Fujita, Daishi et al. published their research in Chem in 2016 | CAS: 3268-21-1

1,4-Diiodo-2,3,5,6-tetramethylbenzene (cas: 3268-21-1) belongs to iodide derivatives. Iodide-containing intermediates are common in organic synthesis, because of the easy formation and cleavage of the C–I bond. A typical method for synthesis of aromatic iodides is diazotization of primary aromatic amines followed by treatment of potassium iodide. Aliphatic alcohols are converted to alkyl iodides by treating with hydrogen iodide.Synthetic Route of C10H12I2

Self-Assembly of M30L60 Icosidodecahedron was written by Fujita, Daishi;Ueda, Yoshihiro;Sato, Sota;Yokoyama, Hiroyuki;Mizuno, Nobuhiro;Kumasaka, Takashi;Fujita, Makoto. And the article was included in Chem in 2016.Synthetic Route of C10H12I2 This article mentions the following:

Self-assembly is invaluable in the construction of giant mol. structures via a bottom-up approach. Although living organisms naturally make the most use of self-assembly and freely handle the mechanism at will, scientists are still far behind the level of nature. Inspired by the elegant structures of virus capsids, the authors have previously constructed roughly spherical giant metal complexes with the symmetry of an octahedron, cuboctahedron, and rhombicuboctahedron M6L12, M12L24, and M24L48, resp. Here, the authors report the 1st successful synthesis of an M30L60 mol. icosidodecahedron that consists of âˆ?00 components: 30 Pd(II) ions and 60 (2,5-bis(4-pyridyl-1,4-tetramethylphenylene)thiophene) ligands that assemble into the largest well-defined spherical macromol. to date (diameter of âˆ?.2 nm). Tuning the flexibility of the ligand was the key for successful self-assembly. A highly complex but sym. organized structure was identified through x-ray crystallog. anal. The interior space of the mol. complex is large enough (157,000 Å3) to enclose proteins. In the experiment, the researchers used many compounds, for example, 1,4-Diiodo-2,3,5,6-tetramethylbenzene (cas: 3268-21-1Synthetic Route of C10H12I2).

1,4-Diiodo-2,3,5,6-tetramethylbenzene (cas: 3268-21-1) belongs to iodide derivatives. Iodide-containing intermediates are common in organic synthesis, because of the easy formation and cleavage of the C–I bond. A typical method for synthesis of aromatic iodides is diazotization of primary aromatic amines followed by treatment of potassium iodide. Aliphatic alcohols are converted to alkyl iodides by treating with hydrogen iodide.Synthetic Route of C10H12I2

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