54300-24-2Relevant articles and documents
Does the ethanolammonium acetate ionic liquid mix homogeneously with molecular solvents?
Zhu, Xiao,Zhang, Huan,Xu, Yingjie
, p. 205 - 212 (2016)
In order to study micro-structural heterogeneities in the solutions of ionic liquids (ILs), ethanolammonium acetate (EOAA) IL has been synthesized and 1H NMR spectra of its binary solutions, namely EOAA/DMSO and EOAA/n-butanol, have been measured at 298.15 K. Then the concentration-dependent chemical shifts δ (-CH3, EOAA), δ (-CH3, DMSO) and δ (-CH3, n-butanol) have been correlated separately using the local composition (LC) model. The results indicated that self-association of EOAA played the leading role within EOAA-rich region in mixtures. However with the molecular solvents increasing, the interactions between EOAA and solvents gradually predominated. Moreover the comparisons between DMSO and n-butanol have demonstrated that DMSO could break the network of IL more easily, indicating that the influence of DMSO on the properties of EOAA should be more obvious, which was consistent with experimental results of viscosity and conductivity. Furthermore the maximum difference between the local and the bulk appeared at x(EOAA) ≈ 0.5 for both systems, which reflected remarkable nonideality of mixtures at this concentration.
Binary Mixture of Double Protic Ionic Liquid: Density, Viscosity, Refractive Index, Surface Tension, and Derivative Properties
Buarque, Filipe S.,Camêlo, Lídia C. A.,Soares, Cleide M. F.,Mattedi, Silvana,Ferreira, Ailton F. B.,Feitosa, Filipe X.,Souza, Ranyere L.,de Sant’Ana, Hosiberto B.,Lima, álvaro S.
, p. 4309 - 4325 (2021/11/18)
This work presents density (ρ), dynamic viscosity (η), refractive index (nD), and surface tension (γ) experimental data for three pure protic ionic liquids: 2-hydroxyethylammonium acetate ([2-HEA][Ac]), bis(2-hydroxyethyl)ammonium acetate ([BHEA][Ac]), and bis(2 hydroxyethyl)ammonium butyric ([BHEA][Bu]), along with experimental data for two binary systems, as follows: ([2-HEA][Ac] + [BHEA][Ac]) and ([2-HEA][Ac] + [BHEA][Bu]), at a temperature range ofT= 278.15 to 343.15 K and atmospheric pressure (101.3 kPa). For the ([2-HEA][Ac] + [BHEA][Ac]) binary system, excess volume and refractive index deviation values are negative, while for the ([2-HEA][Ac] + [BHEA][Bu]) binary system are positive. For the first, there is a volume contraction, with higher probability of ion interactions. For the latter system, an expansive trend and lower ion interactions were found when compared to the ([2-HEA][Ac] + [BHEA][Ac]) system. Viscosity deviations values show a negative behavior for both binary systems studied. These results could indicate the predominance of dispersive forces. Furthermore, for the [2-HEA][Ac] + [BHEA][Ac] system, surface tension deviation values are positive. On the other hand, for the [2-HEA][Ac] + [BHEA][Bu] system this derivative property are negative. From these results, the [2-HEA][Ac] + [BHEA][Ac] binary system could be characterized by presenting prevalent dispersion forces and an unequal distribution of the mixture components between the bulk and interface.
Hydroxyl alkyl ammonium ionic liquid assisted green and one-pot regioselective access to functionalized pyrazolodihydropyridine core and their pharmacological evaluation
Patel, Divyang M.,Sharma, Mayank G.,Vala, Ruturajsinh M.,Lagunes, Irene,Puerta, Adrián,Padrón, José M.,Rajani, Dhanji P.,Patel, Hitendra M.
, p. 137 - 150 (2019/01/30)
Herein our team explored a promising synthetic trail to Functionalized pyrazolodihydropyridine core using hydroxyl alkyl ammonium ionic liquid via one-pot fusion of 3-methyl-1-phenyl-1H-pyrazole-5-amine, different heterocyclic aldehydes and 1, 3-Cyclic diones. The aimed compounds were obtained by Domino-Knoevenagel condensation and Michael addition followed by cyclization. The reaction transformation involves the formation of two C–C and one C–N bond formation. The perspective of the present work is selectively approached to Functionalized pyrazolodihydropyridine core excluding other potential parallel reactions under environmentally benign reaction condition. The present protocol show features such as the low E-factor, ambiphilic behavior of ionic liquid during reaction transformation, scale-up to a multigram scale, reusability of the ionic liquid, mild reaction condition, and produce water as a byproduct. All newly derived compounds were evaluated for their in vitro biological activities. In preliminary biological studies compound, 4c showed better potency than the standard drug ampicillin against Gram-negative bacteria (E. coli); the compound 4i exhibited outstanding activity against S. aeruginosa which is far better than ampicillin, chloramphenicol, and ciprofloxacin. The compound 4m was found more potent against C. albicans, than that of griseofulvin and show equipotency to nystatin whereas, in preliminary antitubercular screening, compound 4o was exhibited more potency than rifampicin. Noteworthy compounds 4f and 4i were found most active in antiproliferative screening.
