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Relevant bibliographies by topics / Nickel complexe

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Academic literature on the topic 'Nickel complexe'

Author: Grafiati

Published: 4 June 2021

Last updated: 18 February 2022

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Journal articles on the topic "Nickel complexe"

1

Liu, Xuan Wen, Xi Wi Qi, and Feng Liu. "Synthesis, Structures, Properties and DFT Studies of a New Bicopper Complexe [Cu(Hdmg)₄(Hdmg)(teda)]·6H₂O." Applied Mechanics and Materials 470 (December 2013): 104–7. http://dx.doi.org/10.4028/www.scientific.net/amm.470.104.

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A new copper complexe [Cu (Hdmg)4(teda)]6H2O(H2dmg=dimethyl glyoxime;teda=triethylenediamine) was synthesized by solution method of nickel nitrate with corresponding ligands. Single crystal X-ray diffraction analysis reveals that crystal belongs to monoclinic, space group C2/c. The Cu2+ is five-coordinated with five N atoms of two dmg molecules and one teda molecule. The pdc anions, as a bridging ligand, link two adjacent Cu ions, forming a dinuclear structure. The structures and properties of complexes have been characterized by elemental analysis and IR spectrum. We also studied the electronic structure and orbital energies of the title complex by DFT methods, and the results reveals that the energy gap between LUMO and HOMO is disappeared. CCDC: 952374

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Masotti, H., G. Peiffer, Ch Siv, R. Valls, and R. Faure. "Cyclodimérisation Asymétrique du Penta-2,4-Dienoate de Méthyle Activée Par Un Complexe du Nickel." Bulletin des Sociétés Chimiques Belges 102, no. 7 (September 1, 2010): 461–65. http://dx.doi.org/10.1002/bscb.19931020705.

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Julien-Pouzol, M., S. Jaulmes, P. Laruelle, S. Carvalho, and E. D. Paniago. "Structure d'un complexe du nickel(II) avec l'aminoacétohydroxamate monosodique, Na[Ni(C2H4N2O2)(C2H5N2O2)].3H2O." Acta Crystallographica Section C Crystal Structure Communications 41, no. 5 (May 15, 1985): 712–15. http://dx.doi.org/10.1107/s0108270185005224.

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Siove, A., D. Ades, C. Chevrot, and G. Froyer. "Polymérisation électroinduite du 3,6 dibromo N-éthylcarbazole catalysée par un complexe du nickel zéro-valent." Journal de Chimie Physique 86 (1989): 155–61. http://dx.doi.org/10.1051/jcp/1989860155.

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Cheng, Xue Hua, Xiu Lan Xin, Li Hua Yin, and Yang Yu. "Syntheses and Spectral Properties of Tetra-(4,4-Dimethyl-Phenyl) Dithiolene Nickel Complex." Applied Mechanics and Materials 469 (November 2013): 81–86. http://dx.doi.org/10.4028/www.scientific.net/amm.469.81.

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Tetra-(4,4-dimethyl-phenyl) dithiolene nickel complex was synthesized by sulfuration with P2S5 and nickel complexs using bis-(4,4-dimethyl-phenyl) ethanedione as raw material. The structure of dithiolene nickel complexes was characterized by melting point, IR and 1HNMR. The maximum absorption spectra of this dithiolene nickel complexes in different solvent was measured by Ultraviolet-Visible-near Infrared Spectrum, and the photo stability and thermal stability were discussed. The results showed that this new method was used to synthesis bis-(4,4-dimethyl-phenyl) ethanedione, which greatly reduces the synthesis time compared to previous methods.

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Safavi, A., and L. Fotouhi. "Electrochemical reduction of nickel(II) dithiocarboxylates at the mercury electrode." Canadian Journal of Chemistry 75, no. 7 (July 1, 1997): 1023–29. http://dx.doi.org/10.1139/v97-122.

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The reduction mechanisms of a series of nickel(II) dithiocarboxylate complexes have been investigated in dimethyl sulphoxide at the mercury electrode. Various electrochemical techniques, including polarography, cyclic voltammetry, chronoamperometry, and controlled potential coulometry, were employed. The reduction of the complexes of the acid derivatives of 2-aminocyclopentene-1-dithiocarboxylate (ACD) proceeds initially by an ECE mechanism (electron transfer – chemical reaction – electron transfer) followed by a one-electron irreversible process. The nature of the complete electrode reaction suggests a metal-centered reduction. The nickel complexes of the ester derivatives of ACD underwent a one-electron reduction that was subject to a follow-up catalytic reaction (EC′ mechanism) and the original complex is regenerated through this regeneration reaction. Keywords: reduction, nickel(II) dithiocarboxylate, mercury electrode.

