Synthesis, structural characterization, Hirshfeld surface analysis and spectroscopic studies of cadmium (II) chloride complex with 4-hydroxy-1-methylpiperidine

被引:15
作者
Soudani, S. [1 ]
Ferretti, V. [2 ,3 ]
Jelsch, C. [4 ]
Lefebvre, F. [5 ]
Ben Nasr, C. [1 ]
机构
[1] Univ Carthage, Fac Sci Bizerte, Lab Chim Mat, Zarzouna 7021, Tunisia
[2] Dept Chem & Pharmaceut Sci, Via Fossato di Mortara 17, I-44121 Ferrara, Italy
[3] Ctr Struct Diffractometry, Via Fossato di Mortara 17, I-44121 Ferrara, Italy
[4] Univ Lorraine, CNRS, Inst Jean Barriol, CRM2, Vandoeuvre Les Nancy, France
[5] Ecole Super Chim Phys Elect, Lab Chim Organometall Surface LCOMS, F-69626 Villeurbanne, France
关键词
4-Hydroxy-1-methylpiperidine; Hexachloridocadmate; X-ray diffraction; Hirshfeld surface analysis; NMR; DFT calculations; DENSITY-FUNCTIONAL THEORY; VIBRATIONAL-SPECTRA; CRYSTAL-STRUCTURES; AMMONIUM-SALTS; PIPERIDINE; MOLECULES; CONTACTS;
D O I
10.1016/j.jssc.2015.12.029
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The chemical preparation, crystal structure, Hirshfeld surface analysis and spectroscopic characterization of the novel cadmium (II) 4-hydroxy-1-methylpiperidine complex, Cd4Cl10(C6H14NO)(2)center dot 2H(2)O, have been reported. The atomic arrangement can be described as built up by an anionic framework, formed by edge sharing CdCl6 and CdCl5O octahedral linear chains spreading along the a-axis. These chains are interconnected by water molecules via O-H center dot center dot center dot Cl and O-H center dot center dot center dot O hydrogen bonds to form layers parallel to (011) plane. The organic cations are inserted between layers through C-H center dot center dot center dot Cl hydrogen bonds. Investigation of intermolecular interactions and crystal packing via Hirshfeld surface analysis reveals that the H-C center dot center dot center dot Cl and H-C center dot center dot center dot H-C intermolecular interactions are the most abundant contacts of the organic cation in the crystal packing. The statistical analysis of crystal contacts reveals the driving forces in the packing formation. The C-13 and N-15 CP-MAS NMR spectra are in agreement with the X-ray structure. The vibrational absorption bands were identified by infrared spectroscopy. DFT calculations allowed the attribution of the NMR peaks and of the IR bands. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:7 / 13
页数:7
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