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  • 1
    ISSN: 0044-8249
    Keywords: Elektronentransfer ; Porphyrinoide ; Supramolekulare Chemie ; Wirt-Gast-Chemie ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0570-0833
    Keywords: electron transfer ; host-guest chemistry ; porphyrinoids ; supramolecular chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 3
    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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  • 4
    ISSN: 0947-6539
    Keywords: asymmetric ring-opening ; carnitine ; cyclizations ; β-lactones ; nucleophilic substitutions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The syntheses of the enantiomerically pure, carnitine-related β-lactones 10 and 12 starting from various carnitine precursors of opposite configuration (or carnitine itself) are described. (R)-3-Chlorocarnitine (20) has also been directly prepared from (S)-carnitine (14) and has been cyclized to 12 by a second inversion of configuration of the stereogenic centre. By nucleophilic attack at the carbonyl carbon, the β-lactone carnitine derivatives have been converted into esters, amides and guanidino congeners. Following this route, it is possible to obtain the biologically active isomer (R)-carnitine (1) starting from the otherwise useless industrial by-product (S)-carnitine (14). Nucleophilic attack by selected ambidient nucleophiles at the β-carbon of the same β-lactone derivatives results in a second inversion of configuration of the stereogenic centre. Besides aminocarnitine (3), chiral acetylcarnitine (2) and acetylthiocarnitine (5) have been synthesized in homochiral forms following this latter procedure.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 219-225 
    ISSN: 0947-6539
    Keywords: arenes ; C-C coupling ; dyes ; fluorescence ; terrylenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Terrylenimides 3 and 4 represent a new class of blue colorants, exhibiting absorption maxima at 650 to 700 nm and fluorescence emissions in the NIR region (673 to 750 nm). The terrylenimides were synthesized by means of various organometallic coupling reactions, catalyzed by transition metal complexes (Nio, Pdo) and starting from the aromatic bromides, boronic acids, or organotin compounds. The terrylenimides have all the properties expected of excellent fluorescent dyes: high extinction coefficients, high fluorescence quantum yields, and very good thermal, chemical, and photochemical stabilities. Owing to its extended π system, 3 can reversibly accept four negative charges. By varying the substituents, 3 and 4 can be modified to serve either as soluble dyes or as insoluble pigments.
    Additional Material: 4 Ill.
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  • 6
    ISSN: 1434-1948
    Keywords: Rhodium ; N ligands ; Carbonyl complexes ; Methoxycarbonyl ; Dinuclear complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of 1,4,7-trimethyl-1,4,7-triazacyclononane (Cn*) with [{(CO)2Rh(μ-Cl)}2] in methanol at 0°C, followed by the addition of NH4PF6, results in the formation of the mononuclear carbonyl complex [Cn*Rh(μ-CO)2]PF6 ([1]PF6), the dinuclear carbonyl complex [Cn*Rh(μ-CO)3RhCn*](PF6)2 {[2](PF6)2} and the dinuclear methoxycarbonyl complex [Cn*Rh(C(O)OMe)(μ-CO)2RhCn*]PF6 ([3]PF6). The reaction of [2](PF6)2 with NaOMe results in formation of [3]PF6 by the attack of the methoxide at a bridging carbonyl. Treatment of [3]PF6 with NH4PF6 regenerates [2](PF6)2, thus showing that the methoxylation of [2](PF6)2 is reversible. The structures of [1]PF6, [2](PF6)2 and [3]PF6 have been determined by single-crystal X-ray diffraction. For [3]PF6 an unprecendented facile, reversible, migration of the C(O)OMe ligand between the two rhodium centres of the Rh(μ-CO)2Rh core is observed.
