The title compound,2,6-bis（2-pyridinylmethyl）-3,5-bis（2-hydroxyl-5-chlorophe nyl）-pyrazine（C26H12Cl2N4O2C2H8O2,Mr=551.41）,has been synthesized and characterized by LC-ESIMS,NMR,UV and IR spectroscopy as well as ...The title compound,2,6-bis（2-pyridinylmethyl）-3,5-bis（2-hydroxyl-5-chlorophe nyl）-pyrazine（C26H12Cl2N4O2C2H8O2,Mr=551.41）,has been synthesized and characterized by LC-ESIMS,NMR,UV and IR spectroscopy as well as by X-ray single-crystal diffraction.The compound behaves as a substituted pyrazine.The hydrogen atoms on C（2） and C（3） are substituted by 2-pyridinyl,whereas those on C（1） and C（4） are substituted by 2-hydroxyl-5-chlorophenyl.It crystallizes in the monoclinic system,space group P21/c with a=8.9433（12）,b=32.003（4）,c=10.5209（18）,β=111.199（2）°,V=2807.5（7）3,Z=4,Dc=1.305 mg/m3,F（000）=1144 and μ=0.094 mm-1.A total of 13235 reflections were collected in the range of 2.17～25.01o by using a phi and omega scan mode,of which 4923 were unique（Rint=0.0692） and 2872 observed reflections with Ⅰ 〉2σ（Ⅰ） were used in the structure solution and refinement.展开更多
The new title compound （2E,6E）-2,6-bis（2,3-dimethoxybenzylidene）cyclohexanone （C 24 H 26 O 5,M r=394.45） has been synthesized,and its crystal structure was studied.The title compound crystallizes in the orthorho...The new title compound （2E,6E）-2,6-bis（2,3-dimethoxybenzylidene）cyclohexanone （C 24 H 26 O 5,M r=394.45） has been synthesized,and its crystal structure was studied.The title compound crystallizes in the orthorhombic system,space group Pca2 1 with a=17.536（2）,b=14.8515（16）,c=8.0512（9）,V=2096.8（4） 3,Z=4,D c=1.250 g/cm 3,λ=0.71073,μ=0.087 mm-1 and F（000）=840.The structure was solved by direct methods and refined to R=0.0533 and wR=0.1248 from 2727 observed reflections （I 2σ（Ⅰ））.The title molecules are connected through hydrogen bonds to generate a 3-D supramolecule.The preliminary biological tests showed definitely biological activity for the title compound.展开更多
Homopolymer（PBIP） containing 2,6-bis（1＇-methylbenzimidazolyl）pyridine（Me BIP） ligands in the side chain was synthesized by RAFT polymerization and its kinetics was studied. Polymeric complex PBIP-Nd^3＋ was pre...Homopolymer（PBIP） containing 2,6-bis（1＇-methylbenzimidazolyl）pyridine（Me BIP） ligands in the side chain was synthesized by RAFT polymerization and its kinetics was studied. Polymeric complex PBIP-Nd^3＋ was prepared by chelating PBIP with lanthanide ion Nd^3＋. The homopolymers and PBIP-Nd^3＋ complex were investigated by NMR, FTIR, GPC and TGA. The optical property of PBIP-Nd^3＋ complex was characterized by UV-Vis spectroscopy. The magnetic property of PBIP-Nd^3＋ complex was measured as a function of temperature（5 K to 300 K） and as a function of field（-3.98×10^6 A/m to 3.98×10^6 A/m）. These results indicated that PBIP-Nd^3＋ complex is paramagnetic.展开更多
