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  • Chemistry  (8)
  • Acoustic Doppler Current Profiling (ADCP), Nortec AWAC 1 Mhz; CTM2008-04517; CTM2009-06269-E; CTM2010-11955-E/MAR; DATE/TIME; EMSODEV; EMSO implementation and operation: DEVelopment of instrument module; EMSO-Link; ES5110020; Fixed Point Open Ocean Observatories Network; FixO3; Implementation of the Strategy to Ensure the EMSO ERICs Long-term Sustainability; Instalació de sensors en observatorio submari expansible OBSEA; Instalacion de equipos en superfície para la ampliación de las prestaciones del observatorio submarino obsea; Instrumentación y tecnologías aplicadas al estudio, caracterización y explotación sostenible del medio marino; Integración de sensores para monitorización submarina en una red con sincronización temporal; Interoperabilidad e instrumentación de plataformas autónomas marinas para la monitorización sísmica; Interoperabilidad en redes de sensores marinos y ambientales; Interoperabilitat en xarxes de sensors marins i ambientals; INTIMAS; INTMARSIS; JERICO-NEXT; Joint European Research Infrastructure network for Coastal Observatory – Novel European eXpertise for coastal observaTories; MarInTech; MELOA; MeteoMet2; Metrology for essential climate variables; Multi-purpose/Multi-sensor Extra Light Oceanography Apparatua; NeXOS; Next generation, Cost-effective, Compact, Multifunctional Web Enabled Ocean Sensor Systems Empowering Marine, Maritime and Fisheries Management; Nuevas tecnologías para el seguimiento de la acidificación marina en el espacio natural Costa del Garraf; OBSEA:OBSEA:2009-05; Operatividad laboratorio submarino obsea; OPOBSEA; Pressure, water; PT2009-0080; Redes de sensores submarinos acústicos aplicados al seguimiento de especies de interes comercial; Redes de sensores submarinos autónomos y cableados aplicados a la monitorización remota de indicadores biológicos; RESBAC; RESBIO; SARTI-MAR; SINEOS; Sismòmetre marí digital amb connexió per cable; Sistemas inalambricos para la extension de observatorios submarinos; Sistemes dAdquisició Remota de dades i Tractament de la Informació en el Medi Marí; VALTEC09-1-0059; Wave directional spread; Wave height, maximum; Wave height, significant; Wave height, tenth; Wave height, third; Wave mean direction; Wave peak direction; Wave period, maximum; Wave period, mean, zero crossing
  • Biomass
  • Length-weight relationships
  • 2015-2019
  • 1995-1999  (8)
  • 1997  (8)
Collection
Keywords
  • Chemistry  (8)
  • Acoustic Doppler Current Profiling (ADCP), Nortec AWAC 1 Mhz; CTM2008-04517; CTM2009-06269-E; CTM2010-11955-E/MAR; DATE/TIME; EMSODEV; EMSO implementation and operation: DEVelopment of instrument module; EMSO-Link; ES5110020; Fixed Point Open Ocean Observatories Network; FixO3; Implementation of the Strategy to Ensure the EMSO ERICs Long-term Sustainability; Instalació de sensors en observatorio submari expansible OBSEA; Instalacion de equipos en superfície para la ampliación de las prestaciones del observatorio submarino obsea; Instrumentación y tecnologías aplicadas al estudio, caracterización y explotación sostenible del medio marino; Integración de sensores para monitorización submarina en una red con sincronización temporal; Interoperabilidad e instrumentación de plataformas autónomas marinas para la monitorización sísmica; Interoperabilidad en redes de sensores marinos y ambientales; Interoperabilitat en xarxes de sensors marins i ambientals; INTIMAS; INTMARSIS; JERICO-NEXT; Joint European Research Infrastructure network for Coastal Observatory – Novel European eXpertise for coastal observaTories; MarInTech; MELOA; MeteoMet2; Metrology for essential climate variables; Multi-purpose/Multi-sensor Extra Light Oceanography Apparatua; NeXOS; Next generation, Cost-effective, Compact, Multifunctional Web Enabled Ocean Sensor Systems Empowering Marine, Maritime and Fisheries Management; Nuevas tecnologías para el seguimiento de la acidificación marina en el espacio natural Costa del Garraf; OBSEA:OBSEA:2009-05; Operatividad laboratorio submarino obsea; OPOBSEA; Pressure, water; PT2009-0080; Redes de sensores submarinos acústicos aplicados al seguimiento de especies de interes comercial; Redes de sensores submarinos autónomos y cableados aplicados a la monitorización remota de indicadores biológicos; RESBAC; RESBIO; SARTI-MAR; SINEOS; Sismòmetre marí digital amb connexió per cable; Sistemas inalambricos para la extension de observatorios submarinos; Sistemes dAdquisició Remota de dades i Tractament de la Informació en el Medi Marí; VALTEC09-1-0059; Wave directional spread; Wave height, maximum; Wave height, significant; Wave height, tenth; Wave height, third; Wave mean direction; Wave peak direction; Wave period, maximum; Wave period, mean, zero crossing
  • Biomass
  • Length-weight relationships
  • Polymer and Materials Science  (4)
  • +
Publisher
Years
  • 2015-2019
  • 1995-1999  (8)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 41 (1997), S. 721-729 
