High molecular weight（Mw） poly（L-lactic acid）s（PLLAs） were synthesized using multifunctional epoxy compound（Joncryl-ADR4370） as chain extender. The products were characterized by gel permeation chromatography...High molecular weight（Mw） poly（L-lactic acid）s（PLLAs） were synthesized using multifunctional epoxy compound（Joncryl-ADR4370） as chain extender. The products were characterized by gel permeation chromatography（GPC） and spectroscopy（1HNMR and FTIR）. The results indicated that the Mw of PLLA increased with the increasing of the ratio of epoxy compound and the extending of reaction time. The highest Mw of PLLA reached 360 000 g/mol when the ratio of epoxy compound was 1.5 wt%. However, the reactants turned to cross-linking when the ratio of epoxy compound was over 1.5 wt%. Differential scanning calorimetry（DSC） measurements demonstrated that the glass transition（Tg） and melting temperatures（Tm） of products increased slightly as the increase of the molecular weight. Analysis of the hydrolytic degradation in vitro showed that the branched PLLA possessed the quicker degradability than that of the linear PLLA.展开更多
The Zn2＋, Ni2＋ and Co3＋ doped Sr14Cu24041 compounds were synthesized by standard solid state method. X-ray diffraction results show that the changes in lattice parameters are very small. Selected area electron diff...The Zn2＋, Ni2＋ and Co3＋ doped Sr14Cu24041 compounds were synthesized by standard solid state method. X-ray diffraction results show that the changes in lattice parameters are very small. Selected area electron diffraction patterns （EDPs） show that the diffraction spots corresponding to the CuO2 chain substructure are extended to streaks along a＊ and b＊ directions for all the samples, while the diffraction spots produced merely by the Cu203 ladder substructure are still very sharp. This means that the periodicities of chains in a＊ and b＊ directions are partially destroyed upon doping ofZn, Ni and Co due to that the initial phase of each chain becomes a random variable. The temperature dependence of magnetic properties was measured for every sample. And the number of dimers in CuO2 chain per formula unit （f.u.） and dimer coupling constant are obtained by fitting the temperature dependence of the magnetic susceptibility. It is found that the degree of initial phase disorder is related to the order degree of magnetic sequence in CuO2 chain. For the un-doped sample, the decoupling of dimers is weak, the magnetic sequence is slightly destroyed, and the streaks in EDP are also very weak, which implies the degree of initial phase disorder in CuO2 chain is very low. When Zn2~ and Ni2＋ ions are doped, the number of dimers per f.u. decreases, and the intensity of diffraction streaks increases in comparison with the corresponding spots. Furthermore, when the high spin magnetic ions Co3＋ are doped, the number of holes in Sr14Cu24041 decreases, the magnetic sequence is destroyed very seriously, and the spots in EDP are extended to streaks almost completely. The phenomenon that the diffraction spots ofCuO2 chain extend to streaks in EDP appears as evidence that the magnetic sequence in the CuO2 chain is destroyed by doping of Zn, Ni, Co.展开更多
Ta_4(Te_2)_4Te_4I,Mr=2381.90,Monoclinic,C2/c,a=21.987(2),b=6.153(2),c= 19.936(3),β=122.42(14),V=2276.7 ~3,z=4,Dm=6.8(5)g/cm^3,Dc=6.95g/cm^3,λ(Mok)= 0.71073,μ=354.0cm^(-1),F(000)=3876,T=296(1)k,R=5.3%,Rw=6.8%,for 11...Ta_4(Te_2)_4Te_4I,Mr=2381.90,Monoclinic,C2/c,a=21.987(2),b=6.153(2),c= 19.936(3),β=122.42(14),V=2276.7 ~3,z=4,Dm=6.8(5)g/cm^3,Dc=6.95g/cm^3,λ(Mok)= 0.71073,μ=354.0cm^(-1),F(000)=3876,T=296(1)k,R=5.3%,Rw=6.8%,for 1118 unique observed reflections(1>3σ(Ⅰ)).The structure is composed of [Ta_4(Te_2)_4Te_4I]_∞~ chains,which are formed by the four-nuclear butterfly cluster units "Ta_4(Te_2)_4Te_4" with the Ⅰ atoms as the bridging atoms between different cluster units.展开更多
