Relevant bibliographies by topics / Osmium compounds. Ruthenium compounds. Porphyrins

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'Osmium compounds. Ruthenium compounds. Porphyrins'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Osmium compounds. Ruthenium compounds. Porphyrins"

1

Lewis, Jack, and Paul R. Raithby. "Reflections on osmium and ruthenium carbonyl compounds." Journal of Organometallic Chemistry 500, no. 1-2 (September 1995): 227–37. http://dx.doi.org/10.1016/0022-328x(95)00512-o.

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Clark, G. R., C. E. F. Rickard, W. R. Roper, D. M. Salter, and L. J. Wright. "Compounds with ruthenium-silicon and osmium-silicon bonds." Pure and Applied Chemistry 62, no. 6 (January 1, 1990): 1039–42. http://dx.doi.org/10.1351/pac199062061039.

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Puerta, M. Carmen, and Pedro Valerga. "Ruthenium and osmium vinylidene complexes and some related compounds." Coordination Chemistry Reviews 193-195 (October 1999): 977–1025. http://dx.doi.org/10.1016/s0010-8545(99)00166-6.

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LEWIS, J., and P. R. RAITHBY. "ChemInform Abstract: Reflections on Osmium and Ruthenium Carbonyl Compounds." ChemInform 27, no. 8 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199608303.

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Cerón-Camacho, Ricardo, Manuel A. Roque-Ramires, Alexander D. Ryabov, and Ronan Le Lagadec. "Cyclometalated Osmium Compounds and beyond: Synthesis, Properties, Applications." Molecules 26, no. 6 (March 12, 2021): 1563. http://dx.doi.org/10.3390/molecules26061563.

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The synthesis of cyclometalated osmium complexes is usually more complicated than of other transition metals such as Ni, Pd, Pt, Rh, where cyclometalation reactions readily occur via direct activation of C–H bonds. It differs also from their ruthenium analogs. Cyclometalation for osmium usually occurs under more severe conditions, in polar solvents, using specific precursors, stronger acids, or bases. Such requirements expand reaction mechanisms to electrophilic activation, transmetalation, and oxidative addition, often involving C–H bond activations. Osmacycles exhibit specific applications in homogeneous catalysis, photophysics, bioelectrocatalysis and are studied as anticancer agents. This review describes major synthetic pathways to osmacycles and related compounds and discusses their practical applications.
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Chen, Hong, Zi-Chao Tang, Rong-Bin Huang, and Lan-Sun Zheng. "Photodissociation Mass Spectrometry of Trinuclear Carbonyl Clusters M3(CO)12 (M = Fe, Ru, Os)." European Journal of Mass Spectrometry 6, no. 1 (February 2000): 19–22. http://dx.doi.org/10.1255/ejms.301.

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Photodissociation of trinuclear carbonyl cluster compounds of Fe, Ru and Os was studied by recording the mass spectra produced from laser ablation of the cluster compounds. Under the experimental conditions, dissociation of the cluster compounds is very extensive, but the dissociation pathway of the osmium cluster is different from those of the iron and ruthenium clusters. The iron and ruthenium clusters not only lost their carbonyl ligands, but their cluster cores were also fragmented. As the osmium cluster dissociated, it ejected three pairs of oxygen atoms, in sequence, before losing the carbonyl ligands, but the trinuclear osmium core did not fragment. This specific dissociation scheme of the osmium cluster reveals its special structural stability. Not only does it have stronger metal-metal bonds, but also a relatively stable coordination bond formed between osmium and carbonyl ligands. In addition, different distributions of positive and negative fragment ions were observed in the experiment. This difference is interpreted as the result of different stabilities of their electronic structures.
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Licona, Cynthia, Jean-Baptiste Delhorme, Gilles Riegel, Vania Vidimar, Ricardo Cerón-Camacho, Bastien Boff, Aina Venkatasamy, et al. "Anticancer activity of ruthenium and osmium cyclometalated compounds: identification of ABCB1 and EGFR as resistance mechanisms." Inorganic Chemistry Frontiers 7, no. 3 (2020): 678–88. http://dx.doi.org/10.1039/c9qi01148j.

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8

Walter, Michael G., Alexander B. Rudine, and Carl C. Wamser. "Porphyrins and phthalocyanines in solar photovoltaic cells." Journal of Porphyrins and Phthalocyanines 14, no. 09 (September 2010): 759–92. http://dx.doi.org/10.1142/s1088424610002689.

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This review summarizes recent advances in the use of porphyrins, phthalocyanines, and related compounds as components of solar cells, including organic molecular solar cells, polymer cells, anddye-sensitized solar cells. The recent report of a porphyrin dye that achieves 11% power conversion efficiency in a dye-sensitized solar cell indicates that these classes of compounds can be as efficient as the more commonly used ruthenium bipyridyl derivatives.
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Gianino, Jacqueline, and Seth N. Brown. "Highly covalent metal–ligand π bonding in chelated bis- and tris(iminoxolene) complexes of osmium and ruthenium." Dalton Transactions 49, no. 21 (2020): 7015–27. http://dx.doi.org/10.1039/d0dt01287d.

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Chambron, Jean-Claude, Jean-Paul Collin, Isabelle Dixon, Valérie Heitz, Xavier J. Salom-Roig, and Jean-Pierre Sauvage. "Synthesis of one-dimensional bis-porphyrinic compounds with a transition metal complex as bridging unit." Journal of Porphyrins and Phthalocyanines 08, no. 01 (January 2004): 82–92. http://dx.doi.org/10.1142/s1088424604000076.

