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Christine Goze

Publications and source records attributed to Christine Goze.

7 recordsLinked to original sources

Tetrahedral boron chemistry for the preparation of highly efficient "cascatelle" devices.

The replacement of the two fluorine atoms on the boron center of the well-known Bodipy fluorophore by functionalized acetylenic groups opens the way to a new family of highly luminescent, redox active, and stable fluorophores termed "E-Bodipy" species. The substitution is effective for ethynyl-lithium reagents incorporating tolyl, naphthyl, pyrenyl, fluorenyl, and terpyridinyl units. The protocol also tolerates the presence of various functional groups in the dipyrromethene meso position such as pyrene, phenylethynylpyrene, 4'-terpyridine, and iodophenyl. The last of these is particularly useful for a further coupling reaction enabling introduction of a flexible arm bearing a succinimidyl unit reactive toward primary amines. X-ray structure determinations of two E-Bodipy compounds confirm the introduction of the ethynyl units and show the boron atoms to have a distorted tetrahedral environment, with B-C(ethynyl) approximately 1.59 A and both boron atoms lying essentially in the mean planes of the dipyrromethene units. All the new compounds show intense electronic absorption bands (epsilon 60,000-70,000 M-1 cm-1), high quantum yields (>80%), and slow rates of nonradiative decay. Absorption by the aromatic substituents results in a "cascatelle" process leading to emission exclusively through the boradiazaindacene entity and thus large virtual Stokes' shift (>10,000 cm-1). The new compounds are also redox active, with the formation of both Bodipy+* and Bodipy-* occurring more readily than for F-Bodipy species. The molecules in their excited states are strong reducing agents.

Boron Compounds↗

Unusual fluorescent monomeric and dimeric dialkynyl dipyrromethene-borane complexes.

Novel monomeric and dimeric dialkynyl borondipyrromethene dyes (E-Bodipy) have been prepared in two different ways, providing systems in which the boron center is attached to either two similar or two dissimilar acetylenic units incorporating chromophores such as pyrene or anthracene. Both families exhibit interesting fluorescence and redox properties in which almost quantitative intramolecular energy transfer occurs.

Boranes↗

Synthesis and photophysical properties of borondipyrromethene dyes bearing aryl substituents at the boron center.

Several borondipyrromethene (Bodipy) dyes bearing an aryl nucleus linked directly to the boron center have been prepared under mild conditions. The choice of Grignard or lithio organo-metallic reagents allows the isolation of B(F)(aryl) or B(aryl)2 derivatives; where aryl refers to phenyl, anisyl, naphthyl, or pyrenyl fragments. A single crystal, X-ray structure determination for the bis-anisyl compound shows that the sp3 hybridized boron center remains pseudo-tetrahedral and that the B-C bond distances are 1.615 and 1.636 A. All compounds are electrode active but replacement of the fluorine atoms by aryl fragments renders the Bodipy unit more easily oxidized by 100 mV in the B(F)(aryl) and 180 mV in the B(aryl)2 compounds whereas reduction is made more difficult by a comparable amount. Strong fluorescence is observed from the Bodipy fluorophore present in each of the new dyes, with the radiative rate constant being independent of the nature of the aryl substituent. The fluorescence quantum yields are solvent dependent and, at least in some cases (aryl = anisyl or pyrenyl), nonradiative decay from the first-excited singlet state is strongly activated. There is no indication, however, for population of a charge-transfer state, in which the aryl substituent acts as donor and the Bodipy fragment functions as acceptor, that is strongly coupled to the ground state. Instead, it is conjectured that nonradiative decay involves a conformational change driven by the solvophobic effect. Thus, the rate of nonradiative decay in any given solvent increases with increasing surface accessibility (or molar volume) of the aryl substituent. Intramolecular energy transfer from pyrene or naphthalene residues to Bodipy is quantitative.

Boron Compounds↗

Intramolecular energy transfer in pyrene-bodipy molecular dyads and triads.

