The title compound 2 (C15H22NO4PS, Mr = 343.38) was prepared by the reaction of α-benzoylthioformmorpholine 1 with trimethyl phosphite. The crystal is of monoclinic, space group P21/c with a = 14.906(2), b = ...The title compound 2 (C15H22NO4PS, Mr = 343.38) was prepared by the reaction of α-benzoylthioformmorpholine 1 with trimethyl phosphite. The crystal is of monoclinic, space group P21/c with a = 14.906(2), b = 8.4711(12), c = 13.343(2) ?, β = 96.761(4)o, Z = 4, V = 1673.1(5) ?3, Dc = 1.363 g/cm3, μ(MoKα) = 3.06 cm-1, F(000) = 728, the final R = 0.0590 and wR = 0.1740 for 3036 observed reflections (I > 2σ(I)). X-ray analysis revealed that the interatomic distance of C(5)–C(6) is 1.353(4) ?, indicating it is a normal C=C double bond. The P(1) atom takes a distorted tetrahedral geometry, and the morpholine ring adopts a chair conformation. The morpholino group is located at the 1-position of vinylphosphonate, and the phenyl and thiomethyl groups at the 2-position.展开更多
A novel fluorescent probe 9-（4-（1,2-diamine）benzene-N1-phenyl）acridine（DABPA） was synthesized for the detection of nitric oxide（NO） and characterized by IR, 1H-NMR and EI-MS spectroscopy. Based on a photoelect...A novel fluorescent probe 9-（4-（1,2-diamine）benzene-N1-phenyl）acridine（DABPA） was synthesized for the detection of nitric oxide（NO） and characterized by IR, 1H-NMR and EI-MS spectroscopy. Based on a photoelectron transfer mechanism, the fl uorescence intensities of DABPA were investigated with the different concentrations of NO. Under the optimal experimental conditions, the fl uorescence intensity of DABPA had a good linear relationship（R2=0.9977） with NO concentration in the range from 1×10-7 to 1.5×10-6 mol/L with a detection limit of 1×10-8 mol/L. The cytotoxicity induced by DABPA was evaluated by the MTT（3-（4,5-dimethylthiazol-2-yl）-2,5diphenyl tetrazolium bromide） assay for biological application. Furthermore, the probe DABPA had also been successfully applied to real-time image NO produced in PC12 cells in the presence of L-arginine.展开更多
A more feasibly convergent synthesis of selective estrogen receptor degrading agent(S)-8-(4-((1-(3-fluoropropyl)-pyrrolidin-3-yl)oxy)phenyl)-7-(4-hydroxyphenyl)-5,6-dihydronaphthalen-2-ol was reported,featured with co...A more feasibly convergent synthesis of selective estrogen receptor degrading agent(S)-8-(4-((1-(3-fluoropropyl)-pyrrolidin-3-yl)oxy)phenyl)-7-(4-hydroxyphenyl)-5,6-dihydronaphthalen-2-ol was reported,featured with concise work up and absence of regioselectivity dilemma.展开更多
1-(2-chlorophenyl) ethanol (CPE) is of health and environmental concern due to its toxicity and its use as an inter-mediate in pharmaceutical manufacturing. The current work deals with the catalytic reductive dechlori...1-(2-chlorophenyl) ethanol (CPE) is of health and environmental concern due to its toxicity and its use as an inter-mediate in pharmaceutical manufacturing. The current work deals with the catalytic reductive dechlorination and detoxification of CPE by Pd/Fe bimetal. CPE was effectively dechlorinated to 1-phenyl ethanol (PE) accompanied by the equivalent release of chloride. The extent of CPE dechlorination increased with temperature,Fe dosage and Pd loading. A decrease in solution pH increased CPE dechlorination,resulting