@article {2319,
	title = {Adsorption of small gas molecules onto Pt-doped single-walled carbon nanotubes},
	journal = {J. Phys. Chem. C},
	volume = {112},
	number = {19},
	year = {2008},
	note = {ISI Document Delivery No.: 297XATimes Cited: 15Cited Reference Count: 108Yeung, Charles See Liu, Lei Vincent Wang, Yan Alexander},
	month = {May},
	pages = {7401-7411},
	abstract = {<p>The adsorption of small gaseous molecules to the metal center in Pt-doped (5,5) single-walled carbon nanotubes has been explored within density functional theory. A model system consisting of a single Pt atom residing in the middle of a carbon nanotube with capping H atoms is used for our investigation. For all gases studied, the overall process of adsorption was found to be exothermic, where the affinity strongly depended on the orientation of the molecule. By examining the density of states and molecular orbitals of these nanotube-adsorbate complexes in comparison to the bare Pt-doped nanotube, we show that the electronic structure of these materials is strongly influenced by the presence of gases. Hence, we propose an application of Pt-doped single-walled carbon nanotubes as gas sensors and hope to motivate experimental work in this field.</p>},
	keywords = {AB-INITIO, COVALENT FUNCTIONALIZATION, ELECTRONIC-PROPERTIES, INTERMOLECULAR INTERACTIONS, LASER-ABLATION, NO, PLATINUM COMPLEXES, PT(111), SIDEWALL FUNCTIONALIZATION, TRANSITION-METAL},
	isbn = {1932-7447},
	url = {<Go to ISI>://000255649500014},
	author = {Yeung, C. S. and Liu, L. V. and Y. A. Wang*}
}
@article {904,
	title = {"Spectrum-only" assignment of core-penetrating and core-nonpenetrating Rydberg states of calcium monofluoride},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {82},
	number = {6},
	year = {2004},
	note = {ISI Document Delivery No.: 861XATimes Cited: 3Cited Reference Count: 38},
	month = {Jun},
	pages = {791-803},
	type = {Article},
	abstract = {Rydberg states of calcium monofluoride in the n* = 17-20 region have been observed by ionization-detected optical-optical double-resonance spectroscopy via the D(2)Sigma(+) v = 1 intermediate state. All members of the six core-penetrating Rydberg series in the n* = 17-20 region and several components of the 17f and 17g core-nonpenetrating Rydberg states have been assigned. While the assignment of core-penetrating Rydberg states is straightforward without use of an effective Hamiltonian model, "spectrum-only" assignment of core-nonpenetrating states is complicated because strong l-uncoupling causes the core-nonpenetrating states to evolve rapidly from Hund{\textquoteright}s case (b) to Hund{\textquoteright}s case (d) coupling. We describe "spectrum-only" assignment procedures, developed in the spirit of Gerhard Herzberg, that can be used to assign optical-optical double-resonance spectra of core-penetrating and core-nonpenetrating Rydberg states using only information contained in the spectrum rather than predictions derived from an effective Hamiltonian model. The ambiguities that arise in the assignment of each class of states are discussed in detail.},
	keywords = {ANGULAR-MOMENTUM STATES, AUTOIONIZATION, CaF, DECAY DYNAMICS, electric quadrupole moment, EXCITED-STATES, HIGHER, IONIZATION, laser spectroscopy, MAGNETIC-FIELD, NO, QUANTUM-DEFECT THEORY, Rydberg states, TRIPLE-RESONANCE SPECTROSCOPY},
	isbn = {0008-4042},
	url = {<Go to ISI>://000224450700014},
	author = {Kay, J. J. and Byun, D. S. and Clevenger, J. O. and Jiang, X. and Petrovi, V. S. and Seiler, R. and Barchi, J. R. and Merer, A. J. and Field, R. W.}
}
@article {393,
	title = {Differing reactivities of (trimpsi)M(CO)(2)(NO) complexes [M = V, Nb, Ta; trimpsi = (BuSi)-Bu-t(CH2PMe2)(3)] with halogens and halogen sources},
	journal = {Inorganic Chemistry},
	volume = {41},
	number = {21},
	year = {2002},
	note = {ISI Document Delivery No.: 605KHTimes Cited: 11Cited Reference Count: 55},
	month = {Oct},
	pages = {5388-5396},
	type = {Article},
