Chloro ethane dimethyl sulfoxide,C_2H_5Cl·DMSO(ECI·DMSO)was prepared by interaction of acrylic acid with conc.Hydrochloric acid in dimethyl sulfoxide(DMSO)and subsequent decarboxylation with H_2O_2 solution....Chloro ethane dimethyl sulfoxide,C_2H_5Cl·DMSO(ECI·DMSO)was prepared by interaction of acrylic acid with conc.Hydrochloric acid in dimethyl sulfoxide(DMSO)and subsequent decarboxylation with H_2O_2 solution.The formation of the compound was confirmed by spectral and analytical methods;the molecular weight was determined by cryoscopic method.The solubility of poly(vinyl alcohol)(PVA)in different solvents or mixed solvents at 40℃,50℃and 60℃temperature in the presence of 0.01% of EC1·-DMSO was determined.It tu...展开更多
Poly(3-hydroxyalkanoates) (PHAs) are a promising class of biodegradable polymers,exhibiting properties comparable to traditional petroleum-based counterparts.Nonetheless,the widespread commercialization of PHAs is hin...Poly(3-hydroxyalkanoates) (PHAs) are a promising class of biodegradable polymers,exhibiting properties comparable to traditional petroleum-based counterparts.Nonetheless,the widespread commercialization of PHAs is hindered by the absence of an efficient and economically viable catalytic system,impeding their competitiveness against non-biodegradable polymers.In an effort to address this challenge,we present a study on a newly developed chloro-bridged dimeric salphen zirconium cobaltate complex for the direct synthesis of PHAs via carbonylative polymerization of epoxides.The catalytic system demonstrates favorable activity under mild reaction conditions,enabling complete monomer conversion and an impressive 92% selectivity towards PHA formation.Through meticulous control experiments and mechanistic studies,we have gained crucial insights into the polymerization process.Remarkably,our findings challenge the prevailing notion of sequential ring-opening polymerization of in-situ generated β-lactones as the primary pathway.Instead,we demonstrate that the polymerization predominantly proceeds through direct co-polymerization of epoxide and carbon monoxide,unveiling a unique and efficient mechanism for PHA synthesis.展开更多
Little is known about the toxic activity of the atrazine (a herbicide, commonly used in agricultural production) on the thyroid gland. In this study the compound was administered orally in female albino rats at sublet...Little is known about the toxic activity of the atrazine (a herbicide, commonly used in agricultural production) on the thyroid gland. In this study the compound was administered orally in female albino rats at sublethal exposure equivalent to 0.2 LD50 doses for 6 and 12 days. At termination of dosing the anesthetized animals were killed and blood was drawn for the determination of serum triiodothyronine (T3) and thyroxin (T4). A dose-dependent decrease of serum T3 concentration was observed in all the groups (control: 0.57 nmol·L-1; 6 days: 0.35 nmol·L-1; 12 days: 0.21 nmol·L-1). The thyroid gland was examined light-microscopically. Bouin's solution-fixed thyroids were embedded in paraffin and sections cut at 6 μm, stained separately with toluidine blue according to Slinchenko's method. Histologically in experimental groups epithelium featured small cuboidal cells and occasional structures of the follicles confluence within epitheliomers. A dose-dependent changes of the following parameters were observed: (a) increasing of number of follicle-building thyroid cells; (b) increasing of follicular volume, (c) decreasing of nucleus volume. Investigation of the whole population of thyroid mast cells disclosed no change in degranulation intensity. By contrast, degranulation intensity was decreased in perifollicular mast cells from groups treated with atrazine in dose-dependent manner.There are no changes observed in degranulation of stromal mast cells. These results suggesting that differences in response to the atrazine might account for an aspect of the functional heterogeneity within the rat thyroid mast cell population.展开更多
