Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 13 to 24 of 265 entries
Sorted by: Best Match Show Resources per page
Pulsed fluorescence measurements of trapped molecular ions with zero background detection.

Journal of the American Society for Mass Spectrometry

Khoury JT, Rodriguez-Cruz SE, Parks JH.
PMID: 12056569
J Am Soc Mass Spectrom. 2002 Jun;13(6):696-708. doi: 10.1016/S1044-0305(02)00364-1.

Sensitive methods have been developed to measure laser-induced fluorescence from trapped ions by reducing the detection of background scattering to zero levels during the laser excitation pulse. The laser beam diameter has been reduced to approximately 150 microm to...

Cite
Khoury JT, Rodriguez-Cruz SE, Parks JH. Pulsed fluorescence measurements of trapped molecular ions with zero background detection. J Am Soc Mass Spectrom. 2002;13(6):696-708doi: 10.1016/S1044-0305(02)00364-1.
Khoury, J. T., Rodriguez-Cruz, S. E., & Parks, J. H. (2002). Pulsed fluorescence measurements of trapped molecular ions with zero background detection. Journal of the American Society for Mass Spectrometry, 13(6), 696-708. https://doi.org/10.1016/S1044-0305(02)00364-1
Khoury, Joseph T, et al. "Pulsed fluorescence measurements of trapped molecular ions with zero background detection." Journal of the American Society for Mass Spectrometry vol. 13,6 (2002): 696-708. doi: https://doi.org/10.1016/S1044-0305(02)00364-1
Khoury JT, Rodriguez-Cruz SE, Parks JH. Pulsed fluorescence measurements of trapped molecular ions with zero background detection. J Am Soc Mass Spectrom. 2002 Jun;13(6):696-708. doi: 10.1016/S1044-0305(02)00364-1. PMID: 12056569.
Copy Download .nbib Format: NLM
Sandia octahedral molecular sieves (SOMS): structural and property effects of charge-balancing the M(IV)-substituted (M = Ti, Zr) Niobate framework.

Journal of the American Chemical Society

Nyman M, Tripathi A, Parise JB, Maxwell RS, Nenoff TM.
PMID: 11853447
J Am Chem Soc. 2002 Feb 27;124(8):1704-13. doi: 10.1021/ja017081z.

Sandia octahedral molecular sieves (SOMS) is an isostructural, variable composition class of ion exchangers with the general formula Na(2)Nb(2-x)M(IV)(x)O (6-x)(OH)(x).H(2)O (M(IV) = Ti, Zr; x = 0.04-0.40) where up to 20% of the framework Nb(V) can be substituted with...

Cite
Nyman M, Tripathi A, Parise JB, et al. Sandia octahedral molecular sieves (SOMS): structural and property effects of charge-balancing the M(IV)-substituted (M = Ti, Zr) Niobate framework. J Am Chem Soc. 2002;124(8):1704-13doi: 10.1021/ja017081z.
Nyman, M., Tripathi, A., Parise, J. B., Maxwell, R. S., & Nenoff, T. M. (2002). Sandia octahedral molecular sieves (SOMS): structural and property effects of charge-balancing the M(IV)-substituted (M = Ti, Zr) Niobate framework. Journal of the American Chemical Society, 124(8), 1704-13. https://doi.org/10.1021/ja017081z
Nyman, May, et al. "Sandia octahedral molecular sieves (SOMS): structural and property effects of charge-balancing the M(IV)-substituted (M = Ti, Zr) Niobate framework." Journal of the American Chemical Society vol. 124,8 (2002): 1704-13. doi: https://doi.org/10.1021/ja017081z
Nyman M, Tripathi A, Parise JB, Maxwell RS, Nenoff TM. Sandia octahedral molecular sieves (SOMS): structural and property effects of charge-balancing the M(IV)-substituted (M = Ti, Zr) Niobate framework. J Am Chem Soc. 2002 Feb 27;124(8):1704-13. doi: 10.1021/ja017081z. PMID: 11853447.
Copy Download .nbib Format: NLM
Experimental and theoretical methods to investigate extraframework species in a layered material of dodecaniobate anions.

Inorganic chemistry

Nyman M, Larentzos JP, Maginn EJ, Welk ME, Ingersoll D, Park H, Parise JB, Bull I, Bonhomme F.
PMID: 17298051
Inorg Chem. 2007 Mar 19;46(6):2067-79. doi: 10.1021/ic061454l. Epub 2007 Feb 14.

