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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1517-1520 
    ISSN: 0009-2940
    Keywords: Interstellar chemistry ; Heterocumulenes ; Charge-reversal mass spectrometry ; Neutralization-reionization mass spectrometry ; Collisional activation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Neutralization-reionization mass spectrometry as well as charge reversal and collisional activation experiments serve to distinguish and assign the connectivities NNCCN and NCNCN to isomeric pairs of anions, neutral radicals and cations of C2N3. Loss of N2 to generate C2N+ is the critical discriminant, and the assignment is further substantiated by subjecting these fragment ions to collisional activation experiments by using tandem-mass spectrometry facilities.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1481-1483 
    ISSN: 0009-2940
    Keywords: Interstellar chemistry ; Polycarbon nitride radicals ; Neutralization-reionization mass spectrometry ; Tandem mass spectrometry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title radicals, thought to be of prime importance in the genesis of interstellar organic molecules, are accessible in the gas phase by neutralization of the corresponding CnN+ ions (n = 2-5) using tandem mass spectrometry methods (neutralization-reionization mass spectrometry). Collision-induced dissociation reactions of mass-selected CnN+ are in keeping with the connectivity of a “carbon rod” bearing a nitrogen atom at one terminus.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 1803-1805 
    ISSN: 0009-2940
    Keywords: Beam experiments ; Interstellar chemistry ; Dicarbon sulfide ; Butatrienedithione ; Neutralization-reionization mass spectrometry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title compounds are generated and characterized in the gas phase by mass spectrometric methods (neutralization-reionization mass spectrometry), and for dicarbon sulfide the experimental results are supported by ab initio MO calculations (HF/6-31G*).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 2069-2071 
    ISSN: 0009-2940
    Keywords: Interstellar chemistry ; Polycarbon disulfides ; Neutralization-reionization mass spectrometry ; Beam experiments ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title compounds are generated and characterized in the gas phase by tandem mass spectrometry (neutralization-reionization mass spectrometry); it is demonstrated that both even and odd-numbered polycarbon disulfides S(Cn)S(n = 2-6) are stable species. The elusiveness of the even-numbered analogues (n = 2, 4, 6) in the condensed phase must be due to facile intermolecular reactions.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 279-283 
    ISSN: 0009-2940
    Keywords: Interstellar chemistry ; Heterocumulenes ; Neutralization-reionization mass spectrometry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The isomeric [C2,N,O2]+ ions OCNCO+, OCCNO+, and NCCO2- have been generated and structurally characterized on the basis of their collisional activation, charge reversal, and neutralization-reionization mass spectra. The open-shell neutrals formed in the neutralization step undergo facile unimolecular decomposition. A recovery signal is obtained only for OCCNO.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2353-2355 
    ISSN: 0009-2940
    Keywords: Ylides ; Distonic ions ; Neutralization-reionization mass spectrometry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The recently described (Maier et al.[2]) title compound is not only viable in an argon matrix (10 K) but is also accessible in the gas phase. Electron impact ionization of (CH3)3CCX2NC (X = H, D) gives rise to HCNCX2+, which can be successfully neutralized in a beam experiment.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0947-6539
    Keywords: gas-phase chemistry ; mass spectrometry ; periodic trends ; peroxides ; transition-metal ions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The bimolecular gas-phase reactions of d-block transition-metal cations M+ with dimethyl peroxide were screened by means of Fourier transform ion cyclotron resonance mass spectrometry. The rich chemistry can be classified into four types of reactions: i) Oxygen-atom transfer to generate MO+, ii) elimination of radicals, mostly CH3O·, iii) intramolecular redox reaction of dimethyl peroxide to form CH3OH, CH2O and CO, and iv) charge transfer from the metal cation to produce CH3OOCH3+. Some general trends became apparent from this study. For example, the “early” transition metals almost exclusively induce oxygen transfer to generate MO+, in line with the notoriously high oxophilicities of these metals, and electron transfer is only observed for Zn+ and Hg+. Both the radical loss and the disproportionation reaction emerge from a rovibrationally highly excited insertion intermediate (CH3O)2M+, and for the first-row metals the branching ratio of the competing processes seems to be affected by the M+—OR bond strengths as well as the electronic groundstate configurations of M+. For the 4d and 5d cations Ru+—Ag+ and Pt+—Au+, respectively, products resulting from intramolecular redox reactions dominate; this probably reflects the higher propensity of these metal ions to facilitate β-hydrogen atom shifts.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0947-6539
