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Journal ArticleDOI: 10.1021/ACS.INORGCHEM.1C00310

Isostructural Single- And Dual-Lanthanide Metal-Organic Frameworks Based On Substituent-Group-Modifying Tetracarboxylate Ligands for Ratiometric Temperature Sensing.

04 Mar 2021-Inorganic Chemistry (American Chemical Society (ACS))-Vol. 60, Iss: 6, pp 4133-4143
Abstract: In this study, two substituent-group-modifying tetracarboxylate ligands, 2',5'-dimethoxy-[1,1':4',1″-terphenyl]-3,3″,5,5″-tetracarboxylic acid (H4TPTC-2OMe) and 2',5'-dimethyl-[1,1':4',1″-terphenyl]-3,3″,5,5″-tetracarboxylic acid (H4TPTC-2Me), with similar geometries were used as the organic linkers to construct isostructural lanthanide metal-organic frameworks (LnMOFs). The as-prepared LnTPTC-2OMe and LnTPTC-2Me were structurally elucidated by means of single-crystal and powder X-ray diffraction in addition to thermogravimetric analysis and were assessed as luminescence ratiometric thermometers by obtaining the temperature dependence of the luminescence behaviors. We found that both the single lanthanide EuTPTC-2OMe and the dual lanthanide Eu0.05Tb0.95TPTC-2Me exhibited a distinct S-type luminescence response to temperatures in the range from 313 to 473 K, and their ratiometric parameters can be understood on the basis of the classic Mott-Seitz model. Energy transfers from the ligand to Tb3+ (or Eu3+) and from Tb3+ to Eu3+ in these two systems were investigated theoretically as well as with low-temperature (77 K) time-resolved photoluminescence spectroscopy, quantum yield, and lifetime analysis. Therefore, these two materials possess a good relative sensitivity, a small temperature uncertainty, and a favorable spectral repeatability in addition to a remarkable emission color change, enhancing their potential use for temperature measurement and in situ monitoring in microelectronics.

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Topics: Lanthanide (53%), Luminescence (53%), Isostructural (52%)

5 results found

Journal ArticleDOI: 10.1107/S2053229621010639
Abstract: A novel three-dimensional (3D) CdII coordination polymer, namely, poly[[μ2-4,4'-bis(2-methylimidazol-1-yl)-[1,1'-biphenyl]](μ2-5-methylisophthalato)cadmium(II)], [Cd(C9H6O4)(C20H18N4)]n or [Cd(MIP)(4,4'-BMIBP)]n, (I), was synthesized by the hydrothermal method using 5-methylisophthalic acid (H2MIP), 4,4'-bis(2-methylimidazol-1-yl)-[1,1'-biphenyl] (4,4'-BMIBP) and Cd(NO3)2·6H2O, and characterized by single-crystal X-ray diffraction, elemental analysis, IR spectroscopy and thermogravimetric analysis. Compound (I) exhibits a novel fivefold interpenetrating 3D diamondoid framework. Additionally, it shows fluorescence emission in the solid state and promising photocatalytic activities for the degradation of methylene blue (MB) in water at room temperature.

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Topics: Coordination polymer (55%)

Journal ArticleDOI: 10.1039/D1DT01550H
Alexandru Topor1, Daniel Avram, Radu Dascalu, Catalin Maxim1  +2 moreInstitutions (1)
Abstract: Three 1D coordination polymers with benzoate bridges have been assembled in the presence of 18-crown-6-ether (18C6): 1∞[Tb(PhCOO)3(H2O)(EtOH)]·0.5(18C6) 1, 1∞[Eu(PhCOO)3(H2O)2]·0.5(18C6) 2, 1∞[Nd(PhCOO)3(H2O)2]·0.5(18C6) 3. Compounds 2 and 3 are isomorphous. The crown ether molecules co-crystallize with the resulting 1D coordination polymers and play an important role in the supramolecular architecture of the crystals. A molecular alloy was prepared in a similar way to compound 1 using TbCl3·6H2O and EuCl3·6H2O in a molar ratio of 95 : 5. The EuIII ions have statistically substituted the TbIII ions in the host lattice The luminescence thermometry performance of the Tb0.95Eu0.05 system was investigated using pulsed excitation into TbIII absorption at 352 nm. The maximum Sr value is 1.88% K−1 at 80 K which is slightly reduced at 1.60% K−1 at 313 K. Time-gated emission spectroscopy, employed here for the first time, allows us to reduce the spectral overlap of Tb and Eu emissions in the 610 to 625 nm range by 100% at 80 K, from 18 to 9%. Compound 1 as well as the molecular alloy, Tb0.95Eu0.05, show X-ray induced luminescence.

