1965
DOI: 10.1246/bcsj.38.859
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The Polymerization of Acetylene with Dicyclopentadienyl-titanium

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Cited by 15 publications
(4 citation statements)
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“…Over the next decade, other synthetic methods such as the hydrogenation of (η 5 -C 5 H 5 ) 2 TiMe 2 and the reduction of (η 5 -C 5 H 5 ) 2 TiCl 2 with sodium naphthalenide or sodium metal were reported to produce titanocene. Also around this time, reports began to appear suggesting that the proposed sandwich structure may not be correct.…”
Section: Bis(cyclopentadienyl)titanium Compounds: “The Titanocenes”mentioning
confidence: 99%
“…Over the next decade, other synthetic methods such as the hydrogenation of (η 5 -C 5 H 5 ) 2 TiMe 2 and the reduction of (η 5 -C 5 H 5 ) 2 TiCl 2 with sodium naphthalenide or sodium metal were reported to produce titanocene. Also around this time, reports began to appear suggesting that the proposed sandwich structure may not be correct.…”
Section: Bis(cyclopentadienyl)titanium Compounds: “The Titanocenes”mentioning
confidence: 99%
“…Journal of the American Chemical Society / 92:21 j October » Given in the table are the monisotopic species with 12C, S5C1, and 48Ti; assignments are based on the polyistopic distribution patterns for each of the ions. 6 Ionizing voltage, 18 ev. c Ionizing voltage, 15 eV.…”
Section: Reaction To ((C5h5)(c6h4)ticl)2mentioning
confidence: 99%
“…Chemical evidence4 suggests that the 3 (6) position of the 1.2-BioC2Hi2 carborane is the most electrophilic BH position on the icosahedral surface. This further suggests, when coupled with the observed value seen at the 3 (6) position, that substitutents placed further away from the carbon atom pair (7, 8, 9, 10, 11, and 12) would be subject to a detectable +1 effect of the icosahedron.…”
Section: Discussionmentioning
confidence: 78%
“…Repeated preparations always resulted in oil formation, as was observed in the initial preparation, but these now could be seeded with previously prepared (CH3)3NH+ compound. The compound was purified by recrystallization from water; e.g., 6.0 g was dissolved in 500 ml of hot water and the insoluble yellowish material remaining was filtered off. The solution was allowed to cool slowly, seeded with a few particles of the crude starting material, and left in the refrigerator overnight.…”
Section: Methodsmentioning
confidence: 99%