2019
DOI: 10.1016/j.catcom.2019.03.011
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Atmospherical oxidative coupling of amines by UiO-66-NH2 photocatalysis under milder reaction conditions

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Cited by 42 publications
(18 citation statements)
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“…The XPS survey spectrum, as shown in Figure A, demonstrated the difference between yeast and yeast@UiO-66-NH 2 composites was that the Zr element only existed in the latter. In the yeast@UiO-66-NH 2 composites, the Zr 3d 5/2 and Zr 3d 3/2 are observed at around 182.57 and 185.02 eV in high-resolution XPS spectrum of Zr 3d (Figure B), respectively, indicating the existence of Zr 4+ . , The peaks at 182.57 and 185.02 eV were assigned to the Zr–O, and Zr–N bond, respectively. This is similar to the results reported in the literature to the formation of ZrO 2 and ZrN. , Figure C is the high-resolution XPS spectrum of C 1s, the peaks at 284.33 eV, 285.64 eV, and 287.20 eV are assigned to the C–C or C–H, carboxylate carbon (OCO) and carbonyl carbon (CO) bonds of the yeast cell wall functional groups.…”
Section: Resultssupporting
confidence: 89%
See 1 more Smart Citation
“…The XPS survey spectrum, as shown in Figure A, demonstrated the difference between yeast and yeast@UiO-66-NH 2 composites was that the Zr element only existed in the latter. In the yeast@UiO-66-NH 2 composites, the Zr 3d 5/2 and Zr 3d 3/2 are observed at around 182.57 and 185.02 eV in high-resolution XPS spectrum of Zr 3d (Figure B), respectively, indicating the existence of Zr 4+ . , The peaks at 182.57 and 185.02 eV were assigned to the Zr–O, and Zr–N bond, respectively. This is similar to the results reported in the literature to the formation of ZrO 2 and ZrN. , Figure C is the high-resolution XPS spectrum of C 1s, the peaks at 284.33 eV, 285.64 eV, and 287.20 eV are assigned to the C–C or C–H, carboxylate carbon (OCO) and carbonyl carbon (CO) bonds of the yeast cell wall functional groups.…”
Section: Resultssupporting
confidence: 89%
“…In the yeast@UiO-66-NH 2 composites, the Zr 3d 5/2 and Zr 3d 3/2 are observed at around 182.57 and 185.02 eV in high-resolution XPS spectrum of Zr 3d (Figure 3B), respectively, indicating the existence of Zr 4+ . 51,52 The peaks at 182.57 and 185.02 eV were assigned to the Zr−O, and Zr−N bond, respectively. This is similar to the results reported in the literature to the formation of ZrO 2 and ZrN.…”
mentioning
confidence: 99%
“…This intermediate could form benzaldimine by removing the H 2 O 2 molecule. Meanwhile, H 2 O 2 also acts as an additional oxidant to further oxidize carbon-centered radicals to generate benzaldimines. , Finally, the benzaldimine molecule and additional benzylamine undergo an addition reaction to obtain the desired imine product.…”
Section: Resultsmentioning
confidence: 99%
“…Overall, the observed byproducts are the same, regardless of the mechanism. Some research has even reached the anaerobic version (Scheme 9, bottom), where protons act as oxidants, generating hydrogen as byproduct [105]. As a result of this electron transfer, electron holes are generated, which also trigger the formation of the amine radical cation transient species.…”
Section: Oxidative Couplingmentioning
confidence: 99%
“…Otherwise, a ligand functionalization protocol of UiO-66 allowed the obtaining of different UiO-66-NH 2 MOFs, that enabled the isolation of the corresponding imine products under both aerobic and anaerobic conditions. [105]. There are also two recent examples of hybrid structures of MOFs capable of performing this organic transformation.…”
Section: Oxidative Couplingmentioning
confidence: 99%