PdCl 2 (CH 3) 3CC 6H 4SC 4H 9- S 2, C 28 H 44 Cl 2S 2Pd, M r =622.0756, triclinic, space group P1, a=10.403(2), b=12.346(2), c=13.475(2) , α=89 11(1)°, β=75.44(1)°, γ=69.52(...PdCl 2 (CH 3) 3CC 6H 4SC 4H 9- S 2, C 28 H 44 Cl 2S 2Pd, M r =622.0756, triclinic, space group P1, a=10.403(2), b=12.346(2), c=13.475(2) , α=89 11(1)°, β=75.44(1)°, γ=69.52(1)°, V=1564.2(5) 3, Z=2, D c =1.32 g/cm 3, Mo Kα radiation, μ =9.00 cm -1 , F(000)=647.95, R =0.0316 for 4561 observed reflections with I≥3σ(I) . Pd(Ⅱ) is coordinated by two chloride atoms and two sulfur atoms of organic ligands, forming a rhombic quadrilateral plane with Pd-S of 2.325(1) and Pd-Cl of 2.295(1) .展开更多
A series of new complexes, CpTiCl[S2P(OR)2]2 (where R) Et, n-Pr, i-Pr, Bui, Ph) and CpTiCl [S2POGO]2 (where G) –CH2CMe2CH2-, -CMe2CMe2-) have been prepared by the drop wise addition of the appropriate O, O’-dialkyl ...A series of new complexes, CpTiCl[S2P(OR)2]2 (where R) Et, n-Pr, i-Pr, Bui, Ph) and CpTiCl [S2POGO]2 (where G) –CH2CMe2CH2-, -CMe2CMe2-) have been prepared by the drop wise addition of the appropriate O, O’-dialkyl or -alkylene dithiophosphoric acid to cyclopentadienyl titanium trichloride in 1:2 molar ratio and refluxed in benzene solution. The new compounds were characterized by molecular weight measurements elemental analyses and spectroscopic studies (1H, 13C, and 31P NMR, and in-frared). We suggest a distorted tetrahedron structure of these new complexes and the dithioligand behaves as bidentate ligand.展开更多
Six sterically hindered chloro meso-tetra-ortho-alkylphenylporphinato irons (T(o-R)PPFe(III)Cl, R = Me, Et, n-Pr, i-Pr, n-Bu, t-Bu) were synthesized and used to catalyze the monooxygenation of cyclohexane with PhIO. B...Six sterically hindered chloro meso-tetra-ortho-alkylphenylporphinato irons (T(o-R)PPFe(III)Cl, R = Me, Et, n-Pr, i-Pr, n-Bu, t-Bu) were synthesized and used to catalyze the monooxygenation of cyclohexane with PhIO. Both the yields of cyclohexanol and the relative rates of monooxygenation of cyclohexane catalyzed by T(o-R) PPFe(IIl)Cl were higher than those of TPPFe(III)Cl respectively. The order of the yields(%) of cyclohexanol and the rate of cyclohexanol formation in the monooxygenation of cyclohexane catalyzed by T(o-R)PPFe(III)Cl for the different substituents are: i-Pr(58) > Et(57) > n-Pr(52) > Me(51) > n-Bu(48) > t-Bu(46) > H(35) and i-Pr > Et > t-Bu > n-PT greater than or equal to Me greater than or equal to n-Bu greater than or equal to H respectively. The special steric effect on the catalytic character of these different alkyl substituents in T(o-R)PPFe(III)Cl is proposed on the basis of the results.展开更多
Chloro 2 diethylaminoethyl 3(2H) pyridazinone was synthesized by the reaction of 6 chloro 3(2H) pyridazinone and 2 diethylamionethyl chloride reaction in methylbenzene. Then the structure was characterized by...Chloro 2 diethylaminoethyl 3(2H) pyridazinone was synthesized by the reaction of 6 chloro 3(2H) pyridazinone and 2 diethylamionethyl chloride reaction in methylbenzene. Then the structure was characterized by means of 1H NMR, IR, UV. By the method of ab initio HF and density functional theory (DFT) B3LYP, the geometric structures of the reagent intermediate, the product and its isomer were optimized and their total energies were calculated. The properties for the frontier molecular orbitals and the rules for energy distribution were analyzed systematically. It was shown that the energy of the nitrogen alkyl compound is lower than that of the oxy alkyl compound and the former is stable than the latter . This result is in accordance with the fact that 6 chloro 2 diethylaminoethyl 3(2H) pyridazinone is synthesized by the reaction of \{6 chloride \}2 diethylaminoethyl 3(2H) pyridazinone and 2 diethylaminoethyl chloride.展开更多
