Academic literature on the topic '2-N'

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Journal articles on the topic "2-N"

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Ananda Mohan, P. V. "Reverse Converters for the Moduli Set { $$2^{n}, 2^{n-1}-1,2^{n}-1, 2^{n+1}-1\}(n\,\hbox {Even})$$ 2 n , 2 n - 1 - 1 , 2 n - 1 , 2 n + 1 - 1 } ( n Even )." Circuits, Systems, and Signal Processing 37, no. 8 (December 5, 2017): 3605–34. http://dx.doi.org/10.1007/s00034-017-0725-0.

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Tarasova, Ol'ga A., Ludmila V. Klyba, Vladimir Yu Vvedensky, Nina A. Nedolya, Boris A. Trofimov, Lambert Brandsma, and Hermann D. Verkruijsse. "One-Pot Syntheses of 2-N-Alkylamino-, 2-N-Phenylamino-, 2-N, N-Dialkylamino-, and 2-N-Alkyl-N-phenylaminothiophenes." European Journal of Organic Chemistry 1998, no. 2 (February 1998): 253–56. http://dx.doi.org/10.1002/(sici)1099-0690(199802)1998:2<253::aid-ejoc253>3.0.co;2-e.

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Noorimehr, Mohammad Reza, Mehdi Hosseinzadeh, and Keivan Navi. "Efficient Reverse Converters for 4-Moduli Sets {2 $$^{2n-1}-1$$ 2 n - 1 - 1 , 2 $$^{n}$$ n , 2 $$^{n}+1$$ n + 1 , 2 $$^{n}-1$$ n - 1 } and {2 $$^{2n-1}$$ 2 n - 1 , 2 $$^{2n-1}-1$$ 2 n - 1 - 1 , 2 $$^{n}+1$$ n + 1 , 2 $$^{n}-1$$ n - 1 } Based on CRTs Algorithm." Circuits, Systems, and Signal Processing 33, no. 10 (April 29, 2014): 3145–63. http://dx.doi.org/10.1007/s00034-014-9798-1.

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Gao, Yang, Rui Wang, Jiehong Lei, Yu Zhu, Danhui Li, Lei Zhang, Weiyu Xie, and Zhigang Wang. "Fully Active Nitrogen Energetic Chains Mg 2 (N 5 ) 2 N 2 [Mg 2 (N 5 ) 2 N 2 ] n under Ambient Conditions." Advanced Theory and Simulations 4, no. 5 (March 25, 2021): 2000283. http://dx.doi.org/10.1002/adts.202000283.

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Rompel, Annette, Andrew D. Bond, and Christine J. McKenzie. "N-Methyl-N-(2-pyridiniomethyl)-2-[N-(2-pyridiniomethyl)methylamino]-N-(2-pyridylmethyl)ethanaminium tris(perchlorate)." Acta Crystallographica Section E Structure Reports Online 60, no. 11 (October 9, 2004): o1987—o1988. http://dx.doi.org/10.1107/s1600536804025103.

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Michels, Janel T., Briana G. O'Malley, Eric L. Klein, Lei Yang, Andreas Grohmann, and Robert P. Houser. "2-Methyl-N,N′-bis[2-(methylsulfanyl)ethyl]-2-(2-pyridyl)-N,N′-ditosylpropane-1,3-diamine." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (October 27, 2005): o3834—o3836. http://dx.doi.org/10.1107/s1600536805033726.

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Balalaie, Saeed, Yaghoub Haghighatnia, Frank Rominger, and Vahid Amani. "N-[2-(N-Cyclohexylcarbamoyl)propan-2-yl]-N-(2-iodophenyl)prop-2-ynamide." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (January 7, 2012): o272. http://dx.doi.org/10.1107/s1600536811055140.

