2017
DOI: 10.1016/j.apcata.2017.07.026
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Highly efficient C Cl bond cleavage and unprecedented C C bond cleavage of environmentally toxic DDT through molecular electrochemical catalysis

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Cited by 13 publications
(5 citation statements)
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“…The redox couples with different oxidation states serve as conduits for electron transfer, enabling electrons flow into halogenated organic compounds. [107][108][109][110][111][112][113] Chen et al 114 employed ZnCl 2 as the media to facilitate the electrocatalytic reduction of PCP. It indicated that the electrocatalytic mechanism of PCP reduction predominantly follows an indirect electroreduction pathway involving Zn/Zn 2þ as the redox media.…”
Section: Indirect Electrocatalytic Dehalogenation Via Mediamentioning
confidence: 99%
See 1 more Smart Citation
“…The redox couples with different oxidation states serve as conduits for electron transfer, enabling electrons flow into halogenated organic compounds. [107][108][109][110][111][112][113] Chen et al 114 employed ZnCl 2 as the media to facilitate the electrocatalytic reduction of PCP. It indicated that the electrocatalytic mechanism of PCP reduction predominantly follows an indirect electroreduction pathway involving Zn/Zn 2þ as the redox media.…”
Section: Indirect Electrocatalytic Dehalogenation Via Mediamentioning
confidence: 99%
“…Introducing redox couples as media for indirect electrocatalytic dehalogenation are the third mechanism presented in Figure 4C. The redox couples with different oxidation states serve as conduits for electron transfer, enabling electrons flow into halogenated organic compounds 107–113 . Chen et al 114 .…”
Section: Mechanisms Of Electrocatalytic Reduction Dehalogenationmentioning
confidence: 99%
“…A number of transition metal macrocycles have shown promise in catalytic reductive dehalogenation, an important transformation to degrade many common water pollutants. Cobalt macrocycles, including cobalt phthalocyanines and cobaloximes, , have shown promise in electrocatalytically reducing chlorinated compounds. Cobalt and iron porphyrins immobilized on TiO 2 nanoparticles make use of favorable interfacial kinetics to support multiple electron transfer and enable photocatalytic C–Cl bond breaking following visible-light excitation. Recognizing that these examples are productive toward carbon–halogen bond breaking, these molecular catalysts may be a good place to look for developing treatment systems for the degradation of particularly challenging per- and polyfluoroalkyl substances (PFAS) pollutants.…”
Section: Reactivitymentioning
confidence: 99%
“…330 A number of transition metal macrocycles have shown promise in catalytic reductive dehalogenation, an important transformation to degrade many common water pollutants. Cobalt macrocycles, 331 including cobalt phthalocyanines 332 and cobaloximes, 333,334 have shown promise in electrocatalytically reducing chlorinated compounds. Cobalt and iron porphyrins immobilized on TiO 2 nanoparticles make use of favorable interfacial kinetics to support multiple electron transfer and enable photocatalytic C−Cl bond breaking following visiblelight excitation.…”
Section: Zeolitesmentioning
confidence: 99%
“…[11][12][13][14][15] Based on the similar structure with vitamin B 12 , metalloporphyrinoids can also be used as efficient catalysts for the C-Cl bond cleavage of environmentally harmful organochloride through an electrocatalytic reduction process. [16][17][18][19][20][21] An in-depth study of the mechanism has demonstrated that the first step is a dissociative electron transfer from the reduced metal-center to the organochloride, leading to chloride elimination and the formation of a radical species. The re-oxidized metal complexes can then be re-used for the next catalytic cycle.…”
Section: Introductionmentioning
confidence: 99%