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  • Chemistry  (6)
  • Sunflower mutant  (2)
  • 161-976B; Alboran Sea; Biogenic material, total; Calcite; Calcium carbonate; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Deviation; Dolomite; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Epoch; Grain size, mean; Joides Resolution; Kurtosis; Leg161; Lithologic unit/sequence; Ocean Drilling Program; ODP; Phyllosilicate; Quartz; Sample code/label; Sand; Silt; Size fraction 〈 0.002 mm, clay; Skewness; Terrigenous; X-ray diffraction (XRD)  (1)
  • 1995-1999  (9)
  • 1965-1969
  • 1999  (9)
Collection
Keywords
Publisher
Years
  • 1995-1999  (9)
  • 1965-1969
Year
  • 1
    Electronic Resource
    Electronic Resource
    Syntheses and Characterization by NMR Spectroscopy and X-ray Diffraction of Complexes Derived from Metals of Groups 2 and 13 and the Ligand Bis(3,5-di-tert-butyl-1-hydroxy-2-phenyl)amine (1999)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1021-1027 
    Details
    ISSN: 1434-1948
    Keywords: Alkaline earth metals ; Group-13 metals ; Coordination chemistry ; Bis(3,5-di-tert-butyl-1-hydroxy-2-phenyl)amine ligand ; Nonacoordinated strontium compound ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of 3,5-di-tert-butylcatechol and aqueous ammonia with boron, aluminum, gallium, or strontium chloride, or with calcium or barium acetate produce, under oxidizing conditions, neutral complexes of stoichiometric formulae ML (M = BCl), ML2, [M = Al (2), Ga (3), Ca (4), and Ba (5)], and ML3H [M = Sr (6)] [L = different oxidation states of bis(3,5-di-tert-butyl-1-hydroxy-2-phenyl)amine]. The structures of 1 and 4-6 were established by 1H- and 13C-NMR spectroscopy and of 2, 3, and 6 by X-ray diffraction. The coordination compound ClBL (1) was obtained by transmetallation of ZnL2 with BCl3. It is a tetracyclic compound with tetracoordinated boron and nitrogen atoms, the ligand being in the reduced form, bis(hydroxyphenyl)amine. The paramagnetic complexes 2 and 3 crystallized in the triclinic system and are hexacoordinated with two orthogonal planar ligands bonded to the metal atoms. The ligands appear in two different oxidation states: one as the monoanion and another as a radical dianion. Based on their X-ray diffraction molecular structures, it is deduced that both ligands have similar structures, confirming electronic delocalization and fast interconversion of their oxidation states. Ca and Ba complexes are diamagnetic and hexacoordinated, both ligands being monoanions The strontium complex crystallized in the monoclinic system, the metal atom is nonacoordinated, having two ligands as monoanions, and a third one is a neutral protonated diquinone. Its structure is a distorted helix with three paddles in a C3 geometry and its unexpected diamagnetic behaviour is due to the presence of a reduced protonated ligand.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Inheritance of high palmitic acid content in the seed oil of sunflower mutant CAS-5 (1999)
    Springer
    Theoretical and applied genetics 98 (1999), S. 496-501 
    Details
    ISSN: 1432-2242
    Keywords: Key words Helianthus annuus ; Sunflower mutant ; Palmitic acid ; Inheritance ; Fatty acid composition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  Sunflower genotypes with increased levels of palmitic acid (C16 : 0) in the seed oil could be useful for food and industrial applications. The objective of the present study was to determine the inheritance of the high C16 : 0 content in the sunflower mutant line CAS-5 (〉25% of the total oil fatty acids). This mutant was reciprocally crossed with the lines HA-89 (5.7% C16 : 0) and BSD-2-691 (5.4% C16 : 0), the latter being the parental line from which CAS-5 was isolated. No maternal effect for the C16 : 0 content was observed from the analysis of F1 seeds in any of the crosses. The inheritance study of the C16 : 0 content in F1, F2 and BC1F1 seeds from the crosses of CAS-5 with its parental line BSD-2-691 indicated that the segregation fitted a model of two alleles at one locus with partial dominance for the low content. The analysis of the fatty acid composition in the F2 populations from the crosses with HA-89 revealed a segregation fitting a ratio 19 : 38 : 7 for low (〈7.5%), middle (7.5–15%), and high (〉25%) C16 : 0 content, respectively. This segregation was explained on the basis of three loci (P1, P2, P3) each having two alleles showing partial dominance for low content. The genotypes with a high C16 : 0 content were homozygous for the recessive allele p1 and for at least one of the other two recessive alleles, p2 or p3. This model was further confirmed with the analysis of the F3 and the BC1F1 generations. It was concluded that both the recessive alleles p2 and p3 were already present in the BSD-2-691 line, the allele p1 being the result of a mutation from P1. This genetic study will facilitate breeding strategies associated with the incorporation of the high C16 : 0 trait into agronomically acceptable sunflower hybrids.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s001220051097
