Hydrazine-Containing Heterocycle Cytochalasan Derivatives From Hydrazinolysis of Extracts of a Desert Soil-Derived Fungus Chaetomium madrasense 375

“Diversity-enhanced extracts” is an effective method of producing chemical libraries for the purpose of drug discovery. Three rare new cytochalasan derivative chaetoglobosins B1-B3 (1–3) were obtained from chemically engineered crude broth extracts of Chaetomium madrasense 375 prepared by reacting with hydrazine monohydrate and four known metabolite chaetoglobosins (4–7) were also identified from the fungus. The structures were identified by NMR and MS analysis and electronic circular dichroism simulation. In addition, the antiproliferative activities of these compounds were also evaluated, and the drug-resistant activities of cytochalasans were evaluated for the first time. Compound 6 possessed potent activity against four human cancer cells (A549, HCC827, SW620, and MDA-MB-231), and two drug-resistant HCC827 cells (Gefitinib-resistant, Osimertinib-resistant) compared with the positive controls.

Molybdenum-assisted reduction of VO2+ for low cost electrolytes of vanadium redox flow batteries

Efficient and affordable energy storage systems are indispensable to accomplish a successful energy transition from fossil fuels to renewable sources. Although all-vanadium redox flow batteries (VRFB) possess many distinctive advantages, much improvement in the process for electrolyte preparation is needed to overcome low productivity and complexity of the current electrolysis process. Herein, we demonstrate a simple one-pot process for the preparation of V3.5+ electrolytes from V2O5 by utilizing hydrazine monohydrate as a residue-free reducing agent and molybdenum as a homogeneous catalyst accelerating the reduction of VO2+. It is confirmed that the performance of the electrolytes prepared by the newly developed process is identical to that by electrolysis in terms of charge-discharge efficiency and capacity up to current density of 200 mA cm-2. This study can contribute to the wide spread of VRFB by providing a scalable process suitable for the mass production of V3.5+ electrolyte.

On-water synthesis of glycosyl selenocyanate derivatives and their application in the metal free organocatalytic preparation of nonglycosidic selenium linked pseudodisaccharide derivatives

Glycosyl selenocyanate derivatives were prepared in water using KSeCN as selenium precursor. Reaction of glycosyl selenocyanate with sugar electrophiles in the presence of hydrazine monohydrate furnished Se-linked pseudodisaccharides.

Ultra-highly active Ir-Ru-B/CeO2 catalyst for hydrogen generation from hydrazine monohydrate

On-demand hydrogen generation from catalytic decomposition of hydrazine monohydrate (N2H4·H2O) represents a promising chemical hydrogen storage technology for onboard and portable applications. But the performances of existing catalysts are still...

Magnetically recyclable Co/ZnO@NiFe2O4 nanoparticles as highly active and reusable catalysts for hydrazine monohydrate hydrogen generation

The novel and cost-effective highly magnetic nanoparticle (NP) catalysts for hydrazine monohydrate dehydrogenation were successfully developed. It will provide a high gravimetric hydrogen storage capacity.

Possible detection of hydrazine on Saturn’s moon Rhea

We present the first analysis of far-ultraviolet reflectance spectra of regions on Rhea’s leading and trailing hemispheres collected by the Cassini Ultraviolet Imaging Spectrograph during targeted flybys. In particular, we aim to explain the unidentified broad absorption feature centred near 184 nm. We have used laboratory measurements of the UV spectroscopy of a set of candidate molecules and found a good fit to Rhea’s spectra with both hydrazine monohydrate and several chlorine-containing molecules. Given the radiation-dominated chemistry on the surface of icy satellites embedded within their planets’ magnetospheres, hydrazine monohydrate is argued to be the most plausible candidate for explaining the absorption feature at 184 nm. Hydrazine was also used as a propellant in Cassini’s thrusters, but the thrusters were not used during icy satellite flybys and thus the signal is believed to not arise from spacecraft fuel. We discuss how hydrazine monohydrate may be chemically produced on icy surfaces.

