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dc.contributor.authorKanamori, Hidetoen_US
dc.contributor.authorDehghani, Zeinab. T.en_US
dc.contributor.authorMizoguchi, Asaoen_US
dc.contributor.authorEndo, Yasukien_US
dc.date.accessioned2019-04-03T06:40:59Z-
dc.date.available2019-04-03T06:40:59Z-
dc.date.issued2017-10-25en_US
dc.identifier.issn0031-9007en_US
dc.identifier.urihttp://dx.doi.org/10.1103/PhysRevLett.119.173401en_US
dc.identifier.urihttp://hdl.handle.net/11536/143977-
dc.description.abstractMicrowave transitions between the ortho and para states of the S2Cl2 molecule in a free isolated condition are observed for the first time. In the theoretical treatment, we derive eigenfunctions of an effective Hamiltonian including the ortho-para interaction to calculate the intensities and frequencies of forbidden ortho-para transitions in the cm-wave region and pick up some promising candidates for the spectroscopic detection. In the experiment, transitions of the S2Cl2 molecule under a supersonic jet condition are observed with a Fourier transform microwave spectrometer. Seven hyperfine resolved rotational transitions including the lowest rotational level are detected as the ortho-para transitions at the predicted frequencies within the experimental errors. The observed intensities are about 10(-3) times the allowed transitions, which are consistent with the predictions based on the intensity-borrowing model. This result suggests that the orthopara conversion of this molecule occurs in a few thousand years through spontaneous emission even in a circumstance where molecular collisions occur rarely like in interstellar space.en_US
dc.language.isoen_USen_US
dc.titleDetection of Microwave Transitions between Ortho and Para States in a Free Isolated Moleculeen_US
dc.typeArticleen_US
dc.identifier.doi10.1103/PhysRevLett.119.173401en_US
dc.identifier.journalPHYSICAL REVIEW LETTERSen_US
dc.citation.volume119en_US
dc.citation.issue17en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000413663300005en_US
dc.citation.woscount3en_US
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