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Journal articles on the topic 'Group viii metal complexes'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 February 2022

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1

WATANABE, Yoshihisa, and Teruyuki KONDO. "Novel organic syntheses using group VIII metal complexes." Journal of Synthetic Organic Chemistry, Japan 47, no. 12 (1989): 1132–45. http://dx.doi.org/10.5059/yukigoseikyokaishi.47.1132.

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2

Cho, Ook-Jae, Ik-Mo Lee, Kun-You Park, and Hoon-Sik Kim. "Selective hydrogenolysis of CFC-113a by group VIII transition metal complexes." Journal of Fluorine Chemistry 71, no. 1 (1995): 107–9. http://dx.doi.org/10.1016/0022-1139(94)03159-w.

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3

Zinovieva, Elena G., and Vladimir A. Efimov. "Complexes of metal salts of groups I-VIII with trialkyl (aryl) phosphates." Butlerov Communications 58, no. 5 (2019): 49–53. http://dx.doi.org/10.37952/roi-jbc-01/19-58-5-49.

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The reactions of various inorganic salts of metals of groups I-VIII in the Periodic Table with trialkyl(aryl)phosphate compounds obtained new multifunctional complexes. Modern methods of physicochemical analysis studied the laws of complexation reactions. The influence of the nature and molar ratio of the starting trialkyl(aryl)phosphates, metal salts and their crystalline hydrates on the nature of the reactions between them has been revealed. It has been shown that organic phosphates with aromatic radicals are less reactive compared to trialkylphosphates. The presence of crystallization water

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4

Tchertanov, L., and C. Pascard. "Statistical Analysis of Noncovalent Interactions of Anion Groups in Crystal Structures. III. Metal Complexes of Thiocyanate and their Hydrogen-Donor Accepting Function." Acta Crystallographica Section B Structural Science 53, no. 6 (1997): 904–15. http://dx.doi.org/10.1107/s0108768197008549.

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The bidentate function of the thiocyanate anion was studied using the Cambridge Structural Database System. Complexing properties (metal–thiocyanate interactions) with respect to metal cations were analysed. Two main classes were distinguished: (a) alkali and alkaline earth metals, and (b) metals of Zn and Cu groups and transition metals (group VIII). Good correlations were found between the nature of the metal (radius, oxidation state and charge) and its position relative to the thiocyanate unit. Hydrogen-bond acceptor properties of discrete and complexed SCN units were compared. The extraord

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5

De La Piscina, Pilar Ramirez, Narcis Homs та Jose-Luis G. Fierro. "Adsorption of group VIII metal cyanide complexes on acid-modified γ-alumina". Applied Catalysis 49, № 2 (1989): 259–71. http://dx.doi.org/10.1016/s0166-9834(00)83022-5.

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6

Qin, Xiaofei, Xiaoyan Liu, Caihong Guo, and Haishun Wu. "Reaction Mechanisms of Carbonyl Compounds Hydrosilylation Catalyzed by Group VIII Transition Metal Complexes." Chinese Journal of Organic Chemistry 36, no. 1 (2016): 60. http://dx.doi.org/10.6023/cjoc201507037.

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7

Harsy, Stephen G. "Homogeneous hydrogenation of nitroaliphatic compounds catalyzed by group VIII transition metal phosphine complexes." Tetrahedron 46, no. 21 (1990): 7403–12. http://dx.doi.org/10.1016/s0040-4020(01)89056-6.

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8

Quiroga, M E, E A Cagnola, D A Liprandi, and P C L'Argentière. "Cyclohexene hydrogenation using Group VIII metal complexes as catalysts in heterogeneous and homogeneous conditions." Journal of Chemical Technology & Biotechnology 76, no. 2 (2001): 215–19. http://dx.doi.org/10.1002/jctb.365.

