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Journal articles on the topic "C.020.673.440"

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Smith, Alice M., Jürgen Agreiter, and Vladimir E. Bondybey. "Laser-induced fluorescence of matrix-isolated HCCCCCN+ and HCCCCCCCN+." Chemical Physics Letters 244, no. 5-6 (October 1995): 379–87. http://dx.doi.org/10.1016/0009-2614(95)00915-q.

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Bartel, Christoph, Peter Botschwina, Hans Bürger, Antonio Guarnieri, Änne Heyl, Aiko Huckauf, Dieter Lentz, Tatjana Merzliak, and El Bachir Mkadmi. "Cyanisocyanacetylen, N≡C−C≡C−N≡C." Angewandte Chemie 110, no. 20 (October 16, 1998): 3036–40. http://dx.doi.org/10.1002/(sici)1521-3757(19981016)110:20<3036::aid-ange3036>3.0.co;2-n.

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Bartel, Christoph, Peter Botschwina, Hans Bürger, Antonio Guarnieri, Änne Heyl, Aiko Huckauf, Dieter Lentz, Tatjana Merzliak, and El Bachir Mkadmi. "Cyanoisocyanoacetylene, N≡C−C≡C−N≡C." Angewandte Chemie International Edition 37, no. 20 (November 2, 1998): 2879–82. http://dx.doi.org/10.1002/(sici)1521-3773(19981102)37:20<2879::aid-anie2879>3.0.co;2-0.

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Okabayashi, T., M. Tanimoto, K. Tanaka, and E. Hirota. "Microwave spectroscopy of fluorocyanobutadiyne (F-CC-CC-CN)." Chemical Physics Letters 230, no. 6 (December 1994): 530–35. http://dx.doi.org/10.1016/0009-2614(94)01205-9.

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Makovicky, Emil, and Sven Karup-Møller. "Exploratory studies of the Cu–Pd–Se system at 650°C, 550°C, 400°C, and 300°C." European Journal of Mineralogy 29, no. 4 (October 10, 2017): 645–52. http://dx.doi.org/10.1127/ejm/2017/0029-2651.

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Sinha, Narayan, Dorus Heijnen, Ben L. Feringa, and Michael G. Organ. "Murahashi Cross‐Coupling at −78 °C: A One‐Pot Procedure for Sequential C−C/C−C, C−C/C−N, and C−C/C−S Cross‐Coupling of Bromo‐Chloro‐Arenes." Chemistry – A European Journal 25, no. 39 (June 24, 2019): 9180–84. http://dx.doi.org/10.1002/chem.201901678.

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Bartel, Christoph, Peter Botschwina, Hans Buerger, Antonio Guarnieri, Aenne Heyl, Aiko Huckauf, Dieter Lentz, Tatjana Merzliak, and El Bachir Mkadmi. "ChemInform Abstract: Cyanoisocyanoacetylene, NC-CC-NC." ChemInform 30, no. 14 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199914088.

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Smith, Alice M., Günter Schallmoser, Anton Thoma, and Vladimir E. Bondybey. "Infrared spectral evidence of N≡C–C≡C–N≡C: Photoisomerization of N≡C–C≡C–C≡N in an argon matrix." Journal of Chemical Physics 98, no. 3 (February 1993): 1776–85. http://dx.doi.org/10.1063/1.464266.

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A. Adrio, Luis, and King Kuok (Mimi) Hii. "Palladium-Catalyzed Heterofunctionalization of C-H, C=C and C≡ C Bonds." Current Organic Chemistry 15, no. 18 (September 1, 2011): 3337–61. http://dx.doi.org/10.2174/138527211797248003.

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Allen, Gregory W., Robert S. Armstrong, Manuel J. Aroney, Raymond K. Pierens, and Alan J. Williams. "Polarisability anisotropies of C—H, C—C, C—Cl and C—Br bonds." J. Chem. Soc., Faraday Trans. 2 84, no. 11 (1988): 1775–78. http://dx.doi.org/10.1039/f29888401775.

