Relevant bibliographies by topics / C. P. E

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  2. Dissertations / Theses
  3. Books
  4. Book chapters
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Academic literature on the topic 'C. P. E'

Author: Grafiati
Published: 4 June 2021
Last updated: 20 February 2023

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Journal articles on the topic "C. P. E"

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Hietkamp, Sibbele, Thomas Lebbe, Gerd U. Spiegel, and Othmar Stelzer. "Oligophosphaalkane, XVII Funktionalisierte Tri-, Tetra-und Pentaphosphaalkane mit der Donorsequenz P-C-C-P und P-C-C-C-P/Oligophosphaalkanes, XVII Functionalized Tri-, Tetra-and Pentaphosphaalkanes with the Donor Sequence P-C-C-P and P-C-C-C-P." Zeitschrift für Naturforschung B 42, no. 2 (February 1, 1987): 177–85. http://dx.doi.org/10.1515/znb-1987-0210.

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Abstract Starting with the secondary phosphanes R2PH (R = Me, Ph, iPr) and the vinyl-or allylmethylphosphinic acid isopropylesters, the triphosphaalkanes R2P-[CH2]3 -PMe -[CH2]2 -PMeH containing one terminal PH-group have been synthesized in a multiple step synthesis. The tertiary-secondary phosphanes R2P-[CH2]3 -PMeH obtained as intermediates may be used for the syntheses of hybrid donor systems PPN. The P-C-skeletons of the tetra-and pentadentate oligophosphaalkanes have been built up by a free radical initiated addition of the vinyl or allyl compounds CH2=CH-P(NEt2)2 or CH2 =CH-CH2-P(O)(OiPr)Me to disecondary or disecondary-tertiary phosphanes, HMeP-[CH2]n-PMeH (n = 2, 3) or HMeP-[CH2]3 -PPh-[CH2]3 -PMeH, respectively. Methanolysis of the tetra-and pentaphosphaalkanes with terminal P-NEt2 functional groups affords the methoxy derivatives in almost quantitative yield. While the terminal P(NEt2)2 groups in the oligophosphaalkanes cannot be reduced by LiAlH4 , the corresponding methoxy derivatives react immediately to give the primary-tertiary phosphanes.
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Pol, Roman. "On metrizable E with C p ( E ) ≇ C p ( E ) × C p ( E )." Mathematika 42, no. 1 (June 1995): 49–55. http://dx.doi.org/10.1112/s0025579300011347.

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Krupski, Mikołaj, and Witold Marciszewski. "A metrizable X with C p (X) not homeomorphic to C p (X) × C p (X)." Israel Journal of Mathematics 214, no. 1 (July 2016): 245–58. http://dx.doi.org/10.1007/s11856-016-1373-y.

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Yoshifuji, Masaaki. "Chemistry of Several Sterically Bulky Molecules with P=P, P=C, and C≡P Bond." Molecules 27, no. 5 (February 25, 2022): 1557. http://dx.doi.org/10.3390/molecules27051557.

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Several sterically protected, low-coordinate organophosphorus compounds with P=P, P=C, and C≡P bond are described in this study. Molecules such as diphosphenes, phosphaalkenes, 1-phosphaallenes, 1,3-diphosphaallenes, 3,4-diphosphinidenecyclobutenes, and phosphaalkynes are stabilized with an extremely bulky 2,4,6-tri-t-butylphenyl (Mes*) group. The synthesis, structures, physical, and chemical properties of these molecules are discussed, together with some successful applications in catalytic organic reactions.
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Schlapp-Hackl, Inge, Christoph Falschlunger, Kathrin Zauner, Walter Schuh, Holger Kopacka, Klaus Wurst, and Paul Peringer. "Syntheses and crystal structures of [IrIII{C(CHCO2Et)(dppm)2-κ4 P,C,C′,P′}ClH]Cl·2.75CH2Cl2 and its derivatives, [IrIII{C(CHCO2Et)(dppm)2-κ4 P,C,C′,P′}(CH2CO2Et)Cl]Cl·CH3OH·0.5H2O, [IrIII{C(CHCO2Et)(dppm)2-κ4 P,C,C′,P′}Cl2]Cl·CH3OH·2H2O and [IrIII{C(CHCO2Et)(dppm)2-κ4 P,C,C′,P′}(CH2CO2Et)(CO)]Cl2·2CH2Cl2·1.5H2O." Acta Crystallographica Section E Crystallographic Communications 75, no. 1 (January 1, 2019): 12–20. http://dx.doi.org/10.1107/s2056989018017024.

