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A Double Isotopic Labelling Study of the Infrared Spectra of the Linkage Isomers [Pd(bipy)(SCN)2], [Pd(bipy)(NCS)2] and Related Complexes
Authors:Carola Engelter  David A. Thornton  Gareth M. Watkins
Affiliation:Department of Inorganic Chemistry , University of Cape Town , Rondebosch , 7700 , South Africa
Abstract:Abstract

The IR spectra of the linkage isomers [Pd(bipy)(SCN)2] and [Pd(bipy)(NCS)2] have been determined in the C≡N stretching region (2200–2000 cm?1) and below 500 cm?1. The band shifts resulting from deuteration of the 2,2′-bipyridine (bipy) ring and 15NCS-labelling are shown to provide a ready means for distinguishing between the internal ligand modes, the μPd-N(bipy) and μPd-SCN/μPd-NCS vibrations. The assignment technique has been further extended to the complexes [Pt(bipy)(SCN)2] and [Pd(phen)(SCN)2] (phen = 1,10-phenanthroline). Finally, a comparison between the IR spectra of [Pd(bipy)(NCO)2], [Pd(bipy)(NCS)2] and [Pd(bipy)(SCN)2] reveals that the frequencies μM-NCO, μM-NCS and μM-SCN decrease in the sequence NCO > NCS > SCN.
Keywords:Europium  LSR  Eu (FOD)3  Eu (HFC)3  Eu (FACAM)3  4,5-Dihydro-5-methyl-4-oxo-5-phenyl-2-furancarboxylic acid methyl ester  Antihyperlipoproteinemic  Enantiomeric excess  Lanthanide-induced shifts  Analysis  Stereoisomer.
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