@article {1417,
	title = {Threshold ion-pair production spectroscopy of HCN},
	journal = {Journal of Chemical Physics},
	volume = {124},
	number = {7},
	year = {2006},
	note = {ISI Document Delivery No.: 014IPTimes Cited: 4Cited Reference Count: 32},
	month = {Feb},
	pages = {5},
	type = {Article},
	abstract = {The spectroscopic technique of threshold ion-pair production spectroscopy (TIPPS) has been applied to the triatomic molecule HCN. We have recorded the total ion-pair yield and TIPP spectra for the HCN -> H++CN- process using coherent vacuum ultraviolet excitation. From the simulation of our high-resolution TIPP spectrum we have precisely measured the HCN ion-pair threshold E-IP(0) to be 122 244 +/- 4 cm(-1). This value could be used to determine the bond dissociation energy D-0(H-CN) to unprecedented accuracy. Our fitting result also showed that rotationally excited instead of cold CN- fragment is favored as the ion-pair dissociation product in the threshold region.},
	keywords = {CN, DCN, DYNAMICS, ELECTRONIC STATES, MOLECULE, NM, PHOTO-DISSOCIATION, PHOTODISSOCIATION, PHOTOIONIZATION, TIPPS},
	isbn = {0021-9606},
	url = {<Go to ISI>://000235473500018},
	author = {Hu, Q. J. and Zhang, Q. and Hepburn, J. W.}
}
@article {1316,
	title = {The 4051-angstrom band of C-3 ((A)over-tilde(1)Pi(u)-(X)over-tilde(1)Sigma(+)(g), 000-000): Perturbed low-J lines and lifetime measurements},
	journal = {Journal of Chemical Physics},
	volume = {122},
	number = {24},
	year = {2005},
	note = {ISI Document Delivery No.: 943DNTimes Cited: 5Cited Reference Count: 31},
	month = {Jun},
	pages = {8},
	type = {Article},
	abstract = {Rotational analyses have been carried out at high resolution for the 000-000 and 000-100 bands of the A (1)Pi(u)-X (1)Sigma(g)(+) transition of supersonic jet-cooled C-3. Two different spectra have been recorded for each band, using time gatings of 20-150 and 800-2300 ns. At the shorter time delay the spectra show only the lines observed by many previous workers. At the longer time delay many extra lines appear, some of which have been observed previously by [McCall Chem. Phys. Lett. 374, 583 (2003)] in cavity ring-down spectra of jet-cooled C-3. Detailed analysis of these extra lines shows that at least two long-lived states perturb the A (1)Pi(u), 000 state. One of these appears to be a (3)Sigma(u)(-) vibronic state, which may possibly be a high vibrational level of the b (3)Pi(g) state, and the other appears to be a P=1 state with a low rotational constant B. Our spectra also confirm the reassignment by McCall of the R(0) line of the 000-000 band, which is consistent with the spectra recorded towards a number of stars that indicate the presence of C-3 in the interstellar medium. Fluorescence lifetimes have been measured for a number of upper-state rotational levels. The rotational levels of the A (1)Pi(u) state have lifetimes in the range of 230-190 ns, decreasing slightly with J; the levels of the perturbing states have much longer lifetimes, with some of them showing biexponential decays. An improved value has been obtained for the nu(1) vibrational frequency of the ground state, nu(1)=1224.4933 +/- 0.0029 cm(-1). (c) 2005 American Institute of Physics.},
	keywords = {C3, CHAIN, EMISSION-SPECTRA, INTERSTELLAR C-3, MOLECULE, SPECTROSCOPY, STATES, TRANSITION, TRANSLUCENT SIGHT LINES},
	isbn = {0021-9606},
	url = {<Go to ISI>://000230332400023},
	author = {Zhang, G. Q. and Chen, K. S. and Merer, A. J. and Hsu, Y. C. and Chen, W. J. and Shaji, S. and Liao, Y. A.}
}
@article {1149,
	title = {Quantitative proteomic analysis of sokotrasterol sulfate-stimulated primary human endothelial cells},
	journal = {Molecular \& Cellular Proteomics},
