Relevant bibliographies by topics / Organic compounds

Academic literature on the topic 'Organic compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 31 July 2024

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Journal articles on the topic "Organic compounds"

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Ciganek, M., and J. Neca. "Chemical characterization of volatile organic compounds on animal farms." Veterinární Medicína 53, No. 12 (December 29, 2008): 641–51. http://dx.doi.org/10.17221/1969-vetmed.

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More than one hundred volatile organic substances were identified by gas chromatography and mass spectrometry (GC/MS) in the indoor and outdoor air, stable and farm road dust and farm soil samples from two pig and cattle farms in the South Moravian Region. Volatile fatty acids (acetic, propanoic, butanoic and pentanoic acids) and their esters dominated along with aldehydes (butanal, pentanal and hexanal) and 4-methylphenol in the indoor and outdoor air samples. Road dust and soil samples contained mainly volatile aromatic compounds (toluene, benzene, ethylbenzene, styrene and xylenes), aliphatic hydrocarbons (largely n-alkanes), dichloromethane and carbon disulphide. The health risks associated with particular volatile compounds detected in the indoor and outdoor samples from the farms need to be assessed.
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Shibata, M., K. Nakamura, and Y. Miyaji. "Biological Decomposition of Trace Organic Compounds." Water Science and Technology 19, no. 3-4 (March 1, 1987): 417–27. http://dx.doi.org/10.2166/wst.1987.0222.

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Biological decomposition of trace organic compounds was investigated to apply to the reclamation system of the rinse water recovered from semiconductor manufacturing processes. First, growth characteristics of microorganisms grown at low concentrations of organics were examined and extremely low saturation constants for acetate and methanol were obtained. Based on the growth characteristics, a biological fluidized bed reactor was operated to remove low concentrations of organics in a laboratory scale. One milligram per liter of acetate carbon was degraded to less than 10µg/l carbon with 10 minutes of hydraulic retention time. Low concentrations of methanol and isopropanol, which are main organics contained in the recovered rinse water, were also decomposed effectively. For a full scale operation, a pilot study was also carried out to examine treatability and stability of a fluidized bed reactor. Effluent organic concentrations decreased gradually and had been stable below 5µg/l carbon during 5 month operation.
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Gee, Ivan. "Volatile Organic Compounds." Indoor and Built Environment 5, no. 3 (1996): 187–88. http://dx.doi.org/10.1159/000463709.

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Gee, Ivan. "Volatile Organic Compounds." Indoor and Built Environment 5, no. 3 (May 1996): 187–88. http://dx.doi.org/10.1177/1420326x9600500311.

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Eaborn, Colin. "Naming organic compounds." Journal of Organometallic Chemistry 393, no. 3 (September 1990): C56—C57. http://dx.doi.org/10.1016/0022-328x(90)85182-x.

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Crans, Debbie, Anastasios Keramidas, and Chryssoula Drouza. "Organic Vanadium Compounds - Transition State Analogy with Organic Phosphorus Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 109, no. 1 (1996): 245–48. http://dx.doi.org/10.1080/10426509608545136.

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Ariefin, Mokhamat, and Vety Sri Harlinda Ayudha. "Synthesis and Characterization of Benzodithiophene (BDT) Quinoid Compounds as a Potential Compound for n-Type Organic Thin-Film Transistors (OTFT)." Jurnal Kimia Sains dan Aplikasi 23, no. 7 (July 17, 2020): 261–66. http://dx.doi.org/10.14710/jksa.23.7.261-266.

