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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Journal of the American Chemical Society 117 (1995), S. 9671-9678 
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Journal of the American Chemical Society 117 (1995), S. 9679-9685 
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Structural chemistry 10 (1999), S. 429-431 
    ISSN: 1572-9001
    Schlagwort(e): Supramolecular Chemistry ; crystallization ; X-Ray crystal structures ; crystal engineering
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The preparation of a three component crystal of 2,2′-dihydroxybiphenyl (1), phenazine (2) and acridine (3) is described whose possible existence was produced from the structure of a 2:3 cocrystal of 2,2′-dihydroxybiphenyl (1) and phenazine (2). X-Ray structures of both crystals are reported. Inspection of the crystal lattice of the 2:3 cocrystal shows that one phenazine molecule forms one and the other two hydrogen bonds to hydroxygroups of the diol. The molecule forming only one hydrogen bond can be replaced successfully by acridine, a one-hydrogen bond acceptor.
    Materialart: Digitale Medien
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  • 4
    ISSN: 1572-9001
    Schlagwort(e): Molecular recognition ; crystal engineering ; supramolecular chemistry
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The crystal structures of molecular complexes betweenmeso- 1,2-diphenyl-1,2-ethanediol and two bisimines (N,N′-(dibenzylidene)-ethylenediamine and glyoxylidene-bis(2,4-dimethyl-3-pentyl-amine) are reported at different temperatures. The structure-determining motif of the cocrystalline arrangement is one single O-H ⋯. N hydrogen bond resulting in infinite ladderlike polymers. The supramolecular structure is formed by recognition of fitting species: Thed- orl-isomers do not arrange in such structures.1H NMR experiments show that no prearrangements take place by forming complexes in solution.
    Materialart: Digitale Medien
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  • 5
    ISSN: 0947-3440
    Schlagwort(e): Diels-Alder cycloaddition ; Electron transfer ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Electron transfer as initiating step in [4 + 2] cycloadditions was studied with 2,3-bis(dimethylaminomethylene)bicyclo-[2.2.1]heptane (1) and 2,3-bis(dimethylaminomethylene)bicyclo[2.2.2]octane (2) as models. These dienes, having the necessary synperiplanar configuration for a concerted [4 + 2] cycloaddition were allowed to react with dienophiles of increasing acceptor capacity. Slightly activated alkenes like methyl acrylate and acrylonitrile undergo smooth cycloaddition in contrast to the corresponding open-chain dienes where cycloaddition with these dienophiles could not be observed. The use of dimethyl fumarate and dimethyl maleate lead to identical cycloaddition products due to an isomerization of dimethyl maleate catalyzed by 1 and 2. Fumaronitrile and maleonitrile proved to be stable under the reaction conditions and lead to different stereoisomers in the cycloaddition to 2. The introduction of three and four acceptor groups, different combinations of cyano and methoxycarbonyl groups, leads to a sudden increase in reactivity towards 1 and 2. At the same time the cycloadditions are no longer stereospecific in those cases where they could be checked, and radical ions could be detected either by ESR spectroscopy or by stopped-flow visible spectroscopy. This applies in particular to dichloromethane as solvent. Stopped-flow measurements in combination with a rapid-scan unit reveals a transient absorption at λ ∽ 420 nm in acetonitrile for 1,1-dicyano-2,2-bis(methoxycarbonyl)ethene and dimethyl dicyanofumarate as dienophiles which is ascribed to zwitterionic intermediates by a comparison with related systems. The cycloadditions of TCNE to 1 and 2 lead to thermally unstable adducts in both cases. Electron transfer was not only observed in solution but could also be detected in the isolated solid products, in particular if they were placed in a polar environment like KBr where complete dissociation in radical ions seems to take place. The relevance of these studies for the mechanism of Diels-Alder reactions is that suitable model systems can be constructed where electron transfer can be observed. Due to the loss of stereospecificity in these cases it is concluded that complete electron transfer is not the principal mechanism of these [4 + 2] cycloadditions which in their majority occur with retention of stereochemistry in the reactants.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 6
    ISSN: 0947-3440
    Schlagwort(e): 2H-Imidazole ; 1,4-Diazadienes ; [4 + 2] Cycloadditions ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 2,2-Diethyl-4,5-dimethyl-2H-imidazole 1, formally a 1,4-di-azadiene, does not produce [4 + 2] cycloadducts with various electronically-different dienophiles. In the presence of tri-fluoroacetic acid, it tautomerizes to 2,2-diethyl-4-methyl-5-methylene-3-imidazoline 2 and forms a dimer, the structure of which was determined by X-ray crystallography.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 7
    ISSN: 0947-3440
