Nestive ions zue shown to lad to so!vated ions in 'he \_ms phzsse by rcsction with estew of formic acid w&n two requirements ar"-mat: (1) the bond energy of the cluster is grezter than 9.3 kczljmole, and (2) the proton nfimity of the negative ion is gcater tisn 3:9 kcaliniole. A likely mechanism for
Formation of metal cluster ions by gas-phase ion-molecule reactions: The bond energies of Cr2+ AND Mn2+
β Scribed by R. Houriet; T. Vulpius
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 272 KB
- Volume
- 154
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
Ion-molecule reactions occurring in Cr(CO)*, Fe(CO),, and Mns(C0) !,, systems are carried out in a Fourier transform ion cyclotron resonance (FTICR) spectrometer. Abundant intensities of bare metal cluster ions can be formed by employing a multiple pulse sequence including selective ejections and photodissociation.
In subsequent collisional activation experiments, the binding energies of Cr: and Mn$ are determined as 1.6? 0.2 and 2.1 ? 0.3 eV, respectively, the latter being in conflict with a previously reported value
Recent experiments with atomic metal ions have provided a growing amount of information on the reactivity and thermochemistry of transition-metal compounds. The interest in these systems lies in their importance as intermediates in catalytic reactions
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Ions in an externally generated laser plasma of heavy metals have been directly confined in an RF ion trap and subjected to ion-molecule reactions. Trapped metal ions as well as their chemical reaction products have been detected with a quadrupole mass spectrometer. The first four ions of Sd transit
Thermodynamic quantities, AH:\_ ,,\* and AS:\_ ,,", for the clustering reactions, X-(CSI),\_,+CSz=X-(CS,),, X=F, Cl, Br and I, were measured with a pulsed electron-beam high-pressure mass spectrometer. A large binding energy, 35.0 kcal/mol, for F-...CS2 has been obtained, whereas those for other X-.
Under chemical ionization (CI) conditions, cis and trans 1,2-indanediols mainly react with the NH 3 /NH 4 + system via a nucleophilic substitution process. In the CI source several mechanisms can occur yielding the substituted [M + NH 4 -H 2 O] + ions at m/z 150. Collisionally activated reaction (CA
## Abstract The preceeding paper presents a critical tabular compilation of 2βcenter homoβ and heteropolar bond dissociation energies. This paper deals with some empirically derived general aspects of these data, particularly regarding relationships between structure and reactivity, __i.e__. substi