1990
DOI: 10.1039/dt9900001935
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Technetium(V) nitrido complexes with tetra-azamacrocycles: monocationic and neutral octahedral complexes containing the [TcN]2+core. Crystal structure of [TcN(L1)H2O]·2H2O (H2L1= 1,4,8,11-tetra-azacyclotetradecane-5,7-dione)

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Cited by 23 publications
(4 citation statements)
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“…As in the other few complexes containing the mer -{Tc­(CO) 3 } + motif, , the bonds between Tc and the two carbonyl ligands in the trans -position to each other are weakened compared to the third CO ligand, which has another ligand (here water) in the trans -position. The Tc–O­(water) bond lengths are similar to those in other Tc complexes containing aqua ligands. One of the few structural differences between the three solid-state structures are the C1–Tc–O10 and C3–Tc–O10 angles. They are significantly smaller (83.9(1)°, 86.9(1)) in the BArF 24 – salt than in the two hydrogen-bridged dimers (90.34(7)° to 93.20(8)°), in which the two carbonyl ligands are slightly bent away from the H-bonded anions.…”
Section: Results and Discussionmentioning
confidence: 58%
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“…As in the other few complexes containing the mer -{Tc­(CO) 3 } + motif, , the bonds between Tc and the two carbonyl ligands in the trans -position to each other are weakened compared to the third CO ligand, which has another ligand (here water) in the trans -position. The Tc–O­(water) bond lengths are similar to those in other Tc complexes containing aqua ligands. One of the few structural differences between the three solid-state structures are the C1–Tc–O10 and C3–Tc–O10 angles. They are significantly smaller (83.9(1)°, 86.9(1)) in the BArF 24 – salt than in the two hydrogen-bridged dimers (90.34(7)° to 93.20(8)°), in which the two carbonyl ligands are slightly bent away from the H-bonded anions.…”
Section: Results and Discussionmentioning
confidence: 58%
“…Despite the importance of the technetium chemistry in aqueous media, there are surprisingly few structural reports about Tc complexes with aqua ligands. Of course, there are a number of oxido and nitrido complexes, where water sometimes appears as a strongly labilized ligand trans to O 2– and N 3– ; but this is the most labile coordination position in such molecules, and the replacement of such aqua ligands does not represent a synthetic approach to stable ligand exchange products. In addition to some instable chlorido complexes of technetium­(V) and -(IV), there exist to the best of our knowledge hitherto only three compounds, in which aqua ligands have been proven by X-ray structural analysis (Chart ).…”
Section: Introductionmentioning
confidence: 99%
“…The nitrido ligand is a powerful π-electron donor and shows a high capacity to stabilize the Tc(V) oxidation state. The [Tc⋮N] 2+ core forms technetium(V) nitrido complexes with a variety of chelators. The technetium(V) nitrido complex, [ 99m TcN(noet) 2 ] (noet = N -ethyl- N -ethoxydithiocarbamato), has been developed as a new myocardial imaging agent by CIS−Bio International . However, very little effort has been made to use the [Tc⋮N] 2+ core for the 99m Tc-labeling of biomolecules.…”
Section: [Tc⋮n]2+ Corementioning
confidence: 99%
“…Some years ago, Baldas and co-workers first explored nitrido technetium chemistry. Following these pioneering investigations, our research group and others have further studied the coordination chemistry and biological properties of technetium complexes characterized by the presence of the terminal Tc⋮N multiple bond. Extensive studies have been carried out on the synthesis and biological evaluation of square pyramidal nitrido technetium(V) complexes with dithiocarbamate, , dithiocarboxylate, , and dithiophosphinate ligands, and with ONS-type Schiff base ligands. , Five- and six-coordinated nitrido technetium(V) complexes have been also prepared with N 2 S 2 -type ligands, , diphosphines, and polyphosphines, , and cyclic and acyclic polydentate amine ligands. …”
Section: Introductionmentioning
confidence: 99%