    ISSN: 0006-3525
    Keywords: Poly(β-L-aspartate)s ; helical conformations ; quantum mechanical calculations ; cooperative energy effects ; helix stability ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformational preferences of the monomeric units of a series of poly(α-alkyl-β-L-aspartate)s were examined by quantum mechanical calculations. α-Alkyl-β-aspartamyl m-oligopeptides with a number of residues m ranging from 1 to 7 and arranged in the conformations experimentally observed for their corresponding polymers were computed. Both their total relative energies and their cooperative energy differences were compared as a function of the length of the oligopeptide and the nature of the alkyl side group. Results revealed that the 13/4 helical arrangement is the most stable structure for the isolated polymer chain for any side group, although a 17/4 helix becomes favored in the case of methyl and ethyl groups due to the packing effects. On the other hand, the stability of the 4/1 helix appears to be the preferred conformation for side groups with a branched constitution. © 1997 John Wiley & Sons, Inc. Biopoly 41: 721-729, 1997
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A comprehensive study of the alkaline hydrolysis of the β-lactam ring of azetidin-2-one was carried out using ab initio molecular-orbital calculations at the RHF/6-31 + G* level. The influence of the solvent on this reaction was investigated by using the reaction field method (SCRF); the solvent was found to suppress the interference of some gas-phase reactions and allow the presence of a transition state to be detected as the nucleophile approaches the β-lactam ring. The transition state corresponds to a structure where the OH- group lies at a distance of 1.927 Å from the C=O group of the β-lactam ring and exhibits a potential barrier of 13.6 kcal/mol.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1997 (1997), S. 527-532 
    ISSN: 0947-3440
    Keywords: Centaurea paui ; Sesquiterpenes ; Heliangolides ; Elemanolides ; Terpenoids ; Natural products ; Phytochemistry ; Lactones ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aerial parts of Centaurea paui afforded, in addition to several known sesquiterpene lactones, the two new elemanolides 2-4, the new elemane derivative 5 as well as the five new heliangolides 14-18. Their structures were elucidated by spectroscopic methods, especially high-field NMR spectroscopy. The structure of the heliangolide 12 previously isolated from this plant, has been confirmed by X-ray diffraction.
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  • 4
    ISSN: 0006-3525
    Keywords: helix/coil transition ; multiple sequence approximation ; AGADIR ; Zimm-Bragg theory ; Lifson-Roig theory ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this work we present the development of the multiple sequence approximation (AGADIRms) and the standard one-sequence approximation (AGADIRIs) within the framework of AGADIR's α-helix formation model. The extensive comparison between these new formulations and the original one [AGADIR; v. Muñoz and L. Serrano (1994),Nat. Struct. Biol., Vol. 1, pp. 399-409] indicates that the standard one-sequence approximation is virtually identical to the multiple sequence approximation, while the previously used residue partition function approximation [Muñoz and Serrano (1994); (1995), J. Mol. Biol., Vol. 245, pp. 275-296] is less precise. The calculations of the average helical content performed with AGADIR are precise for peptides of less than 30 residues and progressively diverge from the multiple sequence formulation for longer peptides. The helicity distribution of heteropolypeptides with less than 50% average helical content is also well described, while those of quasi-homopolymers with high helical content tend to be flattened. These inaccuracies lead to an underestimation of 0.017 kcal/mol for the mean-residue enthalpic contribution in AGADIR, as compared to AGADIRms and AGADIRIs. The other energy contributions to α-helix stability are not affected by the original statistical approximation. We also discuss the particularities of the model for α-helix formation utilized in AGADIR and compare it with the classical Zimm-Bragg and Lifson-Roig theories. Moreover, we develop the mathematical relationships between the basic AGADIR energy contributions and helix nucleation and elongation, which permit the quantitative comparison between formalisms. Remarkably, the comparison between AGADIRms and the Lifson-Roig formalism shows that, despite the differences on treating helix/coil cooperativity, both theories give virtually identical results when an equivalent set of parameters is used. This indicates that the helix/coil transition is a solid theory independent of the particularities of the model for α-helix formation. © 1997 John Wiley & Sons, Inc. Biopoly 41: 495-509, 1997.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 591-599 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extrusion rheometry experiments with a commercial thermotropic liquid crystalline copolyester show concave Bagley plots and convex pressure profiles. A loss of the orientation produced at the entrance of the capillary and the slit can explain these non-linearities. Assuming that the order parameter, S, relaxes exponentially with time, the Doi-Edwards model for the shear flow of rod-like polymers is used to adjust experimental data.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 8 (1997), S. 85-89 
