Abstract
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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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2384–2386, October, 2005.
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Nekrasov, Y.S., Skazov, R.S., Simenel, A.A. et al. Reactivity of ferrocenylalkylazoles under conditions of dissociative ionization. Russ Chem Bull 54, 2460–2462 (2005). https://doi.org/10.1007/s11172-006-0138-x
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DOI: https://doi.org/10.1007/s11172-006-0138-x