With constant economic development and continuous improvement of living standards in Northeast China,rural tourism,as a new type of tourism,is increasingly favored. From the perspective of symbolic interaction theory,...With constant economic development and continuous improvement of living standards in Northeast China,rural tourism,as a new type of tourism,is increasingly favored. From the perspective of symbolic interaction theory,taking the current situation of rural tourism in Northeast China as an example,this paper explained the semiotic significance between hosts and guests in rural tourism. It established the evaluation indicators for authentic symbolic perception of rural tourism. Also,combined with the theories of sociology and anthropology,it studied the interaction between hosts and tourists of rural tourism in Northeast China.展开更多
Viologen,as a type of strong electron acceptor,is prone to undergo electron transfer(ET)and change color under external stimuli.However,due to the easy aggrega-tion of viologen molecules,they usually suffer from poorfl...Viologen,as a type of strong electron acceptor,is prone to undergo electron transfer(ET)and change color under external stimuli.However,due to the easy aggrega-tion of viologen molecules,they usually suffer from poorfluorescence emission in the condensed phase.Herein,a new viologen derivative of VioCl_(2)⋅2Cl(1^(2+)⋅2Cl)was designed and synthesized,in which thefluorescence was enhanced by intro-ducing Me-β-CD to weaken the interactions between viologen molecules.Then a viologen-based host-guest supramolecule of 1^(2+)@Me-β-CD was obtained by elec-trostatic interactions.Photo-/chemo-responded guest 1^(2+)supplies 1^(2+)@Me-β-CD,a green and dark purple caused by intramolecular and intermolecular ET.Further-more,1^(2+)@Me-β-CD displays an additional thermal responsive purple color.The triple chromic behaviors all exhibit excellent reversibility and cycling stability.As expected,1^(2+)@Me-β-CD exhibits strong photoluminescence(PL)in solid-liquid dual states,presenting an improved quantum yield(Φ)from 1^(2+)(Φ_(s)=0.37%,Φ_(1)= 16.74%)to=1^(2+)@Me-β-CD(Φ_(s)= 10.45%,Φ_(1)= 25.86%),and thefluores-=cence intensity can be dynamically modulated by light,heat,and acid/base vapors.The multi-responsive chromism and tunablefluorescence of 1^(2+)@Me-β-CD allow for potential applications in information security and smart windows.展开更多
Organic molecules that exhibit long persistent luminescence (LPL) are rapidly gaining attention for a variety of applications. In this study, organic molecules with simple structures were selected and organic long per...Organic molecules that exhibit long persistent luminescence (LPL) are rapidly gaining attention for a variety of applications. In this study, organic molecules with simple structures were selected and organic long persistent luminescence (OLPL) crystals were prepared. The crystal structure of the prepared OLPL crystal was elucidated and the guideline for the design of OLPL crystal was clarified. LPL was observed in OLPL crystals prepared with TMB as the guest molecule and 1,2-bis(diphenylphosphino)ethane as the host molecule. XRD measurements of the OLPL crystals suggest that the guest molecule is a solid solution substituted in the stable crystal structure of the host molecule in a lattice-shrinking direction.展开更多
Ordered mesoporous silica were synthesized under different conditions:hydrothermal synthesis in basic medium,room temperature synthesis in acid medium and sol gel synthesis in neutral medium,and pore structure,specif...Ordered mesoporous silica were synthesized under different conditions:hydrothermal synthesis in basic medium,room temperature synthesis in acid medium and sol gel synthesis in neutral medium,and pore structure,specific surface area and pore size distribution of samples were studied and compared in detail by means of SAXRD,HRTEM,BET,FT IR.The results show that the mesopores in the samples obtained via above three methods all possess uniform hexagonal arrays in short range.Mesoporous silica obtained in acid medium possesses narrow pore size distribution centered around 1.24nm with specific surface area of 1220 m 2·g -1 ;Mesoporous silica obtained in basic medium by hydrothermal synthesis at 160℃ possesses narrow pore size distribution centered