z-logo
Premium
13 C and proton nuclear magnetic resonance spectra of trans ‐[arylbromobis(triethyl phosphine)palladium(II)] and related compounds. The π‐donor ability of the Ni(PEt 3 ) 2 X, Pd(PEt 3 ) 2 X and Pt(PEt 3 ) 2 X groups
Author(s) -
Granell Jaume,
Muller Guillermo,
Rocamora Mercè,
Vilarrasa Jaume
Publication year - 1986
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.1260240311
Subject(s) - chemistry , palladium , substituent , phosphine , proton , ring (chemistry) , spectral line , nmr spectra database , proton nmr , proton magnetic resonance , paramagnetism , medicinal chemistry , crystallography , stereochemistry , nuclear magnetic resonance , catalysis , organic chemistry , quantum mechanics , astronomy , physics
13 C and proton NMR spectra of several arylpalladium and some arylnickel and arylplatinum complexes have been compared. The Ni(PEt 3 ) 2 X and Pd(PEt 3 ) 2 X substituents induce a paramagnetic shift of C ipso (of the phenyl ring) which is much larger than that induced by Pt(PEt 3 ) 2 X. However, there are no significant differences along the Ni/Pd/Pt series for the ortho, meta and para positions. For the six compounds of general formula trans ‐[ArPdBr(PEt 3 ) 2 ] reported here, the mean Δ(δ) C values induced on the ArH by the introduction of the PdBr(PEt 3 ) 2 substituent are found to be 26.9 (C ipso ), 7.2 (C ortho ), −1.1 (C meta ), −5.5 (C para ), −0.03 (H ortho ), −0.28 (H meta ) and −0.38 ppm (H para ).

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