z-logo
Premium
Cyclopalladation of 1,1′‐Azonaphthalene (= Di(naphthalen‐1‐yl)diazene): Isolation and characterization of two isomeric complexes
Author(s) -
Kind Lothar,
Klaus Alfred J.,
Rys Paul,
Gramlich Volker
Publication year - 1998
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19980810211
Subject(s) - chemistry , palladium , stereochemistry , medicinal chemistry , organic chemistry , catalysis
The cyclopalladation of 1,1′‐azonaphthalene (= di(naphthalen‐1‐yl)diazene; 2 ) with bis(hexafluoroacetyl‐acetonato)palladium(II) (3; [Pd(hfa) 2 ]) yields the ortho ‐palladated complex (1,1,1,5,5,5‐hexafluoropentane‐2,4‐dionato‐κ 2 O , O ′)[1‐(naphthalen‐1‐ylazo‐κ N 2 )naphthalen‐2‐yl‐κ C 2 ]palladium(II) ( 4 ) as well as the peri ‐palladated complex (1,1,1,5,5,5‐hexafluoropentane‐2,4‐dionato‐κ 2 O , O ′)[8‐(naphthalen‐1‐ylazo‐κ N 2 )naphthalen‐1‐yl‐κ C 1 ]‐palladium(II) ( 5 ); their structures were corroborated by X‐ray analyses. The formation of the novel peri ‐metallated product 5 containing a six‐membered palladacycle strongly depends upon the reaction conditions.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom