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Relevant bibliographies by topics / Resolution (Chemistry)

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Academic literature on the topic 'Resolution (Chemistry)'

Author: Grafiati

Published: 4 June 2021

Last updated: 24 January 2023

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Journal articles on the topic "Resolution (Chemistry)"

1

Geiss, Andrew, Sam J. Silva, and Joseph C. Hardin. "Downscaling atmospheric chemistry simulations with physically consistent deep learning." Geoscientific Model Development 15, no. 17 (September 5, 2022): 6677–94. http://dx.doi.org/10.5194/gmd-15-6677-2022.

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Abstract. Recent advances in deep convolutional neural network (CNN)-based super resolution can be used to downscale atmospheric chemistry simulations with substantially higher accuracy than conventional downscaling methods. This work both demonstrates the downscaling capabilities of modern CNN-based single image super resolution and video super-resolution schemes and develops modifications to these schemes to ensure they are appropriate for use with physical science data. The CNN-based video super-resolution schemes in particular incur only 39 % to 54 % of the grid-cell-level error of interpolation schemes and generate outputs with extremely realistic small-scale variability based on multiple perceptual quality metrics while performing a large (8×10) increase in resolution in the spatial dimensions. Methods are introduced to strictly enforce physical conservation laws within CNNs, perform large and asymmetric resolution changes between common model grid resolutions, account for non-uniform grid-cell areas, super-resolve lognormally distributed datasets, and leverage additional inputs such as high-resolution climatologies and model state variables. High-resolution chemistry simulations are critical for modeling regional air quality and for understanding future climate, and CNN-based downscaling has the potential to generate these high-resolution simulations and ensembles at a fraction of the computational cost.

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Steinwandel, Ulrich P., Benjamin P. Moster, Thorsten Naab, Chia-Yu Hu, and Stefanie Walch. "Hot phase generation by supernovae in ISM simulations: resolution, chemistry, and thermal conduction." Monthly Notices of the Royal Astronomical Society 495, no. 1 (March 29, 2020): 1035–60. http://dx.doi.org/10.1093/mnras/staa821.

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ABSTRACT Supernovae (SNe) generate hot gas in the interstellar medium (ISM), help setting the ISM structure, and support the driving of outflows. It is important to resolve the hot gas generation for galaxy formation simulations at solar mass and sub-parsec resolution that realize individual SN explosions with ambient densities varying by several orders of magnitude in a realistic multiphase ISM. We test resolution requirements by simulating SN blast waves at three metallicities (Z = 0.01, 0.1, and 1 Z⊙), six densities and their respective equilibrium chemical compositions (n = 0.001–100 cm−3), and four mass resolutions (0.1–100 M⊙), in three dimensions. We include non-equilibrium cooling and chemistry, a homogeneous interstellar radiation field, and shielding with a modern pressure–energy smoothed particle hydrodynamics method including isotropic thermal conduction and a meshless-finite-mass solver. We find stronger resolution requirements for chemistry and hot phase generation than for momentum generation. While at 10 M⊙ the radial momenta at the end of the Sedov phase start converging, the hot phase generation and chemistry require higher resolutions to represent the neutral-to-ionized hydrogen fraction at the end of the Sedov phase correctly. Thermal conduction typically reduces the hot phase by 0.2 dex and has little impact on the chemical composition. In general, our 1 and 0.1 M⊙ results agree well with previous numerical and analytic estimates. We conclude that for the thermal energy injection SN model presented here resolutions higher than 10 M⊙ are required to model the chemistry, momentum, and hot phase generation in the multiphase ISM.

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Yu, Karen, Daniel J. Jacob, Jenny A. Fisher, Patrick S. Kim, Eloise A. Marais, Christopher C. Miller, Katherine R. Travis, et al. "Sensitivity to grid resolution in the ability of a chemical transport model to simulate observed oxidant chemistry under high-isoprene conditions." Atmospheric Chemistry and Physics 16, no. 7 (April 7, 2016): 4369–78. http://dx.doi.org/10.5194/acp-16-4369-2016.

