New cyclic and spirocyclic aminosilanes

New cyclic and spirocyclic aminosilanes were synthesised using ethylenediamine, 2-aminobenzylamine, 1,8-diaminonaphthalene, o-phenylenediamine, and trans-cyclohexane-1,2-diamine as starting material. These diamines were converted into aminosilanes using silicon tetrachloride and dimethyldichlorosila...

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Autores principales: Herbig Marcus, Scholz Henrik, Böhme Uwe, Günther Betty, Gevorgyan Lia, Gerlach Daniela, Wagler Jörg, Schwarzer Sandra, Kroke Edwin
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Lenguaje:EN
Publicado: De Gruyter 2021
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Acceso en línea:https://doaj.org/article/ba071241cfdd45e084ef2da1ecf93fa1
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spelling oai:doaj.org-article:ba071241cfdd45e084ef2da1ecf93fa12021-12-05T14:10:55ZNew cyclic and spirocyclic aminosilanes0792-12412191-021910.1515/mgmc-2021-0007https://doaj.org/article/ba071241cfdd45e084ef2da1ecf93fa12021-04-01T00:00:00Zhttps://doi.org/10.1515/mgmc-2021-0007https://doaj.org/toc/0792-1241https://doaj.org/toc/2191-0219New cyclic and spirocyclic aminosilanes were synthesised using ethylenediamine, 2-aminobenzylamine, 1,8-diaminonaphthalene, o-phenylenediamine, and trans-cyclohexane-1,2-diamine as starting material. These diamines were converted into aminosilanes using silicon tetrachloride and dimethyldichlorosilane directly and via the N,N’-bis(trimethylsilylated) amino derivatives. 15 new compounds of the type (diamino)(SiMe3)2, (diamino)2Si, (diamino)SiMe2, and (diamino)SiCl2 have been prepared. The formation of two cyclotrisilazane derivatives was observed starting from (N,N’-2-aminobenzylamino)dichlorosilane by trimerisation. All synthesised compounds have been characterised with NMR-, Raman-, or IR-spectroscopy, mass-spectrometry, and boiling or melting point. Single-crystal X-ray structure analyses of several derivatives have been performed.Herbig MarcusScholz HenrikBöhme UweGünther BettyGevorgyan LiaGerlach DanielaWagler JörgSchwarzer SandraKroke EdwinDe Gruyterarticlespiro compoundspirocyclicaminosilanesilazaneChemistryQD1-999ENMain Group Metal Chemistry, Vol 44, Iss 1, Pp 51-72 (2021)
institution DOAJ
collection DOAJ
language EN
topic spiro compound
spirocyclic
aminosilane
silazane
Chemistry
QD1-999
spellingShingle spiro compound
spirocyclic
aminosilane
silazane
Chemistry
QD1-999
Herbig Marcus
Scholz Henrik
Böhme Uwe
Günther Betty
Gevorgyan Lia
Gerlach Daniela
Wagler Jörg
Schwarzer Sandra
Kroke Edwin
New cyclic and spirocyclic aminosilanes
description New cyclic and spirocyclic aminosilanes were synthesised using ethylenediamine, 2-aminobenzylamine, 1,8-diaminonaphthalene, o-phenylenediamine, and trans-cyclohexane-1,2-diamine as starting material. These diamines were converted into aminosilanes using silicon tetrachloride and dimethyldichlorosilane directly and via the N,N’-bis(trimethylsilylated) amino derivatives. 15 new compounds of the type (diamino)(SiMe3)2, (diamino)2Si, (diamino)SiMe2, and (diamino)SiCl2 have been prepared. The formation of two cyclotrisilazane derivatives was observed starting from (N,N’-2-aminobenzylamino)dichlorosilane by trimerisation. All synthesised compounds have been characterised with NMR-, Raman-, or IR-spectroscopy, mass-spectrometry, and boiling or melting point. Single-crystal X-ray structure analyses of several derivatives have been performed.
format article
author Herbig Marcus
Scholz Henrik
Böhme Uwe
Günther Betty
Gevorgyan Lia
Gerlach Daniela
Wagler Jörg
Schwarzer Sandra
Kroke Edwin
author_facet Herbig Marcus
Scholz Henrik
Böhme Uwe
Günther Betty
Gevorgyan Lia
Gerlach Daniela
Wagler Jörg
Schwarzer Sandra
Kroke Edwin
author_sort Herbig Marcus
title New cyclic and spirocyclic aminosilanes
title_short New cyclic and spirocyclic aminosilanes
title_full New cyclic and spirocyclic aminosilanes
title_fullStr New cyclic and spirocyclic aminosilanes
title_full_unstemmed New cyclic and spirocyclic aminosilanes
title_sort new cyclic and spirocyclic aminosilanes
publisher De Gruyter
publishDate 2021
url https://doaj.org/article/ba071241cfdd45e084ef2da1ecf93fa1
work_keys_str_mv AT herbigmarcus newcyclicandspirocyclicaminosilanes
AT scholzhenrik newcyclicandspirocyclicaminosilanes
AT bohmeuwe newcyclicandspirocyclicaminosilanes
AT guntherbetty newcyclicandspirocyclicaminosilanes
AT gevorgyanlia newcyclicandspirocyclicaminosilanes
AT gerlachdaniela newcyclicandspirocyclicaminosilanes
AT waglerjorg newcyclicandspirocyclicaminosilanes
AT schwarzersandra newcyclicandspirocyclicaminosilanes
AT krokeedwin newcyclicandspirocyclicaminosilanes
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