around 1.90nm with specific surface area of 542.8 m 2·g -1 ;and mesoporous silica obtained in neutral medium by sol gel synthesis possesses broader pore size distribution centered around 4.01nm,specific surface area of 485.0 m 2·g -1 .Therefore,ordered mesoporous silicas with different pore sizes can be prepared using various synthetic methods and conditions.After heat treatment,Si O Si bending vibration strengthens and the adsorption peak of asymmetrical Si O Si stretching vibration broadens,and the crosslinking and condensation reaction of silica skeleton strengthen, meanwhile the amount of active centers of hydroxyl group on the surface of mesopores may be influenced,thus chemical assembly activity of mesopores may also be influenced.展开更多
The bitterness of a drug is a major challenge for patient acceptability and compliance,especially for children.Due to the toxicity of medication,a human taste panel test has certain limitations.Atomoxetine hydrochlori...The bitterness of a drug is a major challenge for patient acceptability and compliance,especially for children.Due to the toxicity of medication,a human taste panel test has certain limitations.Atomoxetine hydrochloride(HCl),which is used for the treatment of attention deficit/hyperactivity disorder(ADHD),has an extremely bitter taste.The aim of this work is to quantitatively predict the bitterness of atomoxetine HCl by a biosensor system.Based on the mechanism of detection of the electronic tongue(Etongue),the bitterness of atomoxetine HCl was evaluated,and it was found that its bitterness was similar to that of quinine HCl.The bitterness threshold of atomoxetine HCl was 8.61μg/ml based on the Change of membrane Potential caused by Adsorption(CPA)value of the BT0 sensor.In this study,the taste-masking efficiency of 2-hydroxypropyl-β-cyclodextrin(HP-β-CyD)was assessed by Euclidean distances on a principle component analysis(PCA)map with the SA402B Taste Sensing System,and the host–guest interactions were investigated by differential scanning calorimetry(DSC),powder X-ray diffraction(XRD),nuclear magnetic resonance(NMR)spectroscopy and scanning electron microscopy(SEM).Biosensor evaluation and characterization of the inclusion complex indicated that atomoxetine HCl could actively react with 2-hydroxypropyl-β-cyclodextrin.展开更多
The preparation of two types of molecular sieves AlPO 4-11 and MAPO-11 is reported. The particle size of the latter is hundreds of microns, about 10 times larger than that of the former. The XRD, IR and DTA spectra h...The preparation of two types of molecular sieves AlPO 4-11 and MAPO-11 is reported. The particle size of the latter is hundreds of microns, about 10 times larger than that of the former. The XRD, IR and DTA spectra have demonstrated that magnesium has been introduced into the framework of AlPO 4-11. The successful preparation of large single crystal of MAPO-11 will open up a new area for the preparation of large molecular sieves crystals in the future. The large MAPO-11 crystal compound is a promising host for the host-guest assembly of composite materials.展开更多
The parasitic plant Cistanche deserticola attaches to Haloxylon ammodendron, a perennial shrub with high tolerance to salinity and drought. However, little was known about the parasite-host relation between the two sp...The parasitic plant Cistanche deserticola attaches to Haloxylon ammodendron, a perennial shrub with high tolerance to salinity and drought. However, little was known about the parasite-host relation between the two species. Effects of the parasite on chlorophyll a fluorescence and nutrient accumulation in the host plant (H. am- modendron) were investigated in the Taklimakan Desert. Some photosynthetic parameters of both host and non-host H. ammodendron plants were measured by in vivo chlorophyll a fluorescence technology in the field. The assimilating branches of host and non-host plants were collected and nutrient and inorganic ion contents were analyzed. The results from field experiments showed that the infection of C. deserticola reduced the non-photochemical quenching of the variable chlorophyll fluorescence (NPQ) and the potential maximum quantum yield for primary photochemistry (Fv/Fm) of the host. Compared with non-host plants, the host H. ammodendron had low nutrient, low inorganic ion contents (Na~ and K~) and low K~/Na~ ratios in the assimilating branches. It suggested that C. deserticola infection reduced the nutrient acquisition and caused damage to the photoprotection through thermal dissipation of the energy of the photosystem II in the host, resulting in a decrease in the tolerance to salinity and high radiation. It was concluded that the attachment of the parasite plant (C. deserticola) had negative effects on the growth of its host.展开更多