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De Maré, George R., Niny Z. Rao, and Charles W. Bock. "The structure and C C vibrational frequencies of the all- trans polyenes C 2 n H 2 n +2 ( n = 2 − 15), C 2 n H 2 n (Me) 2 ( n = 2 – 13), and C 2 n H 2 n ( tert -Butyl) 2 ( n = 2 – 5): Computational results." Chemical Data Collections 11-12 (December 2017): 25–35. http://dx.doi.org/10.1016/j.cdc.2017.07.005.

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TARASOVA, O. A., L. V. KLYBA, V. YU VVEDENSKY, N. A. NEDOLYA, B. A. TROFIMOV, L. BRANDSMA, and H. D. VERKRUIJSSE. "ChemInform Abstract: One-Pot Syntheses of 2-N-Alkylamino-, 2-N-Phenylamino-2-N,N-dialkylamino-, and 2-N-Alkyl-N-phenylaminothiophenes." ChemInform 29, no. 23 (June 22, 2010): no. http://dx.doi.org/10.1002/chin.199823111.

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Tadee, Suton. "On the Diophantine Equations (n + 2)x - 2.n y = z 2 and (n + 2)x + 2.n y = z 2." Annals of Pure and Applied Mathematics 27, no. 01 (2023): 19–22. http://dx.doi.org/10.22457/apam.v27n1a04899.

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In this article, we solve the Diophantine equations (n + 2)x - 2.n y = z 2 and (n + 2)x + 2.n y = z 2 , where x, y, z are non-negative integers and n is a positive integer with n ≡ 2 or n ≡ 3 (mod 4).
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Dissertations / Theses on the topic "2-N"

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Bermúdez, Hermida Marta Maria. "Estudio Estructural de nylons N, 2/N y N,N+2." Doctoral thesis, Universitat Politècnica de Catalunya, 1998. http://hdl.handle.net/10803/6459.

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El trabajo realizado en la Tesis tiene como objetivo general el estudio estructural de nylons fundamentalmente mediante la difracción de rayos-x y la microscopía electrónica. Los nylons estudiados se agrupan en tres familias:

a) Nylons n con elevado número de metilenos: nylon 12 y nylon 16. El nylon 16 ha sido sintetizado y caracterizado por primera vez.

b) Nylons 2/n: nylon 2/12 y nylon 2/16. Síntesis y caracterización de ambos productos siguiendo el método general de síntesis de nylons 2/n.

c) Nylons (n, n+2): Nylons 4,6, 6,8, 8,10 3,5 y 5,7. Se ha realizado la síntesis de todos ellos excepto del nylon 4,6 el cuál se ha estudiado a partir de una muestra comercial (DSM, Holanda).

Se han determinado las condiciones experimentales apropiadas para la preparación selectiva de las formas alfa y del nylon 12 en monocristales y películas. Los datos cristalográficos registrados para la fase y están en total acuerdo con la estructura descrita en la literatura. Los datos obtenidos para la fase alfa nos llevan a proponer para
esta forma una estructura triclínica basada en un modelo de empaquetamiento de láminas progresivo.

Se ha llevado a cabo la síntesis del nylon 16 mediante policondensación térmica del ácido 16- aminohexadecanoico y efectuado su caracterización físico química. Presenta una Tf de 164 C. El análisis estructural se ha realizado sobre cristales crecidos en disolución y se determina una forma y.

Se han sintetizado las copoliamidas 2/12 y 2/16 por condensación de ésteres activos y posterior postpolicondensación en estado sólido. Presentan Tf a 230 y 215 C respectivamente. El nylon 2/12 presenta dimorfismo mientras que en el 2/16 sólose ha observado la forma II; la forma II tiene una estructura pseudohexagonal con cadenas en conformación de hélices 6 y puentes de hidrógeno dirigidos en tres direcciones a 120 ; la forma I es minoritaria y sólo se observa bajo condiciones especiales.
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de, lechtenf@itp uni-hannover. "N=(2$|$2) Supersymmetric Toda Lattice Hierarchy in N=(2$|$2) Superspace." J. Nonlinear Math. Phys. 8 (2001) 183-195, 2000. ftp://ftp.esi.ac.at/pub/Preprints/esi913.ps.

