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  • 1990-1994  (59)
  • Chemistry  (53)
  • Computational Chemistry and Molecular Modeling  (3)
  • Evolution  (3)
  • 1
    ISSN: 1432-0819
    Schlagwort(e): Key wordsZoned magma body ; Chemical variation ; ash-flow sheets ; Tephra sequence ; Differentiation ; time constraints ; Evolution
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie
    Notizen: Abstract The Rainier Mesa ash-flow is a large (1200 km3), 11.6 My old, chemically zoned unit that ranges in composition from 55 to 76% SiO2– one of the largest chemical ranges ever observed in a large volume ash-flow sheet. Two chemical trends occur in this sheet, a low silica (55–66% SiO2) and a high silica (〉66% SiO2) trend. Ninety per cent of the Rainier Mesa sheet occurs in the high silica trend. Immediately beneath the Rainier Mesa sheet is a thick tephra sequence. The chemical variation of this sequence is nearly equivalent to the high silica portion of the Rainier Mesa ash-flow sheet (about 66–78% SiO2). Throughout the tephra sequence numerous small ash-flow layers occur, and each ash-flow layer is chemically zoned from more evolved at the base to less evolved at the top. This is consistent with having been erupted from a zoned magma body. The lowest silica tephra units are at the base of the sequence and the highest silica units are at the top – that is, the large-scale chemical trend of the entire sequence is opposite to that of the individual ash-flow layers. These ash-flow layers are of very small volume. The tephra sequence provides a unique record of the incremental development of the zoned, high silica portion of the Rainier Mesa magma body.
    Materialart: Digitale Medien
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  • 2
    ISSN: 1432-0819
    Schlagwort(e): Zoned magma body ; Chemical variation ash-flow sheets ; Tephra sequence ; Differentiation time constraints ; Evolution
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie
    Notizen: Abstract The Rainier Mesa ash-flow is a large (1200 km3), 11.6 My old, chemically zoned unit that ranges in composition from 55 to 76% SiO2 — one of the largest chemical ranges ever observed in a large volume ash-flow sheet. Two chemical trends occur in this sheet, a low silica (55–66% SiO2) and a high silica (〉66% SiO2) trend. Ninety per cent of the Rainier Mesa sheet occurs in the high silica trend. Immediately beneath the Rainier Mesa sheet is a thick tephra sequence. The chemical variation of this sequence is nearly equivalent to the high silica portion of the Rainier Mesa ash-flow sheet (about 66–78% SiO2). Throughout the tephra sequence numerous small ash-flow layers occur, and each ash-flow layer is chemically zoned from more evolved at the base to less evolved at the top. This is consistent with having been erupted from a zoned magma body. The lowest silica tephra units are at the base of the sequence and the highest silica units are at the top — that is, the large-scale chemical trend of the entire sequence is opposite to that of the individual ash-flow layers. These ash-flow layers are of very small volume. The tephra sequence provides a unique record of the incremental development of the zoned, high silica portion of the Rainier Mesa magma body.
    Materialart: Digitale Medien
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  • 3
    ISSN: 1432-072X
    Schlagwort(e): Eubacterium ; Thermophile ; Evolution ; Fervidobacterium ; Lipids ; Thermotoga
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract An extremely thermophilic anaerobic fermentative eubacterium growing at temperatures between 50 and 80°C (opt.: 65°C) was isolated from an Icelandic hot spring. The cells were Gram-negative motile rods, about 1.8 μm in length, and 0.6 μm in width occurring singly and in pairs. About 50% of the cells formed large spheroids at one end similar to Fervidobacterium nodosum. The new isolate H 21 differed from Fervidobacterium nodosum by a 6 mol % higher GC-content of its DNA (41 mol %), its ability to grow on cellulose, and insignificant DNA homology. The lipids of isolate H 21 were similar to that of members of “Thermotogales”. 16S rRNA sequencing of isolate H 21 and Fervidobacterium nodosum indicated (a) that isolate H 21 represents a new species of the genus Fervidobacterium which we name Fervidobacterium islandicum and (b) that the genus Fervidobacterium belongs to the “Thermotogales” branch.