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Abstract. Formation of ozone and organic aerosol in continental atmospheres depends on whether isoprene emitted by vegetation is oxidized by the high-NOx pathway (where peroxy radicals react with NO) or by low-NOx pathways (where peroxy radicals react by alternate channels, mostly with HO2). We used mixed layer observations from the SEAC4RS aircraft campaign over the Southeast US to test the ability of the GEOS-Chem chemical transport model at different grid resolutions (0.25° × 0.3125°, 2° × 2.5°, 4° × 5°) to simulate this chemistry under high-isoprene, variable-NOx conditions. Observations of isoprene and NOx over the Southeast US show a negative correlation, reflecting the spatial segregation of emissions; this negative correlation is captured in the model at 0.25° × 0.3125° resolution but not at coarser resolutions. As a result, less isoprene oxidation takes place by the high-NOx pathway in the model at 0.25° × 0.3125° resolution (54 %) than at coarser resolution (59 %). The cumulative probability distribution functions (CDFs) of NOx, isoprene, and ozone concentrations show little difference across model resolutions and good agreement with observations, while formaldehyde is overestimated at coarse resolution because excessive isoprene oxidation takes place by the high-NOx pathway with high formaldehyde yield. The good agreement of simulated and observed concentration variances implies that smaller-scale non-linearities (urban and power plant plumes) are not important on the regional scale. Correlations of simulated vs. observed concentrations do not improve with grid resolution because finer modes of variability are intrinsically more difficult to capture. Higher model resolution leads to decreased conversion of NOx to organic nitrates and increased conversion to nitric acid, with total reactive nitrogen oxides (NOy) changing little across model resolutions. Model concentrations in the lower free troposphere are also insensitive to grid resolution. The overall low sensitivity of modeled concentrations to grid resolution implies that coarse resolution is adequate when modeling continental boundary layer chemistry for global applications.

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Sanchez, Sergio I., Matthew W. Small, Shankar Sivaramakrishnan, Jian-guo Wen, Jian-Min Zuo, and Ralph G. Nuzzo. "Visualizing Materials Chemistry at Atomic Resolution." Analytical Chemistry 82, no. 7 (April 2010): 2599–607. http://dx.doi.org/10.1021/ac902089f.

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Grewe, Volker, Martin Dameris, Christine Fichter, and Robert Sausen. "Impact of aircraft NOx emissions. Part 1: Interactively coupled climate-chemistry simulations and sensitivities to climate-chemistry feedback, lightning and model resolution." Meteorologische Zeitschrift 11, no. 3 (August 2, 2002): 177–86. http://dx.doi.org/10.1127/0941-2948/2002/0011-0177.

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Charlton-Perez, C. L., M. J. Evans, J. H. Marsham, and J. G. Esler. "The impact of resolution on ship plume simulations with NO<sub>x</sub> chemistry." Atmospheric Chemistry and Physics 9, no. 19 (October 9, 2009): 7505–18. http://dx.doi.org/10.5194/acp-9-7505-2009.

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Abstract. A high resolution chemical transport model of the marine boundary layer is designed in order to investigate the detailed chemical evolution of a ship plume in a tropical location. To estimate systematic errors due to finite model resolution, otherwise identical simulations are run at a range of model resolutions. Notably, to obtain comparable plumes in the different simulations, it is found necessary to use an advection scheme consistent with the Large Eddy Model representation of sub-grid winds for those simulations with degraded resolution. Our simulations show that OH concentration, NOx lifetime and ozone production efficiency of the model change by 8%, 32% and 31% respectively between the highest (200 m×200 m×40 m) and lowest resolution (9600 m×9600 m×1920 m) simulations. Interpolating to the resolution of a typical global composition transport model (CTM, 5°×5°), suggests that a CTM overestimates OH, NOx lifetime and ozone production efficiency by approximately 15%, 55% and 59% respectively. For the first time, by explicitly degrading the model spatial resolution we show that there is a significant reduction in model skill in accurately simulating the aforementioned quantities due to the coarse resolution of these CTMs and the non-linear nature of atmospheric chemistry. These results are significant for the assessment and forecasting of the climate impact of ship NOx and indicate that for realistic representation of ship plume emissions in CTMs, some suitable parametrisation is necessary at current global model resolutions.

