@article {2438,
	title = {A DNAzyme with Three Protein-Like Functional Groups: Enhancing Catalytic Efficiency of M2+-Independent RNA Cleavage},
	journal = {Chembiochem},
	volume = {10},
	number = {12},
	year = {2009},
	note = {ISI Document Delivery No.: 487MWTimes Cited: 5Cited Reference Count: 76Hollenstein, Marcel Hipolito, Christopher J. Lam, Curtis H. Perrin, David M.},
	month = {Aug},
	pages = {1988-1992},
	type = {Article},
	keywords = {BEACON SENSOR, biology, CLEAVING DNA ENZYME, CYTOSOLIC FREE MAGNESIUM, DEOXYRIBOZYMES, DNAzymes, enzyme catalysis, EVOLUTION, HAIRPIN RIBOZYME, HIGH-DENSITY, IN-VITRO SELECTION, ION, nucleic acids, NUCLEIC-ACIDS, RNAse A mimics, synthetic},
	isbn = {1439-4227},
	url = {<Go to ISI>://000269279700012},
	author = {Hollenstein, M. and Hipolito, C. J. and Lam, C. H. and Perrin,David M.}
}
@article {2426,
	title = {Products and kinetics of the reactions of an alkane monolayer and a terminal alkene monolayer with NO3 radicals},
	journal = {Journal of Geophysical Research-Atmospheres},
	volume = {114},
	year = {2009},
	note = {ISI Document Delivery No.: 401ZETimes Cited: 10Cited Reference Count: 95Gross, Simone Bertram, Allan K.},
	month = {Jan},
	pages = {14},
	type = {Article},
	abstract = {The reactions of an alkanethiol and a terminal alkenethiol self-assembled monolayer with NO3 radicals (in the presence of NO2 and O-2) were studied. For the alkane monolayer, infrared (IR) spectroscopy and time-of-flight secondary ion mass spectrometry (ToF-SIMS) confirmed the formation of organonitrates (RONO2). The observation of organonitrates is in contrast to the recent X-ray photoelectron spectroscopy (XPS) data, which showed very little nitrogen-containing surface species. The identification of organonitrates may help explain why significant volatilization of the organic chain was not observed in recent studies of alkane monolayer oxidation by NO3 radicals. The reactive uptake coefficient (gamma) of NO3 on alkene monolayers determined in our study is higher than the values obtained in a recent study using liquid and solid alkene bulk films. A possible reason for this difference may be the location of the double bond at the interface. Using the g value determined in our studies, we show that under conditions where NO3 is high the lifetime of an alkene monolayer in the atmosphere may be short ( approximately 20 min). XPS, IR, and ToF-SIMS were used to identify surface functional groups after the oxidation of the alkene monolayers by NO3. The results are consistent with the formation of C-O, aldehyde/ketone, carboxylic groups, and nitrogen containing species.},
	keywords = {GAS-PHASE, HETEROGENEOUS OXIDATION, ION, MASS-SPECTROMETRY, NITROGEN-DIOXIDE, OH RADICALS, OLEIC-ACID, POLYCYCLIC AROMATIC-HYDROCARBONS, REACTIONS, RELATIVE RATE CONSTANTS, SELF-ASSEMBLED MONOLAYERS, VOLATILE ORGANIC-COMPOUNDS},
	isbn = {0148-0227},
	url = {<Go to ISI>://000262982300003},
	author = {Gross, S. and Bertram, A. K.}
}
@article {1416,
	title = {Energetics and dynamics of threshold photoion-pair formation in HF/DF},
	journal = {Journal of Chemical Physics},
	volume = {124},
	number = {7},
	year = {2006},
	note = {ISI Document Delivery No.: 014IPTimes Cited: 4Cited Reference Count: 36},
	month = {Feb},
	pages = {10},
	type = {Article},
