Bisphosphonate salts as covalent and non-covalent task-specific ionic liquid synthesis

IF 1.3 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR Phosphorus, Sulfur, and Silicon and the Related Elements Pub Date : 2024-09-02 Epub Date: 2024-10-12 DOI:10.1080/10426507.2024.2416215
Abdoul Razak Halidou Dougourikoye , Mina Hariri , Jean-Noël Volle , Amadou Tidjani Ilagouma , Moussa Idrissa , Fatemeh Darvish , Jean Luc Pirat , David Virieux
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Abstract

Functionalized ionic liquids, commonly referred to as task-specific ionic liquids (TSILs), represent a distinct subset within the realm of ILs. They stand out by having a functional group covalently bonded to either the cationic or the anionic counterpart of the ionic liquid. These tailored modifications confer specific properties to TSILs, making them well-suited for various applications, including catalysis, liquid–liquid extraction, and synthesis. Notably, they also find relevance in the field of nanomaterials. In this paper, we delineate the synthetic pathway for TSILs featuring imidazolinium or pyridinium cores functionalized with a bisphosphonate unit. Furthermore, we provide detailed insights into the green synthesis of imidazolinium salts constituted by a bisphosphonate moiety as the counterion. These innovative TSILs, characterized by a bisphosphonate group, pave the way for a new avenue in the selective complexation of strategic metals and the development of new drugs.1 This underscores their potential utility in strategic metal recovery by extraction and related endeavors.
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作为共价和非共价任务特异性离子液体合成的双膦酸盐
功能化离子液体,通常被称为任务特异性离子液体(TSILs),代表了任务特异性离子液体领域内的一个独特子集。它们的突出之处在于其官能团与离子液体的阳离子或阴离子对应物共价结合。这些量身定制的修饰赋予TSILs特定的性质,使其非常适合各种应用,包括催化、液-液萃取和合成。值得注意的是,它们也在纳米材料领域找到了相关性。在本文中,我们描述了以咪唑或吡啶为核心的双膦酸盐单元功能化的TSILs的合成途径。此外,我们提供了详细的见解,绿色合成咪唑盐构成了一个反离子的双膦酸盐部分。这些创新的TSILs以双膦酸基团为特征,为战略性金属的选择性络合和新药的开发开辟了新的途径这强调了它们在通过提取和相关努力实现战略性金属回收方面的潜在效用。
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来源期刊
CiteScore
2.60
自引率
7.70%
发文量
103
审稿时长
2.1 months
期刊介绍: Phosphorus, Sulfur, and Silicon and the Related Elements is a monthly publication intended to disseminate current trends and novel methods to those working in the broad and interdisciplinary field of heteroatom chemistry.
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