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Dissertations / Theses on the topic "C.020.673.440"

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Huang, Xiaohua 1973. "Palladium-catalyzed C-C, C-N and C-O bond formation." Thesis, Massachusetts Institute of Technology, 2003. http://hdl.handle.net/1721.1/29639.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2003.
Vita.
Includes bibliographical references.
New methods for Pd-catalyzed cross-coupling reactions of aryl halides or arenesulfonates are described. Key to the success of these transformations is the proper choice of ligand and reaction conditions. Palladium catalysts supported by bulky, monodentate phosphine ligands with a biaryl backbone or the bidentate ligand, Xantphos, effectively promote the formation of ca-aryl carbonyl compounds. Base-sensitive functional groups are better tolerated when a weak base, such as K3PO4, is used. One of the most difficult transformations in Pd catalysis, the intermolecular C-O bond formation between primary alcohols and electron-neutral or even electron-rich aryl halides, was effectively promoted by the use of a new generation of ligands, 3-methyl-2-di-t-butylphosphinobiaryl. The one-step synthesis of ligands from cheap starting materials, as well as the mild reaction conditions employed for the coupling reactions, enables the practical use of Pd catalysis to access aryl alkyl ethers for the first time. Continuing study of Pd-catalyzed C-N bond-forming processes using biaryl monophosphine ligands led to the discovery of a structural derivative of these ligands, 2-dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl. This ligand, in combination with a Pd source, produces a catalyst system with both a greater degree of activity and of stability than those that use our previous ligands. Substrates that were not amenable to Pd catalysis previously are reexamined using this new catalyst system, and excellent results are obtained.
by Xiaohua Huang.
Ph.D.
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Raghuvanshi, Keshav. "Ruthenium(II)-Catalyzed C-N, C-O and C-C Formations by C-H Activation." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2017. http://hdl.handle.net/11858/00-1735-0000-002B-7D4C-2.

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Voigtländer, David. "Neue Platin-katalysierte C-C- und C-O-Verknüpfungsreaktionen." [S.l. : s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=961741740.

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Qian, Xin. "Cobalt-Catalyzed C-C and C-N Coupling reactions." Phd thesis, Ecole Polytechnique X, 2013. http://pastel.archives-ouvertes.fr/pastel-00943479.

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Ce travail de these a permis le déveloippement de nouvelles reactions de couplage catalysées par des sels de cobalt(II) Le premier chapitre décrit l'allylation cobalta catalysée d'halogénures d'alkyles. La méthode est facile à mettre en œuvre, efficace avec une grande variété d'halogénures d'alkyes et des acétates ou carbonates d'allyle substitués. Les rendements vont de bons à excellents et la tolérance fonctionnelle élevée. Dans le cas d'acétates d'allyle substitués le produit linéaire est obtenu majoritairement ou exclusivement. Quelques expériences ont permis de mettre en lumière la formation d'espèce radicalaire lors du cycle catalytique. Les premiers essais pour étendre cette méthodologie aux couplages allyle-allyle et alkyle-alkyle sont également décrits. Le deuxième chapitre porte sur l'amination catalysée au cobalt d'organozinciques fonctionnalisés en utilisant des N-chloroamines. La procédure est simple et générale et demande des conditions plus douces que celles précédemment décrite, tout en tolérant un très large éventail de substrats, avec une bonne tolérance à de nombreux groupes fonctionnels. Les premiers essais pour étendre la méthodologie à la réaction entre un organozincique et une source électrophile de soufre en vue de former des liaisons C-S sont également exposés. Enfin le dernier chapitre décrit la réaction d'organozinciques engendrés par catalyse au cobalt avec une source " verte " de cyanure électrophile, N-cyano-N-phenyl-p-methyl-benzenesulfonamide (NCTS), pour conduire avec de bons rendements aux arylnitriles correspondants. Des sources analogues de CN+ ont également été testées.
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Luyten, Marcel Andre. "Zur Synthese von (c,c,c,t)-[5.5.5.5]Fenestran /." [S.l : s.n.], 1985. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

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Liu, Weiping. "Ruthenium- and Manganese-Catalyzed C−O and C−C Formation via C−H Activation." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2016. http://hdl.handle.net/11858/00-1735-0000-0028-8771-3.

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Fabris, Massimo <1980&gt. "Innovative green methodologies for C-C, C-N and C-O bond forming reactions." Doctoral thesis, Università Ca' Foscari Venezia, 2011. http://hdl.handle.net/10579/1096.

