Shu-Jen Han, Dharmendar Reddy, et al.
ACS Nano
We have described the synthesis of a variety of 1,3, 1,4, and 1,5 donor-acceptor conjugation extended substituted pyrazole derivatives and have studied their spectroscopic and nonlinear optical properties. These materials are thermally stable and absorb strongly in the UV-visible region, albeit at much shorter wavelengths than comparably substituted cyclic azapolyenes such as 2-pyrazolines. Quadratic hyperpolarizability measurements suggest that the pyrazoles are significantly nonlinear, and that 1,3 and 1,4 substitution is preferred. 1,5 substitution causes a significant drop in the nonlinearity and a blue shift in the long-wavelength absorption maximum, presumably due to a twisting and partial deconjugation of the substituents to relieve unfavorable steric interactions. The experimental results are compared with those predicted by simple “finite field” computational procedures. © 1993, American Chemical Society. All rights reserved.
Shu-Jen Han, Dharmendar Reddy, et al.
ACS Nano
O.F. Schirmer, W. Berlinger, et al.
Solid State Communications
B.A. Hutchins, T.N. Rhodin, et al.
Surface Science
Sharee J. McNab, Richard J. Blaikie
Materials Research Society Symposium - Proceedings