Reactions of lead cluster cations and anions with ethylene, propene, and trans ‐and cis ‐butene have been studied using a home‐built reflectron time‐of‐flight mass spectrometer. Both the high‐ and low‐energy pathway reactions were observed in the lead cluster reactions. For ethylene, only association products [Pb k (C 2 H 4 ) n + ] were observed. For propene, both association products [Pb k (C 3 H 6 ) n + ], high‐energy pathway products [Pb k (CH 3 ) + ] and their further association products [Pb k (CH 3 ) m (C 3 H 6 ) n + ] were observed, while for butenes, besides the three kinds of products mentioned above, Pb k (C 4 H 8 ) n + ,Pb k CH 3 + and Pb k (CH 3 ) m (C 4 H 8 ) n + , low‐energy pathway products [Pb k C 4 H 6 + ,Pb k C 3 H 3(5) + , Pb k C 3 H 2(3) + (for cis‐butene only)] and their further association products [Pb k C 4 H 6 (C 4 H 8 ) n + , Pb k C 3 H 3(5) (C 4 H 8 ) n + ,Pb k C 3 H 2(3) (C 4 H 8 ) n + (for cis‐butene only)] were also observed. Bond selectivity and effects of steric hindrance were observed in the low‐energy pathway reactions of lead cluster cations with trans ‐ and cis ‐butene. The same anionic products, Pb k C m − , with nearly the same intensity distribution, were observed in the reactions of lead cluster anions with all four alkenes studied here. Some reaction mechanisms are proposed for these reactions.
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Tian et al. (2002) studied this question.
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