Acid-soluble collagen(ASC) and pepsin-soluble collagen(PSC) from the spine(ASC-SP and PSC-SP) and skull(ASC-SK and PSC-SK) of the skipjack tuna, Katsuwonus pelamis, were successfully isolated and characterized. The yi...Acid-soluble collagen(ASC) and pepsin-soluble collagen(PSC) from the spine(ASC-SP and PSC-SP) and skull(ASC-SK and PSC-SK) of the skipjack tuna, Katsuwonus pelamis, were successfully isolated and characterized. The yields of ASC-SP, PSC-SP, ASC-SK and PSC-SK were(2.47 ± 0.39)%,(5.62 ± 0.82)%,(3.57 ± 0.40)%, and(6.71 ± 0.81)%, respectively, on the basis of dry weight. The four collagens contained Gly(330.2-339.1 residues/1 000 residues) as the major amino acid, and their imino acid contents were between 168.8 and 178.2 residues/1 000 residues. Amino acid composition, SDS-PAGE, and FTIR investigations confirmed that ASC-SP and ASC-SK were mainly composed of type I collagen, and had higher contents of high-molecular weight cross-links than those of PSC-SK and PSC-SP. The FTIR investigation also certified all the collagens had triple helical structure. The denaturation temperatures of ASC-SK, PSC-SK, ASC-SP, and PSC-SP were 17.8, 16.6, 17.6, and 16.5 °C, respectively. All isolated collagens were soluble at acidic pH(1-5) and lost their solubilities when the NaCl concentration was above 2%(W/V). The isolated collagens from the spines and skulls of skipjack tuna could serve as an alternative source of collagens for further application in food, cosmetic, biomedical, and pharmaceutical industries.展开更多
Four novel calix[4]arene derivatives 5-8 bearing four fluorogenic coumarin units attached via imino group acting also as binding sites at the upper rim have been prepared and characterized by IR, IH NMR and MS. Compou...Four novel calix[4]arene derivatives 5-8 bearing four fluorogenic coumarin units attached via imino group acting also as binding sites at the upper rim have been prepared and characterized by IR, IH NMR and MS. Compounds 5-8 adopt a cone conformation. Their complexation properties to different heavy and transition metal ions have been studied by UV-vis spectroscopy. Compounds 5, 6, 8 show selective recognition to Fe^3＋ and Cr^3＋.展开更多
Two novel fluorescent calix[4]arene derivatives la and lb with benzoxazole or benzothiazole units in 1,3-alternate conformation have been synthesized and characterized by IR, ^1H NMR, ^13C NMR and MS. Their complexati...Two novel fluorescent calix[4]arene derivatives la and lb with benzoxazole or benzothiazole units in 1,3-alternate conformation have been synthesized and characterized by IR, ^1H NMR, ^13C NMR and MS. Their complexation properties to different heavy and transition metal ions have been studied by UV-vis spectroscopy and fluorescence spectrometer. Compounds 1a and 1b show selective recognition to Fe^3＋ and Cr^3＋.展开更多
A novel heterospin complex {[(CuL)Ni(IM 2Py) 2](ClO 4) 2} 2·2H 2O (L=2,3 dioxo 5,6:14,15 dibenzo 1,4,8,12 tetraazacyclo pentadeca 7,12 diene, IM 2Py=2 (2′ pyridyl) 4,4,5,5 tetra^methyl 4,5 d...A novel heterospin complex {[(CuL)Ni(IM 2Py) 2](ClO 4) 2} 2·2H 2O (L=2,3 dioxo 5,6:14,15 dibenzo 1,4,8,12 tetraazacyclo pentadeca 7,12 diene, IM 2Py=2 (2′ pyridyl) 4,4,5,5 tetra^methyl 4,5 dihydro 1 H imidazoline 1 oxyl) has been synthesized and its crystal structure was determined by X ray diffraction analysis. In order to interpret the exchange interaction of this asymmetric heterospin system, a theoretical model has been established. Using this theoretical model the magnetic susceptibility data have been fitted and lead to coupling constant values equal to 1 4 cm -1 (Ni Rad) and -38 0 cm -1 (Ni Cu), respectively.展开更多
