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High-valent technetium complexes with the [(99)TcO(3)](+) core from in situ prepared mixed anhydrides of [(99)TcO(4)](-) and their reactivities


Tooyama, Y; Braband, H; Spingler, B; Abram, U; Alberto, R (2008). High-valent technetium complexes with the [(99)TcO(3)](+) core from in situ prepared mixed anhydrides of [(99)TcO(4)](-) and their reactivities. Inorganic Chemistry, 47(1):257-264.

Abstract

The highly reactive mixed anhydrides [TcO3(OCOPh)] and [TcO3(OBF3)]- were synthesized by treatment of [TcO4]- with strong Lewis acids benzoyl chloride and BF3.OEt2. These mixed anhydrides, prepared in situ, were used as precursors for the synthesis of complexes containing the [TcO3]+ core. Subsequent reactions with bi- or tridentate ligands resulted in new complexes comprised of the [TcO3]+ core. As examples with bidentate ligands, the classical complexes [TcO3Cl(bipy)] (1) (bipy = 2,2'-bipyridine) and [TcO3Cl(phen)] (2) (phen = 1,10-phenanthroline) have been prepared by this strategy and structurally characterized. The new compounds [TcO3(bpza)] (3) (bpza = di-1H-pyrazol-1-ylacetate), [TcO3(bpza*)] (4) (bpza* = bis(3,5-dimethyl-1H-pyrazol-1-yl)acetate), [TcO3(tpzm*)]+ (6) (tpzm* = 1,1,1-methanetriyltris(3,5-dimethyl-1H-pyrazole), and [ReO3(tpzm*)][ReO4] (7) are examples of complexes with tripod ligands. The complexes have been structurally characterized, and their 99Tc NMR spectra have been recorded. As a common feature, the X-ray structures show a distinct widening of the O-Tc-O angles, almost to a tetrahedral angle. With the perspective of radiopharmaceutical applications, water stability and reactivities toward alkenes are described.

Abstract

The highly reactive mixed anhydrides [TcO3(OCOPh)] and [TcO3(OBF3)]- were synthesized by treatment of [TcO4]- with strong Lewis acids benzoyl chloride and BF3.OEt2. These mixed anhydrides, prepared in situ, were used as precursors for the synthesis of complexes containing the [TcO3]+ core. Subsequent reactions with bi- or tridentate ligands resulted in new complexes comprised of the [TcO3]+ core. As examples with bidentate ligands, the classical complexes [TcO3Cl(bipy)] (1) (bipy = 2,2'-bipyridine) and [TcO3Cl(phen)] (2) (phen = 1,10-phenanthroline) have been prepared by this strategy and structurally characterized. The new compounds [TcO3(bpza)] (3) (bpza = di-1H-pyrazol-1-ylacetate), [TcO3(bpza*)] (4) (bpza* = bis(3,5-dimethyl-1H-pyrazol-1-yl)acetate), [TcO3(tpzm*)]+ (6) (tpzm* = 1,1,1-methanetriyltris(3,5-dimethyl-1H-pyrazole), and [ReO3(tpzm*)][ReO4] (7) are examples of complexes with tripod ligands. The complexes have been structurally characterized, and their 99Tc NMR spectra have been recorded. As a common feature, the X-ray structures show a distinct widening of the O-Tc-O angles, almost to a tetrahedral angle. With the perspective of radiopharmaceutical applications, water stability and reactivities toward alkenes are described.

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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Department of Chemistry
Dewey Decimal Classification:540 Chemistry
Language:English
Date:January 2008
Deposited On:23 Feb 2009 13:50
Last Modified:06 Dec 2017 18:23
Publisher:American Chemical Society
ISSN:0020-1669
Publisher DOI:https://doi.org/10.1021/ic701908q
PubMed ID:18076160

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