Siliciumverbindungen mit starken intramolekularen sterischen Wechselwirkungen, XX [1] 1,1-Di-tert-butyl-2,2-dimesityldisilane: Synthese, Molekülstruktur, Radikale / Silicon Compounds with Strong Intramolecular Steric Interactions, XX [1] 1,1-Di-tert-butyl-2,2-dimesityldisilanes: Synthesis, Molecular Structure, Radicals

1985 ◽  
Vol 40 (5) ◽  
pp. 601-606 ◽  
Author(s):  
Manfred Weidenbruch ◽  
Klaus Kramer
Keyword(s):  
Molecular Structure ◽  
Radical Anion ◽  
Alkali Metals ◽  
Force Field Calculations ◽  
Silicon Compounds ◽  
X Ray ◽  
Tert Butyl ◽  
Anti Conformation ◽  
Empirical Force Field ◽  
Empirical Force Field Calculations

The sterically congested disilanes tBu2XSiSiXMes2 [X = H (1), X = Cl (2)] have been prepared. An X-ray structure analysis of 1 reveals a preference for the anti-conformation in the solid state. Similar results have been obtained by empirical force field calculations and DNMR spectroscopy. Reaction of 2 with an electron rich olefin leads to a chlorine bridged disilanyl radical whereas treatment with alkali metals yields the corresponding disilenyl radical anion, tBu2Si=SiMes2˙̄.

Empirical force field calculations on sandalwood odor molecules

1987 ◽  
Vol 22 (5) ◽  
pp. 479-480 ◽  
Author(s):  
Anton Beyer ◽  
Peter Wolschann ◽  
Armin Becker ◽  
Gerhard Buchbauer ◽  
Karin Mraz
Keyword(s):  
Force Field ◽  
Force Field Calculations ◽  
Empirical Force Field ◽  
Empirical Force Field Calculations

scholarly journals New Spiro-Tin Compounds: Reaction of N,N′-Dialkyl Sulfur Diimides with Cyclic Bis(amino)stannylenes - Unexpected Formation of a N-N Bond

1995 ◽  
Vol 50 (12) ◽  
pp. 1811-1817 ◽  
Author(s):  
Max Herberhold ◽  
Christian Köhler ◽  
Wolfgang Milius ◽  
Bernd Wrackmeyer
Keyword(s):  
Molecular Structure ◽  
Magnetic Resonance ◽  
Single Crystal ◽  
Structure Analysis ◽  
Membered Ring ◽  
Monoclinic Space Group ◽  
Unexpected Formation ◽  
Tin Compounds ◽  
X Ray ◽  
Tert Butyl

N,N′-Dialkyl sulfur diimides (1), R(NSN)R [R = Me (a), Et (b), nPr (c), nBu (d)] react with cyclic bis(amino)stannylenes such as 1,3-di-tert-butyl-4,4-dimethyl-1,3,4,2λ2-diazasilastannetedine (2) or 1,3-di-tert-butyl-4,4,5,5-tetramethyl-1,3,4,5,2λ2-diazadisilastannolidine (3) in a 2:1 ratio to give the new spiro-tin(IV) compounds 5a-d, 6b and 6c, built from the respective cyclic bis(amino)stannylene and a seven-membered ring in which the two sulfur diimide groups are coupled via a N-N bond and across the tin atom. A 1:1 adduct 4 is proposed as an intermediate which is the final product 4e in the case of R = tBu (1e). The products were characterized by multinuclear magnetic resonance (1H, 13C, 15N, 29Si, 119Sn NMR), and in the case of 5c the molecular structure was determined by single crystal X-ray structure analysis [monoclinic, space group C2/c ; a = 1504.1(3), b = 1393.3(3), c = 1688.6(3) pm; β = 115.71(3)°].

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