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Synthesis and Characterizations of Positive-Working Photosensitive Polyimides Having 4,5-Dimethoxy-o-Nitrobenzyl Side Group

机译:具有4,5-二甲氧基-邻硝基苄基侧基的正性光敏聚酰亚胺的合成与表征

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摘要

To synthesize a new positive-working photosensitive polyimide, alkali-soluble polyimide containing carbox-ylic acid side group was synthesized, and parts of its carboxylic acid groups were esterified with 4,5-dimethoxy-2-nitrobenzyl bromide. The chemical structure of the resulting polymer was characterized by ~1H-NMR and FT-IR spectroscopies. The substitution ratio of photosensitive groups was estimated by ~1H-NMR integration values, and the thermal properties were examined by differential scanning calorimetry and thermogravimetric analyses. Upon UV irradiaition, 4,5-dimethoxy-2-nitrobenzyl moiety underwent the photodegradation with generation of carboxylic acid side groups as evidenced by UV/vis spectroscopy. As a result, the polymer became soluble in alkaline developer, and a micron-sized positive pattern was successfully fabricated from the synthesized polymer.
机译:为了合成新的正型感光性聚酰亚胺,合成了具有羧酸-侧基的碱溶性聚酰亚胺,并且其羧酸基的一部分被4,5-二甲氧基-2-硝基苄基溴酯化。所得聚合物的化学结构通过〜1 H-NMR和FT-IR光谱学表征。通过〜1 H-NMR积分值估计光敏基团的取代率,并且通过差示扫描量热法和热重分析分析热性质。在UV照射下,通过UV /可见光谱法证明,4,5-二甲氧基-2-硝基苄基部分经历光降解并产生羧酸侧基。结果,聚合物变得可溶于碱性显影剂,并且由合成的聚合物成功地制造了微米级的正图案。

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