Abstract:A series of rhenium(I) tricarbonyl diimine complexes with crown ether pendants has been synthesized and characterized. The complexes showed selective and specific binding properties for various metal ions of different sizes and degrees of hardness and softness by variation of the cavity size and donor atoms of the crown ether. Upon binding of metal ions, obvious spectral changes were observed in the UV-vis spectra of the complexes and the emission intensity was found to be strongly enhanced. The X-ray crystal … Show more
“…The rhenium atoms are also coordinated by three carbonyl ligands in a fac arrangement, as well as one halogen atom. The average Re\N bond length is 2.338 and 2.182 Å for 1 and 2, respectively, which are consistent with other similar complexes [33][34][35]. The bite angles of N\Re\N (average 59.1°for 1 and 59.71°for 2) are significantly deviating from the ideal value of 90°, imposed by satiric requirement of chelating geometry of the naphthyridine ring.…”
“…The rhenium atoms are also coordinated by three carbonyl ligands in a fac arrangement, as well as one halogen atom. The average Re\N bond length is 2.338 and 2.182 Å for 1 and 2, respectively, which are consistent with other similar complexes [33][34][35]. The bite angles of N\Re\N (average 59.1°for 1 and 59.71°for 2) are significantly deviating from the ideal value of 90°, imposed by satiric requirement of chelating geometry of the naphthyridine ring.…”
“…The red shift of the emission maxima could be explained by the fact that the binding of the cations to imine ligand would decrease σ-donating ability and stabilize the π* orbital of the bipyridine ligand and hence decreased the emission energy [63]. Recently Wang et al and others [22,23,6466] pointed out that the weak luminescence of coumarin derivative containing imine group can be explained by C=N isomerization mechanism which facilitates the decay of the excited state via nonradiative process.…”
“…The incorporation of soft donor atoms such as S or Se in the pendant groups allows for specific binding of soft metal cations. For example, Yam et al [8] have achieved highly selective sensing of Pb 2+ and Hg 2 using complexes 1c and 1d, respectively (Fig. 1).…”
Compounds that change their absorption and/or emission properties in the presence of a target ion or molecule have been studied for many years as the basis for optical sensing. Within this group of compounds, a variety of organometallic complexes have been proposed for the detection of a wide range of analytes such as cations (including H + ), anions, gases (e.g. O 2 , SO 2 , organic vapours), small organic molecules, and large biomolecules (e.g. proteins, DNA). This chapter focuses on work reported within the last few years in the area of organometallic sensors. Some of the most extensively studied systems incorporate metal moieties with intense long-lived metal-to-ligand charge transfer (MLCT) excited states as the reporter or indicator unit, such as fac-tricarbonyl Re(I) complexes, cyclometallated Ir(III) species, and diimine Ru(II) or Os(II) derivatives. Other commonly used organometallic sensors are based on Pt-alkynyls and ferrocene fragments. To these reporters, an appropriate recognition or analyte-binding unit is usually attached so that a detectable modification on the colour and/or the emission of the complex occurs upon binding of the analyte. Examples of recognition sites include macrocycles for the binding of cations, H-bonding units selective to specific anions, and DNA intercalating fragments. A different approach is used for the detection of some gases or vapours, where the sensor's response is associated with changes in the crystal packing of the complex on absorption of the gas, or to direct coordination of the analyte to the metal centre.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.