X-ray crystal structures of co-crystals involving tetra-iso-butyl-resorcin[4]arene 1 with both acetone and acetonitrile solvents were reported. The component 1?2(CH3)2CO 2 assembles such that the resorcin[4]arene adop...X-ray crystal structures of co-crystals involving tetra-iso-butyl-resorcin[4]arene 1 with both acetone and acetonitrile solvents were reported. The component 1?2(CH3)2CO 2 assembles such that the resorcin[4]arene adopts a C2v conformation and the acetone serves as hydrogen bond acceptors, forming a 1D hydrogen-bonded polymer. 2 (C50H68O10) crystallizes in the triclinic, space group P1 with a = 10.0440(7), b = 13.7498(9), c = 17.6374(12) ?, α = 77.726(2), β = 86.733(2), γ = 88.634(2)o, V = 2376.1(3) ?3, Dc = 1.159 g/cm3, and Z = 2. The assembly process of component 1?2CH3CN?H2O 3 yields a 2D hydrogen-bonded polymer formed by intermolecular hydrogen bonds between resorcin[4]arene and water molecules. In the case of component 3, the acetonitrile molecule serves as guest inside the bowl of resorcin[4]arene host. 3 (C48H64N2O9) crystallizes in the monoclinic, space group P2/n with a = 13.7570(18), b = 9.0961(12), c = 19.453(3) ?, β = 103.017(3)o, V = 2371.7(5) ?3, Dc = 1.138 g/cm3, and Z = 2.展开更多
This paper reports the synthesis of host-guest nanocomposite material [Fe(bpy)(3)]Y2+ (where bpy=2,2'-bipyridine) using the flexible ligand method. X-ray diffraction analysis. adsorption technique, and cyclic volt...This paper reports the synthesis of host-guest nanocomposite material [Fe(bpy)(3)]Y2+ (where bpy=2,2'-bipyridine) using the flexible ligand method. X-ray diffraction analysis. adsorption technique, and cyclic voltammetry were used to characterize the material. The results show that [Fe(bpy)(3)](2+) has been entrapped in the supercage of zeolite, its electron transfer is realized by electron hopping of [Fe(bpy)(3)](2+) within the supercage of zeolite.展开更多
Quantum chemical calculations were carried out to investigate the structures and properties for the inclusion complexes of nitrobenzene (NB) into β-cyclodextrin. Two low-energy conformations of β-cyclodextrin (A ...Quantum chemical calculations were carried out to investigate the structures and properties for the inclusion complexes of nitrobenzene (NB) into β-cyclodextrin. Two low-energy conformations of β-cyclodextrin (A and B) in the gas phase were initially investigated by the PM3 and B3LYP/6-31+G(d,p) calculations, respectively. Three different orientations were considered in the inclusion process of A and B with NB to form 1:1 complexes. Potential energy scan by PM3 calculations indicated that the phenyl orientation Ab for conformation A and the equator orientation Bc for conformation B are more favorable in energy, respectively. We also considered the 2:1 inclusion complexes of host A or B with guest NB in the gas phase. PM3 calculation indicated that the host-guest interaction energies to form 1:1 complexes are more negative than those to form 2:1 NB/B complexes. Finally, we studied the solvent effect of NB/CD complex, and PM3 results show that the influence of water molecules on the inclusion process is very important. The driving forces for the inclusion process and the geometries of complexes were discussed in detail.展开更多
Zirconium proline-N-methylphosphonate-phosphate (α-ZPMPP) was prepared in the presence of HF for the first time. The a-ZPMPP sample is highly crystallized with interlayer distance of 1.52 nm. The interlayer distance ...Zirconium proline-N-methylphosphonate-phosphate (α-ZPMPP) was prepared in the presence of HF for the first time. The a-ZPMPP sample is highly crystallized with interlayer distance of 1.52 nm. The interlayer distance of complex of α-ZPMPP with n-butylamine (α-ZPMPP-BA) is in 0.45 nm larger than that of α-ZPMPP. The α-ZPMPP possesses different intercalation behavior of host-guest compound from α-ZP.展开更多
