Initial rotational (and for the H, reaction, vibrational) quantum-state distributions of ZnH (ZnD) formed in the exoergic reactions of Zn( ) with H,, D,, and HD were determined. Unusual isotope effects are observed, and is postulated that product rotational energy is a result of an angular dependenc
Dynamics of the reactions of Mg(3s3p1p1) with H2, HD, and D2: Rotational quantum state distributions of MgH (MgD) products
โ Scribed by W.H. Breckenridge; Jiang-Hua Wang
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- English
- Weight
- 625 KB
- Volume
- 137
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
The initial bimodal distributions of product MgH( u=O) rotational states in the reaction of Mg( 'P, ) with H2 or HD are found to be identical. Similar results were found for MgD( v=O) produced from D2 or HD. From these as well as other recent results, it is proposed that both the predominant "high-N" as well as the minor "low-Ap' components of the distributions result from insertion of Mg( 'P,) into the H-H bond, and that there are two different primary modes of decomposition of the isotopic H-Mg-H intermediates.
๐ SIMILAR VOLUMES
Complete quantum state distributions for HD (u= 1) and HD(u=2) are obtained by photolyzing HI at 266 nm m the presence of D2 and detecting the nascent HD product via (2+ 1) resonance-enhanced multiphoton ionization (REMPI). Calibration against an effusive oven source ( d 1800 K) yields any necessary
The state-to-state cross sections for D t Hz(u= 1, j= 1 )+HD(u'= I, j' =O-13) +H are calculated at the (very high) total energy 1.8 eV both by quasiclassical trajectories and by a well-converged quantum dynamical variational calculation on the most accurate available potential energy surface. Result