	volume = {4},
	number = {2},
	year = {2005},
	note = {ISI Document Delivery No.: 902UFTimes Cited: 9Cited Reference Count: 40},
	month = {Feb},
	pages = {191-204},
	type = {Article},
	abstract = {The endothelium forms a continuous monolayer at the interface between blood and tissue and contributes significantly to the sensing and transducing of signals between blood and tissue. New blood vessel formation, or angiogenesis, is initiated by the activation of endothelial cells and is an important process required for various pathological and physiological situations. This study used cleavable isotope-coded affinity tag reagents combined with mass spectrometry to investigate the molecular basis of a recently discovered angiogenesis-promoting steroid, sokotrasterol sulfate. Changes in the relative abundances of over 1000 proteins within human endothelial cells treated with sokotrasterol sulfate and vehicle-treated cells were identified and quantitated using this technique. A method that examines the entire ensemble of quantitative measurements was developed to identify proteins that showed a statistically significant change in relative abundance resulting from treatment with sokotrasterol sulfate. A total of 93 proteins was significantly up-regulated, and 37 were down-regulated in response to sokotrasterol sulfate stimulation of endothelial cells. Among the up-regulated proteins, several were identified that are novel to endothelial cells and are likely involved in cell communication and morphogenesis. These findings are consistent with a role for sokotrasterol sulfate in endothelial sprouting.},
	keywords = {CANCER, DIFFERENTIATION, EXPRESSION, GENE, GROWTH-FACTOR, ISCHEMIC-HEART-DISEASE, MASS-SPECTROMETRY, MOLECULE, THERAPEUTIC ANGIOGENESIS, VEGF},
	isbn = {1535-9476},
	url = {<Go to ISI>://000227381300008},
	author = {Karsan, A. and Pollet, I. and Yu, L. R. and Chan, K. C. and Conrads, T. P. and Lucas, D. A. and Andersen, R. J. and Veenstra, T.}
}
@article {635,
	title = {Threshold ion-pair production spectroscopy of HCl/DCl: Born-Oppenheimer breakdown in HCl and HCl+ and dynamics of photoion-pair formation},
	journal = {Journal of Chemical Physics},
	volume = {119},
	number = {17},
	year = {2003},
	note = {ISI Document Delivery No.: 733FHTimes Cited: 16Cited Reference Count: 31},
	month = {Nov},
	pages = {8938-8945},
	type = {Article},
	abstract = {Threshold ion-pair production spectroscopy (TIPPS) has been applied to two isotopomers, HCl and DCl. From the high-resolution TIPP spectra the ion-pair thresholds of the two molecules have been precisely measured. Combined with the known ionization energy of H(D) and the electron affinity of Cl, the difference between their bond dissociation energies is calculated, and therefore an experimental determination of the effect of Born-Oppenheimer breakdown on the dissociation limit of the ground state potential curve has been obtained. The difference in D-e for the two isotopomers was found to be: D-e(H-Cl)-D-e(D-Cl)=3.2+/-1.0 cm(-1). The bond energy for HCl was in agreement with our previous determination, D-0(H-Cl)=35748.2+/-0.8 cm(-1). These results are compared to a recent study of Born-Oppenheimer breakdown in HCl by Coxon and Hajigeorgiou, where high resolution spectroscopic data was used to fit Born-Oppenheimer breakdown correction terms for the intramolecular potential function. The present study also measured the high resolution spectra for photoion-pair production for HCl and DCl in the threshold region for ion-pair production (similar to86 nm). Although there is qualitative agreement between the current results and previous experimental and theoretical work, there are some important differences. The possible mechanism for ion-pair formation in HCl and DCl is discussed in light of these high resolution results. (C) 2003 American Institute of Physics.},