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The common feature of the four iridium(III) salt complexes, (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}(ethoxyoxoethanylidene)methane-κ4 P,C,C′,P′)chloridohydridoiridium(III) chloride methylene chloride 2.75-solvate (4), (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}(ethoxyoxoethanylidene)methane-κ4 P,C,C′,P′)chlorido(ethoxyoxoethanido)iridium(III) chloride–methanol–water (1/1/0.5) (5), (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}(ethoxyoxoethanylidene)methane-κ4 P,C,C′,P′)dichloridoiridium(III) chloride–methanol–water (1/1/2) (6) and (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}(ethoxyoxoethanylidene)methane-κ4 P,C,C′,P′)carbonyl(ethoxyoxoethanide)iridium(III) dichloride–methylene chloride–water (1/2/1.5) (7) or in terms of their formulae [Ir(C55H50O2P4)ClH]Cl·2.75CH2Cl2 (4), [Ir(C4H7O2)(C55H50O2P4)Cl]Cl·CH3OH·0.5H2O (5), [Ir(C55H50O2P4)Cl2]Cl·CH3OH·2H2O (6) and [Ir(C4H7O2)(C55H50O2P4)(CO)]Cl2·2CH2Cl2·1.5H2O (7) is a central IrIII atom coordinated in a distorted octahedral fashion by a PCCP ligand system and two additional residues, such as chlorides, a hydride, a carbonyl or an alkyl unit. Thereby, the PCP pincer ligand system and the residue trans to the carbodiphosphorane (CDP) C atom surround the iridium(III) transition metal in the equatorial plane under the formation of two five-membered dissimilar chelate rings [C—CCDP—P (4, 5, 6 and 7) for the first ring: 120.2 (3), 121.9 (5), 111.2 (3) and 121.7 (2) °; for the second ring: 112.1 (3), 113.5 (5), 120.5 (3) and 108.3 (2)°]. A cyclopropane-like heterocycle is positioned approximately orthogonal (84.21–88.85°) to the equatorial plane, including an alkylidene bridge connecting the IrIII atom and the coordinating CDP atom of the PCP subunit. In general, the neutral PCCP ligand system coordinates the metal in a tetradentate way via three Lewis acid/base bonds and by an alkylidene unit presenting strengthened interactions. In all the crystal structures, (disordered) solvent molecules are present in the voids of the packed molecules that interact with the positively charged complex and its chloride counter-ion(s) through weak hydrogen bonding.
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Karsch, Hans H., Brigitte Deubelly, Gregor Grauvogl, and Gerhard Müller. "Oxidative Verknüpfung von Phosphinomethanidliganden an Titanocen- und Bismutzentren: selektive CC-, PC- und PP-Bindungsbildung." Journal of Organometallic Chemistry 459, no. 1-2 (October 1993): 95–105. http://dx.doi.org/10.1016/0022-328x(93)86060-u.

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Wesseling, Rein. "Joined Cases C-238/99 P, C-244/99 P, C-245/99 P, C-247/99 P, C-250/99 P to C-252/99 P and C-254/99 P, Limburgse Vinyl Maatschappij NV (LVM) and Others v. Commission, [2002] ECR 1-8375." Common Market Law Review 41, Issue 4 (August 1, 2004): 1141–55. http://dx.doi.org/10.54648/cola2004039.

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KNAZIK, STEPHEN R. "P EDIATRIC P REHOSPITAL C ARE." Prehospital Emergency Care 6, no. 4 (January 2002): 478. http://dx.doi.org/10.1080/10903120290938210.

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Castillo, F. "P? A? E? C?-E? P?" Computers & Chemical Engineering 19, no. 1 (June 11, 1995): S89—S94. http://dx.doi.org/10.1016/0098-1354(95)00157-w.

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Grobe, Joseph, Duc Le Van, and Thomas Großpietsch. "Reaktive E=C(p-p)π-Systeme, XXVIII / Reactive E=C(p-p)π-Systems, XXVIII." Zeitschrift für Naturforschung B 46, no. 8 (August 1, 1991): 978–84. http://dx.doi.org/10.1515/znb-1991-0802.

