Abstract:
:The reaction between [(eta(6)-p-cymene)Ru(H2O)3]X2 and 4,7-phenanthroline (phen) leads to the formation of the rectangular tetranuclear complexes [(eta(6)-p-cymene)4Ru4(mu-4,7-phen-N4,N7)(2)(mu-OH)4]X4 (X=NO3, 1a; SO3CF3, 1b) which have been structurally characterised by X-ray crystallography. 1H NMR spectroscopic studies suggest the presence of a partially dissociated dinuclear species of type [(eta6-p-cymene)2Ru2(mu-4,7-phen-N4,N7)(solv)4]4+ in equilibrium with the tetranuclear cyclic species found in the solid state. The temperature effect for this equilibrium was studied by variable temperature 1H NMR experiments in D2O and MeOD. The results reveal that the proportion of the tetranuclear species increases with the polarity of the solvent which favour stacking interactions between the phenanthroline moieties. In addition, the reactivity of the tetranuclear species towards the nucleosides guanosine (Guo), cytidine (Cyt), 2'-deoxythymidine (Thy) and 2'-deoxyadenosine (dAdo) has been monitored by (1)H NMR as a potential model for the interaction of the 1 species with the probable DNA target. The results reveal that the 1 systems are able to bind the nucleobases endocyclic nitrogen atoms of Guo Cyt, and dAdo.
journal_name
J Inorg Biochemjournal_title
Journal of inorganic biochemistryauthors
Galindo MA,Quirós M,Romero MA,Navarro JAdoi
10.1016/j.jinorgbio.2007.11.009subject
Has Abstractpub_date
2008-05-01 00:00:00pages
1025-32issue
5-6eissn
0162-0134issn
1873-3344pii
S0162-0134(07)00322-4journal_volume
102pub_type
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