Time-resolved luminescence microscopy of bimetallic lanthanide helicates in living cells.

Multiphoton-excited luminescent lanthanide bioprobes: two- and three-photon cross sections of dipicolinate derivatives and binuclear helicates.

Multiphoton excited luminescent properties of water-soluble Eu(III) and Tb(III) complexes with derivatives of dipicolinic acid functionalized with a polyoxyethylene pendant arm and terminal groups, [Eu(L(OMe))(3)](3-), [Eu(L(NH2))(3)](3-), and [Tb(L(OH))(3)](3-), as well as of binuclear helicates with overall composition [Ln(2)(L(CX))(3)] (X = 2, 5) are investigated. Characteristic emission fro...

Synthesis and cell localization of self-assembled dinuclear lanthanide bioprobes.

Lanthanide bioprobes and bioconjugates are ideal luminescent stains in view of their low propensity to photobleaching, sharp emission lines and long excited state lifetimes permitting time-resolved detection for enhanced sensitivity. In this paper, we expand our previous work which demonstrated that self-assembled dinuclear triple-stranded helicates [Ln2(L(C2X))3] behave as excellent cell and t...

A versatile ditopic ligand system for sensitizing the luminescence of bimetallic lanthanide bio-imaging probes.

The homoditopic ligand 6,6'-[methylenebis(1-methyl-1H-benzimidazole-5,2-diyl)]bis(4-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}pyridine-2-carboxylic acid) (H(2)L(C2)) has been tailored to self-assemble with lanthanide ions (Ln(III)), which results in the formation of neutral bimetallic helicates with the overall composition [Ln(2)(L(C2))(3)] and also provides a versatile platform for further derivati...

Bimetallic lanthanide complexes that display a ratiometric response to oxygen concentrations† †Electronic supplementary information (ESI) available: Synthetic procedures, luminescence and NMR spectra, photophysical considerations, time-resolved emission profiles and luminescence lifetimes. See DOI: 10.1039/c4sc03827d Click here for additional data file.

Isolation and characterization of the first circular single-stranded polymetallic lanthanide-containing helicate.

A thorough examination of the disassembly of bimetallic triple-stranded lanthanide helicates [Ln2(Li)3]6+ (stoichiometry S = m/n = 2/3 = 0.67, global complexity GC = m + n = 2 + 3 = 5) in excess of metals shows the competitive formation of standard linear bimetallic complexes [Ln2(Li)2]6+ (S= 1.0, GC = 4), and circular trimetallic single-stranded helicates [Ln3(Li)3]9+ (S= 1.0, GC = 6).