    Materialart: Digitale Medien
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  • 4
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The three ligands 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetrakis(methylenephosphonic acid) (1), 1,4,7,11-tetraazacyclotridecane-1,4,7,11-tetrakis(methylenephosphonic acid) (2), and 1,4,8,11-tetraazacyclotetradecane-1,4,8,1 1-tetrakis(methylenephosphonic acid) (3) have been synthesized by condensation of the corresponding macrocycles with formaldehyde and phosphorous acid. The protonation and stability constants with the earth-alkali ions have been determined at 25° and I = 0.1 M (Me4)N(NO3) by potentiometric titrations. Because of the high values of the first two protonation constants, 1H-NMR measurements were necessary to determine them. Titrations in different supporting electrolytes (NaNO3, KNO3, RbNO3, CsNO3, and Me4N(NO3)) show that their choice is of paramount importance, as the above ligands can form complexes with alkali-metal ions. The potentiometric results for the earth-alkali ions show that beside mononuclear complexes of different degrees of protonation ([MLHn], n = 0-4), also binuclear species are formed ([M2LHm], m = 0-2). It is interesting that 1 with the smallest macrocyclic ring has the greatest tendency to form binuclear complexes, which are so stable that they partially prevent the formation of the corresponding mononuclear species. For [ML], [MLH], [M2L], and [M2LH], the stability sequence is Mg2+ 〈 Ca2+ 〉 Sr2+ 〉 Ba2+, whereas for [MLH2], [MLH3], and [MLH4], the stability steadily decreases from Mg2+ to Ba2+.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 5
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A new and generally applicable synthetic path for the preparation of heteroditopic bis-macrocycles using tri-N-protected tetraazacycloalkanes as building blocks and bromoacetyl bromide as bridging reagent is described. In the first step, bromoacetyl bromide is used as acylating agent for one of the macrocycles, whereas in the second step it is used as alkylating agent for the second macrocycle, thus giving protected bis-macrocyclic amides (e.g. 6). After reduction of the amide moiety and deprotection, bis-azamacrocycles with an ethylene bridge are obtained (e.g. 8). The corresponding homoditopic bis-macrocycles 16 and 17 are also prepared for comparison purpose. Spectrophotometric studies indicate that bis-macrocycle 8, which consists of a 12- and a 14-membered ring, binds two metal ions with equal affinity, whereas compound 13, in which an unsubstituted (cyclam) and a trimethyl-substituted tetraazacyclotetradecane unit (Me3cyclam) are bridged, shows selective metal-ion binding. The first metal ion is always incorporated into the cyclam unit, whereas the second one binds to the Me3cyclam macrocycle. Thus, by sequential addition of two different metal ions, heterobinuclear complexes can easily be prepared. The electrochemistry of the binuclear Ni2+ complexes, studied by CV and DPV, as well as the EPR spectra of the binuclear Cu2+ complexes clearly indicate metal-metal interactions.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 6
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Solution studies of the Cu2+ complex with 11-(3-aminopropyl)-1,4,7,11-tetraazacyclotetradecane(L) indicate that, depending on the pH and on the age of the solution, different species are present. Dissolving the solid [CuL](ClO4)2 in slightly acidic solution gives the protonated complex AH, characterized by an absorption maximum at 574 nm, by a relatively fast proton-induced dissociation kinetics and by the typical colour change in basic solution to give the deprolonated form A with coordinated side chain. AH slowly interconverts in acidic solution to a new species BH, which has an absorption maximum at 547 nm, and which is kineticaily more stable against acid dissociation and shows no coordination of the amino group of the side chain. In alkaline solution, however, the deprotonated form B deliver A in a base induced reaction. The X-ray diffraction studies of A and BH allow to determine the geometry of the metal ion and the configuration of the macrocycle. In A, the Cu2+ is pentacoordinated by the five N-atoms of the ligand and the macrocycle is in the RRSR configuration, whereas in BH the Cu2+ is octahedrally coordinated by the four N-atoms of the macrocycle and two axial perchlorate O-atoms with the macrocycle in the RRRS configuration. The amino group of the side chain is protonated and not coordinated. Thus, the on/off equilibrium of the side chain not only changes the geometry of the metal ion, as is generally found, but also alters the macrocyclic moiety.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 7
