OPTICAL MATERIALS
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2019
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IF 2.687
Jiang Wu,Haowen Bai,Wenjie Qu,Guanying Cao,Yanjie Zhang,Jingjie Yu
CsPbBr 3 quantum-dot borosilicate microcrystals and Eu 3+ -doped CsPbBr 3 quantum-dot microcrystals with different concentrations of Eu 3+ are successfully prepared by high temperature melting. The particle morphology of the microcrystals is characterized by scanning electron microscopy (SEM). The fluorescence characteristics are analyzed by fluorescence spectroscopy and CIE chromaticity coordinates . In this research, CsPbBr 3 quantum dots are effectively coated with borosilicate microcrystals to improve the stability of CsPbBr 3 quantum dots while ensuring its strong green emission at 517 nm. The energy transfer from CsPbBr 3 quantum dots to Eu 3+ occurs after doping. When changing the concentration of Eu 3+ , the emission peaks of perovskite broaden and blue shift occurs (517 nm→474 nm). The CIE color coordinate moves from (0.0807, 0.7200) to (0.4537, 0.2724). Therefore, the continuous adjustment of solid perovskite materials from green light to blue light and then to red light region is realized.
研究领域:
材料科学
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纳米光学
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无机非金属材料
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光电子学
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发光材料
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固态化学
✓ 已验证
DOI
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2016
·
IF 2.653
Xue-Dong Xiao,Lin Shi,Li-Hui Guo,Jun-Wen Wang,Xiang Zhang
The supramolecular interaction between the water-soluble pillar[5]arene (WP[5]) as host and dopamine hydrochloride (DH) as guest was studied by spectrofluorometry . The fluorescence intensity of DH gradually decreased with increasing WP[5] concentration, and the possible interaction mechanism between WP[5] and DH was confirmed by 1 H NMR, 2D NOESY , and molecular modelling. Based on significant DH fluorescence, a highly sensitive and selective method for DH determination was developed for the first time. The fluorescence intensity was measured at 312 nm, with excitation at 285 nm. The effects of pH, temperature, and reaction time on the fluorescence spectra of the WP[5]-DH complex were investigated. A linear relationship between fluorescence intensity and DH concentration in the range of 0.07–6.2 μg mL − 1 was obtained. The corresponding linear regression equation is Δ F = 25.76 C + 13.56 (where C denotes the concentration in μg mL − 1 ), with the limit of detection equal to 0.03 μg mL − 1 and the correlation coefficient equal to 0.9996. This method can be used for the determination of dopamine in injection and urine samples. In addition, the WP[5]-DH complex has potential applications in fluorescent sensing and pharmacokinetics studies of DH.
研究领域:
分析化学
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超分子化学
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药物代谢
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生物分析
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药代动力学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2014
·
IF 2.354
Ni Cheng,Xiaoyuan Ma,Xiang Sheng,Tao Wang,Rui Wang,Jingjing Jiao,Li Yu
Two structurally similar imidazolium-based anionic surface active ionic liquids (SAILs) with double hydrocarbon chains, viz. 1-butyl-3-methylimidazolium bis(2-ethylhexyl) sulfosuccinate (C 4 mim-AOT) and 1-butyl-3-methylimidazolium bis(2-ethylhexyl) phosphate (C 4 mim-DEHP), were synthesized by a straightforward ion-exchange technique. A comparative investigation of their aggregation behavior with the corresponding traditional anionic surfactants, sodium bis(2-ethylhexyl) sulfosuccinate (Na-AOT) and sodium bis(2-ethylhexyl) phosphate (Na-DEHP) in aqueous solution was performed in detail by surface tension, electric conductivity, fluorescence spectra and dynamic light scattering measurements. The critical micelle concentration (CMC) values for the surfactants with double hydrocarbon chains obtained by different techniques are in good agreement. The surface activity of C 4 mim-AOT and C 4 mim-DEHP is superior to that of the corresponding traditional anionic surfactants, Na-AOT and Na-DEHP. It is also found that for anionic SAILs the nature of the anionic active group is a dominant factor in the determination of their aggregation behavior in aqueous solution, e.g. CMC and aggregation number, while the introduced organic cation plays a minor role. Theoretical calculations show that more conformations and electronegativity for DEHP anion leads to higher aggregation number and CMC values for C 4 mim-DEHP. This work is expected to be of practical values for the environmental friendly anion SAILs in nanomaterial synthesis and phase separation, etc.
