Since the discovery of classical chiral oxazoline ferrocene ligands in 1995, they have become pivotal in transition metal-catalyzed asymmetric transformations. Over the past decade, a notable evolution has been observed with the emergence of siloxane-substituted oxazoline ferrocenes, demonstrating significant potential as chiral ligands and catalysts. These compounds have consistently delivered exceptional results in diverse and mechanistically distinct transformations, surpassing the capabilities of classical oxazoline ferrocene ligands. This review meticulously delineates the research progress on siloxane-substituted oxazoline ferrocene compounds. It encompasses the synthesis of crucial precursors and desired products, highlights their achievements in asymmetric catalysis reactions, and delves into the exploration of the derivatization of these compounds, emphasizing the introduction of ionophilic groups and their impact on the recovery of transition metal catalysts. In addition to presenting the current state of knowledge, this review propels future research directions by identifying potential topics for further investigation concerning the siloxane-tagged derivatives. These derivatives are poised to be promising candidates for the next generation of highly efficient ligands and catalysts.

Ionic liquids have been utilized in numerous significant applications within the field of chemistry, particularly in organic chemistry, due to their unique physical and chemical properties. In the realm of asymmetric transition-metal-catalyzed transformations, chiral ionic-liquid-supported ligands and their corresponding transition-metal complexes have facilitated these processes in unconventional solvents, especially ionic liquids and water. These innovative reaction systems enable the recycling of transition-metal catalysts while producing optically active organic molecules with comparable or even higher levels of chemo-, regio-, and stereoselectivity compared to their parent catalysts. In this short review, we aim to provide an overview of the structures of chiral ionic-liquid-supported ligands and the synthetic pathways for these ligands and catalysts. Various synthetic methodologies are demonstrated based on the conceptual frameworks of diverse chiral ionic-liquid-supported ligands. We systematically present the structures and comprehensive synthetic pathways of the chiral ionic-liquid-supported ligands and the typical corresponding transition-metal complexes that have been readily applied to asymmetric processes, categorized by their parent ligand framework. Notably, the crucial experimental procedures are delineated in exhaustive detail, with the objective of enhancing comprehension of the pivotal aspects involved in constructing chiral ionic-liquid-tagged ligands and compounds for both scholars and readers. Considering the current limitations of such ligands and catalysts, we conclude with remarks on several potential research directions for future breakthroughs in the synthesis and application of these intriguing ligands.

The deposition of Yellow River sediment in the middle and lower reaches is a significant factor in the siltation of reservoirs and the occurrence of serious flooding along the river. The efficient and valuable utilization of Yellow River sediment has already become a key research topic in this field. In this study, we have employed Yellow River sediment as the primary material, in conjunction with commercially available slag, fly ash, and quicklime as the binder, to develop a novel type of artificial flood-prevention stone. Following a 28-day standard curing procedure, the highest compressive strength of the prepared artificial stone was recorded at 4.29 MPa, with a value exceeding 0.7 MPa under wet conditions. The results demonstrated that the prepared artificial stone met the specifications for artificial flood-prevention stones. The curing mechanism, as evidenced by analyses from SEM and XRD testing, indicated that the alkali excitation process in the binder, which produced C-A-S-H gel, was the key factor in enhancing the compressive strength of the specimens. Notably, an evaluation of the amount of CO₂ emissions and the cost of the artificial stone concluded that the preparation process was both environmentally friendly and cost-effective.

A new mononuclear phenoxyimine nickel (II) catalyst with a xanthene skeleton was synthesized and applied to polymerization of ethylene/propylene. Higher activities were achieved in comparison with the catalyst lacking the axial steric hindrance and the catalyst with a synergistic effect. Moreover, the synthetic method was easier than that for the bimetallic catalyst.