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Two potential compounds as an n-Type organic thin-film transistor (OTFT) from benzodithiophene (BDT) derivatives have been synthesized and characterized. BDT was chosen as the core because it has π-conjugated bonds, rigid structures, and planar. Quinoid structure with end-cap (terminal group) in the form of dicyanomethylene is used because it can lower the LUMO value of the compound, and side chains are selected in the form of alkoxy so that two BDT derivatives are obtained namely BDTQ-6 (hexyloxy) and BDTQ-10 (decyloxy). Based on the results of TGA, BDTQ-6 and BDTQ-10 have decomposition points of 183°C and 203°C, which indicate the compound has excellent thermal stability. From the UV-Vis measurement, the λmax value of the two compounds is 599 nm with optical gap energy (Eg°pt) of 1.7 eV. From the DPV measurement, the LUMO value for the two compounds is -4.3 eV, with an energy gap (Eg) of 1.69 eV (BDTQ-6) and 1.70 eV (BDTQ-10). Based on observations of the crystal structure through x-ray diffraction, it was found that the BDTQ-10 crystal has a "brick type" layer arrangement with a distance between layers of 3.55 Å. With excellent thermal stability and suitable LUMO values and energy gaps, it is expected that BDTQ-6 and BDTQ-10 compounds have the potential to be n-Type OTFT materials.
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Chen, J., R. J. Griffin, A. Grini, and P. Tulet. "Modeling secondary organic aerosol formation through cloud processing of organic compounds." Atmospheric Chemistry and Physics Discussions 7, no. 3 (June 26, 2007): 8951–82. http://dx.doi.org/10.5194/acpd-7-8951-2007.

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Abstract. Interest in the potential formation of secondary organic aerosol (SOA) through reactions of organic compounds in condensed aqueous phases is growing. In this study, the potential formation of SOA from irreversible aqueous-phase reactions of organic species in clouds was investigated. A new proposed aqueous-phase chemistry mechanism (AqChem) is coupled with the existing gas-phase Caltech Atmospheric Chemistry Mechanism (CACM) and the Model to Predict the Multiphase Partitioning of Organics (MPMPO) that simulate SOA formation. AqChem treats irreversible organic reactions that lead mainly to the formation of carboxylic acids, which are usually less volatile than the corresponding aldehydic compounds. Zero-dimensional model simulations were performed for tropospheric conditions with clouds present for three consecutive hours per day. Zero-dimensional model simulations show that 48-h averaged SOA formation are increased by 27% for a rural scenario with strong monoterpene emissions and 7% for an urban scenario with strong emissions of aromatic compounds, respectively, when irreversible organic reactions in clouds are considered. AqChem was also incorporated into the Community Multiscale Air Quality Model (CMAQ) version 4.4 with CACM/MPMPO and applied to a previously studied photochemical episode (3–4 August 2004) focusing on the eastern United States. The CMAQ study indicates that the maximum contribution of SOA formation from irreversible reactions of organics in clouds is 0.28 μg m−3 for 24-h average concentrations and 0.60 μg m−3 for one-hour average concentrations at certain locations. On average, domain-wide surface SOA predictions for the episode are increased by 8.6% when irreversible, in-cloud processing of organics is considered.
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SOBOLEVA, E. A., Ya A. VISURKHANOVA, N. M. IVANOVA, М. Е. BEISENBEKOVA, and S. O. KENZHETAEVA. "ULTRAFINECOPPER AND NICKEL POWDERS INTHE ELECTRO-CATALYTICHYDROGENATIONOF ORGANIC COMPOUNDS." Chemical Journal of Kazakhstan 74, no. 2 (June 30, 2021): 32–48. http://dx.doi.org/10.51580/2021-1/2710-1185.26.

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Ultrafine copper and nickel powders are synthesized by a chemical reduction of the metal cations from their salts in an aqueous ethanol solution without and with the addition of a polymer stabilizer (polyvinylpyrrolidone and polyvinyl alcohol). The structure and morphological features of the prepared metal powders were investigated by X-ray phase analysis and electron microscopy. The electrocatalytic properties of the Cu and Ni powders have been studied in the electrohydrogenation of acetophenone, nitrobenzene, p-nitroaniline, and cyclohexanone. A higher electrocatalytic activity of Cu powders, as well as skeletal copper, was established in the electrohydrogenation of the first three of the listed compounds in comparison with nickel powders, which is explained by the ability of copper cations to be reduced from its oxides in the electrochemical system under investigation. It is shown that the use of polymer stabilizers in the synthesis of Cu and Ni powders contributes to reducing metal particle sizes, but does not increase the electrocatalytic activity of the corresponding metal powders.
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Scheide, Marcos R., Celso R. Nicoleti, Guilherme M. Martins, and Antonio L. Braga. "Electrohalogenation of organic compounds." Organic & Biomolecular Chemistry 19, no. 12 (2021): 2578–602. http://dx.doi.org/10.1039/d0ob02459g.

