The role of weak interactions in the crystal packing of two novel 1D Hg(II) coordination polymers and investigation for preparation of their rod and spherical structures

被引:3
|
作者
Mahmoudi, Ghodrat [1 ]
Hayati, Payam [2 ]
Mohammadi, Khosro [3 ]
Masoudiasl, Ardavan [1 ]
Mague, Joel T. [4 ]
Zangrando, Ennio [5 ]
机构
[1] Univ Maragheh, Fac Sci, Dept Chem, POB 55181-83111, Maragheh, Iran
[2] Nano Gostaran Navabegh Fardaye Dashtestan Co, Persian Gulf Sci & Technol Pk, Borazjan, Iran
[3] Persian Gulf Univ, Fac Sci, Dept Chem, Bushehr 75169, Iran
[4] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
[5] Univ Trieste, Dept Chem & Pharmaceut Sci, Via L Giorgieri 1, I-34127 Trieste, Italy
关键词
Hg coordination polymer; Crystal structure; Ultrasound irradiation; Topology; Hirshfeld surface analysis; Morphology; HIRSHFELD SURFACE-ANALYSIS; INTERMOLECULAR INTERACTIONS; SONOCHEMICAL SYNTHESIS; DFT CALCULATIONS; REACTION-TIME; COUNTER-ION; COMPLEXES; LIGANDS; SPECTROSCOPY; TEMPERATURE;
D O I
10.1016/j.ica.2019.119243
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two novel 1D mercury(II) polymeric coordination compounds, namely {[Hg-2(L)(Cl)(4)].0.5(H2O)}(n) (1) and [Hg-2(L)(Br)(4)](n) (2) (where L = bis(2-pyridylmethyl)-ketazine), C14H15N4) were synthesized using either a branched tube or sonochemical method. The XRD powder spectra confirmed the same crystalline phase for compounds produced by both the methods. Single crystal X-ray analysis of 1 and 2 obtained using the branched tube revealed isomorphous and isostructural structures of 2,2,3C6 topology, comprising penta-coordinated Hg2+ ions. The Hirshfeld surface analysis of the crystal packing of complexes 1 and 2 was discussed in detail to evaluate the interactions among the polymers that are affected by the different halogen atoms present. The effects of experimental conditions utilized for the sonochemical method (power and reaction time) were analyzed with respect to the growth and final morphology of the nanostructures obtained. While reaction time directly affected the final size of the nanostructures of 1 and 2, the sonication power showed an inverse trend. The microcrystals of 1 and 2 thus obtained were further analyzed by IR spectroscopy, X-ray powder diffraction (XRD) and scanning electron microscopy (SEM).
引用
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页数:8
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