Skip to main content

  | मौसम…

411 समाचार
Public archive edition · Attributed source reporting with original dates · AI drafts are excluded

411 REFERENCE · Wikipedia

1,3,5,7-Tetramethyl-1,3,5,7-tetrasilaadamantane

Reference material by Wikipedia contributors. This retains its source identity and is not 411 news reporting.

1,3,5,7-tetramethyl-1,3,5,7-tetrasilaadamantane.svg 1,3,5,7-Tetramethyl-1,3,5,7-tetrasilaadamantane 17995-33-4 correct FDA SQY6S5MRB7 123745 140316 1S/C10H24Si4/c1-11-5-12(2)8-13(3,6-11)10-14(4,7-11)9-12/h5-10H2,1-4H3 XMNIPURNPMVXKW-UHFFFAOYSA-N C[Si]12C[Si]3(C[Si](C1)(C[Si](C2)(C3)C)C)C 6 4 24 colorless solid 244 10.1002/zaac.19693650102 Bildung siliciumhaltiger Verbindungen, XXVII. Carbosilane mit vier Si-Atomen 1969 Fritz G. Haase R. Kummer D. Zeitschrift für Anorganische und Allgemeine Chemie 365 1–2 1–13 1,3,5,7-Tetramethyl-1,3,5,7-tetrasilaadamantane is the organosilicon compound with the formula (CH2)6(SiCH3)4. It is a colorless solid that is soluble in organic solvents. The compound is one of the iconic carbosilanes, featuring alternating \sSi\sC\sSi\sC\s linkages.10.1007/978-3-642-70800-8 Carbosilanes 1986 Fritz Gerhard Matern Eberhard 978-3-642-70802-2 Otherwise it can be described as a diamondoid cluster. It arises as one of many products from the pyrolysis of tetramethylsilane. A more efficient route involves the reaction of the cyclic carbosilane (CH2Si(CH3)2)3 (1,1,3,3,5,5-hexamethyl-1,3,5-trisilacyclohexane) with aluminium tribromide.10.1021/ja00724a069 1,3,5,7-Tetrasilaadamantanes. Facile synthesis via catalyzed ligand redistribution 1970 Frye Cecil L. Klosowski Jerome M. Weyenberg Donald R. Journal of the American Chemical Society 92 21 6379–6380 thumb|left|Carbosilanes are known for several diamondoid structures. References Category:Adamantane-like molecules Category:Carbosilanes