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In this review we target sp, sp2 and sp3 carbon fluorination, chlorination, bromination and iodination reactions using electrolysis as a redox medium. Mechanistic insights and substrate reactivity are also discussed.
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Dissertations / Theses on the topic "Organic compounds"

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Ojala, S. (Satu). "Catalytic oxidation of volatile organic compounds and malodorous organic compounds." Doctoral thesis, University of Oulu, 2005. http://urn.fi/urn:isbn:9514278704.

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Abstract This thesis describes efforts made on the development of an existing catalytic incinerator. The development work, called process characterization, consists of four general parts. These are the development of measurement methodology, the studying of construction materials, the selection of suitable catalysts and the testing of the effects of process operation conditions. The two application areas for catalytic incineration considered in this thesis are solvent emission abatement (VOC, volatile organic compounds) and chip bin emission abatement (SVOC, sulphur-containing volatile organic compounds). As a baseline, the process characterization is started with the development of measurement methodology. In general, the methodology will decrease costs and simplify the carrying out of the actual measurements and thereby make the measurement time more effective. In the methodology it is proposed that continuous total concentration measurement should be used in connection with qualitative sampling to obtain reliable measurement data. The selection of suitable construction materials for the application is very important. As shown in this thesis, the end conversions in solvent emission abatement may even be improved through the selection of the proper construction materials. In chip bin emission abatement, the problem arises from corrosive oxidation products that set limits on the construction materials used as well as on oxidation conditions. Catalyst selection is based on the following catalytic properties: activity, selectivity and durability. These catalytic properties are studied either at the laboratory or on an industrial scale. The catalytic materials tested are Pt, Pd, Pt-Pd, Cu-Mn oxides, MnO2-MgO, CuxMg(1-x)Cr2O4 and CuxCr2O4. The most important selection criteria in solvent emission abatement are proposed to be activity and selectivity. In the case of chip bin-SVOC-abatement, these are selectivity and durability. Based on these criteria, catalysts containing Cu-Mn oxides and Pt were demonstrated to be the best catalysts in VOC oxidation, and catalyst containing MnO2-MgO was shown to be best catalyst in SVOC oxidation. A study on the effect of process operation parameters (temperature, concentration and gas hourly space velocity (GHSV)) and moisture was carried out with the aid of factorial design. In VOC (n-butyl acetate) oxidation, the most influential process parameter was GHSV, which decreased the end conversion when it was increased. In SVOC (DMDS) oxidation, the effect of temperature was most significant. The end conversions increased as the temperature increased. Moisture slightly decreased the formation of by-products in n-butyl acetate oxidation. In DMDS oxidation, moisture slightly increased the end conversions at a lower temperature level (300°C). At the end of the thesis, these process parameters are also discussed from the standpoint of the catalysts' activity, selectivity and durability. Finally, proposals for process improvements are suggested.
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Taylor, Paul. "Organic thionitroso compounds." Thesis, Durham University, 1989. http://etheses.dur.ac.uk/6482/.

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A series of novel N-substituted phthalimide-2-sulplienamides was prepared. The N-aryl analogues were shown to be efficient precursors to thionitrosoarenes. Extension of the methodology to heteroaroraatic and acyl derivatives was unsuccessful, with the exception of 3-thionitroso- pyridine, the first known thionitrosoheteroarene. Thionitrosoarenes are shown to be versatile dienophiles and enophiles. Reactions with various substituted dienes proceeded with high stereoselectivity and some regioselectivity to afford 3,6-dihydro- 1,2-thiazines. Cycloadditions of thionitrosoarenes generated independently from imidosulphurous chloride precursors showed similar selectivities. The mechanism of cycloaddition is discussed in the light of molecular orbital calculations.
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Hunter, James Freeman. "Oxidation of atmospheric organic carbon : interconnecting volatile organic compounds, intermediate-volatility organic compounds, and organic aerosol." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/97794.

