Synthesis of Chiral Resorcinarene-based Hosts and a Mass Spectrometric Study of their Chemistry in Solution and the Gas Phase
✍ Scribed by Ngong K. Beyeh; Domonkos Fehér; Minna Luostarinen; Christoph A. Schalley; Kari Rissanen
- Publisher
- Springer Netherlands
- Year
- 2006
- Tongue
- English
- Weight
- 550 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0923-0750
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
N-Methylaniline (NMA) was ethylated and N-ethylaniline (NEA) was methylated under chemical ionization conditions using C(2)H(5)I and CH(3)I, respectively, as reagent gases. The structures of the resulting m/z 136 adduct ions have been probed using metastable ion and collision-induced dissociation (C
Fast-atom bombardment mass spectrometry has been used to investigate the chemical behavior of Fe(III) and Mn(III) tetraarylporphyrins (TAP) in both the condensed and gas phases and to clarify the mechanisms responsible for the production of positive and negative ions. The differences in the behavior
The chemical behavior of Fe(III) and M(III) tetraarylporphorin (TAP) complexes with N-alkylimidazoles and other suitable ligands was studied by direct reaction in the fast-atom bombardment matrix and in the gas phase. The coordination reaction occurs at the metal center and yields molecular adducts
The liquid secondary ion mass spectrometry and electron impact ionization fragmentation pathways of 1,9bis(dimethylamino)-2,8-dimethoxy-dibenzofuran (l), a new proton-sponge base with increased steric compression (buttressing) and much higher basicity (pK, = 14.3), and of its monoprotonated (2) and