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9

Arzoumanian, Henri, André Baldy, Marcel Pierrot, and Jean-François Petrignani. "Reaction of molybdenum—molybdenum triple bonded compounds with group VIII peroxo-transition metal complexes." Journal of Organometallic Chemistry 294, no. 3 (1985): 327–31. http://dx.doi.org/10.1016/0022-328x(85)87448-9.

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10

HARSY, S. G. "ChemInform Abstract: Homogeneous Hydrogenation of Nitroaliphatic Compounds Catalyzed by Group VIII Transition Metal Phosphine Complexes." ChemInform 22, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199107091.

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11

Zanello, Piero. "Structural aspects of the redox flexibility of group VIII metal complexes with tripodal polyphosphine ligands." Pure and Applied Chemistry 67, no. 2 (1995): 323–30. http://dx.doi.org/10.1351/pac199567020323.

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12

Barone, Vincenzo, Ivo Cacelli, Alessandro Ferretti, and Michele Visciarelli. "Transport properties of binuclear metal complexes of the VIII group using a simplified NEGF-DFT approach." Physical Chemistry Chemical Physics 15, no. 27 (2013): 11409. http://dx.doi.org/10.1039/c3cp50974e.

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13

Williams, Daniel J., Robert L. Jones, and Patricia H. Poor. "Main group metal halide complexes with sterically hindered thioureas. VIII. Complexes of lead(II) halides with 1,3-dimethyl-2(3H)-imidazolethione." Inorganica Chimica Acta 144, no. 2 (1988): 237–40. http://dx.doi.org/10.1016/s0020-1693(00)86293-3.

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14

Dzhemilev, U. M., R. I. Khusnutdinov, Z. S. Muslimov, O. M. Nefedov, and G. A. Tolstikov. "Homodimerization of spiro{bicyclo[2.2.1]Hepta-2,5-Diene-7,1?-cyclopropane}, catalyzed by group VIII transition metal complexes." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 11 (1988): 2337–43. http://dx.doi.org/10.1007/bf00959891.

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15

Simón-Manso, Eugenio, та Mauricio Valderrama. "Group VIII transition metal complexes with the chiral diphosphazane ligand (S)-α-(Ph2P)2N(CHMePh): Synthesis and structural characterization". Journal of Organometallic Chemistry 691, № 3 (2006): 380–86. http://dx.doi.org/10.1016/j.jorganchem.2005.09.004.

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16

Casoli, Antonella, Alessandro Mangia, Giovanni Predieri, and Enrico Sappa. "Behaviour of mono-, bi- and trinuclear group VI, VII and VIII metal carbonyl complexes in high-performance liquid chromatography." Journal of Chromatography A 355 (January 1986): 285–90. http://dx.doi.org/10.1016/s0021-9673(01)97325-x.

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17

Decken, Andreas, Robert A. Gossage, and Paras N. Yadav. "Oxazoline chemistry. Part VIII. Synthesis and characterization of a new class of pincer ligands derived from the 2-(o-anilinyl)-2-oxazoline skeleton Applications to the synthesis of group X transition metal catalysts." Canadian Journal of Chemistry 83, no. 8 (2005): 1185–89. http://dx.doi.org/10.1139/v05-163.

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The synthesis and characterization of a new and readily synthesized class of potentially anionic pincer ligands with C1 point group symmetries is described. These materials can be made via amide coupling of a 2-(2′-anilinyl)-2-oxazoline unit with picolinic acid; the incorporation of enantiopure oxazoline fragments facilitates the construction of chiral C1 pincers. Treatment of the free ligands with Pd metal sources leads to the formation of amidoPd pincer complexes in good yield. One of these Pd complexes has been characterized by single crystal X-ray diffraction methods, which confirms the p

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18

Jiang, Ting, Yusong Bai, Peng Zhang, Qiwei Han, David B. Mitzi, and Michael J. Therien. "Electronic structure and photophysics of a supermolecular iron complex having a long MLCT-state lifetime and panchromatic absorption." Proceedings of the National Academy of Sciences 117, no. 34 (2020): 20430–37. http://dx.doi.org/10.1073/pnas.2009996117.

