This critical review outlines the current state-of-the-art research on the reversibly switchable wettability of surface brought about by external stimuli and the exchange of counterions. Chemical composition and surface topography are the two key factors in the wettability of solid substrates. Applying external stimuli and exchanging counterions of ionic liquids and polyelectrolyte films are valuable approaches for rendering the change in surface chemistry and/or topography, and for driving the transition between hydrophilicity and hydrophobicity of surfaces. Through the combination of stimuli-responsive films and micro-/nanostructural surfaces, smart surfaces with reversible switching between superhydrophobicity and superhydrophilicity have been achieved. As an important advancement in reversibly switchable wettability, this review briefly introduces ionic liquids (ILs) as on-off systems to obtain reversibly switchable wettability and then discusses in more detail the methods to induce the reversibly switchable wettability of surfaces modified by ILs, additives, or thin films. In addition to reversibly switchable wettability mechanisms, open problems and potential solutions are discussed (157 references).
Supported ionic liquids (SILs), which refer to ionic liquids (ILs) immobilized on supports, are among the most important derivatives of ILs. The immobilization process of ILs can transfer their desired properties to substrates. Combination of the advantages of ILs with those of support materials will derive novel performances while retaining properties of both moieties. SILs have been widely applied in almost all of fields involving ILs, and have brought about drastic expansion of the ionic liquid area. As green media in organic catalytic reactions, based on utilizing the ability of ILs to stabilize the catalysts, they have many advantages over free ILs, including avoiding the leaching of ILs, reducing their amount, and improving the recoverability and reusability of both themselves and catalysts. This has critical significance from both environmental and economical points of view. As novel functional materials in surface science and material chemistry, SILs are ideal surface modifying agents. They can modify and improve the properties of solids, such as wettability, lubricating property, separation efficiency and electrochemical response. With the achievements in the field of ILs, using magnetic nanoparticles (MNPs) to SILs has drawn increasing attention in catalytic reactions and separation technologies, and achieved substantial progress. The combination of MNPs and ILs renders magnetic SILs, which exhibit the unique properties of ILs as well as facile separation by an external magnetic field. In this article, we focus on imidazolium-based ILs covalently grafted to non-porous and porous inorganic materials. The excellent stability and durability of this kind of SILs offer a great advantage compared with free ILs and IL films physically adsorbed on substrates without covalent bonds. Including examples from our own research, we overview mainly the applications and achievements of covalent-linked SILs in catalytic reactions, surface modification, separation technologies and electrochemistry.
A highly efficient palladium acetate-catalyzed ligand-free Suzuki reaction in aqueous phase was developed in short reaction times (0.5-1 h) at 35 degrees C in air. The key for such a successful catalytic system was the use of a suitable amount of cosolvents in the aqueous phase. The method could be extended to the consecutive multi-Suzuki coupling, and polyaryls were prepared in a single one-pot step in high selectivity and excellent yield under mild reaction conditions (60 degrees C).
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