EventsThe 1st International Electronic Conference on Crystals
Published
This submission belongs to the session D. Interactions in Crystal Structures and Crystal Engineering of the event The 1st International Electronic Conference on Crystals
Published date
21 May, 2018
Citation
Ana M. Garcia-Deibe, Matilde Fondo, Julio Corredoira, Jesus Sanmartin-Matalobos, 2D supramolecular structure for a chiral heterotrinuclear ZnII₂HoIII complex through varied H-bonds connecting solvates and counterions, in Proceedings of The 1st International Electronic Conference on Crystals, 21 May–31 May 2018, MDPI: Basel, Switzerland, doi: 10.3390/IECC_2018-05247
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2D supramolecular structure for a chiral heterotrinuclear ZnII2HoIII complex through varied H-bonds connecting solvates and counterions

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1. Dpt. of Inorganic Chemistry. Universidade de Santiago de Compostela. 15782. SPAIN
Abstract

We report the crystal structure of [Zn2HoIII(L)(ald)(HO)(H2O)3(MeCN)](NO3)2·EtOH [being H3L = 2-(5‑bromo-2-hydroxy-3-methoxyphenyl)-1,3-bis[4-(5-bromo-2-hydroxy-3-methoxy phenyl)-3-azabut-3-enyl]-1,3-imidazolidine); and Hald = 5‑bromo-2-hydroxy-3-methoxybenzaldehyde]. Despite the presence of two bulky multidentate ligands, as well as several monodentate ligands surrounding the nonacoordinated holmium cation, and the two pseudooctahedral zinc ions, the intricate H-bonded system formed by this chiral heterotrinuclear complex is only expanded in a 2D supramolecular structure. The interactions involve the nitrate counterions and the solvated ethanol, in such way that each complex unit is connected to an identical enantiomer, and to two units of inverted chirality through H bonds

Keywords
H-bond system
metallosupramolecular structure
heterotrinuclear complex
holmium
lanthanide
Manuscript
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