Modified novolac phenol resin, resist material, coating film, and resist permanent film

US2016017083A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016017083-A1
Application numberUS-201414773769-A
CountryUS
Kind codeA1
Filing dateJan 21, 2014
Priority dateMar 14, 2013
Publication dateJan 21, 2016
Grant date

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  1. Title

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present invention provides a modified novolac phenol resin having excellent developability and heat resistance, a method for producing the same, a photosensitive composition, a resist material, and a permanent film. The modified novolac phenol resin has a molecular structure in which hydrogen atoms of phenolic hydroxyl groups possessed by a novolac phenol resin (C) are partially or entirely substituted by acid dissociable groups, the novolac phenol resin (C) being produced by condensing an aromatic compound (A) represented by structural formula (1) below with an aldehyde compound (B).

First claim

Opening claim text (preview).

1 . A modified novolac phenol resin having a molecular structure in which hydrogen atoms of phenolic hydroxyl groups possessed by a novolac phenol resin (C) are partially or entirely substituted by acid dissociable groups, the novolac phenol resin (C) being produced by condensing an aromatic compound (A) represented by structural formula (1) below with an aldehyde compound (B), [in the formula, Ar is a structural moiety represented by structural formula (2-1) or (2-2) below (in the formula, k is an integer of 0 to 2, p is an integer of 1 to 5, q is an integer of 1 to 7, and R 3 is any one of a hydrogen atom, an alkyl group, an alkoxy group, an aryl group, an aralkyl group, and a halogen atom), R 1 and R 2 are each any one of an alkyl group, an alkoxy group, an aryl group, an aralkyl group, and a halogen atom, and m and n are each an integer of 1 to 4]. 2 . The modified novolac phenol resin according to claim 1 , wherein the acid dissociable group is any one of a tertiary alkyl group, an alkoxyalkyl group, an acyl group, an alkoxycarbonyl group, a heteroatom-containing cyclic hydrocarbon group, and a trialkylsilyl group. 3 . The modified novolac phenol resin according to claim 2 , wherein the acid dissociable group is any one of an alkoxyalkyl group, an alkoxycarbonyl group, and a heteroatom-containing cyclic hydrocarbon group. 4 . The modified novolac phenol resin according to claim 1 , wherein a presence ratio [(α)/(β)] of phenolic hydroxyl group (α) to acid dissociable group (β) in the resin is within a range of 95/5 to 10/90. 5 . The modified novolac phenol resin according to claim 1 , produced by reacting a phenol compound (a1) having any one of an alkyl group, an alkoxy group, an aryl group, an aralkyl group, and a halogen atom as a substituent on an aromatic nucleus with an aromatic aldehyde (a2) to produce an aromatic compound (A), condensation-reacting the resultant aromatic compound (A) with an aldehyde compound (B), and then reacting the resultant novolac phenol resin (C) with a compound represented by any one of structural formulae (3-1) to (3-8) (in the formulae, X represents a halogen atom, Y represents a halogen atom or a trifluoromethanesulfonyl group, R 4 to R 8 each independently represent an alkyl group having 1 to 6 carbon atoms or a phenyl group, and n is 1 or 2). 6 . A method for producing a modified novolac phenol resin, the method comprising reacting a phenol compound (a1) having any one of an alkyl group, an alkoxy group, an aryl group, an aralkyl group, and a halogen atom as a substituent on an aromatic nucleus with an aromatic aldehyde (a2) to produce an aromatic compound (A), condensation-reacting the resultant aromatic compound (A) with an aldehyde compound (B), and then reacting the resultant novolac phenol resin (C) with a compound represented by any one of structural formulae (3-1) to (3-8) (in the formulae, X represents a halogen atom, Y represents a halogen atom or a trifluoromethanesulfonyl group, R 4 to R 8 each independently represent an alkyl group having 1 to 6 carbon atoms or a phenyl group, and n is 1 or 2). 7 . A photosensitive composition comprising the modified novolac phenol resin according to claim 1 and a photoacid generator. 8 . A resist material comprising the photosensitive composition according to claim 7 . 9 . A coating film comprising the photosensitive composition according to claim 7 . 10 . A resist permanent film comprising the resist material according to claim 8 .

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Classifications

  • C08G8/30Primary

    by unsaturated compounds, e.g. terpenes · CPC title

  • Macromolecular compounds which are rendered insoluble or differentially wettable (G03F7/075 takes precedence; macromolecular azides G03F7/012; macromolecular diazonium compounds G03F7/021) · CPC title

  • Chemically modified polycondensates · CPC title

  • Modified phenol-aldehyde condensates · CPC title

  • the macromolecular compound being present in a chemically amplified positive photoresist composition · CPC title

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What does patent US2016017083A1 cover?
The present invention provides a modified novolac phenol resin having excellent developability and heat resistance, a method for producing the same, a photosensitive composition, a resist material, and a permanent film. The modified novolac phenol resin has a molecular structure in which hydrogen atoms of phenolic hydroxyl groups possessed by a novolac phenol resin (C) are partially or entirely…
Who is the assignee on this patent?
Dainippon Ink & Chemicals
What technology area does this patent fall under?
Primary CPC classification C08G8/30. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jan 21 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).