A novel transition-metal ion coordination-linked network compound {Na4[Co- (H2O)2(NH2NH2)2Mo8O27]?16H2O}n 1 was synthesized by the reduction reaction of Na2MoO4? 2H2O, NH2NH2?2HCl and Co(OAc)2?4H2O in aq...A novel transition-metal ion coordination-linked network compound {Na4[Co- (H2O)2(NH2NH2)2Mo8O27]?16H2O}n 1 was synthesized by the reduction reaction of Na2MoO4? 2H2O, NH2NH2?2HCl and Co(OAc)2?4H2O in aqueous solution at ambient temperature and structurally characterized. Crystal data for 1: triclinic system, space group P1, a = 9.5544(2), b = 9.8640(2), c = 11.6338(3) ?, α = 103.3790(10), β = 100.5600(10), γ = 96.2750(10)o, V = 1035.32(4) ?3, Z = 1, Dc = 2.789 g/cm3 and R = 0.0453. The X-ray crystal structure analysis shows that 1 is constructed by octamolybdate anions linked via corner-sharing interactions and hetero-metal links into the polymeric anionic sheet [Co(H2O)2(NH2NH2)2Mo8O27]n 4n-, and further allied by [Na4(H2O)12]n 4n+ sodium chains into a 3D framework with z-shaped channels. The mag- netic study of compound 1 indicates that weak antiferromagnetic coupling interaction occurs be- tween the cobalt centers.展开更多
The title compounds 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxylic acid（C11H9Cl N2O2, HL）（1） and [Cu（L）2（H2O）]（2） were prepared and structurally characterized by elemental analysis, IR and single-crysta...The title compounds 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxylic acid（C11H9Cl N2O2, HL）（1） and [Cu（L）2（H2O）]（2） were prepared and structurally characterized by elemental analysis, IR and single-crystal X-ray diffraction. Compound 1（C11H9Cl N2O2） crystallizes in the monoclinic system, space group P21/n with a = 7.249（3）, b = 20.515（10）, c = 7.249（3）,β= 96.30°, V = 1071.6（9） ？3, Z = 4, Mr = 236.65, Dc = 1.467 g/cm3, F（000） = 488, GOOF = 1.029, μ= 0.341 mm-1, the final R = 0.0736 and w R = 0.1966 for 1500 observed reflections with I 〉 2σ（I）. Compound 2（C22H18Cl2Cu N4O5） crystallizes in the monoclinic system, space group P21/c with a = 7.2931（6）, b = 24.548（2）, c = 13.2726（11）, β= 99.4040（10）°, V = 2344.2（3） ？3, Z = 4, Mr = 552.84, Dc = 1.566 g/cm3, F（000） = 1124, GOOF = 1.050, μ= 1.201 mm-1, the final R = 0.0376 and w R = 0.1000 for 3626 observed reflections with I 〉 2σ（I）. 1 and 2 are connected through hydrogen bonding interactions to generate 2D and 3D supramolecular structures, respectively. Moreover, the preliminary antibacterial activities of 1 and 2 against the gram positive bacteria（S. aureus, C. albicans and B. subtilis） and gram negative bacteria（E. coli and P. aeruginosa） have been tested by using the microdilution method, and the results indicate that 2 is more active than 1 against the tested bacteria.展开更多
A new organo-directed titanium phosphate, [NH3CH2CH2NH3]·[TiO(HPO4)2], was synthesized by the solvothermal method and its structure was determined by single crystal X-ray diffraction. The structure consists of 1-...A new organo-directed titanium phosphate, [NH3CH2CH2NH3]·[TiO(HPO4)2], was synthesized by the solvothermal method and its structure was determined by single crystal X-ray diffraction. The structure consists of 1-D zigzag chains built up from trans-corner-sharing titanium oxo octahedra running along the b axis, with fused Ti2P three-membered rings being attached to the ( Ti ( O ( Ti ( O ( backbone.展开更多
This paper presents a synthesis method for a new dwell mechanism that is composed of cam mechanism, guide-bar mechanism and chain transmission. And then it gives an actual engineering example.
