The syntheses of N,N '-bis-[(2-pyridylmethyl)]-1,3-diamido-Ni(II) Ο½ Cu(II), and this is confirmed by the potentiometric data (papH 2 , aqueous solutions; logΞ² ML [Co(II)] = 1.75; propane (papH 2 ) and N,N '-bis-[(2-pyridylmethyl)]-1,3diamido-2-hexadecylpropane (C 16 papH 2 ) are reported logΞ² MLH-2
Hydrosoluble transition-metal coordination compounds of triphenylphosphine m-trisulfonate
β Scribed by Chantel Larpent; Henri Patin
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 455 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0268-2605
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β¦ Synopsis
By using 31P NMR and IR techniques it is established that the basicities of triphenylphosphine rn-trisulfonate (TPPTS) and triphenylphosphine (PPh,) are in the same order of magnitude. This highly hydrosoluble phosphine is a convenient ligand for the synthesis of hydrosoluble coordination compounds of molybdenum(O), palladium(II), platinum(I1) and rhodium(1). The exchange of TPPTS with ligands other than PPh, (nitriles, carbon monoxide, olefins, chloride) can be used to obtain the desired complexes. However, because redox reactions between metal salts, water and TPPTS are possible, the synthesis of low- valent precursors must be carried out and the experimental conditions have to be carefully controlled to avoid side-reactions and the participation of the sulfonate anions in competitive reactions.
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Reaction between deprotonated p-tert-butyltetrathiacalix[4]arene and Co II or Zn II under strictly defined conditions leads to the formation of sandwich species in which a trimetallic unit is held between two opposed, divergently oriented, staggered O-and S-bound calixarene ligands in the cone confo