Octupolar dendrimers with large first hyperpolarizability

被引:38
作者
Jeong, HC
Piao, MJ
Lee, SH
Jeong, MY
Kang, KM
Park, G
Jeon, SJ
Cho, BR
机构
[1] Korea Univ, Mol Optoelect Lab, Dept Chem, Seoul 136701, South Korea
[2] Korea Univ, Mol Optoelect Lab, Ctr Electro & Photo respons Mol, Seoul 136701, South Korea
[3] Kookmin Univ, Seoul 136702, South Korea
关键词
D O I
10.1002/adfm.200304478
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of 1,3,5-tricyano-2,4,6-tris(styryl)benzene derivatives (1,2) and dendrimers (3) have been synthesized and their first hyperpolarizabilities (beta) were determined. Whereas the lambda(max) values of 1-3 are similar, the oscillator strength increases with the molecular size. For all compounds, the Stokes shifts are significantly larger when NAr2 is used as the donor. The beta(0) values of 1-3 range from 252 to 507 x 10(-30) esu and increases with the number of octupolar units in the molecule. When the octupolar molecules are linked to the 1,3,5-position of the benzene ring by flexible ether linkages, the beta(O) value increases by 1.7 fold. On the other hand, octupolar monodendron based on the nitrogen atom core and 1,3,5-tricyano-2,4,6-tris(p-diarylaminostyryl)benzene moieties at the periphery exhibits beta(O) = 507 x 10(-30) esu, which is one of the largest (O) values reported for the octupolar molecules.
引用
收藏
页码:64 / 70
页数:7
相关论文
共 37 条
[1]  
BUNEL J, 2002, J AM CHEM SOC, V124, P4560
[2]  
Cho BR, 2002, B KOR CHEM SOC, V23, P1253
[3]   Synthesis and nonlinear optical properties of 1,3,5-methoxy-2,4,6-tris(styryl)benzene derivatives [J].
Cho, BR ;
Chajara, K ;
Oh, HJ ;
Son, KH ;
Jeon, SJ .
ORGANIC LETTERS, 2002, 4 (10) :1703-1706
[4]   Octupolar crystals for nonlinear optics: 1,3,5-trinitro-2,4,6-tris(styryl)benzene derivatives [J].
Cho, BR ;
Lee, SJ ;
Lee, SH ;
Son, KH ;
Kim, YH ;
Doo, JY ;
Lee, GJ ;
Kang, TI ;
Lee, YK ;
Cho, MH ;
Jeon, SJ .
CHEMISTRY OF MATERIALS, 2001, 13 (05) :1438-+
[5]   1,3,5-tricyano-2,4,6-tris(vinyl)benzene derivatives with large second-order nonlinear optical properties [J].
Cho, BR ;
Park, SB ;
Lee, SJ ;
Son, KH ;
Lee, SH ;
Lee, MJ ;
Yoo, J ;
Lee, YK ;
Lee, GJ ;
Kang, TI ;
Cho, MH ;
Jeon, SJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (26) :6421-6422
[6]   Highly unusual effects of π-conjugation extension on the molecular linear and quadratic nonlinear optical properties of ruthenium(II) ammine complexes [J].
Coe, BJ ;
Jones, LA ;
Harris, JA ;
Brunschwig, BS ;
Asselberghs, I ;
Clays, K ;
Persoons, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (04) :862-863
[7]   From molecules to opto-chips: organic electro-optic materials [J].
Dalton, LR ;
Steier, WH ;
Robinson, BH ;
Zhang, C ;
Ren, A ;
Garner, S ;
Chen, AT ;
Londergan, T ;
Irwin, L ;
Carlson, B ;
Fifield, L ;
Phelan, G ;
Kincaid, C ;
Amend, J ;
Jen, A .
JOURNAL OF MATERIALS CHEMISTRY, 1999, 9 (09) :1905-1920
[8]   Synthesis and nonlinear optical, photophysical, and electrochemical properties of subphthalocyanines [J].
del Rey, B ;
Keller, U ;
Torres, T ;
Rojo, G ;
Agulló-López, F ;
Nonell, S ;
Martí, C ;
Brasselet, S ;
Ledoux, I ;
Zyss, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (49) :12808-12817
[9]  
DHNAULT CJ, 1998, J OPT SOC AM B, V15, P257
[10]  
*FUJ LIM, 1999, MOPAC 2002