psi * psi Posted December 14, 2011 Posted December 14, 2011 I'm not sure if this is in the right forum, but it's not a homework problem, so I thought I'd ask it here. This may be an obvious answer that I'm overlooking, but I'm curious. In the case of a complex such as [Ru(phen)2(qdppz)]2+, I KNOW that qdppz (quinone phased dipyridophenazine) is the intercalating ligand, but I don't know why. Why does qdppz intercalate and not the phen ligand? Thanks!
mississippichem Posted December 14, 2011 Posted December 14, 2011 I'm not sure if this is in the right forum, but it's not a homework problem, so I thought I'd ask it here. This may be an obvious answer that I'm overlooking, but I'm curious. In the case of a complex such as [Ru(phen)2(qdppz)]2+, I KNOW that qdppz (quinone phased dipyridophenazine) is the intercalating ligand, but I don't know why. Why does qdppz intercalate and not the phen ligand? Thanks! You do mean DNA intercalation right? I assume so because the compound you have posted is similar to a class of DNA intercalcting poly-pyridyl Ruthenium(II) complexes I'm familiar with. Well off hand I would say that anything with a quinone, two pyridinyl groups and a phenazine is going to have a lot of [imath] \pi-\pi [/imath] stacking interactions with any purines or pyrimidines. I'm not sure of the structure of "qdppz" (do you have a structure or IUPAC name?) but from how you describe it there should be available hydrogen bond acceptors as well.
Recommended Posts
Create an account or sign in to comment
You need to be a member in order to leave a comment
Create an account
Sign up for a new account in our community. It's easy!
Register a new accountSign in
Already have an account? Sign in here.
Sign In Now