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首页> 外文期刊>Bulletin of the Korean Chemical Society >Electronic Photodepletion Spectroscopy of Dibenzo-18-crown-6 with a Potassium Ion
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Electronic Photodepletion Spectroscopy of Dibenzo-18-crown-6 with a Potassium Ion

机译:钾离子对二苯并-18-冠-6的电子光耗尽光谱

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Electronic photodepletion spectrum of dibenzo-18-crown-6 with a potassium ion (K+-DB18C6) was obtained in the gas phase using electrospray ionization and quadrupole ion-trap reflectron time-of-flight mass spectrometry. The spectrum exhibited rather a broad absorption band at 36350 cm?1, which was tentatively assigned as the origin of the S1 band. The photodepletion spectrum of Cs+-DB18C6 was also obtained to elaborate the effects of metal cations on electronic and geometric structures of metal cation-DB18C6 complexes. We found that the S1 band of Cs+-DB18C6 was red-shifted by 180 cm?1 from that of K+-DB18C6. With the results of quantum theoretical calculations using the density functional theory, we suggested that the red-shift arose mainly from weaker binding of Cs+ to DB18C6 than that of K+, which resulted from a larger size of Cs+ than that of the cavity in DB18C6.
机译:使用电喷雾电离和四极杆离子阱反射电子飞行时间质谱仪,在气相中获得了带有钾离子的二苯并18-18冠-6的电子光耗尽光谱。该光谱在36350cm?1处显示出相当宽的吸收带,该吸收带暂定为S1带的起源。还获得了Cs + -DB18C6的光耗尽光谱,以阐明金属阳离子对金属阳离子-DB18C6配合物的电子和几何结构的影响。我们发现,Cs + -DB18C6的S1带比K + -DB18C6的S1带红移了180 cm?1。根据使用密度泛函理论的量子理论计算结果,我们认为红移主要是由于Cs +与DB18C6的键合比K +弱,这是由于Cs +的尺寸大于DB18C6中空腔的尺寸引起的。

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