The title compound [Cu（C11H29N5）]（ClO4）2 was synthesized and characterized by elemental analysis, IR and X-ray single-crystal diffraction. The compound crystallizes in the monoclinic system, space group P21/n with...The title compound [Cu（C11H29N5）]（ClO4）2 was synthesized and characterized by elemental analysis, IR and X-ray single-crystal diffraction. The compound crystallizes in the monoclinic system, space group P21/n with α = 9.405（2）, b = 14.495（3）, c = 14.715（3） A, β= 90.262（3）°, V=2006.1（7） A^3,M,=493.83,Z=4,F）（000）= 1028,Dc= 1.635 g/cm^3, T= 298（2） K,μ= 1.403 mm^-1 and = 0.71073 A. The was refined to R = 0.0508 and wR = 0. 1250 for 2293 observed reflections with I 〉 2σ（I）. The Cu（Ⅱ） atom possesses a five-coordtinate CuN5 environment which shows a slightly distorted square-pyramidal geonetry. Antimicrobial activity study found that the complex is active against Salmonella species, Staphylococcus aureu, Bacillus pumilus and Bacillus coliforms.展开更多
The heterobinuclear complex of formula Cu (oxap )Gd(phen)2 (CIO4 )3 has been synthesized, where oxap denotes the N, N'-bis (2-aminopropyl )oxamido dianion and phen represents 1,10-phenanthroline. The complex was c...The heterobinuclear complex of formula Cu (oxap )Gd(phen)2 (CIO4 )3 has been synthesized, where oxap denotes the N, N'-bis (2-aminopropyl )oxamido dianion and phen represents 1,10-phenanthroline. The complex was characterized with ESR and variable temperature magnetic susceptibility (4- 300K). The least-squares fit of the experimental sosceptibilities yielded J=2. 25cm-1. The observed Gd (Ⅲ)-Cu (Ⅱ) coupling is ferromagnetic.One Plausible mechanism that can cause a ferromagnetic coupling between Gd(Ⅱ) and Cu (Ⅱ) is discussed in terms of spin-polarization.展开更多
The title complex [Cu（ampym）（bapa）Cl]（ClO4） （C10H22Cl2CuN6O4） was synthesized and characterized by elemental analysis, IR and X-ray single-crystal diffraction. The crystal crystallizes in the orthorhombic syst...The title complex [Cu（ampym）（bapa）Cl]（ClO4） （C10H22Cl2CuN6O4） was synthesized and characterized by elemental analysis, IR and X-ray single-crystal diffraction. The crystal crystallizes in the orthorhombic system, space group Pna21 with a = 11.9904（12）, b = 15.9796（16）, c = 8.9 i 43（9） A^°, V = 1708.0（3）A^°3 Mr = 424.78, Z = 4, F（000） = 876, Dc = 1.652 g/cm^3, T = 293 K,μ =1 .619 mm^-1 and λ=0.71073 A^°. The structure was refined to R = 0.0240 and wR ： 0.0564 for 2905 observed reflections with I 〉 2σ（I）. Flack = 0.039（12）.展开更多
An efficient, environmentally friendly procedure is developed for the condensation of aldchydcs/kctoncs and activated methylene compounds by using an aminopropyl-functionalized MCM-41 catalyst in aqueous solution. Dif...An efficient, environmentally friendly procedure is developed for the condensation of aldchydcs/kctoncs and activated methylene compounds by using an aminopropyl-functionalized MCM-41 catalyst in aqueous solution. Different aldchydcs/kctoncs and activated methylene compounds gave the corresponding alkcncs in 78-97% isolated yields in mild reaction conditions. In comparison with organic solution, the aqueous solution gives higher yields in the same reaction conditions. Further more, the aminopropyl-functionalizcd MCM-41 in aqueous system can be reused for 8 flints without significant decrease of activity.展开更多
