Author:
Liantonio Rosalba,Logothetis Thomas A.,Messina Maria T.,Metrangolo Pierangelo,De Santis Alessandra,Pilati Tullio,Resnati Giuseppe
Abstract
2,2':6',2''-Terpyridine (1) is a well-known electron donor module in metal coordination chemistry and typically works as a tridentate ligand. Here it is shown that 1 can also work as electron donor towards iodoperfluorocarbons both in solution and in the solid phase. Halogen-bonded supramolecular systems are thus obtained. Specifically, terpyridine 1 self-assembles with 1,2,4,5-tetrafluoro-3,6-diiodobenzene (2) and affords the trimeric adduct 3, which is stable and crystalline in the air at room temperature. Single crystal X-ray analysis shows how in adduct 3 both iodine atoms of one molecule of 2 are halogen-bonded to the nitrogen atoms of external pyridine rings of two molecules of 1 that act as monodentate electron donors.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
14 articles.
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1. Halogen bonding in the co-crystallization of potentially ditopic diiodotetrafluorobenzene: a powerful tool for constructing multicomponent supramolecular assemblies;National Science Review;2020-08-07
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5. Pentaerythritol tetrakis(4-iodo-2,3,5,6-tetrafluorophenyl) ether: a tecton for the self-assembly of double strand 1D infinite chains;Journal of Fluorine Chemistry;2005-02