Molecular-level properties of ionic liquids (ILs) draw an increasing interest. Several informative experimental approaches for investigation of nano/miscrostructuring phenomena and local viscosity/rigidity of ILs use probe molecules sensitive to microenvironment along with suitable detection techniques. In this work, we for the first time investigate capabilities of photoexcited triplet fullerenes to probe local properties of ILs, with time-resolved electron paramagnetic resonance (TR EPR) being a sensitive detection tool. We have selected C and its derivative phenyl-C-butyric acid methyl ester (PCBM) as probes and ILs [Bmim]BF and [Cmim]BF as solvents. C and PCBM demonstrate different sensitivities to microenvironment in ILs. Spin dynamics of photoexcited C is strongly contributed by pseudorotation of the Jahn-Teller axis, making its use as a probe for microenvironment challenging. This behavior is strongly suppressed in PCBM, which, in addition, is more soluble in ILs than C. The in-depth analysis of variable-temperature two-dimensional TR EPR data shows that spectral shapes are sensitive to the restricted mobility of PCBM in ILs. In this way, the information on local environment and heterogeneities in ILs can be obtained by TR EPR. PCBM usefully complements the other spin probes previously implemented for EPR studies in ILs. It is larger in size and in addition allows high-sensitivity TR EPR measurements up to a room temperature, which is an important improvement for characterization of heterogeneities in room-temperature ILs.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.jpcb.8b04000DOI Listing

Publication Analysis

Top Keywords

ils
10
time-resolved electron
8
electron paramagnetic
8
paramagnetic resonance
8
ionic liquids
8
epr
5
pcbm
5
resonance study
4
study photoexcited
4
photoexcited fullerenes
4

Similar Publications

Designing dicationic organic salts and ionic liquids exhibiting high fluorescence in the solid state.

J Ion Liq

December 2024

Department of Chemistry and Biochemistry, University of Nevada Las Vegas, 4505 S. Maryland Parkway, Box 454003, Las Vegas, NV 89154, United States.

Dicationic ionic liquids (DILs) are emerging as a powerful, next-generation approach to designing applied ILs because of their superior physicochemical properties as well as their diverse complexity and tunability for task specific applications. DILs are scarce in the literature compared to monocationic ILs (MILs), and one of their main issues is their expected tendency to possess higher melting temperatures. A series of 1,4-bis[2-(4-pyridyl)ethenyl] benzene and 1,4-bis[2-(2-pyridyl)ethenyl]benzene quaternary salts (Q-BPEBs) with different counterions (bromide, tosylate, and triflimide) and carbon chain lengths (C, C, and C) have been synthesized for their potential as DILs with strong photoluminescent properties in the solid state.

View Article and Find Full Text PDF

This study focuses on two types of phosphonium cation-based ionic liquids (P-ILs) with different alkyl chains: triethylalkylphosphonium (P222R) and tributylalkylphosphonium (P444R) cations. Broadband dielectric spectroscopy showed that the translational motion of the ions accelerated with an increasing number of alkyl chains by coupling with their rotational motion in both P-ILs. Raman spectroscopy revealed that P222R cations, despite dielectric similarities to P444R cations, can form all-trans conformations and cation-rich nanodomains because they have a relatively polar, short alkyl chain moiety with a central P atom and less-polar alkyl chains than those of P444R cations.

View Article and Find Full Text PDF

Sigal peptides have garnered remarkable efficacy in rejuvenating photoaged skin and delaying senescence. Nevertheless, their low solubility and poor permeability bring about a formidable challenge in their transdermal delivery. To address this challenge, bioactive ionic liquids (ILs) synthesized from natural glycyrrhizic acid (GA) and oxymatrine (OMT) with eminent biocompatibility is first prepared.

View Article and Find Full Text PDF

Characterization of 1,8-diazabicyclo(5.4.0)undec-7-ene-hydroxyl-based ionic liquid for CO capture.

R Soc Open Sci

January 2025

Fundamental and Applied Sciences Department, Centre of Ionic Liquids, Universiti Teknologi PETRONAS, Seri Iskandar, Perak Darul Ridzuan 32610, Malaysia.

Six 1,8-diazabicyclo(5.4.0)undec-7-ene-based ionic liquids (ILs) linked with ethyl or propyl hydroxyl cations, coupled with thiocyanate, dicyanamide and bistriflimide anions, were synthesized through a two-step reaction: quaternization and ion exchange.

View Article and Find Full Text PDF

Isoniazid (INH) and rifampicin (RIF) are the two main drugs used for the management of tuberculosis. They are often used as a fixed drug combination, but their delivery is challenged by suboptimal solubility and physical instability. This study explores the potential of active pharmaceutical ingredient-ionic liquids (API-ILs) to improve the physicochemical and pharmaceutical properties of INH and RIF.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!