Itsukashi, Masako’s team published research in Journal of Photochemistry and Photobiology, A: Chemistry in 2018 | CAS: 624-73-7

1,2-Diiodoethane(cas: 624-73-7) is one of organic iodides. Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Recommanded Product: 624-73-7

In 2018,Itsukashi, Masako; Nakashima, Nobuaki; Yatsuhashi, Tomoyuki published 《Coulomb explosion of a series of α, ω-diiodoalkanes in intense laser fields》.Journal of Photochemistry and Photobiology, A: Chemistry published the findings.Recommanded Product: 624-73-7 The information in the text is summarized as follows:

The kinetic energy of ions produced by a Coulomb explosion, in which multiply charged mol. cations dissociate, is determined by the charge number, mass, and geometric configuration of the ions upon explosion. Although the importance of the structural deformation and migration of atoms on kinetic energy variations is well known, there has been little investigation into the effect of charge localization before the ions are released. In this study, the angular distributions of iodine and carbon ions ejected from linear alkanes, which have one iodine atom on each side of an alkyl chain having one to six carbon atoms, are measured. The highly charged iodine ions (I4+, I5+) are emitted mostly along the laser polarization direction, whereas the angular distribution of iodine ions becomes isotropic the longer the alkyl chain and the lower the charge number of iodines are. Furthermore, the longer the alkyl chain, the higher the kinetic energy of iodine and carbon ions. The emission of ions is discussed in terms of the selective ionization of aligned mols. based on their MOs. The charge localization during ionization in strong alternating elec. fields followed by two-body Coulomb explosion via a C-I bond cleavage is proposed. The experimental process involved the reaction of 1,2-Diiodoethane(cas: 624-73-7Recommanded Product: 624-73-7)

1,2-Diiodoethane(cas: 624-73-7) is one of organic iodides. Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons–Smith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.Recommanded Product: 624-73-7

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com