Small Carbon Clusters (Cn(0), Cn(+), Cn(-)) from Acyclic and Cyclic Precursors. Neutralization-Reionization Mass Spectrometry and Theory

Abstract

Ab initio calculations of isomeric carbon clusters C sub n(0) and C sub n(+), n = 2-4, yield structures and energies similar to previous reports, although five (not two) C4(+) structures have local energy minima. Dissociative ionization of structurally varied precursors was used to prepare C3 and C4 ionic and neutral isomers; however, their mass spectra from collisionally activated dissociation (CAD) and neutralization-reionization (NR) under a wide variety of conditions are indistinguishable, indicating only one isomer or the same mixture of isomers. Likewise, CAD and NR spectra of C4(+) and C4(0) from (13) CH2=CHCH=(13)CH2 and C3(+) and C3(0) from CH2=(13)CHCH3 show complete (13)C/(12) C scrambling. CAD cross sections are consistent with C4(+) - C6(+) ions as mainly linear isomers and C7(+) ions from cyclic precursors as mainly cyclic. Product abundances from the unimolecular dissociation of C sub (0), C sub n(-), and C sub n(+) allow the selection of thermodynamic data that should be of higher relative accuracy, such as 11.4 eV for the C3 ionization energy from reported values of 10.0-13.0 eV.

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 1993
Accession Number
ADA281166

Entities

People

  • Aberra Fura
  • Frantisek Turecek
  • Fred W. Mclafferty

Organizations

  • Cornell University

Tags

Communities of Interest

  • Biomedical
  • C4I
  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Accuracy
  • Chemistry
  • Dissociation
  • Electronic States
  • Electrons
  • Energy
  • First Principles Calculations
  • Geometry
  • Heat Energy
  • Ionization
  • Mass Spectra
  • Mass Spectrometers
  • Mass Spectrometry
  • Measurement
  • Spectra
  • Spectrometry
  • Spectroscopy

Readers

  • Molecular Photonics/Laser Physics
  • Organic Chemistry
  • Quantum Chemistry

Technology Areas

  • Fully Networked C3