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13798-24-8

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13798-24-8 Usage

Uses

Different sources of media describe the Uses of 13798-24-8 differently. You can refer to the following data:
1. Terbium Chloride has important role as an activator for green phosphors used in colour TV tubes, is also used in special lasers and as a dopant in solid-state devices. Chloride compounds can conduct electricity when fused or dissolved in water.
2. Terbium(III) chloride hexahydrate is used in the primary chemical intermediates and in chemical research.

Chemical Properties

white crystalline powder, crystals and/or chunks

Check Digit Verification of cas no

The CAS Registry Mumber 13798-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,9 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13798-24:
(7*1)+(6*3)+(5*7)+(4*9)+(3*8)+(2*2)+(1*4)=128
128 % 10 = 8
So 13798-24-8 is a valid CAS Registry Number.
InChI:InChI=1/3ClH.H2O.Tb/h3*1H;1H2;/q;;;;+3/p-3

13798-24-8 Well-known Company Product Price

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  • Alfa Aesar

  • (44472)  Terbium(III) chloride hexahydrate, REacton?, 99.999% (metals basis)   

  • 13798-24-8

  • 5g

  • 984.0CNY

  • Detail
  • Alfa Aesar

  • (44472)  Terbium(III) chloride hexahydrate, REacton?, 99.999% (metals basis)   

  • 13798-24-8

  • 25g

  • 3628.0CNY

  • Detail
  • Alfa Aesar

  • (11210)  Terbium(III) chloride hexahydrate, REacton?, 99.99% (REO)   

  • 13798-24-8

  • 10g

  • 1049.0CNY

  • Detail
  • Alfa Aesar

  • (11210)  Terbium(III) chloride hexahydrate, REacton?, 99.99% (REO)   

  • 13798-24-8

  • 50g

  • 3744.0CNY

  • Detail
  • Alfa Aesar

  • (11209)  Terbium(III) chloride hexahydrate, REacton?, 99.9% (REO)   

  • 13798-24-8

  • 10g

  • 998.0CNY

  • Detail
  • Alfa Aesar

  • (11209)  Terbium(III) chloride hexahydrate, REacton?, 99.9% (REO)   

  • 13798-24-8

  • 50g

  • 2459.0CNY

  • Detail
  • Aldrich

  • (204560)  Terbium(III)chloridehexahydrate  99.999% trace metals basis

  • 13798-24-8

  • 204560-1G

  • 402.48CNY

  • Detail
  • Aldrich

  • (204560)  Terbium(III)chloridehexahydrate  99.999% trace metals basis

  • 13798-24-8

  • 204560-5G

  • 3,499.47CNY

  • Detail
  • Aldrich

  • (212903)  Terbium(III)chloridehexahydrate  99.9% trace metals basis

  • 13798-24-8

  • 212903-5G

  • 733.59CNY

  • Detail
  • Aldrich

  • (212903)  Terbium(III)chloridehexahydrate  99.9% trace metals basis

  • 13798-24-8

  • 212903-25G

  • 1,819.35CNY

  • Detail

13798-24-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Terbium(III) chloride hexahydrate

1.2 Other means of identification

Product number -
Other names terbium(3+),trichloride,hexahydrate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13798-24-8 SDS

13798-24-8Relevant articles and documents

Homochiral porous lanthanide phosphonates with 1D triple-strand helical chains: Synthesis, photoluminescence, and adsorption properties

Yue, Qi,Yang, Jin,Li, Guang-Hua,Li, Guo-Dong,Chen, Jie-Sheng

, p. 4431 - 4439 (2006)

Four homochiral porous lanthanide phosphonates, [Ln(H2L) 3]·2H2O, (H3L = (S)-HO 3PCH2-NHC4H7-CO2H, Ln = Tb (1), Dy (2), Eu (3), Gd (4)), have been synthesized under hydrothermal conditions. These compounds are isostructural, and they possess a 3D supramolecular framework built up from 1D triple-strand helical chains. Each of the helical chain consists of phosphonate groups bridging adjacent Ln(III) ions. The helical chains are stacked through hydrogen bonds to form 1D tubular channels along the c axis. Moreover, helical water chains are located in the 1D channels, and after removal of these water chains, the compounds exhibit selective adsorption capacities for N2, H2O, and CH 3OH molecules. Compounds 1 and 3 show strong green and red fluorescent emissions, respectively, in the solid state at room temperature. Crystal data for 1: TbP3O17N3C 18H37, tetragonal (No.76), space group P41, a = 12.4643(3) A, b = 12.4643(3) A, c = 18.7577(5) A, V = 2914.17(13) A3, and Z = 4. For 2: DyP3O 17N3C18H37, a = 12.4486(3) A, b = 12.4486(3) A, c = 18.7626(5) A, V = 2907.60(13) A3, and Z = 4. For 3, EuP3O17N 3C18H37, a = 12.4799(3) A, b = 12.4799(3) A, c = 18.8239(5) A, V = 2931.78(13) A3, and Z = 4. For 4: GdP3O17N3C18H 37, a = 12.4877(18) A, b = 12.4877(18) A, c = 18.824(4) A, V = 2935.5(8) A3, and Z = 4.