	abstract = {Threshold ion-pair production spectroscopy (TIPPS) has been applied to two isotopomers, HF and DF. From the high resolution (similar to 0.3 cm(-1)) TIPP spectra, the ion-pair thresholds of HF/DF have been precisely measured. Combined with the ionization energy of H(D), the electron affinity of F, and the zero point energies of HF/DF, the difference between their classical bond dissociation energies was obtained as D-e(H-F)-D-e(D-F)=12.4 +/- 0.5 cm(-1). Our result provides an experimental estimate of the Born-Oppenheimer breakdown in the ground electronic state. The present work also measured the total ion-pair yield spectra of HF and DF in the threshold region, and the ion-pair formation mechanisms of these two molecules were discussed in light of the high resolution results.},
	keywords = {Born-Oppenheimer breakdown, DIATOMIC HYDRIDES, DISSOCIATION-ENERGIES, ELECTRONIC-SPECTRUM, HF, ION, ISOTOPIC DEPENDENCE, PHOTOELECTRON-SPECTROSCOPY, PRODUCTION SPECTROSCOPY, X1-SIGMA+ STATES},
	isbn = {0021-9606},
	url = {<Go to ISI>://000235473500019},
	author = {Hu, Q. J. and Hepburn, J. W.}
}
@inbook {1136,
	title = {Dynamics and energetics of photoion-pair formation in HF/DF},
	booktitle = {DR2004: Sixth International Conference on Dissociative Recombination: Theory, Experiments and Applications},
	series = {Journal of Physics Conference Series},
	volume = {4},
	year = {2005},
	note = {ISI Document Delivery No.: BCE13Times Cited: 5Cited Reference Count: 23Proceedings Paper6th International Conference on Dissociative RecombinationJUL 12-16, 2004Mosbach, GERMANYDIRAC HOUSE, TEMPLE BACK, BRISTOL BS1 6BE, ENGLAND},
	pages = {267-271},
	publisher = {Iop Publishing Ltd},
	organization = {Iop Publishing Ltd},
	address = {Bristol},
	abstract = {Preliminary results of a high resolution coherent vacuum ultraviolet study of photoion-pair formation in HF/DF are reported. These results include threshold ion-pair production (TIPPS) and total photoion-pair yield spectra, which show sharp resonances due to predissociating Rydberg states. Detailed analysis of the spectra provides precise energies for the ion-pair thresholds, and insight into the mechanism for ion-pair formation.},
	keywords = {DF, DISSOCIATION, F2, HCL, HF, ION, PRODUCTION SPECTROSCOPY, STATES, THRESHOLD},
	isbn = {1742-6588},
	url = {<Go to ISI>://000228817000040},
	author = {Hu, Q. J. and Hepburn, J. W.},
	editor = {Wolf, A. and Lammich, L. and Schmelcher, P.}
}
@article {639,
	title = {N-bromosuccinimide promoted ring expansion reactions: Diastereoselective formation of functionalized azaspirocyclic cyclopentanones},
	journal = {Synlett},
	number = {14},
	year = {2003},
	note = {ISI Document Delivery No.: 741GTTimes Cited: 10Cited Reference Count: 30},
	month = {Nov},
	pages = {2131-2134},
	type = {Article},
	abstract = {N-Bromosuccinimide (NBS) induces ring enlargements of 2-(1-hydroxycyclobutyl)-p-toluenesulfonylenamides such as 1. These high yielding reactions typically occur with good diastereoselectivity. This ring expansion protocol under neutral conditions forms compounds that are potentially versatile intermediates for the construction of spirocycle-containing alkaloids.},
	keywords = {bromine, CONSTRUCTION, entry, HALICHLORINE, ION, KETONES, PINNAIC ACID, piperidines, REDUCTION, ring expansion, spiro compounds, SPIROCYCLIC CORE, STEREOSELECTIVE},
	isbn = {0936-5214},
	url = {<Go to ISI>://000186450900005},
	author = {Hurley, P. B. and Dake, G. R.}
}
@inbook {423,
	title = {Pre-steady-state kinetics of enzymatic reactions studied by electrospray mass spectrometry with on-line rapid-mixing techniques},
