Structures and Considerable Static First Hyperpolarizabilities: New Organic Alkalides (M+@n6adz)M‘- (M, M‘ = Li, Na, K; n = 2, 3) with Cation Inside and Anion Outside of the Cage Complexants

Abstract

Eighteen structures of new organic alkalides (M+@n6adz)M'- (M, M'=Li, Na, K; n=2, 3) with the alkali-metal cation M+ lying near the center of the adz cage and the alkali-metal anion M'- located outside are obtained with all real frequencies. They exhibit very large static first hyperpolarizabilities (beta0) up to 3.2x10(5) au, which exceeds the record value of beta0=1.7x10(5) au for nonlinear optical compounds [Chem.-Eur. J. 1997, 3, 1091]. All potassides (M+@n6adz)K- (M=Li, Na, K; n=2, 3) have considerably large beta0 values (1.6x10(5)-3.2x10(5) au) much larger than the beta0 value (3.6x10(4) au) of the previously designed cuplike alkalide Li+(calix[4]pyrrole)K- [J. Am. Chem. Soc. 2006, 128, 1072]. This shows that the 26adz and 36adz cage complexants are preferable to cuplike calix[4]pyrrole complexant in enhancing the first hyperpolarizability. The effect of cage size of the complexant on the first hyperpolarizability is also presented here: in most cases, the smaller cage complexant corresponds to the larger beta0 value. Moreover, the crucial role by the alkali-metal anion in the large first hyperpolarizability of these alkalides is revealed. These results may provide new means for designing high-performance nonlinear optical materials.