Mixed salts containing croconate violet, lanthanide and potassium ions: Crystal structures and spectroscopic characterization of supramolecular compounds

被引:6
作者
Faria, Luiz Felipe O. [1 ]
Soares, Antonio L., Jr. [1 ]
Diniz, Renata [1 ]
Yoshida, Maria I. [2 ]
Edwards, Howell G. M. [3 ]
de Oliveira, Luiz Fernando C. [1 ]
机构
[1] Univ Fed Juiz de Fora, Nucleo Espectroscopia & Estrutura Mol, Dept Quim, BR-36036900 Juiz De Fora, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Quim, Belo Horizonte, MG, Brazil
[3] Univ Bradford, Raman Spect Grp, Univ Analyt Ctr, Div Chem & Forens Sci, Bradford BD7 1DP, W Yorkshire, England
关键词
Croconate violet; Lanthanide ions; Crystal structure; Vibrational spectra; Pseudo-oxocarbons; BOND-DELOCALIZED DIANION; X-RAY-DIFFRACTION; PSEUDO-OXOCARBON; VIBRATIONAL-SPECTRA; THERMAL-BEHAVIOR; SINGLE-CRYSTAL; SQUARATE; ACID; COPPER(II); COMPLEXES;
D O I
10.1016/j.ica.2009.09.050
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The vibrational spectra and crystal structures of four lanthanide and potassium salts of 3,5-bis(dicyanomethylene)cyclopentane-1,2,4-trionate (C(1)1N(4)O(3)(2-)), known as croconate violet (CV), are described in this work. All LnKC(22)N(8)O(6) (Ln = La+3, Nd+3, Gd+3 and Ho+3) compounds are isostructural, crystallizing in the triclinic P (1) over bar space group. In each compound the lanthanide ion is acting as both monodentate and chelate metal sites, whereas the potassium presents only monodentate coordination. The crystal structure shows the formation of a periodic 2D structure extended by K-N bonds parallel to the crystallographic [0 0 1] direction; these 2D sheets form hydrogen bonds with water molecules giving rise to a 3D extended arrangement. It is not possible to observe any type of pi-interaction and the main forces responsible to stabilize the structures are the hydrogen bonds. The vibrational spectra of all the compounds are very similar, and the most important vibrational markers for the croconate violet ion, namely the nu(C N) and nu(C O) modes, behave differently: the nu(C N) modes are not shifted by the presence of the lanthanide ion species, only showing small band intensity differences, whereas the nu(C O) bands are shifted to higher wavenumbers, due to their coordination to the metal sites. (C) 2009 Elsevier B.V. All rights reserved.
引用
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页码:49 / 56
页数:8
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