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The reaction of perfluoro-2-phosphapropene F3CP=CF2 (1) with tert-butylamine or isopropylamine in a 1:3 molar ratio leads to the novel iminomethylene phosphanes F3CP=C=N(tBu) [(2), 30% yield] and F3CP=C=N(iPr) [(3), 5%], respectively. 2 slowly decomposes at room temperature giving tert-butylisonitrile and the cyclophosphanes (F3CP)n (n = 3, 4, 5). 3 is found to be less stable than 2 and for example is attacked by primary amines. The reaction of 2 with 2,3-dimethyl-1,3-butadiene or trimethylphosphane yields, on the one hand, the cycloaddition product of bis(trifluormethyl)diphosphene (4), and on the other hand, the phosphorus ylid Me3P=PCF3 (5) together with (tBu)NC.2 and 3, respectively, are not obtained from (F3C)2PH and the corresponding primary amines in a series of HF elimination and H2NR addition reactions. The main products formed from a 1:4 molar mixture of (F3C)2PH and H2N(iPr) in a one-pot procedure were shown to be the chiral phosphanes F3CP[NH(iPr)]C[=N(iPr)]H (6), F3CP[NH(iPr)]CHF2 (7) and F3CP[NH(iPr)]CH2F (8) (60:35:5). The corresponding reaction of (F3C)2PH with H2N(tBu) mainly yields the compound F3CP[NH(tBu)]CH2F (10).
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Dissertations / Theses on the topic "C. P. E"

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Ouhsaine, Fatima. "Phosphamétallapropènes -P=C(X)-E(X')< et phosphamétallaallènes -P=C=E<(E=Si, Ge)." Phd thesis, Université Paul Sabatier - Toulouse III, 2009. http://tel.archives-ouvertes.fr/tel-00450166.

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Ce travail concerne l'étude des hétéroallènes E=C=E', analogues supérieurs des allènes, pour lesquels E et E' sont des éléments lourds des groupes 14 et 15. L'engouement suscité par ces hétéroallènes est dû au fait qu'ils apparaissent comme des briques moléculaires de choix en synthèse hétérocyclique et organométallique grâce notamment à la présence de deux doubles liaisons juxtaposées; de plus ils sont également très intéressants d'un point de vue théorique avec notamment la détermination de la nature des doubles liaisons et de la géométrie de la molécule pour déterminer s'ils présentent une structure proche de celle des allènes ou non. Ce travail est développé en quatre parties : après un rappel bibliographique dans le premier chapitre sur la chimie des hétéroallènes possédant des atomes de phosphore, de germanium et de silicium, nous avons présenté dans les deuxième et troisième chapitres la synthèse, la première structure aux rayons X et l'étude de la réactivité du premier phosphagermaallène stable vis-à-vis des chalcogènes (S, Se, Te), de dérivés carbonylés (aldéhydes et cétone α-éthyléniques, acrylates, cétone énolysable) et du disulfure de carbone. Dans le quatrième chapitre, après un rappel bibliographique sur les phosphasilaallènes –P=C=Si<, la synthèse de nouveaux phosphasilapropènes –P=C(X)-Si(X')< est ensuite décrite ainsi que leurs structures aux rayons X. Un premier essai d'obtention de phosphasilaallène à partir de ces nouveaux phosphasilapropènes est décrit
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Briquet-Duhazé, Sophie. "Les performances en lecture dans les classes à cours multiples SE/C. P. ET S. E. /C. P. /C. E. 1." Rouen, 1996. http://www.theses.fr/1996ROUEL239.

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Une étude statistique, réalisée auprès d'un échantillon de 905 élèves, montre que les résultats en lecture en fin de C. P. Sont supérieurs dans les classes S. E. C. P. Et S. E. C. P. C. E. 1 par rapport aux classes de C. P. à cours unique. Les classes S. E. C. P. Et S. E. C. P. C. E. 1 sont examinées, notamment le rôle de la section enfantine lors du passage maternelle C. P. Ainsi que les interactions entre élèves des différents niveaux
A study based upon statistics made from the observation of a group of 905 pupils, shows that reading competences are superior in classes S. E. C. P. And S. E. C. P. C. E. 1 to those obtained in C. P. Classes with only one section. S. E. C. P and S. E. C. P. C. E. 1 classes are assayed and tested in this study, with an emphasis on the part played by kindergarden when young children leave the French ecole maternelle to acquire reading skills, in C. P. Without forgetting the various interactions between pupils of different degrees of proficiency
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Waller, Bradley A. "Properties of p-adic C^k Distributions." The Ohio State University, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=osu1385485834.

