PINKAS, Jiri and Jiri LOBL. Adduct formation and dealkylsilylation reactions of alumazene. In Pacifichem 2005 - INOR 166. 1st ed. Honolulu, USA: ACS, 2005, p. 166-166.
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Basic information
Original name Adduct formation and dealkylsilylation reactions of alumazene
Name in Czech Tvorba aduktu a dealkylsilylační reakce alumazenu
Authors PINKAS, Jiri (203 Czech Republic, guarantor) and Jiri LOBL (203 Czech Republic).
Edition 1. vyd. Honolulu, USA, Pacifichem 2005 - INOR 166, p. 166-166, 1 pp. 2005.
Publisher ACS
Other information
Original language English
Type of outcome Proceedings paper
Field of Study 10402 Inorganic and nuclear chemistry
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14310/05:00013018
Organization unit Faculty of Science
Keywords in English iminoalane; alumazene; dealkylsilylation
Tags alumazene, dealkylsilylation, Iminoalane
Changed by Changed by: prof. RNDr. Jiří Pinkas, Ph.D., učo 627. Changed: 31/5/2009 22:21.
Abstract
Trimeric iminoalane alumazene, [2,6-(i-Pr)2C6H3NAlMe]3, possesses a central six-membered Al3N3 planar ring. Its high reactivity is caused by a polarity of the Al-N bonds and a small delocalization of the ŕ electrons in the ring. We will present the results of our studies on the reactivity of alumazene with a variety of oxygen and nitrogen bases and trimethylsilyl esters of acids of phosphorus and sulfur with the aim of obtaining new polycyclic and polyhedral molecules. Trimethylester of phosphoric acid in the reaction with alumazene at room temperature forms a cis-adducts A and on heating affords intractable mixtures of products. On the other hand, mono- and bisadduct of triphenylphosphine oxide were structurally characterized and a trans isomer B was revealed by X-ray diffraction analysis. Dealkylsilylation reactions of trimethylsilyl esters of phosphonic acids (RP(O)(OSiMe3)2, R = Me, Ph, CCl3) lead to bicyclic products C or D, depending on the size of R. Phosphoric acid ester, OP(OSiMe3)3, provided a heteroadamantane compound E. Analogous dealkylsilylation reaction was observed with trimethylsilyl esters of sulfonic acids and provided bicyclic moieties similar to C that assemble into a hexameric supramolecular ring in the solid state. The reactions of pyridines and nitriles (RCN, R = Me3Si, i-Pr, 4-MeOC6H4, 4-MeC6H4, 2,6-F2C6H3) with alumazene were studied in analogy to their reactions with AlMe3. Mono-, bis- and tris-adducts were observed spectroscopically and also were structurally characterized. The cis- and trans isomers were observed for the bis-adducts of 2,6-X2C6H3CN (X = F, Cl) and MeC6H4CN, respectively.
Abstract (in Czech)
Tvorba aduktu a dealkylsilylační reakce alumazenu
Links
GA203/04/0296, research and development projectName: Sonochemická syntéza oxidových a fosfátových materiálů
Investor: Czech Science Foundation, Sonochemical Synthesis of Oxide and Phosphate Materials
MSM0021622410, plan (intention)Name: Fyzikální a chemické vlastnosti pokročilých materiálů a struktur
Investor: Ministry of Education, Youth and Sports of the CR, Physical and chemical properties of advanced materials and structures
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