Academic literature on the topic 'Chlorofluoromethane'

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Journal articles on the topic "Chlorofluoromethane"

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Blanco, S., A. Lesarri, J. C. López, J. L. Alonso, and A. Guarnieri. "The Rotational Spectrum of Chlorofluoromethane." Journal of Molecular Spectroscopy 174, no. 2 (December 1995): 397–416. http://dx.doi.org/10.1006/jmsp.1995.0011.

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Favero, Laura B., Assimo Maris, Sonia Melandri, Paolo Ottaviani, and Walther Caminati. "Non covalent interactions stabilizing the chiral dimer of CH2ClF: a rotational study." Physical Chemistry Chemical Physics 21, no. 7 (2019): 3695–700. http://dx.doi.org/10.1039/c8cp06288a.

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Two C–H⋯Cl–C and one C–H⋯F–C bonds stabilize (by 5.9 kJ mol−1) the dimer of chlorofluoromethane observed by rotational spectroscopy in the gas phase. The spectral analysis is complicated by the quadrupolar effects of the two nonequivalent Cl nuclei.
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Ottaviani, Paolo, Walther Caminati, and Jens-Uwe Grabow. "Tunneling motions of argon on chlorofluoromethane." Journal of Chemical Physics 125, no. 19 (November 21, 2006): 194302. http://dx.doi.org/10.1063/1.2378625.

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Binbrek, Omar S., Bruce H. Torrie, and Ian P. Swainson. "Neutron powder-profile study of chlorofluoromethane." Acta Crystallographica Section C Crystal Structure Communications 58, no. 11 (October 22, 2002): o672—o674. http://dx.doi.org/10.1107/s0108270102017328.

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Puzzarini, Cristina, Riccardo Tarroni, and Paolo Palmieri. "The anharmonic force field of chlorofluoromethane." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 53, no. 8 (July 1997): 1123–31. http://dx.doi.org/10.1016/s1386-1425(96)01865-3.

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Schlitzer, Reiner, Wolfgang Roether, Harald Oster, Hans-Georg Junghans, Martin Hausmann, H. Johannsen, and A. Michelato. "Chlorofluoromethane and oxygen in the Eastern Mediterranean." Deep Sea Research Part A. Oceanographic Research Papers 38, no. 12 (December 1991): 1531–51. http://dx.doi.org/10.1016/0198-0149(91)90088-w.

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Schlueter, S. A., T. S. Davison, J. M. Fraser, and A. Anderson. "Raman and infrared spectra of solid chlorofluoromethane." Journal of Raman Spectroscopy 25, no. 6 (June 1994): 429–33. http://dx.doi.org/10.1002/jrs.1250250609.

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OKAZAKI, Susumu, and Kiyoshi SHINODA. "Surface Modification of TiO2 Using Chlorofluoromethane or Hydrofluoromethane." Journal of the Japan Society of Colour Material 63, no. 12 (1990): 750–56. http://dx.doi.org/10.4011/shikizai1937.63.750.

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Baldacci, A., P. Stoppa, S. Giorgianni, R. Visinoni, and S. Ghersetti. "Diode Laser Spectroscopy of the ν8 Band of Chlorofluoromethane." Journal of Molecular Spectroscopy 166, no. 2 (August 1994): 264–72. http://dx.doi.org/10.1006/jmsp.1994.1192.

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Fine, Rana A., Mark J. Warner, and Ray F. Weiss. "Water mass modification at the Agulhas retroflection: chlorofluoromethane studies." Deep Sea Research Part A. Oceanographic Research Papers 35, no. 3 (March 1988): 311–32. http://dx.doi.org/10.1016/0198-0149(88)90013-1.

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Dissertations / Theses on the topic "Chlorofluoromethane"

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Messias, Marie-José. "Les chlorofluoromethanes, traceurs des eaux profondes dans les zones de fracture romanche et chain en atlantique equatorial." Paris 6, 1994. http://www.theses.fr/1994PA066409.