Dendritic cyclophane tetramer and octamer were prepared by aminolysis of succinimidyl ester derivative of tetraaza [6.1.6.1] paracyclophane with the corresponding poly(amidoamine) dendrimers as a scaffold, followed by...Dendritic cyclophane tetramer and octamer were prepared by aminolysis of succinimidyl ester derivative of tetraaza [6.1.6.1] paracyclophane with the corresponding poly(amidoamine) dendrimers as a scaffold, followed by removal of the protecting groups. The present cyclophane tetramer and octamer showed enhanced guest-binding affinities toward fluorescent guests such as 6-p-toluidinonaphthalene-2-sulfonate and 6-anilinonaphthalene-2-sulfonate, in comparison with those of monocyclic cyclophane, reflecting multivalency effects in macrocycles.展开更多
A water-soluble cyclophane (1) having poly(ethylene glycol) (PEG) moieties has been prepared from a tetraazide-functionalized cyclophane derivative and four poly(ethylene glycol) methyl ether acetylenes by Cu(I)-catal...A water-soluble cyclophane (1) having poly(ethylene glycol) (PEG) moieties has been prepared from a tetraazide-functionalized cyclophane derivative and four poly(ethylene glycol) methyl ether acetylenes by Cu(I)-catalyzed 1,3 dipolar cycloadditions (click chemistry). An analogous derivative having a pyrene moiety (2) was also prepared in a similar manner. The guest-binding behavior of 1 and 2 toward anionic guests such as 6-p-toluidinonaphthalene-2-sulfonate was investigated by fluorescence spectroscopy. The binding constants (K) of the host-guest complexes were evaluated.展开更多
In attempts to fabricate thermally stable second-order nonlinear polymer thin films, we have investigated the second harmonic generation (SHG) from both nonlinear polymer and guest-host thin films. We have also invest...In attempts to fabricate thermally stable second-order nonlinear polymer thin films, we have investigated the second harmonic generation (SHG) from both nonlinear polymer and guest-host thin films. We have also investigated the role of capping on the SHG, temporal stability and relaxation of dipole alignment. Corona poling techniques were employed to orient the dopants into the noncentrosymmetric structure required to obtain the SHG. The effect of capping with a polymeric encapsulant below the glass transition temperature of the polymers on the unpoled and corona poled thin films was studied. Capping of the nonlinear polymer and guest host thin films have resulted in high SHG with good temporal stability. SHG signal falls drastically during the first 8 days after poling while no further significant decay in SHG signal was observed after about 33 days. Our investigations have identified the characteristics required for a good encapsulant on a non-con-ductive surface.展开更多
A tetranuclear complex [Co(III)(2)(L)(2)(AcO)(2)(OH)](AcO)(2I). 4H(2)O (L = N-ferrocenylmethyl-1,4,7-triaza-cyclononane) was prepared from ligand L . HI and its crystal structure was determined. The crystal exists in ...A tetranuclear complex [Co(III)(2)(L)(2)(AcO)(2)(OH)](AcO)(2I). 4H(2)O (L = N-ferrocenylmethyl-1,4,7-triaza-cyclononane) was prepared from ligand L . HI and its crystal structure was determined. The crystal exists in P2(1)(/)a space group and its cell parameters are a = 14.285(3)Angstrom, b = 19.888(3)Angstrom, c = 19.133(3)Angstrom; beta = 109.12(2)degrees; V = 5135.8 Angstrom(3); Z = 4. Electrochemical investigation reveals that the oxidation potential of ferrocenyl group in 1 has a 0.11V-positive-shift from that of the ferrocenyl group in L.HI.展开更多
基金Supported by Student Innovation Project of University of Science and Technology Liaoning in 2017(201710146000016)
文摘With constant economic development and continuous improvement of living standards in Northeast China,rural tourism,as a new type of tourism,is increasingly favored. From the perspective of symbolic interaction theory,taking the current situation of rural tourism in Northeast China as an example,this paper explained the semiotic significance between hosts and guests in rural tourism. It established the evaluation indicators for authentic symbolic perception of rural tourism. Also,combined with the theories of sociology and anthropology,it studied the interaction between hosts and tourists of rural tourism in Northeast China.
