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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.


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Synthesis and characterization of techne
✍ Dennis W. Wester; David H. White; Fred W. Miller; Richard T. Dean; John A. Schre 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 729 KB

## 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