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Complexation and enantioselectivity of novel bridge-like uranyl- 2-((1Z,9Z)-9-(2-Hydroxyphenyl)-3,5,6,8-tetrahydrobenzo[h][1,4,7,10] dioxadiazacyclododecin-2-yl)-5-methoxyphenol with chiral organophosphorus pesticide enantiomers of R/S-malathions
Published in Environmental Technology, 2022
Xuebing Tao, Rong Yang, Yang Xiao, Lifu Liao, Xilin Xiao, Changming Nie
In the field of actinide chemistry, the research on uranyl-salophens has always been a hot field that researchers are keen to study. The core of uranyl-salophen is uranyl ion (), and 5f-6d orbital hybridization leads to linear structure, the 5f orbital can form multiple coordination bonds [1–6]. The equatorial plane of perpendicular to the line usually forms four-, five- or six-dentate complexes [6–8]. In uranyl complexes, the uranium and oxygen atoms at both ends are usually in a straight line. This spatial position causes the donor atoms at the equatorial position to be on the same plane. In addition, the oxygen atoms on the equatorial plane are easily bridged to other atoms to form the coordination polymer [9].