The highly charged dodecaniobate Keggin ions [XNb12O40](-16) (X = Si, Ge) and [XNb12O40](-15) (X = P) serve as building blocks of self-assembled, low-dimensional anionic framework materials. In addition to its high charge, the Keggin ion provides optimal binding geometries...

Cite
Nyman M, Larentzos JP, Maginn EJ, et al. Experimental and theoretical methods to investigate extraframework species in a layered material of dodecaniobate anions. Inorg Chem. 2007;46(6):2067-79doi: 10.1021/ic061454l.
Nyman, M., Larentzos, J. P., Maginn, E. J., Welk, M. E., Ingersoll, D., Park, H., Parise, J. B., Bull, I., & Bonhomme, F. (2007). Experimental and theoretical methods to investigate extraframework species in a layered material of dodecaniobate anions. Inorganic chemistry, 46(6), 2067-79. https://doi.org/10.1021/ic061454l
Nyman, May, et al. "Experimental and theoretical methods to investigate extraframework species in a layered material of dodecaniobate anions." Inorganic chemistry vol. 46,6 (2007): 2067-79. doi: https://doi.org/10.1021/ic061454l
Nyman M, Larentzos JP, Maginn EJ, Welk ME, Ingersoll D, Park H, Parise JB, Bull I, Bonhomme F. Experimental and theoretical methods to investigate extraframework species in a layered material of dodecaniobate anions. Inorg Chem. 2007 Mar 19;46(6):2067-79. doi: 10.1021/ic061454l. Epub 2007 Feb 14. PMID: 17298051.
Copy Download .nbib Format: NLM
Quantitative high-pressure pair distribution function analysis.

Journal of synchrotron radiation

Parise JB, Antao SM, Michel FM, Martin CD, Chupas PJ, Shastri SD, Lee PL.
PMID: 16120977
J Synchrotron Radiat. 2005 Sep;12:554-9. doi: 10.1107/S0909049505022612. Epub 2005 Aug 16.

The collection of scattering data at high pressure and temperature is now relatively straightforward thanks to developments at high-brightness synchrotron radiation facilities. Reliable data from powders, that are suitable for structure determination and Rietveld refinement, are routinely collected up...

Cite
Parise JB, Antao SM, Michel FM, et al. Quantitative high-pressure pair distribution function analysis. J Synchrotron Radiat. 2005;12:554-9doi: 10.1107/S0909049505022612.
Parise, J. B., Antao, S. M., Michel, F. M., Martin, C. D., Chupas, P. J., Shastri, S. D., & Lee, P. L. (2005). Quantitative high-pressure pair distribution function analysis. Journal of synchrotron radiation, 12554-9. https://doi.org/10.1107/S0909049505022612
Parise, John B, et al. "Quantitative high-pressure pair distribution function analysis." Journal of synchrotron radiation vol. 12 (2005): 554-9. doi: https://doi.org/10.1107/S0909049505022612
Parise JB, Antao SM, Michel FM, Martin CD, Chupas PJ, Shastri SD, Lee PL. Quantitative high-pressure pair distribution function analysis. J Synchrotron Radiat. 2005 Sep;12:554-9. doi: 10.1107/S0909049505022612. Epub 2005 Aug 16. PMID: 16120977.
Copy Download .nbib Format: NLM
The structures of Ag55+ and Ag55- : trapped ion electron diffraction and density functional theory.

Nano letters

Schooss D, Blom MN, Parks JH, v Issendorff B, Haberland H, Kappes MM.
PMID: 16218720
Nano Lett. 2005 Oct;5(10):1972-7. doi: 10.1021/nl0513434.

We report the experimental structure determination of cold, mass selected Ag(55)(+/-) cluster ions using the recently developed technique of trapped ion electron diffraction. By comparison of experimental and theoretical molecular scattering functions and consideration of computed total energies, we...

Cite
Schooss D, Blom MN, Parks JH, et al. The structures of Ag55+ and Ag55- : trapped ion electron diffraction and density functional theory. Nano Lett. 2005;5(10):1972-7doi: 10.1021/nl0513434.
Schooss, D., Blom, M. N., Parks, J. H., v Issendorff, B., Haberland, H., & Kappes, M. M. (2005). The structures of Ag55+ and Ag55- : trapped ion electron diffraction and density functional theory. Nano letters, 5(10), 1972-7. https://doi.org/10.1021/nl0513434
Schooss, Detlef, et al. "The structures of Ag55+ and Ag55- : trapped ion electron diffraction and density functional theory." Nano letters vol. 5,10 (2005): 1972-7. doi: https://doi.org/10.1021/nl0513434
Schooss D, Blom MN, Parks JH, v Issendorff B, Haberland H, Kappes MM. The structures of Ag55+ and Ag55- : trapped ion electron diffraction and density functional theory. Nano Lett. 2005 Oct;5(10):1972-7. doi: 10.1021/nl0513434. PMID: 16218720.
Copy Download .nbib Format: NLM
THE TEXAS ACADEMY OF SCIENCE.

