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Two roaming pathways in the photolysis of CH3CHO between 328 and 308 nm
被引:52
作者:
Lee, Kin Long K.
[1
]
Quinn, Mitchell S.
[1
]
Maccarone, Alan T.
[2
]
Nauta, Klaas
[1
]
Houston, Paul L.
[3
]
Reid, Scott A.
[2
]
Jordan, Meredith J. T.
[2
]
Kable, Scott H.
[1
]
机构:
[1] Univ New S Wales, Sch Chem, Kensington, NSW 2052, Australia
[2] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[3] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
基金:
澳大利亚研究理事会;
关键词:
PHOTODISSOCIATION DYNAMICS;
THERMAL-DECOMPOSITION;
VINYL ALCOHOL;
ACETALDEHYDE;
STATE;
MECHANISM;
RADICALS;
PRODUCTS;
KINETICS;
D O I:
10.1039/c4sc02266a
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The correlated speed and rotational energy distributions of the CO fragment from photodissociation of CH3CHO have been measured at a range of wavelengths from 308 to 328 nm. The distributions are bimodal, showing low J, slow speed, and high J, fast speed components. The cold component disappears for lambda > 325 nm. This threshold corresponds to C-H bond cleavage and we assign these CO products as arising from roaming of a H-atom about a CH3CO core. We attribute the hot component to CO formed through CH3-roaming. No evidence was observed for the presence of a transition state mechanism. This is the first time two distinct roaming channels have been observed from the same electronic state. The results support the growing understanding that roaming can be significant in chemical reactions and outweigh traditional pathways.
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页码:4633 / 4638
页数:6
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