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Synthesis, Crystal Structure and Properties of a Novel Vanadium(Ⅴ) Oxoperoxo Complex Incorporating a Tridentate Hydrazone Ligand
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作者 耿磊珍 邢婧 周荫庄 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2012年第2期185-190,共6页
A novel vanadium(V) oxoperoxo complex [VOO2(APTCH)(CH3OH)] (HAPTCH = 2-acetylpyridine thiophene-2-carboxylic hydrazone) has been synthesized and characterized by IR, TGA and X-ray single-crystal structure dete... A novel vanadium(V) oxoperoxo complex [VOO2(APTCH)(CH3OH)] (HAPTCH = 2-acetylpyridine thiophene-2-carboxylic hydrazone) has been synthesized and characterized by IR, TGA and X-ray single-crystal structure determination. The complex crystallizes in the monoclinic system, space group P21/c with a = 11.232(2), b = 10.762(2), c = 112.613(3), β = 99.44(3)°, V = 1504.1(5)3, Dc = 1.657 g·cm-3, Z = 4, F(000) = 768, μ = 0.827 mm-1, the final R = 0.0392 and wR = 0.1073 for 2266 observed reflections with I 〉 2σ(I). Single-crystal X-ray diffraction studies reveal that the vanadium(V) is coordinated by a tridentate ligand, methanol molecule and peroxo group to form a pentagonal-bipyramidal geometry. The crystal structure is stabilized by intermolecular hydrogen bonds of O-H···N and C-H···O. 展开更多
关键词 vanadium(V) oxoperoxo complex hydrazone crystal structure TGA
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Synthesis and Crystal Structure of a Vanadium(V) Complex with 2-Hydroxy-1-naphthaldehyde Isonicotinoyl Hydrazone 被引量:2
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作者 于青 李春英 +3 位作者 边贺东 梁宏 宋海斌 王宏根 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2007年第1期37-40,共4页
The mononuclear vanadium(V) complex with 2-hydroxyl-l-naphthaldehyde isonicotinoyl hydrazone was synthesized and characterized by single-crystal X-ray diffraction. The crystal is of monocfinic, space group P2 1/n wi... The mononuclear vanadium(V) complex with 2-hydroxyl-l-naphthaldehyde isonicotinoyl hydrazone was synthesized and characterized by single-crystal X-ray diffraction. The crystal is of monocfinic, space group P2 1/n with α = 10.3153(15), b = 7.4024(11 ), c = 24.413(4) A, β = 101.911(2)°, V= 1824.0(5) A^3, Z= 4, Mr = 427.28, Dc = 1.556 g/cm^3, F(000) = 880,μ(MoKα) = 0.591, the final R = 0.0372 and wR = 0.0926. The vanadium(V) atom adopts a distorted square-pyramidal geometry coordinated by the tridentate ligand and two oxygen atoms. The hydrogen bonds and strong π-π stacking interactions link the complex molecules into a 3-D network structure. 展开更多
关键词 crystal structure vanadium complex tridentate ligand hydrazone
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Synthesis and Crystal Structure of Binuclear Ytterbium Complex with Isonicotinoyl Hydrazone
