生物氧化是生物化学代谢部分的重要内容,因其复杂性和抽象性不易被学生理解。采用非变性聚丙烯酰胺凝胶电泳(Native polyacrylamide gel electrophoresis, Native-PAGE)构建了适用于本科实验教学的“线粒体复合体酶I活性方法”。从锥虫...生物氧化是生物化学代谢部分的重要内容,因其复杂性和抽象性不易被学生理解。采用非变性聚丙烯酰胺凝胶电泳(Native polyacrylamide gel electrophoresis, Native-PAGE)构建了适用于本科实验教学的“线粒体复合体酶I活性方法”。从锥虫中提取线粒体粗体物,以10μg/孔样品蛋白上样量,进行非变性聚丙烯酰胺凝胶电泳, NADH脱氢酶酶促反应时间为30分钟,可得到分辨率高、条带清晰的特异性酶活性条带。将Native-PAGE方法应用到本科生化实验中,可有效拓展教学内容,有助于教学紧密联系科研,对本科生化实验教学的开展有借鉴意义。展开更多
Introduction: The role of high-sensitive cardiac troponin (hs-cTn) assays has higher analytical precision at lower concentrations to detect myocardial injury. The changes in troponin concentration between two assays c...Introduction: The role of high-sensitive cardiac troponin (hs-cTn) assays has higher analytical precision at lower concentrations to detect myocardial injury. The changes in troponin concentration between two assays conducted within a specified time interval refers to “Delta troponin”. This study aimed to assess the correlation between the complexity of coronary lesions and significant delta high-sensitivity troponin I levels in patients with non-ST elevation myocardial infarction. Methods: This cross-sectional study was conducted in the Department of Cardiology, Ibrahim Cardiac Hospital & Research Institute, Dhaka, Bangladesh from July 2022 to June 2023. A total of 70 patients with significant delta hs-cTnI were included and divided into two groups: Group-A (n = 36) with a delta hs-cTnI rise between >20% to 49%, and Group-B (n = 34) with a delta hs-cTnI rise ≥ 50%. Coronary angiography was performed and the SYNTAX Score was calculated for both groups. Data were collected using SPSS version 25.0. Result: Patients with a high-rise delta cTnI (≥50%) showed a significantly higher proportion of lesions in major coronary arteries LCx and LAD compared to those with a low-rise of cTnI (20% - 49%) (p = 0.007 and 0.004, respectively). The presence of triple vessel diseases was higher in the former group than in the latter (p 22, compared to none in the low-rise group (p Conclusion: A high rise in delta hs-cTnI is linked to higher SYNTAX scores, signifying complex coronary lesions in NSTEMI patients, with a significant linear correlation between them. Patients with a high rise in delta cTnI may exhibit more significant coronary artery lesions and triple vessel diseases compared to those with a low rise in cTnI.展开更多
目的探讨循环可溶性MHC-I类链相关蛋白A[soluble major histocompatibility complex class I-related chain A,sMICA)、可溶性MHC-I类链相关蛋白B(soluble major histocompatibility complex class I-related chain B,sMICB]与系统性红...目的探讨循环可溶性MHC-I类链相关蛋白A[soluble major histocompatibility complex class I-related chain A,sMICA)、可溶性MHC-I类链相关蛋白B(soluble major histocompatibility complex class I-related chain B,sMICB]与系统性红斑狼疮(systemic lupus erythematosus,SLE)疾病活动性、自身抗体的关系。方法选择2020年1月~2023年1月重庆大学附属黔江医院收治的156例SLE患者(SLE组)和门诊体检中心体检的103例健康志愿者(对照组)。根据SLE疾病活动度评分(SLE disease activity index,SLEDAI)将SLE患者分为轻度活动组(n=43)、中度活动组(n=69)和重度活动组(n=44)。检测血清sMICA,sMICB水平以及自身抗体、外周血NK细胞占比,Spearman或Pearson分析sMICA,sMICB与评分、自身抗体、外周血NK细胞占比的相关性,受试者工作特征(ROC)曲线用来分析sMICA和sMICB诊断SLE活动度的价值。