@article {2476,
	title = {The ground state rotational spectrum of the fluorosulfate radical},
	journal = {Journal of Chemical Physics},
	volume = {130},
	number = {18},
	year = {2009},
	note = {ISI Document Delivery No.: 448LDTimes Cited: 2Cited Reference Count: 26Kolesnikova, Lucie Varga, Juraj Striteska, Lucie Nova Beckers, Helmut Willner, Helge Aubke, Friedhelm Urban, Stepan},
	month = {May},
	pages = {9},
	type = {Article},
	abstract = {The rotational spectra of the fluorosulfate (FSO3 center dot) molecular radical in its vibronic ground state were measured in the millimeter-wave region and analyzed in detail using the matrix elements of the rotational, fine, and hyperfine Hamiltonian terms. The analysis of the assigned transition frequencies made it possible to derive very precise values of the rotational, centrifugal distortion and fine structure constants and to confirm the C-3v molecular symmetry of the vibronic ground state unambiguously. In addition, an effective parameter of the "A(1)-A(2) splitting" was determined. The rotational transitions of the FSO3 center dot free radical were observed, identified, and analyzed for the first time.},
	keywords = {ASSIGNMENTS, BANDS, CLASSIFICATION, fluorine compounds, free radical reactions, ground states, HYPERFINE, LASER EXCITATION, lifetimes, millimetre wave spectra, molecular configurations, radiative, rotational states, STRUCTURE, SYMMETRIC-TOP MOLECULES, SYSTEM, vibronic states},
	isbn = {0021-9606},
	url = {<Go to ISI>://000266263200023},
	author = {Kolesnikova, L. and Varga, J. and Striteska, L. N. and Beckers, H. and Willner, H. and Aubke, F. and Urban, S.}
}
@article {1344,
	title = {Solid state NMR investigation of the structure of AlPO4-14A},
	journal = {Microporous and Mesoporous Materials},
	volume = {88},
	number = {1-3},
	year = {2006},
	note = {ISI Document Delivery No.: 004TCTimes Cited: 5Cited Reference Count: 14},
	month = {Jan},
	pages = {163-169},
	type = {Article},
	abstract = {The as-synthesized aluminophosphate framework material AlPO4-14A has a number of unique structural features related to the connectivities in the network of Al and P atoms. One tetrahedral Al atom is present that is linked, via Al-O(H)-Al bonds to two octahedral Al atoms and, consequently to only two P atoms. However, ail Al/P ratio of one is maintained as each of these octahedral Al atoms is connected to five P atoms in addition to the Al-O(H)-Al linkage. This connectivity network means that a framework made up of alternating Al and P atoms cannot be obtained by calcination. A variety of H-1, Al-27, and P-31 solid state NMR experiments have been employed to characterize the AlPO4-14A structure. A fast H-1 MAS experiment showed that the template was in the protonated form and a H-1 {Al-27} TRAPDOR experiment identified the resonance of the {\textquoteright}framework{\textquoteright} proton. The Al-27 and P-31 resonances were completely assigned by the Al-27 -> P-31 INEPT heteronuclear correlation experiment and the quadrupolar parameters of the Al-27 signals determined from the Al-27 MQMAS experiment. Lastly, the complete assignment of both Al-27 and P-31 resonances made it possible to qualitatively determine the location and orientation of the template molecule within the framework from two-dimensional dipolar-based H-1 -> P-31 cross-polarization and H-1 -> Al-27 TEDOR heteronuclear correlation experiments. The data from these experiments confirm in detail the AlPO4-14A structure and will be useful benchmarks for the investigation of other structures for which diffraction data are limited. (c) 2005 Elsevier Inc. All rights reserved.},
