Reaction of *NO with W(phen)(CO)(2)(SPh)(2) (phen = 1,10-phenanthroline) results in clean conversion to W(phen)(CO)(2)(NO)(SPh). Reduction of the W(II) bisthiolates to the W(0) nitrosyl thiolate occurs with simultaneous reductive elimination of PhS-NO, which is unstable but could be detected spectroscopically. Reaction of W(phen)(CO)(2)(1,2-S(2)-Arene), however, does not result in reductive elimination of either free or bound nitrosothiol. Carbon monoxide is displaced, forming W(phen)(NO)(2)(1,2-S(2)-Arene) (1,2-S(2)-Arene = 1,2-benzene dithiolate or toluene-3,4-dithiolate). Complexes of butanethiol and thiophenol W(phen)(CO)(3)(RSH) react with excess *NO to form nitrosyl thiolate complexes W(phen)(CO)(2)(NO)(SR). These reactions also produce N(2)O and HNO(2), which are attributed to decomposition of initially formed HNO. These observations indicate that *NO may be capable of direct attack on complexed thiols. Crystal structures of W(phen)(CO)(2)(NO)(SPh) and W(phen)(NO)(2)(toluene-3,4-dithiolate) are reported.
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http://dx.doi.org/10.1021/ic990830h | DOI Listing |
ACS Nano
January 2025
School of Chemistry and Chemical Engineering, National Special Superfine Powder Engineering Research Center, Nanjing University of Science and Technology, Nanjing 210094, China.
Constructing a strong bonded interface is highly desired to build fast charge-transfer channels and tune reactive sites for optimizing CO photoreduction. In this work, a covalent triazine framework (CTF) combined with a BiSBr heterojunction is designed using an electrostatic self-assembly process. Due to the oppositely charged states between two components and ultrasonic treatment, a strong coupled interface is realized with the formation of Bi-C/N/O bonds, leading to robust interfacial polarization.
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December 2024
Grupo Química-Física Molecular y Modelamiento Computacional (QUIMOL), Escuela de Ciencias Químicas, Universidad Pedagógica y Tecnológica de Colombia, Sede Tunja, Avenida Central del Norte, Boyacá 150003, Colombia.
Silylation is a widely used derivatization technique for the gas chromatographic analysis of benzodiazepines, a class of psychoactive drugs commonly encountered in forensic and biological samples. This study investigated the optimal experimental conditions for the silylation of benzodiazepines using ,-bis(trimethylsilyl)trifluoroacetamide containing 1% trimethylchlorosilane (BSTFA + 1% TMCS), a widely employed silylating agent. Ten structurally different benzodiazepines, including variations within the classic 1,4-benzodiazepine core and triazolo ring derivatives, were selected to address the effect of structural diversity on silylation.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
College of Polymer Science & Engineering, Sichuan University, Chengdu 610065, China. Electronic address:
While single-atom catalysts (SACs) have been extensively investigated as a high-atom-efficiency heterogeneous catalyst for peroxymonosulfate (PMS) oxidation reaction, the stable constructing and activation efficacy of the reaction sites remains less clarified. Herein, we employed gelatin as a N,O-bidentate ligand for Co (II) to form for a N-doped carbon precursor, while introducing NaCl as a template agent to induce the adoption of a Co-N conformation and disorganize the Co-O moiety. This approach facilitates uniform spatial isolation and atomic-level dispersion of Co atoms within the aerogel, effectively inhibiting the aggregation of Co during synthesis and enabling precise and controllable preparation of Co single-atom catalysts (SACs).
View Article and Find Full Text PDFNat Commun
December 2024
College of Engineering and Applied Sciences, Jiangsu Key Laboratory of Artificial Functional Materials, Nanjing University, Nanjing, China.
Early disease diagnosis hinges on the sensitive detection of signaling molecules. Among these, hydrogen sulfide (HS) has emerged as a critical player in cardiovascular and nervous system signaling. On-chip immunoassays, particularly nanoarray-based interfacial detection, offer promising avenues for ultra-sensitive analysis due to their confined reaction volumes and precise signal localization.
View Article and Find Full Text PDFMolecules
November 2024
Department of General and Inorganic Chemistry, University of Pécs, Ifjúság u. 6., H-7624 Pécs, Hungary.
Palladium-catalyzed carbonylation reactions of -phenylene dihalides were studied using aminoethanols as heterobifunctional ,-nucleophiles. The activity of aryl-iodide and -bromide as well as the chemoselective transformation of amine and hydroxyl functionalities were studied systematically under carbonylation conditions. Aminocarbonylation can be selectively realized under optimized conditions, enabling the formation of amide alcohols, and the challenging alkoxycarbonylation can also be proved feasible, enabling amide-ester production.
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