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conditions are:FR=1mL/min(isocratic);Mp=CH3OH:THF:Buffer pH-6=30:30:40;C18 Luna from Phenomenex.
Suggestions required to slve this issue.
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Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
What would you suggest me to go ahead in seperation of those complexes?A lot of metal complexes do not survive chromatography. It is possible that whatever you see is a portion the complex (organic molecule) and if it the same for all three you might see only one peak,
the same ligand complexed with different metals not same metal complexed with different ligands.Regarding complex stability in chromatography - if those compounds form complexes with the same metal, would adding metal salt to mobile phase help?
[edited for clarity]
Cobalt and copper complexed with quinolyl azo dimethyl amino phenolwhat are your complexes?
Check the paper at this link.Cobalt and copper complexed with quinolyl azo dimethyl amino phenolwhat are your complexes?
i tried that method.That method was reproducable.Check the paper at this link.Cobalt and copper complexed with quinolyl azo dimethyl amino phenolwhat are your complexes?
http://www.ncbi.nlm.nih.gov/pubmed/12509050
If you think that it works and cannot reach full paper let me know
i am planning to quantify Cu,Co,Zn,Mn and Fe simultaneously in single run.will this method help?What is the task? If you task is to quantify each complex you can look at cobalt and copper in ELSD, and your ligand in UV and do calculation on each complex assuming that you know structure of the complex and you don't have excess of free metal ions and free ligand floating around.
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