	booktitle = {Enzyme Kinetics and Mechanism, Pt F: Detection and Characterization of Enzyme Reaction Intermediates},
	series = {Methods in Enzymology},
	volume = {354},
	year = {2002},
	note = {ISI Document Delivery No.: BV53FTimes Cited: 8Cited Reference Count: 42Review525 B STREET, SUITE 1900, SAN DIEGO, CA 92101-4495 USA},
	pages = {50-64},
	publisher = {Academic Press Inc},
	organization = {Academic Press Inc},
	address = {San Diego},
	keywords = {ACID, BETA-LACTAMASE, CATALYSIS, COMPLEXES, INTERMEDIATE, ION, IONIZATION, MECHANISM, REAL-TIME},
	isbn = {0076-6879},
	url = {<Go to ISI>://000179267700003},
	author = {Konermann, L. and Douglas, D. J.}
}
@article {4843,
	title = {Chirally modified zeolites as reaction media: Photochemistry of an achiral tropolone ether},
	journal = {Organic Letters},
	volume = {2},
	number = {2},
	year = {2000},
	note = {ISI Document Delivery No.: 278ZETimes Cited: 49Cited Reference Count: 26},
	month = {Jan},
	pages = {119-121},
	type = {Article},
	abstract = {[GRAPHICS] Zeolites modified with chiral inductors serve as media for performing chiral induction during photochemical reactions of organic molecules. The photochemical behavior of achiral tropolone ethyl phenyl ether illustrates this unique feature of a zeolite.},
	keywords = {AROMATICS, benzene, CATION-PI INTERACTIONS, CHEMISTRY, interactions, ION, MODEL, MOLECULE, STATE ORGANIC-PHOTOCHEMISTRY, WATER},
	isbn = {1523-7060},
	url = {<Go to ISI>://000085018200006},
	author = {Joy, A. and Scheffer, J. R. and Ramamurthy, V.}
}
@article {4208,
	title = {Analyte-additive interactions in nonaqueous capillary electrophoresis: a critical review},
	journal = {Trac-Trends in Analytical Chemistry},
	volume = {17},
	number = {7},
	year = {1998},
	note = {ISI Document Delivery No.: 107HPTimes Cited: 54Cited Reference Count: 40},
	month = {Aug},
	pages = {424-434},
	type = {Review},
	abstract = {This article reviews the recent developments in nonaqueous capillary electrophoresis and discusses the effect of the solvent on analyte-additive interactions. When nonaqueous solvents are used, solvophobic interactions are generally weaker than those in water; therefore, those additives that can change the analyte mobility through electrostatic or donor-acceptor interactions should be further explored. (C) 1998 Elsevier Science B.V. All rights reserved.},
	keywords = {ANIONS, CHIRAL SEPARATION, cohesion energy, density, dielectric constant, electron donor-acceptor interaction, FORMAMIDE, ION, MEDIA, nonaqueous capillary electrophoresis, SEPARATION SELECTIVITY, solvent effect, SOLVENTS, SURFACTANTS, WATER, ZONE ELECTROPHORESIS},
	isbn = {0165-9936},
	url = {<Go to ISI>://000075202300022},
	author = {Bowser, M. T. and Kranack, A. R. and Chen, D. D. Y.}
}
@article {4232,
	title = {Conjugate Bronsted-Lewis superacids in fluorosulfuric acid - Hammett acidity function and electrical conductivity studies of Ta(V), Nb(V) and Sb(V) Lewis acids},
	journal = {Journal of Fluorine Chemistry},
	volume = {89},
	number = {1},
	year = {1998},
	note = {ISI Document Delivery No.: ZJ736Times Cited: 0Cited Reference Count: 41},
	month = {Apr},
	pages = {117-123},
	type = {Article},