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  • 3
    Electronic Resource
    Electronic Resource
    Genetic control of high stearic acid content in the seed oil of the sunflower mutant CAS-3 (1999)
    Springer
    Theoretical and applied genetics 99 (1999), S. 663-669 
    Details
    ISSN: 1432-2242
    Keywords: Key words Helianthus annuus ; Sunflower mutant ; Stearic acid ; Oil quality ; Genetic control
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  A sunflower mutant, CAS-3, with about 25% stearic acid (C18:0) in the seed oil was recently isolated after a chemical-mutagen treatment of RDF-1-532 seeds (8% C18:0). To study the inheritance of the high C18:0 content, CAS-3 was reciprocally crossed to RDF-1–532 and HA-89 (5% C18:0). Significant reciprocal-cross differences were found in one of the two crosses, indicating possible maternal effects. In the CAS-3 and RDF-1–532 crosses, the segregation patterns of the F1, BC1, and F2 populations fitted a one-locus (designated Es1) model with two alleles (Es1, es1) and with partial dominance of low over high C18:0 content. Segregation patterns in the CAS-3 and HA-89 crosses indicated the presence of a second independent locus (designated Es2) with two alleles (Es2, es2), also with partial dominance of low over high C18:0 content. From these results, the proposed genotypes (C18:0 content) of each parent were as follows: CAS-3 (25.0% C18:0) =es1es1es2es2; RDF-1–532 (8.0% C18:0) =Es1Es1es2es2; and HA-89 (4.6% C18:0) =Es1Es1Es2Es2. The relationship between the proposed genotypes and their C18:0 content indicates that the Es1 locus has a greater effect on the C18:0 content than the Es2 locus. Apparently, the mutagenic treatment caused a mutation of Es1 to es1 in RDF-1–532.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s001220051282
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  • 4
    Electronic Resource
    Electronic Resource
    HRGC/FID and HRGC/MSD Analysis of the Secondary Metabolites Obtained by Different Extraction Methods from Lepechinia schiedeana, and in Vitro Evaluation of Its Antioxidant Activity (1999)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 22 (1999), S. 343-349 
    Details
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; gas chromatography-mass spectrometry ; essential oil analysis ; Lepechinia schiedeana ; antioxidant activity ; lipid peroxidation ; Ledol; Ledol HMQC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Steam distillation (SD), simultaneous distillation-solvent extraction (SDE), microwave-assisted solvent extraction (MWE), and supercritical (CO2) extraction (SFE) were used to isolate secondary metabolites from Lepechinia schiedeana. The various extracts were analyzed by capillary gas-chromatography, on poly (dimethylsiloxane) (DB-1) and poly(ethyleneglycol) (INNOWAX), 60 m columns, using FID or MSD (EI, 70 eV). Kováts indexes, mass spectra, or standard compounds were employed for compound identification. 43, 61, 67, and 79 compounds at concentrations above 0.01% were detected in the SD, SDE, MWE, and SFE extracts, respectively. Ledol, C15H26O, was the major constituent (20.04-36.87%) in all extracts. Oxygenated sesquiterpenes (24.36-43.14%), C10H16, monoterpenes (27.70-39.87%), and C15H24, sesquiterpenes (10.04-22.22%) were the main groups of compounds present in SD, SDE, MWE, and SFE extracts. Heavy hydrocarbons (Cn 〉 15), diterpenoids, and phytosterols were found only in MWE and SFE extracts. The antioxidant activity of Lepechinia schiedeana was measured by the HRGC quantification of the volatile carbonyl compounds, final products of lipoxidation, released in a model lipid system (sunflower oil) by the effect of the Fenton reagent. The concentration of volatile carbonyl compounds decreased by 65% when lipid oxidation was induced in the presence of macerated Lepechinia plant. The protection of polyunsaturated acids in sunflower oil was also studied by measuring their concentrations after heating of the oil (180°C, 2 h) with and without macerated Lepechinia plant.
