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Chemical ionization proton transfer

The bis-trimethylsilyl ethers of stereoisomeric 5,7-undecanediol 78 (as well as the free diols) give upon chemical ionization (protonation with QH9) MH+ ions, which show two major processes (reaction 41). One corresponds to a Grob-type fragmentation 05-cleavage) of the ion 79 (formed by loss of Me3SiOH from protonated 78) to yield the silylated aldehyde 80. The second major reaction path involves loss of CH4 from MH+, followed by cyclization of the intermediate 81 (siloxy transfer) to 82 and ft-cleavage (loss of 1-hexene) to generate 8467. This reaction sequence, in which a centrally located structural unit rather than a peripheral one is eliminated, is rarely observed under chemical ionization and deserves further study. [Pg.460]

A third method for generating ions in mass spectrometers that has been used extensively in physical chemistry is chemical ionization (Cl) [2]. Chemical ionization can involve the transfer of an electron (charge transfer), proton (or otlier positively charged ion) or hydride anion (or other anion). [Pg.1330]

Chemical ionization (Cl) The formation of new ionized species when gaseous molecules interact with ions. This process may involve the transfer of an electron, proton, or other charged species between the reactants in an ion-molecule reaction. Cl refers to positive ions, and negative Cl is used for negative ions. [Pg.372]

Thus the reactant ions for chemical ionization formed in the methane plasma consists of approximately equal amounts of a strong gaseous Bronsted acid (CH5+) and ions which can act either as Lewis acids or Bronsted acids (C2H5+ + C3H5+). These reactant ions will effect the chemical ionization with an added substance by proton transfer or hydride ion transfer, both of which may be accompanied by fragmentation of the ion initially formed. [Pg.174]

We have previously shown (8) that the chemical ionization spectra using methane as reactant are generated by the combination of dissociative proton transfer from CH5 + and hydride ion abstraction and alkyl ion... [Pg.177]

The extension of analytical mass spectrometry from electron ionization (El) to chemical ionization (Cl) and then to the ion desorption (probably more correctly ion desolvation ) techniques terminating with ES, represents not only an increase of analytical capabilities, but also a broadening of the chemical horizon for the analytical mass spectrometrist. While Cl introduced the necessity for understanding ion—molecule reactions, such as proton transfer and acidities and basicities, the desolvation techniques bring the mass spectrometrist in touch with ions in solution, ion-ligand complexes, and intermediate states of ion solvation in the gas phase. Gas-phase ion chemistry can play a key role in this new interdisciplinary integration. [Pg.315]

Chemical ionization (Cl) has proven to be a useful technique for the MS analysis of many pollutants [533 - 537]. Cl uses a reagent ion to react with the analyte molecules to form ions by either a proton or hydride transfer ... [Pg.74]

Not all ionization methods rely on such strictly unimolecular conditions as El does. Chemical ionization (Cl, Chap. 7), for example, makes use of reactive collisions between ions generated from a reactant gas and the neutral analyte to achieve its ionization by some bimolecular process such as proton transfer. The question which reactant ion can protonate a given analyte can be answered from gas phase basicity (GB) or proton affinity (PA) data. Furthermore, proton transfer, and thus the relative proton affinities of the reactants, play an important role in many ion-neutral complex-mediated reactions (Chap. 6.12). [Pg.50]

Proton transfer is one of the prominent representatives of an ion-molecule reaction in the gas phase. It is employed for the determination of GBs and PAs (Chap. 2.11.2) by either method the kinetic method makes use of the dissociation of proton-bound heterodimers, and the thermokinetic method determines the equilibrium constant of the acid-base reaction of gaseous ions. In general, proton transfer plays a crucial role in the formation of protonated molecules, e.g., in positive-ion chemical ionization mass spectrometry (Chap. 7). [Pg.60]

Chemical ionization (Cl) sources (48, 49) use electron bombardment of a reagent gas at higher pressures than normally found in a mass spectrometer ion source, i.e., torr. Sample ionization follows via an ion-molecule reaction, often accompanied by a proton transfer to yield a quasi-molecular ion ... [Pg.233]

We turn to the chemical behavior of cycloalkane holes. Several classes of reactions were observed for these holes (1) fast irreversible electron-transfer reactions with solutes that have low adiabatic IPs (ionization potentials) and vertical IPs (such as polycyclic aromatic molecules) (2) slow reversible electron-transfer reactions with solutes that have low adiabatic and high vertical IPs (3) fast proton-transfer reactions (4) slow proton-transfer reactions that occur through the formation of metastable complexes and (5) very slow reactions with high-IP, low-PA (proton affinity) solutes. [Pg.323]

Atmospheric pressure chemical ionization APCI is a method closely related to electrospray ionization. It uses ion-molecule reactions to produce ions from analyte molecules. The sample is electrohydrodynamically sprayed into the source (Figure 14.3). The evaporation of the solvent is often supported by a heated gas at temperatures between 80 and 400°C. Within the source, a plasma is created using a corona discharge needle that is placed close to the end of the metal capillary. In this plasma, proton transfer reactions occur, leading to the ionization of the analyte, mainly by the formation of [M+H]+ ions. Compared to ESI MS, APCI MS is very well suited for the analysis of less-polar components and can therefore... [Pg.375]

Figure 14.3 Principle of atmospheric pressure chemical ionization. The dissolved analyte is sprayed through a capillary. Evaporation of the solvent is supported by a heated gas stream. Within the source, a plasma is formed by a Corona discharge needle, which creates the charged reagent gas (here HgO+j. The ionization of the analyte (M) is performed by the transfer of the charge (proton) via ion-molecule reactions. Figure 14.3 Principle of atmospheric pressure chemical ionization. The dissolved analyte is sprayed through a capillary. Evaporation of the solvent is supported by a heated gas stream. Within the source, a plasma is formed by a Corona discharge needle, which creates the charged reagent gas (here HgO+j. The ionization of the analyte (M) is performed by the transfer of the charge (proton) via ion-molecule reactions.

See other pages where Chemical ionization proton transfer is mentioned: [Pg.550]    [Pg.110]    [Pg.73]    [Pg.438]    [Pg.482]    [Pg.989]    [Pg.107]    [Pg.510]    [Pg.718]    [Pg.234]    [Pg.158]    [Pg.163]    [Pg.512]    [Pg.155]    [Pg.11]    [Pg.12]    [Pg.58]    [Pg.198]    [Pg.203]    [Pg.321]    [Pg.695]    [Pg.78]    [Pg.41]    [Pg.56]    [Pg.68]    [Pg.477]    [Pg.1085]    [Pg.210]    [Pg.8]    [Pg.195]    [Pg.85]    [Pg.225]    [Pg.3]    [Pg.15]    [Pg.194]    [Pg.241]   
See also in sourсe #XX -- [ Pg.19 ]




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