one-electron

This mechanism appears to operate only in the absence of one-electron donors.

The energy eigenfunctions are assumed to be products of one-electron wavefunctions.

It is used as a one-electron reducing agent.

In this way, a set of self-consistent one-electron orbitals are calculated.

The matrix element of the one-electron operator appearing on the right hand side is finite.

The spatial components of these one-electron functions are called atomic orbitals.

The reversible one-electron reduction step gives stable 11π species.

Corannulene can be reduced up to a tetraanion in a series of one-electron reductions.

The addition of two one-electron ligands is called oxidative addition.

It remains a one-electron approximation to a multitudinous many-body problem.

The one-electron reduction potential of a molecule can be used to obtain an electron affinity.

Electrochemical studies show that 3 undergoes a reversible one-electron reduction.

In others words with this model the well-known one-electron two-photon ionization law is recovered.

For light one-electron ions, which are important for the experiment, this contribution has, so far, not been known.

One-electron reduction reactions with enzymes in solution: a pulse radiolysis study.

Then, this is a one-electron operator s defined by its Cartesian components:

Many aromatic compounds can undergo one-electron reduction by alkali metals.

One-electron changes are also possible and in fact some oxidative addition reactions proceed via series of 1e changes.

The completeness profile is used to provide a visual assessment of the quality of one-electron basis sets.

EPR measurements confirm that it serves as a one-electron shuttle.

The monovalent dihelium cation is stabilised by a one-electron bond.

Conclusions from these results suggest that several one-electron properties have a predictable, although not monotonic convergence pattern.

This means that cannot be written as a product of one-electron wave functions and the wave function is entangled.

Sodium also reacts with polycyclic aromatic hydrocarbons via one-electron reduction.

Nitric oxide can serve as a one-electron pseudohalide.