Artigo Revisado por pares

Propargylene: A C3H2 isomer with unusual bonding

1989; American Institute of Physics; Volume: 91; Issue: 8 Linguagem: Inglês

10.1063/1.456765

ISSN

1520-9032

Autores

Günther Maier, Hans Peter Reisenauer, Wolfgang Schwab, Petr Čárský, V. Špirko, B. Andes Hess, L. J. Schaad,

Tópico(s)

Molecular Junctions and Nanostructures

Resumo

Propargylene was identified in a matrix as a product of photolysis of cyclopropenylidene and diazopropyne. The molecule is a triplet. The optimum geometry predicted by ab initio calculations corresponds to a structure HC≡C–C̈H. The transition structure in the interconversion HC≡C–C̈H⇄HĊ=C=ĊH⇄HC̈–C≡CH is very low in energy and close to the energy of the vibrational ground state. Owing to this nonrigidity, computed infrared (IR) frequencies based on a harmonic treatment do not match the experimental spectrum. When this nonrigidity is taken into account by using a nonharmonic approximation calculated UMP2/6-31G** IR spectra are in good agreement with the observed spectra of HCCCH and DCCCD.

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