JOURNAL OF COORDINATION CHEMISTRY
·
2017
·
IF 1.795
Shan-Shan Zhao,Peng Wang,Li-Na Wang,Lin Fu,Xiao-Meng Han,Jie Qin,Shao-Song Qian
The multidentate Schiff-base ligand N′-(1-(pyrazin-2-yl)ethylidene)isonicotinohydrazide (HL) has been prepared. Reaction with zinc, copper, and silver nitrate afford three complexes, [Zn(HL′)2](NO3)2·3H2O (1), {[Cu2(L)2(NO3)(H2O)2]·NO3}n (2) and {[Ag2(L)2]·3H2O}n (3). These complexes have been characterized by elemental analysis, IR spectroscopy, and single-crystal X-ray diffraction. In 1, HL is a neutral tridentate ligand, whereas in 2 and 3, HL is a deprotonated tetradentate ligand. The hydrogen bonding interactions between NO3− and the host framework result in various supramolecular polymeric structures: a 2-D layer for 1 and 3-D network for 2 and 3. The antibacterial activities of these complexes have been investigated and the results indicate that 3 showed good antibacterial activities.
研究领域:
无机化学
·
材料科学
·
药物化学
✓ 已验证
DOI
高影响因子
JOURNAL OF COORDINATION CHEMISTRY
·
2024
·
IF 2.2
Ying Zhou,Xiao-Tong Song,Hui-Chao Guan,Shu-Mei Yue
In this investigation, six new metal complexes with 2-(pyridin-2-yl)benzo[d]imidazole (bpm) were synthesized and analyzed by single-crystal X-ray diffraction (XRD), including catena-bis[(µ-2,2-bis(4-carobxyphenyl)hexafluoropropane)-(2-(pyidin-2-yl)-1H-benzimidazole)-aqua-zinc] (1), catena-[(µ-2,2-bis(4-carobxyphenyl)hexafluoropropane)-(2-(pyidin-2-yl)-1H-benzimidazole)-aqua-cadmium] (2), aqua-[2,2-bis(4-carobxyphenyl)hexafluoropropane]-bis[2-(pyridin-2-yl)-1H-benzimidazole]-manganese (3), μ-[2-nitrobenzene-1,4-dicarboxylato]-μ-[2-nitrobenzene-1,4-dicarboxylato]-bis[2-(pyridin-2-yl)-1H-benzimidazole]-di-zinc (4), catena-[bis(µ-2-nitrobenzene-1,4-dicarboxylato)-diaqua-bis(2-(pyridin-2-yl)-1H-benzimidazole)-di-cadmium] (5), aqua-[pyridine-2,6-dicarboxylato]-[2-(pyridin-2-yl)-1H-benzimidazole]-copper hydrate (6) (H2hfipbb = 2,2-bis(4-carboxyphenyl)hexafluoropropane, H2nbdc acid = Nitroterephthalic acid, and H2pda = 2,6-pyridinedicarboxylic acid). Complex 1 crystallized in a monoclinic system with space group P21/n; 2 crystallized in a monoclinic system with space group C2/c; 3 crystallized in an orthorhombic system with space group Pna21; 5 crystallized in a monoclinic system with space group P21/c; 4 and 6 crystallized in triclinic systems with space group P-1. The DNA-binding modes of the complexes were investigated by several analysis methods (e.g. viscosity analysis, circular dichroism spectroscopy, fluorescent spectroscopic analysis, as well as UV spectroscopic analysis). Complexes 1-6 bind to calf thymus DNA via an intercalative mode. The results of this study provide insights into the mechanism of DNA binding and provide a basis for rationally designing new powerful reagents for DNA detection and targeting.