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Ditschar, Bernd. "C, P and water dynamics in Mycorrhiza." Doctoral thesis, [S.l.] : [s.n.], 2005. http://webdoc.sub.gwdg.de/diss/2005/ditschar.

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Roucaute, Yves. "Le P. C. F face à l'état." Paris 10, 1985. http://www.theses.fr/1985PA100232.

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Ferré, Louis. "Problemes de representation optimale par l'a. C. P." Toulouse 3, 1988. http://www.theses.fr/1988TOU30242.

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Les delicats problemes de choix de metrique et de dimension de representation en analyse en composantes principales sont etudiees par une approche de type choix de modele. L'analyse en composantes principales est presentee dans le cadre du modele a effets fixes et l'etude de l'efficacite des estimateurs conduit d'une part a une propriete de type gauss-markov et d'autre part a un critere pour la determination de la dimension optimale de representation. Ces deux resultats sont ensuite appliques a l'analyse factorielle des correspondances et a l'analyse factorielle discriminante pour lesquelles ils trouvent leur pleine justification. L'auteur propose par ailleurs une revue bibliographique sur le theme du choix de dimension en analyse en composantes principales
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Boillet, Pierre-Yves. "Ecbatane et la Médie d'Alexandre aux Arsacides (c. 331 a. C. -c. 228 p. C. ) : histoire monétaire et économique." Bordeaux 3, 2009. http://www.theses.fr/2009BOR30048.

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Depuis l'époque achéménide, la Médie occupe une place singulière entre la Mésopotamie et les pays du Plateau iranien. Elle commande l’accès de l’une et de l’autre et est traversée par la Grande Route Royale qui permet de relier Bactres. Les souverains achéménides ont d’ailleurs fait d’Ecbatane leur résidence estivale, ce qui leur a permis de contrôler un territoire réputé hostile, celui des montagnes du Zagros, habitées ici par les Cosséens. Ce sont en réalité les auteurs grecs postérieurs à Alexandre qui nous livrent un témoignage négatif de ces peuples montagnards : aussi, l’étude conjointe de la documentation disponible – littéraire, numismatique et épigraphique – suggère une analyse diachronique nouvelle de l’organisation territoriale en Médie de la conquête macédonienne à l’avènement de la dynastie sassanide. Les Séleucides firent à leur tour d'Ectabane un relais important du pouvoir royal, l’autorité du satrape de Médie s’étendant également aux Hautes Satrapies. Mais, jusqu’au règne d’Antiochos III, le contrôle de la Médie séleucide paraît tout de même avoir été inachevé. D’ailleurs, si Ecbatane conservait son statut de capitale politique des Hautes Satrapies, Séleucie du Tigre en était, semble-t-il, devenue la capitale économique et financière. La politique des souverains parthes, pour partie héritage de celle des Séleucides, a marqué une étape supplémentaire dans l’appropriation de l’espace, avec une intégration territoriale à l’échelle interrégionale, englobant la Médie et la Babylonie : les monogrammes séleucides communs et contemporains des ateliers de Séleucie et d’Ecbatane puis la division du travail opérée à l’époque parthe entre les deux ateliers en sont la preuve
Since the achaemenid period, Media lies a singular place between Mesopotamia and countries of the Iranian Plateau. It orders the access of both and is crossed by the Royal Main road which allows to connect Bactra. The Achaemenid kings make moreover of Ecbatana their summer residence, allowing them to control a hostile renowned territory, that of the mountains of Zagros, lived here by Cosseans. In fact, these are the Greek authors posterior to Alexander that deliver us a negative testimony of these mountain peoples : so, a re-examination of the literary documentation, numismatics and epigraphy allows to encircle the consequences of the Macedonian conquest in Media and to see the evolution of the territorial organization from the Seleucids to the Parthians. Seleucid kings make Ecbatana an important relay of the royal power, the authority of the satrap of Media also extending farther East, but, until the reign of Antiochus III, the territory of seleucid Media appears all the same to have missed coherence. Moreover, since Antiochos I, if Ecbatana certainly keeps its status of political capital of the High Satrapies, it is Seleucia on the Tigris who henceforth seems to have become the economic and financial capital. The policy of the Parthian kings, partly inheritance of that of Seleucid, marks a supplementary stage in the appropriation of the space, with a territorial integration in the interregional scale, containing Media and Babylonia : seleucid commons and contemporaries monograms of the mints of Seleucia and Ecbatana, then the division of labor operated in the parthian period between both mints are the proof
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Jäschke, Britta [Verfasser]. "Neue multinäre nitridische Keramiken in den Systemen B/P/N/(C), Al/P/N/(C) und Si/N/C aus molekularen und polymeren Vorläufern / Britta Jäschke." Aachen : Shaker, 2003. http://d-nb.info/1172611645/34.