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Thesis: Ph. D. in Environmental Chemistry, Massachusetts Institute of Technology, Department of Civil and Environmental Engineering, 2015.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 101-110).
.Organic molecules have many important roles in the atmosphere, acting as climate and biogeochemical forcers, and in some cases as toxic pollutants. The lifecycle of atmospheric organic carbon is extremely complex, with reaction in multiple phases (gas, particle, aqueous) and at multiple timescales. The details of the lifecycle chemistry (especially the amount and properties of particles) have important implications for air quality, climate, and human and ecosystem health, and need to be understood better. Much of the chemical complexity and uncertainty lies in the reactions and properties of low-volatility oxidized intermediates that result from the oxidation of volatile organic precursors, and which have received comparatively little study thus far. This thesis describes three projects that link together the entire chain of oxidation (volatile to intermediate to condensed) in an effort to improve our understanding of carbon lifecycle and aerosol production. Laboratory studies of atmospherically relevant aerosol precursors show that the slow oxidation of intermediates is critical to explaining the yield and properties of aerosol under highly oxidized ("aged") conditions, and that the production of organic particles is significantly increased when intermediates are fully oxidized. This aging process is a strong function of molecular structure, and depends on aerosol concentration through the phenomenon of condensational trapping. Further laboratory studies of a series of (poly)cyclic 10 carbon alkanes show that structural effects are largely explained through fragmentation reactions, and that more generally, carbon-carbon bond scission is a ubiquitous and important reaction channel for oxidized intermediates. Finally, direct measurement of oxidized intermediate compounds in field studies shows that these compounds are abundant and important in the ambient atmosphere, with concentrations and properties in between those of volatile and particulate organic compounds. Together with other co-located measurements and complementary techniques, this enables estimates of emission, oxidation, and deposition to be constructed. The results from this thesis can be used to inform more sophisticated models of atmospheric organic carbon cycling, and to improve prediction of organic particulate matter concentrations.
by James Freeman Hunter.
Ph. D. in Environmental Chemistry
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Szecsödy, James Edward. "Sorption Kinetics of Hydrophobic Organic Compounds onto Organic Modified Surfaces." Diss., The University of Arizona, 1988. http://hdl.handle.net/10150/219433.

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The sorption of five chlorinated benzenes and sixteen other organic solutes was investigated by determining the extent of sorption and the sorption rates in a series of 40 batch and 139 column experiments using surface-modified silica of known chemical composition. These surfaces were used to represent important functional groups in soil, and consisted of porous silica with patchy surface coatings of aliphatic chains (C₁, C₈, and C₁₈), and other substituent groups (phenyl, amine, alcoholic, and carboxylic). Three possible rate-limiting steps were examined: diffusion through immobile pore fluid, diffusion through bound organic matter, and the chemical binding and release rate. First-order desorption rate coefficients were observed to be 10⁻¹ to 10⁻² s⁻¹ on unbonded, and C₈, C₁₈, amine, and alcoholic modified surfaces, and 10⁻³ to 10⁻⁵ s⁻¹ on C₁ and phenyl-polymer modified surfaces. Diffusion through immobile pore fluid had only a minor effect on the sorption rate, as evidenced by similar rates on organic-bound porous and solid particles. The diffusion rate through the bound organic layer is not rate limiting due to the small organic layer thickness. The observed slow desorption on the phenyl-polymer surface is consistent with the rate limiting step being the chemical binding and release rate. The changes in the rate with temperature and within a series of chlorinated benzenes support this conclusion. The free energies for sorption onto the phenyl-polymer surface ranged from -4.0 kcal mol⁻¹ for chlorobenzene to -6.9 kcal mol⁻¹ for pentachlorobenzene, which are within the range expected for van der Waals interactions. The observed sorption energies are slightly stronger than predicted for hydrophobic surfaces, possibly reflecting strong binding due to multiple pi-pi electron interactions on the phenyl-polymer surface. Hydrophobic solute partitioning onto natural soils, as observed by others, is less than that observed on aliphatic and phenyl hydrophobic surfaces in this study, but greater than on amine or alcoholic modified surfaces. The sorption of di-, tri-, and tetra-chlorobenzenes onto the phenyl-polymer surface is apparently driven by the overall sorption enthalpy (ΔH° = -3.9 to -4.9 kcal mo1⁻¹) and to a lesser extent by the entropy (TΔS° = 0.5 to 1.5 kcal mol⁻¹). As equilibrium of the reactions observed in this study are reached within hours, these reactions are important at small field scales where residence times are hundreds of hours or less.
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Sephton, Mark A. "Organic compounds in meteorites." Thesis, Open University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.339860.

