Nicolis, Ioannis et al. published their research in Journal of the American Chemical Society in 1993 | CAS: 53784-83-1

Heptakis(6-Bromo-6-Deoxy)-閻?Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon闂佺偨鍎茶ぐ绲﹐mine bond is electrophilic, i.e. alkyl bromides are alkylating agents. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Synthetic Route of C42H63Br7O28

Molecular organization in the 6-bromo-6-deoxycyclodextrins, formation of molecular layers, and the first crystal structure of a selectivity perfunctionalized 閻?cyclodextrin was written by Nicolis, Ioannis;Coleman, Anthony W.;Charpin, Pierrette;Villain, Francoise;Zhang, Ping;Ling, Chang Chung;de Rango, Colette. And the article was included in Journal of the American Chemical Society in 1993.Synthetic Route of C42H63Br7O28 This article mentions the following:

6-Bromo-6-deoxycyclodextrins form stable monomol. at the air-H2O interface, with mol. areas of 180, 220 and 260 闁?sup>2 for 濞?, 閻? and 缂?Br-CD. In the case of the heptakis-bromo-閻?CD compound 3 dimensional crystal structure was determined The heptakis-Br-閻?CD compound is monoclinic, space group P21, with a 15.714(3), b 15.917(6), c 30.102(4) 闁? 閻?90.55(2)闁? Z = 2. The structure is as a novel packing of dimeric 閻?cyclodextrin systems in a square arrangement. The layers are held together by Br-Br Van der Waals interactions giving rise to a quasi-continuous hydrophobic interface between the layers. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-閻?Cyclodextrin (cas: 53784-83-1Synthetic Route of C42H63Br7O28).

Heptakis(6-Bromo-6-Deoxy)-閻?Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon闂佺偨鍎茶ぐ绲﹐mine bond is electrophilic, i.e. alkyl bromides are alkylating agents. The principal reactions for organobromides include dehydrobromination, Grignard reactions, reductive coupling, and nucleophilic substitution.Synthetic Route of C42H63Br7O28

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary