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1.
Armelao L Bottaro G Quici S Cavazzini M Scalera C Accorsi G 《Dalton transactions (Cambridge, England : 2003)》2011,40(43):11530-11538
Innovative Tb(3+) antenna complexes employing two different substituted 2-hydroxyphthalamide ligands (HxOH-IAM and bis-HxOH-IAM) acting simultaneously as coordinating sites and light collector units have been synthesized and successively anchored in silica layers by the sol-gel technique. The complexes show remarkable photoluminescence (PL) quantum yields in methanol solution, as high as 0.30 and 0.40 for (HxOH-IAM)(4)?Tb(3+) and (bis-HxOH-IAM)(2)?Tb(3+), respectively. The grafting of the Tb(3+) complexes in silica single layers accomplished by exploiting the terminal hydroxyl groups of the IAM chains results in highly transparent and homogeneous films displaying bright green emission and PL efficiencies of up to 0.40. The silica layers containing the (bis-HxOH-IAM)(2)?Tb(3+) show remarkable photostability even under prolonged and continuous irradiation (up to 3.5 h). The nature of the IAM ligands allows the photoexcitation of the complexes at wavelengths even longer than 350 nm, which is a spectral window suitable to develop luminescent lanthanide probes dedicated to bioanalyses and bioimaging applications. 相似文献
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Wang D Yang P Cheng Z Wang W Hou Z Dai Y Li C Lin J 《Journal of colloid and interface science》2012,365(1):320-325
Gd(2)(WO(4))(3) doped with Eu(3+) or Tb(3+) thin phosphor films with dot patterns have been prepared by a combinational method of sol-gel process and microcontact printing. This process utilizes a PDMS elastomeric mold as the stamp to create heterogeneous pattern on quartz substrates firstly and then combined with a Pechini-type sol-gel process to selectively deposit the luminescent phosphors on hydrophilic regions, in which a Gd(2)(WO(4))(3):Ln(3+) (Ln=Eu, Tb) precursor solutions were employed as ink. X-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence (PL) spectra, as well as low voltage cathodoluminescence (CL) spectra were carried out to characterize the obtained samples. Under ultraviolet excitation and low-voltage electron beams excitation, the Gd(2)(WO(4))(3):Eu(3+) samples exhibit a strong red emission arising from Eu(3+)(5)D(0,1,2)-(7)F(1,2) transitions, while the Gd(2)(WO(4))(3):Tb(3+) samples show the green emission coming from the characteristic emission of Tb(3+) corresponding to (5)D(4)-(7)F(6,5,4,3) transitions. The results show that the patterning of rare earth-doped phosphors through combining microcontact printing with a Pechini-type sol-gel route has potential for field emission displays (FEDs) applications. 相似文献
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Tb掺杂SiO2-B2O3-NaF玻璃的制备及发光性质 总被引:5,自引:0,他引:5
使用正硅酸乙酯、硼酸和氟化钠为前驱体,0.10 mol•L-1TbCl3溶液为掺杂剂,通过溶胶-凝胶方法制备了Tb3+掺杂的SiO2-B2O3-NaF玻璃,研究了Tb3+在SiO2-B2O3-NaF体系中的发光性质,结果显示发光体能产生强的绿色发光(544 nm),归属于Tb3+的5D4—7F5电子跃迁.Tb3+含量不同时,除发光强度不同外,其发射光谱基本相同,并且在低掺杂Tb3+样品和低退火温度样品中检测到了来自5D3跃迁产生的峰,其跃迁随Tb3+掺杂浓度的增加和退火温度的升高而发生猝灭,这种现象归因于5D3-5D47F6—7F0和/或5D3—7F07F6—5D4跃迁中发生了交叉弛豫现象.Tb3+在SiO2-B2O3-NaF玻璃中的激发光谱由一个宽峰和一系列窄峰组成,宽峰最大波长位于230 nm,对应于Tb3+的4f 8—4f 75d 1跃迁,一系列窄峰位于300~380 nm处,归属于4f 8跃迁,所有发光材料的XRD和TEM测试显示材料是非晶态的. 相似文献
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A mild sol-gel technique was used to incorporate terbium dibenzoyl-L-cystine complex into silica and green luminescent hybrid material was fabricated. (1)H NMR and fluorescence spectroscopy revealed the hybrids can recognize F(-) anions through hydrogen bonding formation and had no sense in binding other halide or HSO(4)(-). Furthermore, a luminescent hydrogel was successfully designed by immobilizing a terbium activated phosphor (Gd(0.1)Ce(0.9)PO(4):Tb) into molecular hydrogelator (dibenzoyl-L-cystine). The Tb(III) emission in hydrogel media gave a distinguished enhancement based on temperature increase and the function conforms to exponential equation y = 1160.6 exp(0.03x). The stability of the green luminescent gel was rather excellent and the reversibility of the gel can be recycled at least five times. 相似文献
