Porous nonprecious metal-based nanomaterials have gained considerable attention in heterogeneous catalysis owing to their low price, high specific surface area, efficient mass/electron transfer, tunable pore structure, and unique physicochemical properties. Controlling the phase and compositions of these porous nonprecious metal-based materials is critical to their applications. Porous nonprecious transition-metal borides (TMBs), typical metal−metalloid alloys, have recently received much interest because of their optimized electronic structure, adjustable crystal phase, and abundant active site. The controlled tuning of the porous structure of TMBs, exploring the relationship between the structure and performance, and understanding the function of B are essential for developing catalysts with excellent performance; however, these factors have rarely been reviewed. Herein, a detailed summary of the synthesis methods of porous TMBs is provided by precisely defining their shape, composition, and pore size/structure. Incorporating B into metals can significantly alter their performance due to the unique metalloid properties of B. Further, we focus on the key roles of B in porous TMBs for related heterogeneous catalytic applications, including phase control, regulated electronic structure, optimized adsorption of reaction intermediates, and enhanced charge transfer and stability. Finally, we outline the shortcomings, challenges, and possible development of porous TMBs, which need to be further explored to increase TMBs' contribution to heterogeneous catalyst applications and beyond.
New experimental procedures for the preparation of dibenziodolium salts by oxidative cyclization of 2-iodobiphenyl in the presence of appropriate strong acids are described. Particularly useful is a convenient one-pot synthesis of dibenziodolium hydrogen sulfate from 2-iodobiphenyl using Oxone as an inexpensive and environmentally safe oxidant. Dibenziodolium hydrogen sulfate, bis(triflyl)imidate, or triflate can be readily converted to various other dibenziodolium derivatives (chloride, bromide, thiocyanate, azide, cyanide, phenylsulfinate) by anion exchange. Structures of key products have been established by single-crystal X-ray diffraction analysis. Particularly interesting is the X-ray structure of dibenziodolium thiocyanate, which represents the first example of a structurally characterized hypervalent iodine compound with a relatively short iodine-sulfur secondary bond distance.
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