BackgroundExcessive exposure to manganese (Mn), an essential trace element, has been shown to be neurotoxic, especially when inhaled. Few studies have examined potential effects of Mn on cognitive functions of environmentally exposed children.ObjectiveThis study was intended to estimate environmental exposure to Mn resulting from mining and processing and to explore its association with intellectual function of school-age children.MethodsChildren between 7 and 11 years of age from the Molango mining district in central Mexico (n = 79) and communities with similar socioeconomic conditions that were outside the mining district (n = 93) participated in the cross-sectional evaluation. The revised version of the Wechsler Intelligence Scale for Children adapted for the Mexican population was applied. Concentrations of Mn in blood (MnB) and hair (MnH) were used as biomarkers of exposure.ResultsExposed children had significantly higher median values for MnH (12.6 μg/g) and MnB (9.5 μg/L) than did nonexposed children (0.6 μg/g and 8.0 μg/L, respectively). MnH was inversely associated with Verbal IQ [β = −0.29; 95% confidence interval (CI), −0.51 to −0.08], Performance IQ (β = −0.08; 95% CI, −0.32 to 0.16), and Total Scale IQ (β = −0.20; 95% CI, −0.42 to 0.02). MnB was inversely but nonsignificantly associated with Total and Verbal IQ score. Age and sex significantly modified associations of MnH, with the strongest inverse associations in young girls and little evidence of associations in boys at any age. Associations with MnB did not appear to be modified by sex but appeared to be limited to younger study participants.ConclusionsThe findings from this study suggest that airborne Mn environmental exposure is inversely associated with intellectual function in young school-age children.

Surfactant molecules are tested as water-in-crude emulsion breakers to attain the quickest separation rate in the so-called “proportional regime”. A concept of demulsifier performance is proposed on the basis of the required demulsifier concentration to offset the effect of a given amount of asphaltenes. The experimental evidence allows one to rank the tested products and relate their performance to their hydrophilicity and molecular weight. Some evidence indicates that the presence of acids in the crude makes it easier to break emulsions and suggests that so-called “extended surfactants” can significantly shorten the demulsifying process.

The synthesis of simple imidazolium-based ligand precursors containing a 1,3-alkylidene-2,4,6-trimethylbenzene spacer was examined and different synthetic protocols were applied depending on the nature of the alkylidene arm. For a methylene arm, simple dications 5a,b.2CI were obtained directly. The higher homologue counterparts were conveniently prepared by general multistep routes following a five-step sequence for ethylene dications 6a,b.2Br or a six-step sequence for propylene dications 7a,b.2Br in > or = 52% overall yield. Imidazolium salts based on the shorter methylene spacer were used to prepare palladium complexes (17-20) with N-heterocyclic carbenes via transmetallation from well-defined silver compounds or directly in basic conditions. In order to facilitate spectroscopic characterisation of the palladium species two [Pd(allyl)(bis-oxazoline)]+ (25-26) complexes with the same ligand bridge were synthesized. [PdX2bisL] complexes appeared in solution as mixtures of species, mononuclear with cis- or trans-geometry or oligomeric compounds. The reaction of [PdCl(allyl)]2 and micro-bis(carbene)(AgX)2 complexes in 1 : 1 or in 0.5 : 1 ratio leads to binuclear compounds [Pd2Cl2(allyl)2(micro-bis-carbene)] (19a,19b) and to very labile monomeric [Pd(allyl)(bis-carbene)]+ (20a,20b) compounds, respectively. The preparation of analogous [Pd(allyl)(bis-oxazoline)]+ complexes showed the formation of one of the four possible isomers. [Pd(allyl)(bis-oxazoline)]PF6 complexes were inactive as catalytic precursors in the allylic substitution reaction.

No abstract

Excess nitrogen (N) leading to the eutrophication of water and impacts on ecosystems is a serious environmental challenge. Wetlands can remove significant amounts of N from the water, primarily through the process of denitrification. Most of our knowledge on wetland denitrification is from temperate climates; studies in natural tropical wetlands are very scarce. We measured denitrification rates during a dry and a wet season in five floodplain forests dominated by Melaleuca spp., a coastal freshwater wetland of tropical Australia. We hypothesised that the denitrification potential of these wetlands would be high throughout the year and would be limited by N and carbon (C) availability. Mean potential denitrification rates (Dt) were 5.0±1.7mgm2h–1, and were within the reported ranges for other tropical and temperate wetlands. The rates of Dt were similar between the dry and the wet seasons. From the total unamended denitrification rates (Dw, 3.1±1.7mgm2h–1), 64% was derived from NO3– of the water column and the rest from coupled nitrification–denitrification. The factor most closely associated with denitrification was background water NO3–-N concentrations. Improved management and protection of wetlands could play an important role in improving water quality in tropical catchments.

Optimization studies allowed the efficient synthesis of a simple structural motif based on meta‐bis(1‐imidazolyl)benzenes 1 through copper‐catalyzed coupling of 1,3‐diiodobenzene and imidazole under mild reaction conditions. This protocol was then used to prepare a representative sterically hindered N‐arylimidazole 2a, the most common structural motif among N‐heterocyclic carbenes (NHC). Having optimized the main variables governing CuI‐catalyzed imidazole N‐arylation, the first Ullmann‐type synthesis of N‐mesitylimidazole (2a) is reported. Moreover, the coupling between boronic acids as the aryl donor partners and either imidazole or benzimidazole was examined; in all cases the reactions proceeded in very low yield. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)

An instrument was constructed to assess faculty attitudes toward university students with disabilities and accommodations in the United States and México. Faculty in the United States were more positive about their professional development and had more positive general assumptions about students with disabilities. Faculty in both countries were very similar in their willingness to accommodate most types of students with disabilities and to become friends with people with disabilities.

The enantioselective synthesis of tropanols has been accomplished through chiral phosphoric acid catalyzed pseudotransannular ring opening of 1‐aminocyclohept‐4‐ene‐derived epoxides. The reaction proceeds together with the desymmetrization of the starting material and leads to the direct formation of the 8‐azabicyclo[3.2.1]octane scaffold with excellent stereoselectivity. The synthetic applicability of the reaction was demonstrated by the enantioselective synthesis of the two natural products (−)‐α‐tropanol and (+)‐ferruginine.