	keywords = {aluminophosphate, DIFFRACTION, HETCOR, solid state NMR, SPECTRA, SPINS, STRUCTURE, zeolite},
	isbn = {1387-1811},
	url = {<Go to ISI>://000234774100021},
	author = {Brouwer, D. H. and Chezeau, J. M. and Fyfe, C. A.}
}
@article {1053,
	title = {The state of the filament},
	journal = {Embo Reports},
	volume = {6},
	number = {3},
	year = {2005},
	note = {ISI Document Delivery No.: 901QMTimes Cited: 22Cited Reference Count: 30},
	month = {Mar},
	pages = {220-226},
	type = {Review},
	abstract = {Movement is a defining characteristic of life. Macroscopic motion is driven by the dynamic interactions of myosin with actin filaments in muscle. Directed polymerization of actin behind the advancing membrane of a eukaryotic cell generates microscopic movement. Despite the fundamental importance of actin in these processes, the structure of the actin filament remains unknown. The Holmes model of the actin filament was published 15 years ago, and although it has been widely accepted, no high-resolution structural data have yet confirmed its veracity. Here, we review the implications of recently determined structures of F-actin-binding proteins for the structure of the actin filament and suggest a series of in silico tests for actin-filament models. We also review the significance of these structures for the arp2/3-mediated branched filament.},
	keywords = {actin filament, ACTIN-FILAMENT, ACTIVATION, ALDRICH-SYNDROME PROTEIN, arp2/3, ARP2/3 COMPLEX, BETA-ACTIN, CRYSTAL-STRUCTURE, DOMAIN, gelsolin, STRUCTURAL BASIS, STRUCTURE, WASp, WH2},
	isbn = {1469-221X},
	url = {<Go to ISI>://000227297000009},
	author = {Aguda, A. H. and Burtnick, L. D. and Robinson, R. C.}
}
@article {Yamani2004,
	title = {Cu \{NMR\} study of detwinned single crystals of Ortho-II YBCO6.5},
	journal = {Physica C: Superconductivity},
	volume = {405},
	number = {3{\textendash}4},
	year = {2004},
	pages = {227 - 239},
	abstract = {Copper \{NMR\} has been used as a local probe of the oxygen ordering in Ortho-II YBa2Cu3O6.5 crystals grown in BaZrO3 crucibles. Line assignments have been made to each of the expected crystallographically inequivalent sites. The presence of distinct and narrow lines for these sites as well as the lack of a line known to be associated with oxygen defects indicates that these crystals are highly stoichiometric. Our estimate of the lower limit on the chain length is consistent with that derived from X-ray diffraction measurements. In addition, we have found no evidence for static magnetic moments, in contrast to some previous results.},
	keywords = {STRUCTURE},
	issn = {0921-4534},
	doi = {http://dx.doi.org/10.1016/j.physc.2004.02.010},
	url = {http://www.sciencedirect.com/science/article/pii/S092145340400156X},
	author = {Z. Yamani and W.A. MacFarlane and B.W. Statt and D. Bonn and R. Liang and W.N. Hardy}
}
@article {826,
	title = {Microwave spectra, nuclear field shift effects, geometries and hyperfine constants of bismuth mononitride, BiN, and bismuth monophosphide, BiP},
	journal = {Journal of Molecular Structure},
	volume = {695},
	year = {2004},
	note = {ISI Document Delivery No.: 827SVTimes Cited: 11Cited Reference Count: 66Sp. Iss. SI},
