نتایج جستجو برای: electron delocalization

تعداد نتایج: 310383  

Journal: :Acta Crystallographica Section A Foundations of Crystallography 2002

Journal: :Physical review 2021

We use field-cycling-assisted dynamic nuclear polarization and continuous radio-frequency (RF) driving over a broad spectral range to demonstrate magnetic-field-dependent activation of spin transport from strongly hyperfine-coupled $^{13}\mathrm{C}$ sites in diamond. interpret our observations with the help theoretical framework where interactions are mediated by electron spins. In particular, ...

Journal: :Inorganic chemistry 2012
Alexey Potapov Kyle M Lancaster John H Richards Harry B Gray Daniella Goldfarb

Hard-ligand, high-potential copper sites have been characterized in double mutants of Pseudomonas aeruginosa azurin (C112D/M121X (X = L, F, I)). These sites feature a small A(zz)(Cu) splitting in the EPR spectrum together with enhanced electron transfer activity. Due to these unique properties, these constructs have been called "type zero" copper sites. In contrast, the single mutant, C112D, ...

2005
N. Silvis-Cividjian C. W. Hagen P. Kruit

Electron-beam-induced deposition EBID is a versatile microand nanofabrication technique based on electron-induced dissociation of metal-carrying gas molecules adsorbed on a target. EBID has the advantage of direct deposition of three-dimensional structures on almost any target geometry. This technique has occasionally been used in focused electron-beam instruments, such as scanning electron mic...

2000
Haranath Ghosh Alok Shukla Sumit Mazumdar

Electron-electron interactions in general lead to both ground state and excited state confinement. We show, however, that in phenyl-substituted polyacetylenes electron-electron interactions cause enhanced delocalization of quasiparticles in the optically excited state from the backbone polyene chain into the phenyl groups, which in turn leads to enhanced confinement in the chain direction. This...

Journal: :Physical chemistry chemical physics : PCCP 2009
Marco García-Revilla Jesús Hernández-Trujillo

The electronic structure of the benzenium cation, [C6H7]+, the simplest intermediate of electrophilic aromatic substitution reactions, was analyzed in terms of the properties of electron densities obtained from multiconfigurational quantum theoretical methods. The indirect C-H coupling constants and the physical contributions to their values were calculated and rationalized in terms of the elec...

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