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In questo lavoro di tesi è riportato l'impiego di alcuni strumenti della Green Chemistry (come la CO2, i liquidi ionici e i dialchilcarbonati) per la messa a punto di metodologie innovative a ridotto impatto ambientale per la formazione di legami C-C, C-N e C-O. Sono state investigate le seguenti reazioni: la metatesi dell'1-ottene catalizzata da sistemi a base di Re ossido, in presenza di CO2 densa come solvente; l'addizione di Michael di nitroalcani e beta-dichetoni a chetoni alfa,beta-insaturi catalizzata da liquidi ionici; la selettiva mono-idrossialchilazione di aniline con la glicerina carbonato, catalizzata da faujasiti; la selettiva bis-N-alchilazione di aniline da parte del dimetilcarbonato prodotto in situ via transesterificazione di carbonati ciclici con metanolo, catalizzata da faujasiti; l'alchilazione di aniline con carbonati ciclici catalizzata da liquidi ionici; la reazione di decarbossilazione dei dialchilcarbonati in presenza di diversi catalizzatori eterogenei; la reazione tra fenolo e glicerina carbonato catalizzata da faujasiti.
In this PhD thesis it is presented the use of some Green Chemistry Tools (supercritical carbon dioxide, ionic liquids and dialkylcarbonates) for the set up of new green methodologies for C-C, C-N and C-O bond forming reactions. The following reactions have been investigated: the self-metathesis of 1-octene catalysed by supported Re oxide systems, carried out using dense CO2 as solvent; the Michael addition of nitroalkanes and beta-diketones to alpha,beta-unsaturated ketons catalyzed by task specific phosphonium based ionic liquids; the selective mono-hydroxyalkylation of anilines with glycerol carbonate catalysed by alkali metal exchanged faujasites; the selective bis-N-methylation of anilines carried by dimethylcarbonate prepared in situ via the transesterification of alkylene carbonate with methanol catalysed by alkali metal exchanged faujasites; the alkylation of primary aromatic amines with alkylene carbonates, catalysed by phosphonium based ionic liquids; the decarboxylation reaction of dialkyl carbonates catalyzed by different heterogeneous systems; the reaction of glycerol carbonate with phenol, in the presence of faujasites as catalysts.
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Pagès, Lucas. "Hydrofonctionnalisation d'allénamides terminaux par catalyse au cuivre : formation de liaisons C-C, C-S, C-P et C-O." Electronic Thesis or Diss., Montpellier, Ecole nationale supérieure de chimie, 2022. http://www.theses.fr/2022ENCM0017.

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L'objectif de la thèse consiste à découvrir de nouveaux procédés économiques, non toxiques et non polluants pour réaliser la synthèse de molécules à haute valeur ajoutée (dans le domaine de la pharmacie et des matériaux), à partir de molécules de départ simple pouvant éventuellement être issues directement du monde végétal. Ces nouveaux procédés feront principalement appel à la catalyse homogène et à des catalyseurs métalliques peux coûteux et peu toxiques à base par exemple de cuivre (les méthodes que ces nouveaux procédés sont destinés à remplacer font en général appel à des catalyseurs très coûteux et très toxiques à base de palladium et de ligands sophistiqués). Les recherches reposeront sur l'expertise de l'équipe d'accueil dans le domaine l'hydrofonctionnalisation1 de liaisons insaturées (dont l'hydroamination) ainsi que dans celui de l'arylation de nucléophiles carbonés, oxygénés ou azotés,2 par catalyse au cuivre (formation de liaisons C-C et C-hétéroatome). Le projet comportera une partie méthodologie de synthèse ainsi qu'une partie d'étude mécanistique très poussée sur les systèmes catalytiques découverts (RMN, études cinétique, isolation de complexes métalliques intermédiaires, calculs DFT). L'application et le transfert vers le milieu industriel, domaine dans lequel l'équipe a une très grande expérience, seront alors ensuite envisagés et mis en œuvre s'il y a lieu. 1. a) Chem. Comm, 2015, 51, 11210. b) Org. Lett. 2015, 17, 1224. c) Org. Lett. 2016, 18, 1482. d) Adv. Sytnh. Cat., 2017, 349, 4388. e) ACS. Catal. 2017, 7, 425. f) Org. Lett. 2018, 20, 223. g) Synthesis, 2019, 51, 1225. 2. a) Angewandte Chemie, 2007, 46(6), 934. b) Angew. Chem. Int. Ed. 2009, 48, 337. c) Angew. Chem. Int. Ed. 2009, 48, 6954. d) Angew. Chem. Int. Ed. 2009, 48, 8725. d) Angew. Chem. Int. Ed. 2012, 51, 12815. e) Chem. Comm, 2013, 49, 7412. f) Angewandte Chemie, 2015, 54, 1058. g) Angewandte Chemie, 2016, 55, 3785
One of the main objective of the thesis is to discover new economic, non-toxic and non-polluting processes for the synthesis of targets with high added value (in the field of pharmacy and materials), starting from simple starting molecules (possibly issues from the plant world). These new processes will mainly use homogeneous catalysis and inexpensive and low-cost metal catalysts based for example on copper (the methods that these new processes are intended to replace generally make use of very expensive and highly toxic palladium based catalysts and sophisticated ligands). The research will be based on the expertise of the host team in the field of hydrofunctionalization (ref 1) of unsaturated bonds (including hydroamination) as well as in the arylation of carbon, oxygenated or nitrogenous nucleophiles (ref 2) by copper catalysis (formation of C-C and C-heteroatom bonds). The project will include a synthesis methodology part as well as a very advanced mechanistic study of the discovered catalytic systems (NMR, kinetic studies, isolation of intermediate metal complexes, DFT calculations). Application and transfer to industry, where the team has a great deal of experience, will then be considered and implemented if necessary. 1. a) Chem. Comm, 2015, 51, 11210. b) Org. Lett. 2015, 17, 1224. c) Org. Lett. 2016, 18, 1482. d) Adv. Sytnh. Cat., 2017, 349, 4388. e) ACS. Catal. 2017, 7, 425. f) Org. Lett. 2018, 20, 223. g) Synthesis, 2019, 51, 1225. 2. a) Angewandte Chemie, 2007, 46(6), 934. b) Angew. Chem. Int. Ed. 2009, 48, 337. c) Angew. Chem. Int. Ed. 2009, 48, 6954. d) Angew. Chem. Int. Ed. 2009, 48, 8725. d) Angew. Chem. Int. Ed. 2012, 51, 12815. e) Chem. Comm, 2013, 49, 7412. f) Angewandte Chemie, 2015, 54, 1058. g) Angewandte Chemie, 2016, 55, 3785
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Hu, Ying. "C/C++ preprocessing directive analysis." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/MQ65583.pdf.