Science (New York, N.Y.)

Parks HB.
PMID: 17831527
Science. 1933 Jun 09;77(2006):565. doi: 10.1126/science.77.2006.565.

No abstract available.

Cite
Parks HB. THE TEXAS ACADEMY OF SCIENCE. Science. 1933;77(2006):565doi: 10.1126/science.77.2006.565.
Parks, H. B. (1933). THE TEXAS ACADEMY OF SCIENCE. Science (New York, N.Y.), 77(2006), 565. https://doi.org/10.1126/science.77.2006.565
Parks, H B. "THE TEXAS ACADEMY OF SCIENCE." Science (New York, N.Y.) vol. 77,2006 (1933): 565. doi: https://doi.org/10.1126/science.77.2006.565
Parks HB. THE TEXAS ACADEMY OF SCIENCE. Science. 1933 Jun 09;77(2006):565. doi: 10.1126/science.77.2006.565. PMID: 17831527.
Copy Download .nbib Format: NLM
Elasticity of agr-Cristobalite: A Silicon Dioxide with a Negative Poisson's Ratio.

Science (New York, N.Y.)

Yeganeh-Haeri A, Weidner DJ, Parise JB.
PMID: 17740733
Science. 1992 Jul 31;257(5070):650-2. doi: 10.1126/science.257.5070.650.

Laser Brillouin spectroscopy was used to determine the adiabatic single-crystal elastic stiffness coefficients of silicon dioxide (SiO(2)) in the alpha-cristobalite structure. This SiO(2) polymorph, unlike other silicas and silicates, exhibits a negative Poisson's ratio; alpha-cristobalite contracts laterally when compressed...

Cite
Yeganeh-Haeri A, Weidner DJ, Parise JB. Elasticity of agr-Cristobalite: A Silicon Dioxide with a Negative Poisson's Ratio. Science. 1992;257(5070):650-2doi: 10.1126/science.257.5070.650.
Yeganeh-Haeri, A., Weidner, D. J., & Parise, J. B. (1992). Elasticity of agr-Cristobalite: A Silicon Dioxide with a Negative Poisson's Ratio. Science (New York, N.Y.), 257(5070), 650-2. https://doi.org/10.1126/science.257.5070.650
Yeganeh-Haeri, A, et al. "Elasticity of agr-Cristobalite: A Silicon Dioxide with a Negative Poisson's Ratio." Science (New York, N.Y.) vol. 257,5070 (1992): 650-2. doi: https://doi.org/10.1126/science.257.5070.650
Yeganeh-Haeri A, Weidner DJ, Parise JB. Elasticity of agr-Cristobalite: A Silicon Dioxide with a Negative Poisson's Ratio. Science. 1992 Jul 31;257(5070):650-2. doi: 10.1126/science.257.5070.650. PMID: 17740733.
Copy Download .nbib Format: NLM
Tribasic lead maleate and lead maleate: synthesis and structural and spectroscopic characterizations.

Inorganic chemistry

Bonhomme F, Alam TM, Celestian AJ, Tallant DR, Boyle TJ, Cherry BR, Tissot RG, Rodriguez MA, Parise JB, Nyman M.
PMID: 16212365
Inorg Chem. 2005 Oct 17;44(21):7394-402. doi: 10.1021/ic050611y.

We report on the synthesis and structure of tribasic lead maleate hemihydrate ([Pb4O3]C2H2(CO2)2.(1/2)H2O, TRIMAL) and lead maleate (PbC2H2(CO2)2, PBMAL). The structure of [Pb4O3]C2H2(CO2)2.(1/2)H2O, solved ab initio from X-ray powder diffraction data, consists of infinite slabs of edge-sharing OPb4 tetrahedra,...

