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Host-specific attractants structures

Figure (2). Structure of some host-specific attractants for oomycete zoospores... Figure (2). Structure of some host-specific attractants for oomycete zoospores...
Figures 53 and 54 show the structure of the 3/98d complex as it exists in the unit cell [154, 303], Unlike the complexes with 98a-c, the 98d complex has both hydroxyl groups of one 3 hydrogen bonded to both carbonyl groups of one molecule of 98d. As a result, the diyne backbone is curved (Figure 53) [154, 303], There is no reason to believe that the walls of the reaction cavity experienced by 98d or by transients, lOld and 102d derived from it, in optically active 3 complexes are any more rigid or contain less free volume than do the other complexes. The enantiomeric purity of the product must result from specific attractive host-guest interactions retained along the... Figures 53 and 54 show the structure of the 3/98d complex as it exists in the unit cell [154, 303], Unlike the complexes with 98a-c, the 98d complex has both hydroxyl groups of one 3 hydrogen bonded to both carbonyl groups of one molecule of 98d. As a result, the diyne backbone is curved (Figure 53) [154, 303], There is no reason to believe that the walls of the reaction cavity experienced by 98d or by transients, lOld and 102d derived from it, in optically active 3 complexes are any more rigid or contain less free volume than do the other complexes. The enantiomeric purity of the product must result from specific attractive host-guest interactions retained along the...
Comparatively, the walls of a reaction cavity of an inclusion complex are less rigid but more variegated than those of a zeolite. Depending upon the constituent molecules of the host lattice, the guest molecules may experience an environment which is tolerant or intolerant of the motions that lead from an initial ketone conformation to its Norrish II photoproducts and which either can direct those motions via selective attractive (NB, hydrogen bonding) and/or repulsive (steric) interactions. The specificity of the reaction cavity is dependent upon the structure of the host molecule, the mode of guest inclusion, and the mode of crystallization of the host. [Pg.195]

Insects are so successful because of their mobility, high reproductive potential, ability to exploit plants as a food resource, and to occupy so many ecological niches. Plants are essentially sessile and can be seen to produce flowers, nector, pollen, and a variety of chemical attractants to induce insect cooperation in cross-pollination. However, in order to reduce the efficiency of insect predation upon them, plants also produce a host of structural, mechanical, and chemical defensive artifices. The most visible chemical defenses are poisons, but certain chemicals, not intrinsically toxic, are targeted to disrupt specific control systems in insects that regulate discrete aspects of insect physiology, biochemistry, and behavior. Hormones and pheromones are unique regulators of insect growth, development, reproduction, diapause, and behavior. Plant secondary chemicals focused on the disruption of insect endocrine and pheromone mediated processes can be visualized as important components of plant defensive mechanisms. [Pg.225]

Symmetric polymer blends do not exist in reality. A host erf asymmetries are present in real chemical alloys of interest These include attractive potential asymmetries (present even for isotopic blends) and specific interactions, molecular weight asymmetries and polydispersity, and single chain structural differences between the blend components (e.g., monomer shape and volume, backbone stiffness, and tacticity). Realistic accounting for most of these effects would seem to require an off-lattice description which includes local interchain density and concentration correlations, and compressibility effects [1, 2, 63, 66, 67, 80]. [Pg.363]


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See also in sourсe #XX -- [ Pg.1056 ]




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Host structures

Specific structure

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