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Cáceres, Salazar Jorge Cristián, and Acuña Patricio Carreño. "C&C Power Technologies." Tesis, Universidad de Chile, 2015. http://repositorio.uchile.cl/handle/2250/137038.

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Tesis para optar al grado de Magíster en Administración (MBA)
Jorge Cáceres Salazar [Parte I], Patricio Carreño Acuña [Parte II]
Patricio Carreño Acuña [Parte II],no envía autorización para acceso a texto completo de su documento.
El presente trabajo consiste en el desarrollo de un plan de negocio para la empresa C&C Power Technologies, cuyo giro corresponde a la provisión de servicios energéticos con el objetivo de aumentar los niveles de eficiencia energética de sus clientes, esto en base a un modelo de negocio ESCO, cuya sigla en inglés significa Energy Services Company. Dentro de la industria de servicios energéticos, las empresas que operan bajo el modelo ESCO se caracterizan principalmente por dirigir íntegramente un proyecto de eficiencia energética en las instalaciones del cliente, incluyendo una auditoría energética, propuestas técnicas, propuestas de financiamiento, instalación y mantenimiento de equipamiento tecnológico y monitoreo de ahorros energéticos logrados. Este modelo de negocio se caracteriza por crear una relación a largo plazo con el cliente, donde los servicios son pagados durante años a través del ahorro monetario generado en base al mayor ahorro energético logrado en los procesos productivos de los clientes. Bajo este modelo de negocios, el cliente normalmente transfiere los riesgos técnicos y financieros a C&C Power Technologies. En relación al sector servicios energéticos a la cual pertenece C&C Power Technologies, este se encuentra inmersa en un contexto en donde los desafíos en el ámbito de la energía a nivel nacional son relevantes. A nivel país estamos frente a múltiples y complejos retos que exigen soluciones eficientes: el crecimiento en la demanda de energía, la dependencia energética, el cambio climático y la expansión del sistema eléctrico, entre otros. Frente a todos estos desafíos, la eficiencia energética surge como una solución factible y sustentable para nuestro país. Al respecto, muchas empresas han comenzado a responder a esta necesidad en dicho ámbito, es así como se ha ido consolidando la industria de servicios energéticos, cuyos esfuerzos se han orientado en alcanzar mayores niveles de eficiencia energética en los diversos rubros económicos. De esta forma, la eficiencia energética es parte de la solución, ya que disminuye el consumo de energía del país, reduce la dependencia de los energéticos importados, aumenta la seguridad de suministro y disminuye las emisiones de gases efecto invernadero. Adicionalmente, contribuye a incrementar la competitividad del país, al haber menores costos de producción. La idea de desarrollar este proyecto nace fundamentalmente como una respuesta a necesidades concretas al interior de las empresas, particularmente en relación al alza sostenido del precio de las distintas fuentes energéticas, lo cual incide directamente en la necesidad de las empresas para bajar sus costos productivos, así como también a la necesidad de lograr mayores niveles de responsabilidad social empresarial, mediante la menor emisión de elementos contaminantes hacia el medioambiente. Los servicios que C&C Power Technologies pretende comercializar en el mercado son: i) auditorías energéticas; ii) consultorías en eficiencia energética, e; iii) implementación de proyectos de eficiencia energética. El modelo de negocios que se quiere implementar en C&C Power Technologies va más allá de limitarse a entregar un diagnóstico energético a sus clientes tal como lo hace la mayor parte de las empresas consultoras en el ámbito de la eficiencia energética establecidas en el país. Este modelo ofrece soluciones prácticas y con un alto valor agregado dado que se ofrece llevar a cabo la dirección integra de proyectos de eficiencia energética, asegurando resultados en términos de ahorros energéticos a ser logrados. Es por esto que el modelo de negocios de C&C Power Technologies posee un mayor atractivo en relación a otros tipos de proyectos que en la actualidad se comercializan en el ámbito de la eficiencia energética, en donde la implementación y monitoreo de los resultados finalmente queda a cargo del cliente. Dentro del plan financiero, se da a conocer el VAN esperado de la empresa, el cual asciende a $418.820.330 (TIR 75,2%). Mediante una simulación de escenarios se demuestra un significativo nivel de sensibilidad del VAN sujeto al cambio en el número de servicios comercializados por la empresa durante los próximos diez años, lo cual da cuenta de que el negocio tiene un nivel de riesgo medio/alto.
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Books on the topic "C.020.673.440"

