RADIATIVE LIFETIME FOR NUCLEAR SPIN CONVERSION OF WATER-ION, H$_2$O$^+$

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Nuclear spin conversion interaction of the water ion, H2O+, has been studied to derive the spontaneous emission lifetime between the {\em ortho}- and {\em para}-levels. The H2O+ ion is a radical with 2B1 electronic ground state and the off-diagonal electron spin-nuclear spin interaction term, Tab(SaΔIb+SbΔIa), connects {\em para} and {\em ortho} levels, because $ \Delta \mbox{\boldmath I} = \mbox{\boldmath I}_1 - \mbox{\boldmath I}2$ has nonvanishing matrix elements between I=0 and 1. The $ T{ab}$ coupling constant, derived by an ab initio calculation in MRD-CI/Bk level to be 72 MHz, is larger than that of H2O by 4 orders of magnitude, makes the ortho to para conversion of H2O+ faster than that of H2O by 8 orders of magnitude and possibly competitive with other astrophysical processes. Last year we reported {\em ortho} and {\em para} coupling channels below 900 cm−1 caused by accidental near degeneracy of rotational levels. MG06, 2012.} For example, hyperfine components of the 42,2(o) and 33,0(p) levels mix each other by 1.2 x 10−3 due to the near degeneracy (ΔE = 0.417 cm−1), but the lower lying 10,1(p) and 11,1(o) levels mix only by 8.9 x 10−5 because of their large separation (ΔE = 16.27 cm−1). In the present study, we solved the radiative rate equations including all the rotational levels below 900 cm−1 to give the {\em o}-{\em p} conversion lifetime to be 0.451, 3.27, 398 and 910 years for the equilibrium o/p ratio of 3.00, 3.00, 4.52, and 406 when the radiation temperature Tr is 100, 60, 20 and 5 K. These results qualitatively help to understand the observed high o/p ratio of 4.8 ± 0.5 (corresponding to the nuclear spin temperature of 21 K) toward Sgr B2, \textbf{521}, L11 (2010).} but they are too slow to compete with the reaction by collision unless the number of density of H2 in the region is very low ($n\sim1cm^{-3})ortheradiativetemperatureisveryhigh(T_r >$ 50K). , in press.}

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Author Institution: Department of Applied Chemistry, National Chiao Tung University, Hsinchu, 30010, TAIWAN and Department of Chemistry, Faculty of Sciences, Kyushu University, Fukuoka, 812-8581 JAPAN; Department of Chemistry, Faculty of Sciences, Kyushu University, Fukuoka, 812-8581 JAPAN; Department of Astronomy and Astrophysics and Department of Chemistry, the Enrico Fermi Institute, the University of Chicago, Chicago, Illinois, 60637, USA

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