	abstract = {{Conjugate Bronsted-Lewis superacids in fluorosulfuric acid are studied by two techniques. Hammett acidity function studies on HSO3F-Ta(SO3F)(5) in the concentration range of 0-3.4 mol\% of Lewis acid are reported. The conjugate system HSO3F-Ta(SO3F)(5) shows in this range of Lewis acid concentration acidities equal or higher to those of HSO3F-3SO(3)-SbF5, which is commonly assumed to be the strongest conjugate protonic acid. Electrical conductivities of the neat Lewis acids of the type MFn(SO3F)(5-n)},
	keywords = {BEHAVIOR, BIS(FLUOROSULFATE), Bronsted-Lewis, conjugate, CONVENIENT, FLUORIDE, GOLD(III) FLUOROSULFATE, H2SO4-HSO3F, ION, MOLECULAR-STRUCTURES, protonic acid, SYSTEMS, TETRAKIS(FLUOROSULFATO)AURATE(III)},
	isbn = {0022-1139},
	url = {<Go to ISI>://000073247800022},
	author = {Cicha, W. V. and Zhang, D. L. and Aubke, F.}
}
@article {4418,
	title = {Structural, spectroscopic, thermodynamic and kinetic properties of copper(II) complexes with tripodal tetraamines},
	journal = {Inorganic Chemistry},
	volume = {37},
	number = {16},
	year = {1998},
	note = {ISI Document Delivery No.: 110GETimes Cited: 87Cited Reference Count: 38},
	month = {Aug},
	pages = {4022-4029},
	type = {Article},
	abstract = {Spectroscopic, thermodynamic, and kinetic measurements have been made on aqueous solutions of copper(II) complexes of hexamethylated tren and trimethylated tren (one methylation per primary amine group of tren) with the objective of correlating: the influence of geometry (trigonal bipyramidal, evident from UV/vis spectroscopy) and N-alkyl substitution in the ligand on these inherent properties. At 25.0 degrees C the protonation constants of Me(3)tren are not significantly different from those of tren and Me(6)tren, and the stability constant for the Cu(II) complex is of the same order of magnitude as that for the [Cu(tren)(H2O)](2+) complex ion; The pK(a) for deprotonation of the coordinated water molecule of [Cu(Me(3)tren)(H2O)](2+) is intermediate between the values for the complexes containing the unsubstituted and the fully substituted tren ligand. Substitution (pyridine for water) kinetics measurements employing stopped-flow and temperature-jump methods revealed different patterns of reactivity: pyridine replaces water in [Cu(Me(3)tren)(H2O)](2+) with a second-order rate constant of (4.4 +/- 0.8) x 10(2) M-1 s(-1) at 25.0 degrees C, whereas the corresponding process for [Cu(Me(6)tren)(H2O)](2+) is relatively complex and is discussed in more detail. Substitution in the former complex ion is characterized in the forward and reverse directions, by Delta H-double dagger = 60 +/- 8 and 51.9 +/- 0.9 kJ mol(-1), Delta S-double dagger = 5 +/- 27 and -23 +/- 3 J mol(-1) K-1, and Delta V-double dagger = -8.7 +/- 4.6 and -6.2 +/- 1.1 cm(3) mol(-1), respectively, It is concluded that this reaction follows an I-a mechanism, similar to that reported for the comparable reaction of [Cu(tren)(H2O)](2+). An X-ray structural determination on a crystal of [Cu-2(Me(3)tren)(2)(CN)] (ClO4)(3) . 2CH(3)CN demonstrated trigonal bipyramidal geometry about each copper(II) center. As has been found in comparable complexes of tren and Me(6)tren, the axial nitrogen to copper bond is shorter than the equatorial nitrogen-copper bonds, and the angle made by N(axial)-Cu-N(equatorial) is less than 90 degrees (84.6-85.4 degrees), signifying that each copper ion lies below the plane of the equatorial nitrogen atoms.},
	keywords = {AQUEOUS-SOLUTION, CRYSTAL-STRUCTURE, ELECTRONIC-PROPERTIES, IMIDAZOLE, ION, MECHANISM, PHENANTHROLINE, PRESSURE-DEPENDENCE, RESONANCE, SUBSTITUTION KINETICS},