Intercalation of lanthanide cations to a layer-like metal-organic framework for color tunable white light emission

Xu, Xiao-Yu,Yan, Bing

, p. 1178 - 1185 (2015)

One gallium carboxylate of MOF (Ga2(OH)4(C9O6H4) or MIL-124) has been synthesized by a facile solvothermal approach, and the luminescence was tuned by encapsulating lanthanide(iii)(Ln3+) cations into the channels through the active-COOH group in MIL-124 post-synthesis. PXRD, TEM, FTIR, and TGA were performed to determine the structure and thermal stability of the obtained products. The photophysical properties of these Ln3+ incorporated products are studied in detail, whose luminescent color can be tuned by controlling the composition of different Ln3+ cations in MOF. Furthermore, with careful adjustment of the excitation wavelength and concentration of the Ln3+ cations, the color of the luminescence can be modulated, and dichromatic (MIL-124@Eu3+) and trichromatic (MIL-124@Eu3+/Tb3+) white-light-emission can indeed be achieved. One of the optimized chromaticity coordinates in white-light-emission is (0.3693, 0.3362) which is very close to the value for ideal white-light (0.333, 0.333). The versatile luminescence, good thermal stability, and compatibility with aqueous conditions reveal that these materials based on MOF may have some potential applications in luminescent devices for display or lighting. This journal is

Study of the luminescence properties of a novel rare earth complex Tb(DPC)22H2O

Lv, Yuguang,Li, Qiuping,Shi, Chunhui,Liu, Hairan,Liu, Fenghua,Wu, Lili,Wu, Dongmei,Liu, Hong,Xie, Jie

, p. 26 - 29 (2009)

Rare earth complex Tb(DPC)22H2O was synthesized by introducing Pyridine-2,6-dicarboxylic acid(H2DPC) as the ligand and characterized by UV, fluorescent and infrared spectra as well as elemental analysis. The complex exhibi

Synthesis, crystal structure and luminescence properties of two novel lanthanide coordination polymers containing double chain

Song, Hui-Hua,Li, Ya-Juan

, p. 1421 - 1425 (2008)

Two novel lanthanide(III) two-dimensional (2D) coordination polymers [Ln2(PDC)2(OH)2(H2O)2] · H2O (Ln = Eu (1) and Tb (2), H2PDC = pyridine-3,4-dicarboxylic acid) have been prepa

Luminescence enhancement of Tb3+ ion in assemblies of amphiphilic linear-dendritic block copolymers: Antenna and microenvironment effects

Zhu, Linyong,Tong, Xiaofeng,Li, Miaozhen,Wang, Erjian

, p. 2461 - 2464 (2001)

The luminescence enhancement of Tb3+ ion bound to amphiphilic linear-dendritic block copolymers [poly-(acrylic acid)-dendritic polyether, PAA-Dendr.PE] was investigated. Tb3+ ion complexes with a PAA chain of block copolymer to form a supramolecular luminophore. The observed prominent enhancement in luminescence properties can be attributed to two important factors. The antenna effect, energy harvest and transfer from the dendritic polyether subunit to the ground state of the Tb3+ ion, leads to a remarkable increase of luminescence intensity of Tb3+ ion, which enlarges obviously with increasing generation of dendrimer. Furthermore, the unique microenvironment surrounding the Tb3+ ion that derives from multimolecular assembly of copolymer results in a large decrease of the number of water molecules coordinated to Tb3+ from 3.5 to 1.3, which is the other factor to greatly enhance the luminescence intensity of Tb3+ ion.

Luminescent hybrid materials of lanthanide β-diketonate and mesoporous host through covalent and ionic bonding with anion metathesis

Li, Qiu-Ping,Yan, Bing

, p. 8567 - 8574 (2012)

Luminescent mesoporous materials were prepared by performing an anion metathesis reaction on ionic liquid modified SBA15, which has imidazolium chloride bridging units. The lanthanide β-diketonate complex anion was successfully anchored onto the SBA15 fra

Luminescent materials of annealed Eu3+-exchanged zeolite L crystals

Fang, Yi,Li, Huanrong,Wang, Yu,Liu, Xiuwu

, p. 11594 - 11598 (2011/02/27)

In this work, we report the luminescence behavior of Eu3+- exchanged zeolite L microcrystals annealed at different temperatures. SEM and XRD techniques were employed to characterize the samples. UV-vis absorption spectroscopy and luminescence spectroscopy were used to study the luminescence properties of the annealed materials. It is shown that Eu3+-exchanged zeolite L crystals are structurally stable at 800 °C, and that its structure is completely collapsed when annealed at 1100 °C. Calcination of Eu3+-exchanged zeolite L crystals at 700 °C leads to a strong violet-blue emission, while a strong red emission is observed when the sample is annealed at 1100 °C. The Royal Society of Chemistry 2010.

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