The Lewis acid–surfactant–SiO ₂ -combined (LASSC) nanocatalyst synthesizes BIMs, and has the advantages of being non-toxic, multi-cycle, highly stable and efficient.

Modified polyaniline self-stabilizing Cu/Pd bimetallic sub-nanocluster composite materials (Cu/Pd@Mod-PANI-3OH) are obtained through the three steps of oxidative polymerization, structural modification, and metal self-trapping. Palladium and copper are confined and coordinated in the composite material by participating in the reaction and are highly uniformly dispersed in the carrier in the form of sub-nano clusters. The Cu/Pd@Mod-PANI-3OH micro–nano reactor catalyst formed by the self-assembly of copper, palladium and polyaniline has excellent electronic effects, including a tunable microenvironment, metal–carrier and metal–metal synergy, and the stabilizing effect of metal by polyaniline materials. It can efficiently catalyse C–C coupling (Sonogashira and Suzuki) reactions in aqueous solution with high catalytic activity and a wide range of applications (40 substrates). The characterization test results show that the Cu/Pd@Mod-PANI-3OH composite material obtained by self-trapping metal is a kind of prefabricated catalyst. During the reaction process, the high-valent metals in the pre-catalyst are in situ converted into active zero-valent metals. The catalyst's pre-fabrication strategy well protects the catalytic active centre, largely prevents agglomeration of the metal particles (can be recycled 8 times) and exhibits excellent interfacial domain-limited catalysis. The research strategy of modulation of catalytic active sites to improve the properties of materials at the molecular and atomic level reported in this article will open a new door in the research of polyaniline materials.

A cellulose sulfonate catalyst (HS-cellulose sulfonate) with high stability, excellent catalytic activity and high acidity value (about 1.55 mmol g⁻¹) was successfully prepared by SO₃ gas phase sulfonation. The basic morphology and nanostructure of the catalyst were determined by HRTEM, XRD, IR, TG, etc. In addition, the catalyst was applied to the catalytic reaction of a dihydroquinazolinone derivative and a xanthene compound, and very valuable results were obtained. The development and preparation of cellulose sulfonate catalysts provide a good approach for the development and application of cellulose, and also an important application of green organic catalytic synthesis methodology.

Polyaluminum chloride (PAC) is an inorganic polymer material that has the advantages of a simple preparation process and special electronic structure. It is considered to be the most efficient and widely used flocculation material for water treatment. In this work, PAC has been used as a Lewis acid catalyst in interdisciplinary fields because of its polynuclear Al–O cation structure. Further, its catalytic mechanism in green organic synthesis has been studied in detail by using the multicomponent Biginelli reaction as the probe. The effect of solvent on the self-assembly and aggregation process of PAC materials was investigated using optical microscopy, UV-Vis spectrophotometry, particle size analysis, XPS, IR, SEM and HR-TEM. The results show that the PAC materials have different morphological characteristics in different solvents. The Al–O–Al cations were transformed in the ethanol solvent to form new multi-nuclear cation aggregates Al_b, which could be used as inorganic micro–nano reactors with unique synergistic catalysis in catalytic reactions. This is the first time the role of PAC in the Biginelli reaction has been analyzed with a liquid in situ infrared instrument, which provided favorable evidence for the speculated reaction mechanism. The PAC–ethanol system is, therefore, considered to be a green, efficient (best yield >99%), economic and recyclable catalyst for catalyzing organic synthesis reactions. The development and utilization of PAC materials in organic synthesis will bring new vitality to this cheap material, which is widely used in industries.