Electron paramagnetic resonance structural studies

Electron paramagnetic resonance (EPR) studies on pyridine solutions of bianthrone by Wasserman (41) suggest that the thermochromic form may have one unpaired electron localized on each half of the molecule. The structure proposed by Woodward and Wasserman (42) is VIII which they consider to be identical to the colored photochromic form. Klochkov (43) has warned that free radicals may be involved in decomposition processes occuring at high temperatures in studies of the bian-... 

Electron Paramagnetic Resonance Spectroscopy Studies of Immobilized Monoclonal Antibody Structure and Function... 

PFPE-based surfactants have been studied extensively by Johnston and coworkers [26-29], Fourier transform infrared (FTIR) measurements on a w = 10 microemulsion based on ammonium carboxylate PFPE [CF30(CF2CF(CF3)0) CF2C00NH4] (MW = 740) indicated the presence of bulk water domains. Water solubility up to w = 14 was reported at 55°C and around 177 bar for 1.4wt% surfactant [26]. Time-resolved fluorescence and electron paramagnetic resonance (EPR) studies suggested the presence of anisotropic or nonspherical micelles. Zielinski et al. [30] studied the phase stability of this system at 35°C, as shown in Fig. 2 SANS was then employed to study droplet structure. Observations with PFPE were similar to the earlier study in H7E7 [11] discrete water droplets of around 25 A radius were found to be present, and as indicated in Fig. 3 the droplet size increased with added water. 

Electron spin is the basis of the experimental technique called electron paramagnetic resonance (EPR), which is used to study the structures and motions of molecules and ions that have unpaired electrons. This technique is based on detecting the energy needed to flip an electron between its two spin orientations. Like Stern and Gerlach s experiment, it works only with ions or molecules that have an unpaired electron. 

In general, several spectroscopic techniques have been applied to the study of NO, removal. X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), nuclear magnetic resonance (NMR), extended X-ray absorption fine structure (EXAFS) and X-ray absorption near-edge structure (XANES) are currently used to determine the surface composition of the catalysts, with the aim to identify the cationic active sites, as well as their coordinative environment. 

The X-ray structure of zinc naphthalocyanate has been determined with Zn—N bond lengths of 1.983(4) A.829 Pentanuclear complexes with a zinc phthalocyanine core and four ruthenium subunits linked via a terpyridyl ligand demonstrate interaction between the photoactive and the redox active components of the molecule. The absorbance and fluorescence spectra showed considerable variation with the ruthenium subunits in place.830 Tetra-t-butylphthalocyaninato zinc coordinated by nitroxide radicals form excited-state phthalocyanine complexes and have been studied by time-resolved electron paramagnetic resonance.831... 

The description theoretical study of defects frequently refers to some computation of defect electronic structure i.e., a solution of the Schrodin-ger equation (Pantelides, 1978 Bachelet, 1986). The goal of such calculations is normally to complement or guide the corresponding experimental study so that the defect is either properly identified or otherwise better understood. Frequently, the experimental study suffices to identify the basic structure of the defect this is particularly true when the system is EPR (electron paramagnetic resonance) active. However, if the computational method properly simulates the defect, we are provided with a wealth of additional information that can be used to reveal some of the more basic and general features of many-electron defect systems and defect reactions. 

McBride and co-workers have studied extensively the reactions of such free-radical precursors as azoalkanes and diacyl peroxides (246). By employing a variety of techniques, including X-ray structure analysis, electron paramagnetic resonance (EPR), and product studies, and comparing reactions in the crystal and in fluid and rigid solvents, they have been able to obtain extremely detailed pictures of the solid-state processes. We will describe here some of the types of lattice control they have elucidated, and the mechanisms that they suggest limit the efficacy of topochemical control. 

---