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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Published on: March 24, 2018
Electron photodetachment from iodide in ionic liquids through charge-transfer-to-solvent band excitation
Ryuzi Katoh1, Yoichi Yoshida, Yosuke Katsumura
1National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan. r-katoh@aist.go.jp
Abstract:
Solvation of iodide and electrons in an ionic liquid (N,N,N-trimethyl-n-propylammonium bis(trifluoromethanesulfonyl)imide; TMPA-TFSI) was studied through the absorption spectra of the charge-transfer-to-solvent (CTTS) state of iodide and of solvated electrons. The interaction between the TMPA cation and iodide was strong, whereas electrons were weakly solvated in TMPA-TFSI. We followed electron photodetachment from iodide to the ionic liquid and formation of the solvated electrons by observing absorption in the visible and near-infrared regions using a nanosecond laser flash photolysis method. The quantum yield of the photodetachment in TMPA-TFSI was estimated to be 0.34, which is much higher than that in a high-concentration aqueous salt solution previously reported. We also examined a reaction of the solvated electrons with the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (Bmim-TFSI) as a solute in TMPA-TFSI. The reaction rate was determined to be 5.3 x 10(8) M(-1) s(-1). The electrons before full solvation (dry electrons) reacted with Bmim cations efficiently. These observations suggest that the electrons in TMPA-TFSI can move easily before solvation.
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