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Topics: Luminescence (53%), Lanthanide (50%), Supramolecular chemistry (50%)


45 results found

Journal ArticleDOI: 10.1103/PHYSREVLETT.52.997
Erich Runge1, E. K. U. Gross1Institutions (1)
Abstract: The response of an interacting many-particle system to a time-dependent external field can usually be treated within linear response theory. Due to rapid experimental progress in the field of laser physics, however, ultra-short laser pulses of very high intensity have become available in recent years. The electric field produced in such pulses can reach the strength of the electric field caused by atomic nuclei. If an atomic system is placed in the focus of such a laser pulse one observes a wealth of new phenomena [1] which cannot be explained by traditional perturbation theory. The non-perturbative quantum mechanical description of interacting particles moving in a very strong time-dependent external field therefore has become a prominent problem of theoretical physics. In principle, it requires a full solution of the time-dependent Schrodinger equation for the interacting many-body system, which is an exceedingly difficult task. In view of the success of density functional methods in the treatment of stationary many-body systems and in view of their numerical simplicity, a time-dependent version of density functional theory appears highly desirable, both within and beyond the regime of linear response.

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6,210 Citations

Journal ArticleDOI: 10.1021/CR200101D
08 Feb 2012-Chemical Reviews
Topics: Luminescent Measurements (67%)

4,507 Citations

Journal ArticleDOI: 10.1021/NN100244A
04 May 2010-ACS Nano
Abstract: Acquiring the temperature of a single living cell is not a trivial task. In this paper, we devise a novel nanothermometer, capable of accurately determining the temperature of solutions as well as biological systems such as HeLa cancer cells. The nanothermometer is based on the temperature-sensitive fluorescence of NaYF4:Er3+,Yb3+ nanoparticles, where the intensity ratio of the green fluorescence bands of the Er3+ dopant ions (2H11/2 → 4I15/2 and 4S3/2 → 4I15/2) changes with temperature. The nanothermometers were first used to obtain thermal profiles created when heating a colloidal solution of NaYF4:Er3+,Yb3+ nanoparticles in water using a pump−probe experiment. Following incubation of the nanoparticles with HeLa cervical cancer cells and their subsequent uptake, the fluorescent nanothermometers measured the internal temperature of the living cell from 25 °C to its thermally induced death at 45 °C.

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1,075 Citations

Journal ArticleDOI: 10.1021/JA2108036
Yuanjing Cui1, Hui Xu1, Yanfeng Yue2, Zhiyong Guo2  +6 moreInstitutions (3)
Abstract: A luminescent mixed lanthanide metal–organic framework approach has been realized to explore luminescent thermometers. The targeted self-referencing luminescent thermometer Eu0.0069Tb0.9931-DMBDC (DMBDC = 2, 5-dimethoxy-1, 4-benzenedicarboxylate) based on two emissions of Tb3+ at 545 nm and Eu3+ 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.

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Topics: Thermometer (51%)

834 Citations

Open accessJournal ArticleDOI: 10.1038/NCOMMS1714
Kohki Okabe1, Noriko Inada2, Chie Gota1, Yoshie Harada3  +2 moreInstitutions (3)
Abstract: Intracellular temperature mapping has not previously been achieved. Now, a fluorescent polymeric thermometer has been developed that can be used in combination with fluorescence-lifetime imaging microscopy to allow thermometry with spatial and temperature resolutions of 200 nm and 0.18–0.58 ° C.

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796 Citations