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Exploiting earth-abundant iron-based metal complexes as high-performance photosensitizers demands long-lived electronically excited metal-to-ligand charge-transfer (MLCT) states, but these species suffer typically from femtosecond timescale charge-transfer (CT)-state quenching by low-lying nonreactive metal-centered (MC) states. Here, we engineer supermolecular Fe(II) chromophores based on the bis(tridentate-ligand)metal(II)-ethyne-(porphinato)zinc(II) conjugated framework, previously shown to give rise to highly delocalized low-lying3MLCT states for other Group VIII metal (Ru, Os) complexes.

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19

Subasi, Elif, and Hamdi Temel. "Photochemical Reactions of VIB and VIIB Group Metal Carbonyl Complexes with a Chiral Schiff Base." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 37, no. 2 (2007): 85–89. http://dx.doi.org/10.1080/15533170601187409.

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20

Kepert, DL, AF Waters, and AH White. "Synthesis and Structural Systematics of Nitrogen Base Adducts of Group 2 Salts. VIII. Some Mixed-Ligand Complexes of Group 2 Metal Halides With Aromatic N,N'-Bidentate and Oxygen Donors." Australian Journal of Chemistry 49, no. 1 (1996): 117. http://dx.doi.org/10.1071/ch9960117.

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Room-temperature single-crystal X-ray structural characterizations have defined an interesting array of species obtained by variously crystallizing Group 2 halides with 2,2'-bipyridine ( bpy ) and 1,10-phenanthroline ( phen ) from hydroxylic solvents. [( phen )2Ca(OH2)3]Br2 (1) is monoclinic, P21/c, a 16.896(5), b 8.620(2), c 17.814(5) Ǻ, β 97.05(2)°, Z = 4 f.u .; conventional R on ׀ F ׀ was 0.057 for 1707 � independent 'observed' (I > 3σ(I)) reflections No, the complex � containing seven-coordinate Ca(N2)2O3 calcium. [( bpy )2CaBr(OH2)( HOPri )] � Br (2) is monoclinic, P21/c, a 9.674(4), b

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21

Knierzinger, Andreas, and Peter Schönholzer. "Axially Dissymmetric diphosphines in the Biphenyl Series: Crystal structures of three new group-VIII metal complexes of (6,6′-dimethyl-1,1′-biphenyl-2,2′-diyl)bis(diphenylphosphine) ( = biphemp)." Helvetica Chimica Acta 75, no. 4 (1992): 1211–20. http://dx.doi.org/10.1002/hlca.19920750421.

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22

Kröcher, Oliver, René A. Köppel, Michael Fröba, and Alfons Baiker. "Silica Hybrid Gel Catalysts Containing Group(VIII) Transition Metal Complexes: Preparation, Structural, and Catalytic Properties in the Synthesis ofN,N-Dimethylformamide and Methyl Formate from Supercritical Carbon Dioxide." Journal of Catalysis 178, no. 1 (1998): 284–98. http://dx.doi.org/10.1006/jcat.1998.2151.

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23

MALISCH, W., K. GRUEN, N. GUNZELMANN, et al. "ChemInform Abstract: Synthesis and Reactivity of Silicon Transition Metal Complex. Part 26. Phosphenium Complexes. Part 25. pH-Functionalized Phosphametallacycles - Metallo-Silanols of Group VI and VIII Metals: Synthesis and Some Transformation Reactions." ChemInform 27, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.199638253.

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24

Zargarian, D. "Group 10 metal indenyl complexes." Coordination Chemistry Reviews 233-234 (November 1, 2002): 157–76. http://dx.doi.org/10.1016/s0010-8545(02)00201-1.