	month = {Jun},
	pages = {13-22},
	type = {Article},
	abstract = {The diatomic molecules BiN and BiP have been prepared using a laser ablation technique and studied by Fourier transform microwave spectroscopy in the frequency range 7-22 GHz. For BiN, only the J = 1-0 transition fell within this range. Transitions for the ground and first excited vibrational states have been observed for both (BiN)-N-14 and (BiN)-N-15. For BiP, which has only one isotopomer, the transitions J{\textquoteright}-J" = 1-0. 2-1 and 3-2 have been observed, but only for the ground vibrational state. Hyperfine structure has been observed for both nuclei in both molecules the Bi-209 nuclear quadrupole coupling constants show that the electronic structures are similar for the two molecules. Improved bond lengths have been obtained for both molecules. Density functional methods have been used to estimate the electron density at the bismuth nucleus in each molecule and hence allow an estimate of the uncertainty due to field shift effects in the experimentally derived bond lengths. (C) 2003 Elsevier B.V. All rights reserved.},
	keywords = {BII, BiN, BiP, BORN-OPPENHEIMER APPROXIMATION, Born-Oppenheimer breakdown, DIATOMIC-MOLECULES, DUNHAM COEFFICIENTS, FOURIER-TRANSFORM SPECTROSCOPY, GROUND-STATE, HIGH-RESOLUTION, HYPERFINE, IODIDE, ISOTOPE DEPENDENCE, microwave spectra, MOMENTS, nuclear field shift effects, QUADRUPOLE, ROTATIONAL SPECTRUM, STRUCTURE},
	isbn = {0022-2860},
	url = {<Go to ISI>://000221922000003},
	author = {Cooke, S. A. and Michaud, J. M. and Gerry, M. C. L.}
}
@article {880,
	title = {The solid-state molecular structure of W(NO)(3)Cl-3 and the nature of its W-NO bonding},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {82},
	number = {2},
	year = {2004},
	note = {ISI Document Delivery No.: 802BHTimes Cited: 1Cited Reference Count: 46},
	month = {Feb},
	pages = {285-292},
	type = {Article},
	abstract = {{The monomeric trinitrosyl complex, W(NO)(3)Cl-3, can be prepared by the treatment of WCl6 in CH2Cl2 with NO gas, and its identity has been unambiguously confirmed by a single-crystal X-ray diffraction analysis. The complex crystallizes in the space group Pmn2(1) as a three-component twin (a = 10.4280(4) Angstrom},
	keywords = {bonding, CARBONYL, CHEMISTRY, CRYSTAL-STRUCTURE, DERIVATIVES, DICHLORODINITROSYLTUNGSTEN, DICHLOROTRINITROSYLVANADIUM, MOLYBDENUM, MONONUCLEAR, NITROSYL, NITROSYL COMPLEXES, STRUCTURE, TUNGSTEN},
	isbn = {0008-4042},
	url = {<Go to ISI>://000220138500024},
	author = {Hayton, T. W. and Patrick, B. O. and Legzdins,Peter and McNeil, W. S.}
}
@article {5115,
	title = {Complexes of phosphine-phenolate ligands with the [Re=O](3+) and [Re(HNNC5H4N)(NNC5H4N)](2+) cores},
	journal = {Journal of the Chemical Society-Dalton Transactions},
	number = {20},
	year = {2001},
	note = {ISI Document Delivery No.: 487VFTimes Cited: 5Cited Reference Count: 62},
	pages = {3015-3024},
	type = {Article},