采用表面活性剂辅助水热法合成了系列γ-Bi2 MoO6微纳米晶粉。考察了 pH 值及不同表面活性剂对产物物相及形貌的影响。以可见光降解罗丹明 B 作为探针反应，研究了不同条件下的降解效果，对γ-Bi2 MoO6的催化活性做出了评价。研究结果...采用表面活性剂辅助水热法合成了系列γ-Bi2 MoO6微纳米晶粉。考察了 pH 值及不同表面活性剂对产物物相及形貌的影响。以可见光降解罗丹明 B 作为探针反应，研究了不同条件下的降解效果，对γ-Bi2 MoO6的催化活性做出了评价。研究结果表明：在反应物 Bi 与 Mo 物质的量比为2∶1及 pH 为3～9时，表面活性剂的加入并不影响正交晶系γ-Bi2 MoO6的形成；pH 值为9时所得产物的催化活性最高，可见光照射3 h 的降解率可达79．62％。十二烷基硫酸钠（SDS）辅助所得纳米片状γ-Bi2 MoO6具有高达98．81％的降解率。展开更多
The enantioseparation of anti-hepatitis new drug （±）-bicyclol was performed by optically active alkaloid. The alcoholic acid, the hydrolysate of bicyclol was reacted with optically active alkaloid, such as bruc...The enantioseparation of anti-hepatitis new drug （±）-bicyclol was performed by optically active alkaloid. The alcoholic acid, the hydrolysate of bicyclol was reacted with optically active alkaloid, such as brucine, strychnine, quinidine etc., the diastereoisomeric salts were obtained by fractional recrystallization, then separately decomposed and esterified to obtain the two enantiomers of bicyclol. The pharmacological study showed that the effect of （-）-bicyclol was more potent than racemic bicyclol two times and the potency of （＋）-bicyclol was incative.展开更多
In this paper,two compounds[Zn_(2)^(2+)(2,6-bis(4΄-pyridyl)-TTF)(TPA)_(2)^(2-)](1)and[Cd^(2+)(2,6(7)-bis(4΄-pyridyl)-TTF)(TPA)2-(H_(2)O)_(2)](TTF=tetrathiafulvalene,TPA=terephthalic acid)(2)were synthesized by using s...In this paper,two compounds[Zn_(2)^(2+)(2,6-bis(4΄-pyridyl)-TTF)(TPA)_(2)^(2-)](1)and[Cd^(2+)(2,6(7)-bis(4΄-pyridyl)-TTF)(TPA)2-(H_(2)O)_(2)](TTF=tetrathiafulvalene,TPA=terephthalic acid)(2)were synthesized by using solvothermal method and characterized by single-crystal X-ray.The purity of the two compounds was confirmed by their PXRD data.We also tested the photocurrent responses of these two compounds,and found they could generate photocurrent signal when exposed to light,but the photocurrent intensity of compound 2 is significantly greater than that of 1.From the crystal structure analysis,the possible reason for this phenomenon is that 2 has a more compact ligand arrangement than 1,leading to a higher carrier density and easier excitation.展开更多
基金supported by the research grant of Phytochemistry Key Laboratory of Shaanxi Province (No. 02js40)
文摘The title compound,2,6-bis（2-pyridinylmethyl）-3,5-bis（2-hydroxyl-5-chlorophe nyl）-pyrazine（C26H12Cl2N4O2C2H8O2,Mr=551.41）,has been synthesized and characterized by LC-ESIMS,NMR,UV and IR spectroscopy as well as by X-ray single-crystal diffraction.The compound behaves as a substituted pyrazine.The hydrogen atoms on C（2） and C（3） are substituted by 2-pyridinyl,whereas those on C（1） and C（4） are substituted by 2-hydroxyl-5-chlorophenyl.It crystallizes in the monoclinic system,space group P21/c with a=8.9433（12）,b=32.003（4）,c=10.5209（18）,β=111.199（2）°,V=2807.5（7）3,Z=4,Dc=1.305 mg/m3,F（000）=1144 and μ=0.094 mm-1.A total of 13235 reflections were collected in the range of 2.17～25.01o by using a phi and omega scan mode,of which 4923 were unique（Rint=0.0692） and 2872 observed reflections with Ⅰ 〉2σ（Ⅰ） were used in the structure solution and refinement.