    Keywords: ab initio calculations ; iron oxide ; iron sulfide ; mass spectrometry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron-transfer behavior of the binary iron chalcogenides FeO and FeS has been examined by means of mass spectrometry and ab initio calculations using the averaged coupled-pair functional (ACPF) method. The experimental and theoretical results are in good agreement with each other and also with previous studies. The ionization energies (IE) of the diatomic species are found to be IE(FeO) = 8.8±0.2 eV, IE(FeO+) = 17.9±0.4 eV, IE(FeS) = 8.3±0.3 eV, and IE(FeS+) = 16.3±0.5 eV. Two new diatomic dications, FeS2+ and FeO2+, are shown to exist as metastable minima on the corresponding potential-energy surfaces. The data enable an evaluation of the intrinsic gas-phase redox properties of FeS and FeO, and the comparison demonstrates that iron sulfide is more prone to undergo facile reduction and oxidation than iron oxide.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 983-987 
    ISSN: 1434-1948
    Keywords: Telluroles ; Neutralization-reionization mass spectrometry ; DFT calculations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,2-Dichloro-1,3-dichalcogena-2-telluroles of sulfur and selenium, C6H4[XTe(Cl)2Y] with X, Y = S, Se, serve as precursors to generate the cation radicals of 1,3-dichalcogena-2-telluroles C6H4[XTeY]+• as well as the corresponding neutral counterparts by means of neutralization-reionization mass spectrometry. These neutral 2-telluroles are intrinsically stable for at least 1 μs in the gas phase. The most abundant fragmentation channel at the neutral and cationic stages is due to loss of atomic tellurium to afford the corresponding benzo-1,2-dichalcogena-cyclobutenes. For the latter, partial isomerization to the related dichalcogena-ortho-quinones is indicated by the mass-spectrometric fragmentation pattern.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1203-1210 
    ISSN: 1434-1948
    Keywords: Organogermanium ions ; Mass spectrometry ; Ab initio theory ; NBO ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cation [Ge,C,H]+ has been generated by the electron ionisation of trichloromethylgermane. Collisional activation experiments were used to establish a Ge-C-H connectivity in this species, for which a significant fraction of the ion population was found to survive neutralisation-reionisation mass spectrometry (NRMS) experiments. Thus, the neutral counterpart [Ge,C,H]0 is stable on a microsecond timescale. Becke's 3 parameter hybrid density functional (B3LYP) was used to map the ion and neutral potential-energy surfaces, in conjunction with double-zeta and triple-zeta basis sets. The computational results obtained using the triple-zeta basis sets suggest that, for the cation, the global minimum is the high spin 3Σ GeCH+, with the first Ge-C-H excited state, 1Σ GeCH+, approximately 39 kcal mol-1 less stable. The lowest energy ion structure with H-Ge-C connectivity is bent (3A′′HGeC+,∠H-Ge-C = 126.3) and 69 kcal mol-1 less stable than the global minimum. For the neutral, a doublet (2π) with Ge-C-H connectivity is predicted to be the global minimum. The classical barrier for the neutral 1,2-hydrogen shift reaction on the doublet surface is negligible (0.1 kcal mol-1), while the smallest barrier for the cation is 13.0 kcal mol-1, corresponding to (3A′′) HGeC+ → (3Σ) GeCH+. Natural bond order analysis has been used to establish the order of the metal-carbon bond for selected states of both the neutral and the ion. Neutral and cationic isomers with Ge-C triple bonds were found to be high-energy excited states, with the metal-carbon bonds in the cation and neutral ground states of order 2.0 and 2.5, respectively. The instability of Ge-C triple bonded species is attributed to the energy required for electronic promotion in the metal in order to achieve a hybrid configuration suitable for the formation of such a bond.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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