	abstract = {{Complexes incorporating the [Re=O](3+) core have been synthesised with ligands containing the new methyl substituted phosphine-phenolate PO and PO2 donor sets, (2-hydroxy-5-methylphenyl) diphenylphosphine (H(MePO)) and bis(2-hydroxy-5-methylphenyl) phenylphosphine (H-2(Me2PO2)). The analogous tert-butyl ligands, (5-tert-butyl-2-hydroxyphenyl)diphenylphosphine (H(t-BuPO)) and bis(5-tert-butyl-2-hydroxyphenyl) phenylphosphine (H-2 (t-Bu2PO2)), were also prepared. Reaction of either mer-[ReOCl3 (PPh3)(2)] or [NH4][ReO4] in CH3OH with H(MePO) led to formation of [ReOCl(MePO)(2)] (1) in good yield. Reaction of [NH4][ReO4] with H-2 (Me2PO2) in CH3OH afforded [ReO(Me2PO2)(H(Me2PO2))] (2), also in good yield. X-Ray crystallographic analyses of 1 and 2 demonstrated that both complexes are neutral and octahedral, and contain the oxo moiety. Two complexes have been structurally characterised from the reaction of (o-hydroxyphenyl) diphenylphosphine (HPO) with [Re(Hhypy)(hypyH)Cl-3]: [Re(Hhypy)(hypy)(PO)(HPO)]Cl (3) and [ReCl(Hypy)(hypy)(PO)] (4) (hypy = NNC5H4N},
	keywords = {CHELATE COMPLEXES, COORDINATION-COMPOUNDS, CRYSTAL-STRUCTURE, IIB/IIIA-RECEPTOR ANTAGONIST, MOLECULAR-STRUCTURES, rhenium, STRUCTURE, TC-99M, TECHNETIUM RADIOPHARMACEUTICALS, WATER-SOLUBLE PHOSPHINES, X-RAY},
	isbn = {1472-7773},
	url = {<Go to ISI>://000171899200011},
	author = {Kovacs, M. S. and Hein, P. and Sattarzadeh, S. and Patrick, B. O. and Emge, T. J. and Orvig, Chris}
}
@article {5216,
	title = {Fourier transform microwave spectroscopy of cyanides and isocyanides of Al, Ga, and In},
	journal = {Journal of Molecular Spectroscopy},
	volume = {209},
	number = {2},
	year = {2001},
	note = {ISI Document Delivery No.: 490JPTimes Cited: 22Cited Reference Count: 44},
	month = {Oct},
	pages = {178-191},
	type = {Article},
	abstract = {Microwave spectra of the three Group 13 metal cyanide pairs AlNC/AlCN, GaNC/GaCN, and InNC/InCN have been measured in the frequency range 6-25 GHz using a pulsed jet cavity Fourier transform microwave spectrometer. The molecules were prepared by ablating the metal with a pulsed Nd:YAG laser and allowing the vapor to react with cyanogen or acetonitrile contained in the Ar backing gas of the jet. The spectra are those of linear molecules. Rotational constants. centrifugal distortion constants. and nuclear quadrupole coupling constants have been precisely evaluated. Molecular geometries determined from the rotational constants using a linear model have revealed unexpectedly short NC bond lengths for the isocyanides, MNC, and are interpreted in terms of a broadened potential well for the bending mode of these molecules. This interpretation is confirmed with ab initio calculations. The centrifugal distortion constants are consistent with this picture. A new formulation of the rigid bender model has produced plausible values for bond lengths and bending amplitudes for the isocyanides. The N-14 quadrupole coupling constants are discussed in terms of the approximate bending amplitudes. A description of the bonding in the molecules has been obtained using Townes-Dailey theory. (C) 2001 Academic Press.},
	keywords = {aluminum, ATOMS, CORRELATED MOLECULAR CALCULATIONS, EQUILIBRIUM, GAUSSIAN-BASIS SETS, IRC+10216, MONOCYANIDES, PARAMETERS, SPECTRUM, STRUCTURE, TRENDS},
	isbn = {0022-2852},
	url = {<Go to ISI>://000172049000004},
	author = {Walker, K. A. and Evans, C. J. and Suh, S. H. K. and Gerry, M. C. L. and Watson, J. K. G.}
}
@article {4780,
	title = {Analysis of the dynamic properties of Bacillus circulans xylanase upon formation of a covalent glycosyl-enzyme intermediate},
	journal = {Protein Science},
	volume = {9},
	number = {3},
	year = {2000},
	note = {ISI Document Delivery No.: 295XWTimes Cited: 16Cited Reference Count: 56},
	month = {Mar},
	pages = {512-524},
	type = {Article},
