“…The oxidation of alcohols to aldehydes is a reaction under continuous investigation due to its importance in synthetic chemistry in both the laboratory and industry. With increasing concern regarding environmental issues, more sustainable approaches, particularly those employing catalytic routes such as cheap-metal based catalysis 1,2 and photocatalysis, [3][4][5] for the conversion are highly desirable compared to the traditional ones. 6,7 Whether a process is environmentally benign or not depends largely on the usage of catalysts, oxidants and reaction conditions (temperature and reaction media).…”
In this piece of work, CuI and its catalysis on aerobic oxidation of alcohols has been mechanistically investigated with N,N,N′,N′-tetramethylethylenediamine (TMEDA) as a ligand and 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) as a co-catalyst....
“…The oxidation of alcohols to aldehydes is a reaction under continuous investigation due to its importance in synthetic chemistry in both the laboratory and industry. With increasing concern regarding environmental issues, more sustainable approaches, particularly those employing catalytic routes such as cheap-metal based catalysis 1,2 and photocatalysis, [3][4][5] for the conversion are highly desirable compared to the traditional ones. 6,7 Whether a process is environmentally benign or not depends largely on the usage of catalysts, oxidants and reaction conditions (temperature and reaction media).…”
In this piece of work, CuI and its catalysis on aerobic oxidation of alcohols has been mechanistically investigated with N,N,N′,N′-tetramethylethylenediamine (TMEDA) as a ligand and 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) as a co-catalyst....
“…Based on the control experiments and literature reports, 1,10,22 a plausible reaction mechanism is proposed in Scheme 3. Initially, the photogenerated electron–hole pairs of gCN/MnO/MnO(OH) are effectively separated upon light illumination.…”
Section: Resultsmentioning
confidence: 99%
“…Initially, the photogenerated electron–hole pairs of gCN/MnO/MnO(OH) are effectively separated upon light illumination. 22 The photo-generated electrons accumulated on the CB of the photocatalyst activate O 2 to superoxide radical anions (O 2 ˙ − ). Alternatively, the photogenerated hole (h + ) of the photocatalyst undergoes a single electron oxidation process with water to produce H 2 O 2 .…”
Section: Resultsmentioning
confidence: 99%
“…Afterwards, the reaction between the nucleophilic ˙CH 3 -radicals and the most-electrophilic carbon of (iso)quinoliniums ( 1 ) provides the desired product 2 . 22 Throughout the procedure, O 2 is converted to H 2 O 2 (Scheme 3). The same mechanism is applicable for the trideuteromethylation of (iso)quinoliniums (Table 3); however, in this instance, ˙CD 3 -radicals will be produced from DMSO-d 6 .…”
In order to activate dimethylsulfoxide (DMSO, CH3SOCH3) for serving as a methylation agent in the C-H functionalization of (iso)quinoliniums (1), a heterogeneous photo-Fenton-like method comprising the in-situ generation of hydroxyl...
“…which directly kill various microbes. [23][24][25] Whereas photocatalytic disinfection has been widely investigated over TiO 2 and the compounds containing precious metals (e.g. AgInS 2 , AgBr, AgVO 3 , etc.…”
Semiconductor heterostructures are of critical importance in steering the flow of photocarriers (i.e. e- and h+). Here, we have fabricated heterostructure-based semiconductor fibers comprising electrospun In2O3 nanofibers coaxially wrapped by...
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