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作者 卜显和 鹿守亮 +1 位作者 陈巍 张若桦 《Journal of Rare Earths》 SCIE EI CAS CSCD 2001年第2期86-89,共4页
The ytterbium complex of isonicotinoyl hydrazone was synthesized and the structure was determined by X-ray diffraction analysis. The crystal and molecular structure of the title complex [Yb-2(L)(3)](OH)(3) shows that ... The ytterbium complex of isonicotinoyl hydrazone was synthesized and the structure was determined by X-ray diffraction analysis. The crystal and molecular structure of the title complex [Yb-2(L)(3)](OH)(3) shows that the complex has two identical nine-coordinated ytterbium ions with each surrounded by N3O6 donor set, Two ytterbium ions are bridged by three phenolate oxygen atoms, The geometry around each ytterbium ions can be considered as a three-capped trigonal prism. 展开更多
关键词 rare earths synthesis ytterbium complex isonicotinoyl hydrazone crystal structure
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Synthesis and Crystal Structure of Lanthanum Nitrate with Methyl-2-pyridyl Ketone Benzoyl Hydrazone 被引量:5
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作者 TAIXi-shi YINXian-hong +2 位作者 LIUDe-bo TANMin-yu YUKai-bei 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2003年第4期434-436,共3页
A novel La complex with methyl-2-pyridyl ketone benzoyl hydrazone has been synthesized and determined by single crystal X-ray diffraction. The crystal is monoclinic with space group C2/c, a =1 7081(3) nm, b =1 ... A novel La complex with methyl-2-pyridyl ketone benzoyl hydrazone has been synthesized and determined by single crystal X-ray diffraction. The crystal is monoclinic with space group C2/c, a =1 7081(3) nm, b =1 5660(3) nm, c =1 3512(3) nm, α=90 00°, β=94 39(1)°, γ=90 00°, V =3 6037(12) nm 3, Z =4 . The complex is a ten-coordinated one with a lanthanum ion surrounded by a N 4O 6 set. The crystal structure is stabilized by hydrogen bonds between water molecules and NO - 3 anions. 展开更多
关键词 synthesis Lanthanum complex Methyl-2-pyridyl ketone benzoyl hydrazone crystal structure
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Synthesis and Characterization of Three Vanadium(Ⅴ) Complexes Incorporating Tridentate Hydrazone Ligands of Thiophene-2-carboxylic Hydrazide and 2-Furoic Acid Hydrazide
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作者 耿磊珍 邢婧 +1 位作者 魏玮 周荫庄 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2012年第4期562-568,共7页
