@article {1147,
	title = {Calorimetric study on self-assembling of two kinds of monometallic nanoparticles in solution},
	journal = {Journal of Thermal Analysis and Calorimetry},
	volume = {81},
	number = {3},
	year = {2005},
	note = {ISI Document Delivery No.: 962VGTimes Cited: 4Cited Reference Count: 233rd International Symposium on New Frontiers of Thermal Studies of MaterialsNOV 28-30, 2004Tsukuba, JAPANJSCTA, Univ Tsukuba, Grad Sch Pure \& Appl Sci, Soc Promot Calorimetry \& Thermal Anal, Ibaraki, Sci \& Technol Promot Fdn},
	month = {Aug},
	pages = {523-527},
	type = {Proceedings Paper},
	abstract = {Recently, we have reported a noble method of preparing Ag/Rh bimetallic nanoparticles with a pseudo-core/shell structure. We simply mix the dispersions of poly(N-vinyl-2-pyrrolidone)(PVP)-protected Ag and Rh nanoparticles in solution at room temperature. We found that the mixture of dispersions forms bimetallic nanoparticles in a pseudo-core/shell structure on standing. We call this process the {\textquoteright}self-assembling{\textquoteright} or {\textquoteright}self-organizing{\textquoteright}. In this study we seek for a thermodynamic driving force for this process by determining the enthalpy of the interaction among three pairs of nanoparticles by isothermal titration calorimetry (ITC). The results indicate that the interaction between each pair is strongly exothermic, and that among the pairs studied here the strength of the exothermic interaction is in the order of Ag/Pt<Ag/Pd<Ag/Rh.},
	keywords = {bimetallic nanoparticles, calorimetric method, CATALYTIC-ACTIVITY, CLUSTERS, CORE-SHELL NANOPARTICLES, core/shell structure, GROWTH, isothermal titration calorimetry, metal nanoparticle, NUCLEATION, palladium, PD, platinum, REDUCTION, rhodium, self-assembling, SELF-ORGANIZATION, silver, STRUCTURAL-ANALYSIS},
	isbn = {1388-6150},
	url = {<Go to ISI>://000231760500004},
	author = {Kanemaru, M. and Shiraishi, Y. and Koga,Yoshikata and Toshima, N.}
}
@article {1296,
	title = {Dynamic C-13 NMR studies of ligand exchange in linear (d(10)) silver(I) and gold(I) and square-planar (d(8)) rhodium(I) homoleptic metal carbonyl cations in superacidic media},
	journal = {Magnetic Resonance in Chemistry},
	volume = {43},
	number = {7},
	year = {2005},
	note = {ISI Document Delivery No.: 936FUTimes Cited: 0Cited Reference Count: 21},
	month = {Jul},
	pages = {520-527},
	type = {Article},
	abstract = {The dynamic CO exchange of the monovalent metal carbonyl cations [Ag((CO)-C-13)](+), [Au((CO)-C-13)(2)](+)-Au((CO)-C-13) SO3F and [Rh((CO)-C-12)(4-x)((CO)-C-13)(x)](+) (x <= 1) in superacidic solutions was studied by variable-temperature C-13 NMR methods. The exchange rates are strongly dependent on the acidity of the solvent, the concentration of metal carbonyl cations and temperature. Whereas a suitable exchange rate of the Ag(I) system is only accessible in magic acid (HSO3F-SbF5), the more stable Au(I) and Rh(I) systems were studied in the less acidic fluorosulfuric acid. Selected solutions of Ag(I), Rh(I) and Au(I) yielded activation barriers Delta G* of 42.7, 43.5, and 56.2 kJ mol(-1) respectively. Copyright (c) 2005 John Wiley \& Sons, Ltd.},
	keywords = {C-13 NMR, CO exchange, CRYSTAL, dynamic NMR, fluorosulfuric acid, GOLD, HINDERED INTERNAL ROTATION, HSO3F-SBF5, magic acid, metal carbonyl cations, NMR, NUCLEAR-MAGNETIC-RESONANCE, rhodium, silver, UNDECAFLUORODIANTIMONATE(V), VIBRATIONAL-SPECTRA},
	isbn = {0749-1581},
	url = {<Go to ISI>://000229841700003},
	author = {von Ahsen, B. and Bach, C. and Balzer, G. and Bley, B. and Bodenbinder, M. and Hagele, G. and Willner, H. and Aubke, F.}
}
@article {5137,
	title = {Analyte ionization in the furnace atomization plasma excitation spectrometry source - spatial and temporal observations},
	journal = {Journal of Analytical Atomic Spectrometry},
	volume = {16},
	number = {3},
	year = {2001},
	note = {ISI Document Delivery No.: 405MHTimes Cited: 7Cited Reference Count: 34},
	pages = {256-262},
	type = {Article},
