A lanthanide metal-organic framework (MOF) compound of the formulation [Eu2(CO3)(ox)2(H2O)2]·4H2O (1, ox = oxalate) was prepared by hydrothermal synthesis with its structure determined crystallographically. Temperature-dependent but humidity-independent high proton conduction was observed with a maximum of 2.08 × 10(-3) S cm(-1) achieved at 150 °C, well above the normal boiling point of water. Results from detailed structural analyses, comparative measurements of conductivities using regular and deuterated samples, anisotropic conductivity measurements using a single-crystal sample, and variable-temperature photoluminescence studies collectively establish that the protons furnished by the Eu(III)-bound and activated aqua ligands are the charge carriers and that the transport of proton is mediated along the crystallographic a-axis by ordered hydrogen-bonded arrays involving both aqua ligands and adjacent oxalate groups in the channels of the open framework. Proton conduction was enhanced with the increase of temperature from room temperature to about 150 °C, which can be rationalized in terms of thermal activation of the aqua ligands and the facilitated transport between aqua and adjacent oxalate ligands. A complete thermal loss of the aqua ligands occurred at about 160 °C, resulting in the disintegration of the hydrogen-bonded pathway for proton transport and a precipitous drop in conductivity. However, the structural integrity of the MOF was maintained up to 350 °C, and upon rehydration, the original structure with the hydrogen-bonded arrays was restored, and so was its high proton-conduction ability.
Isostructural lanthanide metal-organic frameworks (MOFs) are synthesized through the spontaneous self-assembly of H3BTPCA (1,1',1″-(benzene-1,3,5-triyl)tripiperidine-4-carboxylic acid) ligands and lanthanide ions (we term these MOFs Ln-BTPCA, Ln = La(3+), Tb(3+), Sm(3+), etc.). Prompted by the observation that the different lanthanide ions have identical coordination environment in these MOFs, we explored and succeeded in the preparation of mixed-lanthanide analogues of the single-lanthanide MOFs by way of in situ doping using a mixture of lanthanide salts. With careful adjustment of the relative concentration of the lanthanide ions, the color of the luminescence can be modulated, and white light-emission can indeed be achieved. The mechanisms possibly responsible for the observed photophysical properties of these mixed-lanthanide MOFs are also discussed.
Reducing the level of sulfur content in fuel oils has long been desired for environmental reasons. Polyoxometalates (POMs) can act as catalysts to remove sulfur‐containing heterocyclic compounds by the process of oxidative desulfurization under mild conditions. However, one key obstacle to the development of POM‐based catalysts is the poor solubility of POMs in the overall nonpolar environment. We report a novel strategy for the introduction of catalytically active POMs into nonpolar reaction systems by encapsulating the inorganic catalyst within the pores of a metal–organic framework structure in which the organic ligands act as hydrophobic groups. The nanocrystalline catalysts, obtained rapidly and conveniently by both solution and mechanochemical synthesis, showed remarkable activities in catalytic oxidative desulfurization reactions in both a model diesel environment and in real diesel wherein dibenzothiophene was converted rapidly and quantitatively into dibenzothiophene sulfone.
Cold atmospheric plasma has recently emerged as a simple, low-cost and efficient physical method for inducing significant biological responses in seeds and plants without the use of traditional, potentially environmentally-hazardous chemicals, fungicides or hormones. While the beneficial effects of plasma treatment on seed germination, disease resistance and agricultural output have been reported, the mechanisms that underpin the observed biological responses are yet to be fully described. This study employs Fourier Transform Infrared (FTIR) spectroscopy and emission spectroscopy to capture chemical interactions between plasmas and seed surfaces with the aim to provide a more comprehensive account of plasma−seed interactions. FTIR spectroscopy of the seed surface confirms plasma-induced chemical etching of the surface. The etching facilitates permeation of water into the seed, which is confirmed by water uptake measurements. FTIR of exhaust and emission spectra of discharges show oxygen-containing species known for their ability to stimulate biochemical processes and deactivate pathogenic microorganisms. In addition, water gas, CO2, CO and molecules containing −C(CH3)3− moieties observed in FTIR spectra of the exhaust gas during plasma treatment may be partly responsible for the plasma chemical etching of seed surface through oxidizing the organic components of the seed coat.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.