Temperature-Induced Bifurcations in the Cu(II)-Catalyzed and Catalyst-Free Hydrogen Peroxide-Thiosulfate Oscillating Reaction

2010 ◽  
Vol 114 (26) ◽  
pp. 7014-7020 ◽  
Author(s):  
Ling Yuan ◽  
Qingyu Gao ◽  
Yuemin Zhao ◽  
Xiaodong Tang ◽  
Irving R. Epstein
2016 ◽  
Vol 378 ◽  
pp. 375-383 ◽  
Author(s):  
Yayun Zhang ◽  
Yuhui Li ◽  
Yingying Jiang ◽  
Yancai Li ◽  
Shunxing Li

2010 ◽  
Vol 46 (10) ◽  
pp. 1772 ◽  
Author(s):  
Norihiro Tada ◽  
Lei Cui ◽  
Hiroaki Okubo ◽  
Tsuyoshi Miura ◽  
Akichika Itoh

1986 ◽  
Vol 64 (5) ◽  
pp. 897-903 ◽  
Author(s):  
Brian R. James ◽  
Robert H. Morris ◽  
Pal Kvintovics

Synthetic routes to hydridoiridium(III) dimethylsulfoxide complexes via oxidative addition of HCl or H2 to precursor insitu iridium(I) species are described. The complexes, trans, mer-IrHCl2(DMSO)3 (1a) and cis, mer-IrH2Cl(DMSO)3 (2), have been characterized by 1H nmr and ir, and contain only S-bonded sulphoxide, DMSO. Comparison is made with data for other isomers reported in the literature, and some discrepancies are discussed. The decomposition of 1a and 2 in chloroform leads to isomers of IrCl3(DMSO)3, while (2) with HCl generates cis,cis IrHCl2(DMSO)2(DMSO) with the O-bonded sulfoxide trans to hydride. The reaction of 1a in dichloromethane with dioxygen occurs with a 1:1 stoichiometry and generates two complexes tentatively formulated as Ir(OH)Cl2(DMSO)2H2O (3) and IrCl2(O2)(DMSO)2DMSO (4); a hydroperoxide intermediate (Ir—OOH) initially formed from 1a is considered to react with further 1a in the rate-determining step. Oxidation of coordinated DMSO to the sulphone is not observed, implying that such a catalyzed O2-oxidation reported earlier in aqueous 2-propanol proceeds via reaction of IrOOH with free DMSO, or else via free hydrogen peroxide.


2015 ◽  
Vol 347 ◽  
pp. 428-434 ◽  
Author(s):  
Yancai Li ◽  
Yayun Zhang ◽  
Yanmei Zhong ◽  
Shunxing Li

2015 ◽  
Vol 279 ◽  
pp. 151-156 ◽  
Author(s):  
Sun-Mi Shin ◽  
Jin-Young Jung ◽  
Min-Joon Park ◽  
Jae-Won Song ◽  
Jung-Ho Lee

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