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7

Rayabarapu, Dinesh Kumar, and Chien-Hong Cheng. "Novel cyclization and reductive coupling of bicyclic olefins with alkyl propiolates catalyzed by nickel complexes." Pure and Applied Chemistry 74, no. 1 (January 1, 2002): 69–75. http://dx.doi.org/10.1351/pac200274010069.

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In this article, new metal-mediated cyclization and reductive coupling reactions of bicyclic olefins with alkynes are described. Oxabicyclic alkenes undergo cyclization with alkyl propiolates at 80 C catalyzed by nickel complexes to give benzocoumarin derivatives in high yields. The reaction of bicyclic alkenes (oxa- and azacyclic alkenes) with alkyl propiolates at room temperature in the presence of the same nickel complex gave 1,2-dihydro-napthelene derivatives in good-to-excellent yields. This reductive coupling reaction proceeds under very mild conditions in complete regio- and stereoselective fashion. A mechanism to account for the coumarin formation and the reductive coupling is proposed.

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Zhang, Jie, Jiarui Chang, Ting Liu, Bula Cao, Yazhou Ding, and Xuenian Chen. "Application of POCOP Pincer Nickel Complexes to the Catalytic Hydroboration of Carbon Dioxide." Catalysts 8, no. 11 (November 1, 2018): 508. http://dx.doi.org/10.3390/catal8110508.

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The reduction of CO2 is of great importance. In this paper, different types of bis(phosphinite) (POCOP) pincer nickel complexes, [2,6-(R2PO)2C6H3]NiX (R = tBu, iPr, Ph; X = SH, N3, NCS), were applied to the catalytic hydroboration of CO2 with catecholborane (HBcat). It was found that pincer complexes with tBu2P or iPr2P phosphine arms are active catalysts for this reaction in which CO2 was successfully reduced to a methanol derivative (CH3OBcat) with a maximum turnover frequency of 1908 h−1 at room temperature under an atmospheric pressure of CO2. However, complexes with phenyl-substituted phosphine arms failed to catalyze this reaction—the catalysts decomposed under the catalytic conditions. Complexes with iPr2P phosphine arms are more active catalysts compared with the corresponding complexes with tBu2P phosphine arms. For complexes with the same phosphine arms, the catalytic activity follows the series of mercapto complex (X = SH) ≈ azido complex (X = N3) >> isothiocyanato complex (X = NCS). It is believed that all of these catalytic active complexes are catalyst precursors which generate the nickel hydride complex [2,6-(R2PO)2C6H3]NiH in situ, and the nickel hydride complex is the active species to catalyze this reaction.

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9

Lehmkuhl, Herbert, Johannes Elsäßer, Reinhard Benn, Barbara Gabor, Anna Rufińska, Richard Goddard, and Carl Krüger. "Ein-und zweikernige Phosphorinylnickel-Komplexe/Mono-and Binuclear Phosphorinylnickel Complexes." Zeitschrift für Naturforschung B 40, no. 2 (February 1, 1985): 171–81. http://dx.doi.org/10.1515/znb-1985-0206.

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AbstractThe ethylene molecule in the binuclear complex [bis(2-4η-phosphorinyl)nickel](η2 -ethylene)-P,P′-nickel (1) is displaced by 1-alkenes in an equilibration reaction to give the corresponding (η2 -1-alkene)nickel complexes 2-5. The NMR spectra of the octene complex 3 and the propene complex 6 are temperature dependent because of valence isomerization in the phosphorinyl group and rotation of the olefin. The binuclear structure is not maintained upon displacement of the ethylene by butadiene or isoprene. One nickel atom is displaced as the dodecatrienediylnickel complex 9 and the remaining bis(phosphorinyl)nickel fragment B reacts with insertion of the diene into one allyl-Ni bond to give 7 resp. 8. The molecular structure of 7 was determined by X-ray crystallography.

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Lukeš, Ivan, Zdeněk Kváča, and Ivor Dominák. "Complexes of N-methyliminobis(methylenephosphonic) acid with cobalt, nickel, copper, and zinc." Collection of Czechoslovak Chemical Communications 53, no. 5 (1988): 987–94. http://dx.doi.org/10.1135/cccc19880987.

