Add to ORKGe recently reported that there is an optimal combination of donor and acceptor strengths for a given molecular length and bridge structure that maximizes (beta) . For this combination, there is the correct degree of bond length alternation and asymmetry in the molecule. Our recent findings suggest that molecules that can be viewed as asymmetric cyanines with relatively small amounts of bond length alternation are nearly optimal. In this manner, we have identified molecules with nonlinearities many times that of conventional chromophores for a given length. In this paper, we will present a new computational analysis that allows the correlation of bond length alternation with hyperpolarizabilities and will present EFISH data on simple donor-a...
The synthesis and second-order nonlinear optical properties of acceptor-substituted biologically der...
We report on a series of chromophores that have been synthesized with a modulated conjugation path b...
The solvent dependence of the second hyperpolarizability, γ, of a variety of unsaturated organic com...
e recently reported that there is an optimal combination of donor and acceptor strengths for a given...
A computational method was devised to explore the relationship of charge separation, geometry, molec...
A computational method was devised to explore the relationship of charge separation, geometry, molec...
A computational method was devised to explore the relationship of charge separation, geometry, molec...
There has been much recent effort in the design of optimal chromophores for second-order nonlinear o...
The molecular first hyperpolarizabilities (β) of a series of asymmetric squaraine dyes have been mea...
The molecular first hyperpolarizabilities (β) of a series of asymmetric squaraine dyes have been mea...
It has been suggested that optimizing the first hyperpolarizability, β, of donor-acceptor compounds ...
It has been suggested that optimizing the first hyperpolarizability, β, of donor-acceptor compounds ...
Improved nonlinear organic chromophores of varying conjugation length with either thiobarbituric aci...
Improved nonlinear organic chromophores of varying conjugation length with either thiobarbituric aci...
Since many years, researchers are investigating nonlinear optical active materials to obtain high va...
The synthesis and second-order nonlinear optical properties of acceptor-substituted biologically der...
We report on a series of chromophores that have been synthesized with a modulated conjugation path b...
The solvent dependence of the second hyperpolarizability, γ, of a variety of unsaturated organic com...
e recently reported that there is an optimal combination of donor and acceptor strengths for a given...
A computational method was devised to explore the relationship of charge separation, geometry, molec...
A computational method was devised to explore the relationship of charge separation, geometry, molec...
A computational method was devised to explore the relationship of charge separation, geometry, molec...
There has been much recent effort in the design of optimal chromophores for second-order nonlinear o...
The molecular first hyperpolarizabilities (β) of a series of asymmetric squaraine dyes have been mea...
The molecular first hyperpolarizabilities (β) of a series of asymmetric squaraine dyes have been mea...
It has been suggested that optimizing the first hyperpolarizability, β, of donor-acceptor compounds ...
It has been suggested that optimizing the first hyperpolarizability, β, of donor-acceptor compounds ...
Improved nonlinear organic chromophores of varying conjugation length with either thiobarbituric aci...
Improved nonlinear organic chromophores of varying conjugation length with either thiobarbituric aci...
Since many years, researchers are investigating nonlinear optical active materials to obtain high va...
The synthesis and second-order nonlinear optical properties of acceptor-substituted biologically der...
We report on a series of chromophores that have been synthesized with a modulated conjugation path b...
The solvent dependence of the second hyperpolarizability, γ, of a variety of unsaturated organic com...