研究领域:
物理化学
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胶体与界面化学
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纳米材料合成
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环境友好材料
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分子自组装
✓ 已验证
DOI
高影响因子
INORGANIC CHEMISTRY COMMUNICATIONS
·
2022
·
IF 3.428
Baoqin Mu,Bin Li,Bin Qi
Lanthanide metal–organic framework Ln-MOFs(Ln = Sm, Dy, Dy/Sm) were synthesized by hydrothermal method at 100 °C for 12 h using lanthanide metals (Ln = Sm, Dy, Dy/Sm) as metal ion centers and 1,3,5-benzotrioic acid (H 3 BTC) as ligands. The structural characteristics of Ln(BTC)(H 2 O)·(DMF) were characterized by X-ray Diffraction(XRD), Fourier Transform Infrared Spectroscopy(FT-IR) and Thermogravimetric Analysis(TGA). Scanning electron microscopy showed that the samples showed rod-like morphology, and the fluorescence spectra showed 478 nm and 573 nm corresponding to the characteristic transitions of 4 F 9/2 → 6 H 15/2 (blue light) and 4 F 9/2 → 6 H 13/2 (yellow light) of Dy 3+ , respectively, while orange light at 600 nm and red light at 646 nm corresponded to the characteristic transitions of 4 G 5/2 → 6 H 7/2 and 4 G 5/2 → 6 H 9/2 of Sm 3+ , demonstrating that the double-doped lanthanide metal ions MOF were successfully synthesized. H 7 (P(Mo 2 O 7 ) 6 )/(Dy/Sm-MOF) was used as a sensor for the determination of H 2 PO 4 − , the results of performance evaluation showed that the electrochemical sensor showed a linear relationship between 0.01 and 0.17 mM for H 2 PO 4 − , with a detection limit of 0.005 mM/L, good stability and reproducibility, which opened up a new way for the detection of orthophosphate dihydrogen.
研究领域:
分析化学
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材料科学
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电化学
·
无机化学
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传感器技术
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2014
·
IF 2.354
Tianxiang Yin,Miao Qin,Weiguo Shen
The interactions of Gemini surfactants 1-dodecyl- N , N ′-[(1,4-dioxo-1,4-butanediyl)bis(oxy-2,1-ethanediyl)]bis[ N , N ′-dimethylammonium]dibromide (12-su-12) and 1-dodecyl- N , N ′-[((2 E )-1,4-dioxo-2-butene-1,4-diyl)bis(oxy-2,1-ethanediyl)]bis[ N , N ′-dimethylammonium]dibromide (12-fo-12) and the corresponding single-chain surfactant 1-dodecyl- N -[2-(acetyloxy)ethyl]- N , N -dimethyl ammonium bromide (DTAAB) with bovine serum albumin (BSA) were investigated by conductometry, fluorimetry, UV–vis and CD spectrometry, and dynamic light scattering. It was found that the bindings of all three surfactants to BSA were cooperatively driven by electrostatic and hydrophobic interactions. The Gemini surfactants, carrying more charges and hydrophobic tails, showed stronger interactions with BSA than the single-chain surfactant. The presence of the double bond in the spacer of 12-fo-12 enhanced the interaction between the surfactant and BSA and also significantly varied the binding sites as compared to 12-su-12 and DTAAB, which indicated an important role of the property of the spacer in the interaction between the surfactant and BSA.
