13 research outputs found
Microwave-promoted one-pot conversion of alcohols to oximes using 1-methylimidazolium nitrate, [Hmim][NO3], as a green promoter and medium
1-Methyl-1H-imidazol-3-ium methanesulfonate
The structure of the title salt, C4H7N2+·CH3O3S−, has monoclinic (P21/n) symmetry. The 1-methylimidazolium cation and the methylsulfonate anion in the asymmetric unit are held together by a strong N—H...O hydrogen bond
H<sub>3</sub>PW<sub>12</sub>O<sub>40</sub>–[bmim][FeCl<sub>4</sub>]: A novel and green catalyst-medium system for microwave-promoted selective interconversion of alkoxymethyl ethers into their corresponding nitriles, bromides and iodides
A co-crystal of 1,10-phenanthroline with boric acid: a novel aza-aromatic complex
The title compound, C12H8N2·2B(OH)3, is best described as a host–guest complex in which the B(OH)3 molecules form a hydrogen-bonded cyclic network of layers parallel to the ab plane into which the 1,10-phenanthroline molecules are bound. An extensive network of hydrogen bonds are responsible for the crystal stability. No π-stacking interactions occur between the 1,10-phenanthroline molecules
[C<sub>4</sub>mim][InCl<sub>4</sub>]: An efficient catalyst-medium for alkoxymethylation of alcohols and their interconversion to acetates and TMS-ethers
Crystal structure of triphenyl(vinyl)phosphonium tetraphenylborate
The title ionic salt, C21H20P+·C24H20B−, crystallized with two independent vinyltriphenylphosphonium cations and two independent tetraphenylborate anions per asymmetric unit. These four independent moieties contain nearly perfect tetrahedral symmetry about their respective central C atoms. In the crystal, there are no π-stacking or other intermolecular interactions present
Efficient one-pot synthesis of 2,3-dihydroquinazolin-4(1<i>H</i>)-ones from aromatic aldehydes and their one-pot oxidation to quinazolin-4(3<i>H</i>)-ones catalyzed by Bi(NO<sub>3</sub>)<sub>3</sub>·5H<sub>2</sub>O: Investigating the role of the catalyst
Dual functional ionic liquids as plasticisers and antimicrobial agents for medical polymers
Contamination of medical devices with bacteria such as Meticillin resistant Staphylococcus aureus (MRSA) is of great clinical concern. Poly(vinyl chloride) is widely used in the production of medical devices, such as catheters. The flexibility of catheter tubing is derived from the addition of plasticisers. Here, we report the design of two dual functional ionic liquids, 1-ethylpyridinium docusate and tributyl(2-hydroxyethyl)phosphonium docusate, which uniquely provide a plasticising effect, and exhibit antimicrobial and antibiofilm-forming activity to a range of antibiotic resistant bacteria. The plasticisation of poly(vinyl chloride) was tailored as a function of ionic liquid concentration. The effective antimicrobial behaviour of both ionic liquids originates from the chemical structure of the anion or cation and is not limited to the length of the alkyl chain on the anion/cation. The design approach adopted will be useful in developing ionic liquids as multi-functional additives for polymers
Thermophysical Properties of Imidazolium-Based Lipidic Ionic Liquids
The
thermophysical properties of three lipidic ionic liquids, 1-oleyl-3-methylimidazolium
bistriflimide, 1-elaidyl-3-methylimidazolium bistriflimide, and 1-linoleyl-3-methyl-imidazolium
bistriflimide are measured at 1 bar as a function of temperature over
the range of 273 K to 353 K and correlated to appropriate models.
Each of these compounds is a variation on 1-C<sub>18</sub>-3-methylimidazolium
bistriflimide, where the C<sub>18</sub> chain contains one or more
unsaturations, incorporated into the structure to lower the melting
point. Derived properties such as molar volume and volume expansivity
are also calculated. The data are compared with literature values
for shorter chain 1-<i>n</i>-alkyl-3-methylimidazolium bistriflimide
salts. The longer chains impart lower densities and higher viscosities
relative to their shorter chain homologues. Although the subtle structural
differences between the three compounds result in significant differences
in melting points, there is less of an effect on the liquid phase
thermophysical properties
Direct Air Capture of CO<sub>2</sub> via Ionic Liquids Derived from “Waste” Amino Acids
Direct capture of CO2 from anthropogenic emissions
is
an imperative societal task as the concentration of global atmospheric
CO2 continues to increase drastically. The long-term goal
of negative emission requires methods to remove carbon directly from
the atmosphere, oceanwater, and nonpoint sources. Ionic liquids (ILs)
have had a pivotal impact on finding and implementing innovative solutions
that enable a more sustainable future. Here, we report the first example
of an IL-enabled approach for direct CO2 capture from the
atmosphere on a laboratory scale. These de novo bioderived materials
represent an ideal milieu for direct carbon capture applications because
of their nonvolatility and a priori low toxicity. Easily prepared
liquid salts based on a mixture of three common amino acids, valine,
leucine, and isoleucine, were found to be effective sorbents for ready
and reversible CO2 sequestration from air despite its very
low concentration. Collectively known as branched-chain amino acid,
they are commonly derived from biowaste products, for example, feathers,
fur, and even human hair. Therefore, the resultant ILs from the “waste”
amino acids provide an exciting prospect in terms of CO2 transformation and waste utilization. We provided valuable design
insights for engineering structure–property relationships in
amino acid-based ILs. The impact of moisture on the absorption characteristics
and capacity was evaluated in ambient conditions. We postulate that
the high capture efficiency and stability of these ILs make them superior
to present amine- and alkali-assisted approaches for the direct air
capture of CO2 as a scalable process