具有强可见光发光功能和荧光探测应用的耐热聚合物

Macromol Pub Date : 2023-05-12 DOI:10.3390/macromol3020016
M. Hasegawa, Shunichi Horii
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引用次数: 0

摘要

耐热聚合物具有强烈的,可见的光致发光(PL)功能提出。含有六氟异丙基(HFIP)侧基的聚苯并恶唑(PBO)表现出强烈的紫色PL,量子产率ΦPL为0.22(22%),这是由于大体积的HFIP侧基有效地干扰了荧光团单元的浓度猝灭(CQ)。以1,2,3,4-环丁烷四羧酸二酐(CBDA)和4,4 ' -亚甲基双(环己胺)(MBCHA)为原料合成了全环脂肪族聚酰亚胺(PI)。由2,3,6,7-萘四羧酸二酐(2,3,6,7- ntda)和MBCHA得到的PI具有很高的玻璃化转变温度(Tg = 376℃)和S1(π,π*)态的紫色荧光。然而,其ΦPL值低于预期。观察到用CBDA稀释荧光团对PL增强有明显的影响。这与2,3,6,7- ntda基二亚胺单元的平面结构密切相关。相比之下,使用2,3,6,7- ntda异构体的对应物1,4,5,8- ntda实际上是无荧光的,尽管使用CBDA进行了充分的稀释。采用非共面结构的3,3″,4,4″-对terphenyltetraarboxylic dihydridril (TPDA)与MBCHA制备的PI薄膜在434 nm处具有强蓝色荧光光谱(ΦPL = 0.26)。使用CBDA稀释方法将其荧光增强到0.41的高ΦPL值。即使TPDA与芳香二胺2,2′-双(三氟甲基)联苯胺(TFMB)结合,也观察到强烈的蓝色荧光,没有电荷转移荧光。采用由TFMB衍生的半环脂肪族PI和由氢化三苯酸酐衍生物和4,4′-双酚合成的新型环脂肪族四羧基二酐作为9,10-双(4-氨基苯基)蒽(BAPA)的另一宿主聚合物。含有bapa的PI膜导致了显著的PL增强,其ΦPL值相当高,为0.48。该PI膜也具有较高的Tg(265℃)。利用活性染料N,N ' -双[4-(4-氨基-3-甲基苄基)-2-甲基苯基]-3,4,9,10-苝四羧基二亚胺作为荧光探针,研究了溶液中聚酰亚胺前体之间的转酰胺反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heat-Resistant Polymers with Intense, Visible Photoluminescence Functionality and Fluorescence Probing Application
Heat-resistant polymers with an intense, visible photoluminescence (PL) functionality are presented. A polybenzoxazole (PBO) containing hexafluoroisopropylidene (HFIP) side groups exhibited an intense purple PL with a quantum yield, ΦPL, of 0.22 (22%), owing to the effectively disturbed concentration quenching (CQ) in the fluorophore units by the bulky HFIP side groups. The chain ends of a wholly cycloaliphatic polyimide (PI), derived from 1,2,3,4-cyclobutanetetracarboxylic dianhydride (CBDA) and 4,4′-methylenebis(cyclohexylamine) (MBCHA), were modified with conjugated monoamines. The PI derived from 2,3,6,7-naphthalenetetracarboxylic dianhydride (2,3,6,7-NTDA) and MBCHA exhibited a very high glass transition temperature (Tg = 376 °C) and purple fluorescence from the S1(π,π*) state. However, its ΦPL value was lower than expected. A pronounced effect of fluorophore dilution using CBDA on the PL enhancement was observed. This is closely related to the planar structure of the 2,3,6,7-NTDA-based diimide units. By contrast, the counterpart using an 2,3,6,7-NTDA isomer, 1,4,5,8-NTDA, was virtually non-fluorescent, despite its sufficient dilution using CBDA. The PI film obtained using 3,3″,4,4″-p-terphenyltetracarboxylic dianhydride (TPDA) with a non-coplanar structure and MBCHA exhibited an intense blue fluorescence spectrum (ΦPL = 0.26) peaking at 434 nm. The dilution approach using CBDA enhanced its fluorescence up to a high ΦPL value of 0.41. Even when TPDA was combined with an aromatic diamine, 2,2′-bis(trifluoromethyl)benzidine (TFMB), the intense blue fluorescence was observed without charge-transfer fluorescence. A semi-cycloaliphatic PI derived from TFMB and a novel cycloaliphatic tetracarboxylic dianhydride, which was obtained from a hydrogenated trimellitic anhydride derivative and 4,4′-biphenol, was used as another host polymer for 9,10-bis(4-aminophenyl)anthracene (BAPA). The BAPA-incorporating PI film resulted in a significant PL enhancement with a considerably high ΦPL of 0.48. This PI film also had a relatively high Tg (265 °C). A reactive dye, N,N′-bis[4-(4-amino-3-methylbenzyl)-2-methylphenyl]-3,4,9,10-perylenetetracarboxydiimide, was harnessed as a fluorescence probe to explore transamidation between polyimide precursors in solution.
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