研究领域:
化学
·
生物化学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COORDINATION CHEMISTRY
·
2025
·
IF 2.1
Hou Cong Li,Ming Zhu Wang,Ye Fan Zheng,Ning An,Min Hou,Jing Hu,Wen Ge Li
Three chlorinated metal complexes [Ni2(HL)2(C2H5OH)2Cl2]·2C2H5OH (complex 1), [Co(HL)(L)] (complex 2), and [Zn2(HL)2(CH3COO)2] (complex 3) derived from 5-chlorosalicylaldehyde and 2-(2-aminophenyl)-1H-benzimidazole Schiff base ligand (H2L). The crystal structures of the three complexes were characterized by elemental analysis, infrared spectroscopy, thermogravimetric analysis, X-ray single-crystal diffraction, and UV-visible absorption spectrum. The in vitro cytotoxicity of chlorinated ligand and its metal complexes were evaluated on four different tumor cell lines (A-549 lung cancer, SMMC-7721 liver cancer, MDA-MB-231 breast cancer, and CNE-2Z nasopharyngeal carcinoma), and normal ovarian epithelial cell (IOSE 80) was determined by MTT assay. The results indicated that chloro-benzimidazole Schiff base Co (III) complex (complex 2) displayed higher cytotoxicity against MDA-MB-231 cell line than cisplatin, while the cytotoxicity on IOSE 80 was lower than that of cisplatin. The results of further study of MDA-MB-231 cells by complex 2 showed that complex 2 could inhibit MDA-MB-231 cells in the G0/G1 phase, inhibit cell proliferation and migration, promote cell apoptosis, and increase intracellular ROS level. The Western blot analysis demonstrated that complex 2 could increase Bax protein expression and decrease Bcl-2 protein expression in MDA-MB-231 cells.
研究领域:
无机化学
·
药理学
·
肿瘤学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF MOLECULAR STRUCTURE
·
2023
·
IF 3.8
Min Hou,Hou Cong Li,Ning An,Si Yan Pang,Wen Ge Li,Jing Tong
Three metal complexes [Ni 2 (HL) 2 (C 2 H 5 OH) 2 Cl 2 ]·2C 2 H 5 OH (complex 1), [Co (HL) (L)] (complex 2) and [Zn 2 (HL) 2 (CH 3 COO) 2 ] (complex 3) derived from 5-bromosalicylaldehyde-2-(2-aminophenyl)benzimidazole Schiff base ligand (H 2 L) were synthesized and characterized by infrared (IR) spectroscopy, thermogravimetric (TG) analysis and powder X-ray diffraction (XRD). Single crystal X-ray diffraction analysis confirmed that complex 1 crystallized in binuclear octahedral structure with space group P2 1 /C and complex 2 displayed in mononuclear octahedral structure with space group P 121/c 1. While complex 3 produced binuclear pyramid structure with space group P 121/c 1. Herein, cobalt (Ⅱ) salt was oxidized to form Schiff base cobalt (Ⅲ) complex by coordinating three deprotonated groups. The MTT method was employed to determine the three complexes in vitro cytotoxicity effects against human lung cancer cells (A-549), liver cancer cells (SMMC-7721), breast cancer cells (MDA-MB-231) and nasopharyngeal carcinoma cells (CNE-2Z). The results showed that Co (Ⅲ) complex has significant anticancer activity against human breast cancer MDA-MB-231 cells compared with cisplatin. The further study of its anticancer mechanisms exhibited that Co (Ⅲ) complex could inhibit MDA-MB-231 cells proliferation through both apoptosis and DNA replication inhibition.
研究领域:
无机化学
·
药物化学
·
肿瘤学
✓ 已验证
DOI
高影响因子
DYES AND PIGMENTS
·
2025
·
IF 4.2
Yuqing Yang,Shicong Pei,Mingdi Yang,Kehua Zhang,Jie Jin,Yunsheng Ding,Xianhai Hu
Full-color fluorescent tunable materials have attracted much attention due to their broad application prospects in fields such as lighting, display devices, and biological imaging. However, it remains challenging to prepare environmentally friendly full-color fluorescent tunable materials through simple and efficient methods. Herein, a series of amino-functionalized complexes were synthesized, and, via covalent bonding, a color-tunable waterborne polyurethane system (WPU-Eu 1-x-y Tb x Zn y ) was developed, exhibiting both full-color and white fluorescence. In addition, due to the inherent differences in the ultraviolet absorption properties of each complex, the emission color can be further adjusted by changing the excitation wavelength. This dual mechanism enables both preset and dynamic color adjustments, providing various possibilities for applications such as anti-counterfeiting and display technologies. More importantly, WPU-Eu 1-x-y Tb x Zn y uses water as a dispersant, has a low VOC content, and is particularly safe and environmentally friendly.