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Charlton-Perez, C. L., M. J. Evans, J. H. Marsham, and J. G. Esler. "The impact of resolution on ship plume simulations with NO<sub>x</sub> chemistry." Atmospheric Chemistry and Physics Discussions 9, no. 2 (March 31, 2009): 8587–618. http://dx.doi.org/10.5194/acpd-9-8587-2009.

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Abstract. A high resolution chemical transport model of the marine boundary layer is designed in order to investigate the detailed chemical evolution of a ship plume. To estimate systematic errors due to finite model resolution, otherwise identical simulations are run at a range of model resolutions. Notably, to obtain comparable plumes in the different simulations, it is found necessary to use an advection scheme consistent with the Large Eddy Model representation of sub-grid winds for those simulations with degraded resolution. Our simulations show that OH concentration, NOx lifetime and ozone production efficiency of the model change by 8%, 32% and 31% respectively between the highest (200 mx200 mx40 m) and lowest resolution (9600 mx9600 mx1920 m) simulations. Interpolating to the resolution of a typical global composition transport model (CTM, 5°x5°), suggests that a CTM overestimates OH, NOx lifetime and ozone production efficiency by approximately 15%, 55% and 59% respectively. For the first time, it is shown explicitly that the reduction in model skill is due to the coarse resolution of these CTMs and the non-linear nature of atmospheric chemistry. These results are significant for the assessment and forecasting of the climate impact of ship NOx and indicate that for realistic representation of ship plume emissions in CTMs, some suitable parametrisation is necessary at current global model resolutions.

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Li, Yunzhi, Richard L. Hunter, and Robert T. Mclver. "High-resolution mass spectrometer for protein chemistry." Nature 370, no. 6488 (August 1994): 393–95. http://dx.doi.org/10.1038/370393a0.

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Shapiro, Michael J., and John S. Gounarides. "High resolution MAS-NMR in combinatorial chemistry." Biotechnology and Bioengineering 71, no. 2 (2000): 130–48. http://dx.doi.org/10.1002/1097-0290(2000)71:2<130::aid-bit1004>3.0.co;2-r.

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Esler, J. G., G. J. Roelofs, M. O. Köhler, and F. M. O'Connor. "A quantitative analysis of grid-related systematic errors in oxidising capacity and ozone production rates in chemistry transport models." Atmospheric Chemistry and Physics 4, no. 7 (September 8, 2004): 1781–95. http://dx.doi.org/10.5194/acp-4-1781-2004.

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Abstract. Limited resolution in chemistry transport models (CTMs) is necessarily associated with systematic errors in the calculated chemistry, due to the artificial mixing of species on the scale of the model grid (grid-averaging). Here, the errors in calculated hydroxyl radical (OH) concentrations and ozone production rates 3 are investigated quantitatively using both direct observations and model results. Photochemical steady-state models of radical chemistry are exploited in each case to examine the effect on both OH and 3 of averaging relatively long-lived precursor species, such as O3, NOx, CO, H2O, etc. over different spatial scales. Changes in modelled 3 are estimated, independently of other model errors, by calculating the systematic effect of spatial averaging on the ozone production efficiency 1, defined as the ratio of ozone molecules produced per NOx molecule destroyed. Firstly, an investigation of in-flight measurements suggests that, at least in the northern midlatitude upper-troposphere/lower stratosphere, averaging precursor species on the scale of a T42 grid (2.75° x 2.75°) leads to a 15-20% increase in OH concentrations and a 5-10% increase in 1. Secondly, results from CTM model experiments are compared at different horizontal resolutions. Low resolution experiments are found to have significantly higher [OH] and 3 compared with high resolution experiments. The extent to which these differences may be explained by the systematic error in the model chemistry associated with grid size is estimated by degrading the high resolution data onto a low resolution grid and then recalculating 1 and [OH]. The change in calculated 1 is found to be significant and can account for much of the difference in 3 between the high and low resolution experiments. The calculated change in [OH] is less than the difference in [OH] found between the experiments, although the shortfall is likely to be due to the indirect effect of the change in modelled NOx, which is not accounted for in the calculation. It is argued that systematic errors caused by limited resolution need to be considered when evaluating the relative impacts of different pollutant sources on tropospheric ozone.

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Dissertations / Theses on the topic "Resolution (Chemistry)"

1

Parkin, Richard M. "Kinetic resolution strategies." Thesis, University of Oxford, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343475.

