Synthesis of thiol substituted oligoanilines for molecular device candidates

Autor:	James M. Tour, Austen K. Flatt
Rok vydání:	2003
Předmět:	chemistry.chemical_classification Chemistry Organic Chemistry chemistry.chemical_element Salt (chemistry) Biochemistry Sulfur Combinatorial chemistry Metallic electrode Drug Discovery Thiol Moiety Molecule Organic chemistry
Zdroj:	Tetrahedron Letters. 44:6699-6702
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(03)01626-5
Popis:	The synthesis of thioacetate derivatized oligoanilines designed for molecular electronic device purposes is described. Reversible oxidation between the non-conductive leuco base and conductive emeraldine salt forms of these compounds may produce switching effects and device behavior. The targeted compounds contain a sulfur moiety as a means to connect the molecules to metallic electrodes.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::c748e5c463ecf2f77e1a2b64240c05b9 https://doi.org/10.1016/s0040-4039(03)01626-5 Zobrazit plný text záznamu Full Text from ScienceDirect