Open AccessHigh‐accuracy X‐ray absorption spectra from m M solutions of nickel (II) complexes with multiple solutions using transmission XAS
Author(s) -
Chantler Christopher T.,
Islam M. Tauhidul,
Best Stephen P.,
Tantau Lachlan J.,
Tran Chanh Q.,
Cheah Mun Hon,
Payne Andrew T.
Publication year - 2015
Publication title -
journal of synchrotron radiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.172
H-Index - 99
ISSN - 1600-5775
DOI - 10.1107/s1600577515006190
Subject(s) - x ray absorption spectroscopy , x ray absorption fine structure , xanes , nickel , absorption spectroscopy , extended x ray absorption fine structure , chemistry , absorption (acoustics) , analytical chemistry (journal) , spectral line , spectroscopy , coordination number , materials science , optics , physics , ion , organic chemistry , chromatography , quantum mechanics , astronomy , composite material
A new approach is introduced for determining X‐ray absorption spectroscopy (XAS) spectra on absolute and relative scales using multiple solutions with different concentrations by the characterization and correction of experimental systematics. This hybrid technique is a development of standard X‐ray absorption fine structure (XAFS) along the lines of the high‐accuracy X‐ray extended range technique (XERT) but with applicability to solutions, dilute systems and cold cell environments. This methodology has been applied to determining absolute XAS of bis( N ‐n‐propyl‐salicylaldiminato) nickel(II) and bis( N ‐i‐propyl‐salicylaldiminato) nickel(II) complexes with square planar and tetrahedral structures in 15 m M and 1.5 m M dilute solutions. It is demonstrated that transmission XAS from dilute systems can provide excellent X‐ray absorption near‐edge structure (XANES) and XAFS spectra, and that transmission measurements can provide accurate measurement of subtle differences including coordination geometries. For the first time, (transmission) XAS of the isomers have been determined from low‐concentration solutions on an absolute scale with a 1–5% accuracy, and with relative precision of 0.1% to 0.2% in the active XANES and XAFS regions after inclusion of systematic corrections.