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Göttsch, Hans-Joachim. "Untersuchungen zu C.P. Snow's Romansequenz "Strangers and brothers"." Hamburg : [H.-J. Göttsch], 1985. http://catalog.hathitrust.org/api/volumes/oclc/38668802.html.

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Biosca, Brull Maria. "Fitting the catalysts for effective enantioselective C-X bond forming reactions. Theoretically guided ligand design and mechanistic investigations." Doctoral thesis, Universitat Rovira i Virgili, 2018. http://hdl.handle.net/10803/665121.

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La creixent demanda de compostos enantiomèricament purs, ha incrementat l’interès pel desenvolupament de metodologies per l’obtenció d'aquests compostos. Entre elles, la catàlisi asimètrica és la tècnica més emprada. En aquesta metodologia, l'elecció lligand quiral és clau per l'obtenció de elevades activitats i enantioselectivitats. En aquest context, aquesta tesis és centra en la síntesis de diferents famílies de lligands quirals altament modulars a partir de productes de partida d'elevada disponibilitat. Més concretament, s’han sintetitzat diverses famílies de lligands heterodadors P-oxazolina (P= fosfina, fosfinit, fosfit, fosforamidit), P-altres grups N-dadors (P= fosfit, fosforamidit, fosfonit i N= tiazol, sulfoximina, hidrazona, amina, piridina), P-tioèter (P= fosfina, fosfinit, fosfit) i una família de lligands fosfina quiral-fosfit. Aquests lligands s'han aplicat en la reacció d’hidrogenació d’olefines funcionalitzades i mínimament funcionalitzades catalitzada per Rh i Ir, la reacció de substitució al·lílica i la reacció de protonació descarboxilativa d’oxindoles ambdues catalitzades per Pd. A més a més, en alguns casos, s'han dut a terme estudis computacionals en combinació amb assajos experimentals per estudiar l'origen de les enantioselectivitats obtingudes o bé per guiar l'optimització dels lligand.
La creciente demanda de compuestos enantioméricamente puros, ha incrementado el interés por el desarrollo de metodologías para la obtención de dichos compuestos. Entre ellas, la catálisis asimétrica es la técnica mas utilizada. En dicha metodología, la elección del ligando quiral es clave para la obtención de elevada actividades i enantioselectividades. En este contexto, esta tesis se centra en la síntesis de diferentes familias de ligandos quirales altamente modulares a partir de productos de partida de elevada disponibilidad. Más concretamente, se ha trabajado en la síntesis de ligandos heterodadores P-oxazoline (P= fosfina, fosfinito, fosfito, fosforamidito), P-otros grupos N-dadores (P= fosfito, fosforamidito, fosfonito y N= tiazol, sulfoximina, hidrazona, amina, piridina), P-tioéter (P= fosfina, fosfinito, fosfito) i una familia de ligandos fosfina quiral-fosfito. Estos ligandos se han aplicado en la reacción de hidrogenación de olefinas funcionalitzadas i mínimamente funcionalitzadas catalizada por Rh i Ir, la reacción de substitución alílica y la reacción de protonación descarboxilativa de oxindolas ambas catalizadas por Pd. Además, en algunos casos, se han realizado cálculos computacionales en combinación con ensayos experimentales para estudiar el origen de las enantioselectividades obtenidas o bien para guiar la optimización de los ligandos.
The growing demand on enantiomerically pure compounds has stimulated the interest for the development of methodologies to obtain these compounds. Among them, asymmetric catalysis is one of the most employed tools. In this technic, the choice of the chiral ligand is fundamental to obtain high levels of activity and enantioselectivity. In this context, this thesis is focused on the synthesis of several families of highly modular chiral ligands from readily available starting materials. Particularly, we worked on the synthesis of P-oxazoline (P= phosphine, phosphinite, phosphite, phosphoroamidite), P-other N-donor groups (P= phosphite, phosphoroamidite, phosphonite and N= thiazole, sulfoximine, hydrazone, amine, pyridine), P-thioether (P= phosphine, phosphinite, phosphite) and a family of P*-stereogenic phosphine-phosphite ligands. These ligands have been applied in the Rh- and Ir-catalyzed hydrogenation of functionalized and minimally functionalized olefins, Pd-catalyzed allylic substitution reaction and Pd-catalyzed decarboxylative protonation. Furthermore, in some cases, DFT studies in combination with experimental ones have been performed to better understand the origin of the obtained enantioselectivities or in order to guide the ligand optimization.
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Books on the topic "C. P. E"