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Nigond, Laurence. "Propriétés extractantes des N,N,N',N'-tétraalkyl, alkyl-2, propanediamides-1,3 /." Gif-sur-Yvette : Commissariat à l'énergie atomique, 1992. http://catalogue.bnf.fr/ark:/12148/cb35549711h.

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Vinhato, Elisângela. "Análise conformacional das 2-feniltio, 2-fenilsulfinil e 2-fenilsulfonil-N,N-dietilacetamidas e 2-feniltio, 2-fenilsulfinil e 2-fenilsulfonil-cicloexanonas 4\'-substituídas." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-10062008-141011/.

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A presente tese trata da síntese e a análise conformacional de seis séries de compostos: 2-feniltioN;N-dietilacetamidas 4\'-substituídas (I); 2-fenilsulfinil-N,N-dietilacetamidas 4\'-substituídas (II); 2-fenilsulfonil-N,N-dietilacetamidas 4\'-substituídas (III); 2-feniltio-cicloexanonas 4\'-substituídas (IV); 2-fenilsulfonil-cicloexanonas 4\'-substituídas (V); 2-fenilsulfinil-cicloexanonas 4\'substituídas (IV). O estudo conformacional foi realizado por intermédio das espectroscopias no IV e RMN de hidrogênio, apoiados por cálculos teóricos. A análise de vCO no infravermelho para as séries I, II e III, de forma geral, se correlaciona bem com os cálculos em HF e B3LYP os quais demonstram a ocorrência de duas conformações estáveis para os compostos da série (I), tendo o confôrmero gauche mais estável em relação ao confôrmero cis. O efeito dos substituintes da série (I), observado experimentalmente, é mais concordante com os resultados calculados em B3LYP do que em HF. Com relação à série (II), há apenas uma conformação estável, ou seja, a cis, no gás e em solventes de diferentes polaridades. A série (III) apresentou a existência de três conformações estáveis, sendo duas conformações gauche de maior estabilidade que a terceira conformação cis (no gás e no solvente de baixa polaridade: CCl4). Nas séries das cicloexanonas (IV, V e VI) a análise de vCO no infravermelho e RMN de hidrogênio apresentou a conformação axial como preferencial em CCl4, sendo que esta preferência passou para equatorial em CH3CN (CD3CN). Os cálculos ab initio (HF) reproduziram o resultado experimental em CCl4, apenas para os derivados 2-fenilsulfonil-cicloexanonas 4\'-substituídas (V). Por outro lado, para estas cicloexanonas (IV - VI) os cálculos em B3LYP estão mais concordantes com os dados experimentais. O método NBO (Natural Bond Orbital) confirmou que as conformações gauche das séries (I, II e III) são estabilizadas por pelas interações: nN/π*C=O, πC=O/σ*C-S, σC-S/π*C=O, n(S)/π*C=O, π*C=O/σ*C-S, e as séries (IV, V e VI) pelas interações πC=O/σ*C-S, σC-S/π*C=O, n(S)/π*C=O, π*C=O/σ*C-S. Em contraste, estes resultados de NBO demonstraram também a importância das interações: nO(CO)/σC-S, nO(CO)/σ*S-O e nO(CO)/σ*C-H para a estabilização da conformação cis. Adicionalmente, a análise das cargas calculadas sugeriu a participação de interações Coulombicas na estabilização das conformações cis e gauche. Para todas as séries de compostos (I - VI), os cálculos incluindo o efeito do solvente (Onsager e PCM), para alguns compostos representativos, facilitaram a atribuição de cada conformação em solução.
This thesis reports the synthesis and conformational analysis of six sedes of compounds: N,N diethyl-2-[( 4-substituted)phenylthio] acetamides (I); N,N-diethyl-2-[(4-substituted)phenylsulfinyl] acetamides (II); N,N-diethyl-2-[(4-substituted)phenylsulfonyl] acetamides (III); [4 = OMe, Me, H, Cl, Br and N02]; 2-[(4-substituted)phenylthio] cyclohexanones (IV); 2-[(4-substituted)phenylsulfonyl] cyclohexanones (V) and 2-[(4-substituted)phenylsulfinyl] cyclohexanones (VI), [4 = OMe, H and N02]. The conformational study was performed through the IR and 1H NMR spectroscopies, supported by theoretical calculations. The vCO infrared analysis for the series I, II and III in general matches well with the HF and B3LYP calculations which showed the occurrence of two stable conformations for compounds of series (I), being the gauche the most stable and the cis the second one. As for the substituent effect of series (I), the agreement between the experimental results with B3LYP is better than with HF. calculations. Considering the serries (II), there is only one stable conformation, the cis one, in gas and in solvents of different polarity. The series (III) showed the existence of three stable conformations, being the two gauche the most stable and the cis the least stable (both in the gas and in the low polarity solvent, CCl4). In the cyclohexanones series (IV, V and VI) the vCO infrared and 1H NMR analyses showed a preference for the axial conformation, in CCl4, changing the preference to equatorial one in CH3CN (CD3CN). The ab initio (HF) calculations reproduced the experimental preference, in CCl4, for the 2-[(4-substituted)phenylsulfonyl] cyclohexanones only. On the other hand, for these cyclohexanones (IV-VI) the B3LYP calculations improved the agreement with the experimental data. The NBO (Natural Bond Orbital) method confirmed that the gauche conformations of the series (I, II and III) are stabilized by: nN/π*C=O, πC=O/σ*C-S, σC-S/π*C=O, n(S)/π*C=O, π*C=O/σ*C-S, and for the series (IV, V and VI) by the interactions: πC=O/σ*C-S, σC-S/π*C=O, N(S)/π*C=O, π*C=O/σ*C-S. In contrast these NBO results also revealed the importance of the interactions nO(CO)/σ*C-S, nO(CO)/σ*S-O and nO(CO)/σ*C-H for the stabilization of the cis conformation. Additionally, the calculated charge analysis suggested the stabilization of both cis and gauche conformations due to Coulombic interactions. The inclusion of the solvent effect in the computations (Onsager and PCM methods) for some representative compounds of series (I-VI) facilitated the conformer attribution in solution.
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Duffy, Kirby Timothy Hennessy. "N metabolism and its effects on N¦2 fixation, CO¦2 and O¦2 exchange in legumes." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ36024.pdf.

