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Keywords = aminoethylaminomethyl moiety

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23 pages, 8246 KiB  
Article
Some Theoretical and Experimental Evidence for Particularities of the Siloxane Bond
by Alexandru-Constantin Stoica, Madalin Damoc, Corneliu Cojocaru, Alina Nicolescu, Sergiu Shova, Mihaela Dascalu and Maria Cazacu
Molecules 2022, 27(23), 8563; https://doi.org/10.3390/molecules27238563 - 5 Dec 2022
Cited by 3 | Viewed by 3264
Abstract
The specific features of the siloxane bond unify the compounds based on it into a class with its own chemistry and unique combinations of chemical and physical properties. An illustration of their chemical peculiarity is the behavior of 1,3-bis(2-aminoethylaminomethyl)tetramethyldisiloxane (AEAMDS) in the reaction [...] Read more.
The specific features of the siloxane bond unify the compounds based on it into a class with its own chemistry and unique combinations of chemical and physical properties. An illustration of their chemical peculiarity is the behavior of 1,3-bis(2-aminoethylaminomethyl)tetramethyldisiloxane (AEAMDS) in the reaction with carbonyl compounds and metal salts, by which we obtain the metal complexes of the corresponding Schiff bases formed in situ. Depending on the reaction conditions, the fragmentation of this compound takes place at the siloxane bond, but, in most cases, it is in the organic moieties in the β position with respect to the silicon atom. The main compounds that were formed based on the moieties resulting from the splitting of this diamine were isolated and characterized from a structural point of view. Depending on the presence or not of the metal salt in the reaction mixture, these are metal complexes with organic ligands (either dangling or not dangling silanol tails), or organic compounds. Through theoretical calculations, electrons that appear in the structure of the siloxane bond in different contexts and that lead to such fragmentations have been assessed. Full article
(This article belongs to the Special Issue Covalent and Noncovalent Interactions in Crystal Chemistry)
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