Divanadium(Ⅴ) complex [VO(aptch)(μ-OCH3)]2(1) and two monovanadium(Ⅴ) complexes [VO(apfah))(OEt)](2a and 2b,H2aptch = 2-hydroxyacetophenone thiophene-2-car-boxylic hydrazone,H2apfah = 2-hydroxyaceto... Divanadium(Ⅴ) complex [VO(aptch)(μ-OCH3)]2(1) and two monovanadium(Ⅴ) complexes [VO(apfah))(OEt)](2a and 2b,H2aptch = 2-hydroxyacetophenone thiophene-2-car-boxylic hydrazone,H2apfah = 2-hydroxyacetophenone 2-furoic acid hydrazone) have been synthesized and characterized.Single-crystal X-ray diffraction studies reveal that 1 is a cen-trosymmetric dimer bridged by two methoxido O-atoms.Complex 1 crystallizes in the monoclinic crystal system,space groups P21/c with a = 7.4825(4),b = 17.0928(11),c = 11.6961(7) ,β = 98.172(4)o,Z = 2,F(000) = 728,μ = 0.829 mm-1,the final R = 0.0457 and wR = 0.1137 for 2654 observed reflections with I 〉 2(I).The vanadium(V) is coordinated to the tridentate ligand,ethanol molecule to form a distorted square-pyramidal geometry,complexes 2a and 2b.Although 2a and 2b have the same asymmetric unit,they belong to different space groups.Complex 2a crystallizes in the monoclinic crystal system,space groups P21/n with a = 10.2293(2),b = 15.6660(3),c = 10.6298(2) ,β = 116.259(1)o,Z = 4,μ = 0.676 mm-1;complex 2b crystallizes in the triclinic crystal system,space groups P with a = 8.2808(4),b = 9.4704(5),c = 10.0819(5) ,α = 86.133(3),= 81.956(3),γ = 80.248(3)o,Z = 2 and μ = 0.670 mm-1.The hydrogen bonds are found to exist in 2b only.The crystal structure is stabilized by intermolecular hydrogen bonds of C-H···O. 展开更多
关键词 vanadium(ⅴ) complex hydrazone synthesis crystal structure
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Syntheses, Crystal Structures and Antimicrobial Activities of Vanadium(V) Complexes with Similar Tridentate Hydrazone Ligands 被引量:1
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作者 LI Ke LI Shu-Jing +2 位作者 YAO Xin-Jian NIU Jing-Jing QIU Xiao-Yang 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2015年第6期885-893,共9页
Two hydrazone ligands (E)-N'-(2-hydroxy-5-methoxybenzylidene)-2-hydroxybenzo- hydrazide (HLa) and (E)-N'-(3,5-dichloro-2- hydroxybenzylidene)-4-methoxybenzohydrazide (HLb) were prepared and characterized... Two hydrazone ligands (E)-N'-(2-hydroxy-5-methoxybenzylidene)-2-hydroxybenzo- hydrazide (HLa) and (E)-N'-(3,5-dichloro-2- hydroxybenzylidene)-4-methoxybenzohydrazide (HLb) were prepared and characterized by IR, UV-Vis and 1H NMR spectra. Based on the hydrazone ligands, two new structurally similar vanadium(V) complexes, [VOLaL].CH3OH (1) and [vOLbL] (2), where L is the monoanionic form of benzohydroxamic acid (HL), were prepared and characterized by IR and UV-Vis spectra, and single-crystal X-ray diffraction. Complex 1 crystallizes as the monoclinic space group P21/n, with a = 7.5208(10), b = 15.490(2), c = 20.8929(18) A, β = 96.373(2)°, V = 2418.9(5) A3, Z = 4, R = 0.0831, wR = 0.2607 and GOOF = 1.061. Complex 2 crystallizes as the monoclinic space group P21/c, with a = 11.8577(18), b = 16.468(2), c = 12.2288(18) A, β = 106.064(2)°, V= 2294.7(6) A3, Z = 4, R= 0.0741, wR= 0.1745 and GOOF= 1.014. X-ray analysis indicates that the complexes are mononuclear vanadium (V) species, with the V atoms located in the octahedral coordination. The hydrazone ligands and the complexes were evaluated for their antibacterial (Bacillus subtilis, Staphylococcus aureus, Escherichia coli, and Pseudomonas fluorescence) and antifungal (Candida albicans and Aspergillus niger) activities by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) method. 展开更多