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Baru. P C: (post criptum). [Tournai]: Casterman, 2003.

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Sayers, Rod. P. V. C.: Module 33. Rossendale: Footwear OPEN TECH Unit, 1986.

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Committee, Lambeth Area Child Protection. Lambeth A. C. P. C. child protection interagency procedures. London: Lambeth A. C. P. C., 2000.

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P & C hōshiki shin Minji soshōhō. Ōsaka-shi: Tatsumi Hōritsu Kenkyūjo Ōsaka Honkō, 1999.

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C. P. Cavafy: The economics of metonymy. Urbana: University of Illinois Press, 2009.

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Fraser, Marie. C. P. Independently Published, 2018.

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W. C. P. C. Heinemann, 1988.

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Burdick, Michael. C 'N' P. AuthorHouse, 2006.

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CROMWELL. P C Globe +. Charles Merrill, 1989.

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Cavafy, C. P. C. P. Cavafy. Edited by George Savidis. Princeton University Press, 2010. http://dx.doi.org/10.1515/9781400833658.

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Book chapters on the topic "C. P. E"

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von Angerer, S. "Fragments P—C—P—C and P—C." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00919.

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von Angerer, S. "Fragments P—C, P—C, and P—C." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00924.

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Bansal, R. K., and Neelima Gupta. "Fragments P—C, P—C, and P." In Five-Membered Hetarenes with Three or More Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-01130.

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Bansal, R. K., and Neelima Gupta. "Fragments P—P—C and P—C." In Five-Membered Hetarenes with Three or More Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-01135.

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"P C (= C )." In BIOS Instant Notes in Animal Biology, 22–29. Taylor & Francis, 2003. http://dx.doi.org/10.1201/9780203427545-6.

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"p. c." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics, 1457. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_12424.

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"P/C." In The Fairchild Books Dictionary of Textiles. Fairchild Books, 2021. http://dx.doi.org/10.5040/9781501365072.11734.

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Toffano, M. "Formation of C—C Bonds." In Organophosphorus Compounds (incl. RO-P and RN-P), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00429.

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"Appendix C." In Edward P. Dozier, 161–62. University of Arizona Press, 2022. http://dx.doi.org/10.2307/j.ctv2jhjvf5.18.

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Collier, S. J. "Fragments P—P—P—P and C." In Five-Membered Hetarenes with Three or More Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-01197.

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Conference papers on the topic "C. P. E"

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"Prof. C. P. Wong's Biography." In 2007 8th International Conference on Electronic Packaging Technology. IEEE, 2007. http://dx.doi.org/10.1109/icept.2007.4441563.

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Simon, Laurent, David Chisnall, and Ross Anderson. "What You Get is What You C: Controlling Side Effects in Mainstream C Compilers." In 2018 IEEE European Symposium on Security and Privacy (EuroS&P). IEEE, 2018. http://dx.doi.org/10.1109/eurosp.2018.00009.

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Wolfenstein, L. "The symmetries C, P, and T." In Time reversal—the Arthur Rich memorial symposium. AIP, 1991. http://dx.doi.org/10.1063/1.43004.

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Faust, Nickolas L. "P C Based Synthetic Scene Generation." In 1988 Technical Symposium on Optics, Electro-Optics, and Sensors, edited by Marshall R. Weathersby. SPIE, 1988. http://dx.doi.org/10.1117/12.968471.

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Doyle, Rex, and Tad Leblanc. "The Integration of HSE&C--Communities, Contractors, Operators, and Regulators." In E&P Environmental and Safety Conference. Society of Petroleum Engineers, 2007. http://dx.doi.org/10.2118/106425-ms.

