Luigi Fabbrizzi

The design of luminescent sensors for anions and ionisable analytes

Abstract A molecular luminescent sensor for anions can be built through a modular approach, i.e. by covalently linking an appropriate photoactive fragment to the receptor displaying a satisfactory affinity towards the desired substrate. Following the receptor-anion interaction, an intercomponent process must take place, e.g. an electron transfer (eT) or an energy transfer (ET) process, that distinctly modifies the emission of the luminophore, thus signalling the occurrence of the recognition event. In this article, specific molecular sensors are classified according to the type of receptor-anion interaction, whether hydrogen bonding or metal–ligand interactions. Receptors of the latter class are based on a Zn II polyamine platform, which leaves at least a vacant coordination site for the incoming anion. Substrates include natural amino acids, NH 3 + CH( R )COO − , for which the highest selectivity is observed when the receptor subunit specifically interacts with the R portion. An eT process involving R and the nearby excited luminophore may provide the signal transduction mechanism.

Urea vs. thiourea in anion recognition

Neutral anion receptors (LH) form stable 1 : 1 H-bond [LH...X]- complexes with carboxylates, halides and phosphate (X-). Some of the [LH...X]- complexes, in presence of an excess of X-, release an HX fragment, with formation of [HX2]- and the deprotonated receptor L-. The tendency towards deprotonation increases with the acidity of the receptor and with the stability of the [HX2]- self-complex. Thus, the more acidic thiourea containing receptor deprotonates in the presence all the investigated anions except chloride, whereas the less acidic urea containing receptor undergoes deprotonation only in the presence of fluoride, due to the high stability of [HF2]-.

Molecular switches of fluorescence operating through metal centred redox couples

Three-component molecular systems (redox active subunit)-spacer-(light-emitting fragment) can operate as fluorescence switches, following the alternate addition of an oxidizing agent and a reducing agent (or the adjustment of the potential of the working electrode in an electrolysis experiment). The redox active subunit typically consists of a metal centred redox couple (M(n+1)+/Mn+), encircled by a macrocyclic receptor, and switching efficiency requires that one of the two oxidation states quenches the proximate fluorophore and the other does not. Four ON/OFF systems, based on either the CuII/CuI or NiIII/NiII couple, will be discussed. The nature of the quenching process responsible for the OFF state, either electron transfer or energy transfer, is related to the length and to the flexibility-rigidity of the spacer.

A chemosensing ensemble for selective carbonate detection in water based on metal-ligand interactions.

Displacement of the loosely encapsulated fluorescent indicator coumarine 343 (F) from a dicopper(II) cryptate enables the selective fluorimetric detection of the HCO3 (-) ion (A) in water (see scheme, •○=Cu(2+) ). The fluorophore is quenched when encapsulated, but displays its full emission when released to the solution.

A two-channel molecular dosimeter for the optical detection of copper(II)

A cyclam-like macrocycle with an integrated push-pull chromophore selectively detects Cu2+ inclusion through both orange-to-yellow colour change and quenching of the green fluorescence.

Anion recognition by dimetallic cryptates

Abstract Bis-tren cryptands (i.e. octamine cages consisting of two tripodal tetramine subunits covalently linked by given spacers) are able to incorporate first two metal ions, then an ambidentate anion, according to a cascade mechanism. In particular, dicopper(II) cryptates behave as effective receptors for anions, which fill the empty cavity of the cage and place their donor atoms in the two axial sites left available by each Cu(II) centre (which adopts a trigonal bipyramidal stereochemistry). Anion encapsulation by dicopper(II) cryptates often induces the development of a rather intense anion-to-metal charge transfer absorption band in the visible region, so that the recognition process is signalled by the appearance of a bright colour. Two examples are considered in detail: (i) that of a rigid bis-tren cryptate containing 1,3-xylyl spacers, which does not recognise the shape, but the bite of the polyatomic anion (i.e. the distance between two consecutive donor atoms); and (ii) that of the flexible cryptate containing 2,5-furanyl spacers, which is able to include also monoatomic anions, in particular halides, displaying peak selectivity in favour of Cl − .

