Molecular Engineering of Stilbazolium Derivatives for Second-Order Nonlinear Optics
Source abstract
Abstract
Three series of ionic stilbazolium salts with different counteranions have been synthesized to investigate the effect of counteranion size to crystal packing. Single crystals of five new salts were successfully grown from solution by the slow cooling and slow evaporation techniques. X-ray studies revealed that three of them show the triclinic space group P 1 and two crystallize in the monoclinic space group Cc and P 2 1 / c, respectively. Kurtz powder tests revealed that out of the eight new stilbazolium salts, six possess noncentrosymmetric structures and three show large powder second-harmonic generation efficiencies higher or similar to that of 4- N, N -dimethylamino-4‘- N ‘-methyl-stilbazolium tosylate (DAST). The optimal crystalline packing for electro-optics with perfectly aligned chromophores was achieved in three of the investigated compounds. The reasons for considerably different macroscopic nonlinearities of these compounds have been explored in terms of intermolecular interactions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nonlinear Optical Materials Research · Photorefractive and Nonlinear Optics · Crystal Structures and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Nonlinear Optics Laboratory, Institute of Quantum Electronics, and Laboratory of Crystallography, ETH Hönggerberg, CH-8093 Zürich, Switzerland
References (33)
Show source-provided references
1. Bosshard · 2000
2. Molecular Nonlinear Optics · 1994
3. Nalwa H. S. · 1997
4. Meredith G. · 1983 · 56
5. Coe B. J. · Adv. Funct. Mater. · 2003 · 13 · 34710.1002/adfm.200300026 ↗
6. Nicoud, J. F.; Twieg, R. J.Nonlinear Optical Properties of OrganicMolecules and Crystals; Chemla, D. S., Zyss, J., Eds.; Academic Press, Orlando, FL, 1987; Vol. 1, pp 227−296.10.1016/B978-0-12-170611-1.50008-5 ↗
7. Li D. · J. Am. Chem. Soc. · 1990 · 112 · 738910.1021/ja00176a045 ↗
8. Hochberg M. · Nat. Mater. · 2006 · 5 · 70910.1038/nmat1719 ↗
9. Cheng Y. J. · Chem. Mater. · 2007 · 19 · 115410.1021/cm062340a ↗
10. Kim T. D. · J. Am. Chem. Soc. · 2007 · 129 · 48810.1021/ja067970s ↗
11. Nemoto N. · J. Mater. Chem. · 1997 · 7 · 138910.1039/a701214d ↗
12. Marder S. R. · Chem. Mater. · 1994 · 6 · 113710.1021/cm00044a012 ↗
13. Kwon O. P. · Chem. Mater. · 2006 · 18 · 404910.1021/cm0610130 ↗
14. Marder S. R. · Science · 1989 · 245 · 62610.1126/science.245.4918.626 ↗
15. Pan F. · Adv. Mater. · 1996 · 8 · 59210.1002/adma.19960080714 ↗
16. Geis W. · Appl. Phys. Lett. · 2004 · 84 · 3731
17. Cai B. · Jpn. J. Appl. Phys. · 2004 · 43 · L39010.1143/JJAP.43.L390 ↗
18. Pan F. · Appl. Phys. Lett. · 1999 · 74 · 49210.1063/1.123956 ↗
19. Adachi H. · Jpn. J. Appl. Phys. · 2004 · 43 · L112110.1143/JJAP.43.L1121 ↗
20. Schneider A. · Appl. Phys. Lett. · 2004 · 84 · 2231
21. Thakur M. · Opt. Eng. · 2003 · 42 · 45610.1117/1.1532334 ↗
22. Hosokawa Y. · Cryst. Growth Des. · 2005 · 5 · 86110.1021/cg049709y ↗
23. Wong M. S. · J. Opt. Soc. Am. · 1998 · 15 · 42610.1364/JOSAB.15.000426 ↗
24. Okada S. · Jpn. J. Appl. Phys. · 2003 · 42 · 66810.1143/JJAP.42.668 ↗
25. Yang Z. · Adv. Funct. Mater. · 2005 · 15 · 107210.1002/adfm.200500036 ↗
26. Yang, Z.; Mutter, L.; Ruiz, B.; Aravazhi, S.; Stillhart, M.; Jazbinsek, M.; Gramlich, V.; Günter, P.Adv. Funct. Mater.2007, in press.
27. Ruiz B. · J. Mater. Chem. · 2006 · 16 · 283910.1039/B603049A ↗
28. Kurtz S. K. · J. Appl. Phys. · 1968 · 39 · 379810.1063/1.1656857 ↗
29. Manetta S. · Phys. · 2002 · 3 · 449
30. Bosshard · 1995
31. Kwon O. P. · Cryst. Growth Des. · 2006 · 6 · 232710.1021/cg060293t ↗
32. Zyss J. · Phys. Rev. A · 1982 · 26 · 202810.1103/PhysRevA.26.2028 ↗
33. Bosshard · J. Opt. Soc. Am. B · 2001 · 18 · 162010.1364/JOSAB.18.001620 ↗