Herein a novel aminopropyl-containing ionic liquid based organosilica(ILOS-NH_2) is prepared, characterized and applied as effective adsorbent for removal of crystal violet(CV) dye from wastewater. The ILOS-NH2 materi...Herein a novel aminopropyl-containing ionic liquid based organosilica(ILOS-NH_2) is prepared, characterized and applied as effective adsorbent for removal of crystal violet(CV) dye from wastewater. The ILOS-NH2 material was synthesized by hydrolysis and co-condensation of 1,3-bis-(3-trimethoxysilylpropyl)-imidazolium chloride(BTMSPIC) under acidic conditions followed by treatment with 3-aminopropyl-trimethoxysilane in toluene under reflux conditions. This material was characterized using scanning electron microscopy(SEM), diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS), thermal gravimetric analysis(TGA) and energy dispersive X-ray analysis(EDAX). The material was effectively used in the removal of crystal violet at ambient temperature and showed high capacity and stability under applied conditions. The efficacy of p H, contact time, adsorbent dose, initial dye concentration, temperature, and isotherm studies and the applicability of pseudo-first, second order and Elovich kinetic models have also been investigated.展开更多
A novel material, aminopropyl-functionalized manganese-loaded SBA-15（NH2-Mn-SBA-15）, was synthesized by bonding 3-aminopropyl trimethoxysilane（APTMS） onto manganeseloaded SBA-15（Mn-SBA-15） and used as a Cu2＋ads...A novel material, aminopropyl-functionalized manganese-loaded SBA-15（NH2-Mn-SBA-15）, was synthesized by bonding 3-aminopropyl trimethoxysilane（APTMS） onto manganeseloaded SBA-15（Mn-SBA-15） and used as a Cu2＋adsorbent in aqueous solution. Fourier transform infrared spectroscopy（FT-IR）, X-ray diffraction spectra（XRD）, N2adsorption/desorption isotherms, high resolution field emission scanning electron microscopy（FESEM）and X-ray photoelectron spectroscopy（XPS） were used to characterize the NH2-Mn-SBA-15.The ordered mesoporous structure of SBA-15 was remained after modification. The manganese oxides were mainly loaded on the internal surface of the pore channels while the aminopropyl groups were mainly anchored on the external surface of SBA-15. The adsorption of Cu2＋on NH2-Mn-SBA-15 was fitted well by the Langmuir equation and the maximum adsorption capacity of NH2-Mn-SBA-15 for Cu2＋was over two times higher than that of Mn-SBA-15 under the same conditions. The Elovich equation gave a good fit for the adsorption process of Cu2＋by NH2-Mn-SBA-15 and Mn-SBA-15. Both the loaded manganese oxides and the anchored aminopropyl groups were found to contribute to the uptake of Cu2＋. The NH2-Mn-SBA-15 showed high selectivity for copper ions. Consecutive adsorption–desorption experiments showed that the NH2-Mn-SBA-15 could be regenerated by acid treatment without altering its properties.展开更多
Six novel μ-oxamido trinuclear complexes, namely Cu_2(oxap)_2Ln(ClO_4)_3 (Ln: La, Pr, Nd, Gd, Yb, Ho), where oxap is N,N'-bis(2-aminopropyl)oxamido, have been synthesized. The complex Cu_2(oxap)_2Gd(ClO_4)_3 was ...Six novel μ-oxamido trinuclear complexes, namely Cu_2(oxap)_2Ln(ClO_4)_3 (Ln: La, Pr, Nd, Gd, Yb, Ho), where oxap is N,N'-bis(2-aminopropyl)oxamido, have been synthesized. The complex Cu_2(oxap)_2Gd(ClO_4)_3 was characterized with variable temperature magnetic susceptibility (4-300 K). The exchange integrals J (Cu-Gd) and J'(Cu-Cu) were found to be 0.83 cm^(-1) and -1.62 cm^(-1), indi- cating that very weakly ferromagnetic spin-exchange interaction operates between Cu(II) and Gd (III) ions.展开更多