Cite
Bonhomme F, Alam TM, Celestian AJ, et al. Tribasic lead maleate and lead maleate: synthesis and structural and spectroscopic characterizations. Inorg Chem. 2005;44(21):7394-402doi: 10.1021/ic050611y.
Bonhomme, F., Alam, T. M., Celestian, A. J., Tallant, D. R., Boyle, T. J., Cherry, B. R., Tissot, R. G., Rodriguez, M. A., Parise, J. B., & Nyman, M. (2005). Tribasic lead maleate and lead maleate: synthesis and structural and spectroscopic characterizations. Inorganic chemistry, 44(21), 7394-402. https://doi.org/10.1021/ic050611y
Bonhomme, François, et al. "Tribasic lead maleate and lead maleate: synthesis and structural and spectroscopic characterizations." Inorganic chemistry vol. 44,21 (2005): 7394-402. doi: https://doi.org/10.1021/ic050611y
Bonhomme F, Alam TM, Celestian AJ, Tallant DR, Boyle TJ, Cherry BR, Tissot RG, Rodriguez MA, Parise JB, Nyman M. Tribasic lead maleate and lead maleate: synthesis and structural and spectroscopic characterizations. Inorg Chem. 2005 Oct 17;44(21):7394-402. doi: 10.1021/ic050611y. PMID: 16212365.
Copy Download .nbib Format: NLM
Role of the hydroxyl-water hydrogen-bond network in structural transitions and selectivity toward cesium in Cs0.38(D1.08H0.54)SiTi2O7.(D0.86H0.14)2O crystalline silicotitanate.

Inorganic chemistry

Celestian AJ, Parise JB, Smith RI, Toby BH, Clearfield A.
PMID: 17291108
Inorg Chem. 2007 Feb 19;46(4):1081-9. doi: 10.1021/ic0611387.

The crystal structure of the selective Cs+ ion exchanger D1.6H0.4Ti2SiO7.D2.66H0.34O1.5, known as crystalline silicotitanate or CST, has been determined in both native (D-CST) and in the Cs+-exchanged forms ((Cs, D)-CST) from angle-dispersive and time-of-flight neutron diffraction studies. The final...

Cite
Celestian AJ, Parise JB, Smith RI, et al. Role of the hydroxyl-water hydrogen-bond network in structural transitions and selectivity toward cesium in Cs0.38(D1.08H0.54)SiTi2O7.(D0.86H0.14)2O crystalline silicotitanate. Inorg Chem. 2007;46(4):1081-9doi: 10.1021/ic0611387.
Celestian, A. J., Parise, J. B., Smith, R. I., Toby, B. H., & Clearfield, A. (2007). Role of the hydroxyl-water hydrogen-bond network in structural transitions and selectivity toward cesium in Cs0.38(D1.08H0.54)SiTi2O7.(D0.86H0.14)2O crystalline silicotitanate. Inorganic chemistry, 46(4), 1081-9. https://doi.org/10.1021/ic0611387
Celestian, Aaron J, et al. "Role of the hydroxyl-water hydrogen-bond network in structural transitions and selectivity toward cesium in Cs0.38(D1.08H0.54)SiTi2O7.(D0.86H0.14)2O crystalline silicotitanate." Inorganic chemistry vol. 46,4 (2007): 1081-9. doi: https://doi.org/10.1021/ic0611387
Celestian AJ, Parise JB, Smith RI, Toby BH, Clearfield A. Role of the hydroxyl-water hydrogen-bond network in structural transitions and selectivity toward cesium in Cs0.38(D1.08H0.54)SiTi2O7.(D0.86H0.14)2O crystalline silicotitanate. Inorg Chem. 2007 Feb 19;46(4):1081-9. doi: 10.1021/ic0611387. PMID: 17291108.
Copy Download .nbib Format: NLM
The structure of ferrihydrite, a nanocrystalline material.

Science (New York, N.Y.)

Michel FM, Ehm L, Antao SM, Lee PL, Chupas PJ, Liu G, Strongin DR, Schoonen MA, Phillips BL, Parise JB.
PMID: 17525301
Science. 2007 Jun 22;316(5832):1726-9. doi: 10.1126/science.1142525. Epub 2007 May 24.

Despite the ubiquity of ferrihydrite in natural sediments and its importance as an industrial sorbent, the nanocrystallinity of this iron oxyhydroxide has hampered accurate structure determination by traditional methods that rely on long-range order. We uncovered the atomic arrangement...

