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NMR STUDIES ON THE BENZYLATEDMANNOPYRANOSYL CARBOXYLATES
Li Zhongjun, Qiao Liang, Gao Congyuan, Cai Mengshen
Chinese Journal of Magnetic Resonance, 1994, 11(4): 405-409.
series of benzylated niannopyranosyl carboxylatea have been prepared and their NMR spectra have been investigated. At first, a pair of typical benzylated mannopymnose, 1-0-(3, 5-dinitro-benzoyl) -2, 3, 4, 6-tetra-0-benzyl-D-mannopponose liave been thoroughly studied by using NMR techniques. Three important results have been found:(1) PMR is more accumte and reliable than CMR in identifying the configuration of benzylated mannopyranosee; (2) The values of △δ H-1 and 3 JH-1,2 are two main and good bases for the identification of theconfiguration; (3) The δ C values of the two isomers (α and β ) are in order of the following:C-1 > C-5 > C-3 > C-4 > C-2 > C-6.
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NITROGEN-14 REMOTE NUCLEAR QUADRUPOLE RESONANCE SPECTROMETER
Li Geneying, Jiang Yu, Wu Xianqiu, Wu Xuewen
Chinese Journal of Magnetic Resonance, 1994, 11(4): 419-425.
To meet the requirement of NQR measurement of 14 N compounds outside the probe-head, an NQR speetrometer with simplicity and economy was built. It utilizes the pulsed Fourier transform technique to apouire FID or echo signais for coherent accumulations. The whole system consists of two parts. The first part, hardware component, is made up of a radio-frcquency pulse gcnerator with power output of about 500 W, a probe-head, a receiver, an MCS-96 series single-chip micro-processor (8097BH) and an IBM pcrsonal computcr (PC/386). The second part includes softwam running in the single-chip micro-proessor and programs for the PC to handle numerical time-domain NQR data. With this apbectrometer, NQR signals from typical 14 N samples of tens of grarns and within 10cm distance from the probe can be deteded in tens of seconds.