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THE STUDY ON THE DNMR SPECTRA OF Zn(Ⅱ), Cd(Ⅱ) AND Hg(Ⅱ)-1,3PDTA COMPLEXES
Song Ruifang, Li Liang, Li Fei
Chinese Journal of Magnetic Resonance, 1992, 9(2): 113-119.
Reported here are the DNMR spectra of intramolecular processes of some diamagnetic complexes which were synthesized by the reactions of Zn(Ⅱ), Cd(Ⅱ) and Hg(Ⅱ) with 1,3PDTA (1,3-propanediaminetetraacetic acid), respectively. The rate constants and other thermodynamic parameters were obtained by the complete line shape anaylsis. The intramolecular exchange processes are discussed in this paper. It was found that the activation energies of these metal complexes are related to the electrostatic potential of the metal ions.
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STUDY ON COPOLYMERIZATION MECHANISM AND MOLECULAR CHAIN STRUCTURE OF COPOLYMERS OF β -CYCLODEXTRIN WITH EPICHLOROHYDRIN BY 1 H NMR
Du Dingzhun, Wang Yuesheng, Xu Wenying
Chinese Journal of Magnetic Resonance, 1992, 9(2): 121-129.
A series of copolymcrs of β -Cyclodextrin (β -CD) with Epichlorohydrin (EP) was determined by means of 1 H NMR in D2 O or DMSO-d6 at 60,300 and 400 MHz, and their spectral assignments were given out. Copolymerization mechanism could be ascribed to a nucleophilic addition of hydroxyl group to epoxy group as an active centre. When EP:β -CD=n ≤ 3,the copolymeric molecular chains showed linear or branched structure at β -CD matrix; n ≥ 5, crosslinking network appeared in the chains. The larger n value (here, n ≤ 12), the larger M. W., and the higher crosslinking degree.
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IDENTIFICATION OF A NEW TRITERPENE FROM A. ADSURGENS PALL BY 2D NMR
Wang Min, Wang Yi, Wang Hanqing, Zheng Shangzhen, Sun Liping, Shen Xuwei
Chinese Journal of Magnetic Resonance, 1992, 9(2): 131-140.
The structural analysis of compound (1) was carried out using NMR. Several methods,including 1 H-1 H two-dimensional shift correlation spectroscopy, 13 C-1 H two-dimensional shift correlation spectroscopy, COLOC (COrrelation spectroscopy via LOng rang Coupling) and DEPT were used for chemical assignment. This investigation demonstrates the power of two-dimensional NMR techniques in the structural determination of natural products.
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NMR STUDY OF 1,2,4,6-TETRAPHENYL-2-HYDROXYL-8-AZABICYCLO[3、2、1] OCTANE
Jiang Jianping, Liao Haping, Yao Yiming, Gao Ju Shen, Wenbing, Chen Weixing
Chinese Journal of Magnetic Resonance, 1992, 9(2): 177-182.
The chemical structure of a new synthetic product 1,2,4,6-tetraphenyl-2 -hydroxyl-8-azabicyclo[3、2、1] octane was studied and identified by various NMR spectra (including NON, SD, BB, DEPT, COSY and HETCOR).
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THE STUDY ON 13 C NMR OF TETRAHYDRO-β -CARBOLINES
Yang Xianbin, Jiang Tianyi, Peng Shiqi, Zhang Li
Chinese Journal of Magnetic Resonance, 1992, 9(2): 183-188.
13 C NMR spectra for the four pairs of new tetrahydro-β -carbolines are reported. Chemical shift assignments have been made for all carbons of the tetrahydro-β -carbolincs by APT, HETCOR & HETCOLOC spectra. The chemical shifts of 5-C & 6 -C can be used for configurational assignments of tetrahydro-β -carbolines, for 5-C & 6-C chemical shifts are easily recongnizable. The downfield one is assigned to 5-C & the upfield one assigned to 6-C. In the spectra of 3a, b & 4a, b, both 3-C & 5-C undergo downfield shifts, compared with the corresponding carbons of la, b & 2a, b. Meanwile, 2 -C & 6-C undergo upfield shifts, presumably owing to slight difference in polarization of the C -N bonding electrons.