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Sauthier, Mathieu. "1,2-diiminophosphoranes et 2-'2-pyridyl)phospholes : : nouveaux ligands N,N et P,N pour la catalyse homogène." Rennes 1, 2001. http://www.theses.fr/2001REN10040.

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Nous décrivons la synthèse de nouveaux ligands N,N chiraux : les 1,2-diiminophosphoranes. La chimie de coordination de ces ligands dépend de la nature du squelette carboné. Leur utilisation pour la réaction de substitution allylique catalysée par le palladium a permis d'obtenir de bons excès énantiomériques. Ils ont été utilisés pour la préparation de complexes de nickel qui s'avèrent être des catalyseurs très actifs pour la réaction d'oligomérisation de l'éthylène. Nous avons également préparé de nouveaux ligands mixte P,N : les 2-(2-pyridyl)phospholes. Ces composés se comportent comme des chélates vis à vis du palladium et du ruthénium. Les complexes cationiques du palladium sont actifs pour la copolymérisation éthylène-monoxyde de carbone. Les 2,5-di(2-pyridyl)phospholes possèdent une chimie de coordination très originale et conduisent à la formation de systèmes bimétalliques possédant une phosphine pontante symétrique.
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Jünemann, Klaus. "Symmetrien des N=2 Strings." [S.l. : s.n.], 1999. http://deposit.ddb.de/cgi-bin/dokserv?idn=956853765.

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Klemm, Hanno. "N=2 superconformal boundary states." Thesis, King's College London (University of London), 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.423078.

