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The Thermal Stability of Tris(methimazolyl)borates and Their Germanium Complexes
Author(s) -
Wallace Dawn,
Chalmers Kirsten,
Dodds Christopher A.,
Stepek Iain A.,
Armstrong David R.,
Berlouis Leonard E. A.,
Reglinski John,
Spicer Mark D.
Publication year - 2014
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201301588
Subject(s) - chemistry , germanium , boron , thermogravimetric analysis , inorganic chemistry , thermal stability , crystallography , photochemistry , organic chemistry , silicon
A series of methimazole‐based soft scorpionate anions ([RTm Me ] – , R = H, Ph, Me, n Bu) bearing substitution at the bridgehead boron have been used to produce a series of germanium complexes of general formulae [Ge(RTm Me ) 2 ]I 2 . Structural analyses of the germanium complexes by X‐ray crystallography reveal that they all contain an octahedral S 6 coordination sphere. The scorpionate anions (as their Li or Na salts) and their germanium complexes have been studied by thermogravimetric analysis. This analysis suggests that the degradation pathway for the free scorpionate anions differs from that of the complexes. Both pathways involve the loss of a methimazole ring thereby supporting the view that cleavage of the boron–nitrogen bonds can occur under thermally aggressive conditions. As expected, the presence of the germanium alters the degradation profile of the anion. In contrast to the free anions, the four complexes all display a similar mechanism for degradation. Although the presence of the germanium enforces a conformational change in the anions, its presence does not significantly increase the stability of the boron–nitrogen bonds.