## Abstract The ion–molecule reactions of allyl bromide with the molecular ion of allyl bromide and with its major fragment, the allyl ion, yield the C~6~H~7~^+^ and C~6~H~9~^+^ ions. The structure of these product ions was explored by means of photofragmentation with laser light in the 10 μm regio
Low-temperature reactions of some atomic ions with molecules of large quadrupole moment: C6F6 and c-C6H12
✍ Scribed by C. Rebrion; J.B. Marquette; B.R. Rowe; N.G. Adams; D. Smith
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 588 KB
- Volume
- 136
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Reactions of He+, C+ and N+ ions with C,F, and c-C~H,~ were examined at 27, 68 and 297 K using both CRESU and SIFT techniques. Within the experimental uncertainties, all of the rate coeffkients are found to be temperature-independent in this range. The results are discussed in relation to the most recent theoretical models describing the influence of the quadrupole moment on the temperature dependence of ion-molecule reaction rate coefficients.
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Even though Fe~ clusters in the gas phase have been demonstrated to be able to induce the cylotrimerization of added C2H 2 ligands to benzene, the precursor ion Fe4(CzH2) ~ has not yet been structurally characterized. To improve our understanding of this type of ion, we compare the products obtained
## Abstract Recently, we have discovered the unusual inverse temperature dependence of the kinetic isotope effect (KIE) for the OH + __c__‐C~6~H~12~/__c__‐C~6~D~12~ reaction in water. Temperature increase causes a KIE increase; this is valid for both the Fenton system (I) and the HOONOH~2~O system
## Abstract The gas‐phase ion‐molecule chemistry of exohedrally bound C~60~Rh^+^ with CH~3~X, C~6~H~5~X (X = Cl, Br, and I) and CH~2~I~2~ is studied using Fourier transform ion cyclotron resonance mass spectrometry. Reactions with CH~3~I and CH~2~I~2~ yield the buckminsterfullerene derivatives, C~6