gas-phase "nude" anions compared with "solvated" anions. The present review outlines some of
Gas-phase reactions of the benzyne negative ions
β Scribed by Wenthold, Paul G.; Hu, Jun; Squires, Robert R.
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 248 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1076-5174
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β¦ Synopsis
The reactions of o-, m-and p-benzyne anions and the phenide ion with a series of neutral reagents are described. The m-and p-benzyne anions display similar behavior towards acids, NO and
, analogous to that of phenide ion but clearly di β erent from that of o-benzyne anion. The strongly basic and nucleophilic character of m-and p-benzyne anions dominates their reactivity, and radical-type reactions are generally not observed. Novel bifunctional reactions between m-and p-benzyne anions and both and NO are observed in CS 2 which two sequential S-atom abstractions and two NO additions, respectively, take place.
1998 John Wiley & ( Sons, Ltd.
π SIMILAR VOLUMES
These gas phase ion-molecule coupling reactions are analogous to the condensed phase coupling reactions of metallobenzynes with molecules containing multiple bonds.
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This paper reports a gas-phase study of ligand effects on the reactivity of the organometallic distonic ion Fe(p-benzyne) Γ . New organometallic distonic ions are generated by introducing a benzene ligand onto the metal center of Fe(p-benzyne) Γ . We were interested in whether the reactivity of the