Stealth Luminescent Organic Nanoparticles Made from Quadrupolar Dyes for Two-Photon Bioimaging: Effect of End-Groups and Core

Molecular-based Fluorescent Organic Nanoparticles (FONs) are versatile light-emitting nano-tools whose properties can be rationally addressed by bottom-up molecular engineering. A challenging property to gain control over is the interaction of the FONs’ surface with biological systems. Indeed, most types of nanoparticles tend to interact with biological membranes. To address this limitation, we recently reported on two-photon (2P) absorbing, red to near infrared (NIR) emitting quadrupolar extended dyes built from a benzothiadiazole core and diphenylamino endgroups that yield spontaneously stealth FONs. In this paper, we expand our understanding of the structure-property relationship between the dye structure and the FONs 2P absorption response, fluorescence and stealthiness by characterizing a dye-related series of FONs. We observe that increasing the strength of the donor end-groups or of the core acceptor in the quadrupolar (D-π-A-π-D) dye structure allows for the tuning of optical properties, notably red-shifting both the emission (from red to NIR) and 2P absorption spectra while inducing a decrease in their fluorescence quantum yield. Thanks to their strong 1P and 2P absorption, all FONs whose median size varies between 11 and 28 nm exhibit giant 1P (10⁶ M⁻¹.cm⁻¹) and 2P (10⁴ GM) brightness values. Interestingly, all FONs were found to be non-toxic, exhibit stealth behaviour, and show vanishing non-specific interactions with cell membranes. We postulate that the strong hydrophobic character and the rigidity of the FONs building blocks are crucial to controlling the stealth nano-bio interface.     

Functionalisation of mesoporous silica nanoparticles with 3-isocynatopropyltrichlorosilane

The functionalisation of Mesoporous Silica Nanoparticles (MSN) with the isocyanate group was carried out. The excellent reactivity of 3-isocynanatopropyltrichlorosilane allowed its grafting on the surface of MSN in mild conditions. Further reaction with different nucleophiles bearing primary amino groups led to the formation of a urea linkage and thus the covalent grafting of the nucleophiles to the MSN surface.     

Local field corrections to binding energies of substitutional and interstitial donors in Si and Ge

Intervalley Umklapp matrix elements, with inclusion of local field screening effects, are computed for substitutional and interstitial point-charge impurity potentials in Si and Ge. The shallow character of substitutional donors is not affected in Ge and is even reinforced in Si, where a 20% reduction of the binding energy is obtained as a consequence of the local field effect. In both semiconductors the local field corrections strongly reinforce the non-effective-mass, deep-level character of interstitial point-charge donors.     

On the normal form of a system of differential equations with nilpotent linear part

We consider prenormal forms associated to generic perturbations of the system $\text{x}\text{?}\text{=2y,}\text{y}\text{?}\text{=3x}{}^2$. It is known that they have a formal normal form $\text{x}\text{?}\text{=2y+2x}\text{Δ}{}^1\text{,}\text{y}\text{?}\text{=3x}{}^2\text{+3y}\text{Δ}{}^1$, where $\text{Δ}{}^1\text{=x+A}{}_0\text{(y}{}^2\text{?x}{}^3\text{)}$ [Differential Equations 158 (1) (1999) 152–173]. We show that the series A₀ and the normalizing transformations are divergent, but 1-summable. To cite this article: M. Canalis-Durand, R. Schäfke, C. R. Acad. Sci. Paris, Ser. I 336 (2003).     

Concentration of sodium ion as the determining factor for the association of dansyl amino acids with the teicoplanin molecule in reversed-phase liquid chromatography

The mechanism of the binding of D,L dansyl amino acids to teicoplanin was investigated. Na+ was used as an indicator of the interactions between the solutes and teicoplanin. The number (n) of sodium ions, Na+, excluded from the solute-teicoplanin interface when analyte transfer occurred was determined. A thermodynamic study and enthalpy-entropy compensation were performed to further explore the interaction mechanism. From these results, it was shown that teicoplanin was balanced between 2 conformational states characterized by distinct enantioselective properties. This approach indicates that liquid chromatography (LC) is a useful tool to extract physicochemical and molecular information from retention data. Thus, LC can be used as a complementary technique with the conventional techniques of molecular interaction analysis.     

