The intrinsic optical nonlinearities of linear structures, including conjugated chain polymers and nanowires, are shown to be dramatically enhanced by the judicious placement of a charge diverting path sufficiently short to create a large phase disruption in the dominant eigenfunctions along the main path of probability current. Phase disruption is proposed as a new general principle for the design of molecules, nanowires and any quasi-1D quantum system with large intrinsic response and does not require charge donor-acceptors at the ends. © The design and realization of ultrafast nonlinear optical materials with large responses to optical frequency electric fields remains an active field of pure and applied research [1][2][3][4]. To date, no general design rules for obtaining large nonlinearities from any structure have been articulated, and the response of materials remains well below that allowed by quantum physics. In this letter, we propose a general principle that may explain why modern molecules fall short of their potential and use it to demonstrate simple structures with nonlinear responses approaching the physical limits.The off-resonance electronic nonlinear optical response of a molecule is completely determined by its energy spectrum and transition moments. Normalized to its maximum value, the sum over states expression for the intrinsic first hyperpolarizability along the x-axis may be written as [5] where the sum is over all states, x nℓ is the n, ℓ element of the position matrix withx = x − x 00 , E n0 = E n − E 0 is the difference in energy of eigenstates n and 0, N is the number of electrons and m their mass. We include as many as 100 energy eigenstates to calculate β, but systems with large β are always well approximated using only three states. For brevity, we focus on the first hyperpolarizability, though our results also hold for the second hyperpolarizability, γ xxxx . For the remainder of this letter, all hyperpolarizabilities are divided by their maximum values and represent intrinsic tensor properties. It is evident from Eqn.(1) that a system optimized for nonlinear optics will necessarily have eigenfunctions with a large degree of overlap as well as a large change of dipole moment between contributing levels. This is an essential trade-off to achieve a large response. It is generally recognized that the hyperpolarizabilities of most molecules fall at least 30 times short of the limits. [5,6]. Monte Carlo simulations discovered the optimum energy spectrum for such molecules and provided a strong indicator of the origin of the gap [7]. Optimization of the effective potential energy an electron experiences across the main direction of a quasi-linear molecule showed that the hyperpolarizabilities may be increased by tuning a few parameters [8], by modulation of conjugation along a chain [9], or by donor-acceptor substitution and insertion of spacers [10]. However, there is no general rule about how to construct the ideal potential energy profile across a molecule to maximize the nonlinea...