Synthesis and self-assembly of thiol-modified tellurophenes

Author:

Hoover Gabrielle C.11,Ham Jennifer11,Tang Connie11,Carrera Elisa I.11,Seferos Dwight S.11

Affiliation:

1. Department of Chemistry, University of Toronto, Toronto, ON M5S 3H6, Canada.

Abstract

An asymmetric thiol-modified tellurophene was designed and synthesized, and the ability of the compound to form a monolayer on a gold electrode was confirmed. The surface-active tellurophene was synthesized using Cadiot–Chodkiewicz coupling followed by ring closing and thiol modification. The tellurophene compound forms a monolayer on gold surfaces from a concentrated solution within 24 h. The ability of the compound to conjugate to gold is confirmed by X-ray photoelectron spectroscopy (XPS). A surface blocking experiment was used to evaluate the extent of formation of a monolayer on a gold electrode.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

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