Sensing of transition metals through fluorescence quenching or enhancement. A review

A series of fluorescent sensors for transition metal ions were synthesized by linking a light-emitting subunit, anthracene, to a polyaza chelating subunit, either a dioxotetraamine or a tetraamine. Sensing of the divalent cations CuII, NiII and ZnII was investigated through spectrofluorimetric titrations in acetonitrile–N water (4:1) solutions. The selective recognition of CuII and NiII among other transition and non-transition metal ions is signalled through full quenching of fluorescence; discrimination between the two ions can be achieved by performing titrations at controlled pH. The system containing the tetraamine fragment, whose interaction with CuII and NiII induces fluorescence quenching, is also sensitive to ZnII, but in this case the recognition is signalled through a fluorescence enhancement.

Molecular events switched by transition metals

Transition metals can typically give rise to two (or more) distinct states of comparable stability (two consecutive oxidation states; two different stereochemical arrangements). In a multicomponent system, the conversion of one state to the other can modify a given property of a nearby subunit or can induce drastic changes in the system topology. In this sense, the metal behaves as a switch, which can be operated through an external input (the variation of the pH or of the redox potential). Recent examples of molecular switching by transition metals are reviewed: (i) the quenching/enhancement of the emission of a luminescent fragment effected by a nearby metal centred redox couple (e.g. NiII/NiIII); (ii) the pH driven motion of an aminoalkyl side chain in a NiII scorpionate complex, which is signalled by the variation of the light emission intensity of an appended anthracenyl fragment; (iii) the pH controlled translocation of a NiII ion within a multidentate ligand containing two compartments of different coordinating tendencies and (iv) the intramolecular translocation of a Cl− anion between two pre-positioned metal centres CuII and NiII, within a ditopic receptor, electrochemically driven through the NiII/NiIII redox change.

Recognition and sensing of nucleoside monophosphates by a dicopper(II) cryptate.

The dimetallic cryptate [Cu(2)(II)(1)](4+) selectively recognizes guanosine monophosphate with respect to other nucleoside monophosphates (NMPs) in a MeOH/water solution at pH 7. Recognition is efficiently signaled through the displacement of the indicator 6-carboxyfluorescein bound to the receptor, monitoring its yellow fluorescent emission. Titration experiments evidenced the occurrence of several simultaneous equilibria involving 1:1 and 2:1 receptor/NMP and receptor/indicator complexes. It was demonstrated that the added NMP displaces the indicator from the 2:1 receptor/indicator complex, forming the 1:1 receptor/analyte inclusion complex. Recognition selectivity is thus ascribed to the nature of nucleotide donor atoms involved in the coordination and their ability to encompass the Cu(II)-Cu(II) distance within the cryptate.

The Interaction of Fluoride with Fluorogenic Ureas: An ON1–OFF–ON2 Response

The anion binding tendencies of the two fluorogenic ureas L(1)H and L(2)H, containing the 2-anthracenyl and 1-pyrenyl moieties as signaling units, respectively, have been investigated in MeCN and DMSO by absorption, emission, and (1)H NMR spectroscopies. The formation of stable 1:1 receptor:anion H-bond complexes has been confirmed by structural studies on the crystalline [Bu4N][L(1)···Cl] and [Bu4N][L(2)H···CH3COO] salts. Complexation induces significant variations of the emission properties of L(1)H and L(2)H according to a multifaceted behavior, which depends upon the fluorogenic substituent, the solvent, and the basicity of the anion. Poorly basic anions (Cl(-), Br(-)) cause a red shift of the emission band(s). Carboxylates (CH3COO(-), C6H5COO(-)) induce fluorescence quenching due to the occurrence of an electron-transfer process taking place in the locally excited complex [*L-H···X](-). However, this excited complex may undergo an intracomplex proton transfer from one urea N-H fragment to the anion, to give the tautomeric excited complex [L···H-X](-)*, which emits at higher wavelength. F(-) displays a unique behavior: It forms with L(1)H a stable [L-H···F](-) complex which in the excited state undergoes intracomplex proton transfer, to give the poorly emissive excited tautomer [L···H-F](-)*. With L(2)H, on moderate addition of F(-), the 1:1 H-bond complex forms, and the blue fluorescence of pyrene is quenched. Large excess addition of F(-) promotes deprotonation of the ground-state complex, according to the equilibrium [L(2)H···F](-) + F(-) ⇆ [L(2)](-) + HF2(-). The deprotonated receptor [L(2)](-) is distinctly emissive (yellow fluorescence), which generates the fluorimetric response ON(1)-OFF-ON(2) of receptor L(2)H with respect to F(-).