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  • General Chemistry  (77,717)
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  • 1
    Publication Date: 2024-02-26
    Description: Identifcation of ontogenetic age classes plays an important role in the felds of zoology, palaeontology and archaeology, where accurate age classifcations of (sub)fossil remains are a crucial component for the reconstruction \nof past life. Textural ageing\xe2\x80\x94the identifcation of age-related bone surface textures\xe2\x80\x94provides a size-independent \nmethod for age assessment of vertebrate material. However, most of the work so far is limited to qualitative results. \nWhile qualitative approaches provide helpful insights on textural ageing patterns, they are heavily subject to observer \nbias and fall short of quantitative data relevant for detailed statistical analyses and cross-comparisons. Here, we present a pilot study on the application of 3D surface digital microscopy to quantify bone surface textures on the long \nbones of the grey heron (Ardea cinerea) and the Canada goose (Branta canadensis) using internationally verifed \nroughness parameters. Using a standardised measuring protocol, computed roughness values show a strong correlation with qualitative descriptions of textural patterns. Overall, higher roughness values correspond to increased numbers of grooves and pits and vice versa. Most of the roughness parameters allowed distinguishing between diferent \nontogenetic classes and closely followed the typical sigmoidal animal growth curve. Our results show that bone \ntexture quantifcation is a feasible approach to identifying ontogenetic age classes.
    Keywords: General Physics and Astronomy ; General Environmental Science ; General Biochemistry ; Genetics and Molecular Biology ; General Materials Science ; General Chemistry ; Roughness ; Surfaces ; Taphonomy ; Topography ; Bone ; Ontogeny ; Digital microscopy
    Repository Name: National Museum of Natural History, Netherlands
    Type: info:eu-repo/semantics/article
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 1238-1243 
    ISSN: 0947-6539
    Keywords: gels ; electron microscopy ; scanning tunneling microscopy ; self-assembly ; ureas ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New low molecular weight gelators based on the structure R—NHCONH—X—NHCONH—R have been synthesized and tested for their ability to cause gelation of organic solvents. Compounds 2 (R = n-dodecyl, X = -(CH2)9-), 3 (R = n-dodecyl, X = -(CH2)12-), 4 (R = n-dodecyl, X = 4, 4′-biphenyl), and 5 (R = benzyl, X = -(CH2)9-) form thermoreversible gels with a wide range of organic solvents, at concentrations well below 10 mgmL-1. Depending on the nature of the R and X groups, the solvents that undergo gelation include hexadecane, p-xylene, 1-octanol, n-butyl actetate, cyclohexanone, and tetralin. The gels are stable up to temperatures well above 100°C, but are easily disrupted by mechanical agitation. Light microscopic investigations revealed that compounds 2-5 spontaneously aggregate to form thin flat fibers, which can be several hundreds of micrometers long and only 2-10 μm wide. Depending on the solvent, multiple twists in the fibers are observed. In the gels, these fibers form an extended three-dimensional network, which is stabilized by multiple mechanical contacts between the fibers. Electron microscopy and X-ray powder diffraction revealed that the fibers consist of stacks of sheets. The thickness of the sheets is 3.65 and 3.85 nm for 2 and 3, respectively. Scanning tunneling microscopic investigations of 2 absorbed on graphite showed that 2 forms long ribbons with a width of 5.0 nm. In the ribbons the molecules have a parallel arrangement, with the long molecular axis perpendicular to the long ribbon axis. The two urea groups within a given molecule are each part of mutually parallel extended chains of hydrogen bonds. Based on these observations a model is proposed for the arrangement of the molecules in the fibers. In this model the bisurea molecules aggregate through hydrogen-bond formation into long ribbons, which assemble into sheets. In these sheets the ribbons are tilted. Finally, the sheets stack to form long thin fibers. This model is supported by molecular dynamics simulations.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 1254-1268 
    ISSN: 0947-6539
    Keywords: peptide bundles ; peptides ; pseudo-peptides ; template synthesis ; tripodal ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The stereochemical course of the formation of the two diastereomers of trimethyl 2,2′,2″-nitrilotris[2-(benzoylamino)acetate], 2a and 2b, is described. The structures of both isomers were confirmed by X-ray diffraction studies. Diastereomer 2b could be obtained in larger quantities by epimerisation of 2 a to 2 b with catalytical amounts of NaOMe. The (RRR/SSS)-triester 2 b is a suitable template for the synthesis of tripodal peptide bundles. Saponification of 2 b yielded the C3-symmetrical racemic triacid 4 b, which was coupled with amino acid methyl esters and dipeptide esters to give pseudo-hexapeptides and pseudo-nonapeptides, respectively. The resulting mixtures of diastereomers were easily separated by crystallisation. Their absolute configuration at the template unit (RRR or SSS) was established by means of the CD spectra. The pseudo-hexapeptide (SSS)N(BzGly*ValOMe)3 (14) was saponified to yield the optically pure triacid (SSS)N(BzGly*ValOH)3 (23). Compound 23 is an ideally preorganised template for the production of longer tripodal peptides. This was illustrated by the synthesis of two pseudo-pentadecapeptides. Peptide bundles with polar side chains (histidine and serine) or end groups (catechol or hydroxamate units) were synthesised by using the templates 4 b, 22 and 23 as anchors.