基金supported by the National Natural Science Foundation of China (81072683)Project of Wenzhou Sci & Tech Bureau (Y20100006)Natural Science Foundation of Zhejiang Province (Y20101108)
文摘The new title compound （2E,6E）-2,6-bis（2,3-dimethoxybenzylidene）cyclohexanone （C 24 H 26 O 5,M r=394.45） has been synthesized,and its crystal structure was studied.The title compound crystallizes in the orthorhombic system,space group Pca2 1 with a=17.536（2）,b=14.8515（16）,c=8.0512（9）,V=2096.8（4） 3,Z=4,D c=1.250 g/cm 3,λ=0.71073,μ=0.087 mm-1 and F（000）=840.The structure was solved by direct methods and refined to R=0.0533 and wR=0.1248 from 2727 observed reflections （I 2σ（Ⅰ））.The title molecules are connected through hydrogen bonds to generate a 3-D supramolecule.The preliminary biological tests showed definitely biological activity for the title compound.
基金financially supported by the National Natural Science Foundation of China(No.21174129)
文摘Homopolymer（PBIP） containing 2,6-bis（1＇-methylbenzimidazolyl）pyridine（Me BIP） ligands in the side chain was synthesized by RAFT polymerization and its kinetics was studied. Polymeric complex PBIP-Nd^3＋ was prepared by chelating PBIP with lanthanide ion Nd^3＋. The homopolymers and PBIP-Nd^3＋ complex were investigated by NMR, FTIR, GPC and TGA. The optical property of PBIP-Nd^3＋ complex was characterized by UV-Vis spectroscopy. The magnetic property of PBIP-Nd^3＋ complex was measured as a function of temperature（5 K to 300 K） and as a function of field（-3.98×10^6 A/m to 3.98×10^6 A/m）. These results indicated that PBIP-Nd^3＋ complex is paramagnetic.
文摘采用表面活性剂辅助水热法合成了系列γ-Bi2 MoO6微纳米晶粉。考察了 pH 值及不同表面活性剂对产物物相及形貌的影响。以可见光降解罗丹明 B 作为探针反应，研究了不同条件下的降解效果，对γ-Bi2 MoO6的催化活性做出了评价。研究结果表明：在反应物 Bi 与 Mo 物质的量比为2∶1及 pH 为3～9时，表面活性剂的加入并不影响正交晶系γ-Bi2 MoO6的形成；pH 值为9时所得产物的催化活性最高，可见光照射3 h 的降解率可达79．62％。十二烷基硫酸钠（SDS）辅助所得纳米片状γ-Bi2 MoO6具有高达98．81％的降解率。
文摘The enantioseparation of anti-hepatitis new drug （±）-bicyclol was performed by optically active alkaloid. The alcoholic acid, the hydrolysate of bicyclol was reacted with optically active alkaloid, such as brucine, strychnine, quinidine etc., the diastereoisomeric salts were obtained by fractional recrystallization, then separately decomposed and esterified to obtain the two enantiomers of bicyclol. The pharmacological study showed that the effect of （-）-bicyclol was more potent than racemic bicyclol two times and the potency of （＋）-bicyclol was incative.
基金the Natural Science Foundation of Zhejiang Province(LY18B020016)Ningbo Science and Technology Innovation 2025(2018B10033)。
文摘In this paper,two compounds[Zn_(2)^(2+)(2,6-bis(4΄-pyridyl)-TTF)(TPA)_(2)^(2-)](1)and[Cd^(2+)(2,6(7)-bis(4΄-pyridyl)-TTF)(TPA)2-(H_(2)O)_(2)](TTF=tetrathiafulvalene,TPA=terephthalic acid)(2)were synthesized by using solvothermal method and characterized by single-crystal X-ray.The purity of the two compounds was confirmed by their PXRD data.We also tested the photocurrent responses of these two compounds,and found they could generate photocurrent signal when exposed to light,but the photocurrent intensity of compound 2 is significantly greater than that of 1.From the crystal structure analysis,the possible reason for this phenomenon is that 2 has a more compact ligand arrangement than 1,leading to a higher carrier density and easier excitation.