	isbn = {0020-1669},
	url = {<Go to ISI>://000075371200019},
	author = {Thaler, F. and Hubbard, C. D. and Heinemann, F. W. and vanEldik, R. and Schindler, S. and Fabian, I. and Dittler-Klingemann, A. M. and Hahn, F. E. and Orvig, Chris}
}
@article {3913,
	title = {Synthesis, derivatization and structural characterization of octahedral tris(5-phenyl-4,6-dipyrrinato) complexes of cobalt(III) and iron(III)},
	journal = {Inorganica Chimica Acta},
	volume = {263},
	number = {1-2},
	year = {1997},
	note = {ISI Document Delivery No.: YD821Times Cited: 48Cited Reference Count: 43},
	month = {Oct},
	pages = {279-286},
	type = {Article},
	abstract = {{The formation of octahedral tris(5-phenyl-4,6-dipyrrinato) complexes of cobalt(III) and iron(III) of p-substituted (-H, -CO2Me, -NO2) 5-phenyl-4,6-dipyrrins is described. The molecular structure of the parent cobalt(III) complex was determined by X-ray crystallography. Crystals of C45H33N6Co . C3H6O are monoclinic},
	keywords = {5-phenyldipyrromethanes, cobalt(III) chelates, COMPLEXES, COPPER(II), crystal structures, DIPYRROMETHENES, ION, iron(III) chelates, meso-phenyldipyrrinato, meso-phenyldipyrrins, NICKEL(II), PYRROLE PIGMENTS, TRANSITION-METAL COMPLEXES},
	isbn = {0020-1693},
	url = {<Go to ISI>://A1997YD82100035},
	author = {Bruckner, C. and Zhang, Y. J. and Rettig, S. J. and Dolphin, D.}
}
@article {3568,
	title = {FIXATION OF AMMONIACAL COPPER PRESERVATIVES - REACTION OF VANILLIN, A LIGNIN MODEL-COMPOUND WITH AMMONIACAL COPPER-SULFATE SOLUTION},
	journal = {Holzforschung},
	volume = {49},
	number = {6},
	year = {1995},
	note = {ISI Document Delivery No.: TJ868Times Cited: 21Cited Reference Count: 23},
	pages = {483-490},
	type = {Article},
	abstract = {{A model for the fixation of ammoniacal copper preservatives in wood was examined through reaction of vanillin, a lignin model compound, with ammoniacal copper sulphate solution. The compound produced on evaporation of the aqueous ammoniacal solution has been characterized spectroscopically as di(amine)bis(vanillinato)copper(II); [Cu(vanillin)(2)(NH3)(2)]. Single crystal X-ray crystallographic studies showed that the crystals of [Cu(vanillin)(2)(NH3)(2)] are monoclinic with space group P2(1) with a = 5.4172(9)},
	keywords = {AMMONIACAL COPPER PRESERVATIVES, COMPLEXES, DIAMINE, ESR, FIXATION, ION, LIGNIN MODEL COMPOUND, RESONANCE, VANILLIN, WOOD PRESERVATION, X-ray crystal structure},
	isbn = {0018-3830},
	url = {<Go to ISI>://A1995TJ86800001},
	author = {Xie, C. S. and Ruddick, J. N. R. and Rettig, S. J. and Herring, F. G.}
}
@article {2982,
	title = {SOLVATION DYNAMICS IN ELECTROLYTE-SOLUTIONS},
	journal = {Journal of Chemical Physics},
	volume = {100},
	number = {2},
	year = {1994},
	note = {ISI Document Delivery No.: MT007Times Cited: 33Cited Reference Count: 40},
	month = {Jan},
	pages = {1552-1558},
	type = {Article},
	abstract = {A microscopic theory of the dynamics of ion solvation in electrolyte solutions is given. Consistent with the pure solvent case, the theory predicts a very fast and important inertial relaxation at short times. This is followed by oscillations and an extremely slow long-time decay associated with the formation of an equilibrium {\textquoteright}{\textquoteright}ion atmosphere{\textquoteright}{\textquoteright} about the newly charged particle.},
	keywords = {DIELECTRIC-RELAXATION, INVARIANT EXPANSION, ION, LIQUIDS, MEAN SPHERICAL MODEL, ORNSTEIN-ZERNIKE EQUATION, SIMULATIONS, SOLVENT, SPHERES},