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  • 7
    ISSN: 1434-1948
    Keywords: Rhodium ; Iridium ; N ligands ; Coordination modes ; Polymerizations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexation of [RhI(cod)]+ and [IrI(cod)]+ by the new pyridine-amine-pyrrole ligands Py-CH2-N(R)-CH2-Pyr-H (HLR; R = H, Bzl, Bu) and the corresponding pyridine-amine-pyrrolate ligands [Py-CH2-N(R)-CH2-Pyr]- (LR-; R = H, Bzl, Bu, CH2Py) has been investigated. The neutral ligands HLR (R = H, Bu, Bzl) give [(HLR)MI(cod)]+ (M = Rh, Ir) in which HLR acts as a didentate ligand via the pyridine nitrogen (NPy) and the amine nitrogen (NRamine). The crystal structures of [(HLH)MI(cod)]PF6 (M = Rh: [1]PF6 and M = Ir: [2]PF6) have been determined. Deprotonation of [(HLR)MI(cod)]+ (M = Rh, Ir; R = H, Bzl, Bu) results in the neutral complexes [(LR)MI(cod)] (M = Rh, Ir) of the mono-anionic ligands LR- (R = H, Bzl, Bu). In square-planar [(LH)MI(cod)] (M = Rh: 3, M = Ir: 4), LH- is didentate via NHamine and the pyrrolate nitrogen (NPyr). The X-ray structures of 3 and 4 reveal that in both cases the uncoordinated NPy accepts a hydrogen bond from NHamine. The X-ray structures of [(LBzl)MI(cod)] (M = Rh: 5, M = Ir: 6), show that LBzl- is didentate via Namine and NPyr for M = Rh and tridentate for M = Ir. In solution LBzl- is tridentate for both M = Rh and M = Ir. The neutral complexes [{Py-CH2-N(R)-CH2-Pyr}MI(cod)] (M = Rh, Ir) cannot be oxidised selectively with H2O2. This is in marked contrast to the previously observed selective oxidation of the corresponding cationic complexes [{Py-CH2-N(R)-CH2-Py}RhI(cod)]+. Rhodium complex 5 is an active catalyst for the stereoregular polymerisation of phenylacetylene, whereas iridium complex 6 is inactive.
    Additional Material: 6 Ill.
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  • 8
    ISSN: 1434-193X
    Keywords: Asymmetric synthesis ; Chiral synthons ; Configuration inversion ; Hydroxy lactones ; Lactones ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper we report the inversion of configuration of (S)-β-hydroxy-γ-butyrolactone [(S)-1] to its (R) enantiomer (R)-1, with total retention of the enantiomeric purity, by a four-step procedure. The (R)-β-hydroxy-γ-butyrolactone [(R)-1] was thus synthetized with an overall chemical yield of 47% and 〉 97% ee. This transformation opens an economic route to the production of (R)-GABOB and (R)-carnitine, among other biologically active compounds, from a D-hexose source, or, alternatively, from the industrial waste compound (S)-carnitine. During the reaction sequence, the intermediate β-lactone 4 is also prepared, which is now under investigation as a chiral synthon for new synthetic applications.
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  • 9
    ISSN: 1434-193X
    Keywords: Solid-phase peptide synthesis ; Disperse Red 1 ; p-Nitrophenyl ester ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new simple and efficient method for the detection of incomplete coupling reactions during solid-phase peptide synthesis is decribed. Using p-nitrophenyl ester 1 (NF31), free amino groups can be visually detected on the resin by direct coloring of the beads. A specific feature of the assay resides in the possibility of detection of sterically hindered primary amines.
    Additional Material: 3 Ill.
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  • 10
    ISSN: 1434-193X
    Keywords: Cyclic voltammetry ; Fullerenes ; Phase-transfer catalysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several pyrrolidinofullerenes were N-arylated by phase-transfer catalysis in the absence of solvent. The electrochemical behaviour of the novel C60-acceptor dyads was studied by cyclic voltammetry which showed that the nitro groups on the N-phenyl ring have a strong influence on the reduction potential values. Theoretical calculations at the semiempirical PM3 level fully support the experimental redox potential values.
    Additional Material: 2 Ill.
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