Oxidation reactions in triterpenes under chemical ionization conditions

From a collisional activation spectral study it has been found that certain triterpene alcohols with an ursane or oleanane skeleton undergo oxidation to the corresponding ketones under chemical ionization (NH₃) conditions giving rise to abundant [M + NH₄ ? 2]⁺ ions. Mass-analysed ion kinetic energy and B²/E scan results indicate that both [M + NH₄]⁺ and [M + N₂H₇ ? 2]⁺ ions contribute to the formation of the [M + NH₄ ? 2]⁺ ion.     

Substitution reactions under NH3 chemical ionization conditions in cis-/trans-1,2-dihydroxybenzosuberans

The nucleophilic substitution reaction under NH₃ chemical ionization (CI) conditions in cis- and trans-1,2-dihydroxybenzosuberans (1–4) has been studied with the help of ND₃ CI and metastable data. The results indicate that in the parent diols 1 (cis) and 2 (trans), the substitution ion [M_sH]⁺, is produced mainly by the loss of H₂O from the [MNH₄]⁺ ion (S_Ni reaction) while in their 7-methoxy derivatives 3 and 4, the ion-molecule reaction between [M? OH]⁺ and NH₃ seems to be the major pathway for the formation of [M_sH]⁺. The substitution ion from 1 and 2 and the [MH]⁺ ion from trans-1-amino-2-hydroxybenzosuberan give similar collision-induced dissociation mass-analysed ion kinetic energy spectra. Interestingly, their diacetates do not undergo the substitution reaction.     

Adduct ion formation by metal complexes under methane negative chemical ionization conditions

Negative chemical ionization mass spectrometry is used as a probe to examine reactions between hydrocarbon radicals and metal complexes in the gas phase. The methane negative chemical ionization mass spectra of 27 complexes of cobalt(II ), nickel(II ) and copper(II ) in the presence of O₄, O₂N₂ and N₄ donor atom sets are characterized by two dominant series of adduct ions of the form [M + C_nH_2n]^? and [M + C_nH_2n+1]^? at m/z values above the molecular ion, [M]^?. Insertion of the CH radical into the ligand followed by radical/radical recombination and electron capture is proposed as the major mechanism leading to the formation of [M + C_nH_2n]^? adduct ions. A second pathway involves ligand substitution by C_nH_2n+1 radicals concomitant with H elimination and electron capture. Oxidative addition at the metal followed by ionization is suggested as the principal pathway for the formation of [M + C_nH_2n+1]^? adduct ions.     

Oxidation reactions of dibenzothiophene subjected to negative chemical ionization with oxygen

Dibenzothiophene (1) suffers surface-catalyzed oxidation under CI(O₂) conditions. While in the positive mode M^+· is the only major ion and those of the oxidation products are of minor importance in the negative mode, essentially only ions stemming from oxidized species can be seen, the sulfone ion [M + O₂]^−· being the most important one. The ion m/z 184 previously attributed to M^−· is actually the anion of 2-sulfobenzoic acid cyclic anhydride. Structures for the various oxidation products are proposed and the mechanisms leading to their formation are discussed.     

Differentiation of diastereomeric N-aryltetrahydropyrano/tetrahydrofuranochromenylamines under electron ionization and chemical ionization conditions

A series of diastereomeric 4S,5S,6R/S-tetrahydropyrano- and 3S,4S,5R/S-tetrahydrofuranochromenylamine derivatives (a/b isomers; 1-26) has been studied under electron ionization (EI) and chemical ionization (CI) conditions. The EI mass spectra of all diastereomeric compounds show two characteristic fragment ions, of which one is formed by retro-Diels-Alder (RDA) reaction from the molecular ion, retaining the charge on the diene fragment, and the other [M-(HNAr)]+ ion by a simple radical loss. The RDA process is more favorable in all b isomers, whereas the radical loss is dominant in all a isomers; based on these two ions it is easy to differentiate the two diastereomers. The collision-induced dissociation (CID) spectra of all the molecular ions also show the same trend, which reflects the stereoselectivity in the formation of the two characteristic fragment ions. The results of theoretical calculations performed are in accordance with the experimental observations. The CI experiments (methane and isobutane) on all the diastereomeric compounds also enabled the differentiation of the isomers.     

