Studies of Halogen Bonding Induced by Pentafluorosulfanyl Aryl Iodides: A Potential Group of Halogen Bond Donors in a Rational Drug Design

Studies of Halogen Bonding Induced by Pentafluorosulfanyl Aryl Iodides: A Potential Group of Halogen Bond Donors in a Rational Drug Design

The activation of halogen bonding by the substitution of the pentafluoro-&#955;<sup>6</sup>-sulfanyl (SF<sub>5</sub>) group was studied using a series of SF<sub>5</sub>-substituted iodobenzenes. The simulated electrostatic potential values of SF<sub>5<...

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Bibliographic Details
Main Authors: Yuji Sumii, Kenta Sasaki, Seiji Tsuzuki, Norio Shibata
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Molecules
Subjects:
halogen bonding
fluorine
iodine
pentafluorosulfanyl
titration
ab initio calculation
nmr study
drug design
Online Access:https://www.mdpi.com/1420-3049/24/19/3610

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