Highly efficient, thermally and chemically stable second order nonlinear optical chromophores containing a 2-phenyl-tetracyanobutadienyl acceptor

Journal of the American Chemical Society

Volumn 121, Issue 2, 1999, Pages 472-473

  Wu, Xiaoming ^a   Wu, Jianyao ^a   Liu, Yunqi ^a   Jen, Alex K Y ^a  

^a NORTHEASTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BUTADIENE DERIVATIVE; 2 PHENYL TETRACYANOBUTADIENYL POLYMER; POLYMER; UNCLASSIFIED DRUG;

ARTICLE; CHROMATOPHORE; CRYSTAL STRUCTURE; DIFFERENTIAL SCANNING CALORIMETRY; ELECTRON TRANSPORT; LIGHT SCATTERING; OPTICAL ROTATION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOSPECIFICITY; THERMOSTABILITY;

EID: 0033585565     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja983537+     Document Type: Article

References (16)

1. (a) Burland, D. M.; Miller, R. D.; Walsh, C. A. Chem. Rev. 1994, 94, 31-75.
2. (b) Dalton, L. R.; Harper, A. W.; Ghosn, R.; Steier, W. H.; Ziari, M.; Fetterman, H.; Shi, Y.; Mustacich, R. V.; Jen, A. K.-Y.; Shea, K. J. Chem. Mater. 1995, 7, 1060-1081.
3. (c) Marks, T. J.; Ratner, Angew. Chem., Int. Ed. Engl. 1995, 34, 155-173.
4. (a) Park, J.; Marks, T. J.; Yang, J.; Wong, G. K. Chem. Mater. 1990, 2, 229-231.
5. (b) Wu, J. W.; Valley, J. F.; Ermer; S.; Binkley, E. S.; Kenney, J. T.; Lipscomb, G. F.; Lytel, R. Appl. Phys. Lett. 1991, 58, 225-227.
6. (c) Wong, K. Y.; Jen, A. K.-Y. J. Appl. Phys. 1994, 75, 3308-3310.
7. Jen, A. K.-Y.; Rao, V. P.; Wong, K. Y.; Drost, K. J. J. Chem. Soc., Chem. Commun. 1993, 90-91.
8. Rao, V. P.; Jen, A. K.-Y.; Wong, K. Y.; Drost, K. J. J. Chem. Soc., Chem. Commun. 1993, 1118-1120.
9. Jen, A. K.-Y.; Cai, Y.; Bedworth, P. V.; Mader, S. R. Adv. Mater. 1997, 9, 132-135.
10. Rao, V. P.; Jen, A. K.-Y.; Wong, K. Y.; Drost, K. J. Chem. Commun. 1996, 1237-1238.
11. Ermer, S.; Lovejoy, S. M.; Leung, D. S.; Warren, H.; Moylan, C. R.; Twieg, R. J. Chem. Mater. 1997, 9, 1437-1442.
12. Sukwattanasinitt, M.; Ijadi-Maghsoodi, S.; Barton, T. J. Polym. Prepr. (Am. Chem. Soc., Div. Polym. Chem.) 1995, 36(1), 497-498. Diaryl TCBDs are chemically and thermally stable. However, monoaryl TCBDs do not show either good chemical stability or good thermal stability. See Wu, X.; Jen, A. K.-Y. Polym. Prepr (Am. Chem. Soc., Div. Polym. Chem.) 1998, 39(2), 1091- 1092.
13. Sukwattanasinitt, M.; Ijadi-Maghsoodi, S.; Barton, T. J. Polym. Prepr. (Am. Chem. Soc., Div. Polym. Chem.) 1995, 36(1), 497-498. Diaryl TCBDs are chemically and thermally stable. However, monoaryl TCBDs do not show either good chemical stability or good thermal stability. See Wu, X.; Jen, A. K.-Y. Polym. Prepr (Am. Chem. Soc., Div. Polym. Chem.) 1998, 39(2), 1091-1092.
14. 21NS: C, 79.72: H, 6.39, Found: C, 79.57; H, 6.28.
15. 5: C, 73.17; H, 4.61, Found: C, 73.41; H, 4.83.
16. Moylan, C. R.; Twieg, R. J.; Lee, V. Y.; Swanson, S. A.; Betterton, K. M.; Miller, R. D. J. Am. Chem. Soc. 1993, 115, 12599-12600.