Energy Partitioning in the Dissociation of Cyanogen at 193nm,

Abstract

The quantum state distributions of CN radicals produced in the photodissociation of C2N2 at 193nm have been measured. It has been found that the rotational distribution is the same for radicals formed in the v''=0 and v''=1 level. This has been interpreted to mean that the rotational motion is decoupled during the dissociation, from the vibrational and translational motion of the fragments. The partitioning of the 6795/cm of available energy between vibrational and translational motion in turn has been found to be consistent with a simple statistical model. The observed rotational distribution was reproduced by assuming that there is no contribution to the angular momentum of CN other than the original angular momentum of the parent. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Nov 19, 1981
Accession Number
ADA107773

Entities

People

  • Joshua B. Halpern
  • William M. Jackson

Organizations

  • Howard University

Tags

Communities of Interest

  • C4I
  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Absorption
  • Absorption Coefficients
  • Angular Momentum
  • Chemistry
  • Dissociation
  • Dye Lasers
  • Excimer Lasers
  • Ground State
  • Laser Beams
  • Lasers
  • Liquid Dye Lasers
  • Military Research
  • New York
  • Physical Chemistry
  • Quantum States
  • Quantum Yields
  • United States

Fields of Study

  • Physics

Readers

  • Molecular Photonics/Laser Physics

Technology Areas

  • Quantum Computing