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1.
《Arabian Journal of Chemistry》2023,16(6):104672
X-rays are energy sources exhibiting extended penetration depths, and they have attracted increasing attention in industry and for clinical application. With the rapid development of nanomaterials and X-ray excited luminescent nanoparticles (XLNPs), new modalities for bioimaging and cancer therapy have been developed, such as X-ray luminescent computed tomography (XLCT) and X-ray excited photodynamic therapy (X-PDT). To meet the requirements of biomedical applications, XLNPs must exhibit high luminescence intensities, appropriate size distributions (less than100 nm) and negligible cytotoxicity. Due to the optical properties associated with f-electrons, rear earth (RE) elements are highly suitable for creating XLNPs. NaREF4 nanoparticles (NPs) have been shown to be suitable hosts with high luminescence intensities, controllable sizes, and biocompatibility for X-ray-based biomedical applications. Syntheses of NaLuF4 NPs doped with rare earth elements for upconversion applications have been systematically studied. However, for X-ray excited applications, the doping levels of the NPs must be totally different, which greatly affects the morphologies and sizes of the NaLuF4 NPs. Thus, in this paper, nucleation, phase transitions, morphologies and sizes, and luminescence properties of Tb3+-doped NaLuF4 NPs were systematically studied. OA-capped NaLuF4:Tb3+ NPs were synthesized via coprecipitation processes with different reaction temperatures and reaction times to study the nucleation mechanism systematically, and the morphologies, size distributions and crystal phases were characterized with TEM and XRD. The morphologies, size distributions and crystal phases of these NPs were seriously influenced by the reaction temperature and reaction time. At 295 ℃, the NP sizes increased with prolonged reaction time, and the crystalline phase was a mixture of cubic and hexagonal phases. At 300 ℃ and 310 ℃, the pure hexagonal phase was obtained after 20 min and 35 min reaction times, respectively. The luminescence strengths of these NPs were associated with the particle sizes, crystalline phases, and Tb3+ doping levels. Stronger luminescence was achieved with larger particle sizes and purer hexagonal crystal phases. In addition, the 15 % doping level for Tb3+ provided the maximum luminescence intensity. The present work provides insights into the mechanism of NaLuF4:Tb3+ nanocrystal growth. 相似文献
2.
《印度化学会志》2023,100(5):100990
The emerging upconversion nanoparticles (UCNP) have gained substantial consideration in the field of bioanalytical as well as diagnostic applications. Therefore, great progress has been made in the synthesis and surface modification of luminescent UCNPs over the last two decades. In this paper, we have reported monodispersed and high luminescent upconversion nanoparticles NaYF4: 20%Yb3+, 2%Tm3+ have been synthesized using a solvothermal method, followed by a coating of the NaYF4 shell with a thin layer of SiO2 on the surface to afford the core-shell NaYF4:Yb3+, Tm3+@SiO2 nanoparticles (NP@SiO2). The prepared nanoparticles were of strong upconversion fluorescent emission intensity, hexagonal phase, and with an average size of about 8 ± 1 nm, which have been characterized by luminescence spectroscopy, powder X-ray diffraction (P-XRD), Dynamic light scattering (DLS), and Transmission electron microscopy (TEM). The results indicate that the NP@SiO2 can be used for the conjugation of fluorescent probes for various biomolecules and can find applications in cancer cell imaging and disease diagnosis. 相似文献
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4.
Near-infrared upconverting NaYF4:Yb3*,Tm3* nanophosphors modified with poly(acrylic acid) were prepared and characterized by transmission electron microscopy and luminescence spectroscopy.Based on the observed overlap between the emission spectrum of the NaYF4:Yb3*,Tm3* nanophosphors and the absorption spectrum of the gold nanorods,we believe that a new "turn-off luminescence resonance energy transfer aptamer sensor was constructed for sensing thrombin in near-infrared region. 相似文献
5.
1INTRODUCTIONThelasersoperatedataround2mmwavelengthhavegainedmuchinterestbecauseofvariousappli-cations,e.g.(1)groundorspaceremotesensingforLIDARandmetrology,(2)medicalapplicationssinceliquidwaterhasastrongabsorptionbandnear2mm,and(3)eyesafelaser[1,2].The2… 相似文献
6.