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Павловская, Т. А. C/C++. Москва; Санкт-Петербург: Питер, 2006.

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Jamsa, Kris A. Jamsa's C/C++/C# programmer's bible: The ultimate guide to C/C++/C# programming. 2nd ed. [Las Vegas, NV]: Onword Press, 2002.

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Holub, Allen I. C ⁺ C++: Programming with objects in C and C++. New York: McGraw-Hill, 1992.

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Damberger, Arno. C/C++ Werkzeugkasten. Wiesbaden: Vieweg+Teubner Verlag, 1994. http://dx.doi.org/10.1007/978-3-322-83067-8.

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Hoch, Thomas, and Gerd Küveler. C/C++ anwenden. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2.

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Кораблев, В. C и C++. Киев: BHV, 2002.

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Hoch, Thomas, and Gerd Küveler. C/C++ anwenden. Wiesbaden: Springer Fachmedien Wiesbaden, 2023. http://dx.doi.org/10.1007/978-3-658-38093-9.

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Steig, William. C D C? New York: Farrar, Straus & Giroux, 1986.

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Steig, William. C D C? New York: Farrar Straus Giroux, 2003.

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Steig, William. C D C? New York: Farrar, Straus & Giroux, 1986.

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Book chapters on the topic "C.020.673.440"

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Speel, Erika. "C." In Dictionary of Enamelling, 18–36. London: Routledge, 2018. http://dx.doi.org/10.4324/9780429458576-c.

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Manutchehr-Danai, Mohsen. "C c." In Dictionary of Gems and Gemology, 67–122. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-04288-5_3.

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Hoch, Thomas, and Gerd Küveler. "Prozessüberwachung." In C/C++ anwenden, 3–7. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2_1.

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Hoch, Thomas, and Gerd Küveler. "Kondensator/Tiefpass (Objektorientierung)." In C/C++ anwenden, 83–88. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2_10.

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Hoch, Thomas, and Gerd Küveler. "GrafObjectServer (Objektorientierte Grafik-Programmierung)." In C/C++ anwenden, 91–100. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2_11.

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Hoch, Thomas, and Gerd Küveler. "Ebenes Pendel." In C/C++ anwenden, 101–9. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2_12.

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Hoch, Thomas, and Gerd Küveler. "Zeigeruhr (Objektorientierte Version)." In C/C++ anwenden, 111–19. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2_13.

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Hoch, Thomas, and Gerd Küveler. "Wärmeleiter." In C/C++ anwenden, 121–30. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2_14.

