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  • Chemistry  (48)
  • General Chemistry  (38)
  • photochromes  (3)
  • Hydrogen bonding  (2)
  • coordination modes  (2)
  • 1995-1999  (48)
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  • 1
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chiral biyclic bis-lactams of structures 3 and 4 were synthesized from the key intermediate 2′b, the N,N′-bis(4-methoxybenzyl) derivative of 2 (X = MeO) (Scheme 6). The synthesis of this intermediate involved two key steps: (1) a double condensation of glyoxylic acid/anisamide (= oxoacetic acid/4-methoxybenzamide) adduct 11c with veratrole (1,2-dimethoxybenzene; 10) allowed the introduction of two glycine units at the 4,5-positions of the veratrole ring to give 18c (Schemes 3 and 4); (2) in order to circumvent the hydrolysis of 4-methoxybenzoyl protective groups which proved to be unfeasible, these groups were transformed into 4-methoxybenzyl groups through a sequence involving thiocarbonylation followed by reduction (Scheme 5). Thereafter, the double intramolecular cyclization of the resulting diamino diester 22c proceeded easily to afford 2′b. This intermediate may be transformed via the tetrol 2′g or the diol 2′h into the N-protected derivatives of 2 (X = OR) and of 3 (X = OCOR). Cleavage of the 4-alkuxybenzyl groups was achieved by ceric ammonium nitrate. However, when the aromatic ring bore ether functions (N-protected 2), this normal reaction was accompanied by the oxidative ring cleavage to give the diene-diester structure 4 (Schemes 5 and 6).
    Additional Material: 4 Tab.
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three macrobicyclic octamines 1-3 and the macrotricyclic hexadecamine 14 have been synthesized. The octamines 1-3 bind anionic substrates when protonated. The stability constants of the complexes between the protonated forms of the macrobicyclic polyamines and halide anions have been determined by pH-metric measurements. The stability constants in H2O are very high; 1 in its hexaprotonated form binds F- with high selectivity (selectivity F-/Cl- 〉 108), while 3 exhibits strong stability constants for both F- and Cl-. Three X-ray structures have been obtained, one where F- is held inside the cavity of 1 · 6H+, one where Cl- is included in 3 · 6H+, and 3 · 6H+ where the cavity is empty.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 81 (1998), S. 1-13 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chiral supermolecules may be obtained from suitable achiral molecular constituents associated through a dissymmetrizing interaction mode. This is the case for the supermolecules I-IV formed by hydrogen-bonding association between the achiral complementary components 1a,b and 2a,b,c. The crystal structures of the supermolecular pairs I-III and of the homochiral aggregate of two ternary supermolecules IV have been determined. The structural data are discussed.
    Additional Material: 11 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 80 (1997), S. 2277-2285 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and structural characterization of the macrobicyclic ligand 1 containing a reducible hexakis-(phenylthio)benzene electron-acceptor site is described. It is based on the condensation of the tetraoxa-diazamacrocycle 3 with a suitably functionalized derivative 4 of hexakis(phenylthio)benzene. Complexation of a potassium cation by 1 gives the corresponding cryptate 2, with a stability constant of ca. 4000 M-1 as determined by 1H-NMR titration in CD3CN. The reduction potential of the hexakis(phenylthio)benzene electron-acceptor site in 2 is shifted by 170 mV towards more positive values with respect to that in 1 by complexation of potassium.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 78 (1995), S. 1895-1903 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of the macrobicyclic europium(III) complex [Eu3+ ⊂1]3Cl- incorporating a N,N′ - dioxide unit has been determined. It confirms the cryptate nature of this species, the included cation being bound to six N- and two O-sites. The efficient shielding of the bound Eu3+ ion may be related to the efficient luminescence of this cryptate and points to the role played by the N-oxide sites. To further explore the effect of such binding groups, the two macrocyclic ligands 4 and 5 bearing two bipyridine N,N′ -dioxide lateral arms have been synthesized and their EuIII and TbIII complexes prepared.
    Additional Material: 2 Ill.
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  • 6
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the linear tris[terpyridine] 1 with three tridentate binding sites is described. The reaction with metal ions of octahedral coordination geometry, such as FeII or NiII, leads to the self-assembly of trinuclear complexes [M3(1)2]6+, which display properties in agreement with a double helical structure. The trinuclear iron (II) helicate has been resolved into its enantiomers.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 78 (1995), S. 1-12 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Double-helical metal complexes, the helicates H2-H5, were found to bind to double-helical DNA by spectroscopic, DNA-melting, and electrophoretic-mobility measurements. The helicates also inhibited the cleavage of DNA by two restriction enzymes, Sspl and EcoRV, a property which agrees with the binding occurring in the major groove of the double helix. Visible-light irradiation of solutions containing a helicate and the pBR322 plasmid led to single-strand cleavage, indicating that these complexes could be of interest as potential probes for nucleic-acid structure.
    Additional Material: 11 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 80 (1997), S. 786-803 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The macrocyclic polyamine-based receptor BA bearing two acridine units makes use of combined electrostatic and stacking interactions for the binding of nucleotide polyphosphates and for the recognition of ATP and of NADPH (ka 〉 3 · 108 M), with a high selectivity for NADPH vs. NADP (ca. 103) and NAD(H) (〉 106). The binding properties of this receptor towards a variety of substrates led to its in vitro application as a fluorescent probe for ATP. BA also interacts strongly with nucleic acids as shown by spectrophotometric, spectrofluorimetic, and electrophoretic mobility methods.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Advanced Materials 9 (1997), S. 39-42 
    ISSN: 0935-9648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 2 Ill.
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  • 10
    ISSN: 0947-6539
    Keywords: diarylethenes ; molecular devices ; nonlinear optics ; photochromes ; redox switches ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic photochromic systems represent a starting point for the elaboration of light-triggered molecular switching devices. The novel bispyridinium and bispyridine compounds 12+ and 6 were synthesized as their uncyclized isomers from 3,5-dibromo-2-methylthiophene in overall yields of 43 and 44%, respectively. The diarylethene photochromes 2 and 10-13, substituted with electron donors and acceptors, were prepared from 5-methylthiophene-2-carboxaldehyde in 21-32% overall yield. All of the compounds were found to exhibit pronounced photochromic properties. Irradiation with UV light resulted in essentially complete photocyclization of the open forms to the intensely coloured closed isomers which could, in turn, be reconverted back to the open state with visible light of γ〉600 nm. The absorption maxima of the described compounds in their closed forms are shifted far towards, and even into, the near-IR region. Whereas no thermochromic properties were observed for the open isomers, the rates of thermal decolouration of the cyclized forms was found to be highly dependent on the nature of the substituents on the thiophene rings. It was demonstrated that reversible photochemical interconversion between the two photochromic states could be used to effectively switch a number of physical properties. Thus, the molecules 12+ and 12 represent two kinds of redox switches, the former in reduction and the latter in oxidation, in which electron conduction is switched on in the closed state and off in the open state. Compound 12 may also be considered to be a photoswitchable analogue of tetrathiafulvalene type substances. On the other hand, compound 2 displays a marked increase in nonlinear optical activity on conversion from the open to the closed form. Such systems are prototypes of photoswitchable molecular wires where electron conduction and push-pull interaction can be reversibly modulated by an external stimulus, namely, irradiation by light.
    Additional Material: 10 Ill.
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