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Organotin‐Functionalized Crown Ethers as Ditopic Hosts for Lithium Salts: Synthesis, Structures and Complexation Studies of X 3 SnCH 2 [16]‐crown‐5 (X = I, Br, Cl)
Author(s) -
Arens Verena,
Naseer Muhammad Moazzam,
Lutter Michael,
IovkovaBerends Ljuba,
Jurkschat Klaus
Publication year - 2018
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201800054
Subject(s) - chemistry , intramolecular force , acetonitrile , crown ether , crystallography , tin , nuclear magnetic resonance spectroscopy , electrospray ionization , inorganic chemistry , lithium (medication) , octahedron , crystal structure , stereochemistry , organic chemistry , ion , medicine , endocrinology
The syntheses of the organotin‐substituted crown ethers X 3 SnCH 2 [16]‐crown‐5 ( 2 , X = I; 3 , X = Br; 4 , X = Cl), and the organostannate complex Ph 4 P[ 4· Cl] are reported. These compounds are characterized by 1 H, 13 C, and 119 Sn, NMR spectroscopy, elemental analyses, electrospray ionization mass spectrometry, and single‐crystal X‐ray diffraction studies. The solid‐state structure of 2 is characterized by two intramolecular O→Sn interactions, whereas 3 and 4 each contain one intra‐ and one intermolecular O→Sn interactions involving crown ether and water oxygen atoms. The tin atoms are six‐coordinate showing each a distorted octahedral environment. NMR spectroscopic studies indicate that hexacoordination is retained in solution. The compounds 3 and 4 are ditopic hosts for LiBr and LiCl, and have the ability to solubilize these salts in acetonitrile. The preferred selectivity of these compounds containing [16]‐crown‐5 moieties (known to be selective for sodium salts), towards lithium salts is credited to the increased Lewis acidity of the tin atom and hence the strong intramolecular O→Sn interactions.