IP Library › Granted Patent US 7,816,067
Granted Patent B2
US 7,816,067 · App. 11/921,790 · Granted Oct 19, 2010

Coating-type underlayer coating forming composition for lithography containing naphthalene resin derivative

Assignee: Nissan Chemical Industries, Ltd.
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Quick Facts
Patent No.
US 7,816,067
App. No.
11/921,790
Granted
Oct 19, 2010
Kind
B2
Abstract

To provide a coating-type underlayer coating forming composition containing a naphthalene resin derivative. A coating-type underlayer coating forming composition for lithography comprising a compound of formula (1): wherein A is an organic group having an aromatic group, R 1 is hydroxy group, an alkyl group, an alkoxy group, a halogen group, a thiol group, an amino group or an amide group, m1 is the number of A substituted on the naphthalene ring and is an integer of 1 to 6, m2 is the number of R 1 substituted on the naphthalene ring and is an integer of 0 to 5, a sum of m1 and m2 (m1+m2) is an integer of 1 to 6, in cases where the sum is an integer other than 6, the reminder is hydrogen atom, and n is the number of repeating units ranging from 2 to 7000.

Claims (29)

1. A coating-type underlayer coating forming composition for lithography comprising a compound of formula (1):

wherein A is an organic group having an aromatic group, R 1 is hydroxy group, an alkyl group, an alkoxy group, a halogen group, a thiol group, an amino group or an amide group, m1 is the number of A substituted on the naphthalene ring and is an integer of 1 to 6, m2 is the number of R 1 substituted on the naphthalene ring and is an integer of 0 to 5, a sum of m1 and m2 (m1+m2) is an integer of 1 to 6, in cases where the sum is an integer other than 6, the remainder is hydrogen atom, and n is the number of repeating units ranging from 2 to 7000.

2. The coating-type underlayer coating forming composition for lithography according to claim 1 , further comprising a crosslinking compound.

3. The coating-type underlayer coating forming composition for lithography according to claim 2 , further comprising an acid, an acid generator, or both of them.

4. The coating-type underlayer coating forming composition for lithography according to claim 1 , further comprising an acid, an acid generator, or both of them.

5. A coating type underlayer coating for lithography obtained by coating the coating-type underlayer coating forming composition according to claim 1 on a semiconductor substrate and baking it.

6. A method for forming photoresist pattern for use in manufacture of semiconductor device, comprising coating the coating-type underlayer coating forming composition according to claim 1 on a semiconductor substrate, and baking it to form a coating-type underlayer coating.

7. A method for manufacturing semiconductor device comprising the steps of:

forming a coating-type underlayer coating from the coating-type underlayer coating forming composition according to claim 1 ;

forming a resist coating on the coating-type underlayer coating;

forming a resist pattern by exposure to light and development;

etching the coating-type underlayer coating by use of the resist pattern; and

processing the semiconductor substrate by use of the patterned coating-type underlayer coating.

8. A method for manufacturing semiconductor device comprising the steps of:

forming a coating-type underlayer coating from the coating type underlayer coating forming composition according to claim 1 ;

forming a hardmask on the coating-type underlayer coating;

forming a resist coating further thereon;

forming a resist pattern by exposure to light and development;

etching the hardmask by use of the resist pattern;

etching the coating-type underlayer coating by use of the patterned hardmask; and

processing the semiconductor substrate by use of the patterned coating-type underlayer coating.

9. A coating-type underlayer coating forming composition for lithography comprising a compound of formula (2):

wherein A is an organic group having an aromatic group, R 1 is a hydroxy group, an alkyl group, an alkoxy group, a halogen group, a thiol group, an amino group or an amide group, m1 is the number of A substituted on the naphthalene ring and is an integer of 1 to 6, m2 is the number of R 1 substituted on the naphthalene ring and is an integer of 0 to 5, a sum of m1 and m2 (m1+m2) is an integer of 1 to 6, in cases where the sum is an integer other than 6, the remainder is hydrogen atom, n is the number of repeating units ranging from 2 to 7000, and Ar 1 is a substituted or unsubstituted aromatic group.