	keywords = {BAND SYSTEM, DCL, DEPENDENCE, DF, DISSOCIATION-ENERGY, HF, IONIZATION, MOLECULE, STATES, TIPPS},
	isbn = {0021-9606},
	url = {<Go to ISI>://000185988900021},
	author = {Hu, Q. J. and Melville, T. C. and Hepburn, J. W.}
}
@article {410,
	title = {The electronic spectrum of NiCN in the visible region},
	journal = {Journal of Molecular Spectroscopy},
	volume = {215},
	number = {1},
	year = {2002},
	note = {ISI Document Delivery No.: 601LETimes Cited: 18Cited Reference Count: 74},
	month = {Sep},
	pages = {106-127},
	type = {Article},
	abstract = {The electronic spectrum of NiCN in the 500-630 nm region has been observed by laser-induced fluorescence, following the reaction of laser-ablated nickel atoms with cyanogen under free jet expansion conditions. Seven electronic states hake been identified. Three of these, (X) over tilde (1) (2)Delta(5/2), (X) over tilde (2) (2)Delta(3/2), and (W) over tilde (2)(1)Pi(3/2), are derived from the electron configuration Ni+ (3d(8) 4s) CN, and the other four, (A) over tilde (2) Delta(5/2), (B) over tilde (2)Pi(3/2), (C) over tilde (2)Phi(7/2) and (D) over tilde (2)Phi(5/2), are derived from the configuration Ni+ (3d(8) 4s) CN. Rotational analysis of bands of (NiCN)-N-14 and (NiCN)-N-15 at high resolution has given the bond lengths in the (X) over tilde (2)(1)Delta(5/2) ground state as r(0) (Ni-C) = 1.8292 +/- 0.0028 Angstrom; r(0) (C-N) = 1.1591 +/- 0.0029 Angstrom. The orbital angular momentum splits the bending fundamental of the (X) over tilde (2)(1)Delta(5/2) state into two vibronic components, which lie at 243.640 cm(-1) ((2)Pi(3/2)) and 244.964 cm(-1) ((2)Phi(7/2)). Exceptionally strong Fermi resonance occurs in the ground state between the Ni-C stretching vibration, nu(3), and the overtone of the bending vibration. Sixty vibrational levels of the ground state with /l/ = 0 and l have been assigned, They could tie fitted by least squares to a simple matrix representation of the Fermi resonance that ignores the orbital angular momentum the interaction matrix element, as a fraction of the bending frequency, turns out to be larger than that in the "prototype" molecule, CO2. The two low-lying excited electronic states, (X) over tilde (2)Delta(3/2) at 830 cm(-1) and (W) over tilde (2)(1)Pi(3/2) at 2238 cm(-1), have very similar properties to the ground state. The energies of the excited states in the visible region bear a remarkable resemblance to those found in NiH (S, A. Kadavathu et al., 1991, J. Mol. Spectrosc. 147, 448-470). Again, the effects of Fermi resonance in them are large but those of vibronic coupling are surprisingly small. The most significant vibronic coupling occurs between the (A) over tilde (2)Delta(5/2) and (B) over tilde (2)Pi(3/2) states, which are separated by 79 cm(-1), an interval which is less than half the frequency of the bending vibration that couples them large numbers of vibronically induced bands appear in the excitation and dispersed emission spectra, but the splitting between (tie vibronic components of the bending fundamental of the (A) over tilde (2)Delta(5/2) state is only 6.988 cm(-1). Rotational perturbations are widespread in the (A) over tilde (2)Delta(5/2) state, particularly in the levels of the nu(3) (Ni-C stretching) progression, Vibrational assignments have been made on the basis of the Ni-58-Ni-60 isotope shifts at high resolution and the Franck-Condon patterns in dispersed emission spectra, Various weak unassigned bands, both in the excitation and the dispersed emission spectra, give evidence for the existence of at least three more excited electronic states which it has not been possible to characterize in detail. (C) 2002 Elsevier Science (USA)},
