5335-84-2Relevant articles and documents
Mn(III) complex supported on Fe 3O 4 nanoparticles: Magnetically separable nanocatalyst for selective oxidation of thiols to disulfides
Bagherzadeh, Mojtaba,Haghdoost, Mohammad Mehdi,Moghaddam, Firouz Matloubi,Foroushani, Behzad Koushki,Saryazdi, Setareh,Payab, Ebrahim
, p. 3025 - 3036 (2013)
A manganese(III) complex, [Mn(phox)2(CH3OH) 2]ClO4 (phox = 2-(2′-hydroxyphenyl)oxazoline), was immobilized on silica-coated magnetic Fe3O4 nanoparticles through the amino propyl linkage usi
Copper based on diaminonaphthalene-coated magnetic nanoparticles as robust catalysts for catalytic oxidation reactions and C-S cross-coupling reactions
Yarmohammadi, Nasrin,Ghadermazi, Mohammad,Mozafari, Roya
, p. 9366 - 9380 (2021/03/16)
In this work, the immobilization of copper(ii) on the surface of 1,8-diaminonaphthalene (DAN)-coated magnetic nanoparticles provides a highly active catalyst for the oxidation reaction of sulfides to sulfoxides and the oxidative coupling of thiols to disulfides using hydrogen peroxide (H2O2). This catalyst was also applied for the one-pot synthesis of symmetrical sulfidesviathe reaction of aryl halides with thiourea as the sulfur source in the presence of NaOH instead of former strongly basic and harsh reaction conditions. Under optimum conditions, the synthesis yields of sulfoxides, symmetrical sulfides, and disulfides were about 99%, 95%, and 96% respectively with highest selectivity. The heterogeneous copper-based catalyst has advantages such as the easy recyclability of the catalyst, the easy separation of the product and the less wastage of products during the separation of the catalyst. This heterogeneous nanocatalyst was characterized by FESEM, FT-IR, VSM, XRD, EDX, ICP and TGA. Furthermore, the recycled catalyst can be reused for several runs and is economically effective.
Direct NO Reduction by a Biomimetic Iron(II) Pyrazolate MOF
Cai, Zhongzheng,Moore, Curtis E.,Tao, Wenjie,Wade, Casey R.,Zhang, Shiyu
supporting information, p. 21221 - 21225 (2021/08/23)
A novel metal-organic framework (MOF) containing one-dimensional, Fe2+ chains bridged by dipyrazolate linkers and N,N-dimethylformamide (DMF) ligands has been synthesized. The unusual chain-type metal nodes feature accessible coordination sites on adjacent metal centers, resulting in motifs that are reminiscent of the active sites in non-heme diiron enzymes. The MOF facilitates direct reduction of nitric oxide (NO), producing nearly quantitative yields of nitrous oxide (N2O) and emulating the reactivity of flavodiiron nitric oxide reductases (FNORs). The ferrous form of the MOF can be regenerated via a synthetic cycle involving reduction with cobaltocene (CoCp2) followed by reaction with trimethylsilyl triflate (TMSOTf).
