The interaction between KH and Mg(NH(2))(2) is investigated. Results from temperature-programmed desorption measurements on samples of [Mg(NH(2))(2)][KH](x) (x=0.5, 1.0, and 2.0) indicated that dehydrogenation from [Mg(NH(2))(2)][KH] occurred through a two-step reaction with an onset temperature as low as 60 °C. Accompanied by hydrogen release, K(2)Mg(NH(2))(4) and MgNH successively developed at lower temperatures, whereas KMg(NH)(NH(2)) developed at higher temperatures. However, when dehydrogenation was conducted under isothermal and near-equilibrium conditions, a single-step reaction that led to the formation of KMg(NH)(NH(2)) was observed. KMg(NH)(NH(2)) is a new amide-imide complex. The synthesis of KMg(NH)(NH(2)) can be achieved either by dehydrogenation of the [Mg(NH(2))(2)][KH] mixture or by thermal decomposition of the [K(2)Mg(NH(2))(4)][Mg(NH(2))(2)] mixture.
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http://dx.doi.org/10.1002/cssc.201100207 | DOI Listing |
Inorg Chem
December 2024
College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, Hunan, P. R. China.
Inspired by the rapid growth of Ru-based complexes as molecular ammonia oxidation catalysts, we propose novel Ru-dpp complexes bearing a nitrogen donor as the axial ligand into the ammonia oxidation catalysts family. Herein, a series of Ru-dpp complexes [Ru(-,',″-dpp)(bpy)(L)]·PF (where Hdpp = 2-[5-(pyridin-2-yl)-1-pyrrol-2-yl]pyridine; bpy = 2,2'-bipyridine; L = pyridine (); 4-methylpyridine (); pyrimidine (); isoquinoline ()) containing aromatic nitrogen donor axial ligand are synthesized and fully characterized by NMR, IR, and ESI-MS. The structural analysis displays that dpp as a pincer ligand coordinates to ruthenium, and nitrogen donor L binds to ruthenium at an axial ligand.
View Article and Find Full Text PDFFood Chem
May 2023
Department of Chemistry, Faculty of Sciences, Sivas Cumhuriyet University, TR-58140 Sivas, Turkey. Electronic address:
This study describes the development of 2-hydrazinobenzothiazole modified-amide/imide co-polymers for the extraction/pre-concentration of trace As(III), from edible vegetable oils. Their characterization was realized by help of instrumental techniques. The method is based on pH-dependent complexation between As(III) and co-polymeric chelators in presence of 35-fold excess As(V), their selective extraction into the mixed micellar phase, and detected at pH 2.
View Article and Find Full Text PDFMacromolecules
October 2021
Department of Chemical Engineering & Chemistry, Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600 MB Eindhoven, The Netherlands.
The diamide-imide equilibrium was successfully exploited for the synthesis of dynamic covalent polymer networks in which a dissociative bond exchange mechanism leads to high processibility at temperatures above ≈110 °C. Dynamic covalent networks bridge the gap between thermosets and thermoplastic polymers. At the operating temperature, when the network is fixed, dynamic covalent networks are elastic solids, while at high temperatures, chemical exchange reactions turn the network into a processible viscoelastic material.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2021
Functional Materials Division, Materials & Manufacturing Directorate, Air Force Research Laboratory, AFRL/RXA, Wright-Patterson Air Force Base, Ohio 45433-7750, United States.
To discern multiple intertwined effects, a set of azobenzene-functionalized amide-imide block copolymers, azo(PA--PI)-, where is amide-block content, ., [azoPA] = 25, 50, 75 mol %, was synthesized from 2,2-bis{4-[4-(4-aminophenyldiazenyl)phenoxy]phenyl}propane(azoBPA), 4,4'-oxydibenzoyl chloride (ODBC), and 4,4'-oxydiphthalic anhydride (OPDA). Including homopolymers (azoPA and azoPI), this series of amorphous azopolymers possesses a high glass-transition temperature ( > 210 °C) and a modulus (' ∼ 1.
View Article and Find Full Text PDFChem Commun (Camb)
January 2019
Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Delegación Coyoacán, 04510 Ciudad de México, Mexico.
We used our recently proposed acidity-basicity interplay (ABI) model (Chem. Sci., 2018, 9, 4402) and the Jorgensen secondary interactions hypothesis (JSIH) to rationalise the experimentally observed trends in the formation constants of doubly and triply H-bonded systems with -NHO[double bond, length as m-dash]C- and -NHN- interactions.
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