结果SLE组血清sMICA(173.65±23.92 pg/ml),sMICB(96.35±15.74 pg/ml)水平高于对照组(32.51±6.27 pg/ml,12.03±2.47 pg/ml),外周血CD3^(-)CD56^(+)NK细胞(12.02%±2.65%)占比低于对照组(18.35%±3.71%),差异具有统计学意义(t=58.498,53.897,-16.010,均P<0.05)。重度活动组血清sMICA,sMICB水平高于中度活动组和轻度活动组(t=8.192,12.352;19.652,23.742,均P<0.05),外周血CD3^(-)CD56^(+)NK细胞占比低于中度活动组和轻度活动组(t=8.154,10.658,均P<0.05),差异具有统计学意义。不同疾病活动SLE患者抗‐dsDNA抗体、抗核抗体、抗核小体抗体和抗组蛋白抗体阳性率比较,差异具有统计学意义(χ^(2)=8.795,7.216,7.539,8.946,均P<0.05)。SLE患者血清sMICA,sMICB水平与SLEDAI评分、抗‐dsDNA抗体、抗核抗体、抗核小体抗体、抗组蛋白抗体呈正相关(r=0.206~0.402,均P<0.05),与外周血CD3^(-)CD56^(+)NK细胞占比呈负相关(r=-0.563,-0.427,均P<0.05)。sMICA和sMICB诊断SLE重度活动的曲线下面积为0.652,0.704,联合sMICA,sMICB诊断SLE重度活动的曲线下面积为0.812,高于单独诊断(Z=3.050,2.346,均P<0.05)。结论SLE患者血清sMICA和sMICB水平增高,且与SLE自身抗体阳性率增加、外周血NK细胞占比降低、疾病活动性增强有关,可作为SLE的潜在标志物。展开更多
BACKGROUND Ulcerative colitis(UC)is a chronic,nonspecific intestinal inflammatory disease with undefined pathogenesis.Non-SMC condensin I complex subunit D2(NCAPD2)and non-SMC condensin II complex subunit D3(NCAPD3)pl...BACKGROUND Ulcerative colitis(UC)is a chronic,nonspecific intestinal inflammatory disease with undefined pathogenesis.Non-SMC condensin I complex subunit D2(NCAPD2)and non-SMC condensin II complex subunit D3(NCAPD3)play pivotal roles in chromosome assembly and segregation during both mitosis and meiosis.To date,there has been no relevant report about the functional role of NCAPD2 and NCAPD3 in UC.AIM To determine the level of NCAPD2/3 in intestinal mucosa and explore the mechanisms of NCAPD2/3 in UC.METHODS Levels of NCAPD2/3 in intestinal tissue were detected in 30 UC patients and 30 healthy individuals with in situ hybridization(ISH).In vitro,NCM60 cells were divided into the NC group,model group,si-NCAPD2 group,si-NCAPD3 group and si-NCAPD2+si-NCAPD3 group.Inflammatory cytokines were measured by ELISA,IKK and NF-κB were evaluated by western blot,and IKK nucleation and NF-κB volume were analyzed by immunofluorescence assay.RESULTS Compared with expression in healthy individuals,NCAPD2 and NCAPD3 expression in intestinal tissue was significantly upregulated(P<0.001)in UC patients.Compared with levels in the model group,IL-1β,IL-6 and TNF-αin the si-NCAPD2,si-NCAPD3 and si-NCAPD2+si-NCAPD3 groups were significantly downregulated(P<0.01).IKK and NF-κB protein expression in the si-NCAPD2,si-NCAPD3 and si-NCAPD2+si-NCAPD3 groups was significantly decreased(P<0.01).Moreover,IKK nucleation and NF-κB volume were suppressed upon si-NCAPD2,si-NCAPD3 and si-NCAPD2+si-NCAPD3 transfection.CONCLUSION NCAPD2/3 is highly expressed in the intestinal mucosa of patients with active UC.Overexpression of NCAPD2/3 promotes the release of pro-inflammatory cytokines by modulating the IKK/NF-κB signaling pathway.展开更多