关键词 hydrazone vanadium complex mononuclear complex crystal structure antimicrobial activity
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Synthesis and Crystal Structure of Pyridine-2,6-dicarboxylate Vanadium Complex:[(Pyridine-2,6-dicarboxylate)VO_2]_2[4,4'-bipyridine]·4H_2O
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作者 朱龙根 黄锦顺 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1994年第2期83-86,共4页
Crystal structure of pyridine-2,6-dicarboxylate(dipc) vanadium complex:[(dipc)VO_2]_2( 4, 4'-bipyridine)·4H_2O(M_r=724.34) is monoclinic with space group C2/c and a=25.857(8),b=6.896(1),c=16.267(5),β=106.27(... Crystal structure of pyridine-2,6-dicarboxylate(dipc) vanadium complex:[(dipc)VO_2]_2( 4, 4'-bipyridine)·4H_2O(M_r=724.34) is monoclinic with space group C2/c and a=25.857(8),b=6.896(1),c=16.267(5),β=106.27(4)°,V=2784.62 D_c=1.73 g/cm ̄3,F(000)=1472,Z=4.The structural solutions and refinements based on 1661 reflections (I>2σ(I))converged at R=0. 043.The coordinated number of vanadium atom is 5,the geometrical form of the five atoms are coordinated to the vanadium atom is a distorted tetragonal bipyramid of which the four coordinated atoms O(3),O(5),N(1) and O(2) make up the equatorial plane,while the other coordinated atom O(1) is to occupy the apex. 展开更多
关键词 vanadium complexes synthesis crystal structure
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Synthesis,Crystal Structure and Properties of Complex VO(C_(12)H_(12)N_2O_2)(C_(13)H_(10)NO_2) 被引量:1
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作者 MADong-sheng GaoShan HUOLi-hua GAOJing-sheng 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2004年第3期341-344,共4页
Complex VO(C\-\{12\}H\-\{12\}N\-2O\-2)(C\-\{13\}H\-\{10\}NO\-2)(C\-\{12\}H\-\{12\}N\-2O\+\{\{\}\+\{2-\}\}\-2=acetylacetone benzoylhydrozanate,C\-\{13\}H\-\{10\}NO\+_\-2=\%N\%\|phenylbenzohydroxamate) was synthesized a... Complex VO(C\-\{12\}H\-\{12\}N\-2O\-2)(C\-\{13\}H\-\{10\}NO\-2)(C\-\{12\}H\-\{12\}N\-2O\+\{\{\}\+\{2-\}\}\-2=acetylacetone benzoylhydrozanate,C\-\{13\}H\-\{10\}NO\+_\-2=\%N\%\|phenylbenzohydroxamate) was synthesized and characterized by means of elemental analysis,IR and UV spectroscopies,cyclic voltammetry and single crystal X\|ray diffraction. The complex crystallized in the monoclinic system with space group \%P\%2\-1/\%n\% and the crystal cell parameters \%a\%=1\^3003(1) nm,\%b\%=0\^88836(6) nm,\%c\%=2\^0196(2) nm,\%β\%=95\^065(8)°,\%V\%=2\^3238(3) nm\+3,\%M\%\-r=495\^40 