Laboratory detection of the ring-chain carbenes HC4N and HC6N

Research output: Contribution to journalArticleResearchpeer review

Authors

  • M. C. McCarthy
  • J. U. Grabow
  • M. J. Travers
  • W. Chen
  • C. A. Gottlieb
  • P. Thaddeus

External Research Organisations

  • Harvard University
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Details

Original languageEnglish
Pages (from-to)305-310
Number of pages6
JournalAstrophysical Journal
Volume513
Issue number1 PART 1
Publication statusPublished - 1 Mar 1999

Abstract

The highly polar ring-chain carbenes HC4N and HC6N, formed by substituting either CN or CCCN for a hydrogen atom in cyclopropenylidene (C-C3H2), were detected in a supersonic molecular beam with a Fourier transform microwave spectrometer. Seven a- and four b-type rotational transitions of HC4N and 11 a-type transitions of HC6N, each with resolved nitrogen nuclear quadrupole hyperfine structure, were measured between 6 and 21 GHz, yielding precise values for the three rotational constants, the leading centrifugal distortion constants, and the quadrupole coupling constants. Like the hydrocarbon carbenes C5H2, C7H2, and C9H2, both new molecules have a planar ring-chain structures and singlet electronic ground states. The strongest lines of HC4N can be detected with a signal-to-noise ratio exceeding 10 in a total integration time of less than 1 s, but the lines of HC6N were nearly 100 times weaker.

Keywords

    ISM: molecules, Line: identification, Molecular data, Molecular processes, Radio lines: ISM

ASJC Scopus subject areas

Cite this

Laboratory detection of the ring-chain carbenes HC4N and HC6N. / McCarthy, M. C.; Grabow, J. U.; Travers, M. J. et al.
In: Astrophysical Journal, Vol. 513, No. 1 PART 1, 01.03.1999, p. 305-310.

Research output: Contribution to journalArticleResearchpeer review

McCarthy, MC, Grabow, JU, Travers, MJ, Chen, W, Gottlieb, CA & Thaddeus, P 1999, 'Laboratory detection of the ring-chain carbenes HC4N and HC6N', Astrophysical Journal, vol. 513, no. 1 PART 1, pp. 305-310. https://doi.org/10.1086/306851
McCarthy, M. C., Grabow, J. U., Travers, M. J., Chen, W., Gottlieb, C. A., & Thaddeus, P. (1999). Laboratory detection of the ring-chain carbenes HC4N and HC6N. Astrophysical Journal, 513(1 PART 1), 305-310. https://doi.org/10.1086/306851
McCarthy MC, Grabow JU, Travers MJ, Chen W, Gottlieb CA, Thaddeus P. Laboratory detection of the ring-chain carbenes HC4N and HC6N. Astrophysical Journal. 1999 Mar 1;513(1 PART 1):305-310. doi: 10.1086/306851
McCarthy, M. C. ; Grabow, J. U. ; Travers, M. J. et al. / Laboratory detection of the ring-chain carbenes HC4N and HC6N. In: Astrophysical Journal. 1999 ; Vol. 513, No. 1 PART 1. pp. 305-310.
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AU - McCarthy, M. C.

AU - Grabow, J. U.

AU - Travers, M. J.

AU - Chen, W.

AU - Gottlieb, C. A.

AU - Thaddeus, P.

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N2 - The highly polar ring-chain carbenes HC4N and HC6N, formed by substituting either CN or CCCN for a hydrogen atom in cyclopropenylidene (C-C3H2), were detected in a supersonic molecular beam with a Fourier transform microwave spectrometer. Seven a- and four b-type rotational transitions of HC4N and 11 a-type transitions of HC6N, each with resolved nitrogen nuclear quadrupole hyperfine structure, were measured between 6 and 21 GHz, yielding precise values for the three rotational constants, the leading centrifugal distortion constants, and the quadrupole coupling constants. Like the hydrocarbon carbenes C5H2, C7H2, and C9H2, both new molecules have a planar ring-chain structures and singlet electronic ground states. The strongest lines of HC4N can be detected with a signal-to-noise ratio exceeding 10 in a total integration time of less than 1 s, but the lines of HC6N were nearly 100 times weaker.

AB - The highly polar ring-chain carbenes HC4N and HC6N, formed by substituting either CN or CCCN for a hydrogen atom in cyclopropenylidene (C-C3H2), were detected in a supersonic molecular beam with a Fourier transform microwave spectrometer. Seven a- and four b-type rotational transitions of HC4N and 11 a-type transitions of HC6N, each with resolved nitrogen nuclear quadrupole hyperfine structure, were measured between 6 and 21 GHz, yielding precise values for the three rotational constants, the leading centrifugal distortion constants, and the quadrupole coupling constants. Like the hydrocarbon carbenes C5H2, C7H2, and C9H2, both new molecules have a planar ring-chain structures and singlet electronic ground states. The strongest lines of HC4N can be detected with a signal-to-noise ratio exceeding 10 in a total integration time of less than 1 s, but the lines of HC6N were nearly 100 times weaker.

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