The bis-benzimidazolium salt bis[2-（N-ethylbenzimidazoliumyl）ethyl]amine hexafluorophosphate（LH2·（PF6）2） and its N-heterocyclic carbene silver（Ⅰ） complex[L2Ag3]（PF6）3（1）have been prepared and charact...The bis-benzimidazolium salt bis[2-（N-ethylbenzimidazoliumyl）ethyl]amine hexafluorophosphate（LH2·（PF6）2） and its N-heterocyclic carbene silver（Ⅰ） complex[L2Ag3]（PF6）3（1）have been prepared and characterized.In complex 1,a trinuclear silver（Ⅰ） architecture is formed by two tridentate ligands and three silver（I） atoms,in which one 12- and two 7-membered rings are contained.In the crystal packing of 1,1D chain and 2D supramolecular layer are formed via intermolecular weak interactions,including π…π interactions and C-H…π contacts.Additionally,the fluorescence emission spectra of LH2-（PF6）2 and 1 are described.展开更多
Two silver（I）-sulfonate complexes,[Ag（NO3）（4,4＇-bipy）][Ag（HL）（4,4＇-bipy）]·2H2O（1） and[Ag（H2O）（4,4＇-bipy）][AgL（4,4＇-bipy）]·2H2O（2）,have been synthesized by in situ reaction（H2L = 2-fo...Two silver（I）-sulfonate complexes,[Ag（NO3）（4,4＇-bipy）][Ag（HL）（4,4＇-bipy）]·2H2O（1） and[Ag（H2O）（4,4＇-bipy）][AgL（4,4＇-bipy）]·2H2O（2）,have been synthesized by in situ reaction（H2L = 2-formylbenzenesulfonic acid,4,4-bipy = 4,4-bipyridine）.1 displays two parallel 1D chains expending to a 3D supramolecule by n—n interactions and O-H…O hydrogen bonds,in which the[Ag（NO3）]or[Ag（HL）]units are joined by bridging 4,4＇-bipy molecules,respectively.The interactions between the complexes and DNA were studied by means of fluorescence spectra and surface-enhanced Raman scattering（SERS） spectra.The special configuration and intercalation effects between 1 and DNA are stronger than that between 2 and DNA.展开更多
Two new copper（I） halide complexes bearing 2-（2-benzimidazolyl）-6-methylpyridine （Hbmp） and PPh3 ligands, Cu（Hbmp）（PPh3）X （X = Br （1）; I （2））, have been synthesized and characterized. Single-crystal X-...Two new copper（I） halide complexes bearing 2-（2-benzimidazolyl）-6-methylpyridine （Hbmp） and PPh3 ligands, Cu（Hbmp）（PPh3）X （X = Br （1）; I （2））, have been synthesized and characterized. Single-crystal X-ray structure analysis reveals that the halide ligand has a significant impact on the Cu-Npyridyl bond lengths. Complexes 1 and 2 show the solid-state emissions at ambient temperature, varying with the halide bound to the { Cu（Hbmp）（PPh3） } motif, which are perhaps best attributed to the metal-to-ligand charge-transfer （Cu（I） → Hbmp） transition mixed with some ligand-to-ligand charge-transfer （X and PPh3 → Hbmp） character.展开更多
Two silver(I) complexes were prepared by the reaction of [Ag(C≡CPh)]n with NP3 [NP3 = N(CH2CH2PPh2)3] or with NP3 and [Cu(CH3CN)4]ClO4. Complex 1 [(Ag2Cl(NP3)2)(Ag5- (C≡CPh)6)] contains both NP3 and PhC≡C- ligand...Two silver(I) complexes were prepared by the reaction of [Ag(C≡CPh)]n with NP3 [NP3 = N(CH2CH2PPh2)3] or with NP3 and [Cu(CH3CN)4]ClO4. Complex 1 [(Ag2Cl(NP3)2)(Ag5- (C≡CPh)6)] contains both NP3 and PhC≡C- ligands. The complex cation is (Ag2Cl(NP3)2)+, in which two Ag(NP3)+ cations were bridged by a Cl- donor. The anion is (Ag5(C≡CPh)6)-, where five Ag+ ions are linked by six C≡CPh- to form a pentanuclear cluster. Complex 2 only contains NP3 ligand, where the silver center adopts a trigonal-bipyramidal geometry. Crystal data for 1: C133H116Ag7Cl3- N2P6, Mr = 2789.54, triclinic, space group P1, a = 13.0780(2), b = 15.3678(2), c = 31.2041(3) ?, α = 91.3928(7), β = 90.9328(8), γ = 96.0244(4)o, V = 6233.8(1) ?3, T = 293(2) K, Z = 2, Dc = 1.486 g/cm3, F(000) = 2796, μ = 1.266 mm-1, the final R = 0.0746 and wR = 0.1953 for 16475 observed reflections with I > 2σ(I). Crystal data for 2: C42H42AgClNO4P3, Mr = 861.00, trigonal, space group R3, a = 17.451(1), b = 17.451(1), c = 11.3985(7) ?, V = 3006.0(3) ?3, T = 293(2) K, Z = 3, Dc = 1.427 g/cm3, F(000) = 1326, μ = 0.731 mm-1, the final R = 0.0251 and wR = 0.0663 for 1499 observed reflections with I > 2σ(I).展开更多
