Affiliation:
1. Fachbereich Chemie and Material Science Center (WZMW), Philipps-Universität Marburg, Hans Meerwein Straße 4, 35032 Marburg, Germany
Abstract
A reductive one-pot triflylation and silylation of naphthalene diimide is presented. Post-functionalization of the 1,3,6,8-tetratriflato key compound leads to so far non-accessible UHV processable tetraalkynyl and tetraaminyl 2,7-diazapyrenes.
Funder
Hessisches Ministerium für Wissenschaft und Kunst
Publisher
Royal Society of Chemistry (RSC)
Cited by
5 articles.
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