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Weidinger, A., B. Pietzak, M. Waiblinger, K. Lips, B. Nuber, and A. Hirsch. "Study of N@C[sub 60] and P@C[sub 60]." In The 12th international winterschool on electronic properties of novel materials: progress in molecular nanostructures. AIP, 1998. http://dx.doi.org/10.1063/1.56478.

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Taylor, R. "Improving your company's P&C performance." In 2004 57th Annual Conference on Protective Relay Engineers Conference. IEEE, 2004. http://dx.doi.org/10.1109/cpre.2004.238611.

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Bay, Yuly, Yana Malkova, and Anna Buran. "Cybersecurity threats to P&C systems." In INTERNATIONAL YOUTH SCIENTIFIC CONFERENCE “HEAT AND MASS TRANSFER IN THE THERMAL CONTROL SYSTEM OF TECHNICAL AND TECHNOLOGICAL ENERGY EQUIPMENT” (HMTTSC 2019). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5120650.

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Lee, Jae Keum, and Stephen Lars Olsen. "Measurement of the branching fractions for $B+ \rightarrow (c \bar c)K+ \rightarrow p \bar p K+$ decays." In XV International Conference on Hadron Spectroscopy. Trieste, Italy: Sissa Medialab, 2014. http://dx.doi.org/10.22323/1.205.0200.

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Ta-Shan Tsui, Shyr-Shen Yu, Shi-Hwang Lin, Jr-Luen Lin, Huang-Chieh Change, and Chih-Yu Hsu. "The implementation of using P-P-C filter to balloon snake algorithm." In 2013 2nd International Symposium on Next-Generation Electronics (ISNE 2013). IEEE, 2013. http://dx.doi.org/10.1109/isne.2013.6512421.

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Reports on the topic "C. P. E"

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Klinksiek, Stephen A. Finding The Charm In 800 GeV/c p-Cu and p-Be Single Muon Spectra. Office of Scientific and Technical Information (OSTI), December 2005. http://dx.doi.org/10.2172/897271.

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Frank, Thomas Joseph. Inclusive Particle Production in $\pi^+p, K^+p$, and $pp$ interactions at 200 GeV/c. Office of Scientific and Technical Information (OSTI), January 1985. http://dx.doi.org/10.2172/1375751.

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Suchorebrow, Victor. Inclusive $K^+ K^-$ Production in Reactions $\pi^+ p$, $K^+ p$ and $pp$ at 200 GeV/c. Office of Scientific and Technical Information (OSTI), March 1989. http://dx.doi.org/10.2172/1407116.

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Hurvits, Gilhad. Search for the Pentaquark via the Decay $P^0_{\bar{c} s} \to K^{*} K p$. Office of Scientific and Technical Information (OSTI), December 1997. http://dx.doi.org/10.2172/1421701.

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Gogota, Olga. Production of c and b quarks in $p\bar{p}$ collisions at the Tevatron collider at $\sqrt{s}$ = 1.96 ТеV; Народження $c$ та $b$ кварків в $p\bar{p}$ зіткненнях на колайдері Tevatron при $Е_{цм}$ = 1.96 ТеВ. Office of Scientific and Technical Information (OSTI), January 2016. http://dx.doi.org/10.2172/1331108.

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Cho, IlSung. Measurement of Bc production cross section in p$\bar{p}$ collisions at √s = 1.96 TeV. Office of Scientific and Technical Information (OSTI), January 2005. http://dx.doi.org/10.2172/1368361.

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Morgan, Randall. Record of Decision Remedial Alternative Selection for the C, F, K, and P-Area Coal Pile Runoff Basins (189-C, 289-F, 189-K, and 189-P). Office of Scientific and Technical Information (OSTI), July 1998. http://dx.doi.org/10.2172/881506.

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Marschilok, Amy C. Porous Ag/P/C Composite Electrodes: A New Approach for Metal Air Batteries. Fort Belvoir, VA: Defense Technical Information Center, February 2012. http://dx.doi.org/10.21236/ada565200.

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Gollwitzer, Keith Edwin. The charmonium P wave singlet state (h (c)) produced in anti-proton - proton annihilations. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/1425804.

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Jessop, Colin P. Measurement of the Branching Fractions of Lambda(C)+-->P Anti-K N(Pi). Office of Scientific and Technical Information (OSTI), April 2003. http://dx.doi.org/10.2172/813045.

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