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Volumn 46, Issue 21, 2007, Pages 8950-8962

Bifunctional amine-tethered ruthenium(II) arene complexes form monofunctional adducts on DNA

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CISPLATIN; DNA; DNA DIRECTED RNA POLYMERASE; RUTHENIUM DERIVATIVE;

EID: 35648996964     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic700799w     Document Type: Article
Times cited : (91)

References (98)
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    • In the context of hydrolysis of bifunctional complexes, loss of a negatively-charged chloride ligand from a neutral complex (mono-aquation) would be expected to be more favorable than further loss of chloride from a positively-charged complex (i.e, second aquation step, reflected by K2 < K1. For the bifunctional ruthenium arene complex, η6-p-cymene)Ru(pta)Cl2, where pta, 1,3,5-triaza-7-phosphaadamantane, simultaneous hydrolysis of both chloride ligands was proposed.55 However, in subsequent 1H NMR solution studies the presence of only the mono-aqua species was detected A. Dorcier et al, Organometallics 2006, 25, 4090-4096, that is, preferential mono-aquation, which appears not to conform to the proposed hydrolysis pathway and thus the reported equilibrium constants
    • 1H NMR solution studies the presence of only the mono-aqua species was detected (A. Dorcier et al., Organometallics 2006, 25, 4090-4096), that is, preferential mono-aquation, which appears not to conform to the proposed hydrolysis pathway and thus the reported equilibrium constants.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.