	abstract = {NMR spectroscopy was used to search for mechanistically significant differences in the local mobility of the main-chain amides of Bacillus circulans xylanase (BCX) in its native and catalytically competent covalent glycosyl-enzyme intermediate states. N-15 T-1, T-2, and N-15{H-1} NOE values were measured for similar to 120 out of 178 peptide groups in both the apo form of the protein and in BCX covalently modified at position Glu78 with a mechanism-based 2-deoxy-2-fluoro-beta-xylobioside inactivator. Employing the model-free formalism of Lipari and Szabo, the measured relaxation parameters were used to calculate a global correlation time ( tau(m)) for the protein in each form (9.2 +/- 0.2 ns for apo-BCX; 9.8 +/- 0.3 ns for the modified protein), as well as individual order parameters for the main-chain NH bond vectors. Average values of the order parameters for the protein in the apo and complexed forms were S-2 = 0.86 +/- 0.04 and S-2 = 0.91 +/- 0.04, respectively. No correlation is observed between these order parameters and the secondary structure, solvent accessibility, or hydrogen bonding patterns of amides in either form of the protein. These results demonstrate that the backbone of BCX is well ordered in both states and that formation of the,glycosyl-enzyme intermediate leads to little change, in any, in the dynamic properties of BCX on the time scales sampled by N-15-NMR relaxation measurements.},
	keywords = {ACTIVE-SITE NUCLEOPHILE, ANISOTROPIC ROTATIONAL, BACKBONE DYNAMICS, BINDING, BURIED NEUTRAL HISTIDINE, DIFFUSION, glucanase, GLYCOSYL-ENZYME INTERMEDIATE, MAGNETIC-RESONANCE RELAXATION, MODEL-FREE APPROACH, N-15 NMR RELAXATION, NMR, order parameter, PROTEIN, PROTEINS, relaxation dynamics, SIDE-CHAIN RESONANCES, STRUCTURE},
	isbn = {0961-8368},
	url = {<Go to ISI>://000085994800009},
	author = {Connelly, G. P. and Withers, S. G. and McIntosh, L. P.}
}
@article {4991,
	title = {Laser-induced phosphorescence of SO2 in solid neon: Direct observation of the (b)over-tilde(3)A(2) state in the (OSO)-O-16-O-18 molecule},
	journal = {Journal of Physical Chemistry A},
	volume = {104},
	number = {4},
	year = {2000},
	note = {ISI Document Delivery No.: 280WFTimes Cited: 13Cited Reference Count: 41},
	month = {Feb},
	pages = {771-776},
	type = {Article},
	abstract = {Laser excitation of isotopically labeled SO2 molecules in a neon matrix has allowed the measurement of dispersed phosphorescence spectra ((a) over tilde(3)B(1)-(X) over tilde(1)A(1)) in the wavelength region 387.5-526.3 nm (19 000-25 800 cm(-1)). The origin of the (a) over tilde-(X) over tilde transition lies at 25 747 cm(-1) in (OSO)-O-16-O-16, shifted 18 cm(-1) to the red from the gas phase; the three vibrational frequencies of the (X) over tilde state are nearly unperturbed in the neon matrix (1149, 520, and 1362 cm(-1)). As the zero-phonon lines are sharp and well resolved, it has been possible to monitor emission from a specific isotopomer to obtain its excitation spectrum. The excitation spectra of matrix-isolated (OSO)-O-16-O-16 and (OSO)-O-18-O-18 in the region 350.9-388.5 nm (25 740-28 500 cm(-1)) are similar to those previously observed in the gas phase, with strong perturbations affecting all vibrational levels above a(3)B(1)(110) at 27 005 cm(-1) (370 nm). Two additional groups of bands are observed for the unsymmetrical isotopomer (OSO)-O-18-O-16; they are identified as transitions to levels of the (a) over tilde(3)B(1) state with v(3) = 1 and as direct transitions to the (b) over tilde(3)A(2) state, which both become allowed in the lower symmetry. The v(3) frequency of the (a) over tilde(3)B(1) state of (OSO)-O-18-O-16 is 922 cm(-1); for the (b) over tilde(3)A(2) state, v(1) similar or equal to 791 cm(-1) and v(2) similar or equal to 315 cm(-1), while the (b) over tilde (001) level lies 26 653 cm(-1) above the (X) over tilde (000) level.},
