Abstract
The differing geometrical constraints of the tripodal ligands tris(hydroxyphenyl)amine (N-cappedH3) and tris(3,5-di-t-Bu-2-hydroxyphenyl)methane (C-cappedH3) led, on reaction with [Re(t-BuN)3(OSiMe3)], to the isolation of the complexes [Re(t-BuN)2(N-capped)] (1) and [Re(OSiMe3)(t-BuN)2(C-cappedH)] (2), respectively. Both 1·1/2MeCN and 2 have been structurally characterized using X-ray synchrotron radiation.
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