10. A coating-type underlayer coating forming composition for lithography comprising a compound of formula (3):

wherein X is a single bond, methylene group, C 2-10 -alkylene group, a divalent hydrocarbon group having C 2-10 ether bond, or carbonyl group, Z is a linking group of —O— or —OC(═O)—, Ar 2 is an unsubstituted aromatic ring or an aromatic ring substituted with carboxylic acid, a carboxylic acid ester group, hydroxy group, an alkyl group, an alkoxy group, sulfonic acid group, or a halogen group, R 1 is a hydroxy group, an alkyl group, an alkoxy group, a halogen group, a thiol group, an amino group or an amide group, m1 is the number of A substituted on the naphthalene ring and is an integer of 1 to 6, m2 is the number of R 1 substituted on the naphthalene ring and is an integer of 0 to 5, a sum of m1 and m2 (m1+m2) is an integer of 1 to 6, in cases where the sum is an integer other than 6, the remainder is hydrogen atom and n is the number of repeating units ranging from 2 to 7000.

11. A coating-type underlayer coating forming composition for lithography comprising a compound of formula (4):

wherein X is a single bond, methylene group, C 2-10 alkylene group, a divalent hydrocarbon group having C 2-10 ether bond, or carbonyl group, Z is a linking group of —O— or —OC(═O)—, Ar 2 is an unsubstituted aromatic ring or an aromatic ring substituted with carboxylic acid, a carboxylic acid ester group, hydroxy group, an alkyl group, an alkoxy group, sulfonic acid group, or a halogen group, Ar 1 is a substituted or unsubstituted aromatic group, Ar 2 is an unsubstituted aromatic ring or an aromatic ring substituted with carboxylic acid, a carboxylic acid ester group, hydroxy group, an alkyl group, an alkoxy group, sulfonic acid group, or a halogen group R 1 is a hydroxy group, an alkyl group, an alkoxy group, a halogen group, a thiol group, an amino group or an amide group, m1 is the number of A substituted on the naphthalene ring and is an integer of 1 to 6, m2 is the number of R 1 substituted on the naphthalene ring and is an integer of 0 to 5, a sum of m1 and m2 (m1+m2) is an integer of 1 to 6, in cases where the sum is an integer other than 6, the remainder is hydrogen atom, and n is the number of repeating units ranging from 2 to 7000.

12. A coating-type underlayer coating forming composition for lithography comprising a compound of formula (5):

wherein X is a single bond, methylene group, C 2-10 alkylene group, a divalent hydrocarbon group having C 2-10 ether bond, or carbonyl group, Z is a linking group of —O— or —OC(═O)—, Ar 2 is an unsubstituted aromatic ring or an aromatic ring substituted with carboxylic acid, a carboxylic acid ester group, hydroxy group, an alkyl group, an alkoxy group, sulfonic acid group, or a halogen group, Ar 2 is an unsubstituted aromatic ring or an aromatic ring substituted with carboxylic acid, a carboxylic acid ester group, hydroxy group, an alkyl group, an alkoxy group, sulfonic acid group, or a halogen group, R 1 is a hydroxy group, an alkyl group, an alkoxy group, a halogen group, a thiol group, an amino group or an amide group, m1 is the number of A substituted on the naphthalene ring and is an integer of 1 to 6, m2 is the number of R 1 substituted on the naphthalene ring and is an integer of 0 to 5, a sum of m1 and m2 (m1+m2) is an integer of 1 to 6, in cases where the sum is an integer other than 6, the remainder is hydrogen atom and n is the number of repeating units ranging from 2 to 7000.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 7, 2007
From: ENOMOTO, TOMOYUKI; KISHIOKA, TAKAHIRO; SAKAGUCHI, TAKAHIRO
To: NISSAN CHEMICAL INDUSTRIES, LTD.
Reel/Frame 020295/0380 →
Priority Claims (1)
JP 2005-170758 · Jun 10, 2005 · national
Continuity (1)
Related Publication 20090053647A1 · Feb 26, 2009