基金Funded by the National Natural Science Foundation of China (No.30870609)the Natural Science Foundation of Chongqing (Nos.2009BA4025 and CSTC2009BB4382)the Foundation of Chongqing Municipal Education Commission(No.KJ091415)
文摘High molecular weight（Mw） poly（L-lactic acid）s（PLLAs） were synthesized using multifunctional epoxy compound（Joncryl-ADR4370） as chain extender. The products were characterized by gel permeation chromatography（GPC） and spectroscopy（1HNMR and FTIR）. The results indicated that the Mw of PLLA increased with the increasing of the ratio of epoxy compound and the extending of reaction time. The highest Mw of PLLA reached 360 000 g/mol when the ratio of epoxy compound was 1.5 wt%. However, the reactants turned to cross-linking when the ratio of epoxy compound was over 1.5 wt%. Differential scanning calorimetry（DSC） measurements demonstrated that the glass transition（Tg） and melting temperatures（Tm） of products increased slightly as the increase of the molecular weight. Analysis of the hydrolytic degradation in vitro showed that the branched PLLA possessed the quicker degradability than that of the linear PLLA.
基金Funded by the National Natural Science Foundation of China(Nos.10674105 and 50471028)
文摘The Zn2＋, Ni2＋ and Co3＋ doped Sr14Cu24041 compounds were synthesized by standard solid state method. X-ray diffraction results show that the changes in lattice parameters are very small. Selected area electron diffraction patterns （EDPs） show that the diffraction spots corresponding to the CuO2 chain substructure are extended to streaks along a＊ and b＊ directions for all the samples, while the diffraction spots produced merely by the Cu203 ladder substructure are still very sharp. This means that the periodicities of chains in a＊ and b＊ directions are partially destroyed upon doping ofZn, Ni and Co due to that the initial phase of each chain becomes a random variable. The temperature dependence of magnetic properties was measured for every sample. And the number of dimers in CuO2 chain per formula unit （f.u.） and dimer coupling constant are obtained by fitting the temperature dependence of the magnetic susceptibility. It is found that the degree of initial phase disorder is related to the order degree of magnetic sequence in CuO2 chain. For the un-doped sample, the decoupling of dimers is weak, the magnetic sequence is slightly destroyed, and the streaks in EDP are also very weak, which implies the degree of initial phase disorder in CuO2 chain is very low. When Zn2~ and Ni2＋ ions are doped, the number of dimers per f.u. decreases, and the intensity of diffraction streaks increases in comparison with the corresponding spots. Furthermore, when the high spin magnetic ions Co3＋ are doped, the number of holes in Sr14Cu24041 decreases, the magnetic sequence is destroyed very seriously, and the spots in EDP are extended to streaks almost completely. The phenomenon that the diffraction spots ofCuO2 chain extend to streaks in EDP appears as evidence that the magnetic sequence in the CuO2 chain is destroyed by doping of Zn, Ni, Co.
文摘Ta_4(Te_2)_4Te_4I,Mr=2381.90,Monoclinic,C2/c,a=21.987(2),b=6.153(2),c= 19.936(3),β=122.42(14),V=2276.7 ~3,z=4,Dm=6.8(5)g/cm^3,Dc=6.95g/cm^3,λ(Mok)= 0.71073,μ=354.0cm^(-1),F(000)=3876,T=296(1)k,R=5.3%,Rw=6.8%,for 1118 unique observed reflections(1>3σ(Ⅰ)).The structure is composed of [Ta_4(Te_2)_4Te_4I]_∞~ chains,which are formed by the four-nuclear butterfly cluster units "Ta_4(Te_2)_4Te_4" with the Ⅰ atoms as the bridging atoms between different cluster units.
