Synthesis, complete characterization, and enantioselective electrokinetic separation of functionalized ruthenium complex enantiomers

Chirality. 2004 Jul;16(6):363-8. doi: 10.1002/chir.20042.

Abstract

Electrokinetic chromatography was employed to separate the enantiomers of two novel functionalized ruthenium(II) complexes with different polypyridyl coordination spheres. The use of anionic carboxymethyl-beta-cyclodextrin as chiral mobile phase additive resulted in maximum efficiency and resolution for the enantiomer separation of both transition metal complexes. The syntheses of the [4-(3-hydroxypropyl)-4'-methyl-2,2'-bipyridine]-bis(2,2'-bipyridine)rethenium(II)-bis(tetrafluoroborate) and [4-(3-hydroxypropyl)-4'-methyl-2,2'-bipyridine]-bis(4,4'-dimethyl-2,2'-bypyridine)ruthenium(II)-bis(tetrafluoroborate) complexes and their complete characterization by means of two-dimensional (1)H and (13)C[(1)H] NMR techniques ((1)H-(1)H COSY and (1)H-(13)C HMQC) as well as elemental analyses and MALDI-TOFMS are described in detail. The functionalized complexes can be used as building blocks for further reactions with polymers, biopolymers, surfaces and nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chemistry / methods*
  • Cyclodextrins / chemistry*
  • Electrophoresis, Capillary
  • Hydrogen-Ion Concentration
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Models, Chemical
  • Models, Molecular
  • Ruthenium / chemistry*
  • Ruthenium Compounds / chemical synthesis*
  • Ruthenium Compounds / chemistry
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Stereoisomerism
  • Time Factors
  • beta-Cyclodextrins*

Substances

  • Cyclodextrins
  • Ruthenium Compounds
  • beta-Cyclodextrins
  • carboxymethyl-beta-cyclodextrin
  • Ruthenium