基金National Natural Science Foundation of China,Grant/Award Numbers:21571126,62271299Shanghai Key Laboratory of High Temperature Superconductors。
文摘Viologen,as a type of strong electron acceptor,is prone to undergo electron transfer(ET)and change color under external stimuli.However,due to the easy aggrega-tion of viologen molecules,they usually suffer from poorfluorescence emission in the condensed phase.Herein,a new viologen derivative of VioCl_(2)⋅2Cl(1^(2+)⋅2Cl)was designed and synthesized,in which thefluorescence was enhanced by intro-ducing Me-β-CD to weaken the interactions between viologen molecules.Then a viologen-based host-guest supramolecule of 1^(2+)@Me-β-CD was obtained by elec-trostatic interactions.Photo-/chemo-responded guest 1^(2+)supplies 1^(2+)@Me-β-CD,a green and dark purple caused by intramolecular and intermolecular ET.Further-more,1^(2+)@Me-β-CD displays an additional thermal responsive purple color.The triple chromic behaviors all exhibit excellent reversibility and cycling stability.As expected,1^(2+)@Me-β-CD exhibits strong photoluminescence(PL)in solid-liquid dual states,presenting an improved quantum yield(Φ)from 1^(2+)(Φ_(s)=0.37%,Φ_(1)= 16.74%)to=1^(2+)@Me-β-CD(Φ_(s)= 10.45%,Φ_(1)= 25.86%),and thefluores-=cence intensity can be dynamically modulated by light,heat,and acid/base vapors.The multi-responsive chromism and tunablefluorescence of 1^(2+)@Me-β-CD allow for potential applications in information security and smart windows.
文摘Organic molecules that exhibit long persistent luminescence (LPL) are rapidly gaining attention for a variety of applications. In this study, organic molecules with simple structures were selected and organic long persistent luminescence (OLPL) crystals were prepared. The crystal structure of the prepared OLPL crystal was elucidated and the guideline for the design of OLPL crystal was clarified. LPL was observed in OLPL crystals prepared with TMB as the guest molecule and 1,2-bis(diphenylphosphino)ethane as the host molecule. XRD measurements of the OLPL crystals suggest that the guest molecule is a solid solution substituted in the stable crystal structure of the host molecule in a lattice-shrinking direction.
基金theNationalNaturalScienceFoundationofChina (No .50 2 72048)andtheNaturalScienceFoundationofHubeiProvince (No .2 0 0 1ABB0 76)
文摘Ordered mesoporous silica were synthesized under different conditions:hydrothermal synthesis in basic medium,room temperature synthesis in acid medium and sol gel synthesis in neutral medium,and pore structure,specific surface area and pore size distribution of samples were studied and compared in detail by means of SAXRD,HRTEM,BET,FT IR.The results show that the mesopores in the samples obtained via above three methods all possess uniform hexagonal arrays in short range.Mesoporous silica obtained in acid medium possesses narrow pore size distribution centered around 1.24nm with specific surface area of 1220 m 2·g -1 ;Mesoporous silica obtained in basic medium by hydrothermal synthesis at 160℃ possesses narrow pore size distribution centered around 1.90nm with specific surface area of 542.8 m 2·g -1 ;and mesoporous silica obtained in neutral medium by sol gel synthesis possesses broader pore size distribution centered around 4.01nm,specific surface area of 485.0 m 2·g -1 .Therefore,ordered mesoporous silicas with different pore sizes can be prepared using various synthetic methods and conditions.After heat treatment,Si O Si bending vibration strengthens and the adsorption peak of asymmetrical Si O Si stretching vibration broadens,and the crosslinking and condensation reaction of silica skeleton strengthen, meanwhile the amount of active centers of hydroxyl group on the surface of mesopores may be influenced,thus chemical assembly activity of mesopores may also be influenced.
基金Support received from the National Major Scientific and Technological Special Project for“Significant New Drugs Development”during the Thirteenth Five-year Plan Period,P.R.China(2018ZX09721003-002-004)the Major Research Project of Shandong Province,P.R.China(2018GSF118004)the Key Research and Development Program of Shandong Province,P.R.China(2018CXGC1411)for their support and encouragement in carrying out this work.
文摘The bitterness of a drug is a major challenge for patient acceptability and compliance,especially for children.Due to the toxicity of medication,a human taste panel test has certain limitations.Atomoxetine hydrochloride(HCl),which is used for the treatment of attention deficit/hyperactivity disorder(ADHD),has an extremely bitter taste.The aim of this work is to quantitatively predict the bitterness of atomoxetine HCl by a biosensor system.Based on the mechanism of detection of the electronic tongue(Etongue),the bitterness of atomoxetine HCl was evaluated,and it was found that its bitterness was similar to that of quinine HCl.The bitterness threshold of atomoxetine HCl was 8.61μg/ml based on the Change of membrane Potential caused by Adsorption(CPA)value of the BT0 sensor.In this study,the taste-masking efficiency of 2-hydroxypropyl-β-cyclodextrin(HP-β-CyD)was assessed by Euclidean distances on a principle component analysis(PCA)map with the SA402B Taste Sensing System,and the host–guest interactions were investigated by differential scanning calorimetry(DSC),powder X-ray diffraction(XRD),nuclear magnetic resonance(NMR)spectroscopy and scanning electron microscopy(SEM).Biosensor evaluation and characterization of the inclusion complex indicated that atomoxetine HCl could actively react with 2-hydroxypropyl-β-cyclodextrin.
