Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Hafner, T; Stadlbauer, S; Schalli, M.
Ferrocene functionalized oligomeric siloxane building blocks as potential linkers for biological active molecules
INORG CHEM COMMUN. 2024; 162: 112203 Doi: 10.1016/j.inoche.2024.112203
Web of Science FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Schalli Michael
Altmetrics:

Dimensions Citations:
Plum Analytics:


Scite (citation analytics):

Abstract:
Despite the fact, that biologically active molecules (e.g., antioxidants, antibiotics and antiviral reagents) were investigated intensively in the last decades, new linker molecules and building blocks, which can enhance the activity and change the polarity of compounds is still a growing field in pharmaceutic research. The application of a ferrocene moiety in combination with a siloxane linker attached to a biological active molecule is realized in the present study for the first time. A method is introduced that uses mono- (FcLi) and dilithioferrocene (FcLi2) to perform anionic ring opening reactions of hexamethylcyclotrisiloxane (D3). The formation of lithium silanolate species alpha DnLi (alpha = Fc, D3 = (SiMe2O)3) was observed, followed by the termination of the ring opening reactions with chlorosilanes Cl-o) to obtain siloxane oligomers of type alpha Dno). Approaches were investigated to enable o) = SiMe2H and o) = SiMe2Cl functionality. It was shown, that oligomeric siloxanes were able to undergo further hydrosilylation reactions with the introduction of a phenol moiety.

Find related publications in this database (Keywords)
Siloxane
Ring opening reaction
Ferrocene
Linker molecule
Ferrocenyl siloxane oligomers
Phenol
Hydrosilylation
© Med Uni Graz Impressum