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Cerda, Cavieres Christopher David. "Síntesis de Derivados N-Benzoil-2-(2-Nitrofenil)-1-Hbenzimidazoles. Desarrollo de Metodologías Analíticas y Caracterización Fisicoquímica de N-(p-Flúor)-Benzoil-2-(2-Nitrofenil)-Benzimidazol y N-(p-Nitro)-Benzoil -2-(2 Nitrofenil)-Benzimidazol." Tesis, Universidad de Chile, 2008. http://repositorio.uchile.cl/handle/2250/105700.

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La presente Memoria se orientó al estudio y caracterización electro-analítica de una serie de derivados N-(4-R-benzoil)-2-(2-nitrofenil)-1-H-benzimidazoles como sustratos de interés biológico. Los compuestos estudiados fueron sintetizados a partir de 2-(o-nitrofenil)-benzimidazol, generado por condensación entre 1,2-diamino-benceno y 2-nitrobenzaldehído. Posterior reacción del benzimidazol con una serie de cloruros de aroílo, generó la serie de cuatro N-(4-R-benzoil)-2-(2-nitrofenil)-1-H-benzimidazoles en buen rendimiento (R = NO2, Cl, F), con la excepción del producto denominado PMNB (R = OCH3), que obtuvo un rendimiento promedio de un 5%. Los estudios analíticos posteriormente a la síntesis, fueron desarrollados para los compuestos denominados PNB (R= NO2) y PFNB (R= F) y correspondieron al desarrollo y la puesta punto de metodologías analíticas reproducibles y selectivas, y su posterior aplicación en la caracterización de éstos. Dichos estudios se llevaron a cabo usando las técnicas de polarografía de pulso diferencial (PPD), polarografía tast (PTAST), espectrofotometría UV-Vis y cromatografía líquida de alta eficiencia (HPLC). En una primera etapa se llevó a cabo el estudio de influencia del pH por PPD y PTAST, el que por razones de estabilidad fue realizado en un rango de pH entre 2,0 hasta 8,2 para ambos compuestos. En este rango de pH, PFNB y PNB exhibieron dos y tres señales de reducción respectivamente: una señal principal (dos en el caso de PNB) debida a la reducción del grupo nitro y una secundaria, probablemente correspondiente al enlace azometino presente en el anillo benzimidazólico. Ambas señales son dependientes de pH, desplazándose hacia potenciales más negativos mientras más alcalino es el pH. En una segunda etapa se desarrollaron tres metodologías analíticas para la cuantificación de los compuestos en estudio (PPD, HPLC y espectrofotometría UV-Vis), las cuales exhibieron valores adecuados de reproducibilidad (CV< 4,5%) y repetibilidad (CV< 4%), presentando linealidad en un amplio rango de concentración (4,0×10-6 M a 1,0×10-4 M) para ambos compuestos. Por espectrofometría UV-Vis se determinaron las constantes de acidez para cada compuesto, debidas al nitrógeno ubicado en la posición 3 del anillo imidazólico, en ambos casos. Los valores de pKa determinados fueron de 4,79 ± 0,06 para PNB y 4,86 ± 0,06 para PFNB. Utilizando la técnica de HPLC se determinaron los coeficientes de partición respectivos, presentando valores de log P de 2,77 para PNB y de 3,18 para PFNB. Además, por medio de la técnica de PPD se llevó a cabo un estudio preliminar de estabilidad para PNB a pH 3,0 y a temperatura ambiente, observándose que el decaimiento se ajusta a una cinética de seudo orden cero (k= 1,9571×10-7 M/min), con una vida media de alrededor de 4 horas para una concentración inicial de 1×10-4 M.
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Gourmelen, Stéphane. "Théories superconformes d = 2, N = 2 et superalgèbres w." Lyon 1, 1997. http://www.theses.fr/1997LYO10360.

