Volume 43, Issue 2

Metal-Organic Frameworks (MOFs) are a class of crystalline materials that, thanks to their large surface area and high porosity, allow them to be used in various areas of knowledge. This diversity of applications is due to the metal ions and the organic binders that compose them, but it is also important to highlight the ability of MOFs to function as hosts for a great variety of molecules of very different sizes and chemical properties. The first existing approaches for incorporating biomolecules in MOFs are discussed: pore encapsulation, surface binding, covalent binding, and in-situ encapsulation. Next, we discuss the obstacles of designing MOFs for effective gene delivery and how to enhance the gene delivery using different strategies.

Bismuth chloride oxide (BiOCl) is a typical V-VI-VII ternary oxide material, which is one of the widely studied metal oxides due to its unique surface, electronic and photocatalytic properties. However, the broad bandgap and the large number of photogenerated electron-hole pair complexes of BiOCl limit its photocatalytic efficiency. Since the photocatalytic performance of BiOCl is highly dependent on its exposed crystallographic facets, research attention has increasingly focused on the different structures and properties possessed by different crystallographic facets of BiOCl. This article reviews the basic principles of using different crystalline surfaces of BiOCl materials to enhance photocatalytic activity, summarizes the applications of BiOCl single-crystal catalysts and composite catalysts in the environmental field, and provides an outlook on the challenges and new research directions for future development in this emerging frontier area. It is hoped that the crystalline surface-related photocatalysis of BiOCl can be used to provide new guidance for the rational design of novel catalysts for various energy and environment-related applications.

This paper aims to review recent advances on synthesis, crystal structures, thermal, spectroscopic, phase transitions, optical, dielectric, and catalysis properties of hydrate and anhydrous alkylenediammonium halogenometallates materials (Metal: Bi, Sb, Halogen: Cl, Br, I). These hybrid materials present rich structural diversities based on octahedra forming infinite zero dimensional, 1-dimensional chains, 2-dimensional layers, discrete bioctahedra, and discrete tetramer units. The effect, contribution and importance of hydrogen bonding N–H … X (X: Cl, Br, I) are reviewed in terms of solid state relationship. Particularly, a comparative study is made on hydrate and anyhdrous aliphatic chlorobismuthates with alkylenediammonium + NH 3 (CH 2 ) n NH 3 + based on structural data and V/Z variation with (CH 2 ) n chains ( n  = 2–8, 12), and variation of BiCl 6 3− Raman frequencies modes versus (CH 2 ) n chains ( n  = 3–8). Hydrate salts with ( n  = 3, 12) consist of isolated BiCl 6 3− anions and two water molecules, against others ones with isolated anionic chains [BiCl 5 2− ] n or Bi 2 Cl 10 4− dimers, formed by distorted octahedra BiCl 6 3− sharing corners, vices or edges. The reviewed optical and electronic band gaps suggested interesting compounds with band gaps (1.85–2.4 eV), as suitable materials in optoelectronic properties, photoactive layer in solution-processed photovoltaics, and bio-imaging or photovoltaic applications. It was concluded that iodobismuthate salts have generally the lowest bands gap, compared to that of bromo and chlorobismuthate slats. Catalysis proprieties are reviewed n fast (RhB) degradation under dark conditions for (C 4 N 2 H 7 ) 4 Bi 2 Cl 10 , (C 5 H 9 N 2 )BiI 4 , and {(H-BPA) 4 ·[(BiI 6 )I 13 ]·2I 3 } n , and in organic salts synthesis under solvent-free conditions. Herein NH 3 (CH 2 ) n NH 3 BiCl 5 ( n  = 5–7) salts were used as highly efficient catalysts, which is a novel tendency in chlorobismuthate researchs in the green chemistry field.

Transition metal complexes (TMCs) with strong and long-lived excited state absorption (ESA) usually exhibit high-performance optical power limiting (OPL) response. Several techniques, such as transmission vs . incident fluence curves and Z-scan have been widely used to assess the OPL performance of typical TMCs. The OPL performance of TMCs is highly molecular structure-dependent. Special emphasis is placed on the structure-OPL response relationships of Pt(II), Ir(III), Ru(II), and other metal complexes. This review concludes with perspectives on the current status of OPL field, as well as opportunities that lie just beyond its frontier.

As biodiesel (BD)/Fatty Acid Alkyl Esters (FAAE) is derived from vegetable oils and animal fats, it is a cost-effective alternative fuel that could complement diesel. The BD is processed from different catalytic routes of esterification and transesterification through homogeneous (alkaline and acid), heterogeneous and enzymatic catalysis. However, heterogeneous catalysts and biocatalysts play an essential role towards a sustainable alternative to homogeneous catalysts applied in biodiesel production. The main drawback is the supporting material. To overcome this, currently, Metal-Organic Frameworks (MOFs) have gained significant interest as supports for catalysts due to their extremely high surface area and numerous binding sites. This review focuses on the advantages of using various MOFs structures as supports for heterogeneous catalysts and biocatalysts for the eco-friendly biodiesel production process. The characteristics of these materials and their fabrication synthesis are briefly discussed. Moreover, we address in a general way basic items ranging from biodiesel synthesis to applied catalysts, giving great importance to the enzymatic part, mainly to the catalytic mechanism in esterification/transesterification reactions. We provide a summary with recommendations based on the limiting factors.