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  • 5
    Electronic Resource
    Electronic Resource
    Derivative Chemistry of [Ru2(μ-bdt)(CO)6], a Binuclear Ruthenium(I) Carbonyl Complex Containing a Bridging Benzene-1,2-dithiolate Ligand (1999)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1133-1139 
    Details
    ISSN: 1434-1948
    Keywords: Ruthenium ; Thiolate ligands ; Dithiolate ligands ; Substitution reactions ; Electrophilic additions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The known dithiolate-bridged ruthenium(I) complex [Ru2(μ-bdt)(CO)6] (1) (bdt = benzene-1,2-dithiolate) has been prepared in fair yield (55%) by the sequential treatment of RuCl3·nH2O with carbon monoxide, benzene-1,2-dithiol and zinc in a one-pot reaction. Complex 1 reacts readily with monodentate phosphanes to give, stepwise, the penta- and tetracarbonyl derivatives [Ru2(μ-bdt)(CO)6-n(PR3)n] (n = 1, 2; R = Ph, Cy, iPr). However, the reaction of 1 with one equivalent of bis(diphenylphosphanyl)methane (dppm) affords a mixture of complex 1 and the disubstituted derivative [Ru2(μ-bdt)(CO)4(η1-dppm)2], in which the dppm ligands are monodentate. This mixture is subsequently transformed into a polymeric material of formula [{Ru2(μ-bdt)(CO)4}(μ-dppm)]n, which consists of binuclear {Ru2(μ-bdt)(CO)4} units linked to each other by bridging dppm ligands. The use of two equivalents of dppm leads to [Ru2(μ-bdt)(CO)4(η1-dppm)2] in quantitative yield. The X-ray diffraction structure of [Ru2(μ-bdt)(CO)4(PiPr3)2] (3c) confirms that the phosphane ligands are located in axial positions, cis to both sulfur atoms, and that the Ru-Ru distance is short [2.6753(7) Å]. A comparative study of the reactivity of complexes 1 and 3c with the electrophiles H+, [Au(PPh3)]+, and HgCl2 has allowed the isolation of the derivatives [Ru2(μ-H)(μ-bdt)(CO)6-n(PiPr3)n][BF4] (n = 0, 2), [Ru2Au(μ-bdt)(CO)6-n(PiPr3)n(PPh3)][BF4] (n = 0, 2) and [Ru2HgCl2(μ-bdt)(CO)6-n(PiPr3)n] (n = 0, 2), respectively.
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  • 6
    Electronic Resource
    Electronic Resource
    Reactivity of 2-(Diphenylphosphanyl)thiophenol (HSC6H4PPh2) with Ruthenium and Osmium Carbonyl Complexes; Breaking of HSC6H4PPh2 into Sulfide, Phenyl and Diphenylphosphanyl Ligands on a Triruthenium Cluster (1999)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 2000 (1999), S. 499-503 
    Details
    ISSN: 1434-1948
    Keywords: Ruthenium ; Osmium ; Phosphane-thiolate ligands ; C-P bond activation ; C-S bond activation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-(Diphenylphosphanyl)thiophenol (HSC6H4PPh2) reacts with the carbonyl clusters [Ru3(CO)12] and [Os3(CO)10(MeCN)2] to give mixtures of products, the composition of which depends upon the reaction conditions and the ratio of the reactants. The derivatives [M3(μ-H)(μ-η2-SC6H4PPh2)(CO)9] (1a: M = Ru; 1b: M = Os), [Ru3(μ3-S)(μ-η2-Ph)(μ-PPh2)(PPh3)(CO)6] (2), and [Ru2(μ-η2-SC6H4PPh2)2(CO)4] (3) have been isolated. The SC6H4PPh2 ligand of compounds 1a and 1b has the sulfur atom spanning the same M-M edge as the hydride ligand and the phosphorus atom attached to one of the bridged metal atoms. Compound 2, which contains sulfide, phenyl, diphenylphosphanyl and triphenylphosphane ligands that arise from HSC6H4PPh2, has the Ru3 triangle capped by the sulfide and two Ru-Ru edges spanned by bridging phenyl and diphenylphosphanyl ligands. In complex 3, the two SC6H4PPh2 ligands have the same coordination behavior as in 1a or 1b; this binuclear complex is more conveniently prepared by treating [Ru2(μ-η2-MeCO2)2(CO)4(MeCN)2] with HSC6H4PPh2.