4-Amino-3-mercapto-6-methyl-l,2,4-triazin-5（4H）-one 1 converted to 4-amino-6-methy-3-（methylthio）-1,2,4-triazin-5（4H）-one by methylation with methyl iodide.Controlled hydrazination of the resulting compound affo...4-Amino-3-mercapto-6-methyl-l,2,4-triazin-5（4H）-one 1 converted to 4-amino-6-methy-3-（methylthio）-1,2,4-triazin-5（4H）-one by methylation with methyl iodide.Controlled hydrazination of the resulting compound afforded 4-amino-3-hydrazinyl-6- methyl-l,2,4-triazin-5（4H）-one 2 as a building block,to the synthesis of some novel derivatives of[1,2,4]triazino- [4,3,b][1,2,4,5]tetrazepine 3-6,by the reaction with 3-chloropentane-2,4-dione,chloro acetonitrile,1,3-dichloroacetone,and methyl bromoacetate.This general synthetic procedure can be extended to the preparation of wide variety of tetrazepines using 1,2- bielectrophiles derivatives.展开更多
文摘Chloro ethane dimethyl sulfoxide,C_2H_5Cl·DMSO(ECI·DMSO)was prepared by interaction of acrylic acid with conc.Hydrochloric acid in dimethyl sulfoxide(DMSO)and subsequent decarboxylation with H_2O_2 solution.The formation of the compound was confirmed by spectral and analytical methods;the molecular weight was determined by cryoscopic method.The solubility of poly(vinyl alcohol)(PVA)in different solvents or mixed solvents at 40℃,50℃and 60℃temperature in the presence of 0.01% of EC1·-DMSO was determined.It tu...
基金supported by C1 Gas Refinery Program(2018M3D3A1A01018006)Direct Air Capture and Utilization(DACU)grant(RS-2023-00259920)through the National Research Foundation of Korea funded by the Ministry of Science,ICTFuture Planning,Republic of Korea.
文摘Poly(3-hydroxyalkanoates) (PHAs) are a promising class of biodegradable polymers,exhibiting properties comparable to traditional petroleum-based counterparts.Nonetheless,the widespread commercialization of PHAs is hindered by the absence of an efficient and economically viable catalytic system,impeding their competitiveness against non-biodegradable polymers.In an effort to address this challenge,we present a study on a newly developed chloro-bridged dimeric salphen zirconium cobaltate complex for the direct synthesis of PHAs via carbonylative polymerization of epoxides.The catalytic system demonstrates favorable activity under mild reaction conditions,enabling complete monomer conversion and an impressive 92% selectivity towards PHA formation.Through meticulous control experiments and mechanistic studies,we have gained crucial insights into the polymerization process.Remarkably,our findings challenge the prevailing notion of sequential ring-opening polymerization of in-situ generated β-lactones as the primary pathway.Instead,we demonstrate that the polymerization predominantly proceeds through direct co-polymerization of epoxide and carbon monoxide,unveiling a unique and efficient mechanism for PHA synthesis.
文摘Little is known about the toxic activity of the atrazine (a herbicide, commonly used in agricultural production) on the thyroid gland. In this study the compound was administered orally in female albino rats at sublethal exposure equivalent to 0.2 LD50 doses for 6 and 12 days. At termination of dosing the anesthetized animals were killed and blood was drawn for the determination of serum triiodothyronine (T3) and thyroxin (T4). A dose-dependent decrease of serum T3 concentration was observed in all the groups (control: 0.57 nmol·L-1; 6 days: 0.35 nmol·L-1; 12 days: 0.21 nmol·L-1). The thyroid gland was examined light-microscopically. Bouin's solution-fixed thyroids were embedded in paraffin and sections cut at 6 μm, stained separately with toluidine blue according to Slinchenko's method. Histologically in experimental groups epithelium featured small cuboidal cells and occasional structures of the follicles confluence within epitheliomers. A dose-dependent changes of the following parameters were observed: (a) increasing of number of follicle-building thyroid cells; (b) increasing of follicular volume, (c) decreasing of nucleus volume. Investigation of the whole population of thyroid mast cells disclosed no change in degranulation intensity. By contrast, degranulation intensity was decreased in perifollicular mast cells from groups treated with atrazine in dose-dependent manner.There are no changes observed in degranulation of stromal mast cells. These results suggesting that differences in response to the atrazine might account for an aspect of the functional heterogeneity within the rat thyroid mast cell population.
