Academic Journal

Oligosilanylated Silocanes

التفاصيل البيبلوغرافية
العنوان: Oligosilanylated Silocanes
المؤلفون: Meshgi, Mohammad Aghazadeh, Pocheim, Alexander, Baumgartner, Judith, Jouikov, Viatcheslav V., Marschner, Christoph
المساهمون: Technische Universität Graz (TU Graz), Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Austrian Science Fund (Fonds zur Forderung der wissenschaftlichen Forschung) (FWF) Austrian Science Fund (FWF) P 26417, P-30955, Austrian Exchange Service (OeAD) via the Scientific and Technological Cooperation project FR 07/2018, French AMADEUS PHC program 39377YK
المصدر: ISSN: 1420-3049 ; Molecules ; https://hal.science/hal-03127409 ; Molecules, 2021, 26 (1), pp.244. ⟨10.3390/molecules26010244⟩.
بيانات النشر: HAL CCSD
MDPI
سنة النشر: 2021
المجموعة: Université de Rennes 1: Publications scientifiques (HAL)
مصطلحات موضوعية: silanides, hypercoordination, cyclic voltammetry, DFT calculations, [CHIM]Chemical Sciences
الوصف: International audience ; A number of mono- and dioligosilanylated silocanes were prepared. Compounds included silocanes with 1-methyl-1-tris(trimethylsilyl)silyl, 1,1-bis[tris(trimethylsilyl)silyl], and 1,1-bis[tris(trimethylsilyl)germyl] substitution pattern as well as two examples where the silocane silicon atom is part of a cyclosilane or oxacyclosilane ring. The mono-tris(trimethylsilyl)silylated compound could be converted to the respective silocanylbis(trimethylsilyl)silanides by reaction with (KOBu)-Bu-t and in similar reactions the cyclosilanes were transformed to oligosilane-1,3-diides. However, the reaction of the 1,1-bis[tris(trimethylsilyl)silylated] silocane with two equivalents of (KOBu)-Bu-t leads to the replacement of one tris(trimethylsilyl)silyl unit with a tert-butoxy substituent followed by silanide formation via (KOBu)-Bu-t attack at one of the SiMe3 units of remaining tris(trimethylsilyl)silyl group. For none of the silylated silocanes, signs of hypercoordinative interaction between the nitrogen and silicon silocane atoms were detected either in the solid state. by single crystal XRD analysis, nor in solution by Si-29-NMR spectroscopy. This was further confirmed by cyclic voltammetry and a DFT study, which demonstrated that the N-Si distance in silocanes is not only dependent on the energy of a potential N-Si interaction, but also on steric factors and through-space interactions of the neighboring groups at Si and N, imposing the orientation of the p(z)(N) orbital relative to the N-Si-X axis.
نوع الوثيقة: article in journal/newspaper
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/33466467; hal-03127409; https://hal.science/hal-03127409; https://hal.science/hal-03127409/document; https://hal.science/hal-03127409/file/molecules-26-00244-v2.pdf; PUBMED: 33466467
DOI: 10.3390/molecules26010244
الاتاحة: https://hal.science/hal-03127409
https://hal.science/hal-03127409/document
https://hal.science/hal-03127409/file/molecules-26-00244-v2.pdf
https://doi.org/10.3390/molecules26010244
Rights: info:eu-repo/semantics/OpenAccess
رقم الانضمام: edsbas.C2443796
قاعدة البيانات: BASE
الوصف
DOI:10.3390/molecules26010244