Bimolecular rate constants for diffusion in ionic liquidsElectronic supplementary information (ESI) available: Fig. S1: isokinetic plot obtained for the energy transfer reaction of 3BP* and N in five ionic liquids, toluene and acetonitrile. See http://www.rsc.org/suppdata/cc/b2/b202944h/

2002 ◽  
pp. 1880-1881 ◽  
Author(s):  
Andrew J. McLean ◽  
Mark J. Muldoon ◽  
Charles M. Gordon ◽  
Ian R. Dunkin
Keyword(s):  
Energy Transfer ◽  
Ionic Liquids ◽  
Rate Constants ◽  
Transfer Reaction ◽  
Supplementary Information

scholarly journals A study of background emissions enhancements in nitrogen afterglows, due to addition of discharged O2, in connection with the reactions {N2 (A3Σu+, υ) + O(3P)}, {O2 (a1Δg) + N(4S)} and {O2 (a1Δg) + N2 (A3Σu+)}

2005 ◽  
Vol 3 (3) ◽  
pp. 387-403 ◽  
Author(s):  
Efstathios Kamaratos
Keyword(s):  
Energy Transfer ◽  
Rate Constant ◽  
Rate Constants ◽  
Transfer Reaction ◽  
Experimental Results ◽  
Intensity Enhancement ◽  
Emissions Intensity ◽  
Additional Interpretation

AbstractIntensity enhancement due to the addition of discharged O2 is examined for background N2 (B Πg → A3Σu+) emissions in various flowing nitrogen afterglows. Possible implications are reported for the experimentally determined rate constants for the reactions {N2 (A3Σu+, υ) + O(3P)}, and {O2 (a1Δg) + N(4S)}, as a result of the present study. The present, as well as previously reported, N2 (B Πg → A3Σu+) emissions intensity enhancements suggest complementary conclusions. Previous differences in experimental results reported for the {O2 (a1Δg) + N(4S)} reaction [based on studies observing the decay of either O2 (a1Δg) molecules or N(4S) atoms alone] are reconciled by a unifying additional interpretation. This interpretation leads to a rate constant estimate for the energy transfer reaction, {O2 (a1Δg) + N(2(A3Σu+)}, deduced to account for the above N2 (B3Πg → A3Σu+) emissions intensity enhancements.

Machine learning approaches to understand and predict rate constants for organic processes in mixtures containing ionic liquids

2021 ◽  
Vol 23 (4) ◽  
pp. 2742-2752
Author(s):  
Tamar L. Greaves ◽  
Karin S. Schaffarczyk McHale ◽  
Raphael F. Burkart-Radke ◽  
Jason B. Harper ◽  
Tu C. Le
Keyword(s):  
Machine Learning ◽  
Ionic Liquids ◽  
Rate Constants ◽  
Learning Approaches ◽  
Learning Models ◽  
Organic Reaction ◽  
Machine Learning Models ◽  
Selection Of

Machine learning models were developed for an organic reaction in ionic liquids and validated on a selection of ionic liquids.

Rotational Distribution of CO(b3Σ+) Produced in Energy Transfer Reaction from Ar(3P2) to CO

1992 ◽  
Vol 65 (6) ◽  
pp. 1713-1715
Author(s):  
Masaharu Tsuji ◽  
Kazuo Yamaguchi ◽  
Mitsuo Kikukawa ◽  
Hiroyuki Kouno ◽  
Tsuyoshi Funatsu ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Transfer Reaction ◽  
Rotational Distribution

Extraction of energy transfer rate constants from the pulsed laser generated thermal lens spectrometer signal

1982 ◽  
Vol 80 ◽  
pp. 433-436 ◽  
Author(s):  
R.T. Bailey ◽  
F.R. Cruickshank ◽  
R. Guthrie ◽  
D. Pugh ◽  
I.J.M. Weir
Keyword(s):  
Energy Transfer ◽  
Thermal Lens ◽  
Rate Constants ◽  
Transfer Rate ◽  
Pulsed Laser ◽  
Energy Transfer Rate

Probing the microscopic structural organization of neat ionic liquids (ILs) and ionic liquid-based gels through resonance energy transfer (RET) studies

2017 ◽  
Vol 19 (34) ◽  
pp. 23194-23203 ◽  
Author(s):  
Debashis Majhi ◽  
Moloy Sarkar
Keyword(s):  
Ionic Liquid ◽  
Energy Transfer ◽  
Ionic Liquids ◽  
Structural Organization ◽  
Rhodamine 6G ◽  
Resonance Energy Transfer ◽  
Resonance Energy

With the aim to understand the role of the ionic constituents of ionic liquids (ILs) in their structural organization, resonance energy transfer (RET) studies between ionic liquids (donor) and rhodamine 6G (acceptor) have been investigated.

Ultrafast Energy And Electron Transfer In Conjugated Oligomer-Fullerene Molecules

2001 ◽  
Vol 665 ◽  
Author(s):  
P.A. van Hal ◽  
R.A.J. Janssen ◽  
G. Lanzani ◽  
G. Cerullo ◽  
M. Zavelani-Rossi ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Energy Transfer ◽  
Time Constant ◽  
Transfer Reaction ◽  
Polar Solvent ◽  
Phenylene Vinylene ◽  
Intramolecular Electron Transfer ◽  
Pump Probe ◽  
Energy And Electron Transfer ◽  
Probe Spectroscopy

ABSTRACTThe intramolecular photoinduced energy and electron transfer within a fullereneoligothiophene-fullerene triad with nine thiophene units (C60-9T-C60) and an oligo(p-phenylene vinylene)-fullerene dyad with four phenyl groups (OPV4-C60) is investigated with femtosecond pump-probe spectroscopy with sub-10 fs and 200 fs time resolution in solvents of different polarity. Photoexcitation of the π-conjugated oligomer moiety in the triad and dyad results in an ultrafast singlet-energy transfer reaction to create the fullerene singlet-excited state with a time constant of 150-190 fs, irrespective of the polarity of the medium. In a polar solvent, intramolecular electron transfer occurs from the oligomer moiety to the C60 moiety with a time constant of 10-13 ps as a secondary reaction, subsequent to the ultrafast singlet-energy transfer. The charge-separated state has a lifetime of 50-80 ps and recombines to the ground state.

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