TY - JOUR
T1 - Novel luminescent tricarbonylrhenium(I) polypyridine tyraminederived dipicolylamine complexes as sensors for zinc(II) and cadmium(II) Ions
AU - Louie, Man-Wai
AU - Liu, Hua-Wei
AU - Lam, Marco Ho-Chuen
AU - Lau, Tai-Chu
AU - Lo, Kenneth Kam-Wing
PY - 2009/8/10
Y1 - 2009/8/10
N2 - Three luminescent tricarbonylrhenium(I) polypyridine complexes containing a tyramine-derived 2,2'-dipicolylamine (DPAT) unit, [Re(NAN)(CO) 3(py-TU-DPAT)](CF3S03) (py-TU-DPAT = 3-(2(4-hydroxy-3-(2,2'-dipicolylaminomethyl)phenyl)ethylthioureidyl) pyridine;NAN=l,10-phenanthroline (phen) (la), 3,4,7,8-tetramethyl-l, 10-phenanthroline (Me4-phen) (2a), 4,7-diphenyl-l,10-phenanthroline (Ph2-phen) (3a)), and their DPAT-free counterparts, [Re(N AN)(CO)3(py-TU-Et)](CF3S03) (py-TU-Et = 3-(ethylthioureidyl)pyridine; NAN=phen (lb), Me 4-phen (2b), Ph2-phen (3b)), have been synthesized and characterized. Their electrochemical and photophysical properties have been studied. Upon photoexcitation, all the complexes exhibited triplet metal-to-ligand charge-transfer (3MLCT) (dπ(Re)→ π*(NAN)) emission in fluid solutions at 298 K and in low-temperature alcohol glass. The DPAT complexes showed lower emission quantum yields and shorter emission lifetimes compared to those of the DPATfree analogues, indicative of the quenching properties of the appended DPAT unit. The DPAT complexes also exhibited pH-dependent emission, with their emission intensities at pH <3 being ca. 40 fold higher than those at pH > 11. These complexes displayed emission enhancement and lifetime elongation in the presence of zinc(II) and cadmium(II) ions. The cellular uptake of all the complexes by human cervix epithelioid carcinoma (HeLa) cells has been examined by ICP-MS. We have investigated the cytotoxicity of the complexes by the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyltetrazolium bromide (MTT) assay, and the results revealed that all the complexes were more cytotoxic than cisplatin. Furthermore, the cellular uptake of complexes 3a and 3b and the intracellular ion-binding properties of the former complex have been studied by laser-scanning confocal microscopy. © 2009 American Chemical Society.
AB - Three luminescent tricarbonylrhenium(I) polypyridine complexes containing a tyramine-derived 2,2'-dipicolylamine (DPAT) unit, [Re(NAN)(CO) 3(py-TU-DPAT)](CF3S03) (py-TU-DPAT = 3-(2(4-hydroxy-3-(2,2'-dipicolylaminomethyl)phenyl)ethylthioureidyl) pyridine;NAN=l,10-phenanthroline (phen) (la), 3,4,7,8-tetramethyl-l, 10-phenanthroline (Me4-phen) (2a), 4,7-diphenyl-l,10-phenanthroline (Ph2-phen) (3a)), and their DPAT-free counterparts, [Re(N AN)(CO)3(py-TU-Et)](CF3S03) (py-TU-Et = 3-(ethylthioureidyl)pyridine; NAN=phen (lb), Me 4-phen (2b), Ph2-phen (3b)), have been synthesized and characterized. Their electrochemical and photophysical properties have been studied. Upon photoexcitation, all the complexes exhibited triplet metal-to-ligand charge-transfer (3MLCT) (dπ(Re)→ π*(NAN)) emission in fluid solutions at 298 K and in low-temperature alcohol glass. The DPAT complexes showed lower emission quantum yields and shorter emission lifetimes compared to those of the DPATfree analogues, indicative of the quenching properties of the appended DPAT unit. The DPAT complexes also exhibited pH-dependent emission, with their emission intensities at pH <3 being ca. 40 fold higher than those at pH > 11. These complexes displayed emission enhancement and lifetime elongation in the presence of zinc(II) and cadmium(II) ions. The cellular uptake of all the complexes by human cervix epithelioid carcinoma (HeLa) cells has been examined by ICP-MS. We have investigated the cytotoxicity of the complexes by the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyltetrazolium bromide (MTT) assay, and the results revealed that all the complexes were more cytotoxic than cisplatin. Furthermore, the cellular uptake of complexes 3a and 3b and the intracellular ion-binding properties of the former complex have been studied by laser-scanning confocal microscopy. © 2009 American Chemical Society.
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U2 - 10.1021/om900311s
DO - 10.1021/om900311s
M3 - RGC 21 - Publication in refereed journal
SN - 0276-7333
VL - 28
SP - 4297
EP - 4307
JO - Organometallics
JF - Organometallics
IS - 15
ER -