) 6 CHSn(N(CH 3 ) 2 ) 3 and no more than 4 mole % dialkyltin compounds as an impurity relative to the total tin amount.

2. The composition according to claim 1 further comprising one or more alkyl-tin compounds with a different alkyl ligand relative to the cycloheptyl compound and no more than 4 mole % dialkyltin compounds as an impurity relative to the total tin amount.

3. The composition of claim 2 wherein the different alkyl ligand is methyl, ethyl, tert-butyl, tert-amyl, or a combination thereof.

4. A solution comprising an organic solvent and the high purity liquid composition according to claim 1 .

5. The solution of claim 4 having a concentration of the compound represented by the formula (CH 2 ) 6 CHSn(N(CH 3 ) 2 ) 3 of from about 0.01M to about 2M.

6. The solution of claim 4 wherein the organic solvent comprises an alkane, an aromatic hydrocarbon, an ether, an alcohol, or a mixture thereof.

7. The solution of claim 4 further comprising RSnO (3/2−x/2) (OH) x (0<x<3), where R is an alkyl, cycloalkyl, branched alkyl, or substituted alkyl moiety having from 1 to 31 carbon atoms.

8. A method to selectively form a monoalkyltin trialkoxide compound with low dialkyl tin contamination, the method comprising,

reacting a (CH 2 ) 6 CHSn(N(CH 3 ) 2 ) 3 compound with an alcohol represented by the formula HOR″ in an organic solvent to form (CH 2 ) 6 CHSn(OR″) 3 , wherein the (CH 2 ) 6 CHSn(N(CH 3 ) 2 ) 3 reagent comprises the high purity liquid composition according to claim 1 , wherein R″ is a hydrocarbyl group with 1-10 carbon atoms.

9. The method of claim 8 wherein the reaction is performed with a tetradentate chelating agent in an amount from about 0.5 mole % to about 15 mole % relative to the tin molar quantity.

10. A solution comprising an organic solvent and the (CH 2 ) 6 CHSn(OR″) 3 prepared according to the method of claim 8 .

11. The solution of claim 10 having a concentration of from about 0.01M to about 2M and wherein the solvent comprises an alcohol.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2024
From: EDSON, JOSEPH B.; LAMKIN, THOMAS J.; EARLEY, WILLIAM; WAMBACH, TRUMAN
To: INPRIA CORPORATION
Reel/Frame 066020/0141 →
Continuity (4)
Continuation 17198669 · Mar 11, 2021
Continuation 16936861 · Jul 23, 2020
Division 15950292 · Apr 11, 2018
Related Publication 20240182500A1 · Jun 6, 2024
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