The title compound 3 was synthesized and characterized by IR, NMR and HRMS, and its crystal structure was determined by X-ray diffraction analysis. The crystal is of monoclinic system （CI6H23NOTS, Mr = 373.41）, spac...The title compound 3 was synthesized and characterized by IR, NMR and HRMS, and its crystal structure was determined by X-ray diffraction analysis. The crystal is of monoclinic system （CI6H23NOTS, Mr = 373.41）, space group P21, with a = 12.000（2）, b = 5.5970（11）, c = 13.689（3） A. β= 93.25（3）°, V= 917.9（3） A^3, Z= 2, Dc = 1.351 g/cm^3, F（000） = 396, μ = 0.213 mm^-1, the final R = 0.0489 and ωR = 0.0777 for observed reflections （I 〉 2σ（I））. Three intramolecular and three intermolecular hydrogen bonds were found. The absolute configuration of this molecule was confirmed by comparing with the original material.展开更多
Two new M(II)-radical complexes [M(hfac)<sub>2</sub>(IM-<span style="font-size:10.0pt;font-family:;" "=""><i></i></span><i>o<span style="font-...Two new M(II)-radical complexes [M(hfac)<sub>2</sub>(IM-<span style="font-size:10.0pt;font-family:;" "=""><i></i></span><i>o<span style="font-size:10.0pt;font-family:;" "=""></span></i>-QN)] (M = Ni(<strong>1</strong>), Zn(<strong>2</strong>);IM-<span style="white-space:normal;font-size:10pt;font-family:;" "=""><i></i></span><i><span style="white-space:normal;">o</span><span style="white-space:normal;font-size:10pt;font-family:;" "=""></span></i>-QN = 4'-quinoxalinyl-substituted imino nitroxide;<span style="font-family:" font-size:13.3333px;white-space:normal;"=""><i></i></span><i>hfac<span style="font-family:" font-size:13.3333px;white-space:normal;"=""></span></i> = hexafluoroa-cetylacetonate) have been synthesized and characterized by X-ray diffraction analysis, element analyses, IR and UV-Visible spectroscopy. X-ray analysis reveal that the structures of both complexes are similar configuration and differently spatial symmetries. The complex <strong>1</strong> crystallizes in the triclinic <span style="font-family:" font-size:13.3333px;white-space:normal;"=""><i></i></span><i>P<span style="font-family:" font-size:13.3333px;white-space:normal;"=""></span></i>ī space group with the respective cell parameters: <span style="font-family:" font-size:13.3333px;white-space:normal;"=""><i></i></span><i>a<span style="font-family:" font-size:13.3333px;white-space:normal;"=""></span></i> = 9.1189(18) <span style="color:#4F4F4F;font-family:-apple-system, " font-size:16px;white-space:normal;background-color:#f7f7f7;"=""><span style="color:#4F4F4F;font-family:-apple-system, "font-size:16px;white-space:normal;background-color:#F7F7F7;">Å</span></span>, <span style="font-family:" font-size:13.3333px;white-space:normal;"=""><i></i></span><i>b<span style="font-family:" font-size:13.3333px;white-space:normal;"=""></span></i> = 9.836(2) <span style="color:#4F4F4F;font-family:-apple-system, " font-size:16px;white-space:normal;background-color:#f7f7f7;"=""><span style="color:#4F4F4F;font-family:-apple-system, "font-size:16px;展开更多