Molecules bearing a 4,4-difluoro-8-(aryl)-1,3,5,7-tetramethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacene (bodipy) core and 1-pyrenyl-1-phenyl-4-(1-ethynylpyrene), or 1-phenyl-4-[1-ethynyl-(6-ethynylpyrene)pyrene] units were constructed in a step-by-step procedure based on palladium(0)-promoted cross-coupling reactions with the required preconstructed modules. X-ray structures of single crystals reveal a twisted arrangement of the two chromophores. In one case, an almost perfect orthogonal arrangement is found. These dyes are strongly luminescent in solution and display rich electrochemistry in which all redox processes of the bodipy and pyrene fragments are clearly resolved. The absorption spectra indicate that the bodipy and pyrene chromophores are spectrally isolated, thereby inducing a large "virtual" Stokes shift. The latter is realised by efficient transfer of intramolecular excitation energy by the Förster dipole-dipole mechanism. The rate of energy transfer depends on the structure of the dual-dye system and decreases as the centre-to-centre separation increases. The energy transfer efficiency, however, exceeds 90 % in all cases. The linkage of two pyrene residues by an ethyne group leads to a decrease in the energy-transfer efficiency, with the two polycycles acting as a single chromophore. The directly linked bodipy-pyrene dual dye binds to DNA and operates as an efficient solar concentrator when dispersed in plastic.

Boron Compounds↗

Room temperature phosphorescence from ruthenium(II) complexes bearing conjugated pyrenylethynylene subunits.

We describe the synthesis, electrochemistry, and photophysical properties of several Ru(II) complexes bearing different numbers of pyrenylethynylene substituents in either the 5- or 5,5'-positions of 2,2'-bipyridine, along with the appropriate Ru(II) model complexes bearing either bromo- or ethynyltoluene functionalities. In addition, we prepared and studied the photophysical behavior of the diimine ligands 5-pyrenylethynylene-2,2'-bipyridine and 5,5'-dipyrenylethynylene-2,2'-bipyridine. Static and dynamic absorption and luminescence measurements reveal the nature of the lowest excited states in each molecule. All model Ru(II) complexes are photoluminescent at room temperature and exhibit excited-state behavior consistent with metal-to-ligand charge transfer (MLCT) characteristics. In the three Ru(II) molecules bearing multiple pyrenylethynylene substituents, there is clear evidence that the lowest excited state is triplet intraligand (3IL)-based, yielding long-lived room temperature phosphorescence in the red and near IR. This phosphorescence emanates from either 5-pyrenylethynylene-2,2'-bipyridine or 5,5'-dipyrenylethynylene-2,2'-bipyridine, depending upon the composition of the coordination compound. In the former case, the excited-state absorption difference spectra that were measured for the free ligand are easily superimposed with those obtained for the metal complexes coordinated to either one or two of these species. The latter instance is slightly complicated since coordination of the 5,5'-ligand to the Ru(II) center planarizes the diimine structure, leading to an extended conjugation on the long axis with a concomitant red shift of the singlet pi-pi absorption transitions and the observed room temperature phosphorescence. As a result, transient absorption measurements obtained using free 5,5'-dipyrenylethynylene-2,2'-bipyridine show a marked blue shift relative to its Ru(II) complex, and this extended pi-conjugation effect was confirmed by coordinating this ligand to Zn(II) at room temperature. In essence, all three pyrenylethynylene-containing Ru(II) complexes are unique in this genre of chromophores since the lowest excited state is 3IL-based at room temperature and at 77 K, and there is no compelling evidence of interacting or equilibrated excited states.

Journal Article↗

Cation sensors based on terpyridine-functionalized boradiazaindacene.

A new class of highly luminescent dyes is reported. The characteristic feature of these compounds is that a terpyridine fragment is closely appended to a boradiazaindacene moiety in such a way that cation binding to the vacant terpyridine causes strong perturbations of the photophysical properties of the boradiazaindacene unit. In particular, these sensors are especially applicable to the fluorescence detection of trace quantities of zinc(II) ions in solution. The mechanism of the cation-induced quenching process has been investigated by a combination of electrochemistry, UV/Vis absorption, emission, and NMR spectroscopy. Highly luminescent arrays can be formed by doping transparent polymers with low concentrations of these new dyes. In such materials, the change in photophysical properties upon cation binding is so marked that "cation writing" becomes feasible under routine conditions.

Journal Article↗