presumably from an increase in hydrogen production. Under the specific conditions of 20 g/L Pd/Fe,0.10% Pd (w/w) and initial pH 5-6,the CPE dechlorination was completed within 145 min. The dechlorination fol-lowed a pseudo-first-order kinetics with an activation energy of 56.7 kJ/mol. The results of toxicity testing showed that CPE was very toxic to Chlorella,whereas PE showed little toxicity. The toxicity of the reaction solution declined gradually and the pro-moting effects on Chlorella intensified consequently with the dechlorination process. Thus,the reductive dechlorination of CPE to PE by Pd/Fe was a detoxification process. It may be used to effectively reduce the toxicological effects of CPE-contaminated wastewater,thereby enhancing the performance of subsequent biological processes in wastewater treatment.展开更多
A novel phenolic glucoside was isolated from stem barks of Alangium plantanifolium, its structure was elucidated to be 1-O-[2-(1-hydroxy-6-oxocyclohex-2-ene-1-carboxymethyl) -phenyl]-4, 6-O-[(S)-4, 4', 5, 5', ...A novel phenolic glucoside was isolated from stem barks of Alangium plantanifolium, its structure was elucidated to be 1-O-[2-(1-hydroxy-6-oxocyclohex-2-ene-1-carboxymethyl) -phenyl]-4, 6-O-[(S)-4, 4', 5, 5', 6, 6'-hexahydroxydi-phenoyl]-beta -D-glucopyranose 1 by spectroscopic methods including 2D NMR techniques.展开更多
The different interactions between a chemosensor, 1-（naphthalen-2-yl）-3-（6-nitrobenzothiazol-2-yl）-thiourea （1）, and F, acetate （AcO-）, Cl-, and Br- anions have been investigated theoretically at the B3LYP/6-3...The different interactions between a chemosensor, 1-（naphthalen-2-yl）-3-（6-nitrobenzothiazol-2-yl）-thiourea （1）, and F, acetate （AcO-）, Cl-, and Br- anions have been investigated theoretically at the B3LYP/6-31＋G（d,p） level with the basis set superposition error （BSSE） correction. It was found that the high selectivity of compound 1 for F- can be ascribed to the ability of the anion to deprotonate the N-H fragment of the host sensor, while the chemosensor also has a strong affinity for AcO- by virtue of the formation of a hydrogen-bonded complex. Intramolecular charge transfer （ICT） causes the colorimetric signaling of compound 1 after interaction with F-/AcO. A study of substituent effects suggested that the O/NH- and O/S-substituted derivatives are also expected to be promising candidates for chromogenic F3AcO chemosensors.展开更多
基金The project was supported by the Key Laboratory of Organic Synthesis of Jiangsu Province (JSK016)
文摘The title compound 2 (C15H22NO4PS, Mr = 343.38) was prepared by the reaction of α-benzoylthioformmorpholine 1 with trimethyl phosphite. The crystal is of monoclinic, space group P21/c with a = 14.906(2), b = 8.4711(12), c = 13.343(2) ?, β = 96.761(4)o, Z = 4, V = 1673.1(5) ?3, Dc = 1.363 g/cm3, μ(MoKα) = 3.06 cm-1, F(000) = 728, the final R = 0.0590 and wR = 0.1740 for 3036 observed reflections (I > 2σ(I)). X-ray analysis revealed that the interatomic distance of C(5)–C(6) is 1.353(4) ?, indicating it is a normal C=C double bond. The P(1) atom takes a distorted tetrahedral geometry, and the morpholine ring adopts a chair conformation. The morpholino group is located at the 1-position of vinylphosphonate, and the phenyl and thiomethyl groups at the 2-position.
