Reaction of an aminotroponiminato(chloro)germylene
[(i-Bu)2ATIGeCl] (1) (ATI
= aminotroponiminate)
with CuI in acetonitrile afforded an aminotroponiminato(chloro)germylene
stabilized copper(I) iodide complex [{(i-Bu)2ATIGeCl}2(Cu4I4)(CH3CN)2] (2) with a tetrameric distorted cubane
type Cu4I4 core. The reaction of compound 1 in dichloromethane with CuI in the presence of 2 equiv of
pyridine resulted in the first germylene stabilized copper(I) iodide
complex [{(i-Bu)2ATIGeCl}(CuI)(C5H5N)2] (3) with a monomeric CuI
core. A reaction of compound 1 with equimolar amounts
of CuI and pyridine in dichloromethane resulted in a copper(I) iodide
complex [{(i-Bu)2ATIGeCl}2(Cu2I2)(C5H5N)2] (4) with a dimeric Cu2I2 core. Interestingly,
an interconversion between compounds 3 and 4 and conversion of compound 2 to compounds 3 and 4 under suitable conditions are also reported.
The compounds 2–4 have been characterized
by multinuclear NMR spectroscopy and single-crystal X-ray diffraction
studies. The copper atoms in all these complexes are tetracoordinate,
and the Ge(II)–Cu(I) bond lengths in complexes 2, 3, and 4 are 2.341(1), 2.308(1), and
2.345(1) Å, respectively.