Cite
Michel FM, Ehm L, Antao SM, et al. The structure of ferrihydrite, a nanocrystalline material. Science. 2007;316(5832):1726-9doi: 10.1126/science.1142525.
Michel, F. M., Ehm, L., Antao, S. M., Lee, P. L., Chupas, P. J., Liu, G., Strongin, D. R., Schoonen, M. A., Phillips, B. L., & Parise, J. B. (2007). The structure of ferrihydrite, a nanocrystalline material. Science (New York, N.Y.), 316(5832), 1726-9. https://doi.org/10.1126/science.1142525
Michel, F Marc, et al. "The structure of ferrihydrite, a nanocrystalline material." Science (New York, N.Y.) vol. 316,5832 (2007): 1726-9. doi: https://doi.org/10.1126/science.1142525
Michel FM, Ehm L, Antao SM, Lee PL, Chupas PJ, Liu G, Strongin DR, Schoonen MA, Phillips BL, Parise JB. The structure of ferrihydrite, a nanocrystalline material. Science. 2007 Jun 22;316(5832):1726-9. doi: 10.1126/science.1142525. Epub 2007 May 24. PMID: 17525301.
Copy Download .nbib Format: NLM
Photon scanning-tunneling microscopy of unstained Mammalian cells and chromosomes.

Applied optics

Meriaudeau F, Goudonnet JP, Carver E, Parks JE, Jacobson KB, Warmack RJ, Ferrell TL.
PMID: 18301559
Appl Opt. 1998 Nov 01;37(31):7276-88. doi: 10.1364/ao.37.007276.

The photon scanning-tunneling microscope (PSTM) yields optical topographical images of samples that are thin or that are transparent at the wavelength used. A range of sample sizes can be imaged extending to well below the diffraction limit for sufficiently...

Cite
Meriaudeau F, Goudonnet JP, Carver E, et al. Photon scanning-tunneling microscopy of unstained Mammalian cells and chromosomes. Appl Opt. 1998;37(31):7276-88doi: 10.1364/ao.37.007276.
Meriaudeau, F., Goudonnet, J. P., Carver, E., Parks, J. E., Jacobson, K. B., Warmack, R. J., & Ferrell, T. L. (1998). Photon scanning-tunneling microscopy of unstained Mammalian cells and chromosomes. Applied optics, 37(31), 7276-88. https://doi.org/10.1364/ao.37.007276
Meriaudeau, F, et al. "Photon scanning-tunneling microscopy of unstained Mammalian cells and chromosomes." Applied optics vol. 37,31 (1998): 7276-88. doi: https://doi.org/10.1364/ao.37.007276
Meriaudeau F, Goudonnet JP, Carver E, Parks JE, Jacobson KB, Warmack RJ, Ferrell TL. Photon scanning-tunneling microscopy of unstained Mammalian cells and chromosomes. Appl Opt. 1998 Nov 01;37(31):7276-88. doi: 10.1364/ao.37.007276. PMID: 18301559.
Copy Download .nbib Format: NLM
The mechanism responsible for extraordinary Cs ion selectivity in crystalline silicotitanate.

Journal of the American Chemical Society

Celestian AJ, Kubicki JD, Hanson J, Clearfield A, Parise JB.
PMID: 18683931
J Am Chem Soc. 2008 Sep 03;130(35):11689-94. doi: 10.1021/ja801134a. Epub 2008 Aug 07.

Combining information from time-resolved X-ray and neutron scattering with theoretical calculations has revealed the elegant mechanism whereby hydrogen crystalline silicotitanate (H-CST; H2Ti2SiO7 x 1.5 H2O) achieves its remarkable ion-exchange selectivity for cesium. Rather than a simple ion-for-ion displacement reaction...

Cite
Celestian AJ, Kubicki JD, Hanson J, et al. The mechanism responsible for extraordinary Cs ion selectivity in crystalline silicotitanate. J Am Chem Soc. 2008;130(35):11689-94doi: 10.1021/ja801134a.
Celestian, A. J., Kubicki, J. D., Hanson, J., Clearfield, A., & Parise, J. B. (2008). The mechanism responsible for extraordinary Cs ion selectivity in crystalline silicotitanate. Journal of the American Chemical Society, 130(35), 11689-94. https://doi.org/10.1021/ja801134a
Celestian, Aaron J, et al. "The mechanism responsible for extraordinary Cs ion selectivity in crystalline silicotitanate." Journal of the American Chemical Society vol. 130,35 (2008): 11689-94. doi: https://doi.org/10.1021/ja801134a
Celestian AJ, Kubicki JD, Hanson J, Clearfield A, Parise JB. The mechanism responsible for extraordinary Cs ion selectivity in crystalline silicotitanate. J Am Chem Soc. 2008 Sep 03;130(35):11689-94. doi: 10.1021/ja801134a. Epub 2008 Aug 07. PMID: 18683931.
Copy Download .nbib Format: NLM
Showing 13 to 24 of 265 entries