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  • hydrogen bonding  (6)
  • Glomus intraradices  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 28 (1998), S. 931-933 
    ISSN: 1572-8854
    Keywords: Flavone ; hydrate ; hydrogen bonding ; X-ray crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The X-ray crystal structure of 7-hydroxyflavone monohydrate, C14H10O3 · H2O, is determined. The compound crystallizes in the monoclinic space group, P21/n with a = 3.801(3), b = 19.665(4), c = 16. 039(6), β = 93.69(3)°, and μ = 0.68 mm−1 for Z = 4. The phenyl ring of the flavone moiety is rotated 18.6(1)° out of the penzopyran plane, which is a typical value for flavones. In the crystal lattice, there are wide channels which are lined mainly by C–H groups. The water molecules enclosed in these channels are severely disordered.
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  • 2
    ISSN: 1572-8854
    Keywords: Cyclohexane ; alkyne ; hydrogen bonding ; X-ray crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The X-ray crystal structure of the title compound, C18H28O3, is determined. The hydrogen bond scheme does not follow considerations based on hierarchies of donor and acceptor strengths. The hydroxyl group of the molecule accepts only very weak C–H···O interactions.
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  • 3
    ISSN: 1572-8854
    Keywords: alkyne ; hydrogen bonding ; x-ray crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract In the x-ray crystal structure of the alkynol 5β-hydroxy-5α-ethynyl-10β-methyl-Δ1(9)-octalin-2-one [C13H16O2, Pbca, a = 10.244(7), b = 12.734(2), c = 17.125(2) Å, Z = 8], the hydroxyl and ethynyl groups are involved in a hydrogen bond arrangement C—C—H···O···H—O, which is supposed to be anticooperative, i.e., weaker than the sum of two isolated hydrogen bonds.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 29 (1999), S. 99-102 
    ISSN: 1572-8854
    Keywords: Isoflavone ; natural compound ; Dalbergia spinosa ; X-ray crystal structure ; hydrogen bonding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The X-ray crystal structure of the plant isoflavone dalspinin from Dalbergia spinosa is determined. The compound, C17H12O7, is monoclinic in P21/n with a = 3.970(1), b = 23.607(5), c = 14.633(3) Å, β = 94.46(3)°, V = 1367.2(5) Å3, D calc = 1.595 g cm−1 and Z = 4. The molecular structure is characterized by a short intramolecular O–H···O=C hydrogen bond, and a large tilt angle of the two rigid ring systems with respect to each other. The intermolecular interactions in the crystal are discussed.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 28 (1998), S. 581-584 
    ISSN: 1572-8854
    Keywords: Cyclohexane ; alkyne ; hydrogen bonding ; X-ray crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract In the X-ray crystal structure of the alkynol 5β-hydroxy-5α-(prop-2-ynyl)-10β-methyl-Δ1(9)-octalin-2-one [C14H18O2, Pca2 1, a = 13.559(1), b = 7.960(2), c = 21.748(3) Å], the hydroxyl and propynyl groups form a hydrogen bond chain C---C-H⋯O-H⋯O which is supposed to be a cooperative arrangement. Quantum chemical calculations estimate cooperativity enhancement within the array to be 0.4 kcal/mol, which is only a small (but recognizable) effect.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 30 (2000), S. 143-145 
    ISSN: 1572-8854
    Keywords: thian ; oxime ; hydrogen bonding ; x-ray crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The X-ray crystal structure of γ-2-trans-2,6-diphenylthian-1,1-dioxide-4-one oxime is determined [C17H17NO3S, space group P21 n, a = 8.177(1) b = 9.574(1)c = 19.730(5) Å, β = 97.35(5)°]. The oxime group does not form an oxime dimer, but is involved in an O-H···O=S hydrogen bond.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Mycorrhiza 5 (1995), S. 273-278 
    ISSN: 1432-1890
    Keywords: Key words Drought stress ; Tropical maize cultivars ; Glomus intraradices ; Metabolic changes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  A greenhouse experiment was carried out to investigate the influence of the arbuscular mycorrhizal (AM) fungus (Glomus intraradices Schenck & Smith) on metabolic changes in tropical maize (Zea mays L.) under drought. Two cultivars, Tuxpeno sequia C0 (drought sensitive) and C8 (drought resistant), were subjected for 3 weeks to water stress following tasselling (75–95 days after sowing). Fully expanded 7th or 8th leaves were sampled and assessed for levels of chlorophyll, sugars, proteins, and amino acids. Chlorophyll content was not altered either by water stress or the presence of mycorrhizae. Mycorrhizal plants (M+) had higher total and reducing sugars than nonmycorrhizal plants (M–) at the end of 3 weeks of the drought cycle. An increase in protein content was observed with drought stress in M+ plants of the cultivar C0. Most of the amino acids showed a linear increase during the period of water stress in M+ and M– plants for both cultivars. Total amino acids increased by 40.6% and 43.7% in M– plants of C0 and C8, respectively. With the presence of AM fungus, amino acid levels increased by only 10.7% and 19.2% of leaf dry mass in C0 and C8, respectively. Alanine, asparagine, glutamine, and glycine accounted for 70% of the amino acid pool. Under drought, AM inoculation enabled the plants to retain considerable amounts of sugars and proteins, especially in the drought-sensitive cultivar C0. This may be of physiological importance in helping the plant to withstand moderate drought.
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