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Les chlorofluoromethanes (cfm: f11 (cfcl#3) et f12 (cf#2cl#2)) sont des traceurs transitoires anthropiques. Ces composes sont analyses en mer par couplage d'une ligne d'extraction des gaz dissous dans l'eau a un chromatographe en phase gazeuse. Ils ont ete mesures pendant les campagnes romanche 1 (aout 1991) et romanche 2 (novembre 1992) dans les zones de fractures romanche (10w-12w et 030's-050'n) et chain (15w-12w et 130's-1s), passages clef pour les eaux profondes entre les bassins ouest et est de l'atlantique. A l'entree de chaque zone de fracture, la distribution en cfm presente deux noyaux alimentes par les courants profonds de bord ouest. Le signal observe vers 1600 metres marque l'eau profonde nord atlantique superieure (epnas) originaire de la mer du labrador. Il est centre sur 1s et continue a l'est jusqu'a plus de 5w. Le signal a 3800 metres, associes a l'eau profonde nord atlantique inferieure (epnai) originaire du detroit du danemark, passe principalement dans la zone de fracture romanche. Il diminue au niveau des seuils puis plonge dans le bassin est jusqu'a plus de 4500 metres. Le rapport f11/f12 permet de calculer les ages apparents et les dilutions apparentes des masses d'eau. L'epnas a un age apparent de 22-28 ans avec un facteur de dilution de 30. L'epnai apparait plus vieille (30-35 ans) et moins diluee avant les seuils (facteur 4). La dilution apparente de l'epnai augmente apres les seuils (facteur 30) refletant les effets des melanges intenses au franchissement des fractures
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Silva, Filho Arnaldo Fernandes da 1987. "Aplicação do modelo QTAIM/CCFDF para o estudo de estruturas eletrônicas dos clorofluorometanos." [s.n.], 2011. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249355.

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Orientador: Roy Edward Bruns
Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Química
Made available in DSpace on 2018-08-18T09:29:34Z (GMT). No. of bitstreams: 1 SilvaFilho_ArnaldoFernandesda_M.pdf: 1712165 bytes, checksum: ba65ba1932c8a6baa99b265fd3d6770d (MD5) Previous issue date: 2011
Resumo: Foram calculadas as intensidades fundamentais vibracionais no infravermelho e as contribuições QTAIM/CCFDF do tensor polar atômico, nos níveis MP2/6-311++G(3d,3p) e QCISD/cc-pVTZ, para os clorofluorometanos. Um erro rms de 21,2 km/mol foi encontrado entre as intensidades experimentais e as obtidas no nível MP2/6-311++G(3d,3p), e 20,0 km/mol, entre as intensidades experimentais e as obtidas no nível QCISD/cc-pVTZ. O erro rms encontrado entre as intensidades obtidas das funções de onda e as calculadas através dos parâmetros QTAIM/CCFDF foi de 0,016 km/mol para o nível MP2/6-311++G(3d,3p), e 0,018 km/mol para o nível QCISD/cc-pVTZ. O erro para os elementos do tensor polar atômico e derivada média do momento dipolar entre os níveis QCISD/cc-pVTZ, MP2/6-311++G(3d,3p) e os valores experimentais foi da ordem de 0,06 u.a. Apesar do bom resultado para a derivada média do momento dipolar, as contribuições CCFDF não foram calculadas com a mesma exatidão. Apenas os fluorometanos parecem ter estruturas eletrônicas que se ajustam ao modelo simples de eletronegatividade. o átomo de flúor não tem sua capacidade de atrair os elétrons do átomo central saturada, enquanto a carga efetiva do cloro parece depender da quantidade e identidade dos demais átomos substituintes. Esse efeito de saturação separa as moléculas estudadas em três grupos: fluorometanos, clorometanos e clorofluorometanos. As derivadas médias do momento dipolar seguem melhor o modelo de Siegbahn do que cargas de fluxo zero, apesar contribuições dinâmicas que não se anulam completamente. A regra da soma para as derivadas médias do momento dipolar se mostrou eficiente para o átomo de carbono. Os átomos terminais não tiveram a mesma precisão para a regra da soma. A anisotropia calculada no nível QCISD/cc-pVTZ, teve um concordância superior com os valores experimentais, quando comparada com valores do nível MP2/6-311++G(3d,3p)
Abstract: The infrared fundamental intensities and QTAIM/CCFDF contributions to the atomic polar tensor were calculated at MP2/6-311++G(3d, 3p) and QCISD/cc-pVTZ levels, for the chlorofluoromethanes. A rms error of 21.2 km/mol was obtained between experimental and MP2/6-311++G(3d, 3p) intensities. The rms error between experimental and QCISD/cc-pVTZ intensities was 20.0 km/mol. The rms error found between intensities obtained directly from the wave functions and calculated through QTAIM/CCFDF parameters was 0.016 km/mol for the MP2/6-311++G(3d, 3p) level, and 0.018 km/mol for the QCISD/cc-pVTZ level. The error between the theoretical atomic polar tensor elements and mean dipole moment derivatives compared to experimental values is about 0.06 a.u. Despite good results for the mean dipole moment derivatives, the CCFDF contributions have not been calculated with the same accuracy. The fluoromethanes seem to be the only group whose electronic structures fit the simple electronegativity model. The fluorine atom does not has its ability to drain charge from the central atom altered, while the chlorine effective charge seems to depend on the number and identity of other terminal atoms. This saturating effect separates the studied molecules in three groups: fluoromethanes, chloromethane and chlorofluoromethanes. Mean dipole moment derivatives have a better fit to Siegbahn¿s model than zero-flux charges, beside to their dynamic contributions. The sum rule for mean dipole moment derivatives was efficient for the carbon atom. Terminal atoms did not have the same accuracy for the sum rule. QCISD/cc-pVTZ anisotropy values were closer to experimental values, when compared to the MP2/6-311++G(3d, 3p) level
Mestrado
Físico-Química
Mestre em Química
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Mulquiney, John E. "Global atmospheric CFCl3 flux estimation." Phd thesis, 1995. http://hdl.handle.net/1885/138851.