研究领域:
材料科学
·
光学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF STRUCTURAL CHEMISTRY
·
2022
·Vol. 63
·期 8
·1371-1381
·
IF 1.004
Jiang J.,Liu B.,Liu Y.,Jing C.,You Z.
Abstract Two new zinc(II) and nickel(II) complexes, [Zn 2 L(μ 2 -η 1 :η 1 -CH 3 COO)(μ 2 -η 1 :η 2 -CH 3 COO)] n ( 1 ) and [Ni 2 (HL) 2 (H 2 O) 2 (μ 1,3 -N 3 )]Cl·2H 2 O ( 2 ·2H 2 O), where L is the doubly deprotonated form of 4,4′-dimethoxy-2,2′-(propane-1,3-diyldiiminodimethylene)diphenol (H 2 L), were synthesized and characterized by elemental analyses, infrared and electronic spectroscopy, as well as single crystal X-ray diffraction. Complex 1 is a bidentate bridging and chelating bridging acetate bridged polymeric zinc complex. In the asymmetric unit of the complex, one Zn atom is in distorted trigonal bipyramidal coordination, and the other one is in octahedral coordination. Complex 2 ·2H 2 O is an end-to-end azide bridged dinuclear nickel complex. The Ni atoms are in octahedral coordination. The inhibitory property on Jack bean urease of the complexes was studied, and the nickel complex has effective activity.
研究领域:
无机化学
·
生物化学
✓ 已验证
DOI
高影响因子
JOURNAL OF FLUORESCENCE
·
2018
·Vol. 28
·期 6
·1269-1273
·
IF 1.665
Lu Dong,Tang Yiping,Zheng Yuhui
Alcoholic strength is a fundamental variable in industry production and its determination is crucial in technological developments. This study offers a novel strategy for fluorescent sensing of alcoholic content based on a terbium coordination complex. In pure water, the emissive compound displays blue luminescence. However, the addition of ethanol into the aqueous solution has induced the recovery of terbium green emissions. In another case, the achieved Eu(III)-phenanthroline complex shows high sensitivity to solvent polarity and the detection of trace amount of water can be realized through an “on-off” change with a low detection limit of 32.4 ppm.
研究领域:
分析化学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Russian Journal of Physical Chemistry A
·
2018
·Vol. 92
·期 11
·2257-2264
·
IF 0.549
Hong Shao,Ma Qianli,Yu Wensheng,Dong Xiangting,Wang Jinxian,Liu Guixia
Abstract Herein, we describe the innovative one-dimensional nanomaterials, electrospun composite nanoribbons (width 10.119 ± 0.186 μm) containing complexes of Eu(TTA) 3 (TPPO) 2 and Tb(BA) 3 phen in a matrix of polymethylmethacrylate (PMMA). Scanning electron microscopy (SEM), energy dispersive spectrometry (EDS) and fluorescence spectroscopy were used to characterize the final products. The novel luminescent composite nanoribbons exhibit green, orange and red fluorescence emission peaks at 490, 545, 592, and 615 nm, which are ascribed to the 5 D 4 → 7 F 6 (490 nm) and 5 D 4 → 7 F 5 (545 nm) energy transitions of Tb 3+ ions, and the 5 D 0 → 7 F 1 (592 nm), 5 D 0 → 7 F 2 (615 nm) transitions of Eu 3+ ions, respectively. It is observed that the doping percentage and the chosen excitation wavelength could be used to tune the emission color of the samples. The color-tunable luminescent composite nanoribbons have potential applications in the fields of display panels, lasers and bioimaging.
