@Article{JPhysChemA_104_1804,
author = {E. Vauthey},
title = {{Effect of Steric Hindrance on the Dynamics of Charge Recombination within Geminate Ion Pairs}},
journal= {J. Phys. Chem. A},
ISSN = {1089-5639},
volume= {104},
number= {9},
pages = {1804-1810},
url = {http://pubs.acs.org/doi/abs/10.1021/jp993522d},
eprint= {http://www.unige.ch/sciences/chifi/publis/refs_pdf/ref00092.pdf},
doi= {10.1021/jp993522d},
abstract = {{The dynamics of charge recombination within geminate ion pairs formed by electron transfer (ET) quenching of excited aromatic hydrocarbons by aliphatic and aromatic amines was investigated using picosecond transient grating spectroscopy. With aliphatic donors, the rate constant of back ET, {\em k}$_{BET}$, shows a substantial decrease with increasing steric encumbrance around the N atom. No correlation between {\em k}$_{BET}$ and the exergonicity of the process was observed. This effect is ascribed to a decrease of the electronic coupling matrix element, {\em V}, which is affected by both the distance between the N atom of the donor and the aromatic plane of the acceptor and by the delocalization of the hole upon increasing the bulkiness of the alkyl substituents. With aromatic amines, {\em k}$_{BET}$is substantially slower than with the unhindered amines. This is also explained in terms of a smaller value of {\em V} because of charge delocalization.}},
year = {2000}
}
@Article{ChemPhysLett_326_321,
author = {P.-A. Muller and C. Hoegemann and X. Allonas and P. Jacques and E. Vauthey},
title = {{Deuterium Isotope Effect on the Charge Recombination Dynamics of Contact Ion Pairs Formed by Electron-Transfer Quenching in Acetonitrile}},
journal= {Chem. Phys. Lett.},
ISSN = {0009-2614},
volume= {326},
number= {3-4},
pages = {321-327},
url = {http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6TFN-40XNWWD-P&_user=779890&_coverDate=08%2F18%2F2000&_rdoc=20&_fmt=summary&_orig=browse&_srch=%23toc%235231%232000%23996739996%23206079!&_cdi=5231&_sort=d&_docanchor=&_acct=C000043220&_version=1&_urlVersion=0&_userid=779890&md5=f9c8aa45099e9112ad5100e7c2b2ebed},
eprint= {http://www.unige.ch/sciences/chifi/publis/refs_pdf/ref00091.pdf},
doi= {10.1016/S0009-2614(00)00791-0},
abstract = {{The deuterium isotope effect on the fluorescence lifetime of contact ions pairs (CIP) composed of 9,10-dicyanoanthracene and weak aromatic electron donors in acetonitrile has been investigated. For all pairs studied, an increase of the emission lifetime with increasing deuterium substitution on both the electron acceptor and the electron donor was observed. The free ion yield shows the same variation upon deuteration. It is concluded that the efficiency of free ions formation is essentially determined by the competition, within the CIP, between charge recombination and dissociation into free ions and that loose ion pairs do not play a significant role.}},
year = {2000}
}
@InBook{UltrafastPhenomenaXII_485,
author = {E. Vauthey},
title = {{Investigation of the Ultrafast Dynamics of Charge Recombination of Ion Pairs Using Multiplex Transient Grating Spectroscopy}},
booktitle= {Ultrafast Phenomena XII},
editor = {(T. Elsaesser, S. Mukamel, M. M. Murnane and N.F. Scherer Eds), Springer: Berlin},
publisher= {(T. Elsaesser, S. Mukamel, M. M. Murnane and N.F. Scherer Eds), Springer: Berlin},
address = {},
pages = {485},
year = {2000}
}
@Article{EPANewslett__70_30,
author = {E. Vauthey},
title = {{Applications of Transient Grating Techniques for Investigating Ultrafast Processes}},
journal= {EPA Newslett.},
ISSN = {1035-1701},
volume= {70},
pages = {30-57},
year = {2000}
}