Abstract
Reactions of 2,5-bis(benzylthio)-1,3,4-thiadiazole (1) with a common organometallic rhenium starting material [NEt4]2[fac-[Re(I)Br3(CO)3] yielded two distinct types of complexes. Both complexes coordinate only through the nitrogen of the thiadiazole ring. Reaction of 1 with the rhenium starting material alone yielded a bimetallic complex fac-(di-μ-bromo)(μ-2,5-bis(benzylthio)-1,3,4-thiadiazole-κN:κ′N)bis(tricarbonyl rhenium (I)) (2). The nitrogens of the thiadiazole ring of 1 each coordinate to a different rhenium center combined with two bridging bromide ligands in 2. A "2+1" complex was prepared in a two step process by reacting the rhenium starting material with picolinic acid followed by 1 to yield fac-Re(I)(2,5-bis(benzylthio)-1,3,4-thiadiazole)(CO)3(picolinate) (3). Compounds 2 and 3 were characterized by NMR, IR, UV, elemental analysis, and single crystal X-ray diffraction.
| Original language | English |
|---|---|
| Pages (from-to) | 1289-1294 |
| Number of pages | 6 |
| Journal | Inorganica Chimica Acta |
| Volume | 362 |
| Issue number | 4 |
| DOIs | |
| State | Published - Mar 2 2009 |
| Externally published | Yes |
Funding
The work was funded by Department of Defense New Investigator Award Prostate Cancer (Grant # W81XWH0510556), Department of Energy Radiochemistry Education Award Program (Grant # DEFG20705ID14692IDNE006) and the Washington State University Start Up fund. Funding for the X-ray facility at UI was provided by the M.J. Murdock Charitable Trust and NSF-EPSCoR.
Keywords
- Carbonyl
- Organometallic
- Rhenium
- Thiadiazole
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