Lu Yuan Ming Kang Guanjun Chang Xiangmeng Lv Simin Shen Rong Sun 《无机化学与普通化学杂志》2019,645(21):1240-1246
Due to the unique size effects, nanomaterials in infrared absorption have attracted much attention for their strong absorption in the infrared region. To achieve the infrared multi‐band absorption, we propose to synthesize a core‐shell structure nanomaterial consisting of NaYF4:Yb3+, Er3+ core and a layer of SiO2 as shell. A series of NaYF4:Yb3+, Er3+ nanocrystals were synthesized through hydrothermal method by adjusting the ratio of citric acid(CA)‐to‐NaOH, and the effects of CA concentration, and NaOH concentration were studied in detail. NaYF4:Yb3+, Er3+@SiO2 nanoparticles were synthesized by sol‐gel method using TEOS as silica source. The results show that the core‐shell NaYF4:Yb3+, Er3+@SiO2 nanoparticles were successfully synthesized. Up‐conversion spectra of these nanoparticles were recorded with 980 nm laser excitation under room temperature. There are no changes of the emission centers of nanoparticles before or after silica coating, but the emission intensities of nanoparticles after silica coating are weakened. Furthermore, the property of infrared multi‐band absorption was tested through ultraviolet‐visible‐near infrared spectrophotometer and infrared absorption spectra. The results illustrate that the multi‐band infrared absorption nanomaterial was successfully synthesized. 相似文献
7.
将叶酸分子(FA)和2,3-二巯基丁二酸(DMSA)修饰的稀土上转换发光纳米粒子NaYF4:Yb/Er通过酰胺键偶联在多壁碳纳米管(MWCNT)的表面,得到NaYF4:Yb/Er-MWCNT-FA功能化复合纳米材料,并通过透射电子显微镜(TEM)、X射线衍射(XRD)、紫外-可见吸收光谱(UV-vis)、荧光光谱(PL)和共聚焦激光扫描显微镜等手段表征了其形貌、结构、发光性能和靶向成像性能.共聚焦激光扫描显微镜结果表明,相对于正常的HLF细胞,所制备的复合材料能够靶向检测叶酸受体高表达的宫颈癌Hela细胞.此外,将阿霉素进一步通过ππ堆垛吸附在此复合材料后,该载药体系具有明显的抗肿瘤活性,能够实现对肿瘤细胞的一步检测和治疗. 相似文献
8.
Direct Synthesis of Hexagonal NaGdF4 Nanocrystals from a Single‐Source Precursor: Upconverting NaGdF4:Yb3+,Tm3+ and Its Composites with TiO2 for Near‐IR‐Driven Photocatalysis
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Ying Chen Dr. Shashank Mishra Dr. Gilles Ledoux Dr. Erwann Jeanneau Marlene Daniel Prof. Jinlong Zhang Prof. Stéphane Daniele 《化学:亚洲杂志》2014,9(9):2415-2421
A novel single‐source precursor NaGd(TFA)4(diglyme) (TFA=trifluoroacetate) was synthesized, characterized thoroughly, and used to obtain the hexagonal phase of NaGdF4 nanoparticles as an efficient matrix for lanthanide‐doped upconverting nanocrystals (NCs) that convert near‐infrared radiation into shorter‐wavelength UV/visible light. These NCs were then used to prepare well‐characterized TiO2@NaGdF4:Yb3+,Tm3+ nanocomposites to extend the absorption range of the TiO2 photocatalyst from the UV to the IR region. While the visible/near IR part of the photoluminescent spectra remains almost unaffected by the presence of TiO2, the UV part is strongly quenched due to the absorption of TiO2 above its gap at approximately 380 nm by energy transfer or FRET. Preliminary results on the photocatalytic activity of the above obtained nanocomposites are presented. 相似文献
9.
