tris(2-aminoethyl)amine has been researched along with cobalt in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 4 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brewer, CT; Brewer, G; Butcher, RJ; Carpenter, EE; Schmiedekamp, AM; Schmiedekamp, C; Straka, A; Viragh, C; Yuzefpolskiy, Y; Zavalij, P | 1 |
| Bonnitcha, PD; Clegg, JK; Hambley, TW; Hocking, RK; Kim, BJ; Neville, SM; Turner, P | 1 |
| Basallote, MG; Martínez, M; Vázquez, M | 1 |
| Han, S; Li, J | 1 |
4 other study(ies) available for tris(2-aminoethyl)amine and cobalt
| Article | Year |
|---|---|
Synthesis and characterization of homo- and heterodinuclear M(II)-M'(III) (M(II) = Mn or Fe, M'(III) = Fe or Co) mixed-valence supramolecular pseudo-dimers. The effect of hydrogen bonding on spin state selection of M(II).
Topics: Aldehydes; Cobalt; Coordination Complexes; Ethylenediamines; Ferric Compounds; Ferrous Compounds; Hydrogen Bonding; Manganese; Models, Molecular; Pyrazoles; Quantum Theory; Schiff Bases; Spectroscopy, Fourier Transform Infrared; Spectroscopy, Mossbauer; X-Ray Absorption Spectroscopy | 2011 |
Cobalt complexes with tripodal ligands: implications for the design of drug chaperones.
Topics: Cell Line, Tumor; Cobalt; Coordination Complexes; Crystallography, X-Ray; Drug Design; Ethylenediamines; Humans; Ligands; Models, Molecular; Molecular Chaperones | 2012 |
The role of hydroxo-bridged dinuclear species and the influence of "innocent" buffers in the reactivity of cis-[Co(III)(cyclen)(H₂O)₂]³⁺ and [Co(III)(tren)(H₂O)₂]³⁺ complexes with biologically relevant ligands at physiological pH.
Topics: Bridged-Ring Compounds; Buffers; Cobalt; Coordination Complexes; Cyclams; Ethylenediamines; Heterocyclic Compounds; Hydrogen-Ion Concentration; Ligands; Molecular Conformation | 2014 |
A tricorn-rhodamine fluorescent chemosensor for detection of Co
Topics: Cobalt; Ethylenediamines; Fluorescent Dyes; Ions; Molecular Structure; Rhodamines | 2017 |