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Zengpeng Fan Yige Wang Zhixin Xue Li Zhang Yuhuan Chen Shuming Zhang 《Journal of Sol-Gel Science and Technology》2014,72(2):328-333
The sol–gel fabrication of luminescent and transparent thin film of ionogels containing trivalent lanthanide complexes have been obtained from the silylated ionic liquid in the presence of lanthanide salts (Ln3+, Ln=Tb and Eu) and organic ligands. The resulting thin films were investigated by FT-IR spectroscopy, scanning electron microscopy and luminescence spectroscopy. FT-IR spectra reveal the hydrolysis and condensation of the silylated ionic liquid as well as the formation of luminescent lanthanide complexes in the thin films. Scanning electronic microscope images show the homogeneous characteristic of the thin films. 相似文献
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Cui Y Xu H Yue Y Guo Z Yu J Chen Z Gao J Yang Y Qian G Chen B 《Journal of the American Chemical Society》2012,134(9):3979-3982
A luminescent mixed lanthanide metal-organic framework approach has been realized to explore luminescent thermometers. The targeted self-referencing luminescent thermometer Eu(0.0069)Tb(0.9931)-DMBDC (DMBDC = 2, 5-dimethoxy-1, 4-benzenedicarboxylate) based on two emissions of Tb(3+) at 545 nm and Eu(3+) at 613 nm is not only more robust, reliable, and instantaneous but also has higher sensitivity than the parent MOF Tb-DMBDC based on one emission at a wide range from 10 to 300 K. 相似文献
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A supramolecular microfluidic optical chemosensor (muFOC) has been fabricated. A serpentine channel has been patterned with a sol-gel film that incorporates a cyclodextrin supramolecule modified with a Tb(3+) macrocycle. Bright emission from the Tb(3+) ion is observed upon exposure of the (mu)FOC to biphenyl in aqueous solution. The signal transduction mechanism was elucidated by undertaking steady-state and time-resolved spectroscopic measurements directly on the optical chemosensor patterned within the microfluidic network. The presence of biphenyl in the cyclodextrin receptor site triggers Tb(3+) emission by an absorption-energy transfer-emission process. These results demonstrate that the intricate signal transduction mechanisms of supramolecular optical chemosensors are successfully preserved in microfluidic environments. 相似文献
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Armelao L Bottaro G Quici S Cavazzini M Raffo MC Barigelletti F Accorsi G 《Chemical communications (Cambridge, England)》2007,(28):2911-2913
Highly stable Eu(III) and Tb(III) complexes, emitting in the red and green visible regions, respectively, have been anchored onto a single SiO(2) transparent layer, yielding ca. 40 nm thick films; this allows high loading of tailored proportions of the red and green emitters within the films and results in highly uniform and easily colour-tunable luminescent layers. 相似文献
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Anna M. Kaczmarek Ying‐Ya Liu Mariusz K. Kaczmarek Hengshuo Liu Flavia Artizzu Luís D. Carlos Pascal Van Der Voort 《Angewandte Chemie (International ed. in English)》2020,59(5):1932-1940
Covalent Organic Frameworks (COFs), an emerging class of crystalline porous materials, are proposed as a new type of support for grafting lanthanide ions (Ln3+) and employing these hybrid materials as ratiometric luminescent thermometers. A TpBpy‐COF—prepared from 1,3,5‐triformylphloroglucinol (Tp) and 2,2′‐bipyridine‐5,5′‐diamine (Bpy) grafted with Eu/Tb and Dy acetylacetone (acac) complexes can be successfully used as a luminescent thermometer in the 10–360 K (Eu) and 280–440 K (Tb) ranges with good sensing properties (thermal sensitivity up to 1.403 % K?1, temperature uncertainty δT<1 K above 110 K). For the Eu/Tb systems, we observe an unusual and rarely reported behavior, that is, no thermal quenching of the Tb3+ emission, a result of the absence of ion‐to‐ligand/host energy back‐transfer. The LnCOF materials proposed here could be a new class of materials employed for temperature‐sensing applications following up on the well‐known luminescent metal–organic framework thermometers. 相似文献