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The transition-state geometries of retroene elimination reactions of propene from allylamines have been calculated by using the semiempirical AM1 method. The most favored geometry resembles a half chair or a flattened boat. It is also found that the transition states are of polar character and that the negative charge on the N atom decreases in the transition state; thus, the reaction is favored by electron donor substituents on the nitrogen atom, as observed experimentally. © 1997 John Wiley & Sons, Inc.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 8 (1997), S. 97-102 
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diallyltetramethylpiperidinophosphine 1, diallyldiisopropylaminophosphine 2, and diallylmesitylphosphine 3 were pyrolyzed in a stirred flow reactor over the temperature range 400-450°C, using toluene as carrier gas, producing, in all cases, mixtures of phosphorus-containing products. The pyrolysis of 1 produced 1-tetramethylpiperidino-1-phosphabutadiene, in addition to a mixture of phosphines and polyphosphines. Compound 2 produced the azadiphosphole 4, the phosphinine 5, allylphosphine, and diisopropylaminophosphine as major phosphorated products. The pyrolysis of 3 produced a mixture of phosphines and polyphosphines. The complex mixture generated by the three diallylphosphines indicates the formation of free radicals during their pyrolyses. AM1 calculations on the transition state of an expected retroenetype propene elimination reaction showed that, due to the phosphaalkene character of the transition state, the structure of the latter is very rigid and sensitive to steric effects. Steric hindrance of the substituents on the phosphorus atom compels the molecule to distort the half-chair transition structure, causing a rise in the activation energy to values in the range of a homolytic P(SINGLE BOND)C bond dissociation energy. © 1997 John Wiley & Sons, Inc.
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  • 8
    ISSN: 0044-2313
    Keywords: Stibocanes ; dithiophosphinates ; conformational analysis ; x-ray structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Konformative Trends und intermolekulare Assoziation in Dialkyldithiophosphinat-Stibocanen X(CH2CH2S)2SbS2PR2 (X = O, S; R = Me, Et)Alkylstibocanes O/S(CH2CH2S) 2SbS2PMe2/ Et2 1-4 wurden aus den entsprechenden Chlorooxa- und -thiastibocanen bzw. Natriumdialkyldithiophosphinaten in CH2Cl2 dargestellt und durch IR, EI-MS und Multikern-NMR (1H, 13C, 31P{1H}) charakterisiert. Die Kristall- und Molekülstrukturen von O(CH2CH2S) 2SbS2PMe2 1 und S(CH2CH2S) 2PMe2 3 wurden bestimmt. Die Kristallstruktur von 1 zeigt ein Dimer durch zwei Sb … S-intermolekulare Wechselwirkungen (3,960(3) Å). 3 bildet im kristallinen Zustand eine dimere Struktur durch eine sekundäre Sb … Sb-Bindung (4,067(1) Å), 1 und 3 zeigen endocyclische, transannulare Sb … O/S-Wechselwirkungen (1: 2,561(7) Å; 3: 2,972(1) Å) und exocyclische, sekundäre Sb … S-Bindungen (1: 3,454(2) Å; 3: 3,147(2) Å). Die Strukturen von 1 und 3 können als trigonal bipyramidal beschrieben werden mit zusätzlichen sekundären Kontakten über eine Ebene bzw. Kantenverbrückt. Die Konformation des Achtrings in 3 ist Wanne-Sessel, die in 1 Sessel-planar.
    Notes: The alkyl stibocanes O/S(CH2CH2S)2SbS2PMe2/ Et2 1-4 were prepared from the corresponding chloro oxa and thiastibocanes, and sodium dialkyldithiophosphinates in CH2Cl2. Compounds 1-4 were characterized by IR, EI-MS and multinuclear NMR (1H, 13C, 31P{1H}). The crystal and molecular structures of O(CH2CH2S)2SbS2PMe2 1 and S(CH2CH2S)2SbS2PMe2 3 were determined. The crystalline state of 1 has two Sb … S intermolecular interactions [3.960(3) Å] that results in a dimer. The crystalline state of 3 features a dimeric structure through an Sb … Sb secondary bonding [4.067(1) Å]. Compounds 1 and 3 display both an endocyclic, transannular Sb … O/S interaction [1, 2.561(7) Å; 3 2.972(1) Å] and an exocyclic Sb … S secondary bonding [1, 3.454(2) Å, 3, 3.147(2) Å]. The coordination geometry in 1 and 3 could be described as trigonal bipyramidal with additional secondary bonding contacts face capping or edge bridging the polyhedron. The conformation of the eight membered ring in 3 is boat-chair. Whereas in 1, the mean conformation is chair-planar.
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