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The 1 : 1 cobalt, nickel, copper and zinc complexes of N-methyliminobis(methylenephosphonic) acid, and 1 : 2 cobalt and nickel complexes were prepared. The effect of alkali and alkali earth metals as "external cations" on the crystallization and stoichiometry of solid cobalt complex was investigated. Infrared and electronic spectra and magnetic susceptibilities indicate that cobalt and nickel form high-spin complexes. The coordination sphere of the central atom is formed by a distorted octahedron of the ligand oxygen atoms.

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Dissertations / Theses on the topic "Nickel complexe"

1

Sivade, Alain. "EVALUATION DE PHOSPHINO-TRIS(m-METAPHENYLSULFONATES) EN CATALYSE D'OLIGOMERISATION ET DE TELOMERISATION AU CONTACT DE COMPLEXES DU NICKEL OU DU PALLADIUM." Toulouse 3, 1987. http://www.theses.fr/1987TOU30221.

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Filatre-Furcate, Agathe. "Conducteurs moléculaires neutres : complexes bis (dithiolène) d'or et de nickel." Thesis, Rennes 1, 2016. http://www.theses.fr/2016REN1S143.

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Au cours de ce travail, nous nous sommes particulièrement intéressés à une classe de molécules électroactives précurseurs de matériaux moléculaires conducteurs à composant unique, les complexes bis(1,2-dithiolène) d'or et de nickel neutres. Nous avons tout d'abord développé une série originale de complexes radicalaires d'or [Au(R-thiazYdt)2] à partir de ligands dithiolène, riches en électron, les N-alkyl-1,3-thiazoline-2-chalcogénone-4,5-dithiolate (R-thiazYdt)2 avec Y = O, S, Se et R = Pr, iPr, cycloPr, NMe2. Le substituant R de l'hétérocycle joue un rôle majeur sur les propriétés des matériaux, résultant des interactions électroniques intermoléculaires entre ces complexes paramagnétiques. Les complexes de nickel diamagnétiques, [Ni(R-thiazSdt)2], des mêmes ligands dithiolène, présentent quant à eux une organisation à l'état solide très différente, conséquence de leur caractère à "couche fermée". Enfin, la réactivité originale des dérivés avec R = tBu conduit à des ligands dithiolène portés par un cycle aromatique 2-alkylthio-thiazole (RS-tzdt). Leurs complexes d'or neutres [Au(RS-tzdt)2] forment des empilements fortement dimérisés et semi-conducteurs
During this work, we particularly focused on one type of electroactive molecules, precursors of single component molecular conductors, the neutral gold and nickel bis(1,2-dithiolene) complexes. First we developed a series of radical gold complexes [Au(R-thiazYdt)2] derived from electron rich dithiolene ligands, the N-alkyl-1,3-thiazoline-2-chalcogenone-4,5-dithiolate (R-thiazYdt)2 with Y = O, S, Se and R = Pr, iPr, cycloPr, NMe2. The R substituent plays an important role on the properties of these materials resulting from the intermolecular electronic interactions between these paramagnetic complexes. Besides, diamagnetic nickel complexes, [Ni(R-thiazSdt)2], with the same dithiolene ligands exhibit a different organization in the solid state, a consequence of their closed shell nature. Finally, the original reactivity of the derivatives with R = tBu leads to dithiolene ligands with an aromatic 2-alkylthio-1,3-thiazole ring (RS-tzdt). Their neutral gold complexes [Au(RS-tzdt)2] form semi-conducting strongly dimerized stacks

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Boujday, Souhir. "Interaction des complexes aminés du nickel (II) et des halogénoplatinates (IV) avec la silice : vers une reconnaissance moléculaire aux interfaces." Paris 6, 2002. http://www.theses.fr/2002PA066049.

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PETIT, JEAN-FRANCOIS. "Les squarates de lanthanoides : synthese, structure, comportement thermique et proprietes optiques, synthese et structure de dithiosquarates bimetalliques de nickel (ii) et de cerium (iii)." Toulouse 3, 1988. http://www.theses.fr/1988TOU30133.

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Cinq familles de composes isotypes ont ete identifiees en milieu aqueux. Etude radiocristallographique, comportement thermique dans differentes atmospheres, preparation du squarate de cerium anhydre et de trois nouvelles phases hydratees. Etude spectrometrique du derive de l'europium

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De, Souza Roberto Fernando. "Etude des reactions d'oligomerisation, isomerisation et polymerisation de substrats insatures catalysees par des complexes allyle cationiques du nickel." Toulouse 3, 1987. http://www.theses.fr/1987TOU30152.

