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Synthesis, characterization, and structural determination of copper(II) complexes with alkyl derivatives of hydroxybenzophenones.

Authors :
Gonçalves, Cristiane Batista
Marinho, Maria Vanda
Dias, Danielle Ferreira
Dos Santos, Marcelo Henrique
Martins, Felipe Terra
Doriguetto, Antônio Carlos
Source :
Journal of Coordination Chemistry. Mar2017, Vol. 70 Issue 5, p898-913. 16p.
Publication Year :
2017

Abstract

Four mononuclear copper(II) complexes, [Cu(LFQM-115)2] (1), [Cu(LFQM-116)2] (2), [Cu(LFQM-117)2] (3) and [Cu(octyloxy)2] (4) [LFQM-115 = 2-hydroxy-4-O-methylbenzophenone (C14H11O3), LFQM-116 = 2-hydroxy-4-O-butylbenzophenone (C17H18O3), LFQM-117 = 2-hydroxy-4-O-(33-dimethylallyl)benzophenone (C18H18O3) and octyloxy = 2-hydroxy-4-O-octylbenzophenone (C21H25O3)], have been prepared and investigated by infrared spectroscopy, thermal analysis, and powder and single crystal X-ray diffraction. Even though the synthesis and infrared analysis of1,2, and4have been reported previously, their crystal structures were elucidated for the first time here. In addition, the crystal structures of LFQM-116 and LFQM-117 were also determined by single crystal X-ray diffraction. The pseudo-translational symmetry found in LFQM-116 and the isomorphism between LFQM-115 and LFQM-117 are discussed. The complexes were prepared from a reaction of copper(II) nitrate trihydrate and the respective ligand in a (1:2) molar ratio in methanol (for1and2) or THF (for3and4) with addition of NaOH. Furthermore, crystallographic studies show that each copper(II) exhibits a square planar geometry, coordinated by four oxygens of two ligands. The nature and crystal packing of the intermolecular interactions are discussed. Compounds2and3are isomorphic crystals and all structures have the same supramolecular synthon. [ABSTRACT FROM PUBLISHER]

Details

Language :
English
ISSN :
00958972
Volume :
70
Issue :
5
Database :
Academic Search Index
Journal :
Journal of Coordination Chemistry
Publication Type :
Academic Journal
Accession number :
121307504
Full Text :
https://doi.org/10.1080/00958972.2017.1280783