Jakobsen Hans J, Bildsøe Henrik, Skibsted Jørgen, Brorson Michael, Srinivasan Bikshandarkoil R, Näther Christian, Bensch Wolfgang
Instrument Centre for Solid-State NMR Spectroscopy, Department of Chemistry, Aarhus University, Aarhus C, Denmark.
Phys Chem Chem Phys. 2009 Aug 28;11(32):6981-6. doi: 10.1039/b904841n. Epub 2009 Jun 5.
Population transfer from the satellite transitions to the central transition in solid-state (33)S MAS NMR, employing WURST inversion pulses, has led to detection of the most complex (33)S MAS NMR spectrum observed so far. The spectrum is that of (CH(3)NH(3))(2)WS(4) and consists of three sets of overlapping resonances for the three non-equivalent S atoms, in accord with its crystal structure. It has been fully analyzed in terms of three sets of (33)S quadrupole coupling and anisotropic/isotropic chemical shift parameters along with their corresponding set of three Euler angles describing the relative orientation of the tensors for these two interactions. The three sets of spectral parameters have been assigned to the three different sulfur sites in (CH(3)NH(3))(2)WS(4) by relating the changes observed for the spectral parameters to the changes in crystal structures in a comparison with the corresponding data for the isostructural (NH(4))(2)WS(4) analog.
在固态(33)S 核磁共振(MAS NMR)中,利用 WURST 反转脉冲实现从卫星跃迁到中心跃迁的种群转移,从而检测到了迄今为止观察到的最复杂的(33)S MAS NMR 谱。该谱是(CH(3)NH(3))(2)WS(4)的谱,由三组重叠共振峰组成,对应于三个不等价的 S 原子,这与它的晶体结构相符。已根据三组(33)S 四极耦合和各向异性/各向同性化学位移参数,以及描述这两种相互作用张量相对取向的相应三组欧拉角,对其进行了全面分析。通过将观察到的谱参数变化与晶体结构变化相关联,并与同构的(NH(4))(2)WS(4)类似物的相应数据进行比较,将这三组谱参数分配给了(CH(3)NH(3))(2)WS(4)中的三个不同硫位点。