	keywords = {ANION PHOTOELECTRON-SPECTROSCOPY, EXCITED-STATES, FOURIER-TRANSFORM SPECTROSCOPY, LASER-INDUCED FLUORESCENCE, LITHIUM ISOCYANIDE, LOW-LYING STATES, MG-BEARING, MICROWAVE, MOLECULE, POTENTIAL-ENERGY SURFACE, ROTATIONAL SPECTRUM, SPECTROSCOPY},
	isbn = {0022-2852},
	url = {<Go to ISI>://000178446800011},
	author = {Kingston, C. T. and Merer, A. J. and Varberg, T. D.}
}
@article {5040,
	title = {A combined linear ion trap time-of-flight system with improved performance and MSn capabilities},
	journal = {Rapid Communications in Mass Spectrometry},
	volume = {15},
	number = {19},
	year = {2001},
	note = {ISI Document Delivery No.: 477JFTimes Cited: 47Cited Reference Count: 28},
	pages = {1777-1795},
	type = {Article},
	abstract = {A detailed description of a linear ion trap time-of-flight (TOF) mass spectrometer system, capable of sequential mass spectrometry (MS{\textquoteright}), is given. Many improvements have been incorporated since the initial description of this system (Rapid Commun. Mass Spectrom. 1998; 12:1463-1474). The pressure in the trap has been lowered from 7.0 to 1.8 mTorr, resulting in an increase in the mass resolution of ion excitation from 75 to 240. Use of the system for MS3 is demonstrated. Dipole excitation of the n = I harmonic, instead of the n = 0 fundamental frequency of ion motion, is shown to have a higher frequency resolution, f/Deltaf, but lower mass resolution, m/Deltam. Both experiments and modeling demonstrate that at the lower pressure there is less collisional cooling of ions in the axial and radial directions of the trap. The efficiency of trapping is shown to be nearly 100\% for periods up to 5 s. The demonstrated mass range for mass analysis has been extended to greater than m/z 16 250. To avoid the formation of adduct ions when trapping protein ions for extended times requires ultra-high vacuum cleanliness conditions, even though the trap operates in the mTorr-pressure range. Upgrading the TOF to a reflectron with higher quality ion optics results in an increase in the mass resolution of the TOF mass spectrometer to about 5000 at m/z 750. Copyright (C) 2001 John Wiley \& Sons, Ltd.},
	keywords = {COLLISION CELL, EXCITATION, GUIDE, INTERFACE, MOLECULE, QUADRUPOLE MASS-SPECTROMETER, reaction, STORAGE ASSISTED DISSOCIATION},
	isbn = {0951-4198},
	url = {<Go to ISI>://000171279800001},
	author = {Collings, B. A. and Campbell, J. M. and Mao, D. M. and Douglas, D. J.}
}
@article {4843,
	title = {Chirally modified zeolites as reaction media: Photochemistry of an achiral tropolone ether},
	journal = {Organic Letters},
	volume = {2},
	number = {2},
	year = {2000},
	note = {ISI Document Delivery No.: 278ZETimes Cited: 49Cited Reference Count: 26},
	month = {Jan},
	pages = {119-121},
	type = {Article},
	abstract = {[GRAPHICS] Zeolites modified with chiral inductors serve as media for performing chiral induction during photochemical reactions of organic molecules. The photochemical behavior of achiral tropolone ethyl phenyl ether illustrates this unique feature of a zeolite.},
	keywords = {AROMATICS, benzene, CATION-PI INTERACTIONS, CHEMISTRY, interactions, ION, MODEL, MOLECULE, STATE ORGANIC-PHOTOCHEMISTRY, WATER},
	isbn = {1523-7060},
	url = {<Go to ISI>://000085018200006},
	author = {Joy, A. and Scheffer, J. R. and Ramamurthy, V.}
}
@article {4666,
	title = {An analysis of O-H interaction potentials, O-H and O-D collision cross sections, and vibrational states},
	journal = {Planetary and Space Science},
	volume = {47},
	number = {1-2},
	year = {1999},