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Oey, Ching-ching. "Organic-inorganic nanocomposites for organic optoelectronic devices." Click to view the E-thesis via HKUTO, 2005. http://sunzi.lib.hku.hk/hkuto/record/B35321222.

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Oey, Ching-ching, and 黃晶晶. "Organic-inorganic nanocomposites for organic optoelectronic devices." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2005. http://hub.hku.hk/bib/B35321222.

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Sanders, Giles. "The dissolution of organic compounds." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362083.

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Budd, Laura Elizabeth. "Polymorphism in small organic compounds." Thesis, University of Edinburgh, 2010. http://hdl.handle.net/1842/3967.

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The effect of temperature on the crystal structure of deuterated piperidine has been studied using neutron powder diffraction. Differential scanning calorimetry indicates that there are multiple phases accessible via changes in temperature however there is no evidence of this in the neutron powder diffraction study with only one phase observed in the range 2 – 250 K and under various crystallisation conditions. The effect of pressure up to 2.79 GPa has also been determined. The compression of the structure is facilitated through the closing up of voids in the structure and no phase transition is observed. Differential scanning calorimetry has shown N-methyl and N,N-dimethylformamide both exhibit a thermal event prior to melting. Low temperature neutron powder diffraction has shown these transitions are associated with the onset of methyl group rotation. Neutron powder diffraction studies show formamide exhibits remarkable polymorphism at ambient temperature and pressures between 0.1 GPa and 3.6 GPa, forming four new polymorphs. All the structures consist of N-H…O hydrogen bonded chains. The formation of the various polymorphs can be rationalised in terms of the orientation of the molecules within the hydrogen bonded chains and the resultant structures formed by further hydrogen bonds between the chains. This is in stark contrast to the effect of varying conditions of temperature where only one structure exists from 2 K right up to the melting point. The effect of temperature on the crystal structure of pyrazine in the range 8 – 315 K is described. At temperatures below 90 K the structure undergoes a phase transition to a previously uncharacterised phase, designated phase IV, which is closely related to the previously known phase I. The crystal structure of phase III has been determined at 315 K. The crystal structure of pyrazine has been determined at room temperature at pressures between 0.11 GPa and 9.36 GPa. At 0.94 GPa a transition from phase I to phase IV is observed. This is the same phase as observed at low temperatures. Crystal growth at 215 K results in the formation of two different phases of mesitylene; phase II and a new previously unknown phase designated phase IV. The structure of phase IV has been determined and found to be stable in the range 90 – 221 K. On cooling a crystal of deuterated mesitylene in phase II to 90 K a transition to phase III was observed and the resultant crystal structure is closely related to that of phase II.
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Matqi, Khalil Yacoub. "Biodesulphurisation of organic sulphur compounds." Thesis, University of Sheffield, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.251215.

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Books on the topic "Organic compounds"

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chairman, Bennett Andrew F., and Field Barry chairman, eds. Volatile organic compounds. London: HMSO, 1995.

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United States. Environmental Protection Agency. Office of Drinking Water., ed. Volatile organic compounds. Chelsea, Mich: Lewis Publishers, 1991.

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1939-, Michl Josef, Gladysz John A, and American Chemical Society, eds. Strained organic compounds. Washington: American Chemical Society, 1989.

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L, Marinkas Paul, ed. Organic energetic compounds. Commack, N.Y: Nova Science Publishers, 1996.

