A macroscopic solution polarization free-energy functional is combined with semiempirical molecular orbital theory to study shifts of electronic absorption energies for several molecules in solution. The present method requires calculation of the induced electrostatic potential on the van der Waals
Supercyclic Subspaces: Spectral Theory and Weighted Shifts
✍ Scribed by Alfonso Montes-Rodrı́guez; Héctor N Salas
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 540 KB
- Volume
- 163
- Category
- Article
- ISSN
- 0001-8708
No coin nor oath required. For personal study only.
✦ Synopsis
A vector x in a Banach space B is called hypercyclic for a bounded operator T if the orbit {T n x: n \ 0} is dense in B. If the scalar multiples of the elements in the orbit are dense, then the vector x is called supercyclic. We give a general sufficient condition for a bounded operator on a Banach space to have an infinite-dimensional closed subspace of supercyclic vectors. As a consequence, we also obtain a spectral sufficient condition for the existence of such a subspace for an operator. These results allow us to characterize unilateral and bilateral weighted shifts that have an infinite dimensional closed subspace of supercyclic vectors. Surprisingly, there are weighted shift operators that have supercyclic vectors, but in which all closed subspaces of supercyclic vectors are finite dimensional. Our results complement recent work on hypercyclic subspaces and supercyclic subspaces. They also suggest that the problem of the existence of infinite dimensional closed subspaces of supercyclic vectors is not only different, but also more difficult to handle than the corresponding problem for hypercyclic vectors.
📜 SIMILAR VOLUMES
On the basis of continuous medium theory, a model for evaluation of spectral shifts in solution has been developed in this work. The interaction energy between solute dipole and reaction field and the self-energy of the reaction field have been formulated through derivations. Applying the interactio
The shift m E may ior the CTTS spectrum of lodlde on addxtion of alkah chlorxdes is defiitiveiy related to their mean actwIt> coefiic&ents. The reiattve contributions to the coulombrc mteractron of the Debye-Hiickel and expanded4attice models are determined by a new preczse procedure, yteldmg accura