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  • 7
    Electronic Resource
    Electronic Resource
    Isolation of Cross-Coupling Products in Model Studies on the Photochemical Modification of Proteins by Tiaprofenic Acid (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 497-502 
    Details
    ISSN: 1434-193X
    Keywords: Proteins ; Cross coupling ; Drug research ; Photochemistry ; Toxicology ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -To gain insight into the chemical nature of drug-induced photoallergy, model studies have been carried out on the photochemical modification of proteins by tiaprofenic acid. Irradiation of decarboxylated tiaprofenic acid (DTPA) in the presence of p-cresol leads to C-C- and C-O-connected p-cresol “dimers”, together with DTPA hydrodimers. The p-cresol-DTPA cross-coupling product was not detected in this reaction. However, a product of this type is formed using a more hindered phenol, such as 2,6-di-tert-butylphenol. Similar results are obtained when tiaprofenic acid (TPA) or its methyl ester are used as photosensitizers. The observed formation of “dimers” can be related to protein photo-crosslinking, through the coupling of two tyrosine units. On the other hand, phenol-(D)TPA cross-coupling may be relevant to the understanding of drug-protein photobinding.
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  • 8
    Electronic Resource
    Electronic Resource
    Regioselective Lipase-Catalysed Amidation of Dicarboxylic N-Blocked Amino Acid Diesters - Effect of the Side-Chain Length (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 2835-2839 
    Details
    ISSN: 1434-193X
    Keywords: Dicarboxylic amino acids ; Amidation reactions ; Candida antarctica lipase ; Enzyme catalysis ; Regioselectivity ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diethyl esters of both (R)- and (S)-N-blocked α-aminoadipic and α-aminopimelic acids yield exclusively the ω-monoamide when they are subjected to amidation catalysed by the lipase B of Candida antarctica in anhydrous diisopropyl ether. These results are in contrast to the α-monoamide yielded by the equivalent L-glutamic derivatives under the same experimental conditions. These results show that the length of the side chain plays a crucial role in the regioselectivity of the reaction.
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  • 9
    facet.materialart.
    Unknown
    (Table 3) Textural and bulk mineralogy of Pliocene and Pleistocene sediments from ODP Hole 161-976B (1999)
    PANGAEA
    In:  Supplement to: Alonso, Belen; Ercilla, Gemma; Martinez-Ruiz, Francisca C; Baraza, Jesus; Galimont, A (1999): Pliocene-Pleistocene sedimentary facies at Site 976: depositional history in the northwestern Alboran Sea. Zahn, R; Comas, MC; Klaus, A (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 161, 1-12, https://doi.org/10.2973/odp.proc.sr.161.206.1999
    Details
    Publication Date: 2024-01-09
    Description: The Pliocene and Pleistocene deposits recovered at Site 976 from the northwestern Alboran Sea at the Málaga base-of-slope include five main sedimentary facies: hemipelagic, turbidite, homogeneous gravity-flow, contourite, and debris-flow facies. The thickness and vertical distribution of these facies into lithostratigraphic Units I, II, and III show that the turbidites and hemipelagic facies are the dominant associations. The Pliocene and Pleistocene depositional history has been divided into three sedimentary stages: Stage I of early Pliocene age, in which hemipelagic and low-energy turbidites were the dominant processes; Stage II of early Pleistocene/late Pliocene age, in which the dominant processes were the turbidity currents interrupted by short episodes of other gravity flows (debris-flows and homogeneous gravity-flow facies) and bottom currents; and Stage III of Pleistocene age, in which both hemipelagic and low-energy gravity-flow processes occurred. The sedimentation during these three stages was controlled mainly by sea-level changes and also by the sediment supply that caused rapid terrigenous sedimentation variations from a proximal source represented by the Fuengirola Canyon.
    Keywords: 161-976B; Alboran Sea; Biogenic material, total; Calcite; Calcium carbonate; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; Deviation; Dolomite; DRILL; Drilling/drill rig; DSDP/ODP/IODP sample designation; Epoch; Grain size, mean; Joides Resolution; Kurtosis; Leg161; Lithologic unit/sequence; Ocean Drilling Program; ODP; Phyllosilicate; Quartz; Sample code/label; Sand; Silt; Size fraction 〈 0.002 mm, clay; Skewness; Terrigenous; X-ray diffraction (XRD)
    Type: Dataset
    Format: text/tab-separated-values, 2077 data points
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    DATA PANGAEA
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