Details

Autor(en) / Beteiligte

• Ehbets, Julia
• Lorenzen, Sabine
• Mahler, Christoph
• Bertermann, Ruediger
• Berkefeld, Andre
• Poater, Jordi
• Fritz-Langhals, Elke
• Weidner, Richard
• Bickelhaupt, FMatthias
• Tacke, Reinhold

Titel

Synthesis and Hydrolysis of Alkoxy(aminoalkyl)diorganylsilanes of the Formula Type R sub(2)(RO)Si(CH sub(2)) sub(n)H sub(2) (R = Alkyl, n = 1-3): A Systematic Experimental and Computational Study

Ist Teil von

• European journal of inorganic chemistry, 2016-04, Vol.2016 (11), p.1641-1659

Erscheinungsjahr

2016

Quelle

Wiley Online Library Journals Frontfile Complete

Beschreibungen/Notizen

• Alkoxy(aminoalkyl)silanes are important precursors for the formation of amino-functionalized polysiloxanes, which are used in many technical applications. To better understand the mechanism of the hydrolytic cleavage of the Si-alkoxy moiety of alkoxy(aminoalkyl)silanes (an important key step in the formation of amino-functionalized polysiloxanes), a systematic experimental and computational study on the hydrolysis of alkoxy(aminoalkyl)diorganylsilanes of the formula type R sub(2)(RO)Si(CH sub(2)) sub(n)H sub(2) (R = alkyl, n = 1-3) was conducted. For reasons of comparison, silanes of the formula types R sub(2)(RO)SiC(H)MeCH sub(2)NH sub(2) and R sub(2)(RO)Si(CH sub(2)) sub(n) [R = alkyl; n = 1-3; X = N(H)Me, NMe sub(2), piperidino, NMe sub(3) super(+)I super(-), N(H)COOMe, N(Me)COOMe] and compounds Me sub(2)(MeO)Si(CH sub(2)) sub(6)Me and Me sub(2)(MeO)Si(CH sub(2)) sub(6)NH sub(2) were included in this study. For this purpose, the various silanes were synthesized and studied for their hydrolysis kinetics in CD sub(3)CN/D sub(2)O under acidic and basic conditions by using super(1)H NMR spectroscopy as the analytic tool. These experimental investigations were complemented by computational studies (calculation of proton affinities, reaction barriers, and energies relative to reactants of intermediate transition complexes). The different hydrolysis reactivities observed are the result of a number of parameters, such as electronic and steric effects, the strong impact of the pD value, and intramolecular N-H...O hydrogen bonds between the protonated amino group and the alkoxy leaving group. This comprehensive study provided deep insight into the mechanism of hydrolysis of analogous alpha -, beta -, and gamma -amino-functionalized alkoxy(aminoalkyl)diorganylsilanes of the formula type R sub(2)(RO)Si(CH sub(2)) sub(n)H sub(2) (R = organyl, n = 1-3) and a series of related alpha / beta / gamma analogues with other nitrogen-based functional groups. Kinetic studies provided a deep insight into the mechanism of hydrolysis of analogous alpha -, beta -, and gamma -amino-functionalized alkoxy(aminoalkyl)diorganylsilanes of the formula type R sub(2)(RO)Si(CH sub(2)) sub(n)H sub(2) (R = organyl, n = 1-3) and a series of related alpha / beta / gamma analogues with other nitrogen-based functional groups.