Determination of nineteen 4-alkylphenol endocrine disrupters in Geneva municipal sewage wastewater

A preconcentration technique, which involves liquid-liquid-liquid microextraction, was developed to determine phenoxy herbicides in bovine milk. A layer of organic phase was impregnated into the pores of a 3.5 cm long porous hollow fiber, while the internal volume of the fiber was filled with NaOH solution (the acceptor solution) that was connected directly to the needle of a microsyringe. The fiber was then immersed into 8 ml of acidified milk sample. When the sample solution was stirred, acidic analytes were extracted into the organic phase and back extracted simultaneously into the alkaline acceptor medium as the analytes were protonated at low pH and deprotonated at high pH. After extracting for a prescribed time, 5 microl acceptor solution was taken back into the syringe and injected directly into a HPLC system for quantification. The analytes were extracted quantitatively from the sample solution into the acceptor solution with a large enrichment factor of 900. Due to its low cost, the hollow-fiber extraction device was disposed of after a single extraction that eliminated the possibility of carry over effects. In addition, because a small volume of organic solvent was required and little waste is generated, the procedure is environmentally friendly, and is compatible with the "green chemistry" concept.     

DFT study of the ring opening polymerization of ε-caprolactone by grafted lanthanide complexes: 2--Effect of the initiator ligand

The influence of the initiator ligand on the Ring Opening Polymerization (ROP) of ε-caprolactone by lanthanide complexes grafted on silica have been investigated by means of density functional theory (DFT) calculations. Three different initiator ligands (alkyl, dialkylamido and borohydride) and three grating modes (mono-grafted, bi-grafted or bi-grafted after breaking of a Si-O-Si bridge) have been considered. This study highlights that lanthanum grafted complexes (alkyl, amide or borohydride) are active in lactone polymerization. In any case the reaction process is demonstrated to be similar to the one found for homogeneous catalysts. However, even if the different grafting modes are energetically equivalent for the ε-caprolactone ROP initiation reaction, some differences are observed according to the ligand involved in the initiation reaction. In agreement with experimental data, grafted lanthanide amides rapidly polymerise the ε-caprolactone. The grafted alkyl lanthanum complexes are also predicted to be very efficient catalysts. The borohydride is thus predicted to be the least efficient due to the difficulties in the ring opening. Indeed, the rate-determining step is the nucleophilic attack for the methyl and dialkylamido ligands (occuring with a low barrier) whereas it is the ring opening for the borohydride ligands (highest barrier) and the formation of -CH(2)C(=O)(X) (X = CH(3) or NMe(2)) terminal group is more favorable than that of a -CH(2)OBH(2) end group.     

Effects of long‐term exposure to elevated CO2 conditions in slow‐growing plants using a 12C‐enriched CO2‐labelling technique

Despite their relevancy, long‐term studies analyzing elevated CO₂ effect in plant production and carbon (C) management on slow‐growing plants are scarce. A special chamber was designed to perform whole‐plant above‐ground gas‐exchange measurements in two slow‐growing plants (Chamaerops humilis and Cycas revoluta) exposed to ambient (ca. 400 µmol mol^?1) and elevated (ca. 800 µmol mol^?1) CO₂ conditions over a long‐term period (20 months). The ambient isotopic ¹³C/¹²C composition (δ¹³C) of plants exposed to elevated CO₂ conditions was modified (from ca. ?12.8‰ to ca. ?19.2‰) in order to study carbon allocation in leaf, shoot and root tissues. Elevated CO₂ increased plant growth by ca. 45% and 60% in Chamaerops and Cycas, respectively. The whole‐plant above‐ground gas‐exchange determinations revealed that, in the case of Chamaerops, elevated CO₂ decreased the photosynthetic activity (determined on leaf area basis) as a consequence of the limited ability to increase C sink strength. On the other hand, the larger C sink strength (reflected by their larger CO₂ stimulatory effect on dry mass) in Cycas plants exposed to elevated CO₂ enabled the enhancement of their photosynthetic capacity. The δ¹³C values determined in the different plant tissues (leaf, shoot and root) suggest that Cycas plants grown under elevated CO₂ had a larger ability to export the excess leaf C, probably to the main root. The results obtained highlighted the different C management strategies of both plants and offered relevant information about the potential response of two slow‐growing plants under global climate change conditions. Copyright © 2008 John Wiley & Sons, Ltd.     

