Volume 2017, Issue 5 p. 910-914
Full Paper

Synthesis, Structure, and First Reactivity Studies of Functional (Phosphinoamino)boranes

Paresh Kumar Majhi

Institut für Anorganische Chemie der Rheinischen Friedrich‐Wilhelms‐Universität Bonn, Gerhard‐Domagk‐Straße 1, 53121 Bonn, Germany

Search for more papers by this author
José Manuel Villalba Franco

Institut für Anorganische Chemie der Rheinischen Friedrich‐Wilhelms‐Universität Bonn, Gerhard‐Domagk‐Straße 1, 53121 Bonn, Germany

Search for more papers by this author
Gregor Schnakenburg

Institut für Anorganische Chemie der Rheinischen Friedrich‐Wilhelms‐Universität Bonn, Gerhard‐Domagk‐Straße 1, 53121 Bonn, Germany

Search for more papers by this author
Takahiro Sasamori

Institute for Chemical Research, Kyoto University, Gokasho Uji, 611‐0011 Kyoto, Japan

Search for more papers by this author
Rainer Streubel

Corresponding Author

Institut für Anorganische Chemie der Rheinischen Friedrich‐Wilhelms‐Universität Bonn, Gerhard‐Domagk‐Straße 1, 53121 Bonn, Germany

Institut für Anorganische Chemie der Rheinischen Friedrich‐Wilhelms‐Universität Bonn, Gerhard‐Domagk‐Straße 1, 53121 Bonn, Germany

E‐mail: r.streubel@uni‐bonn.de

http://anorganik.chemie.uni‐bonn.de/akstreubel

Search for more papers by this author
Dedicated to the memory of Professor Heinrich Nöth
First published: 06 February 2017
Citations: 2

Abstract

Functional phosphanes having a P–N–B motif were obtained by treatment of chloro(organo)phosphanes with boryl amides. Compounds 4ae are stable up to 100 °C and show no association in solution, even at low temperature (–70 °C). The functional phosphanes were characterized by NMR and IR spectroscopy, MS, and microanalysis, and phosphanes 4a, 4c, and 4e were additionally scrutinized by single‐crystal X‐ray crystallography. Preliminary studies on chlorine/lithium exchange of 4a led to anionic azaphosphaboriridine 5a′.

Abstract

The synthesis and structure of several functional phosphanes having a P–N–B motif are presented. The title compounds exhibit remarkable thermal stability, unlike earlier reported examples, and enable chlorine/lithium exchange leading to the first anionic azaphosphaboriridine.