基金Supported by the National Natural Science Foundation of China(No. 2 99310 10 )
文摘The preparation of two types of molecular sieves AlPO 4-11 and MAPO-11 is reported. The particle size of the latter is hundreds of microns, about 10 times larger than that of the former. The XRD, IR and DTA spectra have demonstrated that magnesium has been introduced into the framework of AlPO 4-11. The successful preparation of large single crystal of MAPO-11 will open up a new area for the preparation of large molecular sieves crystals in the future. The large MAPO-11 crystal compound is a promising host for the host-guest assembly of composite materials.
基金supported by the "Western Light" Talents Training Program of Chinese Academy of Sciences (lhxz200901)
文摘The parasitic plant Cistanche deserticola attaches to Haloxylon ammodendron, a perennial shrub with high tolerance to salinity and drought. However, little was known about the parasite-host relation between the two species. Effects of the parasite on chlorophyll a fluorescence and nutrient accumulation in the host plant (H. am- modendron) were investigated in the Taklimakan Desert. Some photosynthetic parameters of both host and non-host H. ammodendron plants were measured by in vivo chlorophyll a fluorescence technology in the field. The assimilating branches of host and non-host plants were collected and nutrient and inorganic ion contents were analyzed. The results from field experiments showed that the infection of C. deserticola reduced the non-photochemical quenching of the variable chlorophyll fluorescence (NPQ) and the potential maximum quantum yield for primary photochemistry (Fv/Fm) of the host. Compared with non-host plants, the host H. ammodendron had low nutrient, low inorganic ion contents (Na~ and K~) and low K~/Na~ ratios in the assimilating branches. It suggested that C. deserticola infection reduced the nutrient acquisition and caused damage to the photoprotection through thermal dissipation of the energy of the photosystem II in the host, resulting in a decrease in the tolerance to salinity and high radiation. It was concluded that the attachment of the parasite plant (C. deserticola) had negative effects on the growth of its host.
基金This project was supported by the Key Scientific Research Foundation of State Education Ministry of China (No. 204067)
文摘X-ray crystal structures of co-crystals involving tetra-iso-butyl-resorcin[4]arene 1 with both acetone and acetonitrile solvents were reported. The component 1?2(CH3)2CO 2 assembles such that the resorcin[4]arene adopts a C2v conformation and the acetone serves as hydrogen bond acceptors, forming a 1D hydrogen-bonded polymer. 2 (C50H68O10) crystallizes in the triclinic, space group P1 with a = 10.0440(7), b = 13.7498(9), c = 17.6374(12) ?, α = 77.726(2), β = 86.733(2), γ = 88.634(2)o, V = 2376.1(3) ?3, Dc = 1.159 g/cm3, and Z = 2. The assembly process of component 1?2CH3CN?H2O 3 yields a 2D hydrogen-bonded polymer formed by intermolecular hydrogen bonds between resorcin[4]arene and water molecules. In the case of component 3, the acetonitrile molecule serves as guest inside the bowl of resorcin[4]arene host. 3 (C48H64N2O9) crystallizes in the monoclinic, space group P2/n with a = 13.7570(18), b = 9.0961(12), c = 19.453(3) ?, β = 103.017(3)o, V = 2371.7(5) ?3, Dc = 1.138 g/cm3, and Z = 2.
文摘This paper reports the synthesis of host-guest nanocomposite material [Fe(bpy)(3)]Y2+ (where bpy=2,2'-bipyridine) using the flexible ligand method. X-ray diffraction analysis. adsorption technique, and cyclic voltammetry were used to characterize the material. The results show that [Fe(bpy)(3)](2+) has been entrapped in the supercage of zeolite, its electron transfer is realized by electron hopping of [Fe(bpy)(3)](2+) within the supercage of zeolite.