A novel binuclear Ag（I） complex [Ag2（C6H6NaO）2（C6H7N3O）2]·2CH3CN （1） was synthesized by the evaporation reaction of silver nitrate and （E）-1-（pyrazin-2-yl）ethanone oxime （HL）. The complex was charac...A novel binuclear Ag（I） complex [Ag2（C6H6NaO）2（C6H7N3O）2]·2CH3CN （1） was synthesized by the evaporation reaction of silver nitrate and （E）-1-（pyrazin-2-yl）ethanone oxime （HL）. The complex was characterized by elemental analysis, IR spectrum and X-ray single-crystal diffraction analysis. It crystallizes in the monoclinic space group C2/c with a = 22.7089（3）, b = 11.5443（7）, c = 16.1468（4）/A, β = 127.7150（10）°, V= 3348.6（2） A^3, Dc = 1.675 g/cm^3, Mr = 844.42, Z = 4, F（000） = 1696.0,μ = 1.226 mm^-1, the final R =0.0250 and wR = 0.070. The coordination around the silver（I） atom is a distorted trigonal-bipyramidal geometry involving one protonated pyrazinyl oxime ligand （HL）, one deprotonated oxime ligand （L^-） and one CH3CN solvate molecule in the asymmetric unit of complex 1.展开更多
A novel silver（I） complex [Ag（2,2ˊ-bipy）（C14H9O3）]·（C14H10O3） has been synthesized with 2-benzoylbenzoic acid as the ligand. Crystal data for the title complex： monoclinic, space group Cc, a = 27.4089...A novel silver（I） complex [Ag（2,2ˊ-bipy）（C14H9O3）]·（C14H10O3） has been synthesized with 2-benzoylbenzoic acid as the ligand. Crystal data for the title complex： monoclinic, space group Cc, a = 27.4089（13）, b = 10.2897（5）, c = 12.0024（6）A, β = 111.864（4）°, Mr = 715.49, V = 3141.5（3） A3, Dc = 1.513 g/cm^3, Z = 4, μ（Mo Kα） = 0.694 mm^-1, F（000） = 1456, the final R = 0.0473 and w R = 0.1146. In the title complex, the central Ag（I） ion is located in a triangular coordination environment. The electron transfer is quasi-reversible in the electrode reaction and it shows a strong emission peak in the range of 495-520 nm under 502 nm excitation. In addition, it displays diamagnetic property from 3 to 300 K.展开更多
A three-coordinate Ag（I） complex, [Ag（Mepzpy）（PAr3）]BF4·H2O（1, Mepzpy = 3-methyl-1-（2-pyridyl）pyrazole, PAr3 = tri（o-tolyl）phosphine）, was synthesized from the reaction of Ag（CH3CN）4BF4, PAr3 and Me...A three-coordinate Ag（I） complex, [Ag（Mepzpy）（PAr3）]BF4·H2O（1, Mepzpy = 3-methyl-1-（2-pyridyl）pyrazole, PAr3 = tri（o-tolyl）phosphine）, was synthesized from the reaction of Ag（CH3CN）4BF4, PAr3 and Mepzpy in CH3 CN at room temperature. The compound was characterized by UV-vis, NMR and X-ray single-crystal structure analysis. It crystallizes in triclinic space group P1 with a = 10.2251（5）, b = 10.6014（5）, c = 15.7012（5） A, α = 92.963（3）, β = 92.641（3）, γ = 114.647（4）°, V = 1540.6（1）A 3, Z = 2, Mr = 676.24, Dc = 1.458 g/cm3, F（000） = 688, μ = 6.187 mm^-1, GOOF = 1.038, the final R = 0.0530 and wR = 0.1493 for 6371 observed reflections with I 〉 2σ（I）. Compound 1 is ionic. It is composed of a BF4- anion and a [Ag（Mepzpy）（PAr3）]＋ cation. The Ag（I） ion adopts a distorted trigonal pyramidal coordination geometry defined by two nitrogen atoms and a phosphorous atom. The complex emits blue luminescence with maximum peaks at 470 nm in solid state at room temperature.展开更多