and \%Z\%=4. The two oxygen and one nitrogen atoms of the tridentate hydrazone ligand coordinate to the vanadium atom,forming an equatorial plane. And the coordinated vanadium atom exhibits a distorted octahedral geometry. The atom in the transposition to the oxo O atom is the carbonyl oxygen atom of the hydroxamate ligand in the complex. The half\|wave redox potential of the title complex in the three different solvents positively shifts in the order of CH\-2Cl\-2<CH\-3CN<DMF. 展开更多
关键词 Oxovanadium() hydrazone complex Hydroxamate complex crystal structure Spectral property
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Synthesis and Crystal Structure of(Et_4N)_3[{V(o-C_6H_4OS)_3}_2Na] 被引量:1
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作者 Wen Ting-Bin Xu Yong-Jin +5 位作者 Shi Ji-Cheng Deng Yu-Heng Chen Chang-Neng Liu Qiu-Tian Kang Bei-Sheng (State Key Laboratory of Structural Chemistry and Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 3500 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1995年第2期151-156,共6页
Et_4N)_3 [V(mp)_3Na(mp)_3V] was obtained from the reaction of (NH_4)_3VS_4, FeCl_2, Na_2mp(H_2mp=o-mercaptophenol,o-HSC_6H_4OH) and Et_4NCl in CH_3CN. C_(60)H_(84)N_3NaO_6S_6V_2, M_r=1260. 61, monoclinic, space group ... Et_4N)_3 [V(mp)_3Na(mp)_3V] was obtained from the reaction of (NH_4)_3VS_4, FeCl_2, Na_2mp(H_2mp=o-mercaptophenol,o-HSC_6H_4OH) and Et_4NCl in CH_3CN. C_(60)H_(84)N_3NaO_6S_6V_2, M_r=1260. 61, monoclinic, space group C2/c with a=24. 825(8) . b=14.716(5) , c=18. 419(10)A,β=94. 57(3)°, V=6707. 54 A ̄3;Z=4, Dc=1. 248 g/cm ̄3. μ= 5. 002 cm ̄(-1). F(000)=2664. The structure was solved by direct methods and refined to final R(Rω)=0.059(0.059) for 3183 observed reflections with I≥2.5σ(I). The centrosymmetric anion of the title compound contains two [V(mp)_3] ̄(2-) fragments linked by a sodium ion, the crystallographic center of symmetry , through the μ2-O bridges. The Ⅴ(Ⅳ) atom is in a coordination environment intermediate between a trigonal prism and an ideal octahedron. 展开更多
关键词 synthesis crystal structure o-mercaptophenol vanadium complex
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Syntheses and Crystal Structures of 3-Chloro-N'-(3,5-dichloro-2-hydroxybenzylidene)-benzohydrazide and Its Oxovanadium(V) Complex with Antimicrobial Activity
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作者 高栓平 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2012年第3期377-384,共8页