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By using Tb3+ as a luminescent probe, we demonstrate that the phosphorylation state of a 14-residue peptide fragment of alpha-synuclein, a protein implicated in Parkinson's Disease, dramatically affects the metal ion affinity of the peptide. Whereas the unphosphorylated peptide and its phosphoserine analogue show weak Tb3+ binding, its phosphotyrosine analogue shows tight 1:1 binding as well as 2:1 and 3:1 Tb:peptide adducts. Our data suggest that the phosphorylated amino acid must be appropriately positioned among additional ligating residues to establish this phosphorylation-dependent metal binding. 相似文献
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Four new rare earth gallosilicates, Rb 2REGaSi4O12 (RE = Y, Eu, Gd, and Tb, denoted as REGS-1), have been synthesized under high-temperature, high-pressure hydrothermal conditions and characterized by single-crystal X-ray diffraction. They are the first examples of rare earth gallosilicates that contain individually occupied tetrahedral Ga(3+) and Si(4+) centers. The unique structure is formed of two 1D and one 2D substructural units: unbranched achter single chains which are seldom observed in silicates, the PaCl 5-type infinite chains formed of edge-sharing REO7 petagonal bipyramids and the unprecedented mixed-anion double layers with the composition [GaSi4O12]. The photoluminescence properties of EuGS-1 and TbGS-1 have been studied. The Y(3+) ion in YGS-1 can be partially replaced by Eu(3+) and Tb(3+) to yield luminescent materials. 相似文献
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The synthesis and photophysical properties of novel luminescent ruthenium(II) bipyridyl complexes containing one, two, or six lower rim acid-amide-modified calix[4]arene moieties covalently linked to the bipyridine groups are reported which are designed to coordinate and sense luminescent lanthanide ions. All the Ru-calixarene complexes synthesized in this work are able to coordinate Nd(3+), Eu(3+), and Tb(3+) ions with formation of adducts of variable stoichiometry. The absorbance changes allow the evaluation of association constants whose magnitudes depend on the nature of the complexes as well as on the nature of the lanthanide cation. Lanthanide cation complex formation affects the ruthenium luminescence which is strongly quenched by Nd(3+) ion, moderately quenched by the Eu(3+) ion, and poorly or moderately increased by the Tb(3+) ion. In the case of Nd(3+), the excitation spectra show that (i) the quenching of the Ru luminescence occurs via energy transfer and (ii) the electronic energy of the excited calixarene is not transferred to the Ru(bpy)(3) but to the neodymium cation. In the case of Tb(3+), the adduct's formation leads to an increase of the emission intensities and lifetimes. The reason for this behavior was ascribed to the electric field created around the Ru calix[4]arene complexes by the Tb(3+) ions by comparison with the Gd(3+) ion, which behaves identically and can affect ruthenium luminescence only by its charge. However, especially for compounds 1 and 3, it cannot be excluded that some contribution comes from the decrease of vibrational motions (and nonradiative processes) due to the rigidification of the structure upon Tb(3+) complexation. In the case of Eu(3+), compounds 1, 2, and 4 were quenched by the lanthanide addition but the quenching of the ruthenium luminescence is not accompanied by europium-sensitized emission which suggests that an electron-transfer mechanism is responsible for the quenching. On the contrary, compound 3 exhibits enhanced emission upon addition of Eu(3+) (as nitrate salt); it is suggested that the lack of quenching in the [3.2Eu(3+)] adduct is due to kinetic reasons because the electron-transfer quenching process is thermodynamically allowed. 相似文献