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Oligomerisation de l'ethylene. Mecanisme de l'isomerisation des olefines superieures en presence des complexes du titre. Polymerisation catalytique d'autres substrats insatures : styrene, dienes, alcynes. . . La polymerisation du phenylacetylene a ete etudiee en detail car elle conduit a des materiaux semiconducteurs a l'etat non dope

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6

Rodriguez, Gonzalez Vicente. "Le complexe trans-[Ni(glycinate)2(H2O)2] de la synthèse de préparation de catalyseurs Ni/Al2O3." Paris 6, 2004. http://www.theses.fr/2004PA066595.

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Bandyayera, Daniel. "Formation des latérites nickélifères et mode de distribution des éléments du groupe du platine dans les profils latéritiques du complexe de Musongati, Burundi /." Thèse, Chicoutimi : Université du Québec à Chicoutimi, 1997. http://theses.uqac.ca.

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8

Ben, Nasr Chérif. "Complexation du nickel (II) et des lanthanides (III) par des phosphoramides bidentes : Application à l'extraction liquide-liquide." Nancy 1, 1986. http://www.theses.fr/1986NAN10032.

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Les composés de type (NME::(2))::(2)P(O)NRP(O)(NME::(2))::(2) complexent fortement lésions métalliques et peuvent être utilisés en tant qu'agents extractaires dans l'extraction liquide liquide. Synthèse systématique des complexes lanthanides-NDA. L'étude RMN a permis également de trier les contributions de contact et de pseudo-contact au déplacement paramagnétique des protons et des phosphores du ligand engagé dans le complexe et d'obtenir des informations concernant la structure des complexes en solution. Enfin, le problème de l'extraction liquide-liquide des lanthanides par le NIPA dans le nitrométhane a été abordé. Les résultats obtenus ont révélé que le NIPA est un excellent agent extractant, notamment en milieu nitrique, et que l'efficacité de l'extraction augmente quand le rayon atomique diminue

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9

Xiao, Lan. "Etude physico-chimique de la complexation de divers ions metalliques (cu**(2+), ni**(2+) et co**(2+)) avec des dipeptides l-l contenant des chaines laterales non-coordinantes." Paris 7, 1988. http://www.theses.fr/1988PA077170.

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Stabilite des complexes en fonction de l'interaction des chaines laterales du dipeptide et le solvant. Mesures potentiometriques calorimetriques, caracterisation spectrometrique et structure moleculaire

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Daire, Fabrice. "Etude d'electrodes modifiees par fixation de composes de coordination sur un support conducteur du type polypyrrole : application en electrosynthese organique." Paris 6, 1988. http://www.theses.fr/1988PA066176.

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Proprietes electrochimiques des complexes co-l, cu-l, ni-l (ou l=methyl-4, bipyridine-2,2', derive du pyrrole) dans l'acetonitrile. Polymerisation electrolytique de ces complexes sur des electrodes d'or, platine et carbone. Proprietes electrochimiques du polymere co-bipyridyl-polypyrrole; utilisation dans la reduction catalytique des derives allyliques

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Books on the topic "Nickel complexe"

1

Felsher, Dave. Electrowinning of metal: DETA complexes. Montréal, Qué: Dept. of Mining and Metallurgical Engineering, McGill University, 2000.

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Scheenen, Cindy J. H. The reactivity of nickel complexes with sulfur dioxide. Manchester: UMIST, 1998.

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International Conference on Mining and Metallurgy of Complex Nickel Ores (1993 Chin-chang shih, China). Proceedings of the International Conference on Mining and Metallurgy of Complex Nickel Ores: Jinchang, China, September 5-8, 1993. Beijing: International Academic Publishers, 1993.

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4

Karim, Salma. Preparation and characterization of supported and unsupported nickel complexes. Uxbridge: Brunel University, 1991.

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Moreau, S. J. H. The reactions of some Nickel (2) complexes with sulphurdioxide. Manchester: UMIST, 1994.

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Attanasi, E. D. A resource assessment of copper and nickel sulfides within the Mountain View area of the Stillwater Complex, Montana. [Washington]: U.S. G.P.O., 1987.

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Tilus, Pirkko. The formation of aqueous binary and ternary nickel(II) complexes of nitrogen- and carbon-alkylated ethylenediamines, exhibiting octahedral and square planar species. Helsinki: Suomalainen Tiedeakatemia, 1985.