	isbn = {0021-9606},
	url = {<Go to ISI>://A1994MT00700085},
	author = {Chandra, A. and Patey, G. N.}
}
@article {3064,
	title = {THE SYNTHESES AND VIBRATIONAL-SPECTRA OF BIS(CARBONYL)PLATINUM(II) FLUOROSULFATE, PT(CO)2(SO3F)2, AND BIS(CARBONYL)PALLADIUM(II) FLUOROSULFATE, PD(CO)2(SO3F)2},
	journal = {Journal of Fluorine Chemistry},
	volume = {66},
	number = {2},
	year = {1994},
	note = {ISI Document Delivery No.: MX367Times Cited: 26Cited Reference Count: 43},
	month = {Feb},
	pages = {159-166},
	type = {Article},
	abstract = {Reductive carbonylation of platinum(IV) tetrakis(fluorosulfate), Pt(SO3F)4, in fluorosulfuric acid at 80-degrees-C with a CO pressure of 1-2 atm resulted in the quantitative formation of creamy white bis(carbonyl)platinum(II) fluorosulfate, Pt(CO)2(SO3F)2. The corresponding bis(carbonyl)palladium(II) fluorosulfate, Pd(CO)2(SO3F)2, has been formed from solid Pd(II)Pd(IV)(SO3F)6 at room temperature and a CO pressure of 0.5 atm as a yellow solid that was thermally stable up to 117-degrees-C. Both compounds gave nearly identical IR and Raman spectra, which suggests a cis-square-planar configuration. The average CO stretching frequencies were at 2217 and 2201 cm-1 for Pd(CO)2(SO3F)2 and Pt(CO)2(SO3F)2, respectively. They are unusually high and suggest substantially reduced pi-back-donation. Pd(CO)2(SO3F)2 is the first example of a thermally stable mononuclear bis(carbonyl) derivative of dipositive palladium.},
	keywords = {CARBONYL-COMPLEXES, DERIVATIVES, GOLD(III) FLUOROSULFATE, ION, LATE TRANSITION-ELEMENTS, PALLADIUM(II)},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1994MX36700013},
	author = {Hwang, G. and Wang, C. and Bodenbinder, M. and Willner, H. and Aubke, F.}
}
@article {3124,
	title = {THE SYNTHESIS AND VIBRATIONAL-SPECTRA OF FLUOROSULFATE DERIVATIVES OF TITANIUM, ZIRCONIUM AND HAFNIUM},
	journal = {Journal of Fluorine Chemistry},
	volume = {68},
	number = {3},
	year = {1994},
	note = {ISI Document Delivery No.: PE264Times Cited: 3Cited Reference Count: 36},
	month = {Sep},
	pages = {239-248},
	type = {Article},
	abstract = {The syntheses of the binary fluorosulfates, Zr(SO3F), and Hf(SO3F)4, by oxidation of the corresponding metal powders with bis(fluorosulfuryl) peroxide, S2O6F2, in fluorosulfuric acid, HSO3F, are described. The resulting products are white hygroscopic solids which are not sufficiently soluble in HSO3F to allow electrical conductivity and NMR studies or Hammett acidity function (H-0) determinations in order to evaluate their use as Lewis acids in conjugate superacid systems. Oxidation of titanium under similar conditions resulted in the formation of a greenish-yellow resin-like material of limited thermal stability with the approximate composition Ti(SO3F)4. However, infrared spectra indicated the presence of small amounts of HSO3F. In addition, the solvolysis of ZrCl4 in an excess of HSO3F at 25-degrees-C has been investigated as a potential route to Zr(SO3F)4. The results indicate that short reaction times of 1-2 d yielded incompletely substituted products of the approximate composition ZrClx(SO3F)4-x (x = 0.22), while prolonged reaction times of 3-4 weeks gave rise to partially decomposed materials of approximate composition ZrO0.5F1.5(SO3F)1.5. The ability of all three tetrakis(fluorosulfato) metallates to act as SO3F- ion acceptors is evident from the isolation of thermally stable salts of the composition Cs2[M(SO3F)6] (M = Ti, Zr or Hf) when the metal oxidation was carried out in the presence of 2 mol equiv. of CsSO3F. All the materials were characterized by their vibrational spectra, which are extremely similar and closely resemble those of previously reported cesium hexakis(fluorosulfato) metallates.},