	keywords = {ABSORPTION, BAND SYSTEM, FLUORESCENCE, INDUCED EMISSION, MATRICES, REGION, ROTATIONAL, SPECTRA, STRUCTURE, SULFUR-DIOXIDE, VIBRATIONAL STRUCTURE},
	isbn = {1089-5639},
	url = {<Go to ISI>://000085126200014},
	author = {Zen, C. C. and Chen, I. C. and Lee, Y. P. and Merer, A. J.}
}
@article {4787,
	title = {Peak structure with a quadrupole mass filter operated in the third stability region},
	journal = {International Journal of Mass Spectrometry},
	volume = {197},
	year = {2000},
	note = {ISI Document Delivery No.: 291DFTimes Cited: 6Cited Reference Count: 11Sp. Iss. SI},
	month = {Feb},
	pages = {113-121},
	type = {Article},
	abstract = {Peak structure for a quadrupole operated in the third stability region with Mathieu parameters (a, q) approximate to (3, 3) has been studied experimentally and modeled theoretically. It is shown that the structure is due to the imaging properties of the quadrupole field which are caused by the wavelike properties of the ion trajectories. Ions enter the quadrupole through a small inlet aperture on axis. When ions are focused on the center of the exit aperture the transmission is a maximum. Conversely when ions have trajectories that place them near the rods at the exit aperture the transmission is a minimum and a dip appears on a peak. The positions of dips on a peak can be assigned to lines in the stability diagram. These lines follow iso-beta lines, where beta is the parameter that determines the frequencies of ion motion. The positions of the lines are controlled by the number of rf cycles, which ions spend in the quadrupole field. At high resolution (>300) and low ion axial energy (<20 eV) the peak splitting is minimal or absent. (C) 2000 Elsevier Science B.V.},
	keywords = {FREQUENCIES, ION-TRAP, peak, peak shape, quadrupole mass filter, STRUCTURE, third stability region},
	isbn = {1387-3806},
	url = {<Go to ISI>://000085718300007},
	author = {Du, Z. H. and Douglas, D. J. and Glebova, T. and Konenkov, N. V.}
}
@article {4151,
	title = {LEED crystallographic analysis for the structure formed by 2 ML of O at the Zr(0001) surface},
	journal = {Surface Science},
	volume = {380},
	number = {2-3},
	year = {1997},
	note = {ISI Document Delivery No.: XF843Times Cited: 17Cited Reference Count: 29},
	month = {May},
	pages = {540-547},
	type = {Article},
	abstract = {A tensor LEED analysis is reported for the Zr(0001)-(1 x 1)-O surface which involves oxygen at a total coverage of 2 monolayers. The structure is indicated to have two layers of O: one forms an overlayer in which the O atoms bond to hollow sites of three-fold coordination on the regular metal surface. while the other laver has the O atoms in tetrahedral hole sires between the first and second metal layers. The stacking sequence, designated as (C)B(A)AB, corresponds to the first three layers of anion-terminated cubic ZrO2, although some lateral compression is needed for