Páramo Alejandra, Canosa André, Le Picard Sébastien D, Sims Ian R
Laboratoire PALMS-UMR CNRS-Université No. 6627, Equipe Astrochimie Expérimentale, Campus de Beaulieu, Bât. 11C, Université de Rennes 1, 35042 Rennes Cedex, France.
J Phys Chem A. 2006 Mar 9;110(9):3121-7. doi: 10.1021/jp0544787.
A low-temperature gas-phase kinetics study of the reactions and collisional relaxation processes involving C2(X1Sigma(g)+) and C2(a3Pi(u)) in collision with O2 and NO partners at temperatures from 300 to 24 K is reported. The experiments employed a CRESU (Cinétique de Réaction en Ecoulement Supersonique Uniforme) apparatus to attain low temperatures. The C2 species were created using pulsed laser photolysis at 193 nm of mixtures containing C2Cl4 diluted in N2, Ar, or He carrier gas. C2(X1Sigma(g)+) molecules were detected via pulsed laser-induced fluorescence in the (D1Sigma(u)+ <-- X1Sigma(g)+) system, and C2(a3Pi(u)) molecules were detected via pulsed laser-induced fluorescence in the (d 3Pi(g) <-- a 3Pi(u)) system. Relaxation of 3C2 by intersystem crossing induced by oxygen was measured at temperatures below 200 K, and it was found that this process remains very efficient in the temperature range 50-200 K. Reactivity of C2(X1Sigma(g)+) with oxygen became very inefficient below room temperature. Using these two observations, it was found to be possible to obtain the C2(X1Sigma(g)+) state alone at low temperatures by addition of a suitable concentration of O2 and then study its reactivity with NO without any interference coming from the possible relaxation of C2(a3Pi(u)) to C2(X1Sigma(g)+) induced by this reagent. The rate coefficient for reaction of C2(X1Sigma(g)+) with NO was found to be essentially constant over the temperature range 36-300 K with an average value of (1.6 +/- 0.1) x 10(-10) cm3 molecule(-1) s(-1). Reactivity of C2(a3Pi(u)) with NO was found to possess a slight negative temperature dependence over the temperature range 50-300 K, which is in very good agreement with data obtained at higher temperatures.
报道了在300至24K温度下,涉及C2(X1Σ(g)+)和C2(a3Π(u))与O2和NO分子碰撞的反应及碰撞弛豫过程的低温气相动力学研究。实验采用了CRESU(均匀超声速流动中的反应动力学)装置来实现低温。通过在193nm处用脉冲激光光解含稀释于N2、Ar或He载气中的C2Cl4的混合物来产生C2物种。通过在(D1Σ(u)+ ← X1Σ(g)+)体系中的脉冲激光诱导荧光检测C2(X1Σ(g)+)分子,通过在(d 3Π(g) ← a 3Π(u))体系中的脉冲激光诱导荧光检测C2(a3Π(u))分子。在低于200K的温度下测量了氧气诱导的3C2通过系间窜越的弛豫,发现在50 - 200K温度范围内该过程仍然非常有效。C2(X1Σ(g)+)与氧气的反应性在室温以下变得非常低效。利用这两个观察结果,发现通过添加合适浓度的O2可以在低温下单独获得C2(X1Σ(g)+)态,然后研究其与NO的反应性,而不会受到该试剂诱导的C2(a3Π(u))向C2(X1Σ(g)+)可能弛豫的任何干扰。发现C2(X1Σ(g)+)与NO反应的速率系数在36 - 300K温度范围内基本恒定,平均值为(1.6 ± 0.1)×10(-10) cm3 molecule(-1) s(-1)。发现C2(a3Π(u))与NO的反应性在50 - 300K温度范围内具有轻微的负温度依赖性,这与在较高温度下获得的数据非常吻合。