	keywords = {ACIDS, FLUORIDE, GOLD, GOLD(III) FLUOROSULFATE, ION, SUPERACID SYSTEMS},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1994PE26400003},
	author = {Mistry, F. and Aubke, F.}
}
@article {2749,
	title = {THE FREQUENCY-DEPENDENT CONDUCTIVITY OF ELECTROLYTE-SOLUTIONS},
	journal = {Journal of Chemical Physics},
	volume = {99},
	number = {3},
	year = {1993},
	note = {ISI Document Delivery No.: LN782Times Cited: 30Cited Reference Count: 25},
	month = {Aug},
	pages = {2083-2094},
	type = {Article},
	abstract = {The frequency dependent conductivity, sigma(omega), of model electrolyte solutions is investigated employing molecular dynamics simulations. Approximate analytical theories are also derived and evaluated. It is found that sigma(omega) is generally not a simple function and that its detailed frequency dependence contains much useful information about the structure and dynamics of ionic solutions. By varying molecular and state parameters such as the dipole moment and moment of inertia of the solvent, the ionic charge, the solution density, etc., we are able to obtain a physical interpretation of the behavior of sigma(omega). For example, very interesting dynamical solvation effects as well as features associated with ion pairs are identified and described.},
	keywords = {COMPUTER-SIMULATION, CONSTANT, DYNAMICS, ELECTROSTATIC SYSTEMS, FLUID, ION, MOLECULAR THEORY, PERIODIC BOUNDARY-CONDITIONS},
	isbn = {0021-9606},
	url = {<Go to ISI>://A1993LN78200070},
	author = {Chandra, A. and Wei, D. Q. and Patey, G. N.}
}
@article {2831,
	title = {SYNTHESIS AND CHARACTERIZATION OF TETRAKIS(CARBONYL)PLATINUM(II) HEXAKIS(FLUOROSULFATO)PLATINATE(IV), [PT(CO)4][PT(SO3F)6]},
	journal = {Inorganic Chemistry},
	volume = {32},
	number = {21},
	year = {1993},
	note = {ISI Document Delivery No.: MC686Times Cited: 36Cited Reference Count: 27},
	month = {Oct},
	pages = {4667-4669},
	type = {Note},
	keywords = {CATIONS, GOLD(III) FLUOROSULFATE, ION},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1993MC68600036},
	author = {Hwang, G. and Bodenbinder, M. and Willner, H. and Aubke, F.}
}
@article {7380,
	title = {SELECTED REACTIONS OF FLUORINE-FLUOROSULFATE, FOSO2F},
	journal = {Journal of Fluorine Chemistry},
	volume = {59},
	number = {3},
	year = {1992},
	note = {ISI Document Delivery No.: KF321Times Cited: 8Cited Reference Count: 36},
	month = {Dec},
	pages = {333-349},
	type = {Article},
	abstract = {The reactions of fluorine-fluorosulfate, FOSO2F, with SSF2, SeF4, AsF3 and MoF5 have been studied, and its previously reported reactions with SF4, Br2 and I2 re-investigated in order to test its suitability as a synthetic reagent. All substrates reacted exothermically, and sometimes explosively, between 80-298 K. The presence of the byproducts obtained may be rationalized by the thermal decomposition of some of the FOSO2F, which proceeds along two pathways, i.e. FOSO2F {\textendash}> 1/2O2 + SO2F2 and FOSO2F {\textendash}> 1/2F2 + 1/2S2O6F2, during the extremely exothermic reactions via radical intermediates. The fluorine