Tran Thu Huong Le Thi Vinh Hoang Thi Khuyen Le Dac Tuyen Nguyen Duc Van Do Thi Thao Ha Thi Phuong 《Molecules (Basel, Switzerland)》2023,28(1)
We present a visual tool and facile method to detect MCF-7 breast cancer cells by using YVO4:Eu3+@silica-NH-GDA-IgG bio-nanocomplexes. To obtain these complexes, YVO4:Eu3+ nanoparticles with a uniform size of 10–25 nm have been prepared firstly by the hydrothermal process, followed by surface functionalization to be bio-compatible and conjugated with cancer cells. The YVO4:Eu3+@silica-NH-GDA-IgG nanoparticles exhibited an enhanced red emission at 618 nm under an excitation wavelength of 355 nm and were strongly coupled with MCF-7 breast cancer cells via biological conjugation. These bio-nanocomplexes showed a superior sensitiveness for MCF-7 cancer cell labelling with a detection percentage as high as 82%, while no HEK-293A healthy cells were probed under the same conditions of in vitro experiments. In addition, the detection percentage of MCF-7 breast cancer cells increased significantly via the functionalization and conjugation of YVO4:Eu3+ nanoparticles. The experimental results demonstrated that the YVO4:Eu3+@silica-NH-GDA-IgG bio-nanocomplexes can be used as a promising labelling agent for biomedical imaging and diagnostics. 相似文献
10.
《应用有机金属化学》2017,31(7)
Tribenzylammonium tribromide supported onto magnetic nanoparticles (Br3‐TBA‐Fe3O4) as a bromine source was successfully synthesized and characterized using Fourier transform infrared spectroscopy, thermogravimetric analysis, X‐ray diffraction, scanning electron microscopy, energy‐dispersive X‐ray spectroscopy and vibrating sample magnetometry. The synthesized catalyst is shown to be a versatile and highly efficient heterogeneous catalyst for the Knoevenagel condensation and synthesis of 2,3‐dihydroquinazolin‐4(1H )‐one and polyhydroquinoline derivatives. To the best of the authors' knowledge, this is the first report of the use of a bromine source immobilized on Fe3O4 nanoparticles as a magnetically separable catalyst for these reactions. The nanosolid catalyst can be magnetically recovered and reused readily several times without significant loss in catalytic efficiency. 相似文献
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Fe3O4 nanoparticles were prepared and decorated on the surface of nanobentonite (NB), and subsequently modified by the organic and inorganic linkers and then sulfonic acid immobilization on the nanoparticles. The NB-Fe3O4@SiO2@CPTMO@DEA-SO3H catalyst was characterized via Fourier transform-infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, vibrating-sample magnetometer, X-ray diffraction patterns, Brunauer–Emmett–Teller and thermal gravimetric analysis. The new catalyst benefits from a simple preparation method, and environmentally friendly and high magnetic properties of the nanocatalyst, Accordingly, we used it for the synthesis of dihydropyrano[2,3c]pyrazole derivatives in water and ethanol mixture as a green solvent under reflux conditions. Use of mild conditions, easy catalyst separation, cost-effectiveness, short reaction time, reusability of the catalyst, excellent yield and easy work-up are the main advantages of the present method. 相似文献
12.
Wei Lu Meng‐Ling Lu Qing‐Peng Zhang Yong‐Qing Tian Zhi‐Xiang Zhang Han‐Hong Xu 《Journal of polymer science. Part A, Polymer chemistry》2013,51(18):3932-3940
Environment‐friendly and controlled release formulation is highly promising for reducing environmental pollution and achieving the most effective utilization of pesticides. As a novel “green” nanocarrier of pesticides, amphiphilic self‐assembled nanoparticles were prepared by chemical conjugation of octahydrogenated retinoic acid (OR) to the backbone of glycol chitosan (GC). In aqueous media, the synthesized OR‐GC conjugates formed nanosized particles with a diameter of 257 nm. Hydrophobic azadirachtin (AZA) was efficiently loaded into the OR‐GC nanoparticles at a feed weight ratio of up to 1:4 using a simple dialysis method, the maximum drug‐loading efficiency of which was 74%. AZA‐OR‐GC (25 wt %) nanoparticles also showed sustained release of the incorporated AZA (65% of the loaded dose was released in 7 days at 27 °C in phosphate‐buffered saline; pH 7.2). Cytotoxicity tests and cell cycle arrest assays confirmed that OR‐GC exhibits good biocompatibility; AZA‐OR‐GC (25 wt %) nanoparticles also showed favorable inhibition of cell proliferation in Sl‐1 cells compared with free AZA in organic solvents. Overall, controlled release AZA‐OR‐GC may be a promising environment‐friendly formulation for integrated pest management. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 3932–3940 相似文献
13.
