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Title: | Single stranded helical chains of C-H?? interactions further connected by halogen-halogen interactions of type i to construct supramolecular structure of (E)-5-(diethylamino)-2-[(4-iodophenylimino)methyl]phenol compound | Authors: | Kaştaş, G. Albayrak, Ç. Odabaşoğlu, Mustafa Frank, R. |
Keywords: | Halogen-halogen interaction Helical chain Intermolecular hydrogen bond Intramolecular hydrogen bond Schiff base Tautomerism Halogen-halogen interactions Helical chains Intermolecular hydrogen bonds Schiff-base Functional groups Hydrogen bonds Phenols Stereochemistry X ray diffraction Supramolecular chemistry (E) 5 (diethylamino) 2 ((4 iodophenylimino)methyl)phenol (E)-5-(diethylamino)-2-((4-iodophenylimino)methyl)phenol ethylamine halogen phenol derivative solvent article chemical structure chemistry conformation hydrogen bond infrared spectroscopy ultraviolet spectrophotometry X ray crystallography Crystallography, X-Ray Ethylamines Halogens Hydrogen Bonding Models, Molecular Molecular Conformation Solvents Spectrophotometry, Ultraviolet Spectroscopy, Fourier Transform Infrared |
Abstract: | In this study, (E)-5-(diethylamino)-2-[(4-iodophenylimino)methyl]phenol compound was investigated from the point of stacking interactions assembling the supramolecular network, conformational isomerism and tautomerism. For this purpose, X-ray diffraction, FT-IR and UV/Vis spectroscopic techniques were used, giving the following structural and spectroscopic properties of the compound: The title compound has two conformers (anti and eclipsed) in the crystal structure resulting from rotation about C-N single bond of ethyl group. Both conformers prefer enol form in the solid state, adopting E configuration about the CN double bond. The supramolecular architecture of the compound is constructed by two non-covalent interactions as C-H?? and halogen-halogen interactions. The repetition of C-H?? interactions is resulted in a single-stranded helical structure. The helical structures are further connected by C-I?I-C interactions of Type I to construct the two dimensional supramolecular network defined as (6,3)-net in Wells nomenclature. The title compound adopts both enol and keto forms in EtOH (a polar and protic solvent) while enol form is preferred in the solid state. © 2012 Elsevier B.V. All rights reserved. | URI: | https://hdl.handle.net/11499/8537 https://doi.org/10.1016/j.saa.2012.03.058 |
ISSN: | 1386-1425 |
Appears in Collections: | Denizli Teknik Bilimler Meslek Yüksekokulu Koleksiyonu PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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