Behavior of acetals under chemical ionization conditions

Russian Chemical Bulletin -     

Reactivity in the gas phase. Behaviour of isoxazoles under negative ion chemical ionization conditions

[M ? H⁺]^? ions of isoxazole (la), 3-methylisoxazole (1b), 5-methylisoxazole (1c), 5-phenylisoxazole (1d) and benzoylacetonitrile (2a) are generated using NICI/OH^? or NICI/NH₂^? techniques. Their fragmentation pathways are rationalized on the basis of collision-induced dissociation and mass-analysed ion kinetic energy spectra and by deuterium labelling studies. 5-Substituted isoxazoles 1c and 1d, after selective deprotonation at position 3, mainly undergo N ? O bond cleavage to the stable α-cyanoenolate NC ? CH ? CR ? O^? (R = Me, Ph) that fragments by loss of R? CN, or R? H, or H₂O. The same α-cyanoenolate anion (R = Ph) is obtained from 2a with OH^?, or NH₂^?, confirming the structure assigned to the [M ? H⁺]^? ion of 1d, On the contrary, 1b is deprotonated mainly at position 5 leading, via N? O and C(3)? C(4) bond cleavages, to H? C ≡ C? O ^? and CH₃CN. Isoxazole (1a) undergoes deprotonation at either position and subsequent fragmentations. Deuterium labelling revealed an extensive exchange between the hydrogen atoms in the ortho position of the phenyl group and the deuterium atom in the α-cyanenolate NC ? CD = CPh ? O^?.     

Reactions between substrate molecules and chemical ionization reagent gases prior to ionization

A survey of side reactions such as oxidation, hydrogenation, reductive removal of substituents and radical processes is presented, and the implications for mass spectroscopic analysis are pointed out.     

Gas-phase alkylation of 2-methylfuran under chemical ionization conditions

In the gas phase, under chemical ionization conditions, the sites of attachment of [CH₃]⁺ and [C₂H₅]⁺ to 2-methylfuran have been studied by tandem mass spectrometry. Spontaneous metastable and collision-induced fragmentations have been compared to those observed for the protonated alkylfuran isomers. The results obtained show that alkylation occurs preferentially at the β-position.     

Gas-phase reactions of electrons,halide ions and radicals with (meso-tetraphenylporphinato)metal(II) complexes under negative ion chemical ionization conditions

The negative ion chemical ionization mass spectra of a series of (meso-tetraphenylporphinato)metal(II) (metal = Mg, Co, Ni, Cu, Zn) complexes obtained with the electron-energy-moderating/reagent gases argon, NF₃, CF₂Cl₂ and CF₃Br are presented. Formation of the negative ions identified in the mass spectra is accounted for in terms of the chemistry which occurs in the gaseous plasmas. In argon plasmas, the metal complexes undergo resonance electron capture with comparable facility to produce stable molecular ions. In the NF₃, CF₂Cl₂ and CF₃Br plasmas, ionization occurs as a result of ion–molecule reactions as well as resonance electron capture, and is quite selective. Only fluoride ions react with each of the metal complexes, producing metal-containing ions by nucleophilic addition and proton abstraction as well as by inducing ring closure. The less reactive chloride and bromide ions react readily by nucleophilic addition only with the magnesium and zinc complexes. Negative ions are also produced in the plasmas by radical-molecule reactions followed by ionization of the neutral products of these encounters.     

Behavior of aromatic ortho esters under chemical ionization conditions

Conclusions Ortho esters decompose under protolysis conditions in the gas phase to form carboxonium ions [MH-RHO]⁺, which can give stable associates with neutral molecules.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 579–583, March, 1988.     

Tandem radical addition reactions to substituted indoles under atom-transfer and oxidative conditions

The dimethyl methylmalonyl radical was generated upon photolysis of dimethyl bromomethylmalonate or treatment of dimethyl methylmalonate with Mn(OAc)₃·2 H₂O. This radical was added to an exocyclic olefin appended to 1-acyl or 3-acyl indoles, with subsequent cyclization to generate 1,2- or 2,3- fused indole derivatives, respectively.     

Mechanism of reduction of double bond under chemical ionization conditions

The mechanism of double bond reduction occurring in certain conjugated ketones, nitriles, acids and esters under chemical ionization conditions has been studied. The results indicate that the hydrogen radicals present in the chemically ionized plasma are responsible for the reduction of the double bond. This is further supported by experiments with radical traps.     

Differentiation of diastereomeric conduramine derivatives under electron ionization and chemical ionization mass spectral conditions

Diastereomeric conduramine derivatives, i.e., (1R,2S,3R/S,6S)-6-(N-carbomethoxyamino) 1,2-O-isopropylidenecyclohex-4-ene-1,2,3-triol (1 and 2) and their O-acetyl derivatives (3 and 4), were studied using gas chromatography (GC) with electron ionization (EI) and chemical ionization (CI). The EI mass spectra of diastereomeric pairs show consistent differences in the relative abundances of characteristic ions. The EI fragmentation patterns are based on precursor/product ion spectra, high-resolution mass spectrometry (HRMS) and deuterium labelling. The CI spectra show differences from the EI spectra, and the isobutane/CI spectra are much simpler than the methane/CI spectra. The differences shown in the CI spectra are similar to those shown in the product ion spectra of [M+H](+) ions generated under electrospray ionization (ESI) conditions. Theoretical calculations are performed to understand the observed differences. The differences in the relative stabilities of molecular ions, or protonated molecules at different sites, can explain the observed differences in the spectra.