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Year 2005, Month 10 (Section Brief Communications, Page 2460)

Reactivity of ferrocenylalkylazoles under conditions of dissociative ionization

Yu. S. Nekrasov, R. S. Skazov, A. A. Simenel, L. V. Snegur, and V. V. Gumenyuk

Electron ionization mass spectra of biologically active ferrocenylalkylazoles CpFeC5H4CH(R)Az (R = H, Me, Et, Pr, or Ph; AzH is pyrazole, imidazole, indazole, benzoimidazole, benzotriazole, adenine, or their derivatives) were studied. The nature of the heterocyclic fragment (its ionization energy) is the main factor determining the reactivity of these compounds under conditions of dissociative electron ionization.

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