A new emissive mononuclear homoleptic Cu（Ⅰ） complex of 5-rert-butyl-3-（6-methyl-2-pyridyl）-1H-1,2,4-triazole（bmptzH）,[Cu（bmptzH）2]（ClO4）（1）,has been synthesized by treatment of[Cu（PPh_3）2（CH3CN）2]（C...A new emissive mononuclear homoleptic Cu（Ⅰ） complex of 5-rert-butyl-3-（6-methyl-2-pyridyl）-1H-1,2,4-triazole（bmptzH）,[Cu（bmptzH）2]（ClO4）（1）,has been synthesized by treatment of[Cu（PPh_3）2（CH3CN）2]（ClO4） or [Cu（CH3CN）4]（ClO4） with the bmptzH ligand.It is revealed that complex 1 displays a distorted N4 tetrahedral arrangement formed by two bmptzH chelates,in which bmptzH adopts a neutral bidentate chelating coordination mode using the N atom of the pyridyl ring and the 4-N not 2-N atom of the 1,2,4-triazolyl ring.It is shown that complex 1 is highly stable and exhibits good luminescence properties in solution and solid states at room temperature due to the introduction of a methyl group at the ortho-position of the pyridyl ring.展开更多
文摘Introduction: The role of high-sensitive cardiac troponin (hs-cTn) assays has higher analytical precision at lower concentrations to detect myocardial injury. The changes in troponin concentration between two assays conducted within a specified time interval refers to “Delta troponin”. This study aimed to assess the correlation between the complexity of coronary lesions and significant delta high-sensitivity troponin I levels in patients with non-ST elevation myocardial infarction. Methods: This cross-sectional study was conducted in the Department of Cardiology, Ibrahim Cardiac Hospital & Research Institute, Dhaka, Bangladesh from July 2022 to June 2023. A total of 70 patients with significant delta hs-cTnI were included and divided into two groups: Group-A (n = 36) with a delta hs-cTnI rise between >20% to 49%, and Group-B (n = 34) with a delta hs-cTnI rise ≥ 50%. Coronary angiography was performed and the SYNTAX Score was calculated for both groups. Data were collected using SPSS version 25.0. Result: Patients with a high-rise delta cTnI (≥50%) showed a significantly higher proportion of lesions in major coronary arteries LCx and LAD compared to those with a low-rise of cTnI (20% - 49%) (p = 0.007 and 0.004, respectively). The presence of triple vessel diseases was higher in the former group than in the latter (p 22, compared to none in the low-rise group (p Conclusion: A high rise in delta hs-cTnI is linked to higher SYNTAX scores, signifying complex coronary lesions in NSTEMI patients, with a significant linear correlation between them. Patients with a high rise in delta cTnI may exhibit more significant coronary artery lesions and triple vessel diseases compared to those with a low rise in cTnI.