superposition on the regular hcp Zr structure. The absorption of O in the tetrahedral holes results in a significant expansion in the first-to-second Zr-Zr interlayer spacing to about 3.44 Angstrom from the bulk vaue of 2.57 Angstrom. The O-Zr bond lengths are estimated to equal 2.07 Angstrom for the overlayer O atoms, and 2.21 Angstrom for the O atoms in tetrahedral hole sites, Comparisons are made with the structures of the corresponding 0.5 and 1 ML surfaces formed by the O/Zr(0001) system. (C) 1997 Elsevier Science B.V.},
	keywords = {ENERGY-ELECTRON-DIFFRACTION, GROWTH, LEED crystallography, low index single crystal surface, OXIDE THIN-FILMS, OXYGEN, SINGLE-CRYSTAL SURFACES, STRUCTURE, SURFACE, ZIRCONIUM},
	isbn = {0039-6028},
	url = {<Go to ISI>://A1997XF84300044},
	author = {Wang, Y. M. and Li, Y. S. and Mitchell, K. A. R.}
}
@article {3949,
	title = {Synthesis and characterization of the mixed valence Cu(I)/Cu(II) 3,5-bis(trifluoromethyl)-pyrazolate complex, [Cu(II)(2)Cu(I)(F(6)dmpz)(5)]},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {75},
	number = {5},
	year = {1997},
	note = {ISI Document Delivery No.: XF492Times Cited: 18Cited Reference Count: 17},
	month = {May},
	pages = {491-498},
	type = {Article},
	abstract = {{The reaction of molten 3,5-bis(trifluoromethyl)pyrazole (F(6)dmpzH) with copper metal shot under an atmosphere of dioxygen yields the green trimetallic mixed valence [Cu(II)(2)Cu(I)(F(6)dmpz)(5)]. Crystals of [Cu(II)(2)Cu(I)F(6)dmpz)(5)] are triclinic},
	keywords = {3, 5-bis(trifluoromethyl)pyrazolates, ANTIFERROMAGNETISM, copper, COPPER(II) COMPLEX, MAGNETIC-PROPERTIES, METAL PYRAZOLATE POLYMERS, RAY CRYSTAL-STRUCTURE, STRUCTURE, trimetallic, X-RAY},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1997XF49200003},
	author = {Ehlert, M. K. and Storr, A. and Summers, D. A. and Thompson, R. C.}
}
@article {3949,
	title = {Synthesis and characterization of the mixed valence Cu(I)/Cu(II) 3,5-bis(trifluoromethyl)-pyrazolate complex, [Cu(II)(2)Cu(I)(F(6)dmpz)(5)]},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {75},
	number = {5},
	year = {1997},
	note = {ISI Document Delivery No.: XF492Times Cited: 18Cited Reference Count: 17},
	month = {May},
	pages = {491-498},
	type = {Article},
	abstract = {{The reaction of molten 3,5-bis(trifluoromethyl)pyrazole (F(6)dmpzH) with copper metal shot under an atmosphere of dioxygen yields the green trimetallic mixed valence [Cu(II)(2)Cu(I)(F(6)dmpz)(5)]. Crystals of [Cu(II)(2)Cu(I)F(6)dmpz)(5)] are triclinic},
	keywords = {3, 5-bis(trifluoromethyl)pyrazolates, ANTIFERROMAGNETISM, copper, COPPER(II) COMPLEX, MAGNETIC-PROPERTIES, METAL PYRAZOLATE POLYMERS, RAY CRYSTAL-STRUCTURE, STRUCTURE, trimetallic, X-RAY},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1997XF49200003},
	author = {Ehlert, M. K. and Storr, A. and Summers, D. A. and Thompson, R. C.}
}
@article {3597,
	title = {Cationic iridium(III) carbonyl complexes: [Ir(CO)(6)](3+) and [Ir(CO)(5)Cl](2+)},
	journal = {Angewandte Chemie-International Edition in English},
	volume = {35},
	number = {17},
	year = {1996},
	note = {ISI Document Delivery No.: VM029Times Cited: 55Cited Reference Count: 27},
	month = {Sep},
	pages = {1974-1976},
	type = {Article},
	keywords = {carbonyl complexes, ELUCIDATION, FLUOROSULFATE, IR spectroscopy, iridium compounds, MOLECULAR-STRUCTURE, MONOXIDE, SPECTRA, STRUCTURE, UNDECAFLUORODIANTIMONATE(V)},
