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Synthesis, structure, and transition metal complexes of amphiphilic 1,5-diaza-3,7-diphosphacyclooctanes

✍ Scribed by Andrey A. Karasik; Roman N. Naumov; Anna S. Balueva; Yulia S. Spiridonova; Oleg N. Golodkov; Helen V. Novikova; Gennadii P. Belov; Sergey A. Katsyuba; Elena E. Vandyukova; Peter Lönnecke; Evamarie Hey-Hawkins; Oleg G. Sinyashin


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
374 KB
Volume
17
Category
Article
ISSN
1042-7163

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✦ Synopsis


Abstract

Amphiphilic 1,5‐diaza‐3,7‐diphosphacyclooctanes have been synthesized by condensation of hydrophobic primary arylphosphines, formaldehyde, and functionalized hydrophilic primary arylamines (5‐aminoisophthalic acid and the sodium salt of sulfanilic acid). These compounds readily form P,P‐chelate complexes with [PtCl~2~(cod)], which are stable in water. The catalytic activity of palladium catalysts with 1,5‐diaza‐3,7‐diphosphacyclooctane ligands was studied in the copolymerization of ethylene and carbon monoxide. © 2006 Wiley Periodicals, Inc. Heteroatom Chem 17:499–513, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20272


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