基金Funded by the National Natural Science Foundation of China(Nos.50802069,81100890,51272191)the Fundamental Research Funds for the Central Unversities(WUT:2013-IV-010)the Students Innovation and Entrepreneurship Training Program of WHUT(20141049701012)
文摘A novel fluorescent probe 9-（4-（1,2-diamine）benzene-N1-phenyl）acridine（DABPA） was synthesized for the detection of nitric oxide（NO） and characterized by IR, 1H-NMR and EI-MS spectroscopy. Based on a photoelectron transfer mechanism, the fl uorescence intensities of DABPA were investigated with the different concentrations of NO. Under the optimal experimental conditions, the fl uorescence intensity of DABPA had a good linear relationship（R2=0.9977） with NO concentration in the range from 1×10-7 to 1.5×10-6 mol/L with a detection limit of 1×10-8 mol/L. The cytotoxicity induced by DABPA was evaluated by the MTT（3-（4,5-dimethylthiazol-2-yl）-2,5diphenyl tetrazolium bromide） assay for biological application. Furthermore, the probe DABPA had also been successfully applied to real-time image NO produced in PC12 cells in the presence of L-arginine.
基金Science and Technology Development Foundation of Nanjing Medical University(No.NMUB20210013)Key Project of Connotation Construction of Nanjing Medical University,the China Postdoctoral Science Foundation(No.2022M711419)Natural Science Foundation of Jiangsu Province(No.BK20231266)。
文摘A more feasibly convergent synthesis of selective estrogen receptor degrading agent(S)-8-(4-((1-(3-fluoropropyl)-pyrrolidin-3-yl)oxy)phenyl)-7-(4-hydroxyphenyl)-5,6-dihydronaphthalen-2-ol was reported,featured with concise work up and absence of regioselectivity dilemma.
基金Project (Nos. 20977085 and 20688702) supported by the National Natural Science Foundation of China
文摘1-(2-chlorophenyl) ethanol (CPE) is of health and environmental concern due to its toxicity and its use as an inter-mediate in pharmaceutical manufacturing. The current work deals with the catalytic reductive dechlorination and detoxification of CPE by Pd/Fe bimetal. CPE was effectively dechlorinated to 1-phenyl ethanol (PE) accompanied by the equivalent release of chloride. The extent of CPE dechlorination increased with temperature,Fe dosage and Pd loading. A decrease in solution pH increased CPE dechlorination,resulting presumably from an increase in hydrogen production. Under the specific conditions of 20 g/L Pd/Fe,0.10% Pd (w/w) and initial pH 5-6,the CPE dechlorination was completed within 145 min. The dechlorination fol-lowed a pseudo-first-order kinetics with an activation energy of 56.7 kJ/mol. The results of toxicity testing showed that CPE was very toxic to Chlorella,whereas PE showed little toxicity. The toxicity of the reaction solution declined gradually and the pro-moting effects on Chlorella intensified consequently with the dechlorination process. Thus,the reductive dechlorination of CPE to PE by Pd/Fe was a detoxification process. It may be used to effectively reduce the toxicological effects of CPE-contaminated wastewater,thereby enhancing the performance of subsequent biological processes in wastewater treatment.
文摘A novel phenolic glucoside was isolated from stem barks of Alangium plantanifolium, its structure was elucidated to be 1-O-[2-(1-hydroxy-6-oxocyclohex-2-ene-1-carboxymethyl) -phenyl]-4, 6-O-[(S)-4, 4', 5, 5', 6, 6'-hexahydroxydi-phenoyl]-beta -D-glucopyranose 1 by spectroscopic methods including 2D NMR techniques.
基金supported by the Natural Science Foundation of Inner Mongolia Autonomous Region (2011ZD02)
文摘The different interactions between a chemosensor, 1-（naphthalen-2-yl）-3-（6-nitrobenzothiazol-2-yl）-thiourea （1）, and F, acetate （AcO-）, Cl-, and Br- anions have been investigated theoretically at the B3LYP/6-31＋G（d,p） level with the basis set superposition error （BSSE） correction. It was found that the high selectivity of compound 1 for F- can be ascribed to the ability of the anion to deprotonate the N-H fragment of the host sensor, while the chemosensor also has a strong affinity for AcO- by virtue of the formation of a hydrogen-bonded complex. Intramolecular charge transfer （ICT） causes the colorimetric signaling of compound 1 after interaction with F-/AcO. A study of substituent effects suggested that the O/NH- and O/S-substituted derivatives are also expected to be promising candidates for chromogenic F3AcO chemosensors.
