کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1308336 | 975169 | 2009 | 6 صفحه PDF | دانلود رایگان |

The trans-[Cr(cyclam)(nic-O)2]ClO4 (cyclam = 1,4,8,11-tetraazacyclotetradecane; nic-O = O-coordinated nicotinate) has been prepared and structurally characterized by single-crystal X-ray diffraction at 150 K. The chromium atom is in a tetragonally compressed octahedral environment with four N atoms of the macrocyclic ligand in equatorial positions and two O-bonded nicotinates in trans axial positions. The macrocyclic cyclam adopts the centrosymmetric trans-III configuration with six- and five-membered chelate rings in chair and gauche conformation, respectively. The IR and visible spectral properties are consistent with the result of X-ray crystallography. The resolved band maxima of the electronic d–d spectrum are fitted with secular determinant for quartet state energy of d3 configuration in tetragonal field including configurational interaction. It is found that the nitrogen atoms of the cyclam ligand are a strong σ-donors and that O-bonded nicotinato group has strong σ- and π-donor characteristics toward the chromium(III) ion.
The trans-[Cr(cyclam)(nic-O)2]ClO4 has been synthesised and characterized by spectroscopic methods, and its crystal structure is reported. The spectral properties are in agreement with the result of X-ray crystallography, which show that the nicotinato group is bonded to chromium(III) through the one O of its oxygen atoms and the cyclam ligand adopts the most stable trans-III configuration.Figure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 362, Issue 11, 15 August 2009, Pages 4231–4236