基金Supported by National Natural Science Foundation of China,No.81673973Natural Science Foundation of Jiangsu Province,China,No.BK20161577the Developing Program for Highlevel Academic Talent from Jiangsu Hospital of Chinese Medicine,No.y2018rc16
文摘BACKGROUND Ulcerative colitis(UC)is a chronic,nonspecific intestinal inflammatory disease with undefined pathogenesis.Non-SMC condensin I complex subunit D2(NCAPD2)and non-SMC condensin II complex subunit D3(NCAPD3)play pivotal roles in chromosome assembly and segregation during both mitosis and meiosis.To date,there has been no relevant report about the functional role of NCAPD2 and NCAPD3 in UC.AIM To determine the level of NCAPD2/3 in intestinal mucosa and explore the mechanisms of NCAPD2/3 in UC.METHODS Levels of NCAPD2/3 in intestinal tissue were detected in 30 UC patients and 30 healthy individuals with in situ hybridization(ISH).In vitro,NCM60 cells were divided into the NC group,model group,si-NCAPD2 group,si-NCAPD3 group and si-NCAPD2+si-NCAPD3 group.Inflammatory cytokines were measured by ELISA,IKK and NF-κB were evaluated by western blot,and IKK nucleation and NF-κB volume were analyzed by immunofluorescence assay.RESULTS Compared with expression in healthy individuals,NCAPD2 and NCAPD3 expression in intestinal tissue was significantly upregulated(P<0.001)in UC patients.Compared with levels in the model group,IL-1β,IL-6 and TNF-αin the si-NCAPD2,si-NCAPD3 and si-NCAPD2+si-NCAPD3 groups were significantly downregulated(P<0.01).IKK and NF-κB protein expression in the si-NCAPD2,si-NCAPD3 and si-NCAPD2+si-NCAPD3 groups was significantly decreased(P<0.01).Moreover,IKK nucleation and NF-κB volume were suppressed upon si-NCAPD2,si-NCAPD3 and si-NCAPD2+si-NCAPD3 transfection.CONCLUSION NCAPD2/3 is highly expressed in the intestinal mucosa of patients with active UC.Overexpression of NCAPD2/3 promotes the release of pro-inflammatory cytokines by modulating the IKK/NF-κB signaling pathway.
基金supported by the National Natural Science Foundation of China(No.21172172)Tianjin Natural Science Foundation(No.11JCZDJC22000)the Program for Innovative Research Team in University of Tianjin(TD12-5038)
文摘The bis-benzimidazolium salt bis[2-（N-ethylbenzimidazoliumyl）ethyl]amine hexafluorophosphate（LH2·（PF6）2） and its N-heterocyclic carbene silver（Ⅰ） complex[L2Ag3]（PF6）3（1）have been prepared and characterized.In complex 1,a trinuclear silver（Ⅰ） architecture is formed by two tridentate ligands and three silver（I） atoms,in which one 12- and two 7-membered rings are contained.In the crystal packing of 1,1D chain and 2D supramolecular layer are formed via intermolecular weak interactions,including π…π interactions and C-H…π contacts.Additionally,the fluorescence emission spectra of LH2-（PF6）2 and 1 are described.
基金supported by the National Natural Science Foundation of China(No.21173197)
文摘Two silver（I）-sulfonate complexes,[Ag（NO3）（4,4＇-bipy）][Ag（HL）（4,4＇-bipy）]·2H2O（1） and[Ag（H2O）（4,4＇-bipy）][AgL（4,4＇-bipy）]·2H2O（2）,have been synthesized by in situ reaction（H2L = 2-formylbenzenesulfonic acid,4,4-bipy = 4,4-bipyridine）.1 displays two parallel 1D chains expending to a 3D supramolecule by n—n interactions and O-H…O hydrogen bonds,in which the[Ag（NO3）]or[Ag（HL）]units are joined by bridging 4,4＇-bipy molecules,respectively.The interactions between the complexes and DNA were studied by means of fluorescence spectra and surface-enhanced Raman scattering（SERS） spectra.The special configuration and intercalation effects between 1 and DNA are stronger than that between 2 and DNA.