    Additional Material: 14 Ill.
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  • 4
    ISSN: 0947-6539
    Keywords: calixarenes ; hydrogen bonds ; molecular boxes ; noncovalent assembly ; supramolecular chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Calix[4]arenes diametrically substituted at the upper rim with two melamine units spontaneously form well-defined box-like assemblies in the presence of two equivalents of 5,5-diethylbarbituric acid. These assemblies, consisting of nine different components, are held together by 36 hydrogen bonds and are stable in apolar solvents at concentrations of up to 10-4M. This paper reports the first X-ray crystal structure, and the MALDI TOF mass spectra together with the complete 1H NMR spectroscopic characterization of these hydrogen-bonded assemblies. The crystal structure clearly shows that the assemblies are stereogenic, as a result of the antiparallel orientation of the two rosette motifs. Furthermore, the synthesis of twelve new 1,3-bis(melamine)calix[4]arenes carrying different numbers and types of functionalities at the upper rim is described. Detailed 1H NMR spectroscopic studies on the assembly behavior of these functionalized calix[4]arenes shows that 1) polar substituents (e.g. nitro, cyano) hardly affect the stability of the hydrogen-bonded assembly; 2) hydrogen bond donating or accepting groups, like amino and acetamido, can disturb assembly of the boxes under certain conditions by destabilizing the calix[4]arene pinched cone conformation as a result of intramolecular hydrogen bond formation; and 3) sterically bulky groups (e.g. tBu) can significantly inhibit the formation of the hydrogen-bonded assembly, but this effect very much depends on the exact positions of the groups.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 1846-1851 
    ISSN: 0947-6539
    Keywords: disproportionations ; dithiocarba-mate ; homogeneous catalysis ; vulcanization ; zinc ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Model studies have shown that cross-link precursors, that is, intermediates in the sulfur vulcanization of rubber, are transformed into cross-links by a nonsymmetric but regioselective disproportionation mechanism. Thus, two equivalents of the crosslink precursor of the type R—S—S—X are transformed into X—S—X and the actual cross-link R—S—S—S—R. Exchange of sulfur atoms is a prerequisite. A mechanism involving an SNi′ reaction with an allylic moiety, suggested in the literature, has not been observed. The disproportionation reaction is catalyzed by rubber-soluble zinc-dithiocarbamate complexes, an important class of vulcanization accelerators. By virtue of ligand-functional-group exchange reactions these complexes serve to transport and exchange sulfur atoms.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 1852-1859 
    ISSN: 0947-6539
    Keywords: conductivity ; europium ; gold ; magnetic properties ; superstructures ; tin ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title compound was prepared from the elements by reaction in a sealed tantalum tube at 1320 K followed by slow cooling to 970 K. EuAuSn crystallizes with a pronounced subcell of space group Imma (KHg2 type). Additional very weak reflections required a quintupled b axis. The superstructure was refined from single-crystal four-circle diffractometer data (Imm 2, a = 479.1(1) pm, b = 3833.6(5) pm, c = 820.1(1) pm, Z = 20, wR2 = 0.0834, 3675 F2 values and 94 variables). Six crystallographically different europium sites occur in the superstructure. Each europium site has an ordered near-neighbour environment of six gold and six tin atoms in the form of two tilted hexagons. Magnetic susceptibility measurements show Curie-Weiss behaviour above 50 K with an experimental magnetic moment of 7.6(1) μB/Eu, indicating divalent europium. EuAuSn orders antiferromagnetically at about 12 K and undergoes a metamagnetic transition at a critical field of 2.0(2) T. Electrical conductivity measurements show metallic behaviour with a room temperature value of 260 μΩcm. 151Eu and 119Sn Mössbauer spectroscopic experiments are compatible with divalent europium and show complex magnetic hyperfine field splitting at low temperature.