Two novel complexes {[Zn（IM4py）2（tp）（H2O）]2H2O}. 1 and {[Cd（IM4py）2（tp）- （H2O）]1.25H2O},, 2 （IM4py = 2-（4＇-pyridinyl）-4,4,5,5-tetramethylimidazoline-l-oxyl and tp = terephthalate dianion） have been sy...Two novel complexes {[Zn（IM4py）2（tp）（H2O）]2H2O}. 1 and {[Cd（IM4py）2（tp）- （H2O）]1.25H2O},, 2 （IM4py = 2-（4＇-pyridinyl）-4,4,5,5-tetramethylimidazoline-l-oxyl and tp = terephthalate dianion） have been synthesized and characterized by elemental analyses, IR spectrum and single-crystal X-ray diffraction. Crystal data for complex I： monoclinic, space group C2/c, a = 20.648（7）, b = 12.130（4）, c = 14.036（4） A, β = 106.351（5）°, C32H42N6O9Zn, Mr = 720.09, V = 3373.3（2） A3, Z= 4, Dc = 1.418 g/cm^3μt（MoKα） = 0.790 mm^-1, F（000） = 1512, the final R = 0.0407 and wR = 0.0894 for 3480 independent reflections with Rint = 0.0432. Crystal data for complex 2： monoclinic, space group C2/c, a = 21.332（6）, b = 12.063（3）, c = 14.246（4） A, β = 106.704（4）°, C32H40.50N6O8.25Cd, Mr = 753.60, V= 3511.2（2） A^3, Z = 4, Dc = 1.426 g/cm^3,μ（MoKα） = 0.679 mm^--1, F（000） = 1554, the final R = 0.0419 and wR = 0.0961 for 3627 independent reflections with Rint = 0.0440. The framework structures of complexes 1 and 2 are 3-D networks via the hydrogen bonds among 1-D chains. The notable characteristics of the two complexes are that the coordination polyhedron of Zn（Ⅱ） adopts a rare distorted five-coordinate square pyramidal geometry in 1, and the Cd（Ⅱ） complex exhibits an unusual distorted seven-coordinate pentagonal bipyramid in 2.展开更多
Imino Diels-Alder reaction of imines with 2,3-dihydrofuran or 3,4-dihydro-2H-pyran proceeded smoothly in the presence of a catalytic amount (0.5 mol %) of ytterbium triflate to afford furo[3,2-c]- and pyrano[3,2-c] q... Imino Diels-Alder reaction of imines with 2,3-dihydrofuran or 3,4-dihydro-2H-pyran proceeded smoothly in the presence of a catalytic amount (0.5 mol %) of ytterbium triflate to afford furo[3,2-c]- and pyrano[3,2-c] quinolines conveniently in high yield.展开更多
A simple synthesis of medicinally important cis-2-methyl-4-azapan-2-one-1,2,3,4-tetrahydroquinolines/cis-9- （2-methyl-l,2,3,4-tetrahydroquinolin-4-yl）-9H-carbazole was reported. Multicomponent one pot synthesis with...A simple synthesis of medicinally important cis-2-methyl-4-azapan-2-one-1,2,3,4-tetrahydroquinolines/cis-9- （2-methyl-l,2,3,4-tetrahydroquinolin-4-yl）-9H-carbazole was reported. Multicomponent one pot synthesis with ani- lines and N-vinylcaprolactam/N-vinyl carbazole via imino Diels-Alder reaction by using antimony trichloride as catalyst and acetonitrile as solvent was employed. NMR technique （2D） was used to study the regio- and stereo- chemistry of newly synthesized compounds. The cis diastereo-selectivity of the products was predicted by COSY and NOESY studies.展开更多
1,4-Bis-(4-bromobenzoyl)benzene and proflavine,3,6-diaminoacridine free base were synthesized first.Using 1,4- bis-(4-bromobenzoyl)benzene and proflavine,3,6-diaminoacridine free base as the monomers,poly(aryl imino) ...1,4-Bis-(4-bromobenzoyl)benzene and proflavine,3,6-diaminoacridine free base were synthesized first.Using 1,4- bis-(4-bromobenzoyl)benzene and proflavine,3,6-diaminoacridine free base as the monomers,poly(aryl imino) containing acridine units(PAIA) was synthesized via palladium-catalyzed amination.The structure of PAIA was characterized by means of FTIR,~1H-NMR spectroscopy and elemental analysis,the results show an agreement with the proposed structure.The UV absorption and photoluminescence spectra were t...展开更多
A novel compound [Co(IM2-Py)2(NO3)]?(NO3) (IM2-Py = 2-(2?-pyridyl)-4,4,5,5- tetramethylimidazoline-1-oxyl) has been prepared and structurally characterized by X-ray diffrac- tion method. It crystallizes in orthorhom...A novel compound [Co(IM2-Py)2(NO3)]?(NO3) (IM2-Py = 2-(2?-pyridyl)-4,4,5,5- tetramethylimidazoline-1-oxyl) has been prepared and structurally characterized by X-ray diffrac- tion method. It crystallizes in orthorhombic, space group P212121 with a = 11.031(2), b = 13.492(3), c = 20.467(4) ?, V = 3046.0(11) ?3, C24H32CoN8O8, Mr = 619.51, Z = 4, Dc = 1.351 g/cm3, μ(MoKα) = 0.620 mm?1, F(000) = 1292, R = 0.0506 and wR = 0.0845 for 3752 observed reflections with I > 2σ(I). X-ray analysis reveals that the crystal structure consists of [Co(IM2- Py)2(NO3)]+ moiety and a NO3 anion. The cobalt(II) ion is six-coordinated with a distorted octahedral geometry. Tempera- ? ture dependence of susceptibility measurements show that there exist an antiferromagnetic inter- action in the compound.展开更多