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L'etude des theories (super) conformes en dimension 2 se situe a la croisee de deux grands domaines de la physique theorique: l'invariance conforme et la supersymetrie. Leur champ d'applications touche a divers sujets: theories de (super) cordes, phenomenes critiques, systemes integrables, (super) algebres w. Nous traitons des extensions supersymetriques n = 2 des theories conformes dans un formalisme non metrique. Les supersurfaces de riemann (ssr) de type (2,0) et (2,2) sont definies et leurs structures complexes parametrees par des superchamps de beltrami. Definie sur une telle ssr, une theorie de champs superconforme possede une invariance locale liee aux diffeomorphismes et a une symetrie de jauge u(1). L'etude de ces symetries est menee dans le formalisme de brs et appliquee au calcul des anomalies quantiques. Les actions de modeles sigma sont construites sur les ssr (2,0) et (2,2). En outre, nous parametrons les structures projectives des ssr n = 2 grace a une connexion schwarzienne dont l'introduction permet de construire les operateurs superdifferentiels covariants sous les transformations superconformes et globalement definis sur la ssr. Ceux-ci sont classifies et leur ecriture matricielle nous mene, grace a des conditions de courbure nulle, a l'etude des superalgebres w dans le formalisme des superchamps n = 2.
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Books on the topic "2-N"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. 2-(ji-n-bujiruamino) etanōru: 2-(di-n-butylamino)ethanol. Tōkyō: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. N-(2-aminoechiru)-1,2-etanjiamin (betsumei jiechirentoriamin): N-(2-aminoethyl)-1, 2-ethanediamine. Tōkyō: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2007.

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Å, Åkesson Bengt, World Health Organization, International Labour Organisation, United Nations Environment Programme, International Program on Chemical Safety., and Inter-Organization Programme for the Sound Management of Chemicals., eds. N-methyl-2-pyrrolidone. Geneva: World Health Organization, 2001.

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Eckert, Karl-Heinz. Teckningskursen: X=[n over 2] x (n-1). Berlin: Rainer, 1985.

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Belpoliti, M. ;. Grazioli. Italia 2. "Riga" n.17. s.l: Marcos y Marcos, 2000.

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Nambudripad, Devi S. NAETA-2 N: Bowel disorders. Buena Park, CA: Delta Pub. Co., 2007.

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Nambudripad, Devi S. NAETA-2 N: Bowel disorders. Buena Park, CA: Delta Pub. Co., 2007.

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Nambudripad, Devi S. NAETA-2 N: Bowel disorders. Buena Park, CA: Delta Pub. Co., 2007.

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Sigmar. Piensajuegos - N 2. Tandem Library, 1997.

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Crossover n.2. PANINI ESPAÑA S.A., 2022.

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Book chapters on the topic "2-N"

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Morgan, Michael M., MacDonald J. Christie, Thomas Steckler, Ben J. Harrison, Christos Pantelis, Christof Baltes, Thomas Mueggler, et al. "N-Methyl-N-2-Propynylbenzylamine." In Encyclopedia of Psychopharmacology, 768. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4418.

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Hiasat, Ahmad. "A Modulo $$(2^n-2^{n-2}-1)$$ Adder Design." In Communication and Intelligent Systems, 789–802. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1089-9_61.

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Mansel, Heinz-Peter. "Chapter N.2: Nationality." In Encyclopedia of Private International Law, 1289–301. Edward Elgar Publishing, 2017. http://dx.doi.org/10.4337/9781782547235.n.2.

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Solomon, Barry D. "Nash equilibrium." In Dictionary of Ecological Economics, 364–65. Edward Elgar Publishing, 2023. http://dx.doi.org/10.4337/9781788974912.n.2.

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McAndrew, Ian. "Negotiation." In Encyclopedia of Human Resource Management, 273–74. Edward Elgar Publishing, 2023. http://dx.doi.org/10.4337/9781800378841.n.2.