	isbn = {0570-0833},
	url = {<Go to ISI>://A1996VM02900023},
	author = {Bach, C. and Willner, H. and Wang, C. Q. and Rettig, S. J. and Trotter, J. and Aubke, F.}
}
@article {3597,
	title = {Cationic iridium(III) carbonyl complexes: [Ir(CO)(6)](3+) and [Ir(CO)(5)Cl](2+)},
	journal = {Angewandte Chemie-International Edition in English},
	volume = {35},
	number = {17},
	year = {1996},
	note = {ISI Document Delivery No.: VM029Times Cited: 55Cited Reference Count: 27},
	month = {Sep},
	pages = {1974-1976},
	type = {Article},
	keywords = {carbonyl complexes, ELUCIDATION, FLUOROSULFATE, IR spectroscopy, iridium compounds, MOLECULAR-STRUCTURE, MONOXIDE, SPECTRA, STRUCTURE, UNDECAFLUORODIANTIMONATE(V)},
	isbn = {0570-0833},
	url = {<Go to ISI>://A1996VM02900023},
	author = {Bach, C. and Willner, H. and Wang, C. Q. and Rettig, S. J. and Trotter, J. and Aubke, F.}
}
@article {3642,
	title = {Reaction of methanol with perfluorotetracyclobuta-1,3,5,7-cyclooctatetraene},
	journal = {Journal of Fluorine Chemistry},
	volume = {76},
	number = {2},
	year = {1996},
	note = {ISI Document Delivery No.: UA116Times Cited: 4Cited Reference Count: 13},
	month = {Feb},
	pages = {121-124},
	type = {Article},
	abstract = {Perfluorotetracyclobuteno-1,3,5,7-cyclooctatetraene (PCOT) is a planar and centrosymmetric molecule which possesses an extraordinary electron affinity due to the planarity of the eight pi-electron system and the cumulative electron-withdrawing effects of the 16 fluorine atoms. An improved method for the synthesis of PCOT and the product resulting from the spontaneous reaction of PCOT with excess alcohol is reported. Crystal structures of the methyl (1) and ethyl (2) derivatives are described.},
	keywords = {CRYSTAL, IR spectroscopy, MASS SPECTROMETRY, METHANOL, NMR spectroscopy, perfluorotetracyclobutacyclo-octatetraene, reaction, STRUCTURE},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1996UA11600002},
	author = {Cullen, W. R. and Rettig, S. J. and Moore, A. E. and Soulen, R. L.}
}
@article {6968,
	title = {THE APPLICATION OF INTEGRAL-EQUATION THEORIES TO FLUIDS OF NONSPHERICAL PARTICLES NEAR A UNIFORM PLANAR WALL},
	journal = {Journal of Chemical Physics},
	volume = {95},
	number = {7},
	year = {1991},
	note = {ISI Document Delivery No.: GH356Times Cited: 37Cited Reference Count: 39},
	month = {Oct},
	pages = {5281-5288},
	type = {Article},
	abstract = {A general reduction of the Ornstein-Zernike equation is given for molecular fluids near a planar wall. This allows integral equation approximations such as the hypernetted-chain or reference hypernetted-chain (RHNC) theories to be solved numerically for such systems. Dipolar hard sphere fluids near a hard wall are considered in detail and RHNC solutions are obtained. The results are compared with previous calculations for curved surfaces. The RHNC result for the asymptotic behavior of the wall-solvent pair correlation function at large separations is derived and compared with expressions given by classical continuum theory and by exact analysis.},
	keywords = {AQUEOUS-ELECTROLYTE SOLUTIONS, DIPOLAR HARD-SPHERES, ELECTRICAL DOUBLE-LAYER, HYPERNETTED-CHAIN, INFINITE DILUTION, INVARIANT EXPANSION, MEAN, MOLECULAR-SOLVENT MODEL, ORIENTATIONAL, ORNSTEIN-ZERNIKE EQUATION, SPHERICAL MODEL, STRUCTURE},
	isbn = {0021-9606},
	url = {<Go to ISI>://A1991GH35600061},
	author = {Berard, D. R. and Patey, G. N.}
}
