کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1309586 | 975213 | 2009 | 5 صفحه PDF | دانلود رایگان |
The reaction between the 1,4-bis(5-tetrazolyl)benzene ligand (H2btb) and different magnesium salts allowed the recovery of two different molecular salts, namely [Mg(H2O)6](btb) (1) and [Mg(H2O)6](Hbtb)2·2H2O (2). These crystalline materials were fully characterized by spectroscopic, thermal and diffraction methods. In both cases the octahedrally coordinated hexaaquo Mg(II) ions are linked through several strong H-bond interactions of the OH⋯N type to the btb anions, completely or partially deprotonated in 1 and 2, respectively. The thermal analysis has established that, in both cases, all water molecules are lost below 200 °C. Interestingly, the process is completely reversible upon exposure to water-saturated atmosphere. Unfortunately, the anhydrous phases are amorphous, and no structural information could be derived form our PD traces, even if a number of partially crystalline intermediates, formed during the dehydration processes, were observed by thermodiffractometric methods.
Two hexaaquomagnesium salts of the 1,4-bis-(5-tetrazolyl)benzene ligand afford, upon heating, partially, or fully, dehydrated polycrystalline or amorphous phases, depending on the extent of the thermal treatment. These transformations are 100% reversible and have been studied by thermodiffractometric methodsFigure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 362, Issue 12, 15 September 2009, Pages 4630–4634