1984
DOI: 10.1002/cber.19841170916
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Stufenweise Synthese ketten‐ und ringförmiger Siloxane — Kristallstrukturen

Abstract: Disilanole des Typs R,Si(OH), (1, 2: R = CHMe,, CMe,) und das Fluorsilanol (Me,C) Die Hydrolyse von Chlorsilanen als Methode zur Synthese ketten-und ringformiger Siloxane versagt mit zunehmender Crone der Substituenten. Neigen Methylsilanole zur sofortigen Kondensation, so erfordert bereits die H20-Abspaltung aus Isopropylsilanolen drastische Bedingungen I-'). tert-Butylgruppen stabilisieren, wie wir kiirzlich zeigen konnten, bereits Fluorsilanole und deren Lithiumsalze''. Ziel der vorliegenden Arbeit ist nun… Show more

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Cited by 67 publications
(45 citation statements)
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“…1.508 (6) C(5)-C(7) 1.538 (5) C(5)--C (8) 1.519 (7) O (2) shorter than in other hydrogen-bonded silanols (Clegg, 1983;Graalmann, Klingebiel, Clegg, Haase & Sheldrick, 1983). This can be ascribed to the electronwithdrawing fluoro substituent, which has also been observed to shorten adjacent Si-N bonds in silazanes (Clegg, Sheldrick & Stalke, 1984).…”
Section: Table 2 Bond Lengths (A) and Angles (°)mentioning
confidence: 88%
“…1.508 (6) C(5)-C(7) 1.538 (5) C(5)--C (8) 1.519 (7) O (2) shorter than in other hydrogen-bonded silanols (Clegg, 1983;Graalmann, Klingebiel, Clegg, Haase & Sheldrick, 1983). This can be ascribed to the electronwithdrawing fluoro substituent, which has also been observed to shorten adjacent Si-N bonds in silazanes (Clegg, Sheldrick & Stalke, 1984).…”
Section: Table 2 Bond Lengths (A) and Angles (°)mentioning
confidence: 88%
“…[17] As side products, fluoride-containing compounds are formed, which can be potentially used for the regeneration of the depolymerization reagent. [18] We report herein our investigations on the zinc-catalyzed depolymerization of end-of-life polysiloxanes with benzoyl fluoride as the depolymerization reagent.…”
Section: Methodsmentioning
confidence: 99%
“…0,02 mol (7) (1) M+; 'H-NMR: b = 1,09 CMe3, 0.52 SiMe; 2 9 Si-NMR: (3 = 7,19 SiCMe3,6,13 SiMe. 28,78 CC3,20,91 CC3,19,01,18,60 CC7,16,79 CC2;2 9 Si-NMR: (3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)77 SiCMe3,86 SiCHMe2. < 3 = 27,58 NSiCC,,27,36 OSiCC,,20.00 NSiCC3,19,80 OSiCC3,1,56 SiCH3; 2 9 Si-NMR: (3)(4)(5)(6)(7)(8)(9)(10)54 SiN,06 SiOH,97 SiMe.…”
Section: (1) N O (L)mentioning
confidence: 99%
“…Die Verbindungen 9-11 sind gleich dem bekann ten Trisiloxan-l,5-diol 12 [5] sehr gute Startreagen zien zur Darstellung von Achtringen [2].…”
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