The title compound [Cd(IM2py)2Cl2], where IM2py = 2-(2?-pyridinyl)-4,4,5,5-tetra- methylimidazoline-1-oxyl, has been prepared and structurally characterized by X-ray diffraction. It crystallizes in monoclinic, space g...The title compound [Cd(IM2py)2Cl2], where IM2py = 2-(2?-pyridinyl)-4,4,5,5-tetra- methylimidazoline-1-oxyl, has been prepared and structurally characterized by X-ray diffraction. It crystallizes in monoclinic, space group C2/c with a = 18.436(6), b = 9.255(3), c = 15.831(5) ? b = 100.274(5)? C24H32CdCl2N6O2, Mr = 619.86, V = 2658.0(14) ?, Z = 4, Dc = 1.549 g/cm3, m(MoKa) = 1.056 mm-1, F(000) = 1264, the final R = 0.0324 and wR = 0.0659 for 2725 independent reflections with Rint = 0.0378. The title complex exists as discrete mononuclear molecules, adopting a distorted octahedral [cis(Cl)-trans(py)] configuration with the cadmium(II) ion being bonded to two bidentate radicals and two chlorine atoms. There exist p???p stacking interactions between the adjacent parallel pyridyl rings of the complex in the ac plane.展开更多
About 15years have passed since I first attended the International Conference on Fine Chemistry and Functional Polymers(FCFP).One day,I was asked by Prof.Inomata of Kanazawa University to attend the conference,and aft...About 15years have passed since I first attended the International Conference on Fine Chemistry and Functional Polymers(FCFP).One day,I was asked by Prof.Inomata of Kanazawa University to attend the conference,and after a while Prof.Jiang sent me a kind invitation letter.This is the beginning of my first trip to China.Prof.Takemoto of Osaka University was also very active展开更多
基金supported by the National Natural Science Foundation of China(No.31001109)the Public Projects of Zhejiang Province(No.2014C33034)the Special Program for the Science and Technology Plan of Zhejiang Province(Nos.2009C03017-2,2011C02003)
文摘Acid-soluble collagen(ASC) and pepsin-soluble collagen(PSC) from the spine(ASC-SP and PSC-SP) and skull(ASC-SK and PSC-SK) of the skipjack tuna, Katsuwonus pelamis, were successfully isolated and characterized. The yields of ASC-SP, PSC-SP, ASC-SK and PSC-SK were(2.47 ± 0.39)%,(5.62 ± 0.82)%,(3.57 ± 0.40)%, and(6.71 ± 0.81)%, respectively, on the basis of dry weight. The four collagens contained Gly(330.2-339.1 residues/1 000 residues) as the major amino acid, and their imino acid contents were between 168.8 and 178.2 residues/1 000 residues. Amino acid composition, SDS-PAGE, and FTIR investigations confirmed that ASC-SP and ASC-SK were mainly composed of type I collagen, and had higher contents of high-molecular weight cross-links than those of PSC-SK and PSC-SP. The FTIR investigation also certified all the collagens had triple helical structure. The denaturation temperatures of ASC-SK, PSC-SK, ASC-SP, and PSC-SP were 17.8, 16.6, 17.6, and 16.5 °C, respectively. All isolated collagens were soluble at acidic pH(1-5) and lost their solubilities when the NaCl concentration was above 2%(W/V). The isolated collagens from the spines and skulls of skipjack tuna could serve as an alternative source of collagens for further application in food, cosmetic, biomedical, and pharmaceutical industries.