The cationic reagent 1-(3-aminopropyl)-3-butylimidazolium bromide(BAPI) was exploited for the derivatization of carboxyl groups on peptides.Nearly 100% derivatization efficiency was achieved with the synthetic peptide...The cationic reagent 1-(3-aminopropyl)-3-butylimidazolium bromide(BAPI) was exploited for the derivatization of carboxyl groups on peptides.Nearly 100% derivatization efficiency was achieved with the synthetic peptide RVYVHPI(RI-7).Furthermore,the peptide derivative was stable in a 0.1% TFA/water solution or a 0.1%(v/v) TFA/acetonitrile/water solution for at least one week.The effect of BAPI derivatization on the ionization of the peptide RI-7 was further investigated,and the detection sensitivity was improved >42-fold via matrix-assisted laser desorption/ionization time-of-flight mass spectrometry(MALDI-TOF MS),thus outperforming the commercial piperazine derivatization approach.Moreover,the charge states of the peptide were largely increased via BAPI derivatization by electrospray ionization(ESI) MS.The results indicate the potential merits of BAPI derivatization for high sensitivity peptide analysis by MS.展开更多
基金The project was supported by the Natural Science Foundation of Jiangsu Province (No. BK2005045) and Key Marine Biotechnology Lab. of HHIT
文摘The title compound [Cu（C11H29N5）]（ClO4）2 was synthesized and characterized by elemental analysis, IR and X-ray single-crystal diffraction. The compound crystallizes in the monoclinic system, space group P21/n with α = 9.405（2）, b = 14.495（3）, c = 14.715（3） A, β= 90.262（3）°, V=2006.1（7） A^3,M,=493.83,Z=4,F）（000）= 1028,Dc= 1.635 g/cm^3, T= 298（2） K,μ= 1.403 mm^-1 and = 0.71073 A. The was refined to R = 0.0508 and wR = 0. 1250 for 2293 observed reflections with I 〉 2σ（I）. The Cu（Ⅱ） atom possesses a five-coordtinate CuN5 environment which shows a slightly distorted square-pyramidal geonetry. Antimicrobial activity study found that the complex is active against Salmonella species, Staphylococcus aureu, Bacillus pumilus and Bacillus coliforms.
文摘The heterobinuclear complex of formula Cu (oxap )Gd(phen)2 (CIO4 )3 has been synthesized, where oxap denotes the N, N'-bis (2-aminopropyl )oxamido dianion and phen represents 1,10-phenanthroline. The complex was characterized with ESR and variable temperature magnetic susceptibility (4- 300K). The least-squares fit of the experimental sosceptibilities yielded J=2. 25cm-1. The observed Gd (Ⅲ)-Cu (Ⅱ) coupling is ferromagnetic.One Plausible mechanism that can cause a ferromagnetic coupling between Gd(Ⅱ) and Cu (Ⅱ) is discussed in terms of spin-polarization.
基金This project was supported by the Foundation of Science Committee of Jiangsu province (BK2005045)
文摘The title complex [Cu（ampym）（bapa）Cl]（ClO4） （C10H22Cl2CuN6O4） was synthesized and characterized by elemental analysis, IR and X-ray single-crystal diffraction. The crystal crystallizes in the orthorhombic system, space group Pna21 with a = 11.9904（12）, b = 15.9796（16）, c = 8.9 i 43（9） A^°, V = 1708.0（3）A^°3 Mr = 424.78, Z = 4, F（000） = 876, Dc = 1.652 g/cm^3, T = 293 K,μ =1 .619 mm^-1 and λ=0.71073 A^°. The structure was refined to R = 0.0240 and wR ： 0.0564 for 2905 observed reflections with I 〉 2σ（I）. Flack = 0.039（12）.
文摘An efficient, environmentally friendly procedure is developed for the condensation of aldchydcs/kctoncs and activated methylene compounds by using an aminopropyl-functionalized MCM-41 catalyst in aqueous solution. Different aldchydcs/kctoncs and activated methylene compounds gave the corresponding alkcncs in 78-97% isolated yields in mild reaction conditions. In comparison with organic solution, the aqueous solution gives higher yields in the same reaction conditions. Further more, the aminopropyl-functionalizcd MCM-41 in aqueous system can be reused for 8 flints without significant decrease of activity.
