4.5 Article

Photoinduced Bimolecular Electron Transfer from Cyano Anions in Ionic Liquids

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 119, Issue 46, Pages 14790-14799

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.5b09216

Keywords

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Funding

  1. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences at Rutgers [DE-SC0001780]
  2. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences at Penn State [DE-SC0008640]
  3. U.S. Department of Energy (DOE) [DE-SC0008640, DE-SC0001780] Funding Source: U.S. Department of Energy (DOE)

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Ionic liquids with electron-donating anions are used to investigate rates and mechanisms of photoinduced bimolecular electron transfer to the photoexcited acceptor 9,10-dicyanoanthracene (9,10-DCNA). The set of five cyano anion ILs studied comprises the 1-ethyl-3-methylimidazolium cation paired with each of these five anions: selenocyanate, thiocyanate, dicyanamide, tricyanomethanide, and tetracyanoborate. Measurements with these anions dilute in acetonitrile and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)-amide show that the selenocyanate and tricyanomethanide anions are strong quenchers of the 9,10-DCNA fluorescence, thiocyanate is a moderately strong quencher, dicyanamide is a weak quencher, and no quenching is observed for tetracyanoborate. Quenching rates are obtained from both time-resolved fluorescence transients and time-integrated spectra. Application of a Smoluchowski diffusion-and-reaction model showed that the complex kinetics observed can be fit using only two adjustable parameters, D and V-0, where D is the relative diffusion coefficient between donor and acceptor and V-0 is the value of the electronic coupling at donor-acceptor contact.

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