基金the Research Fund for the Doctoral Program of High Education(No.20060056017)Natural Science Foundation of Tianjin(No.07JCZDJC00300)Tianjin International Cooperation Program of Science and Technology(No.08ZCGHHZ00400).
文摘Four novel calix[4]arene derivatives 5-8 bearing four fluorogenic coumarin units attached via imino group acting also as binding sites at the upper rim have been prepared and characterized by IR, IH NMR and MS. Compounds 5-8 adopt a cone conformation. Their complexation properties to different heavy and transition metal ions have been studied by UV-vis spectroscopy. Compounds 5, 6, 8 show selective recognition to Fe^3＋ and Cr^3＋.
基金Natural Science Foundation of Tianjin(No.07JCZDJC00300)Tianjin International Coorperation Program of Science and Technology(No.08ZCGHHZ00400)
文摘Two novel fluorescent calix[4]arene derivatives la and lb with benzoxazole or benzothiazole units in 1,3-alternate conformation have been synthesized and characterized by IR, ^1H NMR, ^13C NMR and MS. Their complexation properties to different heavy and transition metal ions have been studied by UV-vis spectroscopy and fluorescence spectrometer. Compounds 1a and 1b show selective recognition to Fe^3＋ and Cr^3＋.
文摘A novel heterospin complex {[(CuL)Ni(IM 2Py) 2](ClO 4) 2} 2·2H 2O (L=2,3 dioxo 5,6:14,15 dibenzo 1,4,8,12 tetraazacyclo pentadeca 7,12 diene, IM 2Py=2 (2′ pyridyl) 4,4,5,5 tetra^methyl 4,5 dihydro 1 H imidazoline 1 oxyl) has been synthesized and its crystal structure was determined by X ray diffraction analysis. In order to interpret the exchange interaction of this asymmetric heterospin system, a theoretical model has been established. Using this theoretical model the magnetic susceptibility data have been fitted and lead to coupling constant values equal to 1 4 cm -1 (Ni Rad) and -38 0 cm -1 (Ni Cu), respectively.
基金the National Natural Science Foundation of China (No. 20472075)
文摘The title compound 3 was synthesized and characterized by IR, NMR and HRMS, and its crystal structure was determined by X-ray diffraction analysis. The crystal is of monoclinic system （CI6H23NOTS, Mr = 373.41）, space group P21, with a = 12.000（2）, b = 5.5970（11）, c = 13.689（3） A. β= 93.25（3）°, V= 917.9（3） A^3, Z= 2, Dc = 1.351 g/cm^3, F（000） = 396, μ = 0.213 mm^-1, the final R = 0.0489 and ωR = 0.0777 for observed reflections （I 〉 2σ（I））. Three intramolecular and three intermolecular hydrogen bonds were found. The absolute configuration of this molecule was confirmed by comparing with the original material.