研究领域:
生物物理化学
·
分子生物学
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药物递送
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蛋白质科学
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纳米医学
✓ 已验证
DOI
高影响因子
JOURNAL OF LUMINESCENCE
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2013
·
IF 2.144
XiaoDan Zeng,Lin Zhu,FuSheng Zhang,LiYun Feng
The interaction of bovine serum with leucomalachite green (LMG) was investigated by spectroscopic methods . LMG was found to quench the intrinsic fluorescence of BSA by dynamic quenching. High quenching constant suggested that LMG can form a complex with BSA. Binding constant and number of binding site were determined. The thermodynamic parameters suggested the main interacting force is hydrophobic forces . The effect of LMG on the conformation of BSA was analyzed by synchronous fluorescence spectroscopy . RLS spectra were also used to reconfirm the formation of complex between BSA and LMG.
研究领域:
生物化学
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分子生物学
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光谱学
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药物代谢
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蛋白质-配体相互作用
✓ 已验证
DOI
高影响因子
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY
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2016
·
IF 3.035
Xiaoyi Liu,Zhaoxing Ling,Xing Zhou,Farooq Ahmad,Ying Zhou
Butachlor is an effective herbicide to deal with undesired weeds selectively and is used at high levels in Asian countries. However, its interaction and impairment effect on BSA was still not clear. In this study, we investigated the interaction between butachlor and bovine serum albumin (BSA) by multi-spectroscopic methods including UV absorption , circular dichroism (CD) spectra, Fourier transform infrared (FTIR) spectra and fluorescence spectra under physiological conditions (pH = 7.4). The results revealed that there was a static quenching of BSA induced by butachlor stemmed from the formation of complex. Based on thermodynamic data, the interaction of butachlor with BSA was due to happen, and van der Waals force as well as hydrogen bond were the major forces contributed to the interaction. The binding constant K b and number of binding site of butachlor with BSA were 5.158 × 10 5 and 1.372 at 303 K, respectively. The distance r between donor (BSA) and acceptor (butachlor) was 0.113 nm, obtained according to the Förster theory. The results revealed that butachlor induced conformational changes in BSA but the secondary structure of BSA was still retained. In addition, the microenvironment around chromophore residues of BSA, for example, tryptophan , changed as well, resulting from the formation of more hydrogen bonds.
研究领域:
生物化学
·
分子药理学
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药物代谢
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环境毒理学
·
蛋白质科学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2016
·
IF 2.76
Shanshan Zhang,Xuerui Chen,Shiping Ding,Qunfang Lei,Wenjun Fang
The interactions of human serum albumin (HSA) with four cationic gemini surfactants and four single-chain surfactants have been investigated from the measurements of fluorescence spectroscopy, dynamic lights scattering (DLS), zeta potential, and circular dichroism (CD). The fluorescence results show the binding strength of surfactants to HSA, along with the blue shift under the maximum emission wavelength ( λ max ) which is sensitive to the protein conformations. It has been found that the hydrodynamic diameters of the protein aggregates are enlarged and the electrokinetic potentials of them get positive with increasing the concentration of the surfactants. The conformational transformation of the secondary structures of surfactant–HSA aggregates has been confirmed through the quantitative analysis of the CD spectra. The isothermal titration microcalorimetry (ITC) has been employed to further analyze the binding process of single-chain surfactants to HSA. The comprehensive results obtained from various approaches have shown that both hydrophobic and electrostatic interactions are present in the cationic surfactant–HSA systems. Compared with the corresponding single-chain surfactants, the gemini ones have much stronger binding ability to induce the unfolding of HSA. These investigations on the interactions between HSA and surfactants with the altered chain architecture in different concentration regimes can facilitate the application of surfactant-protein systems in pharmaceutical, biotechnology and related fields.
研究领域:
生物物理化学
·
分子生物学
·
药剂学
·
蛋白质科学
·
药物代谢
·
胶体与界面科学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）