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Stevens, Anne Theresa. "The optical resolution of albuterol." Master's thesis, University of Cape Town, 1998. http://hdl.handle.net/11427/19648.

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The acetonide derivative of (rac)-albuterol has been prepared and used as a substrate in cocrystallisation experiments with several acidic resolving agents~ Successful resolution of the acetonide was achieved with both di-0-benzoyl- and di-0-toluoyltartaric acid, with the (2S,3S)enantiomer of the acid selectively co-crystallising with the desired (R)-albuterol acetonide. High performance liquid chromatography on a chiral stationary phase, and 1H NMR experiments using a chiral shift reagent were used to assess the optical purity of the resolved material. Acid hydrolysis of the resolved acetonide gave rise to the target, (R)-albuterol, which was isolated as an acetate salt. The inferred absolute configuration of the resolved acetonide was assessed by 1H NMR analysis of its (R)-Mosher ester, and confirmed by an X-ray structural determination of its (R)-phenylethylurea derivative. The acetonide derivative of (rac)-albuterol has been prepared and used as a substrate in cocrystallisation experiments with several acidic resolving agents~ Successful resolution of the acetonide was achieved with both di-0-benzoyl- and di-0-toluoyltartaric acid, with the (2S,3S)enantiomer of the acid selectively co-crystallising with the desired (R)-albuterol acetonide. High performance liquid chromatography on a chiral stationary phase, and 1H NMR experiments using a chiral shift reagent were used to assess the optical purity of the resolved material. Acid hydrolysis of the resolved acetonide gave rise to the target, (R)-albuterol, which was isolated as an acetate salt. The inferred absolute configuration of the resolved acetonide was assessed by 1H NMR analysis of its (R)-Mosher ester, and confirmed by an X-ray structural determination of its (R)-phenylethylurea derivative.

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Waterman, Naomi Ariane. "Super-resolution imaging with metamaterials." Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8151/.

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The key area of investigation of this research project was the application of metamaterials to super-resolution optical imaging. Specifically, an optical microscope was proposed to emulate a TIRF-SIM microscope, but using metamaterials to create a structured evanescent field. A metamaterial unit cell design of two ‘H’ shape nano-holes at ±45° to the normal in a gold film, with 50nm feature size was developed and simulated in CST Microwave Studio, able to produce structured evanescent illumination patterns. Although this original design proved unsuccessful, both in terms of fabrication and image reconstruction, an alternative design was developed. Alongside this, in MATLAB an algorithm for SIM image reconstruction using the typical sinusoidal masks was created successfully. Then to accommodate atypical SIM masks, such as those produced by the metamaterials, new approaches to SIM image reconstruction were also developed. These approaches modelled the masks as the sum of sinusoids and as the product of sinusoids. These reconstruction approaches were unsuccessful when using the original metamaterial masks, but were successfully able to reconstruct image with improved resolution, compared to standard SIM, using the alternative metamaterial masks. Moreover, resolution enhancement was demonstrated using six masks instead of the nine or more typically used.

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Grange, Andrew H. "Medium resolution atmospheric pressure ionization mass spectrometry /." Full text open access at:, 1988. http://content.ohsu.edu/u?/etd,158.

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Potente, Nina M. "High Resolution Structural Studies of vc-ASADH." University of Toledo / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1271384044.

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Nelson, Keegan Gregory. "Enantioselective hydrolysis of 1-arylpropargylic esters by enzymatic kinetic resolution and dynamic kinetic resolution of 1-arylallylic esters." Thesis, University of Missouri - Kansas City, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=1538847.

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Chiral 1-arylprop-2-en-1-ols and 1-arylprop-2-yn-1-ols are useful building blocks for modern pharmaceuticals. Previous work has found that enzyme catalysis is a potential new enantioselective synthetic route to the former. We found that Candida antarctica lipase is also an effective catalyst for kinetic resolution of various substituted 1 arylpropargylic acetates and haloacetates, affording the respective (R) -1 arylproargylic alcohols with high enantioselectivity (99-100% ee). By varying the substituents on both sides of the ester bond, we discovered that the deacylation of lipase is likely the rate-determining step for our catalytic system. A greater challenge is designing a dynamic kinetic resolution (DKR) system for such substrates, which combines a resolving catalyst (lipase) with a racemizing catalyst, and can potentially lead to quantitative conversion of a racemic substrate into an enantiopure product. We studied the efficacy of various transition-metal complexes for substrate racemization and will report our results for In and Cu compounds.