L-Cysteine Catalyzed Environmentally Benign One-pot Multicomponent Approach Towards the Synthesis of Dihydropyrano[2,3-c]pyrazole Derivatives

Background: The pyrano[2,3-c]pyrazole derivatives are important building blocks of many biologically active compounds owing to their diverse biological potential for example, anti-inflammatory, anticancer, anti-microbial and anti-oxidant properties. Objective: Keeping in mind the wide range of applications of pyrano[2,3-c]pyrazoles, herein we intended to develop a novel synthetic methodology for dihydropyranopyrazoles. We were also interested in determining the influence of amino acids and dipeptides as a catalyst on the synthesis of pyrano[2,3-c]pyrazole derivatives. Methods: To achieve our objectives, we used a one-pot multi-component reaction of ethyl 3-oxobutanoate, propanedinitrile, hydrazine monohydrate and several substituted benzaldehydes by using different catalysts and solvents to synthesize our desired products in the presence of various catalysts. Results and Discussion: We found that optimal conditions for the preparation of pyrano[2,3-c]pyrazoles were L-cysteine (0.5 mol) in the presence of water:ethanol (9:1) at 90 °C. Various 1,4-dihydropyrano[2,3- c]pyrazoles were afforded by using several substituted benzaldehydes in 66-97% yields. Conclusion: We described a green and environmentally benign method to synthesize pyrano[2,3-c]pyrazoles in a one-pot four component reaction of ethyl 3-oxobutanoate, propanedinitrile, hydrazine monohydrate and different substituted benzaldehyde in the presence of L-cysteine in aqueous ethanol (9:1) at 90 oC. Excellent yields of the products, simple work-up, easily available starting materials, use of green solvents, naturally occurring catalyst, non-toxicity, non-chromatographic purification and environmentally benign reaction conditions are some main advantages of this protocol.

SOLVOTHERMAL SYNTHESIS OF TRIPLE NANO COMPOUNDS BISBSE3 IN A LIQUID PHASE

Ternary compounds of bismuth antimony selenide have been synthesized under solvothermal conditions in ethylene glycol medium at the temperature of 453-463 K during 15 hours from bismuth (III) oxide, antimony (III) oxide, elemental selenium (amorph) and hydrazine monohydrate. At a temperature of 453-463 K, after a 15-hour synthesis, a flocculent precipitate is obtained. The thermographic, differential thermal (DTA), X-ray (XRD), chemical, and morphological analyses of the compound were performed and it was found that the crystals of the compound are presented in the form of nano and micro-shelves. The results showed that the composition of selenium compounds of antimony bismuth corresponds to the BiSbSe3 formulas

Selective Synthesis and Photoluminescence Study of Pyrazolopyridopyridazine Diones and N-Aminopyrazolopyrrolopyridine Diones

The newly designed luminol structures of pyrazolopyridopyridazine diones and N-aminopyrazolopyrrolopyridine diones were synthesized from versatile 1,3-diaryfuropyrazolopyridine-6,8-diones, 1,3-diarylpyrazolopyrrolopyridine-6,8-diones, or 1,3-diaryl-7-methylpyrazolopyrrolopyridine-6,8-diones with hydrazine monohydrate. Photoluminescent and solvatofluorism properties containing UV–Vis absorption, emission spectra, and quantum yield (Φf) study of pyrazolopyridopyridazine diones and N-aminopyrazolopyrrolopyridine diones were also studied. Generally, most of pyrazolopyrrolopyridine-6,8-diones 6 exhibited the significant fluorescence intensity and the substituent effect when compared with N-aminopyrazolopyrrolopyridine diones, particularly for 6c and 6j with a m-chloro group. Additionally, the fluorescence intensity of 6j was significantly promoted due to the suitable conjugation conformation. Based on the quantum yield (Φf) study, the value of compound 6j (0.140) with planar structural skeletal was similar to that of standard luminol (1, 0.175).