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Linear multicomponent systems, consisting of two porphyrins attached to a central transition metal center, have been prepared and some of their electron- or energy transfer properties have been studied. Each porphyrin is covalently bound to a bidentate or a terdentate ligand, these coordinating molecules being gathered around the metal to afford the desired structure. The spatial arrangement is such that the porphyrinic components are located at both ends of an axis, the transition metal occupying its center. The edge-to-edge distance between the porphyrins is relatively large (~ 20 to 25 Å) and, due to the rigidity of the connectors, it is very well controlled. Three different strategies have been used to construct such assemblies. In the first approach, the porphyrinic fragments are attached at the back of 2,2′,6′,2″-terpyridine ligands (terpy), on the central position (4′). After reaction with an appropriate metal center (ruthenium(II) or iridium(III)), an octahedral complex is obtained which constitutes the central part of the assembly, whereas the porphyrins are at the periphery of the central complex. The second strategy involves the preparation of a 5,5′-disubstituted 2,2′-bipyridine (bipy) ligand followed by its coordination to ruthenium(II). Subsequently, the porphyrinic nuclei are constructed at both ends of the substituents, leading to a linear geometry with a central complex and two laterally-disposed porphyrins. Finally, a very special ligand has been designed and synthesized, which incorporates two 1,10-phenanthroline nuclei (phen). This ligand can wrap itself around an octahedral center (ruthenium(II)) so as to generate a helical arrangement. Both ends of the single-stranded helix can subsequently be attached to porphyrins.
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Dissertations / Theses on the topic "Osmium compounds. Ruthenium compounds. Porphyrins"

1

Li, Yan, and 李艷. "Synthesis and reactivity of carbene complexes of iron, ruthenium and osmium porphyrins." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B31245730.

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梁嘉茵 and Ka-yan Sarana Leung. "Complexes of iminato, nitrido, imido, and hydrazido ruthenium of osmium porphyrins." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2002. http://hub.hku.hk/bib/B31243307.

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Au, Sze-man Vanessa. "Synthesis, characterization and reactivities of bis(imido)-ruthenium(vi) and -osmium(vi) porphyrins /." Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B21021478.

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區詩敏{272b21} and Sze-man Vanessa Au. "Synthesis, characterization and reactivities of bis(imido)-ruthenium(vi) and -osmium(vi) porphyrins." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B31238117.

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Leung, Ka-yan Sarana. "Complexes of iminato, nitrido, imido, and hydrazido ruthenium of osmium porphyrins /." Hong Kong : University of Hong Kong, 2002. http://sunzi.lib.hku.hk/hkuto/record.jsp?B25212072.

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高寶鴻 and Po-hung Ko. "Syntheses, structures and reactivities of some ruthenium, manganese and osmium complexes of non-porphyrin chelating multi-anionic ligands." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1997. http://hub.hku.hk/bib/B31235906.

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Ko, Po-hung. "Syntheses, structures and reactivities of some ruthenium, manganese and osmium complexes of non-porphyrin chelating multi-anionic ligands /." Hong Kong : University of Hong Kong, 1997. http://sunzi.lib.hku.hk/hkuto/record.jsp?B18611862.

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Luther, Thomas Alan. "Dicationic dihydrogen complexes of osmium and ruthenium /." Thesis, Connect to this title online; UW restricted, 1997. http://hdl.handle.net/1773/11540.

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Lam, Ngai Man. "Synthesis, crystal structures, and reactivity of ruthenium and osmium nitrido complexes /." View abstract or full-text, 2006. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202006%20LAMN.

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劉純晶 and Chunjing Liu. "Nonplanar and sterically encumbered ruthenium porphyrins and catalyticreactivity of ruthenium and manganese porphyrin complexes supported onMCM-41." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1998. http://hub.hku.hk/bib/B31237423.

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Books on the topic "Osmium compounds. Ruthenium compounds. Porphyrins"

1

Knox, G. R., ed. Organometallic Compounds of Ruthenium and Osmium. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4615-5429-5.

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R, Knox G., ed. Organometallic compounds of ruthenium and osmium. London: Chapman and Hall, 1985.

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1934-, Knox G. R., ed. Organometallic compounds of ruthenium and osmium. London: Chapman and Hall, 1985.

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Knox, G. R. Organometallic Compounds of Ruthenium and Osmium (Chapman and Hall Chemistry Sourcebooks) (Chapman and Hall Chemistry Sourcebooks). Springer, 1998.

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Book chapters on the topic "Osmium compounds. Ruthenium compounds. Porphyrins"

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Knox, G. R. "Os Osmium." In Organometallic Compounds of Ruthenium and Osmium, 1–70. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4615-5429-5_1.

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Knox, G. R. "Ru Ruthenium." In Organometallic Compounds of Ruthenium and Osmium, 71–209. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4615-5429-5_2.

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3

Hage, R., J. G. Haasnoot, J. Reedijk, and J. G. Vos. "Electrochemistry and Spectroelectrochemistry of Dinuclear Ruthenium and Osmium Complexes." In Molecular Electrochemistry of Inorganic, Bioinorganic and Organometallic Compounds, 583–88. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1628-2_53.

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"3.5 Transition Metal Compounds and Complexes: 3.5.7 Iron (Fe), Ruthenium (Ru), and Osmium (Os) Compounds." In Synthetic Methods of Organometallic and Inorganic Chemistry, edited by Herrmann and Salzer. Stuttgart: Georg Thieme Verlag, 1996. http://dx.doi.org/10.1055/b-0035-108157.

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Esteruelas, Miguel A., and Ana M. López. "Ruthenium- and Osmium- Hydride Compounds Containing Triisopropylphosphine as Precursors for Carbon-Carbon and Carbon-Heteroatom Coupling Reactions." In Recent Advances in Hydride Chemistry, 189–248. Elsevier, 2001. http://dx.doi.org/10.1016/b978-044450733-4/50007-3.

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