文摘PdCl 2 (CH 3) 3CC 6H 4SC 4H 9- S 2, C 28 H 44 Cl 2S 2Pd, M r =622.0756, triclinic, space group P1, a=10.403(2), b=12.346(2), c=13.475(2) , α=89 11(1)°, β=75.44(1)°, γ=69.52(1)°, V=1564.2(5) 3, Z=2, D c =1.32 g/cm 3, Mo Kα radiation, μ =9.00 cm -1 , F(000)=647.95, R =0.0316 for 4561 observed reflections with I≥3σ(I) . Pd(Ⅱ) is coordinated by two chloride atoms and two sulfur atoms of organic ligands, forming a rhombic quadrilateral plane with Pd-S of 2.325(1) and Pd-Cl of 2.295(1) .
文摘A series of new complexes, CpTiCl[S2P(OR)2]2 (where R) Et, n-Pr, i-Pr, Bui, Ph) and CpTiCl [S2POGO]2 (where G) –CH2CMe2CH2-, -CMe2CMe2-) have been prepared by the drop wise addition of the appropriate O, O’-dialkyl or -alkylene dithiophosphoric acid to cyclopentadienyl titanium trichloride in 1:2 molar ratio and refluxed in benzene solution. The new compounds were characterized by molecular weight measurements elemental analyses and spectroscopic studies (1H, 13C, and 31P NMR, and in-frared). We suggest a distorted tetrahedron structure of these new complexes and the dithioligand behaves as bidentate ligand.
基金Project supported by the National Natural Science Foundation of China.
文摘Six sterically hindered chloro meso-tetra-ortho-alkylphenylporphinato irons (T(o-R)PPFe(III)Cl, R = Me, Et, n-Pr, i-Pr, n-Bu, t-Bu) were synthesized and used to catalyze the monooxygenation of cyclohexane with PhIO. Both the yields of cyclohexanol and the relative rates of monooxygenation of cyclohexane catalyzed by T(o-R) PPFe(IIl)Cl were higher than those of TPPFe(III)Cl respectively. The order of the yields(%) of cyclohexanol and the rate of cyclohexanol formation in the monooxygenation of cyclohexane catalyzed by T(o-R)PPFe(III)Cl for the different substituents are: i-Pr(58) > Et(57) > n-Pr(52) > Me(51) > n-Bu(48) > t-Bu(46) > H(35) and i-Pr > Et > t-Bu > n-PT greater than or equal to Me greater than or equal to n-Bu greater than or equal to H respectively. The special steric effect on the catalytic character of these different alkyl substituents in T(o-R)PPFe(III)Cl is proposed on the basis of the results.
基金Supported by the National Natural Science Foundation of China(No. 2 0 16 2 0 0 5 ) .
文摘Chloro 2 diethylaminoethyl 3(2H) pyridazinone was synthesized by the reaction of 6 chloro 3(2H) pyridazinone and 2 diethylamionethyl chloride reaction in methylbenzene. Then the structure was characterized by means of 1H NMR, IR, UV. By the method of ab initio HF and density functional theory (DFT) B3LYP, the geometric structures of the reagent intermediate, the product and its isomer were optimized and their total energies were calculated. The properties for the frontier molecular orbitals and the rules for energy distribution were analyzed systematically. It was shown that the energy of the nitrogen alkyl compound is lower than that of the oxy alkyl compound and the former is stable than the latter . This result is in accordance with the fact that 6 chloro 2 diethylaminoethyl 3(2H) pyridazinone is synthesized by the reaction of \{6 chloride \}2 diethylaminoethyl 3(2H) pyridazinone and 2 diethylaminoethyl chloride.
文摘4-Amino-3-mercapto-6-methyl-l,2,4-triazin-5（4H）-one 1 converted to 4-amino-6-methy-3-（methylthio）-1,2,4-triazin-5（4H）-one by methylation with methyl iodide.Controlled hydrazination of the resulting compound afforded 4-amino-3-hydrazinyl-6- methyl-l,2,4-triazin-5（4H）-one 2 as a building block,to the synthesis of some novel derivatives of[1,2,4]triazino- [4,3,b][1,2,4,5]tetrazepine 3-6,by the reaction with 3-chloropentane-2,4-dione,chloro acetonitrile,1,3-dichloroacetone,and methyl bromoacetate.This general synthetic procedure can be extended to the preparation of wide variety of tetrazepines using 1,2- bielectrophiles derivatives.
