Recent Progress on the Synthesis and Modified Strategies of Zeolitic-Imidazole Framework-67 Towards Electrocatalytic Oxygen Evolution Reaction

As a class of metal-organic framework, the zeolitic-imidazole framework-67 is constructed from bridging cobalt ions and 2-methylimidazole. The high content of abundant active cobalt species, uniform structure, ultrahigh porosity, and large surface area show the potential for multiple catalytic applications, especially electrocatalytic oxygen evolution reaction (OER). The design and synthetic strategies of catalyst-based ZIF-67 that approach the maximized catalytic performance are still challenging in further development. Herein, the current progress strategy on the structural design, synthetic route, and functionalization of electrocatalysts based on ZIF-67 to boost the catalytic performance of OER is reviewed. Besides, the structurally designed catalyst from various fabricated strategies corresponding to enhancing catalytic activity is discussed. The emphasized review for understanding design and synthetic structure with catalytic performance could guide researchers in further developing catalyst-based ZIF-67 for improving the efficient electrocatalytic OER.     

The effect of synthesis procedure on the catalytic performance of isostructural ZIF‐8

We demonstrate the synthesis of isostructural zeolitic imidazole framework (ZIF‐8) using four distinct synthetic methods. Subsequently, the variations in physicochemical properties were analyzed through the catalytic reaction of CO₂ cycloaddition of epoxide. It was thus demonstrated that simply by changing the type of synthetic method for the preparation of ZIF‐8, the physicochemical properties were changed significantly which in turn influenced the catalytic activity of ZIF‐8. It was found that the synthetic method affected the crystal growth and consequently influenced the physicochemical properties which are crucial aspects in metal–organic framework applications. There is an almost exponential relationship between the reactivity of various ZIF‐8 samples in CO₂ cycloaddition of epoxide and the surface area, CO₂ adsorption and pore volume.     

Identification of Newly Zeaxanthin-Producing Bacteria Isolated from Sponges in the Gulf of Thailand and their Zeaxanthin Production

Sponge-associated bacteria have been found to produce a variety of bioactive compounds including natural pigments. Here, we report the molecular identification of zeaxanthin-producing sponge-associated bacteria isolated from sponges in the Gulf of Thailand and the effect of environmental factors on zeaxanthin production from a bacterium. Three colorful sponge-associated bacteria (CHOB06-6, KODA19-6, and MAKB08-4) were identified based on the 16S rDNA profile. The 16S rDNA sequence-based analyses revealed that CHOB 06-6 and MAKB 08-4 were the closest relatives to Sphingomonas phyllosphaerae FA2^T, and KODA19-6 was a relative of Shingomonas (Blastomonas) natatoria DSM 3183^T. After all bacteria were cultivated in a modified Zobell medium, S. natatoria KODA19-6 was found to produce the highest zeaxanthin at 0.62?mg/l. pH and temperature considerably affected its zeaxanthin production. Its optimal condition for zeaxanthin production was found at a pH of 7 and 30?°C. The bacterium had a maximum specific growth rate (?? _max) of 0.06?1/h with zeaxanthin productivity (Q _p) of 6.27???g/l·h. Therefore, this newly zeaxanthin-producing bacterium has a potential to produce natural zeaxanthin for the food, feed, pharmaceutical, and cosmetic industries.     

Organic electroluminescence devices based on anthracene sulfide derivatives

A series of anthracene derivatives are synthesized and fabricated as light-emitting materials in OLED devices. The incorporation of the chalcogen atoms, either oxygen or sulfur, in between the anthracene moiety and the alkyl or aryl substituents affected drastically the photo- and electroluminescence properties of the materials, especially the HOMO-LUMO band gap and the emitting color of the devices. The new anthracene sulfide derivatives represent a new design for further modification of other light-emitting doped materials.     

Antimicrobial substances from the rare actinomycete Nonomuraea rhodomycinica NR4-ASC07T

Nonomuraea rhodomycinica NR4-ASC07^T is a rare actinomycete isolated from soil in Sirindhorn peat swamp forest. The crude extract of its culture broth exhibited antimicrobial and anticancer against diverse human pathogens and cancer cells. The chemical investigation of the crude extract led to the isolation of two new metabolites named nonomuric acid (1) and 3-hydroxy deoxydaunorubicinol aglycone (2), along with two known bioactive compounds [ε-rhodomycinone (3) and 7-deoxy-13-dihydrocarminomycinone (4)]. Compounds 1 and 3 showed antimalarial activity with the half maximal inhibitory concentration (IC₅₀) of 8.00 and 8.88 μg mL^?1, respectively. Compound 4 inhibited growth of Mycobacterium tuberculosis and Bacillus cereus at the minimum inhibitory concentrations of 50.0 and 12.50 μg mL^?1, respectively. Every compound exhibited cytotoxicity against cancer cells tested at IC₅₀ ≥ 6.34 μg mL^?1. These finding are the first report of bioactive metabolites produced by strain NR4-ASC07^T, suggesting that rare actinomycetes are yet promising sources for novel drug discovery.     

沸石咪唑酯骨架-67高效催化L-丙交酯的开环聚合反应

为了探究沸石咪唑酯骨架材料(Zeolitic Imidazolate Frameworks,ZIFs)结构中的金属单元对其催化活性的影响,我们采用室温法合成了ZIF-8、Zn/Co-ZIF和ZIF-67,并用其催化L-丙交酯的本体开环聚合反应。 在相同的反应条件下,ZIF-67具有最高的催化活性。 与2-甲基咪唑(配体)作为催化剂相比,ZIF-67催化得到的聚乳酸具有高度全同立构结构。 此外,基质辅助激光解吸-飞行时间(MALDI-TOF)质谱表明,ZIF-67催化得到的聚乳酸主要为线状结构。 经过3次循环反应后,ZIF-67的催化活性没有明显降低。