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Journal articles on the topic 'Organocobalt compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 30 July 2024

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1

García-Monforte, M. Angeles, Irene Ara, Antonio Martín, Babil Menjón, Milagros Tomás, Pablo J. Alonso, Ana B. Arauzo, Jesús I. Martínez, and Conrado Rillo. "Homoleptic Organocobalt(III) Compounds with Intermediate Spin." Inorganic Chemistry 53, no. 23 (October 6, 2014): 12384–95. http://dx.doi.org/10.1021/ic501719y.

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2

Bönnemann, H., and W. Brijoux. "Organocobalt Compounds in the Synthesis of Pyridines." Bulletin des Sociétés Chimiques Belges 94, no. 9 (September 1, 2010): 635–49. http://dx.doi.org/10.1002/bscb.19850940903.

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3

Meneghetti, Mario Roberto, Mary Grellier, Michel Pfeffer, Jairton Dupont, and Jean Fischer. "Synthesis of Configurationally Stable, Optically Active Organocobalt Compounds." Organometallics 18, no. 26 (December 1999): 5560–70. http://dx.doi.org/10.1021/om990517n.

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4

Omae, Iwao. "Three characteristic reactions of organocobalt compounds in organic synthesis." Applied Organometallic Chemistry 21, no. 5 (2007): 318–44. http://dx.doi.org/10.1002/aoc.1213.

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5

Meneghetti, Mario Roberto, Mary Grellier, Michel Pfeffer, André De Cian, and Jean Fischer. "Pseudotetrahedral Organocobalt(III) Compounds Containing Specific Coordination Sites for Brønsted Acids." European Journal of Inorganic Chemistry 2000, no. 7 (July 2000): 1539–47. http://dx.doi.org/10.1002/1099-0682(200007)2000:7<1539::aid-ejic1539>3.0.co;2-1.

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6

Levitin, I. Ya, A. N. Kitaigorodskii, A. T. Nikitaev, V. I. Bakhmutov, A. L. Sigan, and M. E. Vol'Pin. "Substitution of bi- and mono- dentate Lewis bases in organocobalt(III) complexes holding a tridentate ligand: Routes to novel series of organocobalt compounds." Inorganica Chimica Acta 100, no. 1 (May 1985): 65–77. http://dx.doi.org/10.1016/s0020-1693(00)88295-x.

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7

Schneider, Jörg J., Richard Goddard, and Carl Krüger. "Oxidative Abbaureaktionen des homonuklearen Cobalthydridclusters [(η5-Cp*)Co]3H4 / Oxidative Degradation Reactions of the Homonuclear Cobalt Hydride Cluster [(η5-Cp*)Co]3H4." Zeitschrift für Naturforschung B 50, no. 4 (April 1, 1995): 448–59. http://dx.doi.org/10.1515/znb-1995-0401.

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The homonuclear cobalt cluster [(η5-Cp*)Co]3H4 2 reacts with various organic and inorganic substrates with complete degradation of the cluster core to afford mainly mononuclear organometallic cobalt compounds. Thus, whereas reaction of the cluster with CO, NO or alkynes results in the retention of the Co3 ring, the cluster reacts with Br2, I2, I2/CO , I2/ P(C 2H5)3, CCl4, HCI3, (CH2)2Br2, Hacac, CH2Br2, (C6H5CO)OOC(CH3)3, HBF4, and BrCN to give mononuclear complexes or bridged dinuclear complexes without a metal-metal bond. In all cases formal oxidation of the metal center is observed. The crystal structures of six organocobalt complexes have been determined by X-ray crystallography.
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8

Parker, Wallace O., Ennio Zangrando, Nevenka Bresciani-Pahor, Patricia A. Marzilli, Lucio Randaccio, and Luigi G. Marzilli. "NMR studies of Costa-type organocobalt compounds. Structural characterization of several 1,5,6-trimethylbenzimidazole complexes." Inorganic Chemistry 27, no. 12 (June 1988): 2170–80. http://dx.doi.org/10.1021/ic00285a032.

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9

Waddell, Walter H., and Larry R. Evans. "Use of Nonblack Fillers in Tire Compounds." Rubber Chemistry and Technology 69, no. 3 (July 1, 1996): 377–423. http://dx.doi.org/10.5254/1.3538378.

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Abstract A variety of nonblack fillers are used in the rubber components of tires. Calcium carbonate, clay, precipitated silica, talc and titanium dioxide are used in white sidewall compounds to impart desired physical properties and appearance. Precipitated silica can be used in black sidewall compounds, including nonstaining EPDM black sidewalls, to significantly improve tear strength, cut-growth resistance and resistance to ozone aging. Precipitated silica is used extensively in wire coat compounds in conjunction with resorcinol and methylene donating resins, and can be used with organocobalt salts to improve adhesive properties, tear strength and cut-growth resistance. Calcium carbonate, clay, mica and talc are found in innerliner compounds, and precipitated silica can be used. Precipitated silica is used in the treads of off-the-road tires such as earthmover tires, in order to improve tear strength and cut-growth resistance. Clay and talc can be used in tire treads. Precipitated silica is also used in the treads of tires of vehicles used for highway driving, such as passenger cars and trucks, in order to reduce the rolling resistance and increase the wet traction of the tire. It is necessary to modify the surface of precipitated silica with a bifunctional organosilane coupling agent in order to maintain tire treadwear for highway vehicles. Figures 16 and 17 are pictorial summaries of the use of nonblack fillers and the benefits of using precipitated silica in the various components of tire compounds, respectively.
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10

Waddell, Walter H., Larry R. Evans, Edward G. Goralski, and Linda J. Snodgrass. "Mechanism by Which Precipitated Silica Improves Brass-Coated Wire-To-Natural Rubber Adhesion." Rubber Chemistry and Technology 69, no. 1 (March 1, 1996): 48–58. http://dx.doi.org/10.5254/1.3538356.

