We investigated the reaction N((4)S,(2)D,(2)P)+SiH(4) in crossed molecular beams at a collision energy of 4.7 kcal mol(-1) with a time-of-flight mass spectrometer and selective photoionization. Ion signals were observed at m/z=42-45, associated with two product channels, HSiNH/SiNH(2)+H+H and HSiN/HNSi+H(2)+H. The species producing the signal at m/z=43 is assigned to product HSiN/HNSi and that at m/z=44 to product HSiNH/SiNH(2). The signal observed at m/z=42 is attributed to daughter ions of those two products and that at m/z=45 to (29)Si and (30)Si isotopic variants. We report time-of-flight spectra as a function of laboratory angle and simulations for the two products, from which both kinetic-energy and angular distributions of products in the center-of-mass (c.m.) frame were derived. The dependence of release of kinetic energy on the c.m. scattering angle is weak. The average translational energy released is 7.7 kcal mol(-1) for product channel HSiNH/SiNH(2)+H+H and 30.3 kcal mol(-1) for product channel HSiN/HNSi+H(2)+H. Through consecutive triple fragmentation, the angular distribution is slightly anisotropic for product HSiNH/SiNH(2) but isotropic for product HSiN/HNSi. Assuming equal efficiencies of detection, we estimate the branching ratios of products HSiNH/SiNH(2) and HSiN/HNSi to be roughly 15:85. To facilitate an understanding of the reaction mechanisms, we calculated the potential-energy surface for reaction N((2)D)+SiH(4) with quantum-chemical methods. Reactions N((2)D)+SiH(4)-->SiNH(2)+H+H and N((2)D)+SiH(4)-->HNSi+H(2)+H account satisfactorily for the present experimental results. Isomeric products HSiNH and HSiN are minor in this work.
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http://dx.doi.org/10.1063/1.3005652 | DOI Listing |
Metal oxides are promising catalysts for small molecule hydrogen chemistries, mediated by interfacial proton-coupled electron transfer (PCET) processes. Engineering the mechanism of PCET has been shown to control the selectivity of reduced products, providing an additional route for improving reductive catalysis with metal oxides. In this work, we present kinetic resolution of the rate determining proton-transfer step of PCET to a titanium-doped POV, TiVO(OCH) with 9,10-dihydrophenazine by monitoring the loss of the cationic radical intermediate using stopped-flow analysis.
View Article and Find Full Text PDFRSC Adv
January 2025
Pharmaceutical Medicinal Chemistry and Drug Design Department, Faculty of Pharmacy (Girls), Al-Azhar University Cairo 11754 Egypt
The current work focuses on the creation of novel derivatives of the quinazolinone ring system, with various substituted thiophene, thienopyrimidine, and thienopyridine scaffolds 3a,b-11. Employing the standard MTT assay, every target compound's antiproliferative efficacy was evaluated in comparison with doxorubicin against both normal WI-38 cells and various cancer cell lines. Derivatives 6, 8a, and 8b demonstrated the most potent activity, alongside their safety profiles against WI-38.
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January 2025
Key Laboratory of Soft Chemistry and Functional Materials of MOE, School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, P. R. China.
2-(2-Hydroxyphenyl)benzothiazole (HBT) derivatives with donor-π-acceptor (D-π-A) structure have received extensive attention as a class of excited state intramolecular proton transfer (ESIPT) compounds in the fields of biochemistry and photochemistry. The effects of electron-donors (triphenylamine and anthracenyl), the position of substituents and solvent polarity on the fluorescence properties and ESIPT mechanisms of HBT derivatives were investigated through time-dependent density functional theory (TDDFT) calculations. Potential energy curves (PECs) and frontier molecular orbitals (FMOs) reveal that the introduction of the triphenylamine group on the benzene ring enhances intramolecular HB, thereby benefiting the ESIPT process.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Chemistry, University of Calgary, 2500 University Dr. NW, T2N 1N4 Calgary, AB Canada.
The extent of coordination-induced bond weakening in aquo and hydroxo ligands bonded to a molybdenum(III) center complexed by a dianionic, pentadentate ligand system was probed by reacting the known complex (BPzPy)Mo(III)-NTf, , with degassed water or dry lithium hydroxide. The aquo adduct was not observed, but two LiNTf-stabilized hydroxo complexes were fully characterized. Computational and experimental work showed that the O-H bond in these complexes was significantly weakened (to ≈57 kcal mol), such that these compounds could be used to form the diamagnetic, neutral terminal molybdenum oxo complex (BPzPy)Mo(IV)O, , by hydrogen atom abstraction using the aryl oxyl reagent ArO• (Ar = 2,4,6-tri--butylphenyl).
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January 2025
Superior Institute of Biomedical Sciences, State University of Ceará, Fortaleza, Ceará 60714-903, Brazil.
Leishmaniasis is a chronic inflammatory zoonotic illness caused by protozoan flagellates belonging to the genus. Current data suggest that over 1 billion people worldwide are susceptible to infection, primarily in tropical and subtropical countries, where up to 2 million new cases are reported annually. Therefore, the development of a vaccine is crucial to combating this disease.
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