Mass spectrometry was used for studying of non-covalent complexes of bioflavonoids with cyclotriveratrylene (CVT). The complexes of cyclotriveratrylene (CVT) with the bioflavonoids (quercetin or dihydroquercetin) have...Mass spectrometry was used for studying of non-covalent complexes of bioflavonoids with cyclotriveratrylene (CVT). The complexes of cyclotriveratrylene (CVT) with the bioflavonoids (quercetin or dihydroquercetin) have been synthesized in subcritical water. The complexe formation was carried out at different temperatures of subcritical water (from 120℃ to 230℃). The structure of the inclusion compounds was confirmed by the data of ESI MS spectroscopy. The mass spectrometry results showed the presence of mixed adducts of CTV monomer, dimer, trimer and tetramer with quercetin and dihydroquercetin. Composition of the CTV complexes with the bioflavonoids, which were obtained in subcritical water medium and by traditional method, was compared.展开更多
Macrocyclic CTV-Br3 reacted with the linear benzene-1,4-diboronic acid and 1,4-diethynylbenzene via Suzuki and Sonogashira-Hagihara coupling reactions producing the rigid porous materials CTV-CMP-1 and CTV-CMP-2. The ...Macrocyclic CTV-Br3 reacted with the linear benzene-1,4-diboronic acid and 1,4-diethynylbenzene via Suzuki and Sonogashira-Hagihara coupling reactions producing the rigid porous materials CTV-CMP-1 and CTV-CMP-2. The porous materials have good thermal and chemical stability. The Brunauer-Emmet-Teller specific surface areas of CTV-CMP-1 and CTV-CMP-2 are 314 and 218 cm2·g^-1, respectively. Physical properties of the porous materi- als were investigated, CTV-CMP-1 showed moderate hydrogen adsorption about 0.81 wt% at 1.13 bar while CTV-CMP-2 showed lower hydrogen adsorption about 0.51 wt%. These materials are analogs to activated carbons which could be potentially used in gas separation and organic compound adsorption.展开更多
Two rigid macrocyclic CTV-based porous organic polymers, Click-POP-1 and Click-POP-2, have been synthe- sized by Click reaction of a cyclotriveratrylene analogue with alkyne groups and aromatic azides in one pot. FTIR...Two rigid macrocyclic CTV-based porous organic polymers, Click-POP-1 and Click-POP-2, have been synthe- sized by Click reaction of a cyclotriveratrylene analogue with alkyne groups and aromatic azides in one pot. FTIR, solid 13C NMR and elemental analysis confirmed the formation of the polymers. Both of them possess high thermo-stability which is up to 410 and 900 ℃, respectively, and moderate hydrogen storage properties with 0.46 wt% at 77 K. Their nitrogen uptake showed type-I isotherm with BET surface areas up to 342 and 317 m2·g ^-1.展开更多
Five organic complexes are prepared by cocrystallization of tri-[（N-methyl-2-imidazoly）methoxy]cyclotriguiacylene （TMIM-CTG） with corresponding acids. While hydrogen bonds are the basic interactions in the five co...Five organic complexes are prepared by cocrystallization of tri-[（N-methyl-2-imidazoly）methoxy]cyclotriguiacylene （TMIM-CTG） with corresponding acids. While hydrogen bonds are the basic interactions in the five complexes, the homo-included motifs with C--H…π interactions also control the molecular arrangement except for complex 5. In complex 1, the two dimensional networks contain 1D zigzag chains formed by hydrogen bonding and 1D chains of homo-included CTG motifs. Complex 2 has 2D 4.82 hydrogen bonding networks, and the chains of homomeric inclusion extend the 2D structure to a 3D framework. Complex 3 contains four-membered rings through hydrogen bonds, and the chains of homo-inclusion link the rings to a novel 2D network. In complex 4, hydrogen bonds construct a novel double-layer 2D network, which is extended to a 3D framework by ＂hand-shake＂ dimeric homomeric inclusion interactions. Interestingly, there is no homomeric inclusion phenomenon in complex 5 and hydrogen bonds solely connect two components to a chiral （6,3） 2D network.展开更多
文摘Mass spectrometry was used for studying of non-covalent complexes of bioflavonoids with cyclotriveratrylene (CVT). The complexes of cyclotriveratrylene (CVT) with the bioflavonoids (quercetin or dihydroquercetin) have been synthesized in subcritical water. The complexe formation was carried out at different temperatures of subcritical water (from 120℃ to 230℃). The structure of the inclusion compounds was confirmed by the data of ESI MS spectroscopy. The mass spectrometry results showed the presence of mixed adducts of CTV monomer, dimer, trimer and tetramer with quercetin and dihydroquercetin. Composition of the CTV complexes with the bioflavonoids, which were obtained in subcritical water medium and by traditional method, was compared.
基金the National Natural Science Foundation of China，the Major State Basic Research Development Program of China，the Chinese Academy of Sciences
文摘Macrocyclic CTV-Br3 reacted with the linear benzene-1,4-diboronic acid and 1,4-diethynylbenzene via Suzuki and Sonogashira-Hagihara coupling reactions producing the rigid porous materials CTV-CMP-1 and CTV-CMP-2. The porous materials have good thermal and chemical stability. The Brunauer-Emmet-Teller specific surface areas of CTV-CMP-1 and CTV-CMP-2 are 314 and 218 cm2·g^-1, respectively. Physical properties of the porous materi- als were investigated, CTV-CMP-1 showed moderate hydrogen adsorption about 0.81 wt% at 1.13 bar while CTV-CMP-2 showed lower hydrogen adsorption about 0.51 wt%. These materials are analogs to activated carbons which could be potentially used in gas separation and organic compound adsorption.
基金the National Natural Science Foundation of China，the Major State Basic Research Development Program of China
文摘Two rigid macrocyclic CTV-based porous organic polymers, Click-POP-1 and Click-POP-2, have been synthe- sized by Click reaction of a cyclotriveratrylene analogue with alkyne groups and aromatic azides in one pot. FTIR, solid 13C NMR and elemental analysis confirmed the formation of the polymers. Both of them possess high thermo-stability which is up to 410 and 900 ℃, respectively, and moderate hydrogen storage properties with 0.46 wt% at 77 K. Their nitrogen uptake showed type-I isotherm with BET surface areas up to 342 and 317 m2·g ^-1.
文摘Five organic complexes are prepared by cocrystallization of tri-[（N-methyl-2-imidazoly）methoxy]cyclotriguiacylene （TMIM-CTG） with corresponding acids. While hydrogen bonds are the basic interactions in the five complexes, the homo-included motifs with C--H…π interactions also control the molecular arrangement except for complex 5. In complex 1, the two dimensional networks contain 1D zigzag chains formed by hydrogen bonding and 1D chains of homo-included CTG motifs. Complex 2 has 2D 4.82 hydrogen bonding networks, and the chains of homomeric inclusion extend the 2D structure to a 3D framework. Complex 3 contains four-membered rings through hydrogen bonds, and the chains of homo-inclusion link the rings to a novel 2D network. In complex 4, hydrogen bonds construct a novel double-layer 2D network, which is extended to a 3D framework by ＂hand-shake＂ dimeric homomeric inclusion interactions. Interestingly, there is no homomeric inclusion phenomenon in complex 5 and hydrogen bonds solely connect two components to a chiral （6,3） 2D network.
