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dc.contributor.authorTanaka, Keiichien_US
dc.contributor.authorHarada, Kensukeen_US
dc.contributor.authorCabezas, Carlosen_US
dc.contributor.authorEndo, Yasukien_US
dc.date.accessioned2018-08-21T05:53:23Z-
dc.date.available2018-08-21T05:53:23Z-
dc.date.issued2018-03-01en_US
dc.identifier.issn0022-2852en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.jms.2017.12.001en_US
dc.identifier.urihttp://hdl.handle.net/11536/144625-
dc.description.abstractFourier transform microwave spectra for the J=1 <- 0 and 2 <- 1 rotational transitions of the SiCl+ ion were observed for two isotopologues (Cl-35 and Cl-37) in the ground and the first excited vibrational states of the ground (1)Sigma(+) electronic state. Thanks to the high resolution of the FTMW spectrometer, hyperfine structures due to the quadrupole moment of the chlorine nucleus and the nuclear spin-rotation interaction were fully resolved. The observed FTMW spectra were combined with previously reported MMW and diode laser spectra in an analysis to determine the mass-independent Dunham coefficients U-k,U-l as well as a mass scaling parameter Delta(Cl)(01) = -0.856(30). The equilibrium bond length of SiCl+ determined is r(e) = 1.9439729(10) angstrom and the nuclear quadrupole coupling constant of (SiCl+)-Cl-35 is eQq(e) = -11.8788(23) MHz. (C) 2017 Elsevier Inc. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleFourier transform microwave spectroscopy of the SiCl+ ionen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jms.2017.12.001en_US
dc.identifier.journalJOURNAL OF MOLECULAR SPECTROSCOPYen_US
dc.citation.volume345en_US
dc.citation.spage39en_US
dc.citation.epage45en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000426538600007en_US
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