16056-77-2

Basic information

• Product Name: GADOLINIUM ACETATE
• Synonyms: GADOLINIUM ACETATE;GADOLINIUM ACETATE HYDRATE;GADOLINIUM ACETATE TETRAHYDRATE;GADOLINIUM (III) ACETATE HYDRATE;GADOLINIUM(III) ACETATE TETRAHYDRATE;gadolinium(3+) acetate;GADOLINIUM ACETATE, 99.9%;Triacetic acid gadolinium salt
• CAS NO: 16056-77-2
• Molecular Formula: 3C₂H₃O₂*Gd
• Molecular Weight: 406.44
• EINECS: 240-204-9
• Mol File: 16056-77-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 117.1 °C at 760 mmHg
• Flash Point: 40 °C
• Appearance: white to off-white crystals, possible acetic odor
• CAS DataBase Reference: GADOLINIUM ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: GADOLINIUM ACETATE(16056-77-2)
• EPA Substance Registry System: GADOLINIUM ACETATE(16056-77-2)

Safety Data

• Hazardous Substances Data: 16056-77-2(Hazardous Substances Data)

Usage

General Description

Gadolinium acetate is a chemical substance commonly utilized in various industrial applications. It is a white, crystalline powder with a slight acetic odor. Its molecular formula is C6H9GdO6. It is often characterized by its solubility in water and non-flammable nature, ensuring safe handling during its use. Gadolinium acetate can be used in different fields such as electronics, ceramics, and medical imaging. It is particularly recognized for its paramagnetic properties, meaning it has uses in magnetic resonance imaging (MRI) and related applications. However, it should be handled with care, considering that direct contact can cause eye and skin irritation, and ingestion or inhalation could be harmful.

InChI:InChI=1/3C2H4O2.Gd/c3*1-2(3)4;/h3*1H3,(H,3,4);/q;;;+3/p-3

Upstream product

• 127-09-3 sodium acetate 
• 10138-52-0 gadolinium(III) chloride 
• 76-05-1 trifluoroacetic acid 
• 64-19-7 acetic acid 

Downstream Products

• 947391-63-1 C₄₀H₅₈GdN₉O₁₀ 
• 947391-69-7 C₂₉H₄₄GdN₇O₈ 

Relevant articles and documents

Photon upconversion in Yb3+-Tb3+ and Yb3+-Eu3+ activated core/shell nanoparticles with dual-band excitation

Exploring novel lanthanide-activated upconversion nanoparticles with distinctive spectral fingerprints and emission lifetimes has long been a great concern for extended optical applications. Herein, we report the study of photon upconversion emissions in Yb3+-Tb3+ and Yb3+-Eu3+ activated nanoparticles with near-infrared excitation. In these nanoparticles, a high content of Yb3+ is required for the simultaneous excitation of two Yb3+ ions, yielding a Yb3+ dimer with a higher excited energy to upconvert photons onto Tb3+ and Eu3+. The optimum doping concentration of Yb3+ ions for Yb3+-Tb3+ and Yb3+-Eu3+ pairs was determined to be 80% and 60%, respectively, which are much higher than that of Yb3+-Er3+/Tm3+ pairs. Notably, the upconversion emission lifetime of the as-prepared nanoparticles was prolonged to 2.3 ms (Tb3+) and 4.0 ms (Eu3+), respectively. Through the epitaxial growth of a Nd3+ doped shell layer, the upconversion emissions of Tb3+ and Eu3+ were intensified 25-fold. At the same time, an extra excitation band in the shorter near-infrared region from Nd3+ at 808 nm was achieved. Moreover, the emissions of Tm3+ were employed to compensate for those of Tb3+ and Eu3+ for multicolor emissions. These results highlight the upconversion emissions of Tb3+ and Eu3+ for potential multicolor imaging and multiplexed detection applications.

Comparative studies of structure, spectroscopic properties and intensity parameters of tetragonal rare earth vanadate nanophosphors doped with Eu(III)

Hydrothermal method was applied in order to synthesize nanocrystalline YVO4, LaVO4 and GdVO4 materials doped with Eu3+ ions. The conditions of synthesis were chosen to allow control of the process based on precipitation reaction in an autoclave, at elevated temperature and pressure. The prepared materials crystallized as single phase spherical-like nanocrystals of the tetragonal I41/amd structure. The average size of the particles was in the range of 7–10 nm in the YVO4- and GdVO4-based products and about 32 nm when LaVO4 was the host compound. The excitation spectra of the materials prepared revealed a broad and intense band in the UV region. The band resulted from charge transfer phenomena: excitation of the VO43+ groups was followed by the energy transfer to Eu3+ ions. Intense, red emission of the samples was a result of electronic transitions in Eu3+ dopant ions. The theoretical Judd-Ofelt intensity parameters Ωλ, obtained using the novel approach to the calculation of Eu-O bond stretching force constant and subsequently charge factors, were compared to the experimental Ωλ. Forced electric dipole part of Ωλ was calculated from scratch (using Eu3+ coordination geometry in REVO4 from DFT calculations), while a single parameter in the dynamic coupling part was fitted to the experimental data. The issues related to the force constant calculation are discussed. Crucial influence of crystal lattice distortions on Ωλ and Eu3+ emission intensities of the materials was shown.