While kinetic resolution has been performed on the 1-arylallylic acetates with excellent yield and enantioselectivity and the DKR regime has been designed, the resulting site-isolation system has required further testing and fine tuning. We have herein investigated the utilization of macroscale site-isolation as well as various factors including solvent, and acyl donor effects in order to optimize conditions of the system.

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Fowkes, Amelia Jane. "High resolution powder neutron diffraction in solid state inorganic chemistry." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299525.

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Bell, W. "High resolution spectroscopy of stratospheric trace species." Thesis, University of Strathclyde, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325275.

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Panov, Sergey I. "Moderate and high resolution spectroscopy of transient molecular ions /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487945015618952.

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Pushkarsky, Michael B. "High resolution spectroscopy and photochemistry of the free radicals /." The Ohio State University, 2000. http://rave.ohiolink.edu/etdc/view?acc_num=osu1488202678773409.

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Books on the topic "Resolution (Chemistry)"

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Hollas, J. Michael. High resolution spectroscopy. 2nd ed. Chichester: J. Wiley, 1998.

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Th, Bley, and SpringerLink (Online service), eds. High Resolution Microbial Single Cell Analytics. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2011.

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3

Hirota, Eizi. High-Resolution Spectroscopy of Transient Molecules. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985.

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4

1935-, Hüfner Stefan, ed. Very high resolution photoelectron spectroscopy. Berlin: New York, 2007.

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Ernst, Frank. High-Resolution Imaging and Spectrometry of Materials. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003.

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6

Breitmaier, Eberhard. Carbon-13 NMR spectroscopy: High resolution methods and applications in organic chemistry and biochemistry. 3rd ed. Germany: VCH Verlagsgesellschaft, 1989.

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7

Stejskal, E. O. High resolution NMR in the solid state: Fundamentals of CP/MAS. New York: Oxford University Press, 1994.

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Drits, Victor A. Electron Diffraction and High-Resolution Electron Microscopy of Mineral Structures. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987.

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9

Michel, Herman, ed. Global and accurate vibration Hamiltonians from high resolution molecular spectroscopy. New York: Wiley, 1999.

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Breitmaier, E. Carbon-13 NMR spectroscopy: High-resolution methods and applications in organic chemistry and biochemistry. 3rd ed. New York: VCH Publishers, 1987.

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Book chapters on the topic "Resolution (Chemistry)"

1

Sakulsombat, Morakot, Yan Zhang, and Olof Ramström. "Dynamic Systemic Resolution." In Constitutional Dynamic Chemistry, 55–86. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/128_2011_203.

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JEFFERSON, D. A. "High Resolution Electron Microscopy." In Solid State Chemistry in Catalysis, 183–203. Washington, D.C.: American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0279.ch011.

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Barrett, G. C. "Resolution of Amino Acids." In Chemistry and Biochemistry of the Amino Acids, 338–53. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-4832-7_10.

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Sakai, Kenichi, Rumiko Sakurai, and Noriaki Hirayama. "Molecular Mechanisms of Dielectrically Controlled Resolution (DCR)." In Topics in Current Chemistry, 233–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/128_071.

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Kenwright, A. M. "High-Resolution NMR and ROMP." In Ring Opening Metathesis Polymerisation and Related Chemistry, 57–67. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0373-5_5.

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Nicholson, J. K. "High Resolution Nuclear Magnetic Resonance Spectroscopy in Clinical Chemistry and Disease Diagnosis." In Clinical Chemistry, 9–26. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0753-2_2.

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Sakai, Kenichi, Rumiko Sakurai, and Hiroyuki Nohira. "New Resolution Technologies Controlled by Chiral Discrimination Mechanisms." In Topics in Current Chemistry, 199–231. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/128_2006_097.

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Potrzebowski, Marek J., and Slawomir Kazmierski. "High-Resolution Solid-State NMR Studies of Inclusion Complexes." In Topics in Current Chemistry, 91–140. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b98649.

