论文标题
硫辅胺和星际搜索的毫米和亚毫米波光谱
Millimeter- and submillimeter-wave spectroscopy of thioformamide and interstellar search toward Sgr B2(N)
论文作者
论文摘要
硫代胺NH2CHS是甲酰胺NH2CHO的含硫类似物。 1970年代,在星际培养基中发现了后者。在星际培养基中检测到的大多数含硫分子是相应含氧化合物的类似物。因此,硫代胺是在星际培养基中进行搜索的有趣候选者。使用Lille光谱仪测量并在150至660 GHz的频率范围内测量硫代氨酰胺的旋转光谱。我们使用Atacama大毫米/亚毫米阵列(ALMA)进行了thiooformamide搜索硫代胺朝向高质量恒星形成区Sagittarius(SGR)B2(N)。从对父母,34S,13C和15N的单独取代的硫代氨基酰胺的同位素物种的基态分析中获得了准确的旋转常数。对于母同位素,最低的两个激发振动状态,即V12 = 1和V9 = 1,使用将科里奥利耦合的模型分析。未检测到硫代胺朝向热核SGR B2(N1S)和SGR B2(N2)。敏感的上限表明硫代酰胺近三个数量级至少比甲酰胺少。这与甲烷硫醇明显不同,甲烷硫醇在两个来源中仅比甲醇少的两个数量级。当CS丰度降低时,甲烷硫醇与硫代氨酰胺所显示的不同行为可能是由于后期(晶粒)和低温时的优先形成(在谷物上)的优先形成。这会降低硫代酰胺与胺的比率,因为在这些条件下HCS自由基不太容易获得。
Thioformamide NH2CHS is a sulfur-bearing analog of formamide NH2CHO. The latter was detected in the interstellar medium back in the 1970s. Most of the sulfur-containing molecules detected in the interstellar medium are analogs of corresponding oxygen-containing compounds. Therefore, thioformamide is an interesting candidate for a search in the interstellar medium. The rotational spectrum of thioformamide was measured and analyzed in the frequency range 150 to 660 GHz using the Lille spectrometer. We searched for thioformamide toward the high-mass star-forming region Sagittarius (Sgr) B2(N) using the ReMoCA spectral line survey carried out with the Atacama Large Millimeter/submillimeter Array (ALMA). Accurate rotational constants were obtained from the analysis of the ground state of parent, 34S, 13C, and 15N singly substituted isotopic species of thioformamide. For the parent isotopolog, the lowest two excited vibrational states, v12 = 1 and v9 = 1, were analyzed using a model that takes Coriolis coupling into account. Thioformamide was not detected toward the hot cores Sgr B2(N1S) and Sgr B2(N2). The sensitive upper limits indicate that thioformamide is nearly three orders of magnitude at least less abundant than formamide. This is markedly different from methanethiol, which is only about two orders of magnitude less abundant than methanol in both sources. The different behavior shown by methanethiol versus thioformamide may be caused by the preferential formation of the latter (on grains) at late times and low temperatures, when CS abundances are depressed. This reduces the thioformamide-to-formamide ratio, because the HCS radical is not as readily available under these conditions.