Flow tube and theoretical study of proton transfer reactions of C3H5+ ions

被引:10
作者
Fairley, DA [1 ]
Milligan, DB [1 ]
Wheadon, LM [1 ]
Freeman, CG [1 ]
Maclagan, RGAR [1 ]
McEwan, MJ [1 ]
机构
[1] Univ Canterbury, Dept Chem, Christchurch, New Zealand
关键词
selected ion flow tube; SIFT; proton transfer; allyl ion; 2-propenyl ion; isomeric structures;
D O I
10.1016/S1387-3806(98)14123-4
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The allyl, CH2CHCH2+, and 2-propenyl, CH3CCH2+, ions have been observed as distinct isomeric species in a flowing afterglow/selected ion flow drift tube (FA/SIFDT). Reaction with methanol is used as a diagnostic for distinguishing the two isomers. The isomeric ratio of allyl:2-propenyl formed via protonation of allene or propyne by a protonated base BH+, is shown to be dependent on the proton affinity of the base B. Proton transfer from H3O+ to allene produces the 2-propenyl cation only, whereas proton transfer from SO2H+ to allene generates a mixture of allyl and 2-propenyl cations, enabling us to estimate the barrier height for the rearrangement allyl --> 2-propenyl as 110 +/- 30 kJ mol(-1). This is in accord with ab initio calculations performed at the G2(MP2) level of theory. The C3H5+ product of the reaction between C2H4.+ and C2H4 was identified as the 2-propenyl cation. Rate coefficients are also reported for reactions of the allyl and 2-propenyl cations with several neutrals. (Int J Mass Spectrom 185/186/187 (1999) 253-261) (C) 1999 Elsevier Science B.V.
引用
收藏
页码:253 / 261
页数:9
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