This study reports the structural and spectroscopic characterization of a novel metal organic compound formulated as [Fe (bpy)3] [Fe (dipic)2]2.7H2O ( 1 ) (dipic = pyridine‐2,6‐dicarboxylate and bpy = 2,2′‐bipyridine). 1 was investigated by elemental analysis, FT‐IR spectroscopy, powder X‐ray diffraction and single crystal X‐ray diffraction (SC‐XRD), which revealed a triclinic structure of expected composition. Thermal degradation of 1 was also investigated. Complex 1 was used as a precursor to prepare superparamagnetic nanoparticles of Fe3O4 by thermal analysis. The obtained Fe3O4 was characterized by Fourier transformed infrared spectroscopy (FT‐IR), powder X‐ray diffraction (XRD) and scanning electron microscopy (SEM). Fe3O4 nanoparticles were used as a nano‐adsorbent to remove Cd2+ from water at room temperature. The results showed that this nano‐adsorbent is effective in removing Cd2+ from contaminated water sources, and that the maximal effectivity of adsorption occurs at pH = 6. Magnetic measurements of complex 1 and Fe3O4 nanoparticles at room temperature revealed paramagnetic and superparamagnetic behavior, respectively. 相似文献
14.
Minoru Nagata Masayuki Nakae 《Journal of polymer science. Part A, Polymer chemistry》2001,39(18):3043-3051
A new series of thermotropic liquid‐crystalline (LC) polyesters were prepared from a diacyl chloride derivative of 4,4′‐(terephthaloyldioxy)‐di‐4‐phenylpropionic acid (PTP) and glycols with a different number of methylene groups (n) [HO(CH2)n OH, n = 6–10, 12] by high‐temperature solution polycondensation in diphenyl oxide. PTP6/10 and PTP6/hydroquinone (H) LC copolyesters were also prepared according to a similar procedure. The chemical structure, LC, phase‐transition behaviors, thermal stability, and solubility were characterized by elemental analysis, Fourier transform infrared spectroscopy, 1H and 13C NMR spectra, differential scanning calorimetry (DSC), thermogravimetric analysis, and a polarizing light microscope. The melting and isotropization temperatures decreased in a zigzag manner as the number of n increased. All of the polyesters formed a nematic phase with the exception of PTP8. The temperature ranges of the mesophase (ΔT) were much wider for the polyesters with an odd number of n's than those with an even number. ΔT increased markedly for the PTP6/10 and PTP6/H copolyesters. The in vitro degradations of the polymers were ascertained by enzymatic hydrolysis and alkaline hydrolysis. The model compound, PTP dihexylester, was synthesized and found to be degraded into terephthalic acid, 3‐(4‐hydroxyphenyl)propionic acid, and 1‐hexanol by Rhizopus delemar lipase, but PTPn homopolyesters and PTP6/10 and PTP6/H copolyesters were resistant to Rhizopus delemar hydrolysis. They were degradable in a sodium hydroxide buffer solution of pH 12 at 60 °C, depending on the number of n's and the copolymer composition. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3043–3051, 2001 相似文献
15.