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Jarvis, Adam P. Nickel complexes of acrylic monomers: Mode of coordination and polymerisation studies. [s.l.]: typescript, 1996.

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9

Shepherd, Jeffrey L. Complex oscillations and chaos during anodic dissolution of nickel in sulphuric acid solutions. Sudbury, Ont: Laurentian University, 1999.

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Blusch, Lina K. The Siamese-Twin Porphyrin and Its Copper and Nickel Complexes: A Non-Innocent Twist. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01674-0.

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Book chapters on the topic "Nickel complexe"

1

Tai, A., and T. Harada. "Asymmetrically Modified Nickel Catalysts." In Catalysis by Metal Complexes, 265–324. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-5261-4_5.

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Ittel, Steven D., H. Berke, H. Dietrich, J. Lambrecht, P. Härter, J. Opitz, and W. Springer. "Complexes of Nickel(0)." In Inorganic Syntheses, 98–104. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch26.

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Blusch, Lina K. "Nickel and Copper Complexes." In Springer Theses, 67–92. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01674-0_5.

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Haworth, D. T., J. D. Brown, Y. Chen, William L. Holder, and William L. Jollv. "Sulfur Nitride Complexes of Nickel." In Inorganic Syntheses, 124–26. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132494.ch20.

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Yamamoto, T., H. M. Büch, and P. Binger. "Nickel-Containing Cyclic Amide Complexes." In Inorganic Syntheses, 204–7. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132579.ch36.

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Haynes, M. Taylor, Evan P. Jackson, and John Montgomery. "Nickel Complexes ofN-Heterocyclic Carbenes." In N-Heterocyclic Carbenes, 371–96. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch13.

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Qiu, Zaozao. "Nickel-1,2-o-Carboryne Complexes." In Late Transition Metal-Carboryne Complexes, 31–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-24361-5_2.

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Adhikary, Anubendu, and Hairong Guan. "Nickel-Catalyzed Cross-Coupling Reactions." In Pincer and Pincer-Type Complexes, 117–48. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527681303.ch5.

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Starzewski, K. A. Ostoja. "Ylide Nickel Catalysis: Progress in Acetylene Polymerization." In Transition Metal Carbyne Complexes, 67–69. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1666-4_6.

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Kowalik-Jankowska, Teresa, Henryk Kozlowski, Etelka Farkas, and Imre Sóvágó. "Nickel Ion Complexes of Amino Acids and Peptides." In Nickel and Its Surprising Impact in Nature, 63–107. Chichester, UK: John Wiley & Sons, Ltd, 2007. http://dx.doi.org/10.1002/9780470028131.ch3.

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Conference papers on the topic "Nickel complexe"

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Lisdiana, Anisya, Solihin, and Djulia Onggo. "Potential application of lateritic nickel as nickel(II) triazole complexes: Electronic spectral studies." In PROCEEDINGS OF THE 3RD INTERNATIONAL SEMINAR ON METALLURGY AND MATERIALS (ISMM2019): Exploring New Innovation in Metallurgy and Materials. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0001453.

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Kijima, M., Y. Sakai, and H. Shirakawa. "Electrochearcal synthesis of carbyne catalyzed by nickel complex." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835618.

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Tailor, Sanjay M., and Urmila H. Patel. "Spectroscopic and thermogravimetric study of nickel sulfaquinoxaline complex." In INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2015): Proceeding of International Conference on Condensed Matter and Applied Physics. Author(s), 2016. http://dx.doi.org/10.1063/1.4946297.

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Castelletto, Stefania, and Andrew Edmonds. "680-890nm spectral range of nickel-nitrogen and nickel-silicon complex single centres in diamond." In SPIE Optical Engineering + Applications, edited by Ronald E. Meyers, Yanhua Shih, and Keith S. Deacon. SPIE, 2012. http://dx.doi.org/10.1117/12.958606.

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Noh, D. Y., M. Mizuno, and J. H. Choy. "Synthesis and magnetic properties of conductive nickel-dmbit complex." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835470.

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Yamashita, M., K. Inoue, T. Furuta, A. Ichikawa, H. Okamoto, N. Kimura, H. Ohki, et al. "Control of charge instabilities in quaspone-dimensional halogen-bridged nickel complexes." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835527.

