2016
DOI: 10.1039/c6dt01264g
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Pyridylphosphinate metal complexes: synthesis, structural characterisation and biological activity

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Cited by 15 publications
(11 citation statements)
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“…The pKa of compound 1 could not be calculated, as the absorbance bands for the aqua-and the hydroxo-compounds overlap; however, changes could only be observed at pH values higher than 10. These pKa values are high, although such a decrease in acidity has been previously reported (generally attributed to an increased electron density on the metal centre) [60,63,64]. As a consequence of such high pKa, only the aqua adduct of the metal complexes is expected to be present at physiological pH (7.4), thus favouring the reaction between the metal complexes with possible ligands such as nucleobases or proteins.…”
Section: Synthesis Stability In Solution Aquation and Pka Determinationmentioning
confidence: 85%
“…The pKa of compound 1 could not be calculated, as the absorbance bands for the aqua-and the hydroxo-compounds overlap; however, changes could only be observed at pH values higher than 10. These pKa values are high, although such a decrease in acidity has been previously reported (generally attributed to an increased electron density on the metal centre) [60,63,64]. As a consequence of such high pKa, only the aqua adduct of the metal complexes is expected to be present at physiological pH (7.4), thus favouring the reaction between the metal complexes with possible ligands such as nucleobases or proteins.…”
Section: Synthesis Stability In Solution Aquation and Pka Determinationmentioning
confidence: 85%
“…These p K a values are high, although such decrease in acidity has been previously reported (generally attributed to an increased electron density on the metal centre). ( Liu and Sadler, 2014 , Peacock et al., 2006 , Cross et al., 2016 ) As a consequence of such high p K a values, only the aqua adduct of the metal complexes is expected to be present at physiological pH (7.4), thus favouring the reaction between the metal complexes with possible ligands such as nucleobases or proteins.…”
Section: Resultsmentioning
confidence: 99%
“…It is worth mentioning here that halide exchange in all Ru(II) complexes does not necessarily follow a common trend. 38,56 In contrast to the NMR data, upon injecting an aliquot of the NMR sample, after necessary dilution with methanol, no m/z peak was observed in the ESI-MS for the halide-exchanged species in 2 and 3. Only the dehalogenated species [(η 6 -pcymene)Ru II Table S5.…”
Section: Solution Stabilitymentioning
confidence: 96%