Some new cationic di- and tricarbonyl complexes of technetium(I)
✍ Scribed by H. H. Knight Castro; C. E. Hissink; J. H. Teuben; W. Vaalburg; K. Panek
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 367 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
Some new low‐valent, cationic complexes of technetium‐99 have been prepared. Oxidation of Tc~2~(CO)~10~ (1) with NOPF~6~ in acetonitrile gave [Tc(CH~3~CN)(CO)~5~]PF~6~ (2) quantitatively. This complex constitutes a useful precursor for cationic carbonyl complexes, as exemplified by a variety of reactions with bi‐ and tridentate ligands from which air‐stable, water‐soluble complexes of type [LTc(CO)~3~]^+^ (L = 1,4,7‐triazacyclononane, 1,4,7‐trimethyl‐1,4,7‐triazacyclononane and 1,4,7‐trithiacyclononane) have been isolated and characterized. A series of mixed complexes of technetium(I) of general formula {Tc(N,N)[P(OR)~3~]~2~(CO)~2~}PF~6~ (N,N = 2,2′‐bipyridine, 4,4′‐dimethyl‐2,2′‐bipyridine and R = methyl, isopropyl) has also been prepared.
📜 SIMILAR VOLUMES
## Technetium(I) complexes of trimethylphosphite (tmp), dimethylmethylphosphonite (dmmp) and methyldiethylphosphinite (mdep) have been synthesized through direct interaction of the ligand with sodium pertechnetate. The homoleptic, hexakis (ligand), cationic complexes can be isolated as tetrapheny