	note = {ISI Document Delivery No.: 179JTTimes Cited: 3Cited Reference Count: 29},
	month = {Jan-Feb},
	pages = {163-174},
	type = {Article},
	abstract = {A detailed comparison of recently published OH, X(2)Pi, (2)Sigma(-), (4)Pi and (4)Sigma(-) potentials is carried out. These potential functions are important in the accurate determination of O-H and O-D collision cross sections. The isotope effect in the O-H and O-D cross sections plays an important role in the enhanced nonthermal escape of H and D from Mars and Venus. The quantum mechanical elastic scattering cross sections for O-H and O-D collisions are determined with a set of potentials which are constructed with a new interpolation of the short range tabulated potentials and the long range asymptotic behaviour. The important role of the asymptotic radial variation of the potential functions in the determination of the elastic cross sections is studied in detail with a semiclassical analysis, and a comparison is made with previous calculations. The vibrational energies for several different X(2)Pi bound potential functions for OH are also calculated and compared with published results. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.},
	keywords = {DISCRETIZATION METHOD QDM, ENERGY, HYDROGEN, MODEL, MOLECULE, OXYGEN, VENUS},
	isbn = {0032-0633},
	url = {<Go to ISI>://000079324100017},
	author = {Shizgal, B. D.}
}
@article {4655,
	title = {Tensor LEED analysis for the Cu(111)-(root x root 7)R19.1 degrees-S surface structure},
	journal = {Surface Science},
	volume = {441},
	number = {2-3},
	year = {1999},
	note = {ISI Document Delivery No.: 253RWTimes Cited: 11Cited Reference Count: 36},
	month = {Nov},
	pages = {425-435},
	type = {Article},
	abstract = {A tensor LEED analysis is reported for the (root 7 x root 7)R19.1 degrees structure formed by S at the Cu(lll)surface. A new structural model is found which corresponds to a modified version of the copper sulphide overlayer model first proposed by Domange and Oudar. In that model, the topmost layer has 3/7 monolayer each of Cu and S atoms, but the modification involves one S atom per unit mesh moving down to displace a Cu atom from the second metal layer. Relaxations among the topmost Cu atoms result in one S atom being effectively three-fold coordinate while the other two are sixfold coordinate and 12-fold coordinate: the averaged S-Cu bond lengths are indicated to equal 2.19, 2.47 and 2.62 Angstrom respectively. Some discussion is included of factors that may influence this choice of surface structure. (C) 1999 Elsevier Science B.V. All rights reserved.},
	keywords = {ADSORPTION, chemisorption, copper, ENERGY-ELECTRON-DIFFRACTION, LAYERS, low energy electron diffraction, LOW INDEX SINGLE CRYSTAL, METAL-SURFACES, MOLECULE, RAY STANDING-WAVE, RECONSTRUCTION, RU(0001), SUBSTRATE, SULFUR, sulphur, SURFACE, surface reconstruction},
	isbn = {0039-6028},
	url = {<Go to ISI>://000083570400024},
	author = {Saidy, M. and Mitchell, K. A. R.}
}
@article {4272,
	title = {Hyperfine constants and nuclear shieldings from the microwave spectra of FBO, CIBO, and FBS},
	journal = {Journal of Molecular Spectroscopy},
	volume = {190},
	number = {1},
	year = {1998},
	note = {ISI Document Delivery No.: ZV968Times Cited: 10Cited Reference Count: 31},
	month = {Jul},
	pages = {157-167},
	type = {Article},
