@article {690,
	title = {New vibrational assignments in the (A)over-tilde(1) A(u)-(X)over-tilde (1)Sigma(+)(g) electronic transition of acetylene, C2H2: the nu({\textquoteright})(1) frequency},
	journal = {Molecular Physics},
	volume = {101},
	number = {4-5},
	year = {2003},
	note = {ISI Document Delivery No.: 657RRTimes Cited: 9Cited Reference Count: 27},
	pages = {663-673},
	type = {Article},
	abstract = {New laser-induced fluorescence spectra of supersonic jet cooled acetylene (C2H2) in the wavelength region 230-205 nm have led to an improved understanding of the vibrational structure of the (A) over tilde (1)A(u) state. Among the new bands observed are two weak perturbed bands at 46008 cm(-1) and 46116 cm(-1). Rotational analyses of these bands, together with the corresponding {\textquoteright}hot{\textquoteright} bands arising from the ground state v(4) fundamental, have shown that the upper states have asymmetric top K structure that is unaffected by a axis Coriolis coupling; this means that they do not involve overtones of the low frequency bending vibrations and therefore must be combinations of a(g) vibrational normal modes. From their positions in the manifold, their vibrational assignments can only be 2(0)(2)3(0)(1) and 1(0)(1)3(0)(1). These assignments lead to values of x(22){\textquoteright}, x(13){\textquoteright}, and a revised value for the symmetric CH stretching frequency, v(1){\textquoteright} = 2880.5 cm(-1); this revised value is 160 cm(-1) lower than the previously accepted value, but consistent with new ab initio calculations that we performed at the EOM-CCSD level using a TZ2P ( triple-zeta plus double polarization) basis set.},
	keywords = {BANDS, MODES, PARTIAL DEPERTURBATION, ROTATION CONSTANTS, SPECTROSCOPY, SPECTRUM, STATE, WAVELENGTH, X BAND SYSTEM},
	isbn = {0026-8976},
	url = {<Go to ISI>://000181680600017},
	author = {Merer, A. J. and Yamakita, N. and Tsuchiya, S. and Stanton, J. F. and Duan, Z. C. and Field, R. W.}
}
