Ladders of relative alkali ion affinities of crown ethers and acyclic analogs were constructed by using the kinetic method. The adducts consisting of two different ethers bound by an alkali metal ion, (M1 + Cat + M2)(+), were formed by using fast atom bombardment ionization to desorb the crown ether
Comparison of the orders of gas-phase basicities and ammonium ion affinities of polyethers by the kinetic method and ligand exchange technique
β Scribed by H.-F. Wu; J.S. Brodbelt
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 577 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1044-0305
No coin nor oath required. For personal study only.
β¦ Synopsis
The orders of relative gas-phase basicities and ammonium ion affinities of a series of polyethers obtained by application of the kinetic method and ligand exchange technique are compared to evaluate the discrepancies of results between the two techniques. The order of gas-phase basicities determined by the ligand exchange technique in a quadrupole ion trap agrees with the order established previously by Kebarle using equilibrium methods in a high-pressure mass spectrometer. The order obtained by the kinetic method in a triple quadrupole mass spectrometer varies for the ranking of one polyether (12-crown-4), and this discrepancy is attributed to a difference in the rates of the competing dissociation pathways from the triethylene glycol dimethyl ether/12-crown4 proton-bound adduct, owing to a substantial variation in the flexibilities of these two ethers. For the order of gas-phase ammonium ion affinities, the kinetic method results agree overall with the ligand exchange results; however, the order of ammonium ion affinities for tetraethylene glycol dimethyl ether and 15-crown-5 could not be differentiated by the ligand exchange method because of the rapidity of ammonium ion transfer between the two polyethers in both directions.
π SIMILAR VOLUMES
## Abstract Ionized benzophenones ([PhC(O)PhY]^+β’^; Y = 4 β NO~2~, 4 β CF~3~, 4βF, 4βBr, 4βMe, 3,4βdiMe, 4βOH, 4βOMe, 2βCl, 2βMe, 2βOH, 2,6βdiMe) undergo competitive dissociation upon collisionβinduced dissociation (CID) at 20 eV collision energy to generate benzoyl cations ([PhCO]^+^ and [YPhCO]^+