An article A microfluidic reactor application for the continuous-flow photocatalytic selective synthesis of aromatic aldehydes WOS:000592362200006 published article about GRAPHITIC CARBON NITRIDE; BENZYL ALCOHOL; AQUEOUS SUSPENSION; OXIDATION; BENZALDEHYDE; NANOSHEETS; WATER in [Lima, Maria J.; Silva, Adrian M. T.; Silva, Claudia G.; Faria, Joaquim L.] Univ Porto, Fac Engn, Dept Engn Quim, Lab Separat & React Engn,Lab Catalysis & Mat LSRE, Rua Dr Roberto Frias S-N, P-4200465 Porto, Portugal; [Lima, Maria J.] Univ Minho, Ctr Phys, P-4800058 Guimaraes, Portugal; [Lima, Maria J.] Univ Minho, Phys Dept, Porto CFUM UP, P-4800058 Guimaraes, Portugal in 2020.0, Cited 48.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6. Safety of Benzyl Alcohol
Benzyl alcohol and a set ofpara-substituted derivatives (-NO2, -Cl, -CH3, -OCH3 and -OH) were converted to the corresponding aldehydes in a commercial continuous-flow microfluidic reactor. Due to the dimension and the rigidity of the commercial microfluidic reactor channels, a stable suspension with few-layer graphitic carbon nitride nanoparticles (GCN-TS) was used to avoid the blockage of the photocatalyst in the channels of the reactor. Preliminary photocatalytic batch experiments revealed that different reaction yields were obtained depending on the aromatic ring activating/deactivating nature of the substituent groups. Regarding the ex-periments under continuous-flow, the highest aldehyde production was obtained for the reactions with 4-methoxybenzyl alcohol as starting molecule, corresponding to 0.19 mM at a retention time of merely 0.75 min. The results show the possibility of employing microfluidic reactors for the selective photocatalytic conversion of aromatic alcohols for both process intensification and screening applications due to the drastic decrease of reaction time.
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Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles