Synthesis of molecularly tunable, dual-reactive poly(4-hydroxystyrene)-based photoresists <i>via</i> anionic polymerization, sequential deprotection, and reprotection reactions

The quantitatively introduced acetoxy and acetal groups in the controlled polymers can be selectively removed under basic and acidic conditions, respectively, enabling the formation of photoresists with precisely controlled compositions.

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Publication Details

Journal
Polymer Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5py00941c
Primary Topic
Photopolymerization techniques and applications
Type
article
Field-Weighted Citation Impact
0.00
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article

Synthesis of molecularly tunable, dual-reactive poly(4-hydroxystyrene)-based photoresists via anionic polymerization, sequential deprotection, and reprotection reactions

Dong Jin Shin, Sang‐Woog Ryu
Polymer Chemistry
Photopolymerization techniques and applications
article

Synthesis of molecularly tunable, dual-reactive poly(4-hydroxystyrene)-based photoresists via anionic polymerization, sequential deprotection, and reprotection reactions

Dong Jin Shin, Sang‐Woog Ryu
article en

Abstract

The quantitatively introduced acetoxy and acetal groups in the controlled polymers can be selectively removed under basic and acidic conditions, respectively, enabling the formation of photoresists with precisely controlled compositions.

Polymer ChemistryVol. 16(45)
Chungbuk National University (KR)
Openalex Percentile: Top 76%
Photopolymerization techniques and applications
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Synthesis of molecularly tunable, dual-reactive poly(4-hydroxystyrene)-based photoresists <i>via</i> anionic polymerization, sequential deprotection, and reprotection reactions — Dong Jin Shin, Sang‐Woog Ryu · Polymer Chemistry (2025) | TGRS Research Map | TGRS