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  • 7
    ISSN: 0947-6539
    Keywords: ab initio calculations ; aluminum ; boron ; pi interactions ; sulfur ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The structures of H2X—Y—XH2 compounds (X = B, Al; Y = O, S) have been studied by means of ab initio calculations at the MP4/6-311 G**/MP2/6-311G** level. The potential energy surface (PES) of the aluminoxane species H2Al—O—AlH2 is rather flat: the energy differences between the various located extrema are less than 1.5 kcal mol-1, and this shows that the observed geometrical preference is not due to electronic factors. For the sulfur analogues H2X—S—XH2 (X = B, Al), three minima are located on the PES: a planar C2v structure, a Cs structure in which one hydrogen atom bridges the two X atoms, and a C2v structure with two bridging hydrogen atoms. For H2Al—S—AlH2, the Cs structure is the most stable, and the planar C2v and the dibridged structures lie 3.2 and 6.7 kcal mol-1 higher, respectively. Qualitatively similar results are obtained for H2B—S—BH2: the Cs and planar C2v structures are nearly isoenergetic, and the dibridged minimum lies 19.4 kcal mol-1 above the planar C2v minimum. These results are rationalized by analyzing the ability of these systems to bend, depending on the nature (oxygen or sulfur) of the central Y atom. The conjugation in these species is also discussed, and calculations on model systems H2X—YH (X = B, Al; Y = O, S) are presented.
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  • 8
    ISSN: 0947-6539
    Keywords: immobilized catalysts ; polysiloxanes ; P ligands ; rhodium ; sol-gel processes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of four equivalents of the monomeric trimethoxysilyl(T)-functionalized ether-phosphine ligand CyP(CH2CH2OCH3)(CH2)3SiR3 (R = OMe [1 a(T0)], Me [1 b]) with [{μ-ClRh(COE)2}2] yielded the monomeric pseudo 14 electron rhodium(I) complexes [ClRh(PO)(P∼O)] (2a(T0)2, 2 b). For the sol-gel process the complex 2 a(T0)2 was protected by introduction of the volatile, reversibly binding ligand pyridine. Thus, the monomeric compound 2 a(T0)2 was co-condensed with two and eight equivalents of the co-condensation agent MeSi(OMe)2(CH2)6(MeO)2SiMe (D0-C6-D0) to give the polysiloxane-bound congeners 2(Tn)2(Di-C6-Di)y (y = 2 and 8, respectively; i = 0-2; n = 0-3). The polysiloxane-bound complex 2(Tn)2-(Di-C6-Di)2 was treated with a variety of small molecules in the gas/solid and liquid/solid interphases. It was shown that a facile cleavage of the Rh-O bond in the ether-phosphine chelate occurred even in the solid state. The reaction of 2(Tn)2-(Di-C6-Di)2 with carbon monoxide, carbon disulfide, and diphenylacetylene resulted in the irreversible coordination of the molecule to the metal. In the presence of pyridine, the polysiloxane-bound complex 2(Tn)2-(Di-C6-Di)2 oxidatively added hydrogen to give the octahedrally configurated complex [ClRhH2(Py)(P ∼ O)2] [6(Tn)2(Di-C6-Di)2]. Treatment of dry 2(Tn)2-(Di-C6-Di)2 with ethene led to the reversible formation of the corresponding complex. Although the materials display low surface areas, at least 75% of the rhodium centers within the matrix are accessible to the rather bulky tolan molecules. The complexes 2(Tn)2(Di-C6-Di)y (y (y = 2, 8) show high activities and selectivities in the hydrogenation of tolan. The conversion was found to depend markedly on the amount of co-condensate (D0-C6-D0) and on the polarity of the solvent. The polysiloxane-bound complexes 2(Tn)2(Di-C6-Di)y are more active than their monomeric congener 2 a(T0)2.
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  • 9
    ISSN: 0947-6539
    Keywords: alkoxy radicals ; Barton reaction ; density functional calculations ; mass spectrometry ; radicals ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactivity of neutral alkoxy radicals in the absence of any interfering intermolecular interactions is investigated by means of the recently introduced method of neutral and ion decomposition difference (NIDD) spectra. These are obtained from quantitative analysis of the corresponding neutralization-reionization (NR) and charge reversal (CR) mass spectra. The following trends emerge: alkoxy radicals with short (C1—C3) or branched alkyl chains give rise to α-cleavage products, whereas longer-chained alkoxy radicals undergo 1,5-hydrogen migrations from carbon to oxygen, that is, Barton-type chemistry. This facile rearrangement has been studied in detail for n-pentoxy radicals by isotopic labeling experiments and computation at the Becke 3 LYP/6-31 G* level of theory. Further, the NIDD spectra of 3-methylpentoxy radicals permit for the first time the identification of the diastereoselectivity of the gas-phase hydrogen migrations. The results from the NIDD method are compared to those from earlier studies in the condensed phase. This new mass spectrometric approach is suggested as a tool for the examination of intramolecular reactions of free alkoxy radicals which can usefully complement theoretical studies.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 1894-1902 
    ISSN: 0947-6539
    Keywords: asymmetric synthesis ; chirality ; diselenides ; selenium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of various nonracemic diselenides by different methods is described. These diselenides are precursors for optically active selenium electrophiles. Their facial selectivity upon addition to styrene was investigated with respect to the chiral moiety neighboring the selenium. Diselenides 1 i, 1 n, and 1 v yielded addition products 7 with diastereomeric excesses up to 95%. Some diselenides, intermediates, and products of the addition reaction were investigated by 77Se NMR spectroscopy.
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