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25

Korolev, Andrey V., Fabien Delpech, Samuel Dagorne, Ilia A. Guzei, and Richard F. Jordan. "Main-Group-Metal Chlorobenzene Complexes." Organometallics 20, no. 16 (2001): 3367–69. http://dx.doi.org/10.1021/om010395a.

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26

VINCETT, M. "Carbon gasification by group VIII metal catalysts." Journal of Catalysis 126, no. 1 (1990): 279–90. http://dx.doi.org/10.1016/0021-9517(90)90066-s.

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27

Hlina, Johann A., James R. Pankhurst, Nikolas Kaltsoyannis, and Polly L. Arnold. "Metal–Metal Bonding in Uranium–Group 10 Complexes." Journal of the American Chemical Society 138, no. 10 (2016): 3333–45. http://dx.doi.org/10.1021/jacs.5b10698.

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28

Lodi, G., G. L. Zucchini, A. De Battisti, A. Giatti, G. Battaglin, and G. Della Mea. "Proton exchange in group VIII metal-oxide films." Surface Science Letters 251-252 (July 1991): A362. http://dx.doi.org/10.1016/0167-2584(91)90980-6.

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29

Lodi, G., G. L. Zucchini, A. De Battisti, A. Giatti, G. Battaglin, and G. Della Mea. "Proton exchange in group VIII metal-oxide films." Surface Science 251-252 (July 1991): 836–40. http://dx.doi.org/10.1016/0039-6028(91)91108-a.

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30

Wolfgramm, Regine, Cristina Ramos, Pascual Royo, Maurizio Lanfranchi, Maria Angela Pellinghelli, and Antonio Tiripicchio. "tert-Butylsilylcyclopentadienyl Group 4 metal complexes." Inorganica Chimica Acta 347 (April 2003): 114–22. http://dx.doi.org/10.1016/s0020-1693(02)01446-9.

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31

Ovcharenko, V. I., A. B. Gel'man, and V. N. Ikorskii. "Complexes with metal-nitroxyl group coordination." Journal of Structural Chemistry 30, no. 5 (1990): 815–36. http://dx.doi.org/10.1007/bf00763808.

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32

López-de-Luzuriaga, José M., Miguel Monge, and M. Elena Olmos. "Luminescent aryl–group eleven metal complexes." Dalton Transactions 46, no. 7 (2017): 2046–67. http://dx.doi.org/10.1039/c6dt04386k.

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This perspective highlights the recent developments in the study of the photoluminescent properties of aryl–group eleven complexes. Related properties and applications such as electroluminescence, triboluminescence, mechanochromism, luminescent liquid crystals, low molecular weight gelators and photocatalysts are also discussed.

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33

Al-Allaf, Talal A. K., and Abeer Z. M. Sheet. "Platinum group metal Schiff base complexes—I. Platinum complexes." Polyhedron 14, no. 2 (1995): 239–48. http://dx.doi.org/10.1016/0277-5387(94)00231-3.

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34

Chiusoli, Gian Paolo. "Group VIII metal-catalyzed CC bond-forming sequences." Journal of Organometallic Chemistry 300, no. 1-2 (1986): 57–80. http://dx.doi.org/10.1016/0022-328x(86)84056-6.

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35

Chiusoli, Gian Paolo. "Group VIII metal-catalyzed organic syntheses via metallacyclic intermediates." Journal of Molecular Catalysis 41, no. 1-2 (1987): 75–88. http://dx.doi.org/10.1016/0304-5102(87)80020-2.

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36

Jaśkowska, Eliza, Iwona Justyniak, Michał K. Cyrański, et al. "Benzoxaborolate ligands in group 13 metal complexes." Journal of Organometallic Chemistry 732 (May 2013): 8–14. http://dx.doi.org/10.1016/j.jorganchem.2013.01.023.

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37

Chandra, S., Rajendra Singh, and R. C. Srivastava. "Platinum Group Metal Complexes of Some Semicarbazones." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 20, no. 1 (1990): 83–95. http://dx.doi.org/10.1080/00945719008049872.

