@article {3125,
	title = {RADICAL FORMATION DURING THE REACTION OF BIS(FLUOROSULFURYL)PEROXIDE, S2O6F2, WITH TETRASULFUR TETRANITRIDE, S4N4, AND ELEMENTAL SULFUR, S-8},
	journal = {Journal of Fluorine Chemistry},
	volume = {66},
	number = {2},
	year = {1994},
	note = {ISI Document Delivery No.: MX367Times Cited: 1Cited Reference Count: 46},
	month = {Feb},
	pages = {147-152},
	type = {Article},
	abstract = {The radical intermediates formed initially in the reaction of S2O6F2 with S4N4 and S8 have been studied by ESR spectroscopy at X-band level. The transient radical formed in the reaction between S2O6F2 and S4N4 has the spin Hamiltonian parameters g(xx) = 2.0014, g(yy) = 2.0054, g(zz) = 2.0249, A(xx) = 22.5 MHz, A(yy) = 4.5 MHz, A(zz) = 2.0 MHz and Q(zz) = 4 MHz as determined by simulation of ESR lineshapes obtained from polycrystalline samples. The spin Hamiltonian parameters are very similar to those previously reported for [S3N2]+., and the spectra are interpreted as being most likely due to the [S3N2]+. radical. The reaction between S2O6F2 and S8 under similar conditions produces a radical that has a g-tensor of the form g(xx) = 2.0026, g(yy) = 2.0184, g(zz) = 2.0258, as determined by simulation. The transient species generated is postulated to be a similar S5+. radical.},
	keywords = {CRYSTAL-STRUCTURE, ELECTRON-SPIN-RESONANCE, HSO3F, NITROGEN, POLYATOMIC CATIONS, S3N2+, SALTS, SPECTRUM},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1994MX36700011},
	author = {Mistry, F. and Herring, F. G. and Haas, A. and Aubke, F.}
}
@article {7258,
	title = {GENERATION OF AU2+ IONS IN THE SOLID-STATE OR IN FLUOROSULFURIC ACID-SOLUTION AND THEIR IDENTIFICATION BY ESR},
	journal = {Journal of the American Chemical Society},
	volume = {114},
	number = {4},
	year = {1992},
	note = {ISI Document Delivery No.: HD978Times Cited: 25Cited Reference Count: 64},
	month = {Feb},
	pages = {1271-1277},
	type = {Article},
	abstract = {{The partial pyrolysis of gold(III) fluorosulfate, Au(SO3F)3, at temperatures below 145-degrees-C allows the generation of Au2+ defects in the solid residue by reductive elimination of SO3F. radicals. Solvated Au2+ is obtained by the reduction of Au(SO3F)3 in HSO3F solution by gold powder at 65-degrees-C. Both systems are studied by ESR and identical high g(iso) values of g = 2.360 are found. Hyperfine splitting due to Au-197},
	keywords = {BR2+, bromine, CATIONS, COMPLEX, GOLD(III) FLUOROSULFATE, HSO3F, I2+, palladium, SILVER(II)},
	isbn = {0002-7863},
	url = {<Go to ISI>://A1992HD97800024},
	author = {Herring, F. G. and Hwang, G. and Lee, K. C. and Mistry, F. and Phillips, P. S. and Willner, H. and Aubke, F.}
}
@article {7387,
	title = {THE STUDY OF SELECTED ACCEPTOR GRAPHITE-INTERCALATION COMPOUNDS BY X-RAY PHOTOELECTRON-SPECTROSCOPY},
	journal = {European Journal of Solid State and Inorganic Chemistry},
	volume = {29},
	number = {4-5},
	year = {1992},
	note = {ISI Document Delivery No.: JJ792Times Cited: 1Cited Reference Count: 37},
	pages = {961-974},
	type = {Article},
	abstract = {X-ray photoelectron spectra of the first-stage acceptor graphite intercalation compounds C7SO3F, C14SO3F.HSO3F, C12SO3CF3, and C8SbF6 are reported. The carbon is core electron binding energy is shifted to slightly lower energies relative to graphite for all four acceptor GICs, largely on account of a Fermi level shift to lower energy upon oxidative intercalation. The shifts in binding energies for the C 1s core electron are compared to those of various fluorinated graphites and to shifts reported previously for related acceptor GICs. In addition, the O 1s, F 1s, and S 2p3/2 XPS spectra are reported. Comparison to those of simple ionic salts formed by the intercalate anions allows an estimation of the Fermi level shift in the acceptor GICs.},
	keywords = {FLUOROSULFATE DERIVATIVES, GOLD, HSO3F},
	isbn = {0992-4361},
	url = {<Go to ISI>://A1992JJ79200027},
	author = {Xia, J. and Hu, H. L. and Frost, D. C. 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.}
}