研究领域:
材料科学
·
光学
·
生物成像
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
·
2019
·Vol. 57
·期 7
·767-775
·
IF 2.591
Xianhui Zhang,Guangqian Zhu,Qaiser Mahmood,Mengmeng Zhao,Liang Wang,Chuyang Jing,Xiaowu Wang,Qinggang Wang
A stereoselectivity switchable polymerization of isoprene has been developed, which is catalyzed by iminoimidazole-Co(II) and -Fe(II) complexes. The influence of substituents ranging from electron donating to the electron withdrawing on the iminoimidazole-Co(II) and -Fe(II) catalysts is investigated for isoprene polymerization. Two sets of iminoimidazole-Co(II) and -Fe(II) complexes have been prepared and fully characterized. X-ray crystallography analysis reveals that the complexes Co1 and Fe1 adopt distorted tetrahedral geometries. In the presence of AlEt 2 Cl as co-catalyst, all the Co(II) complexes are active and the catalytic activity is highly dependent on the molar ratio of Al/Co. All the Co(II) complexes exhibit higher activities at low Al/Co ratio. Compared with the Co(II) complexes, the Fe(II) complexes are essentially inactive under the identical condition. However, on activation with combination of AlEtCl 2 and [Ph 3 C][B(C 6 F 5 ) 4 ], both Co(II) and Fe(II) complexes display high activities with good conversions of isoprene (up to >99%). Additionally, low molecular weight and high trans -1,4-unit (>96%) selectivity are characteristics of the resultant polyisoprene. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57 , 767–775
研究领域:
化学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of the American Chemical Society
·
2018
·
IF 14.357
Weiliang Guo,Hao Ding,Chaoyue Gu,Yanhuan Liu,Xuecheng Jiang,Bin Su,Yuanhua Shao
Electrochemiluminescence (ECL) is a highly successful technique used in commercial immunoassays for clinical diagnosis. Developing an ECL-based multiplex immunoassay, with the potential to enable high-throughput detection of multiple biomarkers simultaneously, remains a current research interest yet is limited by a narrow choice of ECL luminophores. Herein we report the synthesis, photophysics, electrochemistry, and ECL of several new ruthenium(II) and iridium(III) complexes, three of which are eventually used as signal reporters for multiplex immunoassay. The ECL behaviors of individual luminophores and their mixtures were investigated in multiple modes, including light intensity, spectrum, and image measurements. The spectral peak separation between Ru(bpy)2(dvbpy)2+ (bpy = 2,2′-bipyridine, dvbpy = 4,4′-bis(4-vinylphenyl)-2,2′-bipyridine), and Ir(dFCF3ppy)2(dtbbpy)+ (dFCF3ppy = 3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl]phenyl, dtbbpy = 4,4′-bis(tert-butyl)-2,2′-bipyridine) was up to 145 nm, thus providing the spectrum-resolved possibility of identifying light signals. The potential-resolved ECL signals were achieved for the mixtures of Ir(ppy)3 (ppy = 2-phenylpyridine) with either Ru(bpy)2(dvbpy)2+ or Ir(dFCF3ppy)2(dtbbpy)+, due to the self-annihilation ECL of Ir(ppy)3 at higher potentials, as confirmed by electrochemistry-coupled mass spectrometry. A multiplex immunoassay free of spatial spotting antibodies on plates or substrates was ultimately devised by combining luminophore-loaded polymer beads with the homogeneous sandwich immunoreaction. Using potential and spectrum dual-resolved ECL as the readout signal, simultaneous recognition of three antigens, namely, carcinoembryonic antigen (CEA), alpha-fetoprotein (AFP), and beta-human chorionic gonadotropin (β-HCG), was demonstrated in a single run for a sample volume of 300 μL. These results contribute to the understanding of ECL generation by multiple luminophores and devising spot-free multiplex immunoassays with less sample consumption.