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F, Bennett Andrew, and Field Barry, eds. Volatile organic compounds. London: HMSO, 1995.

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Ahluwalia, V. K. Stereochemistry of Organic Compounds. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-84961-0.

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Pattenden, G., J. I. G. Cadogan, and S. V. Ley. Dictionary of Organic Compounds. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-6637-7.

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Buckingham, J., ed. Dictionary of Organic Compounds. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3312-6.

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Madelung, O., U. Rössler, and M. Schulz, eds. Ternary Compounds, Organic Semiconductors. Berlin/Heidelberg: Springer-Verlag, 2000. http://dx.doi.org/10.1007/b72741.

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J, Buckingham, ed. Dictionary of organic compounds. 5th ed. London: Chapman and Hall, 1988.

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Book chapters on the topic "Organic compounds"

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Shankland, Kenneth. "Organic Compounds." In NATO Science for Peace and Security Series B: Physics and Biophysics, 45–52. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5580-2_5.

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Fox, Malcolm A. "Organic Compounds." In Glossary for the Worldwide Transportation of Dangerous Goods and Hazardous Materials, 164–66. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-662-11890-0_54.

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Malainey, Mary E. "Organic Compounds." In Manuals in Archaeological Method, Theory and Technique, 45–72. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-5704-7_5.

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Shallenberger, Robert S. "Organic Compounds." In Taste Chemistry, 253–91. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2666-7_9.

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Berkowitz, Brian, Ishai Dror, and Bruno Yaron. "Organic Compounds." In Contaminant Geochemistry, 79–104. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-54777-5_4.

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Ferguson, G. "Organic Compounds." In Structure Reports, 1–748. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-017-3154-6_1.

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Fromme, Hermann. "Volatile Organic Compounds and Very Volatile Organic Compounds." In Indoor Air Quality, 93–156. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-40078-0_3.

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Uragami, Tadashi. "Volatile Organic Compounds." In Encyclopedia of Membranes, 1–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-40872-4_596-1.

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Voronkov, M. G., N. S. Vyazankin, E. N. Deryagina, A. S. Nakhmanovich, and V. A. Usov. "Organic Sulfur Compounds." In Reactions of Sulfur with Organic Compounds, 173–87. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-0679-5_5.

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Sarkar, Tapan, and Ashok Mulchandani. "Volatile Organic Compounds." In Environmental Analysis by Electrochemical Sensors and Biosensors, 1023–46. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1301-5_14.

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Conference papers on the topic "Organic compounds"

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Syed, Yasir I., Chris Phillips, Davide Deganello, and Keir E. Lewis. "Exhaled Volatile Organic Compounds In COPD Exhaled Volatile Organic Compounds & COPD." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a4598.

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Tumanov, Vladimir Evgen'vich, and Andrei Ivanovich Prokhorov. "Web database on bond dissociation energies of organic compounds." In 23rd Scientific Conference “Scientific Services & Internet – 2021”. Keldysh Institute of Applied Mathematics, 2021. http://dx.doi.org/10.20948/abrau-2021-21.

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The article presents a scientific service on the Internet "Bond Dissociation Energies of Organic Compounds Database". This web database contains experimental values of dissociation energies of homolytic bonds. The service is intended for use by a wide range of chemists, theorists and practitioners in the open access on the Internet. The paper provides a brief overview of the literature sources of the dissociation energies of bonds of organic molecules, which are calculated theoretically, measured experimentally and estimated from kinetic and thermochemical experimental data. Descriptions of experimental data sources, classes of organic compounds and calculation methods are given. The logical structure of the database and the description of the main fields of its tables are given. The architecture of the web database is presented. The main search form of the database interface is presented and examples of search results for a specific organic compound and a fragment of a chemical formula are given. For most compounds, the values of the bond dissociation energy are given at a temperature of 298.15 K, which is usually absent in most sources (taking into account temperature correlations). Currently, work is underway to analyze the published data taking into account the entropy effects.
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Place, M. C. "Dissolved Organic Compounds in Produced Water." In SPE Annual Technical Conference and Exhibition. Society of Petroleum Engineers, 1991. http://dx.doi.org/10.2118/22780-ms.