A hydrazone compound 3-chloro-N'-(3,5-dichloro-2-hydroxybenzylidene)benzo-hydrazide(H2L) derived from the condensation of 3,5-dichlorosalicylaldehyde with 3-chloro-benzohydrazide and its oxovanadium(V) complex ... A hydrazone compound 3-chloro-N'-(3,5-dichloro-2-hydroxybenzylidene)benzo-hydrazide(H2L) derived from the condensation of 3,5-dichlorosalicylaldehyde with 3-chloro-benzohydrazide and its oxovanadium(V) complex [VOL(CH3OH)(OCH3)] have been successfully prepared and characterized by physico-chemical methods and single-crystal X-ray diffraction.The hydrazone ligand coordinates to the V atom through the phenolate O,imine N,and enolic O atoms.The V atom is hexa-coordinated in a distorted octahedral geometry.The antimicrobial activities(MIC) of the hydrazone ligand and the oxovanadium(V) complex have been evaluated against the bacteria Staphylococcus aureus,Baccilus subtilis,Pseudomonas aeruginosa,and Escherichia coli. 展开更多
关键词 hydrazone oxovanadium complex crystal structure synthesis antimicrobial activity
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酰腙氧钒(Ⅴ)配合物的合成、结构及其抑制幽门螺旋杆菌脲酶研究(英文) 被引量:1
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作者 张吉才 李海华 +4 位作者 献冬梅 张梅 甄苗苗 赵月 由忠录 《无机化学学报》 SCIE CAS CSCD 北大核心 2012年第9期1959-1966,共8页
本文合成了2个新的结构类似的酰腙氧钒(Ⅴ)配合物,[VOL(OCH3)(CH3OH)](L=L1=2-氯-N′-(5-氯-2-羟基苯亚甲基)苯甲酰肼(1);L=L2=2-氯-N′-(2-羟基-3-甲氧基苯亚甲基)苯甲酰肼(2)),并通过物理化学方法和单晶X-射线衍射表征了它们的结构。... 本文合成了2个新的结构类似的酰腙氧钒(Ⅴ)配合物,[VOL(OCH3)(CH3OH)](L=L1=2-氯-N′-(5-氯-2-羟基苯亚甲基)苯甲酰肼(1);L=L2=2-氯-N′-(2-羟基-3-甲氧基苯亚甲基)苯甲酰肼(2)),并通过物理化学方法和单晶X-射线衍射表征了它们的结构。在每个配合物中,V原子都采取八面体配位构型,利用配体L中的3个给体原子和1个甲氧配体的氧原子定义其赤道面,利用1个酮氧原子和1个甲醇氧原子占据其2个轴向位置。本文还研究了这2个配合物对幽门螺旋杆菌脲酶的抑制活性。在浓度为100μmol.L-1时,配合物1和2对脲酶的抑制率分别为(82.0%±2.8%)和(28.2%±1.7%)。此外,还做了配合物和幽门螺旋杆菌脲酶的分子对接研究。 展开更多
关键词 酰腙 钒氧()配合物 晶体结构 脲酶 抑制剂
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2-羰基-3-苯基丙酸芳甲酰腙二(2,4-二氯苄基)锡配合物的合成、晶体结构及生物活性 被引量:8
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作者 蒋伍玖 谭宇星 +3 位作者 庾江喜 朱小明 张复兴 邝代治 《无机化学学报》 SCIE CAS CSCD 北大核心 2016年第8期1383-1390,共8页
二(2,4-二氯苄基)二氯化锡分别与2-羰基-3-苯基丙酸苯甲酰腙及2-羰基-3-苯基丙酸水杨酰腙反应,合成了2个取代苄基锡配合物(C1、C2),通过元素分析、IR、1H NMR、13C NMR、119Sn NMR、X射线单晶衍射以及热重分析等表征了配合物结构。测试... 二(2,4-二氯苄基)二氯化锡分别与2-羰基-3-苯基丙酸苯甲酰腙及2-羰基-3-苯基丙酸水杨酰腙反应,合成了2个取代苄基锡配合物(C1、C2),通过元素分析、IR、1H NMR、13C NMR、119Sn NMR、X射线单晶衍射以及热重分析等表征了配合物结构。测试了配合物对癌细胞Hela、MCF7、Hep G2、Colo205、NCI-H460以及正常人体胚肾细胞HEK293、正常人体肝细胞HL7702的体外抑制活性;在Tris-HCl缓冲溶液中,以EB做为荧光探针,用荧光光谱法初步研究了配合物与小牛胸腺DNA的相互作用。结果表明:配合物C1、C2对5种癌细胞都有明显的抑制作用,配合物C2对HEK293、HL7702的细胞毒性远小于C1;配合物C1与小牛胸腺DNA作用是插入结合与静电结合共同作用所致,配合物C2与小牛胸腺DNA作用是插入结合作用所致。 展开更多
关键词 有机锡配合物 酰腙 合成 晶体结构 生物活性
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N-(2-丙酸)-芳甲酰腙二对甲基苄基锡配合物的合成、晶体结构及生物活性 被引量:5
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作者 张志坚 蒋伍玖 +4 位作者 刘洋 邝代治 庾江喜 朱小明 谭宇星 《无机化学学报》 SCIE CAS CSCD 北大核心 2017年第9期1603-1610,共8页
二对甲基苄基二氯化锡分别与N-(2-丙酸)-对硝基苯甲酰腙及N-(2-丙酸)-对叔丁基苯甲酰腙反应,合成了2个取代二苄基锡配合物(C1、C2),通过元素分析、IR、UV-Vis、1H NMR、13C NMR、119Sn NMR、X射线单晶衍射以及热重分析等表征了配合物结... 二对甲基苄基二氯化锡分别与N-(2-丙酸)-对硝基苯甲酰腙及N-(2-丙酸)-对叔丁基苯甲酰腙反应,合成了2个取代二苄基锡配合物(C1、C2),通过元素分析、IR、UV-Vis、1H NMR、13C NMR、119Sn NMR、X射线单晶衍射以及热重分析等表征了配合物结构。测试了配合物对癌细胞H460、HepG2、MCF7以及正常人体肝细胞HL7702的体外抑制活性;在Tris-HCl缓冲溶液中,以EB作为荧光探针,用荧光光谱法初步研究了配合物与小牛胸腺DNA的相互作用。结果表明:配合物C1、C2对3种癌细胞都有较好的抑制作用,配合物C2对HL7702的细胞毒性远小于C1;配合物C1、C2与小牛胸腺DNA作用均是插入结合作用所致。 展开更多
