Xiong, Shuangyu; Sun, Wei; Chen, Rong; Yuan, Zhiqiang; Cheng, Xinjian published an article in 2021. The article was titled 《Fluorescent dialdehyde-BODIPY chitosan hydrogel and its highly sensing ability to Cu2+ ion》, and you may find the article in Carbohydrate Polymers.Safety of 1-Iodopyrrolidine-2,5-dione The information in the text is summarized as follows:
Fluorescent hydrogel with proper hydrophilicity and thermal stability, excellent sensitivity and high selectivity has important practical and scientific significance, especially in heavy metal ion detection. In this work, by adjusting the content of [2, 6-Bis-[4-formylthiophene]]-1,3,5,7-tetramethyl-8-phenyl-4, 4-difluoroborazaindoloene (B3), as a crosslinking agent, a series of chitosan- fluoroboron dipyrrole-chitosan-based fluorescent hydrogels (CBC) with large stokes shift were designed and prepared The hydrogels can be used as fluorescent probes for identifying Cu2+ in aqueous solution The linear quenching range of Cu2+ is 0-50 μM, and the detection limit and quenching constant are 4.75 μM and 3.52 x 104 M-1, resp. Under the interaction of Cu2+, the imine bond C=N was converted to C- N bond, which causes the phenomenon of fluorescence quenching. In addition, relatively high crosslink d. improves hydrophilicity and thermal stability of initial chitosan, and made the swelling ability better. The experimental part of the paper was very detailed, including the reaction process of 1-Iodopyrrolidine-2,5-dione(cas: 516-12-1Safety of 1-Iodopyrrolidine-2,5-dione)
1-Iodopyrrolidine-2,5-dione(cas: 516-12-1) is used in the preparation of vinyl sulfones from olefins and benzenesulfinic acid. It acts as a source for I+ and involved in Hunsdiecker reactions for the conversion of cinnamic acids, and propiolic acids to the corresponding alfa-halostyrenes and 1-halo-1-alkynes respectively. Safety of 1-Iodopyrrolidine-2,5-dione
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com