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Miyazawa, Toshifumi, Hitoshi Iwanaga, Takashi Yamada, and Shigeru Kuwata. "Utilization of proteases for the resolution of non-protein amino acids." In Peptide Chemistry 1992, 94–96. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1474-5_27.

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Sakamoto, Masami, and Takashi Mino. "Total Resolution of Racemates by Dynamic Preferential Crystallization." In Advances in Organic Crystal Chemistry, 445–62. Tokyo: Springer Japan, 2015. http://dx.doi.org/10.1007/978-4-431-55555-1_22.

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Conference papers on the topic "Resolution (Chemistry)"

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HELL, S. W., R. G. EFREMOV, and J. N. HARVEY. "SESSION 4: COMPUTATIONAL MODELING IN HIGH-RESOLUTION IMAGING." In 25th Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811228216_0027.

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HABERL, MATTHIAS G., RAFAEL ARROJO E. DRIGO, MARTIN W. HETZER, and MARK H. ELLISMAN. "TOWARD HIGH RESOLUTION INTRACELLULAR MAPS IN SPACE AND TIME." In 25th Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811228216_0039.

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HUISKEN, JAN. "RECONSTRUCTING EMBRYONIC DEVELOPMENT FROM HIGH-RESOLUTION LIGHT SHEET MICROSCOPY DATA." In 25th Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811228216_0026.

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Fernandes, Carla, Fernando Remião, Barbara Silva, and Paula Pinho. "Synthetic cathinones: Chiral resolution and enantioselectivity studies." In 5th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06331.

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Xing, Fan, Ma Fengyun, and Wei Xianyong. "APPLICATION OF HIGH-RESOLUTION MASS SPECTROMETRY IN COAL CHEMISTRY." In Углехимия и экология Кузбасса. Федеральный исследовательский центр угля и углехимии Сибирского отделения Российской академии наук, 2021. http://dx.doi.org/10.53650/9785902305637_12.

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OBER, RAIMUND J., and MILAD VAHID. "PARAMETER ESTIMATION AND INFORMATION THEORY IN SINGLE-MOLECULE AND SUPER-RESOLUTION MICROSCOPY." In 25th Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811228216_0021.

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Alcantara, Andres R., and Isabel Borreguero-Requejo. "Systematic study of lipase-catalyzed resolution of propanolol precursors." In 4th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05633.

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Frey, Hans M., Paul Beaud, Tobias Lang, and Marcus Motzkus. "High Resolution Femtosecond CARS Spectroscopy." In With Foreword by Prof A H Zewail, Nobel Laureate in Chemistry, 1999. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812777980_0009.

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Endo, Yasuki. "HIGH-RESOLUTION SPECTROSCOPIC STUDIES OF REACTION INTERMEDIATES RELEVANT TO ATMOSPHERIC CHEMISTRY." In 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.wa04.

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ROUILLARD, HERVE, and VALERIE THIERY. "Microwave-assisted kinetic resolution of homochiral diols using lipase." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-c005.

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Reports on the topic "Resolution (Chemistry)"

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Kotula, Paul Gabriel, and Michael J. Rye. Advanced Characterization: 3D chemistry and structure at sub-nm resolution. Office of Scientific and Technical Information (OSTI), October 2014. http://dx.doi.org/10.2172/1172785.

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Drury, Owen Byron. Development of High Resolution X-Ray spectrometers for the Investigation of Bioinorganic Chemistry in Metalloproteins. Office of Scientific and Technical Information (OSTI), January 2007. http://dx.doi.org/10.2172/957593.

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Myton, David. Development and Applications of High Resolution Kinetic Atmospheric Pressure Ionization Mass Spectrometry in Atmospheric Chemistry. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.1208.

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Carpenter, R. W., and M. J. Kim. Planar interfaces: Synthesis and high resolution chemistry and structure analysis. Progress report, March 1, 1997--February 28, 1998. Office of Scientific and Technical Information (OSTI), April 1998. http://dx.doi.org/10.2172/584956.

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Santra, Kalyan. Acquisition and analysis of steady-state and time-resolved fluorescence data for applications in materials science, bioanalytical chemistry, and super-resolution microscopy. Office of Scientific and Technical Information (OSTI), May 2018. http://dx.doi.org/10.2172/1505191.

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