Non-Traditional Squares of Predication and Quantification

Three logical squares of predication or quantification, which one can even extend to logical hexagons, will be presented and analyzed. All three squares are based on ideas of the non-traditional theory of predication developed by Sinowjew and Wessel. The authors also designed a non-traditional theory of quantification. It will be shown that this theory is superfluous, since it is based on an obscure difference between two kinds of quantification and one pays a high price for differentiating in this way: losing the definability between the existence- and all-quantifier. Therefore, a combination of non-traditional predication and classical quantification is preferred here.      

On the independence complex of square grids

The enumeration of independent sets of regular graphs is of interest in statistical mechanics, as it corresponds to the solution of hard-particle models. In 2004, it was conjectured by Fendley et al., that for some rectangular grids, with toric boundary conditions, the alternating number of independent sets is extremely simple. More precisely, under a coprimality condition on the sides of the rectangle, the number of independent sets of even and odd cardinality always differ by 1. In physics terms, this means looking at the hard-particle model on these grids at activity −1. This conjecture was recently proved by Jonsson. Here we produce other families of grid graphs, with open or cylindric boundary conditions, for which similar properties hold without any size restriction: the number of independent sets of even and odd cardinality always differ by 0, ±1, or, in the cylindric case, by some power of 2. We show that these results reflect a stronger property of the independence complexes of our graphs. We determine the homotopy type of these complexes using Forman’s discrete Morse theory. We find that these complexes are either contractible, or homotopic to a sphere, or, in the cylindric case, to a wedge of spheres. Finally, we use our enumerative results to determine the spectra of certain transfer matrices describing the hard-particle model on our graphs at activity −1. These results parallel certain conjectures of Fendley et al., proved by Jonsson in the toric case.     

Isolation of lanthanides from spent nuclear fuel by means of high performance ion chromatography (HPIC) prior to mass spectrometric analysis

Pure and complete fractions of neodymium, samarium, europium, gadolinium and dysprosium were isolated by means of high performance ion chromatography, using a cation exchange column and gradient elution with alpha-hydroxyisobutyric acid solutions (α-HIBA). Intermediate precision and robustness of the isolation method was investigated, identifying eluent pH as the most important parameter. Investigation of the elution behaviour of the most important fission and activation products and actinides indicated that preventing the accumulation of cesium on the cation exchange column required further isocratic elution with a higher concentrated α-HIBA solution after elution of the lanthanides. A sample matrix free of carbon was achieved by means of acid digestion, followed by UV photo-oxidation, resulting in samples suitable for mass spectrometric analysis.

     

Single crystal EPR study of the dinuclear Cu(II) complex [Cu(tda)(phen)](2)·H(2)tda (tda = thiodiacetate, phen = phenanthroline): influence of weak interdimeric magnetic interactions

We report powder and single crystal EPR measurements of [Cu(tda)(phen)](2)·H(2)tda (tda = thiodiacetate, phen = phenanthroline) at 9.7 GHz. This compound consists of centrosymmetric copper(II) ion dimers, weakly ferromagnetically exchange-coupled (J = +3.2 cm(-1)), in which the dimeric units are linked by hydrophobic chemical paths involving the phen molecules. EPR revealed that the triplet spectra are collapsed by interdimeric exchange interactions mediated by that chemical path. Analysis and simulation of the single crystal EPR spectra were performed using Anderson's exchange narrowing model, together with statistical arguments. This approach allowed us to interpret the spectra modulated by the interdimeric interactions in situations of weak, intermediate, and strong exchange. We evaluated an interdimeric exchange constant J' = 0.0070(3) cm(-1), indicating that hydrophobic paths can transmit weak exchange interactions between centers at relatively long distances of the order of ～10 ?.