关键词 有机锡配合物 酰腙 合成 晶体结构 生物活性
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酰腙氧钒(V)配合物的合成、结构及其抑制幽门螺旋杆菌脲酶研究(英文) 被引量:4
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作者 赵月 韩笑 +2 位作者 周晓霞 李海华 由忠录 《无机化学学报》 SCIE CAS CSCD 北大核心 2013年第4期867-874,共8页
为了探索新型高效脲酶抑制剂,本文合成了2个新的酰腙氧钒(V)配合物,[VOL1(OCH3)(CH3OH)](1)和[VOL2(μ-OCH3)]2(2)(H2L1=N′-(5-氯-2-羟基苯亚甲基)-3-硝基苯甲酰肼;H2L2=N′-(5-氯-2-羟基苯亚甲基)-4-氯苯甲酰肼),并通过物理化学方法... 为了探索新型高效脲酶抑制剂,本文合成了2个新的酰腙氧钒(V)配合物,[VOL1(OCH3)(CH3OH)](1)和[VOL2(μ-OCH3)]2(2)(H2L1=N′-(5-氯-2-羟基苯亚甲基)-3-硝基苯甲酰肼;H2L2=N′-(5-氯-2-羟基苯亚甲基)-4-氯苯甲酰肼),并通过物理化学方法和单晶X-射线衍射表征了它们的结构。化合物1是一个单核配合物,而化合物2是由两个甲氧基配体桥连的具有中心对称性的双核配合物。在每个配合物中,V原子都采取八面体配位构型。本文还研究了这两个配合物的热稳定性和它们对幽门螺旋杆菌脲酶的抑制活性。在浓度为100μmol.L-1时,配合物1和2对脲酶的抑制率分别为71.4%和73.3%,其IC50值分别为63.6和37.7μmol.L-1。 展开更多
关键词 酰腙 钒氧(V)配合物 晶体结构 脲酶 抑制剂
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一个新的双核锌(Ⅱ)配合物的水热合成、晶体结构和荧光性质 被引量:6
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作者 王亮 刘娟 +1 位作者 郑长征 吉长友 《精细化工》 EI CAS CSCD 北大核心 2012年第2期105-108,共4页
由5-溴-2-羟基苯基乙酮和4-硝基苯甲酰肼在乙醇溶剂中反应得到5-溴-2-羟基苯基乙酮-4-硝基苯甲酰腙(H2L),以该酰腙为配体,与吡啶、硝酸锌反应,水热合成制得一个新的双核配合物5-溴-2-羟基苯基乙酮-4-硝基苯甲酰腙吡啶锌(Ⅱ)(CCDC:85154... 由5-溴-2-羟基苯基乙酮和4-硝基苯甲酰肼在乙醇溶剂中反应得到5-溴-2-羟基苯基乙酮-4-硝基苯甲酰腙(H2L),以该酰腙为配体,与吡啶、硝酸锌反应,水热合成制得一个新的双核配合物5-溴-2-羟基苯基乙酮-4-硝基苯甲酰腙吡啶锌(Ⅱ)(CCDC:851546),并培养成单晶。通过元素分析、红外分析和X射线单晶衍射对其结构进行了表征。该配合物晶体属单斜晶系,空间群为P21/c,晶胞参数a=1.179 89(9)nm,b=1.648 05(12)nm,c=1.023 00(8)nm,β=96.967 0(10)°,Dc=1.751 mg/m3。荧光光谱表明,配体和配合物均具有荧光性能,在475.0 nm处配合物的荧光强度得到了明显增强。 展开更多
关键词 水热合成 锌(Ⅱ)配合物 5-溴-2-羟基苯基乙酮-4-硝基苯甲酰腙 晶体结构 荧光 功能材料
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二个含水杨酰腙配体的钒配合物的合成与晶体结构研究(英文) 被引量:2
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作者 陈小华 吴琼洁 +2 位作者 吕玮 杨明星 陈丽娟 《无机化学学报》 SCIE CAS CSCD 北大核心 2013年第7期1521-1526,共6页
2种水杨酰腙配体H2L1(H2L1=邻羟基苯乙酮缩水杨酰腙)和H2L2(H2L2=水杨醛缩水杨酰腙)分别与VO(acac)2反应,合成了2个钒配合物[VOL1(C2H5O)]2(1)和[VOL2(i-C3H7O)](2),利用元素分析、红外光谱、紫外光谱和单晶衍射等手段进行表征。配合物... 2种水杨酰腙配体H2L1(H2L1=邻羟基苯乙酮缩水杨酰腙)和H2L2(H2L2=水杨醛缩水杨酰腙)分别与VO(acac)2反应,合成了2个钒配合物[VOL1(C2H5O)]2(1)和[VOL2(i-C3H7O)](2),利用元素分析、红外光谱、紫外光谱和单晶衍射等手段进行表征。配合物1是由酚氧原子桥联2个金属中心形成的具有晶体学中心对称性的双核钒(V)配合物结构,每个V(V)原子具有扭曲的八面体配位构型。配合物2为单核结构,每个V(V)原子具有扭曲的四角锥配位构型,相邻的配合物分子通过分子间氢键作用形成一维超分子链状结构。采用循环伏安法研究了化合物2的电化学性质。 展开更多
关键词 酰腙 钒(V)配合物 晶体结构
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配合物(n-Bu)_2Sn(C_(10)H_8N_2O_4)(C_2H_5OH)的合成和晶体结构 被引量:3
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作者 卢文贯 刘宏文 陶家洵 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2004年第6期600-604,共5页
