Literature DB >> 23713911

Hexafluoridotechnetate(IV) revisited.

Samundeeswari Mariappan Balasekaran1, Matthias Molski, Johann Spandl, Adelheid Hagenbach, Roger Alberto, Ulrich Abram.   

Abstract

Novel synthetic routes to hexafluoridotechnetate(IV) are reported, and for the first time the single-crystal X-ray structures of several M2[TcF6] salts (M = Na, K, Rb, Cs, NH4, and NMe4) were determined. The ammonium and the alkaline metal salts crystallize in the trigonal space group P3m, while the NMe4(+) salt belongs to the space group R3. [TcF6](2-) salts are widely stable in aqueous solution. In alkaline media, however, a slow hydrolysis is observed, and the first hydrolysis product, the dimeric, oxido-bridged complex [F5Tc-O-TcF5](4-), could be studied structurally.

Entities:  

Year:  2013        PMID: 23713911     DOI: 10.1021/ic400775e

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  2 in total

1.  Syntheses, Raman spectroscopy and crystal structures of alkali hexa-fluorido-rhenates(IV) revisited.

Authors:  James Louis-Jean; Samundeeswari Mariappan Balasekaran; Dean Smith; Ashkan Salamat; Chien Thang Pham; Frederic Poineau
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2018-04-06

2.  Coexistence of metamagnetism and slow relaxation of magnetization in ammonium hexafluoridorhenate.

Authors:  James Louis-Jean; Samundeeswari M Balasekaran; Keith V Lawler; Adrián Sanchis-Perucho; José Martínez-Lillo; Dean Smith; Paul M Forster; Ashkan Salamat; Frederic Poineau
Journal:  RSC Adv       Date:  2021-02-03       Impact factor: 3.361

  2 in total

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