文摘Two new M(II)-radical complexes [M(hfac)<sub>2</sub>(IM-<span style="font-size:10.0pt;font-family:;" "=""><i></i></span><i>o<span style="font-size:10.0pt;font-family:;" "=""></span></i>-QN)] (M = Ni(<strong>1</strong>), Zn(<strong>2</strong>);IM-<span style="white-space:normal;font-size:10pt;font-family:;" "=""><i></i></span><i><span style="white-space:normal;">o</span><span style="white-space:normal;font-size:10pt;font-family:;" "=""></span></i>-QN = 4'-quinoxalinyl-substituted imino nitroxide;<span style="font-family:" font-size:13.3333px;white-space:normal;"=""><i></i></span><i>hfac<span style="font-family:" font-size:13.3333px;white-space:normal;"=""></span></i> = hexafluoroa-cetylacetonate) have been synthesized and characterized by X-ray diffraction analysis, element analyses, IR and UV-Visible spectroscopy. X-ray analysis reveal that the structures of both complexes are similar configuration and differently spatial symmetries. The complex <strong>1</strong> crystallizes in the triclinic <span style="font-family:" font-size:13.3333px;white-space:normal;"=""><i></i></span><i>P<span style="font-family:" font-size:13.3333px;white-space:normal;"=""></span></i>ī space group with the respective cell parameters: <span style="font-family:" font-size:13.3333px;white-space:normal;"=""><i></i></span><i>a<span style="font-family:" font-size:13.3333px;white-space:normal;"=""></span></i> = 9.1189(18) <span style="color:#4F4F4F;font-family:-apple-system, " font-size:16px;white-space:normal;background-color:#f7f7f7;"=""><span style="color:#4F4F4F;font-family:-apple-system, "font-size:16px;white-space:normal;background-color:#F7F7F7;">Å</span></span>, <span style="font-family:" font-size:13.3333px;white-space:normal;"=""><i></i></span><i>b<span style="font-family:" font-size:13.3333px;white-space:normal;"=""></span></i> = 9.836(2) <span style="color:#4F4F4F;font-family:-apple-system, " font-size:16px;white-space:normal;background-color:#f7f7f7;"=""><span style="color:#4F4F4F;font-family:-apple-system, "font-size:16px;
基金This work was supported by the National Natural Science Foundation of China (No. 20331010 and 20571045) Natural Science Foundation of Tianjin (No. 043602211)
文摘Two novel complexes {[Zn（IM4py）2（tp）（H2O）]2H2O}. 1 and {[Cd（IM4py）2（tp）- （H2O）]1.25H2O},, 2 （IM4py = 2-（4＇-pyridinyl）-4,4,5,5-tetramethylimidazoline-l-oxyl and tp = terephthalate dianion） have been synthesized and characterized by elemental analyses, IR spectrum and single-crystal X-ray diffraction. Crystal data for complex I： monoclinic, space group C2/c, a = 20.648（7）, b = 12.130（4）, c = 14.036（4） A, β = 106.351（5）°, C32H42N6O9Zn, Mr = 720.09, V = 3373.3（2） A3, Z= 4, Dc = 1.418 g/cm^3μt（MoKα） = 0.790 mm^-1, F（000） = 1512, the final R = 0.0407 and wR = 0.0894 for 3480 independent reflections with Rint = 0.0432. Crystal data for complex 2： monoclinic, space group C2/c, a = 21.332（6）, b = 12.063（3）, c = 14.246（4） A, β = 106.704（4）°, C32H40.50N6O8.25Cd, Mr = 753.60, V= 3511.2（2） A^3, Z = 4, Dc = 1.426 g/cm^3,μ（MoKα） = 0.679 mm^--1, F（000） = 1554, the final R = 0.0419 and wR = 0.0961 for 3627 independent reflections with Rint = 0.0440. The framework structures of complexes 1 and 2 are 3-D networks via the hydrogen bonds among 1-D chains. The notable characteristics of the two complexes are that the coordination polyhedron of Zn（Ⅱ） adopts a rare distorted five-coordinate square pyramidal geometry in 1, and the Cd（Ⅱ） complex exhibits an unusual distorted seven-coordinate pentagonal bipyramid in 2.
基金Project supported by the National Natural Science Fondation of China and Postdoctoral Foundation of China.
文摘 Imino Diels-Alder reaction of imines with 2,3-dihydrofuran or 3,4-dihydro-2H-pyran proceeded smoothly in the presence of a catalytic amount (0.5 mol %) of ytterbium triflate to afford furo[3,2-c]- and pyrano[3,2-c] quinolines conveniently in high yield.