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A novel [2]pseudorotaxane was successfully constructed by the complexation of dibenzo[24]-crown-8 (DB24C8) derivative bearing terpyridine moiety (1) with lanthanide ion (Tb(3+)) and fullerene-containing ammonium salt (2), exhibiting the controlled photophysical behaviors as a reversible luminescent lanthanide switch in the presence of K(+) or 18-crown-6 (18C6). 相似文献
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Yali Li Dr. Yang Xu Prof. Yige Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(31):10976-10982
Highly transparent ultrathin films (UTFs) based on alternative layer‐by‐layer assembly of Eu‐ and Tb‐based lanthanide complexes (LCs) and Mg–Al‐layered double hydroxide (LDH) nanosheets are reported herein. UV–visible absorption and fluorescence spectroscopy showed an orderly growth of the two types of ultrathin films upon increasing the number of deposition cycles. AFM and SEM measurements indicate that the films feature periodic layered structures as well as uniform surface morphology. Luminescent investigations reveal that (LCs/LDH)n UTFs can detect Fe3+ with relative selectivity and high sensitivity (Stern–Volmer constant KSV=8.43×103 L mol?1); this suggests that (LCs/LDH)n UTFs could be a promising luminescent probe for selectively sensing Fe3+ ion. 相似文献
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Zhai X Yu M Cheng Z Hou Z Ma P Yang D Kang X Dai Y Wang D Lin J 《Dalton transactions (Cambridge, England : 2003)》2011,40(48):12818-12825
Rattle-type hollow nanocapsules are among of the most promising candidates as drug carriers owing to their huge inner space and multifunctional material combination. In this paper, rattle-type hollow CaWO(4):Tb(3+)@SiO(2) nanocapsules with a diameter of 100-110 nm and a wall thickness around 10 nm were fabricated. The hollow silica nanospheres were used as nano-reactors and the luminescent core of CaWO(4):Tb(3+) was post-filled into the nano-reactors by a vacuum nano-casting route combined with a Pechini-type sol-gel method. Subsequently, doxorubicin hydrochloride (DOX), a model of an anti-cancer drug, is loaded into the CaWO(4):Tb(3+)@SiO(2) nanocapsules and their cell cytotoxicity, cancer cell uptake and drug release behavior are investigated in vitro. The prepared multifunctional inorganic nanocapsules show a loading capacity for DOX as high as 124 mg g(-1) and sustained-release properties. The release profile of the drug from DOX-loaded nanocapsules can last over five days. Besides, the blank CaWO(4):Tb(3+)@SiO(2) shows very low cytotoxicity against cancer cell lines (HeLa cell) while the DOX-loaded nanocapsules exhibit relatively high efficiency for killing of HeLa cells. The rapid cancer cell uptake process is observed by confocal laser scanning microscopy. The results indicate that a rattle-type hollow CaWO(4):Tb(3+)@SiO(2) nanocapsule has the potential to be used as drug carrier in therapy. Moreover, it is possible to extend the synthetic strategy in this study to other rattle-type multifunctional composites to meet various demands. 相似文献
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A flow-injection chemiluminescence (CL) method, based on the luminescent properties of the Ce(IV)-Na2SO3-lanthanide(III)-grepafloxacin system, was developed for the determination of grepafloxacin {1-cyclopropyl-6-fluoro-1,4-dihydro-5-methyl-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid}. La(III), Tb(III), and Eu(III) ions were tested as possible chemiluminescence sensitizers. The best results were achieved when Tb(III) was used as lanthanide ion, so the technique was optimised working with this ion. Under the optimum experimental conditions, the linear range was 0.05-2.00 μg ml−1 grepafloxacin, with a 0.01 μg ml−1 detection limit and 2.0% relative standard deviation (n=10). The proposed procedure has been applied to the determination of grepafloxacin in tablets and spiked human urine. 相似文献