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38

Bytschkov, Igor, and Sven Doye. "Group-IV Metal Complexes as Hydroamination Catalysts." European Journal of Organic Chemistry 2003, no. 6 (2003): 935–46. http://dx.doi.org/10.1002/ejoc.200390149.

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39

Ohki, Yasuhiro, and Michael D Fryzuk. "Dinitrogen Activation by Group 4 Metal Complexes." Angewandte Chemie International Edition 46, no. 18 (2007): 3180–83. http://dx.doi.org/10.1002/anie.200605245.

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40

Tjaden, Erik B., and Richard F. Jordan. "New cationic group 4 metal alkyl complexes." Macromolecular Symposia 89, no. 1 (1995): 231–35. http://dx.doi.org/10.1002/masy.19950890123.

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41

Havlík, Aleš, Martin Lamač, Jiří Pinkas, Aleš Růžička, and Michal Horáček. "Mixed amido-cyclopentadienyl group 4 metal complexes." RSC Advances 5, no. 73 (2015): 59154–66. http://dx.doi.org/10.1039/c5ra07742g.

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42

Calderazzo, Fausto, and Guido Pampaloni. "Metal carbonyl complexes of group VB metals." Journal of Organometallic Chemistry 303, no. 1 (1986): 111–20. http://dx.doi.org/10.1016/0022-328x(86)80116-4.

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43

Linton, David J., Paul Schooler, and Andrew E. H. Wheatley. "Group 12 and heavier Group 13 alkali metal 'ate complexes." Coordination Chemistry Reviews 223, no. 1 (2001): 53–115. http://dx.doi.org/10.1016/s0010-8545(01)00379-4.

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44

Han-Mou, Gau, Chen Chi-Tain, Jong Ting-Ting, and Chien Mei-Yueh. "Group IV metal-chromium complexes bridged by a benzoate group." Journal of Organometallic Chemistry 448, no. 1-2 (1993): 99–106. http://dx.doi.org/10.1016/0022-328x(93)80074-l.

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45

Nolan, Peter E., David C. Lynch, and Andrew Hall Cutler. "Carbon Deposition and Hydrocarbon Formation on Group VIII Metal Catalysts." Journal of Physical Chemistry B 102, no. 36 (1998): 7073. http://dx.doi.org/10.1021/jp9827882.

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46

Nolan, Peter E., David C. Lynch, and Andrew Hall Cutler. "Carbon Deposition and Hydrocarbon Formation on Group VIII Metal Catalysts." Journal of Physical Chemistry B 102, no. 21 (1998): 4165–75. http://dx.doi.org/10.1021/jp980996o.

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47

Uemiya, Shigeyuki, Masataka Kajiwara, and Toshinori Kojima. "Composite membranes of group VIII metal supported on porous alumina." AIChE Journal 43, S11 (1997): 2715–23. http://dx.doi.org/10.1002/aic.690431317.

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48

Hector, A. L., and I. P. Parkin. "Solid state metathesis preparations of group VIII metal oxide powders." Journal of Materials Science Letters 13, no. 3 (1994): 219–21. http://dx.doi.org/10.1007/bf00278168.

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49

YAMAMOTO, Yasuhiro. "Electrochemical Synthesis of Group 10 Metal Complexes of Isocyanide Containing Metal-Metal Bonds." Journal of Synthetic Organic Chemistry, Japan 51, no. 9 (1993): 804–14. http://dx.doi.org/10.5059/yukigoseikyokaishi.51.804.

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50

Mori, Shigeki, Soji Shimizu, Ji-Young Shin, and Atsuhiro Osuka. "Group 12 Metal Complexes of [26]Hexaphyrin(1.1.1.1.1.1)." Inorganic Chemistry 46, no. 11 (2007): 4374–76. http://dx.doi.org/10.1021/ic7004216.

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