基金support from the NNSFC(Nos21163009 and 21001057)the Key Project of Chinese Ministry of Education(No211088)+2 种基金the Advanced Program for the Retuned Overseas Chinese Scholars of the MOHRSS(No 474[2011])the Training Program for Jiangxi Provincial Young Scientiststhe Foundation of State Key Laboratory of Structural Chemistry(No20110015)
文摘Two new copper（I） halide complexes bearing 2-（2-benzimidazolyl）-6-methylpyridine （Hbmp） and PPh3 ligands, Cu（Hbmp）（PPh3）X （X = Br （1）; I （2））, have been synthesized and characterized. Single-crystal X-ray structure analysis reveals that the halide ligand has a significant impact on the Cu-Npyridyl bond lengths. Complexes 1 and 2 show the solid-state emissions at ambient temperature, varying with the halide bound to the { Cu（Hbmp）（PPh3） } motif, which are perhaps best attributed to the metal-to-ligand charge-transfer （Cu（I） → Hbmp） transition mixed with some ligand-to-ligand charge-transfer （X and PPh3 → Hbmp） character.
基金This work was supported by the NSF of Fujian Province (E0310029) and the Innovation Fund of Fujian Province (2003J044)
文摘Two silver(I) complexes were prepared by the reaction of [Ag(C≡CPh)]n with NP3 [NP3 = N(CH2CH2PPh2)3] or with NP3 and [Cu(CH3CN)4]ClO4. Complex 1 [(Ag2Cl(NP3)2)(Ag5- (C≡CPh)6)] contains both NP3 and PhC≡C- ligands. The complex cation is (Ag2Cl(NP3)2)+, in which two Ag(NP3)+ cations were bridged by a Cl- donor. The anion is (Ag5(C≡CPh)6)-, where five Ag+ ions are linked by six C≡CPh- to form a pentanuclear cluster. Complex 2 only contains NP3 ligand, where the silver center adopts a trigonal-bipyramidal geometry. Crystal data for 1: C133H116Ag7Cl3- N2P6, Mr = 2789.54, triclinic, space group P1, a = 13.0780(2), b = 15.3678(2), c = 31.2041(3) ?, α = 91.3928(7), β = 90.9328(8), γ = 96.0244(4)o, V = 6233.8(1) ?3, T = 293(2) K, Z = 2, Dc = 1.486 g/cm3, F(000) = 2796, μ = 1.266 mm-1, the final R = 0.0746 and wR = 0.1953 for 16475 observed reflections with I > 2σ(I). Crystal data for 2: C42H42AgClNO4P3, Mr = 861.00, trigonal, space group R3, a = 17.451(1), b = 17.451(1), c = 11.3985(7) ?, V = 3006.0(3) ?3, T = 293(2) K, Z = 3, Dc = 1.427 g/cm3, F(000) = 1326, μ = 0.731 mm-1, the final R = 0.0251 and wR = 0.0663 for 1499 observed reflections with I > 2σ(I).
基金supported by the National Natural Science Foundation of China (20871099)the Natural Science Foundation of Gansu Province (0710RJZA113)
文摘A novel binuclear Ag（I） complex [Ag2（C6H6NaO）2（C6H7N3O）2]·2CH3CN （1） was synthesized by the evaporation reaction of silver nitrate and （E）-1-（pyrazin-2-yl）ethanone oxime （HL）. The complex was characterized by elemental analysis, IR spectrum and X-ray single-crystal diffraction analysis. It crystallizes in the monoclinic space group C2/c with a = 22.7089（3）, b = 11.5443（7）, c = 16.1468（4）/A, β = 127.7150（10）°, V= 3348.6（2） A^3, Dc = 1.675 g/cm^3, Mr = 844.42, Z = 4, F（000） = 1696.0,μ = 1.226 mm^-1, the final R =0.0250 and wR = 0.070. The coordination around the silver（I） atom is a distorted trigonal-bipyramidal geometry involving one protonated pyrazinyl oxime ligand （HL）, one deprotonated oxime ligand （L^-） and one CH3CN solvate molecule in the asymmetric unit of complex 1.
