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Aggregate structure, spectroscopic

Reaction conditions can be modified to accelerate the rate of lithiation when necessary. Addition of tertiary amines, especially TMEDA, facilitates lithiation53 by coordination at the lithium and promoting dissociation of aggregated structures. Kinetic and spectroscopic evidence indicates that in the presence of TMEDA lithiation of methoxybenzene involves the solvated dimeric species (BuLi)2(TMEDA)2.54 The reaction shows an isotope effect for the o-hydrogcn, establishing that proton abstraction is rate determining.55 It is likely that there is a precomplexation between the methoxybenzene and organometallic dimer. [Pg.628]

This section is intended as a broad overview of the present knowledge of MTs from the perspective of coordination chemistry the main developments with respect to their metal content, structure, spectroscopic features and chemical properties will therefore be summarized. Moreover, the structural patterns of the metal sulfur aggregates in MTs will be compared with those found... [Pg.213]

Masuo, S., et al. 2003. Fluorescence spectroscopic properties and single aggregate structures of pi-conjugated wire-type dendrimers. J Phys Chem B 107 2471. [Pg.204]

Second, because the proposed novel approach relies on assembling different peptide lipids to organize into desired proteinlike structures, the control and characterization of the assembly process and the aggregate structures are critical steps of the study. More detailed characterizations through microscopic and spectroscopic techniques should be able to bring fmther important insights into this imique molecular assembly technique. [Pg.632]

Chemical models of electrolytes take into account local structures of the solution due to the interactions of ions and solvent molecules. The underlying information stems from spectroscopic, kinetic, and electrochemical experiments, as well as from dielectric relaxation spectroscopy. The postulated structures include ion pairs, higher ion aggregates, and solvated and selectively solvated ions. [Pg.465]

Consequently, due to preferred cis-cis orientation a dimeric structure is observed for the indium complex and an unprecedented cis-trans arrangement in the thallium structure leads to a polymeric aggregate. Further N-NMR spectroscopic studies show that the aluminum and gallium complexes are stable contact ion pairs even in solution whereas the indium and thallium compounds are solvent-separated ion pairs in THE solution. [Pg.96]

Reference [33] describes recent progress on cyanine probes that bind noncova-lently to DNA, with a special emphasis on the relationship between the dye structure and the DNA binding mode. Some of the featured dyes form well-defined helical aggregates using DNA as a template. This reference also includes spectroscopic data for characterizing these supramolecular assemblies as well as the monomeric complexes. [Pg.71]

Extensive biochemical and spectroscopic studies have been undertaken on hCP in order to investigate the nature of the copper centers and their role in structure-function relationships. However, the protein is very susceptible to aggregation, proteolysis, loss of copper, and other chemical degradations and requires careful preparation and handling in these circumstances it is difficult to review all the literature objectively and comprehensively. A three-dimensional crystal structure of hCP has been reported at a nominal resolution of 3.1A [7], but this resolution has been extended to just beyond 3.0 A. This chapter will summarize some of the more important biochemical and spectroscopic studies of the protein. It will then focus on the structural results recently obtained by X-ray crystallographic methods and attempt to explain putative functions of the protein in terms of its molecular structure. [Pg.53]


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Aggregates structure

Structure aggregation

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