Highly Stable trans‐Cyclooctene Amino Acids for Live‐Cell Labeling

trans‐Cyclooctene groups incorporated into proteins via non‐canonical amino acids (ncAAs) are emerging as specific handles for bioorthogonal chemistry. Here, we present a highly improved synthetic access to the axially and the equatorially linked trans‐cyclooct‐2‐ene isomers ( 1 a , b ). We further show that the axially connected isomer has a half‐life about 10 times higher than the equatorial isomer and reacts with tetrazines much faster, as determined by stopped‐flow experiments. The improved properties resulted in different labeling performance of the insulin receptor on the surface of intact cells.     

Grafting of Lanthanum Complexes on a Functionalized Graphene Surface: Theoretical Investigation on Ethylene and 1,3-Butadiene Homo- and Co-Polymerization

In this contribution, we describe the use of graphene as an efficient catalyst support and the role it plays in increasing the Lewis acidity of the supported metal complexes. By a density functional theory study, we show that the [La(N(SiMe₃)₂)₃] complex can be easily grafted on graphene-OH and -COOH functionalized surfaces. Two stable mono-grafted compounds, (gO)-[La(N(SiMe₃)₂)₂] and (gOO)-[La(N(SiMe₃)₂)₂], are formed, behaving as stronger Lewis acids than the previously reported silica grafted analogues. To study the role of the graphene support in catalysis, we also computed the catalytic activity of the alkylated (gO)-[La(CH₃)₂] and (gOO)-[La(CH₃)₂] complexes in the ethylene and 1,3-butadiene homo- and co-polymerization reactions. Both compounds are efficient catalysts for the homo-polymerization of the ethylene and 1,3-butadiene. For the 1,3-butadiene homo-polymerization, the stereoselectivity outcome of the reaction differs according to the grafting site. The results computed for the co-polymerization reaction, finally, show that the high stability of the allylic products leads to the formation of block copolymers.     

Ruthenium nanoparticles canopied by heptagon-containing saddle-shaped nanographenes as efficient aromatic hydrogenation catalysts

The search for new ligands capable of modifying the metal nanoparticle (MNP) catalytic behavior is of increasing interest. Herein we present the first example of RuNPs stabilized with non-planar heptagon-containing saddle-shaped nanographenes (Ru@1 and Ru@2). The resemblance to graphene-supported MNPs makes these non-planar nanographene-stabilized RuNPs very attractive systems to further investigate graphene–metal interactions. A combined theoretical/experimental study allowed us to explore the coordination modes and dynamics of these nanographenes at the Ru surface. The curvature of these saddle-shaped nanographenes makes them efficient MNP stabilizers. The resulting RuNPs were found to be highly active catalysts for the hydrogenation of aromatics, including platform molecules derived from biomass (i.e. HMF) or liquid organic hydrogen carriers (i.e. N-indole). A significant ligand effect was observed since a minor modification on the hept-HBC structure (C CH₂ instead of C O) was reflected in a substantial increase in the MNP activity. Finally, the stability of these canopied RuNPs was investigated by multiple addition experiments, proving to be stable catalysts for at least 96 h.

Ruthenium nanoparticles stabilized with non-planar polycyclic aromatic hydrocarbons (PAHs) are active catalysts in the hydrogenation of aromatic substrates under mild conditions.     

Rotational Spectrum and Conformational Analysis of Perillartine: Insights into the Structure–Sweetness Relationship

We used high-resolution rotational spectroscopy coupled to a laser ablation source to study the conformational panorama of perillartine, a solid synthetic sweetener. Four conformers were identified under the isolation conditions of the supersonic expansion, showing that all of them present an E configuration of the C=N group with respect to the double bond of the ring. The observed structures were verified against Shallenberger–Acree–Kier’s sweetness theory to shed light on the structure–sweetness relationship for this particular oxime, highlighting a deluge of possibilities to bind the receptor.     

