磁性可分离Brønsted酸催化剂合成双愈创木酚- f†

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Komal Tarade, Chandrashekhar Rode and Sanjay Kamble
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引用次数: 0

摘要

目前,聚碳酸酯、环氧树脂和塑料都是由双酚a制成的。然而,众所周知,含有双酚a的材料会造成严重的健康问题,在一些国家已被禁止使用。为了解决这一问题,双愈创木酚- f (BGF)被开发为一种更安全、更可持续的双酚a替代品。我们创造了一种新型的磺酸功能化、磁可分离的多相br / nsted酸催化剂[Fe3O4@SiO2-(Pr)3-N-Bu-SO3H][HSO4−],通过将37%的甲醛与两分子愈创木酚缩合,成功地用于制备BGF。该反应的主要目的是避免使用过量的愈创木酚,同时完成两种起始组分的转化。令人惊讶的是,我们制造的催化剂促进水性甲醛和愈创木酚完全转化为区域异构体,如pp ' -BGF, mp ' -BGF和op ' -BGF,分别有62%,15%和6%的选择性。新型磁可分离多相催化剂在起始物转化和产物分布方面具有较好的催化活性,这可归因于其独特的结构特性。它含有一个悬垂的-SO3H基团,连接到一个很长的丁基链上,使它在反应中很容易接近。我们通过精心优化反应参数,如时间、温度、反应物摩尔比和催化剂负载,为合成双愈木酚- f的有前途和环保意识的方法创建了框架。采用酸碱滴定、FT-IR、XRD、TGA和NMR等技术对催化剂进行了广泛的表征,证实了催化剂的结构,并显示出良好的稳定性和活性。值得注意的是,该催化剂在连续六次运行中表现出可回收性,其有效性没有明显降低。并对愈创木酚与多种醛缩合制备双愈创木酚衍生物的催化活性进行了测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A magnetically separable Brønsted acid catalyst for the synthesis of Bisguaiacol-F†

A magnetically separable Brønsted acid catalyst for the synthesis of Bisguaiacol-F†

Currently, polycarbonates, epoxy resins, and plastics are commercially made from Bisphenol-A. However, BPA-containing materials are well known for causing major health problems and have been banned in several countries. To address this concern, Bisguaiacol-F (BGF) has been developed as a safer and more sustainable alternative to Bisphenol-A. We created a novel sulfonic acid-functionalized, magnetically separable heterogeneous Brønsted acid catalyst, [Fe3O4@SiO2-(Pr)3-N-Bu-SO3H][HSO4], which was successfully utilized for the manufacture of BGF by condensing 37% aq. formaldehyde with two molecules of guaiacol. The main objective for this reaction was to avoid using excess guaiacol while also completing the conversion of both starting components. Surprisingly, our manufactured catalyst promotes the complete conversion of aqueous formaldehyde and guaiacol into regioisomers such as pp′-BGF, mp′-BGF and op′-BGF with 62%, 15%, and 6% selectivity, respectively. Our novel magnetically separable heterogeneous catalyst has improved catalytic activity in terms of starting material conversion and product distribution, which can be attributed to its unique structural characteristics. It contains a pendant –SO3H group that is connected to a lengthy butyl chain, making it conveniently accessible in the reaction. We have created the framework for a promising and environmentally aware approach to the synthesis of Bisguaiacol-F by meticulously optimizing reaction parameters such as time, temperature, reactant molar ratio, and catalyst loading. The catalyst was extensively characterized using acid–base titration, FT-IR, XRD, TGA, and NMR techniques to confirm the structure and reveal remarkable stability and activity. Notably, the catalyst demonstrated recyclability across six consecutive runs, with no noticeable reduction in its effectiveness. The catalytic activity was also tested for guaiacol condensation with a variety of aldehydes to create Bisguaiacol derivatives.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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