Synthesis and Structural Characterization of a Novel Covalently-Bound Corrole Dimer
β Scribed by Atif Mahammed; Ilona Giladi; Israel Goldberg; Zeev Gross
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 158 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0947-6539
No coin nor oath required. For personal study only.
β¦ Synopsis
The (triphenylphosphine)cobalt(iii) complex (2) of 5,10,15-tris(pentafluorophenyl)corrole ( 1) is shown to be an valuable precursor to complexes that have not been fully characterized previously. In contrast to other cobalt corroles, aromatic amines can be substituted for the triphenylphosphine in 2 to form six-coordinate bis(amine)cobalt(iii) complexes. This is demonstrated by spectroscopic methods and by X-ray crystallography of the bis-pyridine complex 4, the first of its kind. While 2 and 4 and even their one-electron oxidized complexes are stable, a spontaneous dimerization of the corrole takes place in the absence of strongly bound ligands. The bis-cobalt complex of the novel corrole dimer 6 was fully characterized by spectroscopic methods and X-ray crystallography.
π SIMILAR VOLUMES
## Reaction of bis(pyrazol-1-yl)acetic acid with n-Bu 2 SnO in a 1 : 1 molar ratio gives dimeric bis[dicarboxylatotetraorganodistannoxanes], {[(n-Bu) 2 (Pz 2 CHCO 2 )Sn] 2 O} 2 (Pz = pyrazol-1-yl or 3,5dimethylpyrazol-1-yl), which are characterized by IR and NMR ( 1 H, 13 C and 119 Sn) spectra and
An o,oΠ-methylene-bridged bisphenol A (BPA) dimer 2 was synthesized by a one-step reaction between formalin and excess BPA in the presence of a cation exchange resin in a polar aprotic solvent. Novel oligomeric polycyclic structures were synthesized by the reaction of reactive difunctional halides,