	abstract = {Rotational spectra of the unstable molecules FBO, CIBO, and FBS have been measured in the 8-26 GHz frequency range using a pulsed jet cavity Fourier transform microwave spectrometer. The samples were prepared by passing electric discharges through mixtures of O-2/BF3, O-2/BCl3, or OCS/BF3, respectively, entrained in Ne. Hyperfine structures in the observed transitions have been resolved and analyzed in terms of nuclear quadrupole, spin-rotation, and spin-spin interactions. The quadrupole and spin-rotation coupling constants have been used to show that the electronic environment surrounding the boron nucleus of all three species is very similar. The spin-rotation constants have been used to determine, for the first time, experimental average shieldings of the Cl, F, and B nuclei of these molecules. Ab initio Values for the nuclear shielding parameters have been calculated for comparison. (C) 1998 Academic Press.},
	keywords = {BORON, CONSISTENT-FIELD CALCULATIONS, DIPOLE-MOMENT, MOLECULAR-STRUCTURE, MOLECULE, QUADRUPOLE-MOMENT, SPECTROSCOPY, SUBSTITUTION STRUCTURE, UNSTABLE, vibration-rotation analysis},
	isbn = {0022-2852},
	url = {<Go to ISI>://000074360400014},
	author = {Gatehouse, B. and Muller, H. S. P. and Gerry, M. C. L.}
}
@article {3914,
	title = {Microwave spectrum and geometry of cyanogen N-oxide, NCCNO},
	journal = {Journal of Molecular Spectroscopy},
	volume = {181},
	number = {2},
	year = {1997},
	note = {ISI Document Delivery No.: WH318Times Cited: 22Cited Reference Count: 32},
	month = {Feb},
	pages = {316-322},
	type = {Article},
	abstract = {The microwave spectrum of cyanogen N-oxide, NCCNO, has been investigated in the frequency region between 4 and 23 GHz, using a pulsed jet Fourier transform microwave spectrometer. The spectrum is that of a linear molecule. Transitions of five isotopomers have been analyzed, and r(0), r(s), and r(I,e), geometries have been determined. The geometry and the N-14 nuclear quadrupole coupling constants have been used to compare NCCNO to similar molecules. Though the present data indicate strongly that the molecule is truly linear, they are insufficient to rule out quasi-linear behavior completely. (C) 1997 Academic Press.},
	keywords = {CONSTANTS, GROUND-STATE, MILLIMETER-WAVE, MOLECULE, NCNCO, PARAMETERS, ROTATIONAL SPECTRA, SPECTROSCOPY},
	isbn = {0022-2852},
	url = {<Go to ISI>://A1997WH31800008},
	author = {Brupbacher, T. and Bohn, R. K. and Jager, W. and Gerry, M. C. L. and Pasinszki, T. and Westwood, N. P. C.}
}
@article {4129,
	title = {Self-assembly of two or more cavitands},
	journal = {Gazzetta Chimica Italiana},
	volume = {127},
	number = {11},
	year = {1997},
	note = {ISI Document Delivery No.: ZN007Times Cited: 0Cited Reference Count: 124th International Conference on CalixarenesAUG 31-SEP 04, 1997PARMA, ITALY},
	month = {Nov},
	pages = {653-655},
	type = {Proceedings Paper},
	abstract = {The linkage of two, three, and four cavitands is described. These macrocycles of macrocycles can lead to covalent linkage of capsules capable of entrapping small molecules.},
	keywords = {MOLECULE},
	isbn = {0016-5603},
	url = {<Go to ISI>://000073598400004},
	author = {Sherman, J. C.}
}
@article {7267,
	title = {THE MICROWAVE-SPECTRUM OF THE VANDERWAALS COMPLEX AR-N2},
	journal = {Chemical Physics Letters},
	volume = {196},
	number = {3-4},
	year = {1992},
	note = {ISI Document Delivery No.: JH787Times Cited: 47Cited Reference Count: 34},
	month = {Aug},
	pages = {274-279},
	type = {Article},
	abstract = {The microwave spectrum of the van der Waals complex Ar-N2 has been investigated. N-15 quadrupole coupling constants, rotational and centrifugal distortion constants, structural parameters and an estimate of the dipole moment have been obtained. A value for the N-14 quadrupole coupling constant for free nitrogen has been derived.},
	keywords = {ENERGY, HCN DIMER, J-DEPENDENCE, MOLECULE, N2-AR, NITROGEN, RADIOFREQUENCY, ROTATIONAL SPECTRUM, SPECTROSCOPY},
	isbn = {0009-2614},
	url = {<Go to ISI>://A1992JH78700009},
	author = {Jager, W. and Gerry, M. C. L.}
}
