Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Silicon Surface-Bound Redox-Active ConjugatedWires Derived From Mono- and Dinuclear Iron(II)and Ruthenium(II) Oligo(phenyleneethynylene) Complexes

Loading...
Thumbnail Image

Date

Authors

Gauthier, Nicolas
Argouarch, Gilles
Paul, Frederic
Toupet, L
Ababou-Girard, Soraya
Sabbah, Hussein
Hapiot, Philippe
Fabre, Bruno
Humphrey, Mark

Journal Title

Journal ISSN

Volume Title

Publisher

Wiley-VCH Verlag GMBH

Abstract

A study has demonstrated the successful covalent assembly of electron-rich mononuclear Fe(II) (21-23) and dinuclear Fe(II) Ru(II) acetylides on monocrystalline silicon surfaces following a novel approach. The experimentation shows that electron-rich mononuclear Fe(II) (2n) or dinuclear Fe(II)/Ru(II) (3) acetylide complexes can be grafted onto hydrogenated silicon surfaces under very mild conditions and following a simple one-step photochemical procedure. These redox-active organometallic monolayers exhibit facile electron transfer between the bound metal centers and the silicon surface through the interfacial Si-C bond. The electron-rich Fe(II) centers in compounds 2n or 3 are oxidized at significantly lower potentials. The data obtained for the Si-3 also unambiguously establish the possibility of generating bound mixed-valence states at the silicon interface.

Description

Citation

Source

Advanced Materials

Book Title

Entity type

Access Statement

License Rights

Restricted until

2037-12-31