کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1335372 | 979526 | 2007 | 8 صفحه PDF | دانلود رایگان |

Reaction of an excess of hydrated LnCl3 (Ln = La, Gd, Ho, Yb, Y) with sodium 5-(2-pyridyl)tetrazolate (Napytz) in water led to the formation of either cationic disubstituted complexes (La, Gd, Ho) or neutral μ-hydroxo-bridged dimers (Y, Yb). Interestingly, there is a lack of propensity for these disubstituted complexes to redistribute forming trisubstituted ones, which is a common behaviour in lanthanoid chemistry. Also, compared to their corresponding lanthanoid carboxylates, all these products are discrete molecular entities forming an extensive hydrogen-bonded and/or π stacking network rather than hybrid polymeric frameworks.
Reaction of an excess of hydrated LnCl3 (Ln = La, Gd, Ho, Yb, Y) with sodium 5-(2-pyridyl)tetrazolate in water led to the formation of either cationic disubstituted complexes (La, Gd, Ho) or neutral μ-hydroxo-bridged dimers (Y, Yb).Figure optionsDownload as PowerPoint slide
Journal: Polyhedron - Volume 26, Issue 18, 20 November 2007, Pages 5406–5413