The (A)over-tilde←(X)over-tilde (1+1) resonance-enhanced multiphoton ionization spectrum of the NO•C2H6 and NO•(C2H6)2 complexes

被引:16
作者
Daire, SE [1 ]
Lozeille, J [1 ]
Gamblin, SD [1 ]
Wright, TG [1 ]
机构
[1] Univ Sussex, Sch Chem Phys & Environm Sci, Brighton BN1 9QJ, E Sussex, England
关键词
D O I
10.1021/jp001858d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The (A) over tilde <-- <(X)over tilde> transitions of NO .C2H6 and NO bullet>(*) over bar * (C2H6)(2) have been recorded using (1 + 1) resonance-enhanced multiphoton ionization spectroscopy. The NO .C2H6 origin is determined to be 44050 +/- 15 cm(-1), and the dissociation energy, D-0', of the (A) over tilde state is measured to be 340 +/- 20 cm(-1). The latter values allow the dissociation energy of the (X) over tilde state, D-0", to be determined as 190 +/- 20 cm(-1). In addition, estimates of the dissociation energies for the processes NO bullet>(*) over bar * (C2H6)(2) + NO .C2H6 + C2H6 and NO bullet>(*) over bar * (C2H6)(2) --> NO + 2C(2)H(6) in the (X) over tilde and (A) over tilde states are obtained; the (A) over tilde state is found to be dissociative along the NO .C2H6. . .C2H6 coordinate. Comparison of the NO .C2H6 (A) over tilde <-- <(X)over tilde> spectrum with that of NO . CH4 is made.
引用
收藏
页码:9180 / 9183
页数:4
相关论文
共 31 条
[1]   VAN-DER-WAALS VIBRATIONS OF NO-METHANE COMPLEXES IN THE A(2)SIGMA(+) STATE [J].
AKIIKE, M ;
TSUJI, K ;
SHIBUYA, K ;
OBI, K .
CHEMICAL PHYSICS LETTERS, 1995, 243 (1-2) :89-93
[2]   Electronic and photoelectron spectroscopy of Rg•NO (Rg = rare gas), NO•N2 and NO•CH4 molecular complexes [J].
Barr, JD ;
Dyke, JM ;
Mack, P ;
Smith, DM ;
Wright, TG .
JOURNAL OF ELECTRON SPECTROSCOPY AND RELATED PHENOMENA, 1998, 97 (1-2) :159-170
[3]   One- and two-color resonance-enhanced multiphoton ionization spectroscopy of the Kr center dot NO complex via the (A)over-tilde(2)Sigma(+) state [J].
Bush, AM ;
Dyke, JM ;
Mack, P ;
Smith, DM ;
Wright, TG .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (22) :9804-9811
[4]   The A 2Σ+ state of Ar•NO studied using resonance-enhanced multiphoton and zero-kinetic-energy pulsed-field ionization spectroscopy [J].
Bush, AM ;
Dyke, JM ;
Mack, P ;
Smith, DM ;
Wright, TG .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (02) :406-415
[5]   High resolution electronic spectroscopy of Kr•OH/D and an empirical potential energy surface [J].
Carter, CC ;
Miller, TA ;
Lee, HS ;
Korambath, PP ;
McCoy, AB ;
Hayes, EF .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (03) :1508-1520
[6]   High resolution electronic spectroscopy and an empirical potential energy surface for Ne.SH/D [J].
Carter, CC ;
Miller, TA ;
Lee, HS ;
McCoy, AB ;
Hayes, EF .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (11) :5065-5078
[7]   The structure of floppy molecules:: the Rg•XH/D (Rg = Ar, Ne, and Kr, X = O or S) family of complexes [J].
Carter, CC ;
Lee, HS ;
McCoy, AB ;
Miller, TA .
JOURNAL OF MOLECULAR STRUCTURE, 2000, 525 :1-45
[8]   Reinvestigation of the emission gamma band system (A(2)Sigma(+)-X(2)Pi) of the NO molecule [J].
Danielak, J ;
Domin, U ;
Kepa, R ;
Rytel, M ;
Zachwieja, M .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1997, 181 (02) :394-402
[9]   Novel magnetic interactions in the open-shell NO-HF complex [J].
Dennis, CR ;
Whitham, CJ ;
Low, RJ ;
Howard, BJ .
CHEMICAL PHYSICS LETTERS, 1998, 282 (5-6) :421-428
[10]  
ENGELMANN R, 1970, LA4364 LOS AL SCI LA