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Tupikova, E. N., I. A. Platonov, and D. S. Khabarova. "Nano catalysts obtained from platinum and cobalt or nickel binary complexes." In EMERGING TECHNOLOGIES: MICRO TO NANO (ETMN-2017): Proceedings of the 3rd International Conference on Emerging Technologies: Micro to Nano. Author(s), 2018. http://dx.doi.org/10.1063/1.5047735.

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Laux, Britta, Sebastian Piegert, and Joachim Ro¨sler. "Advancements in Fast Epitaxial High-Temperature Brazing of Single-Crystalline Nickel-Base Superalloys." In ASME Turbo Expo 2009: Power for Land, Sea, and Air. ASMEDC, 2009. http://dx.doi.org/10.1115/gt2009-59264.

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High temperature diffusion brazing is a very important technology for filling cracks in components from single-crystalline nickel-base superalloys as used in aircraft engines and stationary gas turbines: alloys, which are similar to the base material, are enhanced by a fast diffusing melting-point depressant (MPD) like boron or silicon, which causes solidification by diffusing into the base material. Generally, epitaxial solidification of single-crystalline materials can be achieved by use of conventional braze alloys, however, very long hold times are necessary to provide a complete diffusion of the MPD out of the braze gap. If the temperature is lowered before diffusion is completed, brittle secondary phases precipitate, which serve as nucleation sites for stray grains and, therefore, lead to deteriorating mechanical properties. It was demonstrated in earlier works that nickel-manganese-based braze alloys are appropriate systems for the braze repair of particularly wide gaps in the range of more than 200 μm, which allow a significant shortening of the required hold times. This is caused by the complete solubility of manganese in nickel: epitaxial solidification can be controlled by cooling in addition to diffusion. In this work, it will be shown that the nickel-manganese-based systems can be enhanced by chromium and aluminium, which is with regard to high-temperature applications a very important aspect. Furthermore, it will be demonstrated that silicon, which could be identified as appropriate secondary MPD in recent works, can be replaced by titanium, as this element has additionally a γ′ stabilizing effect. Several braze alloys containing nickel, manganese, chromium, aluminium and titanium will be presented. Previously, the influence of the above mentioned elements on the nickel-manganese-based systems will be visualized by thermodynamic simulations. Afterwards, different compositions in combination with a heat treatment, which is typical for nickel-base superalloys, will be discussed: a microstructure, which is very similar to that within the base material can be presented.

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Inoue, K., M. Yamashita, H. Miyama, T. Ohishi, T. Yosida, and T. Takeuchi. "Haldane gap system: structure and magnetic properties of azide-bridged nickel complexes." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835682.

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Huang, Xiaoping, Yanmin Li, Yong Liu, Henry Peng, and Magdi Azer. "Laser near net shape manufacturing for nickel alloy parts with complex structure." In PICALO 2006: 2nd Pacific International Conference on Laser Materials Processing, Micro, Nano and Ultrafast Fabrication. Laser Institute of America, 2006. http://dx.doi.org/10.2351/1.5056926.

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Reports on the topic "Nickel complexe"

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Smith, Michael Edward. Synthesis, characterization, and reactivity of pentamethylcyclopentadienyl complexes of divalent cobalt and nickel. Office of Scientific and Technical Information (OSTI), October 1993. http://dx.doi.org/10.2172/10108086.

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Pearson, C. D., and J. D. Green. Vanadium and nickel complexes in petroleum resid acid, base, and neutral fractions. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/6745845.

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Pearson, C. D., and J. D. Green. Vanadium and nickel complexes in petroleum resid acid, base, and neutral fractions. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/10133053.

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4

Brugmann, G. E., and A. J. Naldrett. Origin of Copper - Nickel - Platinum Group Element Mineralization in the Ultramafic Part of the Lac Des Iles Complex, Ontario. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1990. http://dx.doi.org/10.4095/131267.

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Wagner, M. R. NMR investigation of dynamic processes in complexes of nickel(II) and zinc(II) with iminodiacetate, n-methyliminodiacetate and n-ethyliminodiacetate. Office of Scientific and Technical Information (OSTI), November 1985. http://dx.doi.org/10.2172/5982240.

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A resource assessment of copper and nickel sulfides within the Mountain View area of the Stillwater Complex, Montana. US Geological Survey, 1987. http://dx.doi.org/10.3133/b1674b.

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Maps, sections, and structure-contour diagrams showing the geology and geochemistry of the Mouat nickel-copper prospect, Stillwater complex, Stillwater County, Montana. US Geological Survey, 1989. http://dx.doi.org/10.3133/mf2038.

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