文摘A simple synthesis of medicinally important cis-2-methyl-4-azapan-2-one-1,2,3,4-tetrahydroquinolines/cis-9- （2-methyl-l,2,3,4-tetrahydroquinolin-4-yl）-9H-carbazole was reported. Multicomponent one pot synthesis with ani- lines and N-vinylcaprolactam/N-vinyl carbazole via imino Diels-Alder reaction by using antimony trichloride as catalyst and acetonitrile as solvent was employed. NMR technique （2D） was used to study the regio- and stereo- chemistry of newly synthesized compounds. The cis diastereo-selectivity of the products was predicted by COSY and NOESY studies.
基金supported by the Foundation of National Key Laboratory of High Temperature and Density Plasma Physics(No.9140C6806030807)the Science and Technology Development Foundation of China Academy of Physics Engineering(No.200708006)
文摘1,4-Bis-(4-bromobenzoyl)benzene and proflavine,3,6-diaminoacridine free base were synthesized first.Using 1,4- bis-(4-bromobenzoyl)benzene and proflavine,3,6-diaminoacridine free base as the monomers,poly(aryl imino) containing acridine units(PAIA) was synthesized via palladium-catalyzed amination.The structure of PAIA was characterized by means of FTIR,~1H-NMR spectroscopy and elemental analysis,the results show an agreement with the proposed structure.The UV absorption and photoluminescence spectra were t...
基金This work was supported by the National Natural Science Foundation of China (No. 20471026) and Natural Science Foundation of Henan Province (No. 0311021200)
文摘A novel compound [Co(IM2-Py)2(NO3)]?(NO3) (IM2-Py = 2-(2?-pyridyl)-4,4,5,5- tetramethylimidazoline-1-oxyl) has been prepared and structurally characterized by X-ray diffrac- tion method. It crystallizes in orthorhombic, space group P212121 with a = 11.031(2), b = 13.492(3), c = 20.467(4) ?, V = 3046.0(11) ?3, C24H32CoN8O8, Mr = 619.51, Z = 4, Dc = 1.351 g/cm3, μ(MoKα) = 0.620 mm?1, F(000) = 1292, R = 0.0506 and wR = 0.0845 for 3752 observed reflections with I > 2σ(I). X-ray analysis reveals that the crystal structure consists of [Co(IM2- Py)2(NO3)]+ moiety and a NO3 anion. The cobalt(II) ion is six-coordinated with a distorted octahedral geometry. Tempera- ? ture dependence of susceptibility measurements show that there exist an antiferromagnetic inter- action in the compound.
基金This work was supported by the NNSFC (No. 20171025 and 20331010) and Natural Science Foundation of Tianjin (No. 033602011)
文摘The title compound [Cd(IM2py)2Cl2], where IM2py = 2-(2?-pyridinyl)-4,4,5,5-tetra- methylimidazoline-1-oxyl, has been prepared and structurally characterized by X-ray diffraction. It crystallizes in monoclinic, space group C2/c with a = 18.436(6), b = 9.255(3), c = 15.831(5) ? b = 100.274(5)? C24H32CdCl2N6O2, Mr = 619.86, V = 2658.0(14) ?, Z = 4, Dc = 1.549 g/cm3, m(MoKa) = 1.056 mm-1, F(000) = 1264, the final R = 0.0324 and wR = 0.0659 for 2725 independent reflections with Rint = 0.0378. The title complex exists as discrete mononuclear molecules, adopting a distorted octahedral [cis(Cl)-trans(py)] configuration with the cadmium(II) ion being bonded to two bidentate radicals and two chlorine atoms. There exist p???p stacking interactions between the adjacent parallel pyridyl rings of the complex in the ac plane.
文摘About 15years have passed since I first attended the International Conference on Fine Chemistry and Functional Polymers(FCFP).One day,I was asked by Prof.Inomata of Kanazawa University to attend the conference,and after a while Prof.Jiang sent me a kind invitation letter.This is the beginning of my first trip to China.Prof.Takemoto of Osaka University was also very active
