作者: J. J. Leventhal , L. Friedman
DOI: 10.1063/1.1671485
关键词:
摘要: Proton transfer from H3+ to H2 has been investigated in a tandem mass‐spectrometer system. Evidence for efficient de‐excitation of approximately one collision obtained by study threshold collision‐induced dissociation D3+ and reactions the H3+–C2H2, H3+–C2H4, H3+–CH4 systems. The results suggest mechanism which leaves behind as product an excited neutral hydrogen molecule containing most internal energy original triatomic molecular ion.