@article {Tsai201523112,
	title = {Roaming as the dominant mechanism for molecular products in the photodissociation of large aliphatic aldehydes},
	journal = {Physical Chemistry Chemical Physics},
	volume = {17},
	number = {35},
	year = {2015},
	note = {<p>cited By 12</p>
},
	pages = {23112-23120},
	abstract = {<p>Photodissociation of isobutyraldehyde (C3H7CHO) at 248 nm is investigated using time-resolved Fourier-transform infrared emission spectroscopy to demonstrate the growing importance of the roaming pathway with increasing molecular size of aliphatic aldehydes. Each acquired CO rotational distribution from v = 1 to 4 is well characterized by a single Boltzmann rotational temperature from 637 to 750 K, corresponding to an average rotational energy of 5.9 {\textpm} 0.6 kJ mol-1. The roaming signature that shows a small fraction of CO rotational energy disposal accompanied by a vibrationally hot C3H8 co-fragment is supported by theoretical prediction. The energy difference between the tight transition state (TS) and the roaming saddle point (SP) is found to be -27, 4, 15, 22, and 30 kJ mol-1 for formaldehyde, acetaldehyde, propionaldehyde, isobutyraldehyde, and 2,2-dimethyl propanal, respectively. The roaming SP is stabilized by a larger alkyl moiety. It is suggested that the roaming photodissociation rate of aldehydes increasingly exceeds those via the tight TS, resulting in the dominance of the CO + alkane products, as the size of aldehydes becomes larger. Along with formaldehyde, acetaldehyde, and propionaldehyde, in this work isobutyraldehyde is further demonstrated that this aldehyde family with special functional group is the first case in the organic compound to follow predominantly a roaming dissociation pathway, as the molecular size becomes larger. {\textcopyright} the Owner Societies 2015.</p>
},
	doi = {10.1039/c5cp03408f},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84940416467\&doi=10.1039\%2fc5cp03408f\&partnerID=40\&md5=1ff2eacfa2dec0b735bb7e108a59f2cc},
	author = {Tsai, P.-Y. and Li, H.-K. and Kasai, T. and Lin, K.-C.}
}