	abstract = {Treatment of (trimpsi)V(CO)(2)(NO) (trimpsi = (BuSi)-Bu-t(CH2PMe2)(3)) with 1 equiv of PhlCl(2) or C2Cl6 or 2 equiv of AgCl affords (trimpsi)V(NO)Cl-2 (1) in moderate yields. Likewise, (trimpsi)V(NO)Br-2 (2) and (trimpsi)V(NO)\(2) (3) are formed by the reactions of (trimpsi)V(CO)(2)(NO) with Br-2 and l(2), respectively. The complexes (trimpsi)M(NO)l(2)(PMe3) (M = Nb, 4; Ta, 5) can be isolated in moderate to low yields when the (trimpsi)M(CO)(2)(NO) compounds are sequentially treated with 1 equiv of l(2) and excess PMe3. The reaction of (trimpsi)V(CO)(2)(NO) with 2 equiv of CINO forms 1 in low yield, but the reactions of (trimpsi)M(CO)(2)(NO) (M = Nb, Ta) with 1 equiv of CINO generate (trimpsi)M(NO)(2)Cl (M = Nb, 6; Ta, 7). Complexes 6 and 7 are thermally unstable and decompose quickly at room temperature; consequently, they have been characterized solely by IR and P-31{H-1} NMR spectroscopies. All other new complexes have been fully characterized by standard methods, and the solid-state molecular structures of 1.3CH(2)Cl(2), 4.(3/ 4)CH2Cl2, and 5.THF have been established by single-crystal X-ray diffraction analyses. A convenient method of generating (ClNO)-N-15 has also been developed during the course of these investigations.},
	keywords = {CHEMISTRY, CRYSTAL-STRUCTURE, DISPROPORTIONATION REACTIVITY, NIOBIUM, NITRIC-OXIDE, NITROSYL COMPLEXES, NO, tantalum, TROPOCORONAND, VANADIUM},
	isbn = {0020-1669},
	url = {<Go to ISI>://000178676700012},
	author = {Hayton, T. W. and Legzdins,Peter and Patrick, B. O.}
}
@article {3857,
	title = {Tensor LEED analyses for the (root 3x root 3)R30 degrees and c(4x2) structures formed by sulphur chemisorbed on the (111) surface of rhodium},
	journal = {Surface Science},
	volume = {345},
	number = {1-2},
	year = {1996},
	note = {ISI Document Delivery No.: TT592Times Cited: 17Cited Reference Count: 16},
	month = {Jan},
	pages = {101-109},
	type = {Article},
	abstract = {Tensor LEED analyses have been made for the Rh(111)-(root 3 x root 3)R30 degrees-S and Rh(lll)-c(4 x 2)-S surface structures formed by S chemisorbed at 1/3 and 1/2 monolayer coverages respectively. For the lower-coverage form, S adsorbs on the regular three-coordinate sites which continue the fee packing sequence; the S-Rh bond lengths are indicated to equal 2.23 Angstrom, and relaxations in the metallic structure are negligible. In the c(4 x 2) form, the adsorption occurs equally on both types of three-coordinate site (fee and hcp), although some surface Rh atoms bond to two S atoms while others bond to just one, and this sets up some interesting relaxations. Specifically, the S atoms displace laterally from the centre of the three-fold sites by 0.20 to 0.29 Angstrom, and the first metal layer is buckled by about 0.23 Angstrom. The first-to-second interlayer spacing in the metal expands to 2.26 Angstrom from the bulk value of 2.20 Angstrom. The average S-Rh bond lengths equal 2.22 Angstrom, and so they are not significantly changed from that in the low-coverage form. The structural evolution for S chemisorbed on the (111) surface of rhodium with increasing coverage is compared with the corresponding evolution on the Rh(110) surface.},
	keywords = {ABSORPTION FINE-STRUCTURE, ASSIGNMENT, chalcogens, CRYSTAL SURFACES, HOLLOW ADSORPTION SITE, LOW ENERGY ELECTRON DIFFRACTION (LEED), LOW INDEX SINGLE, NI(111), NO, rhodium, SURFACE RELAXATION},
	isbn = {0039-6028},
	url = {<Go to ISI>://A1996TT59200014},
	author = {Wong, K. C. and Liu, W. and Saidy, M. and Mitchell, K. A. R.}
}
@article {6898,
	title = {ADDITION AND SPIN EXCHANGE-RATE CONSTANTS BY LONGITUDINAL-FIELD MU-SR - THE MU + NO REACTION},
	journal = {Hyperfine Interactions},
	volume = {65},
	number = {1-4},
	year = {1990},
	note = {ISI Document Delivery No.: EZ856Times Cited: 10Cited Reference Count: 185TH INTERNATIONAL CONF ON MUON SPIN ROTATION RELAXATION AND RESONANCEAPR 09-12, 1990OXFORD, ENGLAND},
	pages = {979-986},
	type = {Proceedings Paper},
	abstract = {{The addition reaction Mu + NO + M {\textendash}> MuNO + M and the spin exchange reaction Mu(arrow-pointing-up) + NO(arrow-pointing-down) {\textendash}> Mu(arrow-pointing-down) + NO (arrow-pointing-up) have been measured by longitudinal field mu-SR at room temperature in the presence of up to 58 atm of N2 as inert collider. The pressure dependence of the longitudinal relaxation rate due to the addition reaction (lambda-c) demonstrates that the system is still in the low pressure regime in this pressure range. The corresponding termolecular rate constant has been determined as k0},
	keywords = {muonium, NO, O-2},
	isbn = {0304-3843},
	url = {<Go to ISI>://A1990EZ85600030},
	author = {Senba, M. and Gonzalez, A. C. and Kempton, J. R. and Arseneau, D. J. and Pan, J. J. and Tempelmann, A. and Fleming, Donald G.}
}