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Yost, C., B. Pacolay, and L. Coyne. "348. Monitoring Volatile Organic Compounds Samplers." In AIHce 2002. AIHA, 2002. http://dx.doi.org/10.3320/1.2766288.

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Barachevsky, Valery A. "Photochromic organic compounds with polyfunctional properties." In ICONO '98: Laser Spectroscopy and Optical Diagnostics--Novel Trends and Applications in Laser Chemistry, Biophysics, and Biomedicine, edited by Andrey Y. Chikishev, Victor N. Zadkov, and Alexei M. Zheltikov. SPIE, 1999. http://dx.doi.org/10.1117/12.340018.

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Wolff, Marcus, Henry Bruhns, and Wenyi Zhang. "Photoacoustic detection of volatile organic compounds." In SPIE Optics + Optoelectronics, edited by Francesco Baldini, Jiri Homola, Robert A. Lieberman, and Kyriacos Kalli. SPIE, 2011. http://dx.doi.org/10.1117/12.888966.

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Henley, Michael V., William R. Bradley, Sheryl E. Wyatt, G. M. Graziano, and J. R. Wells. "Atmospheric transformation of volatile organic compounds." In AeroSense 2000, edited by Patrick J. Gardner. SPIE, 2000. http://dx.doi.org/10.1117/12.394076.

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Monçalves, Matias, Mariana M. Bassaco, Marcos A. Villetti, and Claudio C. Silveira. "Novel Divinyl Sulfides: Potential Luminescent Compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0308-1.

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Xu, D., J. T. Lin, and B. H. T. Chai. "Investigation of spectroscopic properties of nonlinear optical crystals and their relationship to structural radicals." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1989. http://dx.doi.org/10.1364/oam.1989.mw4.

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Abstract:
Since many of the organic conjugated compound crystals have nonlinear optical coefficients of at least 1-2 orders of magnitude higher than those of the inorganic oxide compounds, these crystals have drawn the attention of many researchers. However, the major drawback of these organic compounds is their poor UV transparency which greatly limits their potential applications.
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Khuzina, Liliya L., Airat R. Tuktarov, and Usein M. Dzhemilev. "Catalytic Cycloaddition of Diazo Compounds Based on Pharmacologically Significant and Natural Compounds to C60-Fullerene." In International Electronic Conference on Synthetic Organic Chemistry. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13534.

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Reports on the topic "Organic compounds"

1

Wiberg, K. B. [Energies of organic compounds]. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/79710.

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Wiberg, K. B. Energies of organic compounds. Office of Scientific and Technical Information (OSTI), July 1995. http://dx.doi.org/10.2172/75255.

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Wiberg, K. (Energies of organic compounds). Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/5484131.

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Hites, R. A. Toxic organic compounds from energy production. Office of Scientific and Technical Information (OSTI), November 1990. http://dx.doi.org/10.2172/6150097.

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Hites, R. A. Toxic organic compounds from energy production. Office of Scientific and Technical Information (OSTI), September 1991. http://dx.doi.org/10.2172/6263915.

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Dix, K. Gas chromatographic determination of water in organic compounds and of organic compounds in water after steam distillations. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6783378.

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Gu, B., and R. L. Siegrist. Alkaline dechlorination of chlorinated volatile organic compounds. Office of Scientific and Technical Information (OSTI), June 1996. http://dx.doi.org/10.2172/419269.

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Wiberg, K. B. Energies of organic compounds. Technical progress report. Office of Scientific and Technical Information (OSTI), August 1987. http://dx.doi.org/10.2172/82275.

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John F. Schabron, Jr Joseph F. Rovani, and Theresa M. Bomstad. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS. Office of Scientific and Technical Information (OSTI), July 2003. http://dx.doi.org/10.2172/820761.

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John F. Schabron, Joseph F. Rovani Jr., and Theresa M. Bomstad. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS. Office of Scientific and Technical Information (OSTI), June 2002. http://dx.doi.org/10.2172/822157.

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You might also be interested in the extended bibliographies on the topic 'Organic compounds' for particular source types:
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