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Books on the topic "Chlorofluoromethane"

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Farrokhnia, A. Kinetic and mechanistic study of the reaction of chlorofluoromethanes and hydrochlorofluoromethanes with prefluorided chromia catalyst. Manchester: UMIST, 1998.

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Book chapters on the topic "Chlorofluoromethane"

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "32 CH2ArClF Chlorofluoromethane – argon (1/1)." In Molecules Containing No Carbon Atoms and Molecules Containing One or Two Carbon Atoms, 263. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-540-70614-4_233.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "36 CH2ClFKr Chlorofluoromethane – krypton (1/1)." In Molecules Containing No Carbon Atoms and Molecules Containing One or Two Carbon Atoms, 267. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-540-70614-4_237.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "37 CH2ClFXe Chlorofluoromethane – xenon (1/1)." In Molecules Containing No Carbon Atoms and Molecules Containing One or Two Carbon Atoms, 268. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-540-70614-4_238.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "60 CH4ClFO Chlorofluoromethane – water (1/1)." In Molecules Containing No Carbon Atoms and Molecules Containing One or Two Carbon Atoms, 291. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-540-70614-4_261.

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Vogt, J. "57 CH2ArClF Chlorofluoromethane - argon (1/1)." In Asymmetric Top Molecules. Part 1, 129–30. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10371-1_59.

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Rowland, F. S., and Mario J. Molina. "Chlorofluoromethanes in the Environment." In 1976, Chemistry and Physics of the Stratosphere, 1–35. Washington, DC: American Geophysical Union, 2014. http://dx.doi.org/10.1002/9781118782132.ch1.

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Andrié, C. "Chlorofluoromethanes in the Deep Equatorial Atlantic Revisited." In The South Atlantic, 273–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-80353-6_15.

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"Chlorofluoromethane." In Drugs Handbook 2012–2013. Bloomsbury Academic, 2011. http://dx.doi.org/10.5040/9781350363595.art-338.

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OLÁH, GY, and A. PAVLÁTH. "SYNTHESIS OF ORGANIC FLUORINE COMPOUNDS, VIII: PREPARATION OF CHLOROFLUOROMETHANES (COMPOUNDS OF THE FREON TYPE)." In World Scientific Series in 20th Century Chemistry, 8–11. World Scientific Publishing Company, 2003. http://dx.doi.org/10.1142/9789812791405_0002.

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