    Schlagwort(e): 1,3-Cycloadditions ; Sulfines (thione S-oxides) ; 1,2,4-Oxadithiolanes ; Calculation of TS ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Thione S-oxides (sulfines) harbor the allyl anion MO of 1,3-dipoles, but fail to undergo 1,3-cycloadditions to the usual dipolarophiles with a CC multiple bond. Thioketones stand the test as superdipolarophiles. The thione S-oxides 3 and 9 combined with the thioketones 5 and 7 at 80-100°C, furnishing spiro-1,2,4-oxadithiolanes in high yields despite steric hindrance. The structures of the cycloadducts were clarified by their spectra and an X-ray analysis of 11. Becke3LYP/6-31G* calculations of transition structures and products for the cycloadditions of thioformaldehyde S-oxide to thioformaldehyde support the observed regiochemistry. The activation energy amounts to 3.9 kcal mol-1, in contrast to EA = 17.4 kcal mol-1 for the corresponding addition to ethylene. The transition structures are in accordance with concerted cycloadditions.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 8
    ISSN: 0935-9648
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 9
    ISSN: 1434-193X
    Schlagwort(e): Benzocyclobutenes ; o-Quinodimethanes ; Pericyclic reactions ; Retrodisproportionation ; 9-Anthryl radicals ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: -7,8-Dimethoxy-7,8-diphenyl- (1c), 7,8-dimethyl-7,8-diphenyl- (1d), 7-methoxy-7,8,8-triphenyl- (1e), 7-methyl-7,8,8-triphenyl- (1f), 7-isocyano-7,8,8-triphenyl- (1g), and 7,7,8-triphenylbenzocyclobutene (1h) are amenable to a variety of thermal rearrangements following initial electrocyclic ring-opening to the corresponding 7,8-diphenyl- (2c,d) and 7,8,8-triphenyl-o-quinodimethanes (2e-h). meso-1c was found to undergo a facile meso/rac isomerization at room temperature, indicating that other processes such as a symmetry-forbidden disrotatory ring-opening or a stepwise reaction compete with the symmetry-allowed conrotatory process. An estimate of the energy profile of the 1c/2c reaction system was made by kinetic simulation in combination with oxygen trapping of the intermediate o-quinodimethanes (2c) and semiempirical PM3 calculations, and revealed that the barrier for the symmetry-forbidden pathway is merely about 4 kJ·mol-1 higher than that for the symmetry-allowed one. o-Quinodimethanes 2c, 2g, 2e, and 2h underwent further electrocyclic hexatriene-cyclohexadiene ring-closure to give 4a,10-dihydroanthracene derivatives at temperatures between 20 and 80 °C. The 4a,10-dihydroanthracenes were further transformed to 9,10-disubstituted anthracenes by elimination of methanol or HCN, as well as to 9,10-substituted 9,10-dihydroanthracene derivatives. ESR and ENDOR spectroscopic detection of related 9-anthryl radicals lends support to the view that 9,10-dihydroanthracene products are formed by a homolytic hydrogen-transfer reaction (retrodisproportionation). By way of contrast, the aforementioned transformations play only a minor role in the case of methyl-substituted benzocyclobutenes 1d, 1f as here they are overruled by faster 1,5-H shift reactions of the corresponding o-quinodimethanes 2d, 2f, leading to styrene derivatives.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
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  • 10
    ISSN: 0947-3440
    Schlagwort(e): Diels-Alder cycloaddition ; Electron transfer ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: (E,E)-1 and (E,Z)-1,4-bis(dimethylamino)-1,3-butadiene (2) as model systems for highly electron-rich dienes were allowed to react with olefins of increasing electron-acceptor capacity under standard concentrations (0.4 M solutions of diene and dienophile) and at reaction temperatures from -50°C to a maximum of +60°C (slow decomposition of the diene). Methyl acrylate (3), acrylonitrile (4), and dimethyl methylfumarate (6) did not form cycloadducts with 1 at 35°C in six weeks. Isopropylidenemalononitrile (5) undergoes dimerization. Maleo- (9) and fumaronitrile (10) add to 1 with retention of stereochemistry ( ≥98%). Dimethyl maleate (7) isomerizes under the reaction conditions to dimethyl fumarate (8) and reacts with 1 to the cycloadduct of 8. N-Methylmaleimide (11) gave the expected cycloadduct. The monosubstituted C atoms of the C—C double bond of 1,1,2-tris(methoxycarbonyl)ethene (12) and 2-cyano-1,1-bis(methoxycarbonyl)-ethene (13) add to C-2 of 1 to form zwitterions which stabilize themselves by a 1,3-hydrogen shift to 24 and 25. The reactions of 1 with 1,1-dicyano-2-methoxycarbonylethene (14), 1,1-dicyano-2,2-bis(methoxycarbonyl)ethene (15), and tetracyanoethene (18) provided, though very reactive, no isolable cycloadducts or other identifiable products. Dimethyl dicyanomaleate (16) and dimethyl dicyanofumarate (17) lead in non-stereospecific reactions with 1 to the same cycloadduct even at -50°C in dichloromethane. The same cycloadduct is obtained from 2 and 17. For the reactions of 16 and 17 with 1 electron transfer from diene to dienophile could be demonstrated. Intermediates were detected 1H-NMR-spectroscopically at -95°C which transformed into the cycloadduct when warmed to-50°C. A comparison of the preparative results with oxidation potentials of 1 and 2, and the reduction potentials of the olefins shows, that electron transfer is possible when oxidation and reduction potential are close together. It is concluded from the loss of stereochemistry during the cycloadduct formation in those cases (16 and 17) where electron transfer is observed, and furthermore from retention of stereochemistry (9 and 10) when no electron transfer could be detected, that electron transfer may be a possibility in [4 + 2] cycloadditions, but that it is not the general mechanism of the Diels-Alder reaction.
    Materialart: Digitale Medien
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