基金This project was supported by the 973 Program of the MOST (001CB108906) the NNSFC (90206040+3 种基金 20073048) the NSF of Fujian (2002F015 2002J006) the State Key Lab of Structural Chemistry (030065) and the Chinese Academy of Sciences
文摘A novel transition-metal ion coordination-linked network compound {Na4[Co- (H2O)2(NH2NH2)2Mo8O27]?16H2O}n 1 was synthesized by the reduction reaction of Na2MoO4? 2H2O, NH2NH2?2HCl and Co(OAc)2?4H2O in aqueous solution at ambient temperature and structurally characterized. Crystal data for 1: triclinic system, space group P1, a = 9.5544(2), b = 9.8640(2), c = 11.6338(3) ?, α = 103.3790(10), β = 100.5600(10), γ = 96.2750(10)o, V = 1035.32(4) ?3, Z = 1, Dc = 2.789 g/cm3 and R = 0.0453. The X-ray crystal structure analysis shows that 1 is constructed by octamolybdate anions linked via corner-sharing interactions and hetero-metal links into the polymeric anionic sheet [Co(H2O)2(NH2NH2)2Mo8O27]n 4n-, and further allied by [Na4(H2O)12]n 4n+ sodium chains into a 3D framework with z-shaped channels. The mag- netic study of compound 1 indicates that weak antiferromagnetic coupling interaction occurs be- tween the cobalt centers.
基金Supported by the National Natural Science Foundation of China(No.20662007)the Bureau of Education of Jiangxi Province(No.GJJ09064)Jiangxi Science and Technology Support Program(20112BBF60009)
文摘The title compounds 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxylic acid（C11H9Cl N2O2, HL）（1） and [Cu（L）2（H2O）]（2） were prepared and structurally characterized by elemental analysis, IR and single-crystal X-ray diffraction. Compound 1（C11H9Cl N2O2） crystallizes in the monoclinic system, space group P21/n with a = 7.249（3）, b = 20.515（10）, c = 7.249（3）,β= 96.30°, V = 1071.6（9） ？3, Z = 4, Mr = 236.65, Dc = 1.467 g/cm3, F（000） = 488, GOOF = 1.029, μ= 0.341 mm-1, the final R = 0.0736 and w R = 0.1966 for 1500 observed reflections with I 〉 2σ（I）. Compound 2（C22H18Cl2Cu N4O5） crystallizes in the monoclinic system, space group P21/c with a = 7.2931（6）, b = 24.548（2）, c = 13.2726（11）, β= 99.4040（10）°, V = 2344.2（3） ？3, Z = 4, Mr = 552.84, Dc = 1.566 g/cm3, F（000） = 1124, GOOF = 1.050, μ= 1.201 mm-1, the final R = 0.0376 and w R = 0.1000 for 3626 observed reflections with I 〉 2σ（I）. 1 and 2 are connected through hydrogen bonding interactions to generate 2D and 3D supramolecular structures, respectively. Moreover, the preliminary antibacterial activities of 1 and 2 against the gram positive bacteria（S. aureus, C. albicans and B. subtilis） and gram negative bacteria（E. coli and P. aeruginosa） have been tested by using the microdilution method, and the results indicate that 2 is more active than 1 against the tested bacteria.
文摘A new organo-directed titanium phosphate, [NH3CH2CH2NH3]·[TiO(HPO4)2], was synthesized by the solvothermal method and its structure was determined by single crystal X-ray diffraction. The structure consists of 1-D zigzag chains built up from trans-corner-sharing titanium oxo octahedra running along the b axis, with fused Ti2P three-membered rings being attached to the ( Ti ( O ( Ti ( O ( backbone.
文摘This paper presents a synthesis method for a new dwell mechanism that is composed of cam mechanism, guide-bar mechanism and chain transmission. And then it gives an actual engineering example.