研究领域:
分析化学
·
生物医学工程
·
临床诊断
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Journal of Inorganic and Organometallic Polymers and Materials
·
2013
·Vol. 24
·期 3
·582-590
·
IF 1.174
Li Xin,Bi Cai-Feng,Fan Yu-Hua,Zhang Xia,Zhang Nan,Yan Xing-Chen
A novel transition metal coordination polymer [Co 3 (C 14 H 8 NO 4 Cl) 4 (CH 3 OH) 4 ·4CH 3 OH] n with Schiff base (C 14 H 8 NO 4 Cl: 4-chloroanthranilic acid- 2,4-dihydroxybenzaldehyde) was synthesized using 4-chloroanthranilic acid, 2,4-dihydroxybenzaldehyde and cobalt(II) acetate as source, and its structure was characterized by IR spectroscopy, elemental analysis, 1 H NMR and single crystal X-ray diffraction. X-ray crystallography shows that every cobalt atom is six-coordinated. Two cobalt atoms on the two sides are respective coordinated with two nitrogen atoms from –C=N–, two carboxylic oxygen atoms and two hydroxyl oxygen atoms in different ligands, while the cobalt atom in the middle links two ligands on the side through two carboxylic oxygen atoms and coordinates with four oxygen atoms of methanol, forming a three-nuclear Co(II) complex. The complex forms a two-dimensional layer structure through O–H···O intermolecular hydrogen bonds. The interaction of the Co(II) complex with calf-thymus DNA (CT-DNA) was investigated by UV absorption spectroscopy, fluorescence emission spectroscopy, viscosity and cyclic voltammetry. All measurements revealed that the Co(II) complex binds to DNA via a intercalative mode.
研究领域:
无机化学
·
生物无机化学
·
分子生物学
✓ 已验证
产品关联
DOI
高影响因子
INORGANICA CHIMICA ACTA
·
2024
·
IF 2.7
Shi-Jie Xian,Tao Sun,Yan Li,Kai Wang
Six ternary lanthanide complexes with different β-diketones as primary “antenna” ligand and 2,2’:6’,2’’-terpyridine as neutral ancillary ligand, namely [Ln(hfac) 3 (tpy)] [Ln(III) = Eu ( 1 ), Gd ( 2 ), Tb ( 3 ); hfac = hexafluoroacetylacetone; tpy = 2,2’:6’,2’’-terpyridine] and [Ln(btfa) 3 (tpy)] [Ln(III) = Eu ( 4 ), Gd ( 5 ), Tb ( 6 ); btfa = 4,4,4-trifluoro-1-phenyl-1,3-butanedione], were synthesized and characterized by elemental analysis, infrared spectroscopy, thermogravimetric analysis, single crystal X-ray diffraction and powder X-ray diffraction. The three-dimensional Hirshfeld surface map and two-dimensional fingerprint analysis reveal that the substitution of hfac with btfa result in the decrease of the H···F/F···H and F···F interactions and the increase of the C···H/H···C and H···H interactions. Solid-state luminescence investigations indicate that the Eu(III) complexes ( 1 -Eu and 4 -Eu) and the Tb(III) complexes ( 3 -Tb and 6 -Tb ) display the characteristic lanthanide-centered luminescence upon UV excitations. 1 -Eu and 4 -Eu emit red light at CIE: 0.6827, 0.3172 and CIE: 0.6819, 0.3179 with the quantum yields (QY) of 78.70 % and 68.85 % and the lifetimes ( τ ) of 0.768 and 0.808 ms, respectively. 3-Tb and 6-Tb emit green light at CIE: 0.2677, 0.7221 and CIE: 0.2680, 0.7217 with the QY values of 7.56 % and 1.38 % and the τ values of 0.076 and 0.022 ms, respectively. For the Eu(III) complexes, the substitution of hfac by btfa makes the QY value lower from 78.70 % to 68.85 % and slightly prolong the τ value from 0.768 to 0.808 ms, while for the Tb(III) complexes, both of the QY and τ values decrease. The results suggest that the structures of the primary β-diketone ligands could affect the luminescence performances such as QY and τ values of the Eu(III) and Tb(III) complexes.
研究领域:
无机化学
·
材料科学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）