IP Library Granted Patent US 9,296,879
Granted Patent B2
US 9,296,879 · App. 14/017,281 · Granted Mar 29, 2016

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Quick Facts
Patent No.
US 9,296,879
App. No.
14/017,281
Granted
Mar 29, 2016
Kind
B2
Abstract

This invention provides a composition containing an organometallic compound having a chromophore moiety in the metal polymer backbone which allows a wider range of n/k values such that substrate reflectivity can be controlled under various conditions.

Claims (18)

1. A composition comprising: an organometallic compound of the formula

wherein R 2 =(C 1 -C 20 )hydrocarbyl; M 1 is a Group 3 to Group 14 metal; G=R 3 b -Ch-R 3 b or Ch(OM 1 L 1 m OR 2 ) c ; Ch=a chromophore moiety; R 3 is a divalent linking group having from 1 to 12 carbon atoms; R 4 =H, R 2 or M(L 1 ) m OR 2 ; L 1 is a ligand; m refers to the number of ligands and is an integer from 1-4; a=an integer from 1 to 20; each b is independently an integer from 0 to 25; c=1 or 2; an organic solvent; and a surface treating polymer having a surface energy of 20 to 40 erg/cm 2 and comprising a surface treating moiety chosen from hydroxyl, protected hydroxyl, protected carboxyl, or mixtures thereof.

2. The composition of claim 1 wherein M 1 is chosen from titanium, zirconium, hafnium, tungsten, tantalum, molybdenum, vanadium, indium, germanium, gallium, thallium, and aluminum.

3. The composition of claim 1 wherein each L 1 is chosen from (C 1 -C 20 )alkoxy, (C 2 -C 20 )carboxyl, beta-diketonates, beta-hydroxyketonates, beta-ketoesters, beta-diketiminates, amindinates, guanidinates, or beta-hydroxyiminates.

4. The composition of claim 1 wherein the chromophore moiety comprises one or more of an aromatic ring or an isocyanurate.

5. The composition of claim 4 wherein the aromatic ring is chosen from phenyl, naphthyl, anthracenyl, or phenanthryl.

6. The composition of claim 1 wherein R 3 comprises one or more atoms selected from the group consisting of oxygen, nitrogen, and sulfur.

7. The composition of claim 1 wherein R 3 is selected from the group consisting of (C 2 -C 12 )alkylene-O— and (C 2 -C 12 )alkylidene-O—.

8. The composition of claim 1 wherein G is chosen from Ch, Ch-R 3 b , R a b -Ch, or Ch(OM 1 L 1 m OR 2 ) c .

9. The composition of claim 1 wherein the chromophore moiety is substituted with one or more substituents selected from the group consisting of (C 1 -C 6 )alkyl, cyano, halo, nitro and SO 3 —Y, where Y=H, ammonium or an alkali metal ion.

10. A composition comprising: an organometallic compound of the formula

wherein R 2 =(C 1 -C 20 )hydrocarbyl; M 1 is a Group 3 to Group 14 metal; G=R 3 b -Ch-R 3 b or Ch(OM 1 L 1 m OR 2 ) c ; Ch=a chromophore moiety; R 3 is a divalent linking group having from 1 to 12 carbon atoms; R 4 =H, R 2 or M(L 1 ) m OR 2 ; L 1 is a ligand; m refers to the number of ligands and is an integer from 1-4; a=an integer from 1 to 20; each b is independently an integer from 0 to 25; c=1 or 2; and an organic solvent; wherein the chromophore moiety is an isocyanurate.

11. The composition of claim 10 wherein M 1 is chosen from titanium, zirconium, hafnium, tungsten, tantalum, molybdenum, vanadium, indium, germanium, gallium, thallium, and aluminum.

12. The composition of claim 10 wherein each L 1 is chosen from (C 1 -C 20 )alkoxy, (C 2 -C 20 )carboxyl, beta-diketonates, beta-hydroxyketonates, beta-ketoesters, beta-diketiminates, amindinates, guanidinates, or beta-hydroxyiminates.

13. The composition of claim 10 further comprising a surface treating polymer having a surface energy of 20 to 40 erg/cm 2 and comprising a surface treating moiety chosen from hydroxyl, protected hydroxyl, protected carboxyl, or mixtures thereof.

14. The composition of claim 10 wherein R 3 comprises one or more atoms selected from the group consisting of oxygen, nitrogen, and sulfur.

15. The composition of claim 10 wherein G is chosen from Ch, Ch-R 3 b , R 3 b -Ch, or Ch(OM 1 L 1 m OR 2 ) c .

16. The composition of claim 10 wherein the chromophore moiety is substituted with one or more substituents selected from the group consisting of (C 1 -C 6 )alkyl, cyano, halo, nitro and SO 3 —Y, where Y=H, ammonium or an alkali metal ion.

Assignments (4)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2015
From: YAMADA, SHINTARO; WANG, DEYAN; WONG, SABRINA; LIU, CONG; XU, CHENG-BAI
To: ROHM AND HAAS ELECTRONIC MATERIALS LLC
Reel/Frame 035558/0925 →