	abstract = {Spatially resolved atomic and ionic emission has been measured in a FAPES source at radiofrequency (rf) powers ranging between 10 and 100w. The degree of ionization was spatially dependent, with maxima adjacent to the centre electrode and graphite cuvette wall. Temporally resolved atomic and ionic emission have also been measured in a newly designed FAPES source, and the temporal ionization behaviour of Mg, Cd, Fe, Zn and Cr was derived from these measurements.},
	keywords = {EMISSION-SPECTROMETRY, FAPES, FIGURES, GRAPHITE-FURNACE, LEAD, MERIT, silver, SPECTROSCOPY},
	isbn = {0267-9477},
	url = {<Go to ISI>://000167163200003},
	author = {Lu, S. Y. and LeBlanc, C. W. and Blades, M. W.}
}
@article {5117,
	title = {Tensor LEED analysis for the electrodeposited Pt(111)-(3x3)-Ag,I surface structure},
	journal = {Surface Science},
	volume = {490},
	number = {3},
	year = {2001},
	note = {ISI Document Delivery No.: 473XWTimes Cited: 5Cited Reference Count: 34},
	month = {Sep},
	pages = {256-264},
	type = {Article},
	abstract = {A crystallographic analysis is reported using low-energy electron diffraction (LEED) in the tensor LEED approach for the electrodeposited coadsorption (3 x 3) structure with 4/9 monolayer (ML) of silver and 4/9 ML of iodine on the Pt(1 1 1) surface. The structure approximates a two-layer slice of bulk AgI cut parallel to its (1 1 1) plane and superimposed on the substrate with the Ag atoms in contact with the topmost Pt(1 1 1) layer, and the I atoms forming an overlayer on the Ag atoms. There are two types of Ag atoms in the (3 x 3) unit mesh; one type bonds to a single Pt atom, while the other type bonds to three Pt atoms. The average Ag-Pt bond distances are close to 2.48 and 2.82 (A) over circle respectively for the one and three-coordinate Ag atoms, but both types of Ag atoms bond to three I atoms with an average Ag-I distance of 2.67 (A) over circle. No significant corrugation is observed for either the I layer or the Ag layer. (C) 2001 Elsevier Science B.V. All rights reserved.},
	keywords = {ADSORBATES, ADSORPTION, AG, chemisorption, ELECTROCHEMISTRY, ENERGY-ELECTRON-DIFFRACTION, IODINE, LOW ENERGY ELECTRON DIFFRACTION (LEED), METAL-SURFACES, platinum, PT(111), SCANNING-TUNNELING-MICROSCOPY, silver},
	isbn = {0039-6028},
	url = {<Go to ISI>://000171075300007},
	author = {Labayen, M. and Harrington, D. A. and Saidy, M. and Mitchell, K. A. R.}
}
@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 {7259,
	title = {TEMPORAL EMISSION AND ABSORPTION CHARACTERISTICS OF SILVER, LEAD AND MANGANESE IN FURNACE ATOMIZATION PLASMA EXCITATION SPECTROMETRY},
	journal = {Journal of Analytical Atomic Spectrometry},
	volume = {7},
	number = {7},
	year = {1992},
	note = {ISI Document Delivery No.: JY532Times Cited: 15Cited Reference Count: 37},
	month = {Oct},
	pages = {1039-1046},
	type = {Article},
	abstract = {The temporal behaviour of the signal measured for Ag, Pb and Mn in furnace atomization plasma excitation spectrometry was studied using atomic emission and atomic absorption spectrometry. Analyte was deposited both on the wall and on the r.f. electrode with and without the r.f. power applied. Analyte condensation on the r.f. electrode is observed when no plasma is formed. When the plasma is formed inside the furnace it heats the electrode such that, for Ag and Pb, condensation is not observed except for large amounts of analyte. For Ag and Mn, the appearance temperatures and peak temperatures are not significantly affected by the plasma relative to the response obtained using a graphite furnace. For Pb, appearance and peak temperatures are shifted significantly earlier. For Pb, atom formation may be effected by the presence of CO in the gas phase generated from oxidation of the graphite furnace wall and electrode. The role of carbon in atom formation was studied by depositing the sample on both tungsten and graphite electrodes.},
	keywords = {ASCORBIC-ACID, ATOMIC-ABSORPTION, DOUBLE PEAKS, ELECTROTHERMAL ATOMIZATION, FAPES, FURNACE ATOMIZATION PLASMA EXCITATION SPECTROMETRY, GRAPHITE FURNACE, GRAPHITE-FURNACE, LEAD AND MANGANESE SIGNALS, MECHANISMS, silver, SURFACE, TEMPERATURE, vaporization},
	isbn = {0267-9477},
	url = {<Go to ISI>://A1992JY53200002},
	author = {Hettipathirana, T. D. and Blades, M. W.}
}
