作者: Kesheng Xu , Jingsong Zhang
DOI: 10.1063/1.479680
关键词:
摘要: Photodissociation of C2H3 via its first excited A2A″ state is studied at 327.4 and 366.2 nm using high-n Rydberg-atom time-of-flight technique. C2H2(X1Σg+)+H product channel identified. Product translational energy distributions reveal two highly-inverted vibrational progressions C2H2(X1Σg+) (most likely C≡C stretch combination band with C–H bend). Anisotropic H-atom angular indicate a short lifetime respect to dissociation. D0(C2H2–H)=33.0±0.5 kcal/mol obtained.