We used 1,1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol（A） as the host molecule to selectively recognize the component 1,8-cineole（B） in the volatile oil of Flos Magnoliae（Xin Yi）. The inclusion compound（A+B） was f...We used 1,1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol（A） as the host molecule to selectively recognize the component 1,8-cineole（B） in the volatile oil of Flos Magnoliae（Xin Yi）. The inclusion compound（A+B） was formed as crystalline, and the structure was confirmed by means of IR, （（）1H NMR）, and single crystal X-ray diffraction, with the 1∶2 molar ratios of the host to the guest. The component 1,8-cineole（B） was selectively isolated from the inclusion compound（A+B） by Kugelrohr vaccum technology, and then further characterized by IR, （）1H NMR and （）13C NMR. The whole components in the volatile oil of Flos Magnoliae（Xin Yi） and the isolation effect of 1,8-cineole isolated from inclusion crystals were analyzed by GC and GC-MS, respectively. The result indicate that the good isolation effect is given by the inclusion method, with purity and yield of the component 1,8-cineole（B） separated from the volatile oil of Flos Magnoliae are 100% and 85%, respectively.展开更多
AIM To isolate the chemical components from extracted crude of Psoralea corylifolia L. METHODS Applicate the function of molecular recognition in supramolecular chemistry, use 1,1,6,6 tetraphenylhexa 2,4 diyne 1,6 dio...AIM To isolate the chemical components from extracted crude of Psoralea corylifolia L. METHODS Applicate the function of molecular recognition in supramolecular chemistry, use 1,1,6,6 tetraphenylhexa 2,4 diyne 1,6 diol as the host molecule and chemical components in extracted crude of Psoralea corylifolia L. as guest molecules, which represent different from either in sort, quantity and sites of function groups or in structural topological character, 1,1,6,6 tetraphenylhexa 2,4 diyne 1,6 diol could selectively form inclusion compound with component endowed with interactional complementarity and isolate as crystalline from the extracted crude of Psoralea corylifolia L. RESULTS The isopsoralen as guest molecule is selectively included by 1,1,6,6 tetraphenylhexa 2,4 diyne 1,6 diol in inclusion crystal and removed by acetone from the inclusion compound and total yield is 0 18%. Isopsoralen is determined by UV, IR, 1HNMR and MS and its inclusion compound is determined by means of IR, powder XRD and single crystal XRD. The isolation effect is analyzed by GC/MS. CONCLUSION The method is simple and selective for isolation isopsoralen from extracted crude of Psoralea corylifolia L.展开更多
文摘We used 1,1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol（A） as the host molecule to selectively recognize the component 1,8-cineole（B） in the volatile oil of Flos Magnoliae（Xin Yi）. The inclusion compound（A+B） was formed as crystalline, and the structure was confirmed by means of IR, （（）1H NMR）, and single crystal X-ray diffraction, with the 1∶2 molar ratios of the host to the guest. The component 1,8-cineole（B） was selectively isolated from the inclusion compound（A+B） by Kugelrohr vaccum technology, and then further characterized by IR, （）1H NMR and （）13C NMR. The whole components in the volatile oil of Flos Magnoliae（Xin Yi） and the isolation effect of 1,8-cineole isolated from inclusion crystals were analyzed by GC and GC-MS, respectively. The result indicate that the good isolation effect is given by the inclusion method, with purity and yield of the component 1,8-cineole（B） separated from the volatile oil of Flos Magnoliae are 100% and 85%, respectively.
文摘AIM To isolate the chemical components from extracted crude of Psoralea corylifolia L. METHODS Applicate the function of molecular recognition in supramolecular chemistry, use 1,1,6,6 tetraphenylhexa 2,4 diyne 1,6 diol as the host molecule and chemical components in extracted crude of Psoralea corylifolia L. as guest molecules, which represent different from either in sort, quantity and sites of function groups or in structural topological character, 1,1,6,6 tetraphenylhexa 2,4 diyne 1,6 diol could selectively form inclusion compound with component endowed with interactional complementarity and isolate as crystalline from the extracted crude of Psoralea corylifolia L. RESULTS The isopsoralen as guest molecule is selectively included by 1,1,6,6 tetraphenylhexa 2,4 diyne 1,6 diol in inclusion crystal and removed by acetone from the inclusion compound and total yield is 0 18%. Isopsoralen is determined by UV, IR, 1HNMR and MS and its inclusion compound is determined by means of IR, powder XRD and single crystal XRD. The isolation effect is analyzed by GC/MS. CONCLUSION The method is simple and selective for isolation isopsoralen from extracted crude of Psoralea corylifolia L.