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Garavito Romero, Cristian Camilo. "La doble tributación en el marco de un convenio multilateral para evitarla: un caso desantendido en la normatividad tributaria." In Narrativas tributarias N° 2, 87–158. Ediciones Uniandes, 2020. http://dx.doi.org/10.15425/2017.230.

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Paredes Orjuela, Luis Felipe. "Metáfora de la zanahoria y el garrote: los hoteleros dicen adiós a las rentas exentas." In Narrativas tributarias N° 2, 275–334. Ediciones Uniandes, 2020. http://dx.doi.org/10.15425/2017.233.

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Aguirre García, Iván Felipe. "Entidades Controladas del Exterior (ECE) como vehículo de planeación sucesoral y protección patrimonial: ¿qué dificultades presentan para ser titulares de inversiones en Colombia y en el exterior?" In Narrativas tributarias N° 2, 159–210. Ediciones Uniandes, 2020. http://dx.doi.org/10.15425/2017.231.

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Soto Montenegro, Josue David. "Mecanismos de reparación de víctimas desde el derecho tributario: una historia de vías cruzadas." In Narrativas tributarias N° 2, 211–74. Ediciones Uniandes, 2020. http://dx.doi.org/10.15425/2017.232.

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Álvarez Posada, Santiago. "Cláusula anti-abuso: crítica a la discrecionalidad en su aplicación." In Narrativas tributarias N° 2, 423–524. Ediciones Uniandes, 2020. http://dx.doi.org/10.15425/2017.235.

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Conference papers on the topic "2-N"

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Sadasivam, Saranya, Asif Iqbal Baba, Wei-Shinn Ku, and Haiquan Chen. "A 2 N 2." In SIGSPATIAL'15: 23rd SIGSPATIAL International Conference on Advances in Geographic Information Systems. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/2834126.2834819.

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Chaves, R., and L. Sousa. "{2/sup n/ + 1, 2/sup n+k/, 2/sup n/ - 1} : a new RNS moduli set extension." In Euromicro Symposium on Digital System Design, 2004. DSD 2004. IEEE, 2004. http://dx.doi.org/10.1109/dsd.2004.1333279.

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Phalguna, P. S., Dattaguru V. Kamat, and P. V. Ananda Mohan. "New RNS-To-Binary Converters for Three-Moduli Set $\{2^{n+1}-1,\ 2^{n}-1,\ 2^{n+k}\}$." In 2019 IEEE International Conference on Distributed Computing, VLSI, Electrical Circuits and Robotics (DISCOVER). IEEE, 2019. http://dx.doi.org/10.1109/discover47552.2019.9007938.

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Buldakov, Michail A., Victor N. Cherepanov, and Ivan I. Matrosov. "Dimer polarizability of (N 2 ) 2 and (O 2 ) 2." In Ninth Joint International symposium on Atmospheric and Ocean Optics/ Atmospheric Physics, edited by Gennadii G. Matvienko and Vladimir P. Lukin. SPIE, 2003. http://dx.doi.org/10.1117/12.497171.

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Manochehri, K., S. Pourmozafari, and B. Sadeghian. "Efficient Methods in Converting to Modulo 2^n+1 and 2^n-1." In Third International Conference on Information Technology: New Generations (ITNG'06). IEEE, 2006. http://dx.doi.org/10.1109/itng.2006.60.

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Vassalos, Evangelos, and Dimitris Bakalis. "Residue-to-Binary Converter for the New RNS Moduli Set $\{2^{2n}-2, \ 2^{n}-1, \ 2^{n}+1\}$." In 2019 Panhellenic Conference on Electronics & Telecommunications (PACET). IEEE, 2019. http://dx.doi.org/10.1109/pacet48583.2019.8956249.

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CAMOUZIS, E., R. DEVAULT, and G. PAPASCHINOPOULOS. "PERIOD TWO TRICHOTOMY ON $ X_{N + 1} = {{\alpha + \gamma X_{N - 1} + \delta X_{N - 2} } \over {X_N + X_{N - 2} }} $." In Proceedings of the International Conference (ICCMSE 2003). WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812704658_0022.