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Cu2+ complex of 1, having a non-coordinating carboxylic group, can be reacted under the typical conditions of peptide formation with amines such as 2-methylpropylamine or (pyrid-2-yl)methylamine to give, after removal of Cu2+ with CN-, the amides 4 and 5. The Cu2+ ion is of paramount importance since it protects the four amino groups of the macrocycle so that the amide condensation can specifically be done with the exogenous amine It is also shown that the Cu2+ complex of 1 can be covalently attached to bovine serum albumin (BSA), thus opening the possibility to use this compound as a labelling agent for proteins and antibodies.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 76 (1993), S. 557-562 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The stability constants of the Mn2+, Zn2+, Ni2+, pb2+, and Cd2+ complexes with 1,4,7-triazacylononane-1-acetic acid (noma) were determined at 25° and 0.5M (KNO3) by potentiometric titrations. The species [ML] and [ML(OH)] were found in al cases except for Ni2+, whereas [ML2] was only detected for Cd2+. For the complexes [ML], the order of stability is Mn2+ 〈 Cd2+ 〈 pb2+ 〈 Zn2+ 〈 Zn2+ 〈 Ni2+ 〈 Cu 2+, which is consisten with the Irvin-Williams Series.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 9
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: NMR, potentiometric, and UV/VIS measurements were run to study the protonation and the In3+ and Cu2+ stability constants of 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid (do3a, L). The protonation of do3a follows the typical scheme with two high and several low log KH values. Between pH 11 and 13, the protonation mainly occurs at the N-atom, which is not substituted by an acetate side chain. The In3+ complex is not appreciably protonated even at low pH values (pH ⋐ 1.7), whereas [CuL] can add up to three protons in acidic solution to give the species [CuLH], [CuLH2], and [CuLH3], the stability of which was determined. The formation rates of the Y3+, Gd3+, Ga3+, and In3+ complexes with do3a were measured using a pH-stat technique, whereas that of Cu2+, being faster, was followed on a stopped-flow spectrophotometer. In all cases, the reaction scheme implies the rapid formation of partially protonated intermediates, which rearrange themselves to the final product in the rate-determining process. ([MLH])in, an intermediate, in which the metal ion probably is coordinated by two amino acetate groups, proved to be the reactive species for Y3+, Gd3+, and Ga3+. The formation of [Cu(do3a)] was interpreted by postulating that either ([CuLH])in or ([CuLH])in, and ([CuLH2])in are the reactive complexes. The rates of dissociation of the Y3+, Gd3+, and Cu2+ complexes with do3a were studied spectrophotometrically. For Y3+ and Gd3+, arsenazo III was used as a scavenger, whereas for Cu2+ the absorption associated with d-d* transition was followed. For [Y(do3a)] and [Gd(do3a)], the rate law follows the kinetic expression kobsd = k0 + k1[H+]. The dissociation of [Cu(do3a)] goes through the proton-independent dissociation of [CuLH3], which is the main species at low pH.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 77 (1994), S. 1590-1594 
    ISSN: 0018-019X
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis of benzazepine analogues of the opium alkaloid noscapine (1) is described. The benzazepines 2 and 3 were prepared starting from nornarceine ethyl ester (4; readily available from 1) in several steps. X-Ray analysis of compound 2 revealed that it is not a diastereosisomer mixture but a racemate of the threo-form and thus has the same configuration as 1.
    Materialart: Digitale Medien
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