Synthesis and characterization of sodium polyaspartate‐functionalized silica‐coated magnetite nanoparticles: A heterogeneous,reusable and magnetically separable catalyst for the solvent‐free synthesis of 2‐amino‐4H‐chromene derivatives
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An efficient and facile method was used for the synthesis of sodium polyaspartate‐functionalized silica‐coated magnetite nanoparticles. The structure of this nanoparticle was characterized by scanning electron microscopies, X‐ray diffraction, energy‐dispersive X‐ray, Fourier transform infrared spectroscopies and vibrating sample magnetometry. Then, this compound was used as a reusable heterogeneous catalyst for green synthesis of 2‐amino‐4H‐chromene derivatives via one‐pot three‐component reactions. This novel material showed great catalytic performance and the reactions which were carried out by this catalyst showed good to excellent yields. Besides, the catalyst could easily be separated from the reaction mixture by using an external magnetic field and it was stable enough to reuse several times without any significant reduction in the yield of reactions. Eco‐friendliness, high purity of the desired products, short reaction time and easy workup procedure can be mentioned as the other advantages of this method. 相似文献
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采用微波固相法制备了CaWO4:xEu3+,ySm3+,zLi+红色荧光粉。测量样品的XRD图、激发谱、发射谱及发光衰减曲线,研究并分析了Eu3+、Sm3+、Li+的掺杂浓度,对样品微结构、光致发光特性、能量传递及能级寿命的影响。结果表明,Eu3+、Sm3+、Li+掺杂并未引起合成粉体改变晶相,仍为CaWO4单一四方晶系结构。Eu3+、Sm3+共掺样品中,Sm3+掺杂为3%时,Sm3+对Eu3+的能量传递最有效。Li+掺杂起到了助熔剂和敏化剂的作用,使样品发光更强。在394 nm激发下,与CaWO4:3%Eu3+样品比较,3%Eu3+、3%Sm3+共掺CaWO4及3%Eu3+、3%Sm3+、1%Li+共掺CaWO4样品的发光分别增强2倍及2.4倍。同一激发波长下,单掺Eu3+样品寿命最短,Sm3+、Eu3+共掺样品随Sm3+浓度增加,寿命先减小后增加,且掺杂了Li+的样品比不掺Li+的样品5D0能级寿命有所增加。 相似文献
17.
Fe3O4@Propylsilane@Histidine[HSO4‐] magnetic nanocatalysts: Synthesis,characterization and catalytic application for highly efficient synthesis of xanthene derivatives
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The surface of Fe3O4 magnetic nanoparticles (MNPs) was modified by chloropropylsilane and histidine. The imidazole group of prepared Fe3O4@Propylsilane@Histidine MNPs converted to imidazolium hydrogen sulfate group and Fe3O4@Propylsilane@Histidine [HSO4‐] as a novel environmentally friendly ionic liquid/ magnetite nanoparticle was prepared, successfully. FT‐IR, XRD, SEM and TEM instruments was used to identifiy the histidine ionic liquids/magnetite nanoparticles (HILMNPs). The catalytic activity of synthesized HILMNPs was appraised for the synthesis of 9‐aryl‐1,8‐dioxooctahydroxanthene and spiro[indoline‐3,9′‐xanthene]trione derivatives. The activity of HILMNPs was much better than the other reported heterogeneous and homogeneous catalysts. Furthermore, the prepared catalyst could be separated from the reaction mixture and reused four times without any significant loss in its activity. 相似文献
18.
空气中合成M2B4O7:Eu3+(M=Na,K)荧光体及其性质表征 总被引:7,自引:0,他引:7
以M2B4O7(M=Na,K)为基质,在空气中掺杂稀土元素Eu3+得到了Na2B4O7:Eu3+和K2B4O7:Eu3+荧光体.探讨了体系的烧结条件和荧光性质,分析了晶体的结构.结果表明,虽然两种体系的最佳合成条件不同,但是体系中都同时存在[BO4]和[BO3]结构;稀土离子Eu3+的发光以电偶极跃迁5D0-7F2为主,处于非中心对称的格位上,并且可以很好地存在于基质中,Na2B4O7:Eu3+具有较强的发光强度. 相似文献
19.
通过溶胶-凝胶法合成了上转换发光材料Er~(3+)∶V_(0.01)Y_(2.99)Al_5N_(0.01)F_(0.01)O_(11.98)(Er∶YAG),然后利用水热法合成了BiPO_4,再利用高温煅烧法合成了Er∶YAG/BiPO_4/Pt复合物光催化剂.通过使用X-射线粉末衍射仪(XRD),扫描电子显微镜(SEM),透射电子显微镜(TEM),光致发光光谱(PL)和上转换发射光谱对样品的组成、形貌及光学特征进行了表征.此外,还研究了不同甘油添加量、 Er∶YAG和BiPO_4的摩尔比例和复合温度及光催化剂的循环使用次数对Er∶YAG/BiPO_4/Pt复合物光催化剂活性的影响.实验结果显示Er∶YAG/BiPO_4/Pt复合物光催化剂具有高的光催化活性和较好的稳定性,它可以作为一种高效的光催化剂用于污水中有机污染物的处理. 相似文献