基金Supported by the National Science Foundation of Iran
文摘Herein a novel aminopropyl-containing ionic liquid based organosilica(ILOS-NH_2) is prepared, characterized and applied as effective adsorbent for removal of crystal violet(CV) dye from wastewater. The ILOS-NH2 material was synthesized by hydrolysis and co-condensation of 1,3-bis-(3-trimethoxysilylpropyl)-imidazolium chloride(BTMSPIC) under acidic conditions followed by treatment with 3-aminopropyl-trimethoxysilane in toluene under reflux conditions. This material was characterized using scanning electron microscopy(SEM), diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS), thermal gravimetric analysis(TGA) and energy dispersive X-ray analysis(EDAX). The material was effectively used in the removal of crystal violet at ambient temperature and showed high capacity and stability under applied conditions. The efficacy of p H, contact time, adsorbent dose, initial dye concentration, temperature, and isotherm studies and the applicability of pseudo-first, second order and Elovich kinetic models have also been investigated.
基金supported by the Fundamental Research Funds for the Central Universities (No. TD2010-5)the National Natural Science Research Fund (No. 51278051)the Beijing Forestry University Young Scientist Fund (No. BLX2009018)
文摘A novel material, aminopropyl-functionalized manganese-loaded SBA-15（NH2-Mn-SBA-15）, was synthesized by bonding 3-aminopropyl trimethoxysilane（APTMS） onto manganeseloaded SBA-15（Mn-SBA-15） and used as a Cu2＋adsorbent in aqueous solution. Fourier transform infrared spectroscopy（FT-IR）, X-ray diffraction spectra（XRD）, N2adsorption/desorption isotherms, high resolution field emission scanning electron microscopy（FESEM）and X-ray photoelectron spectroscopy（XPS） were used to characterize the NH2-Mn-SBA-15.The ordered mesoporous structure of SBA-15 was remained after modification. The manganese oxides were mainly loaded on the internal surface of the pore channels while the aminopropyl groups were mainly anchored on the external surface of SBA-15. The adsorption of Cu2＋on NH2-Mn-SBA-15 was fitted well by the Langmuir equation and the maximum adsorption capacity of NH2-Mn-SBA-15 for Cu2＋was over two times higher than that of Mn-SBA-15 under the same conditions. The Elovich equation gave a good fit for the adsorption process of Cu2＋by NH2-Mn-SBA-15 and Mn-SBA-15. Both the loaded manganese oxides and the anchored aminopropyl groups were found to contribute to the uptake of Cu2＋. The NH2-Mn-SBA-15 showed high selectivity for copper ions. Consecutive adsorption–desorption experiments showed that the NH2-Mn-SBA-15 could be regenerated by acid treatment without altering its properties.
基金Project supported by the National Natural Science Foundation or China.
文摘Six novel μ-oxamido trinuclear complexes, namely Cu_2(oxap)_2Ln(ClO_4)_3 (Ln: La, Pr, Nd, Gd, Yb, Ho), where oxap is N,N'-bis(2-aminopropyl)oxamido, have been synthesized. The complex Cu_2(oxap)_2Gd(ClO_4)_3 was characterized with variable temperature magnetic susceptibility (4-300 K). The exchange integrals J (Cu-Gd) and J'(Cu-Cu) were found to be 0.83 cm^(-1) and -1.62 cm^(-1), indi- cating that very weakly ferromagnetic spin-exchange interaction operates between Cu(II) and Gd (III) ions.
基金supported by National Basic Research Program of China (2012CB910604)National Natural Science Foundation of China (21205027,21005079,20935004)+1 种基金Analytical Method Innovation Program of Ministry of Science and Technology of China (2010IM030500)Natural Science Foundation of Hebei Province (B2012201095)
文摘The cationic reagent 1-(3-aminopropyl)-3-butylimidazolium bromide(BAPI) was exploited for the derivatization of carboxyl groups on peptides.Nearly 100% derivatization efficiency was achieved with the synthetic peptide RVYVHPI(RI-7).Furthermore,the peptide derivative was stable in a 0.1% TFA/water solution or a 0.1%(v/v) TFA/acetonitrile/water solution for at least one week.The effect of BAPI derivatization on the ionization of the peptide RI-7 was further investigated,and the detection sensitivity was improved >42-fold via matrix-assisted laser desorption/ionization time-of-flight mass spectrometry(MALDI-TOF MS),thus outperforming the commercial piperazine derivatization approach.Moreover,the charge states of the peptide were largely increased via BAPI derivatization by electrospray ionization(ESI) MS.The results indicate the potential merits of BAPI derivatization for high sensitivity peptide analysis by MS.
