| 1 | Author
| Z. Naturforsch | Requires cookie* | | Title
| Synthese und Dimerisierungsverhalten des l,l-Bis(trimethylsilyl)-2-(2,5-diisopropylphenyl)silens  | | | Abstract
| Tris(trim ethylsilyl)silylmagnesium bromide, (Me^SiX^SiMgBr, reacts with 2.5-diisopropyl-benzaldehyde to give 2,5-diisopropylphenyl-tris(trimethylsilyl)silylmethanol (1). With sodium | | |
Reference
| Z. Naturforsch. 51b, 370—3 (1996); eingegangen am 21. August 1995 | | |
Published
| 1996 | | |
Keywords
| Silenes, Silene Dimerization, 2, 3-Disilanaphthalenes Tetrahydro, 1, 2-Disilacyclobutanes | | |
Similar Items
| Find | | DEBUG INFO
| | | | TEI-XML for
| default:Reihe_B/51/ZNB-1996-51b-0370.pdf | | | Identifier
| ZNB-1996-51b-0370 | | | Volume
| 51 | |
2 | Author
| Clemens Krempner1, Rhett Kempeb, Hartmut Oehme3 | Requires cookie* | | Title
| The Thermal Isomerization of a Tetrahydro-2,3-disilanaphthalene into a 1,2-Disilacyclobutane -The Conversion of a Formal Silene [2+4] Cyclodimer into the [2+2] Cycloadduct  | | | Abstract
| 1,2,3,8a-Tetrahydro-1 -mesityl-5,7,8a-trimethyl-2,2,3,3-tetrakis(trimethylsilyl)-2,3-disila-naphthalene (3), the formal [2+4] cyclodimer of the transient 2-mesityl-l,l-bis(trimethylsilyl)-silene (2), on thermal treatment gradually isomerizes to give a mixture of the [2+2] products (E)-and -predominantly -(Z)-3,4-dimesityl-1,1,2,2-tetrakis(trimethylsilyl)-l,2-disilacyclo-butane [(E/Z)-4], By prolonged heating or at higher temperatures both (E/Z)-3 and (Z)-4 are converted into (E)-4, the thermodynamically most stable head-to-head dimer of 2. Possible pathways of the isomerization processes are discussed. | | |
Reference
| Z. Naturforsch. 52b, 815—818 (1997); received February 14 1997 | | |
Published
| 1997 | | |
Keywords
| Silenes, Silene Dimerization, 2, 3-Disilanaphthalene Tetrahydro, 1, 2-Disilacyclobutane | | |
Similar Items
| Find | | DEBUG INFO
| | | | TEI-XML for
| default:Reihe_B/52/ZNB-1997-52b-0815.pdf | | | Identifier
| ZNB-1997-52b-0815 | | | Volume
| 52 | |
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