Small Changes Have Consequences: Lessons from Tetrabenzyltitanium and ‐zirconium Surface Organometallic Chemistry

Homoleptic benzyl derivatives of titanium and zirconium have been grafted onto silica that was dehydroxylated at 200 and 700 °C, thereby affording bi‐grafted and mono‐grafted single‐site species, respectively, as shown by a combination of experimental techniques (IR, MAS NMR, EXAFS, and elemental analysis) and theoretical calculations. Marked differences between these compounds and their neopentyl analogues are discussed and rationalized by using DFT. These differences were assigned to the selectivity of the grafting process, which, depending on the structure of the molecular precursors, led to different outcomes in terms of the mono‐ versus bi‐grafted species for the same surface concentration of silanol species. The benzylzirconium derivatives were active towards ethylene polymerization in the absence of an activator and the bi‐grafted species displayed higher activity than their mono‐grafted analogues. In contrast, the benzyltitanium and neopentylzirconium counterparts were not active under similar reaction conditions.     

Isolation of C1 through C4 derivatives from CO using heteroleptic uranium(iii) metallocene aryloxide complexes

The conversion of C1 feedstock molecules such as CO into commodity chemicals is a desirable, but challenging, endeavour. When the U(iii) complex, [(C₅Me₅)₂U(O-2,6-^tBu₂-4-MeC₆H₂)], is exposed to 1 atm of CO, only coordination is observed by IR spectroscopy as well as X-ray crystallography, unveiling a rare structurally characterized f element carbonyl. However, using [(C₅Me₅)₂(MesO)U (THF)], Mes = 2,4,6-Me₃C₆H₂, reaction with CO forms the bridging ethynediolate species, [{(C₅Me₅)₂(MesO)U}₂(μ₂-OCCO)]. While ethynediolate complexes are known, their reactivity has not been reported in much detail to afford further functionalization. For example, addition of more CO to the ethynediolate complex with heating forms a ketene carboxylate, [{(C₅Me₅)₂(MesO)U}₂(μ₂:κ²:η¹-C₃O₃)], which can be further reacted with CO₂ to yield a ketene dicarboxylate complex, [{(C₅Me₅)₂(MesO)U}₂(μ₂:κ²:κ²-C₄O₅)]. Since the ethynediolate showed reactivity with more CO, we explored its reactivity further. A [2 + 2] cycloaddition is observed with diphenylketene to yield [{(C₅Me₅)₂U}₂(OC(CPh₂)C( O)CO)] with concomitant formation of [(C₅Me₅)₂U(OMes)₂]. Surprisingly, reaction with SO₂ shows rare S–O bond cleavage to yield the unusual [(O₂CC(O)(SO)]²⁻ bridging ligand between two U(iv) centres. All complexes have been characterized using spectroscopic and structural methods, and the reaction of the ethynediolate with CO to form the ketene carboxylate has been investigated computationally as well as the reaction with SO₂.

Functionalization of CO from C1 to C4 is acheived using a heteroleptic uranium(iii) complex.     

An Experimental and Computational Investigation Rules Out Direct Nucleophilic Addition on the N2 Ligand in Manganese Dinitrogen Complex [Cp(CO)2Mn(N2)]

We have re-examined the reactivity of the manganese dinitrogen complex [Cp(CO)₂Mn(N₂)] ( 1 , Cp=η⁵-cyclopentadienyl, C₅H₅) with phenylithium (PhLi). By combining experiment and density functional theory (DFT), we have found that, unlike previously reported, the direct nucleophilic attack of the carbanion onto coordinated dinitrogen does not occur. Instead, PhLi reacts with one of the CO ligands to provide an anionic acylcarbonyl dinitrogen metallate [Cp(CO)(N₂)MnCOPh]Li ( 3 ) that is stable only below −40 °C. Full characterization of 3 (including single crystal X-ray diffraction) was performed. This complex decomposes quickly above −20 °C with N₂ loss to give a phenylate complex [Cp(CO)₂MnPh]Li ( 2 ). The latter compound was erroneously formulated as an anionic diazenido compound [Cp(CO)₂MnN(Ph)=N]Li in earlier reports, ruling out the claimed and so-far unique behavior of the N₂ ligand in 1 . DFT calculations were run to explore both the hypothesized and the experimentally verified reactivity of 1 with PhLi and are fully consistent with our results. Direct attack of a nucleophile on metal-coordinated N₂ remains to be demonstrated.