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Abstract Quantitative determination of elements in the interfacial growth layer formed on brass-coated wire when reacted in squalene suspensions containing carbon black and curatives, with and without precipitated silica and an organocobalt adhesive, was accomplished by using direct surface characterization techniques: Scanning Electron Microscopy with Energy Dispersive Analysis of X-rays (SEM-EDX), Auger Electron Spectroscopy (AES), X-ray Photoelectron Spectroscopy (XPS) and Proton Induced X-ray Emission (PIXE) Spectroscopy. The effects on elemental changes in the interfacial growth layer upon addition of silica and/or cobalt neodecanoate to the squalene suspensions were statistically analyzed. Since the mechanism for silica improvement of brass-coated wire-to-rubber adhesion was previously shown not to be a simple effect of improving rubber physical properties, a chemical mechanism is proposed involving silica to reduce the thickness of the interfacial growth layer and to change the relative concentration of compounds formed in the interfacial growth layer.
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11

Bönnemann, Helmut. "Organocobalt Compounds in the Synthesis of Pyridines-An Example of Structure-Effectivity Relationships in Homogeneous Catalýsis." Angewandte Chemie International Edition in English 24, no. 4 (April 1985): 248–62. http://dx.doi.org/10.1002/anie.198502481.

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12

Benn, Reinhard, Klaus Cibura, Peter Hofmann, Klaus Jonas, and Anna Rufinska. "Cobalt-59 NMR spectroscopy of organocobalt(I) and -cobalt(III) compounds and its relation to chemical properties of the complexes." Organometallics 4, no. 12 (December 1985): 2214–21. http://dx.doi.org/10.1021/om00131a027.

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13

Nie, Shuming, Patricia A. Marzilli, Luigi G. Marzilli, and Nai-Teng Yu. "Near-IR Fourier transform Raman spectroscopy of photolabile organocobalt B12and model compounds. Identification of the Co–C bond stretch in cobalamins." J. Chem. Soc., Chem. Commun., no. 10 (1990): 770–71. http://dx.doi.org/10.1039/c39900000770.

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14

Nie, Shuming, Patricia A. Marzilli, Luigi G. Marzilli, and Nai Teng Yu. "Near-infrared Fourier transform Raman spectroscopy of photolabile organocobalt B12 and model compounds. 3. Vibrational assessment of factors affecting the cobalt-carbon bond in models." Journal of the American Chemical Society 112, no. 16 (August 1990): 6084–91. http://dx.doi.org/10.1021/ja00172a026.

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15

Nie, Shuming, Luigi G. Marzilli, and Nai Teng Yu. "Near-infrared Fourier transform Raman spectroscopy of photolabile organocobalt B12 and model compounds. 1. Detection of the cobalt-carbon stretching mode in the solid state and in solution." Journal of the American Chemical Society 111, no. 26 (December 1989): 9256–58. http://dx.doi.org/10.1021/ja00208a034.

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16

BOENNEMANN, H., and W. BRIJOUX. "ChemInform Abstract: Organocobalt Compounds in the Synthesis of Pyridines." Chemischer Informationsdienst 17, no. 15 (April 15, 1986). http://dx.doi.org/10.1002/chin.198615387.

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17

Shi, Shu. "Kinetics of electron transfer between macrocyclic organocobalt(III) and nickel(I) compounds." Transition Metal Chemistry 19, no. 1 (February 1994). http://dx.doi.org/10.1007/bf00166288.

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18

LEVITIN, I. YA, A. N. KITAIGORODSKII, A. T. NIKITAEV, V. I. BAKHMUTOV, A. L. SIGAN, and M. E. VOL'PIN. "ChemInform Abstract: Substitution of Bi- und Mono-dentate Lewis Bases in Organocobalt(III) Complexes Holding a Tridentate Ligand: Routes to Novel Series of Organocobalt Compounds." Chemischer Informationsdienst 16, no. 39 (October 1, 1985). http://dx.doi.org/10.1002/chin.198539288.

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19

PARKER, W. O. JUN, E. ZANGRANDO, N. BRESCIANI-PAHOR, P. A. MARZILLI, L. RANDACCIO, and L. G. MARZILLI. "ChemInform Abstract: NMR Studies of Costa-Type Organocobalt Compounds. Structural Characterization of Several 1,5,6-Trimethylbenzimidazole Complexes." ChemInform 19, no. 41 (October 11, 1988). http://dx.doi.org/10.1002/chin.198841056.

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20

BOENNEMANN, H., and W. BRIJOUX. "ChemInform Abstract: An Example of Structure-Effectivity Relationship in Homogeneous Catalysis: Organocobalt Compounds in the Synthesis of Pyridines." ChemInform 19, no. 3 (January 19, 1988). http://dx.doi.org/10.1002/chin.198803387.

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