以2-羰基丙酸水杨酰腙作为配体与二正丁基氧化锡(Ⅳ)在苯/乙醇混合溶剂中反应, 合成了新型配合物(n-Bu)2Sn(C10H8N2O4)(C2H5OH)(C10H8N2O42为2-羰基丙酸水杨酰腙负二价离子)。用单晶X-射线衍射分析法测定了该配合物的晶体结构。晶体属... 以2-羰基丙酸水杨酰腙作为配体与二正丁基氧化锡(Ⅳ)在苯/乙醇混合溶剂中反应, 合成了新型配合物(n-Bu)2Sn(C10H8N2O4)(C2H5OH)(C10H8N2O42为2-羰基丙酸水杨酰腙负二价离子)。用单晶X-射线衍射分析法测定了该配合物的晶体结构。晶体属四方晶系, I41/a空间群, 晶胞参数a = 2.5113(7), b = 2.5113(7), c = 1.5062(6) nm, V = 9.499(5) nm3, Z = 16, Dc = 1.396 g/cm3, m(MoKa) = 1.105 mm1, F (000) = 4096。对于2499 (I >2s(I))个可观测点, 最终可靠因子R = 0.0349, wR = 0.0793。在该配合物的分子结构中, 中心锡原子与3个O原子、1个N原子和2个C原子形成扭曲的八面体几何构型, 其中3个O原子和1个N原子为赤道配位原子, 而CSnC为配合物的轴。相邻配合物分子间因Sn…O的弱相互作用和分子间氢键的作用而以二聚体的结构形式存在。 展开更多
关键词 二有机锡配合物 2-羰基丙酸水杨酰腙 合成 晶体结构 二正丁基氧化锡 抗癌活性
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双水杨醛缩乙二胺氧钒配合物的合成和晶体结构 被引量:1
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作者 李连之 许涛 +1 位作者 王大奇 杜凌云 《化学研究与应用》 CAS CSCD 北大核心 2004年第5期664-666,共3页
The complex VO(SALEN)was synthesized by the reaction of vanadyl sulfate and H2salen.The complex was dissolved in CH2Cl2 and green needle crystal was obtained.It was characterized by elemental analysis,IR and X-ray d... The complex VO(SALEN)was synthesized by the reaction of vanadyl sulfate and H2salen.The complex was dissolved in CH2Cl2 and green needle crystal was obtained.It was characterized by elemental analysis,IR and X-ray diffraction analysis.The complex (C16H14N2O3V,Mr=333.23)belongs to triclinic with space group of Pī.The cell parameters are a=6.678(4)*!,b=1.4663(8)*!,c=15.094,α=102.27(11)°β=92.700(10)°γ=98.387(10)°,V=1424.2(13)*!3,Z=4,Dc=1.554g·cm-3,F(000)=684,μ=0.710mm-1,R1=0.0710,WR2=0.0783.The VO2+ion is five-coordinated to form distorted square pyramid.The thermal decomposition for the complex was investigated and the apparent activation energy was obtained by the Kissinger formula. 展开更多
关键词 钒配合物 合成 晶体结构 热分析
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芳酰腙配体与Ni(Ⅱ)和Co(Ⅱ)配合物的水热合成与晶体结构(英文) 被引量:1
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作者 郑长征 王亮 刘娟 《无机化学学报》 SCIE CAS CSCD 北大核心 2012年第3期637-642,共6页
由苯亚甲基苯乙酮和苯甲酰肼合成一种新型双齿(O、N)酰腙配体(苯亚甲基苯乙酮苯甲酰腙)。由水热法合成了两种配合物[M(babh)2(py)2](M=Ni,1;Co,2;Hbabh=苯亚甲基苯乙酮苯甲酰腙,py=吡啶),并用元素分析、红外、热重及X-射线单晶衍射对其... 由苯亚甲基苯乙酮和苯甲酰肼合成一种新型双齿(O、N)酰腙配体(苯亚甲基苯乙酮苯甲酰腙)。由水热法合成了两种配合物[M(babh)2(py)2](M=Ni,1;Co,2;Hbabh=苯亚甲基苯乙酮苯甲酰腙,py=吡啶),并用元素分析、红外、热重及X-射线单晶衍射对其进行了表征。晶体结构分析结果表明:两个化合物均属单斜晶系,空间群均是P21/n。化合物1和2通过分子间弱的C-H…π堆积形成二维片状超分子层。 展开更多
关键词 席夫碱 酰腙配体 水热合成 配合物 晶体结构
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5-溴-2-羟基苯基甲基酮对甲氧基苯甲酰腙铜(Ⅱ)配合物的合成及其晶体结构 被引量:1
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作者 王亮 刘娟 郑长征 《合成化学》 CAS CSCD 北大核心 2011年第5期648-651,共4页
5-溴-2-羟基苯基甲基酮与对甲氧基苯甲酰肼缩合制得新型配体5-溴-2-羟基苯基甲基酮对甲氧基苯甲酰腙(LH);LH与氯化铜的吡啶溶液在甲醇中于120℃通过水热合成制得铜(Ⅱ)配合物(CuLPy),其结构经XRD,IR和元素分析表征。CuLPy属单斜晶系,空... 5-溴-2-羟基苯基甲基酮与对甲氧基苯甲酰肼缩合制得新型配体5-溴-2-羟基苯基甲基酮对甲氧基苯甲酰腙(LH);LH与氯化铜的吡啶溶液在甲醇中于120℃通过水热合成制得铜(Ⅱ)配合物(CuLPy),其结构经XRD,IR和元素分析表征。CuLPy属单斜晶系,空间群C2/c,晶胞参数a=2.090 4(18)nm,b=1.348 0(12)nm,c=1.473 3(14)nm,β=104.584(2)°,V=4.017 9(6)nm3,Z=8,Dc=1.669 g.cm-3。 展开更多
关键词 酰腙 铜配合物 合成 晶体结构
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