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Hoch, Thomas, and Gerd Küveler. "Multifunktionsplotter." In C/C++ anwenden, 131–50. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2_15.

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Hoch, Thomas, and Gerd Küveler. "Bitoperationen mit C/C++." In C/C++ anwenden, 153–67. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-22165-2_16.

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Conference papers on the topic "C.020.673.440"

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Edmonds, Ernest Alan. "C&C Past, Present and Future." In C&C '21: Creativity and Cognition. New York, NY, USA: ACM, 2021. http://dx.doi.org/10.1145/3450741.3467473.

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Spence, Jocelyn, Boriana Koleva, Martin Flintham, Emily Thorn, Kevin Glover, Rebecca Gibson, Steven David Benford, Hyosun Kwon, Dimitrios Paris Darzentas, and Hanne Gesine Wagner. "C&C Festival of Hybrid Gifting." In C&C '23: Creativity and Cognition. New York, NY, USA: ACM, 2023. http://dx.doi.org/10.1145/3591196.3593052.

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Maver, Tom. "Session details: Keynote Address 1." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/3247463.

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Kerne, Andruid A., and David Shamma. "Session details: Paper Session 1: Textiles and Objects (4 papers)." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/3247464.

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Odom, Will. "Session details: Paper Session 2: Tools and Interfaces (4 papers)." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/3247465.

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Webb, Andrew. "Session details: Paper Session 3: Finding (2 papers 2 notes)." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/3247466.

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Maver, Tom. "Session details: Keynote Address 2." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/3247467.

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Latulipe, Celine. "Session details: Paper Session 4: Moments and Movements (4 papers)." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/3247468.

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Bailey, Brian, and Erin Cherry. "Session details: Posters and Demos Session 1." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/3247469.

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Bailey, Brian, and Erin Cherry. "Session details: Posters and Demos Session 2." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/3247470.

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Reports on the topic "C.020.673.440"

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Gland, J. L. Hydrogen induced C-C, C-N, and C-S bond activation on Pt and Ni surfaces. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10102894.

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Gland, J. L. Hydrogen induced C-C, C-N, and C-S bond activation on Pt and Ni surfaces. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6915688.

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Gland, J. L. Hydrogen Induced C-C, C-N, & C-S Bond Activation on Pt & Ni Surfaces. Office of Scientific and Technical Information (OSTI), July 2004. http://dx.doi.org/10.2172/830711.

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Gland, J. L. [Hydrogen induced C-C, C-N, and C-S bond activities on Pi and Ni surfaces]: Summary. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/10110807.

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AIR FORCE LIFE CYCLE MGMT CENTER. C-130J Hercules Transport Aircraft (C-130J). Fort Belvoir, VA: Defense Technical Information Center, December 2013. http://dx.doi.org/10.21236/ada614735.

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Wuosmaa, A. H., R. R. Betts, and M. Freer. Angular correlation measurements for {sup 12}C{sup 12}C,{sup 12}C{sup 12}C 3{sup -} scattering. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/166299.

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Hara, F. T., J. H. Kaye, R. T. Steele, R. W. Stromatt, D. L. Thomas, and M. W. Urie. SST Sample Characterization Analysis of Archive Samples 102-C, 105-C, and 106-C. Office of Scientific and Technical Information (OSTI), April 1990. http://dx.doi.org/10.2172/1086603.

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Thomas, D. L., F. T. Hara, J. H. Kaye, R. T. Steele, R. W. Stromatt, and M. W. Urie. SST Sample Characterization Analysis of Archive Samples 102-C, 105-C, and 106-C. Office of Scientific and Technical Information (OSTI), February 1991. http://dx.doi.org/10.2172/1086605.

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Stocks, G. M., A. M. Boring, D. M. Nicholson, F. J. Pinski, D. D. Johnson, J. S. Faulkner, and G. L. Gyorffy. Self-consistent electronic structure of alpha-phase Hume-Rothery electron compound alloys Cu/sub c/Zn/sub 1-c/, Cu/sub c/Ga/sub 1-c/, and Cu/sub c/Ge/sub 1-c/. Office of Scientific and Technical Information (OSTI), January 1985. http://dx.doi.org/10.2172/5276443.

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Widener, K., and N. Bharadwaj. C-Band Scanning ARM Precipitation Radar (C-SAPR) Handbook. Office of Scientific and Technical Information (OSTI), November 2012. http://dx.doi.org/10.2172/1054629.

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