formed gives rise to fully fluorinated products, and the SO3F. radicals, initially formed, either dimerize to give S2O6F2 or decompose to O2 and S2O5F2. Element fluoride-fluorosulfates, when formed at all, were obtained in low yields only when SO2F2 or SO2FCl were used as suitable moderators. The complete vibrational spectra of EF5OSO2F (E = S, Se or Te) have been studied and assigned. The reactions of I2, Br2 and AsF3 with FOSO2F yielded viscous liquids of the approximate, non-stoichiometric composition EFn(SO5F)5-n (E = As or I) and EFn(SO3F)3-n (E = Br), with n = non-integral number. All compounds were characterized by their vibrational and F-19 NMR spectra, and in the case of SeF5OSO2F by Se-77 NMR methods.},
	keywords = {DERIVATIVES, GOLD(III) FLUOROSULFATE, halogen, ION, SPECTRA, TRIS(FLUOROSULFATE)},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1992KF32100004},
	author = {Willner, H. and Mistry, F. and Aubke, F.}
}
@article {7148,
	title = {THE CRYSTAL AND MOLECULAR-STRUCTURE OF GOLD TRIS(FLUOROSULFATE)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: FE808Times Cited: 18Cited Reference Count: 49},
	month = {Mar},
	pages = {391-396},
	type = {Article},
	abstract = {{Single crystals of gold(III) tris(fluorosulfate) are obtained by recrystallization from bis(fluorosulfuryl) peroxide, S2O6F2, under O2 pressure. The crystals of [Au(SO3F)3]2 are monoclinic},
	keywords = {CATIONS, CHEMISTRY, COMPLEXES, crystal structure, GOLD(III) FLUOROSULFATE, GOLD(III) TRIS(FLUOROSULFATE), HSO3F, ION, OXIDE, STABILITY},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FE80800005},
	author = {Willner, H. and Rettig, S. J. and Trotter, J. and Aubke, F.}
}
@article {7148,
	title = {THE CRYSTAL AND MOLECULAR-STRUCTURE OF GOLD TRIS(FLUOROSULFATE)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: FE808Times Cited: 18Cited Reference Count: 49},
	month = {Mar},
	pages = {391-396},
	type = {Article},
	abstract = {{Single crystals of gold(III) tris(fluorosulfate) are obtained by recrystallization from bis(fluorosulfuryl) peroxide, S2O6F2, under O2 pressure. The crystals of [Au(SO3F)3]2 are monoclinic},
	keywords = {CATIONS, CHEMISTRY, COMPLEXES, crystal structure, GOLD(III) FLUOROSULFATE, GOLD(III) TRIS(FLUOROSULFATE), HSO3F, ION, OXIDE, STABILITY},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FE80800005},
	author = {Willner, H. and Rettig, S. J. and Trotter, J. and Aubke, F.}
}
@article {7147,
	title = {FLUOROSULFATE DERIVATIVES OF DIVALENT GOLD},
	journal = {Journal of Fluorine Chemistry},
	volume = {52},
	number = {1},
	year = {1991},
	note = {ISI Document Delivery No.: FL539Times Cited: 8Cited Reference Count: 34},
	month = {Apr},
	pages = {13-27},
	type = {Article},
	abstract = {The reduction of gold(III) fluorosulfate, Au(SO3F)3 with either gold powder or carbon monoxide, in fluorosulfuric acid, HSO3F, yields gold(II) fluorosulfate as a yellow-red solid in high yield. Based on magnetic measurements and vibrational spectra, formulation as mixed valency Au(I) Au(III)-(SO3F)4 is suggested. Evidence from ESR measurements for a solvated, paramagnetic Au(II)-species in the supernatant solution is obtained and discussed.},
	keywords = {GOLD(III) FLUOROSULFATE, ION, palladium, SILVER(II), SPECTRA},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1991FL53900003},
	author = {Willner, H. and Mistry, F. and Hwang, G. and Herring, F. G. and Cader, M. S. R. and Aubke, F.}
}
