聚(4-乙烯基吡啶)负载碘作为一种环保、可重复使用的多相催化剂,将二氧化碳高效地化学固定成环碳酸盐

IF 1.1 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Nader Ghaffari Khaligh, Taraneh Mihankhah, Mohd Rafie Johan
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引用次数: 7

摘要

利用二氧化碳以一种环境友好的方法合成有价值的化学物质引起了有机化学家的极大关注。高原子经济的CO2与环氧化物的环加成制备环状碳酸盐是文献中广泛提出的最重要的方法之一。合成的环状碳酸盐被用作聚合物物理加工的加工溶剂、绿色极性非质子溶剂、有价中间体、消泡添加剂、工程塑料以及聚碳酸酯和聚氨酯等聚合物、药品和二次电池中的电解质。[1-6]双功能亲电-亲核催化剂在相对温和的条件下显著促进了这种转化。[7-10]鉴于二氧化碳化学固定的重要性,人们研究了多种均相和非均相催化剂,包括有机碱、离子液体、负载型催化剂、有机共聚物和碳材料,用于二氧化碳与环氧化物的环加成。[11,12]在这些材料中,已经开发出具有理想选择性的不同聚合物负载催化剂[13-32],在催化剂稳定性和催化剂分离方面都优于均相催化剂然而,一些催化剂和方案存在缺点,如使用高温和二氧化碳压力,金属离子,产品分离和/或催化剂合成的成本高,活性低,稳定性差,可重复使用性不理想,需要较长的反应时间。以碱金属盐为催化剂,与天然产物β环糊精、纤维素、卵磷脂、[34-36]和氨基醇[37]等合成环状碳酸盐;但该催化剂存在CO2压力高、反应时间长、不可回收、金属废弃物等缺点,有待进一步完善。因此,在低温、低压条件下,利用二氧化碳作为可回收催化剂,开发环保、无金属的工艺具有很高的研究需求。作为超碱或路易斯碱的有机氮化合物以激活CO2分子[28]和电子给受体与CO2的相互作用而闻名。[38]收稿日期:2018年6月25日|修稿日期:2018年9月9日|收稿日期:2018年9月12日DOI: 10.1002/hc.21440
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficient chemical fixation of CO2 into cyclic carbonates using poly(4-vinylpyridine) supported iodine as an eco-friendly and reusable heterogeneous catalyst

Green and sustainable synthesis is considered as a safer alternative to the conventional synthetic processes owing to its environmental friendly nature, atom economy, cost-effectiveness, and easy handling. Herein, the catalytic efficiency of poly(4-vinylpyridine) supported iodine (P4VP/I2) as a metal-free and organocatalyst system was studied and approved for an efficient chemical fixation of CO2 into cyclic carbonates which is performed via the coupling of CO2 with epoxides. The high conversion and excellent selectivity were obtained for a broad range of epoxides in the presence of catalytic amount of P4VP/I2 under solvent-free conditions. The heterogeneous catalyst could be recovered and regenerated over several times with no significant loss of catalytic activity. The possible mechanism was described for the catalytic performance of P4VP/I2 based on the synergetic effect of the Lewis acid and base sites and nucleophilic anion.

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来源期刊
Heteroatom Chemistry
Heteroatom Chemistry 化学-化学综合
CiteScore
1.20
自引率
0.00%
发文量
5
审稿时长
6 months
期刊介绍: Heteroatom Chemistry brings together a broad, interdisciplinary group of chemists who work with compounds containing main-group elements of groups 13 through 17 of the Periodic Table, and certain other related elements. The fundamental reactivity under investigation should, in all cases, be concentrated about the heteroatoms. It does not matter whether the compounds being studied are acyclic or cyclic; saturated or unsaturated; monomeric, polymeric or solid state in nature; inorganic, organic, or naturally occurring, so long as the heteroatom is playing an essential role. Computational, experimental, and combined studies are equally welcome. Subject areas include (but are by no means limited to): -Reactivity about heteroatoms for accessing new products or synthetic pathways -Unusual valency main-group element compounds and their properties -Highly strained (e.g. bridged) main-group element compounds and their properties -Photochemical or thermal cleavage of heteroatom bonds and the resulting reactivity -Uncommon and structurally interesting heteroatom-containing species (including those containing multiple bonds and catenation) -Stereochemistry of compounds due to the presence of heteroatoms -Neighboring group effects of heteroatoms on the properties of compounds -Main-group element compounds as analogues of transition metal compounds -Variations and new results from established and named reactions (including Wittig, Kabachnik–Fields, Pudovik, Arbuzov, Hirao, and Mitsunobu) -Catalysis and green syntheses enabled by heteroatoms and their chemistry -Applications of compounds where the heteroatom plays a critical role. In addition to original research articles on heteroatom chemistry, the journal welcomes focused review articles that examine the state of the art, identify emerging trends, and suggest future directions for developing fields.
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