基金Supported by the Natural Science Foundation of Hunan Province(No.11JJ9006)Key Project of Science and Technology Plan of Hunan Province(2012FJ2002)the Construct Program of the Key Discipline in Hunan Province
文摘A novel silver（I） complex [Ag（2,2ˊ-bipy）（C14H9O3）]·（C14H10O3） has been synthesized with 2-benzoylbenzoic acid as the ligand. Crystal data for the title complex： monoclinic, space group Cc, a = 27.4089（13）, b = 10.2897（5）, c = 12.0024（6）A, β = 111.864（4）°, Mr = 715.49, V = 3141.5（3） A3, Dc = 1.513 g/cm^3, Z = 4, μ（Mo Kα） = 0.694 mm^-1, F（000） = 1456, the final R = 0.0473 and w R = 0.1146. In the title complex, the central Ag（I） ion is located in a triangular coordination environment. The electron transfer is quasi-reversible in the electrode reaction and it shows a strong emission peak in the range of 495-520 nm under 502 nm excitation. In addition, it displays diamagnetic property from 3 to 300 K.
基金supported by the National Natural Science Foundation of China(51172232)
文摘A three-coordinate Ag（I） complex, [Ag（Mepzpy）（PAr3）]BF4·H2O（1, Mepzpy = 3-methyl-1-（2-pyridyl）pyrazole, PAr3 = tri（o-tolyl）phosphine）, was synthesized from the reaction of Ag（CH3CN）4BF4, PAr3 and Mepzpy in CH3 CN at room temperature. The compound was characterized by UV-vis, NMR and X-ray single-crystal structure analysis. It crystallizes in triclinic space group P1 with a = 10.2251（5）, b = 10.6014（5）, c = 15.7012（5） A, α = 92.963（3）, β = 92.641（3）, γ = 114.647（4）°, V = 1540.6（1）A 3, Z = 2, Mr = 676.24, Dc = 1.458 g/cm3, F（000） = 688, μ = 6.187 mm^-1, GOOF = 1.038, the final R = 0.0530 and wR = 0.1493 for 6371 observed reflections with I 〉 2σ（I）. Compound 1 is ionic. It is composed of a BF4- anion and a [Ag（Mepzpy）（PAr3）]＋ cation. The Ag（I） ion adopts a distorted trigonal pyramidal coordination geometry defined by two nitrogen atoms and a phosphorous atom. The complex emits blue luminescence with maximum peaks at 470 nm in solid state at room temperature.
基金supported by the National Natural Science Foundation of China(Nos.21561013,21501077)the Major Program of Jiangxi Provincial Natural Science Foundation of China for Young Scholar(Nos.20143ACB21017,20161ACB21013)+1 种基金the Jiangxi Provincial Natural Science Foundation of China(Nos.20142BAB203001,20151BAB213003)the Program for Qingjiang Excellent Young Talents of Jiangxi University of Science and Technology
文摘A new emissive mononuclear homoleptic Cu（Ⅰ） complex of 5-rert-butyl-3-（6-methyl-2-pyridyl）-1H-1,2,4-triazole（bmptzH）,[Cu（bmptzH）2]（ClO4）（1）,has been synthesized by treatment of[Cu（PPh_3）2（CH3CN）2]（ClO4） or [Cu（CH3CN）4]（ClO4） with the bmptzH ligand.It is revealed that complex 1 displays a distorted N4 tetrahedral arrangement formed by two bmptzH chelates,in which bmptzH adopts a neutral bidentate chelating coordination mode using the N atom of the pyridyl ring and the 4-N not 2-N atom of the 1,2,4-triazolyl ring.It is shown that complex 1 is highly stable and exhibits good luminescence properties in solution and solid states at room temperature due to the introduction of a methyl group at the ortho-position of the pyridyl ring.
