@article {2205,
	title = {Template-assembled synthetic G-quartets (TASQs)},
	journal = {Angewandte Chemie-International Edition},
	volume = {47},
	number = {26},
	year = {2008},
	note = {ISI Document Delivery No.: 317SSTimes Cited: 8Cited Reference Count: 38Nikan, Mehran Sherman, John C.},
	pages = {4900-4902},
	type = {Article},
	keywords = {cation, CAVITANDS, CHEMISTRY, DEOXYGUANOSINE, DERIVATIVES, G-quartets, GUANOSINE, HOST-GUEST COMPLEXATION, NUCLEOSIDES, NUCLEOTIDE, ORGANIC-SOLVENTS, QUADRUPLEX STRUCTURE, supramolecular, supramolecular chemistry, SYNTHESIS, TELOMERIC DNA OLIGONUCLEOTIDES, TEMPLATE},
	isbn = {1433-7851},
	url = {<Go to ISI>://000257040800022},
	author = {Nikan, M. and Sherman, J. C.}
}
@article {1580,
	title = {Ion pair dissociation: Spectroscopy and dynamics},
	journal = {Annual Review of Physical Chemistry},
	volume = {57},
	year = {2006},
	note = {ISI Document Delivery No.: 044JOTimes Cited: 26Cited Reference Count: 82Suits, Arthur G. Hepburn, John W.},
	pages = {431-465},
	type = {Review},
	abstract = {Ion pair dissociation processes may be studied Using coherent vacuum Ultraviolet laser sources in a manner entirely analogous to photoelectron spectroscopy, albeit with the anion playing the role of a heavy electron. If the excitation energy is above the dissociation energy and the kinetic energy of the fragment is measured Using ion imaging. this approach is termed ion pair imaging spectroscopy (IPIS) and is related to conventional photoelectron spectroscopy. If the excitation energy is just below the dissociation energy and pulsed-field dissociation is employed, this approach is analogous to mass analyzed threshold ionization (MATI) spectroscopy and is termed threshold ion pair production spectroscopy (TIPPS). These approaches provide a novel means of investigating ion thermochemistry and spectroscopy and superexcited state decay dynamics at high resolution.},
	keywords = {cation, ENERGY, HIGH-RESOLUTION, ion imaging, IONIZATION, METHYL, MOLECULAR-OXYGEN, NEGATIVE-IONS, PHOTODISSOCIATION DYNAMICS, PHOTOELECTRON-SPECTROSCOPY, PHOTOIONIZATION, superexcited states, TIPPS, VACUUM-ULTRAVIOLET, velocity map imaging, VUV, ZEKE},
	isbn = {0066-426X},
	url = {<Go to ISI>://000237668700015},
	author = {Suits, A. G. and Hepburn, J. W.}
}
@article {4302,
	title = {Platinum(II)-silver(I) polymers bearing platinum(II) clusters containing chelated P,P- and bridged P, N-2-pyridylphosphine ligands},
	journal = {Journal of Cluster Science},
	volume = {9},
	number = {3},
	year = {1998},
	note = {ISI Document Delivery No.: 168QATimes Cited: 6Cited Reference Count: 32},
	month = {Sep},
	pages = {243-258},
	type = {Article},
	abstract = {Reactions of PtI2L (L = P,P-bonded 1,2-bis(2-pyridyl )phosphino)ethane, d(py)pe, or 1,2-bis((2-pyridyl)phosphino)cyclopentane, d(py)pcp) with excess AgNO3 in acetic acid/ethanol afford the polymers [Pt-2(d(py)pe)(2)Ag-4(NO3)(8) (H2O)(2)](n) (1) and [Pt-2(d(py)pcp)(2) Ag-6(NO3)(10)](n) (2), respectively, which contain Pt2L24+ cores with each L ligand now P,N-bridging two Pt-atoms; these Pt-2 cores are connected via bridging AgNO3 clusters, the Ag being bound to the pyridyl-N or nitrate-O atoms. X-ray crystallographic data reveal Pt-Pt contacts of similar to 2.76 Angstrom indicative of bonding.},
	keywords = {2-PYRIDYL, 2-PYRIDYLPHOSPHINE LIGANDS, =, cation, COMPLEXES, CRYSTAL-STRUCTURE, DIMER, METAL-METAL BOND, OXIDATION, palladium, platinum, pyridylphosphine, silver, SPECTROSCOPY, TETRAKIS(DITHIOACETATO)DIPLATINUM(II)},
	isbn = {1040-7278},
	url = {<Go to ISI>://000078702700004},
	author = {Jones, N. D. and Rettig, S. J. and James, Brian R.}
}
@article {3689,
	title = {Acyclic sulfur-nitrogen compounds. Syntheses and crystal and molecular structures of bis((trifluoromethyl)sulfonyl)amine ((CF3SO2)(2)NH), magnesium hexaaquo bis((trifluoromethyl)sulfonyl)amide dihydrate ([Mg(H2O)(6)][(CF3SO2)(2)N](2)center dot 2H(2)O), an},
	journal = {Inorganic Chemistry},
	volume = {35},
	number = {7},
	year = {1996},
	note = {ISI Document Delivery No.: UC848Times Cited: 58Cited Reference Count: 69},
	month = {Mar},
	pages = {1918-1925},
	type = {Article},
	abstract = {{The syntheses of three acyclic (fluorosulfonyl)- or ((trifluoromethyl)sulfonyl)-nitrogen derivatives and their crystal and molecular structures are reported. The structures of bis((trifluoromethyl)sulfonyl)amine (1; (CF3SO2)(2)NH) and the corresponding anion in magnesium hexaaquo bis((trifluoromethyl)sulfonyl)amide dihydrate (2; [Mg(H2O)(6)][(CF3SO2)(2)N](2) . 2H(2O)) shed some light on the observed high gas-phase acidity of (CF3SO2)(2)NH. Extensive electron delocalization in the anion [(CF3SO)(2)N](-) from planar, sp(2)-hybridized nitrogen into 3d orbitals of sulfur results in a noticeable shortening of the S-N bond on deprotonation. Similar electron delocalization is observed for the third compound, bis(bis(fluorosulfonyl)amino)sulfur (3; (FSO2)(2)NSN(SO2F)(2)), which features planar nitrogens with nearly six equidistant S-N bonds and extremely short S-O and S-F bonds. Compounds 2 and 3 have not been reported previously. Their unexpected, accidental formation and their characterization will be discussed. Compound 1 crystallizes in the space group Peen (No. 56) with a = 16.404(3) Angstrom},
	keywords = {ACIDITY, cation, HEXAHYDRATE, NEUTRON-DIFFRACTION, SALTS, SULFONIMIDES},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1996UC84800027},
	author = {Haas, A. and Klare, C. and Betz, P. and Bruckmann, J. and Kruger, C. and Tsay, Y. H. and Aubke, F.}
}