基金Supported by the National Natural Science Foundation of China (No. 20773107, 20877049)China Postdoctoral Science Foundation (No. 20080431123)Jiangsu Planned Projects for Postdoctoral Research Funds (No. 0801020C)
文摘Quantum chemical calculations were carried out to investigate the structures and properties for the inclusion complexes of nitrobenzene (NB) into β-cyclodextrin. Two low-energy conformations of β-cyclodextrin (A and B) in the gas phase were initially investigated by the PM3 and B3LYP/6-31+G(d,p) calculations, respectively. Three different orientations were considered in the inclusion process of A and B with NB to form 1:1 complexes. Potential energy scan by PM3 calculations indicated that the phenyl orientation Ab for conformation A and the equator orientation Bc for conformation B are more favorable in energy, respectively. We also considered the 2:1 inclusion complexes of host A or B with guest NB in the gas phase. PM3 calculation indicated that the host-guest interaction energies to form 1:1 complexes are more negative than those to form 2:1 NB/B complexes. Finally, we studied the solvent effect of NB/CD complex, and PM3 results show that the influence of water molecules on the inclusion process is very important. The driving forces for the inclusion process and the geometries of complexes were discussed in detail.
文摘Zirconium proline-N-methylphosphonate-phosphate (α-ZPMPP) was prepared in the presence of HF for the first time. The a-ZPMPP sample is highly crystallized with interlayer distance of 1.52 nm. The interlayer distance of complex of α-ZPMPP with n-butylamine (α-ZPMPP-BA) is in 0.45 nm larger than that of α-ZPMPP. The α-ZPMPP possesses different intercalation behavior of host-guest compound from α-ZP.
文摘Dendritic cyclophane tetramer and octamer were prepared by aminolysis of succinimidyl ester derivative of tetraaza [6.1.6.1] paracyclophane with the corresponding poly(amidoamine) dendrimers as a scaffold, followed by removal of the protecting groups. The present cyclophane tetramer and octamer showed enhanced guest-binding affinities toward fluorescent guests such as 6-p-toluidinonaphthalene-2-sulfonate and 6-anilinonaphthalene-2-sulfonate, in comparison with those of monocyclic cyclophane, reflecting multivalency effects in macrocycles.
文摘A water-soluble cyclophane (1) having poly(ethylene glycol) (PEG) moieties has been prepared from a tetraazide-functionalized cyclophane derivative and four poly(ethylene glycol) methyl ether acetylenes by Cu(I)-catalyzed 1,3 dipolar cycloadditions (click chemistry). An analogous derivative having a pyrene moiety (2) was also prepared in a similar manner. The guest-binding behavior of 1 and 2 toward anionic guests such as 6-p-toluidinonaphthalene-2-sulfonate was investigated by fluorescence spectroscopy. The binding constants (K) of the host-guest complexes were evaluated.
文摘In attempts to fabricate thermally stable second-order nonlinear polymer thin films, we have investigated the second harmonic generation (SHG) from both nonlinear polymer and guest-host thin films. We have also investigated the role of capping on the SHG, temporal stability and relaxation of dipole alignment. Corona poling techniques were employed to orient the dopants into the noncentrosymmetric structure required to obtain the SHG. The effect of capping with a polymeric encapsulant below the glass transition temperature of the polymers on the unpoled and corona poled thin films was studied. Capping of the nonlinear polymer and guest host thin films have resulted in high SHG with good temporal stability. SHG signal falls drastically during the first 8 days after poling while no further significant decay in SHG signal was observed after about 33 days. Our investigations have identified the characteristics required for a good encapsulant on a non-con-ductive surface.
文摘A tetranuclear complex [Co(III)(2)(L)(2)(AcO)(2)(OH)](AcO)(2I). 4H(2)O (L = N-ferrocenylmethyl-1,4,7-triaza-cyclononane) was prepared from ligand L . HI and its crystal structure was determined. The crystal exists in P2(1)(/)a space group and its cell parameters are a = 14.285(3)Angstrom, b = 19.888(3)Angstrom, c = 19.133(3)Angstrom; beta = 109.12(2)degrees; V = 5135.8 Angstrom(3); Z = 4. Electrochemical investigation reveals that the oxidation potential of ferrocenyl group in 1 has a 0.11V-positive-shift from that of the ferrocenyl group in L.HI.