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Low, Jeremy Yung Shern, and Chip Hong Chang. "A new RNS scaler for {2n − 1, 2n, 2n + 1}." In 2011 IEEE International Symposium on Circuits and Systems (ISCAS). IEEE, 2011. http://dx.doi.org/10.1109/iscas.2011.5937842.

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Smirnov, Gennady, Pavel Gordeev, Sergey Nikitin, Tatyana Ternikova, Galina Pokhvisneva, and Oleg Luk`yanov. "N-2-NITROXYETHYL AND N-2-AZIDOETHYL DERIVATIVES OF METHYLENE BIS-(1-OXY-1-TRIAZENE-2-OXIDES)." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m739.aks-2019/141-145.

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Apostolova, Lilia N., Stancho Dimiev, Marin S. Marinov, Peter Stoev, George Venkov, Vesela Pasheva, and Ralitza Kovacheva. "Matrix 2[sup n]-holomorphy." In APPLICATIONS OF MATHEMATICS IN ENGINEERING AND ECONOMICS: 36th International Conference. AIP, 2010. http://dx.doi.org/10.1063/1.3515581.

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Reports on the topic "2-N"

1

McQuaid, Michael J. Computational Characterization of 2-Azidocycloalkanamines: Notional Variations on the Hypergol 2-Azido-N,N-Dimethylethanamine (DMAZ). Fort Belvoir, VA: Defense Technical Information Center, September 2002. http://dx.doi.org/10.21236/ada405699.

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Beiersdorfer, P., M. Bitter, S. von Goeler, S. Cohen, K. W. Hill, J. Timberlake, R. S. Walling, M. H. Chen, P. L. Hagelstein, and J. H. Scofield. High resolution n = 3 to n = 2 spectra of neon-like silver. Office of Scientific and Technical Information (OSTI), April 1986. http://dx.doi.org/10.2172/5795102.

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Chen, Chiung-Chu, and Michael McQuaid. A Thermochemical Kinetic-Based Study of Ignition Delays for 2-Azidoethanamine-Red Fuming Nitric Acid Systems: 2-Azido-N-Methylethanamine (MMAZ) Vs. 2-Azido-N,N-Dimethylethanamine (DMAZ). Fort Belvoir, VA: Defense Technical Information Center, January 2014. http://dx.doi.org/10.21236/ada599206.

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Shmakova, Marina. Freezing of Moduli by N=2 Dyons. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/813188.

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Author, Not Given. N sub 2 O formation in combustion systems. Office of Scientific and Technical Information (OSTI), August 1989. http://dx.doi.org/10.2172/5752525.

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Hurth, Tobias. Super Background Field Method for N=2 SYM. Office of Scientific and Technical Information (OSTI), August 2003. http://dx.doi.org/10.2172/815286.

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Slinker, S., and A. W. Ali. Electron Momentum Transfer Collision Frequency in N(2), O(2) and Air. Fort Belvoir, VA: Defense Technical Information Center, July 1985. http://dx.doi.org/10.21236/ada157030.

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Savin, D. W., P. Beiersdorfer, J. C. Lopez-Urrutia, V. Decaux, D. A. Liedahl, K. J. Reed, K. Widmann, G. V. Brown, and S. M. Kahn. Laboratory astrophysics: Measurements of n = n{prime} to n = 2 line emission in Fe{sup 16+} to Fe{sup 23+}. Office of Scientific and Technical Information (OSTI), March 1996. http://dx.doi.org/10.2172/238552.

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Draim, John E., and Henry M. Bowers. Continuous Global N-Tuple Coverage with (2N = 2) Satellites. Fort Belvoir, VA: Defense Technical Information Center, April 1989. http://dx.doi.org/10.21236/ada206522.

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Nahman, N. S. Dielectric constant measurements on n-heptane and 2-heptanone. Office of Scientific and Technical Information (OSTI), January 1994. http://dx.doi.org/10.2172/527432.

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