Please wait a minute...
Frontiers of Chemistry in China

ISSN 1673-3495

ISSN 1673-3614(Online)

CN 11-5726/O6

Front. Chem. China    2010, Vol. 5 Issue (2) : 221-225    https://doi.org/10.1007/s11458-010-0112-x
Research articles
Two-photon absorption of photochromic diarylethene and its application to rewritable holographic recording
Huanhuan LIU1,Yi CHEN1,Baoli YAO2,
1.Laboratory of Organic Optoelectronic Functional Materials and Molecular Engineering, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100080, China; 2.State Key Laboratory of Transient Optics Technology, Xi’an Institute of Optics and Precision Mechanics, Chinese Academy of Sciences, Xi’an 710068, China;
 Download: PDF(238 KB)  
 Export: BibTeX | EndNote | Reference Manager | ProCite | RefWorks
Abstract A new photochromic diarylethene (1a) has been prepared. Both its photochromic behavior and nonlinear optical properties are investigated. 1a shows excellent ring-opening (lmax = 386 nm) and ring-closing (lmax = 652 nm) photoisomerization with UV-Vis light irradiation. With 800 nm femtosecond pulsed laser irradiation, 1a shows two-photon-induced photoisomerization, and a two-photon absorption cross-section (s = 423×1050 cm4·s per photon) is obtained by using two-photon induced fluorescence method. The applications of two-photon absorption of 1a to holographic recording has been also investigated. A two-photon induced micro-pattern is recorded on the diarylethene 1a-PMMA film with an femtosecond laser of 800 nm, 100 fs, 1 kHz, 50 mW.
Keywords diarylethene      photoisomerization      two-photon absorption      holographic recording      rewritablity      
Issue Date: 05 June 2010
 Cite this article:   
Huanhuan LIU,Yi CHEN,Baoli YAO. Two-photon absorption of photochromic diarylethene and its application to rewritable holographic recording[J]. Front. Chem. China, 2010, 5(2): 221-225.
 URL:  
https://academic.hep.com.cn/fcc/EN/10.1007/s11458-010-0112-x
https://academic.hep.com.cn/fcc/EN/Y2010/V5/I2/221
Haw, M.,Nature2003, 422, 556―558

doi: 10.1038/422556a
Huang, G. T., Technol. Rev. 2005, 108, 64―67
Ashley, J.; Bernal, M. P.; Burr, G. W.; Coufal, H.; Guenther, H.; Hoffnagle, J. A.; Jefferson, C. M.; Marcus, B.; et al, IBM J. Res. Develop. 2000, 44, 341―368

doi: 10.1147/rd.443.0341
Hesselink, L.; Orlov, S. S.; Bashaw, M. C., Proc. IEEE2004, 92, 1231―1280

doi: 10.1109/JPROC.2004.831212
Zilker, S. J.,ChemPhysChem2002, 3, 333―334

doi: 10.1002/1439-7641(20020415)3:4<333::AID-CPHC333>3.0.CO;2-W
Wilson, W. L.; Curtis, K.; Tackitt, M.; Hill, A.; Hale, A.; Schilling, M.; Boyd, C.; Campbell, S.; et al, Opt. Quantum Electron. 2000, 32, 393―404

doi: 10.1023/A:1007052522730
Eich, M.; Wendorff, J. H.; Reck, B.; Ringsdorf, H., Makromol. Chem., Rapid. Commun. 1987, 8, 59―63

doi: 10.1002/marc.1987.030080111
Natansohn, A.; Rochon, P., Chem. Rev. 2002, 102, 4139―4176

doi: 10.1021/cr970155y
Imlau, M.; Bieringer, T.; Odoulov, S. G.; Weinheim, T., Germany2003, Ch. 27
Häckel, M.; Kador, L.; Kropp, D.; Schmidt, H. W., Adv. Mater. 2007, 19, 227―231

doi: 10.1002/adma.200601458
Crano, J. C.; Gugliehmetti, R.J., Organic Photochromic and Thermochromic Compounds; Plenum Press: New York, 1999.
Durr, H.; Bouas-Laurent, H., Photochromism:Molecules and Systems; Elsvier: Amsterdam, 1990
Irie, M., Chem. Rev. 2000, 100, 1683―1684

doi: 10.1021/cr980068l
Feringa, B. L., Molecules Switches; Wiley-VCH: New York, 2001

doi: 10.1002/3527600329
Tian, H.; Yang, S., Chem. Soc. Rev. 2004, 33, 85―97

doi: 10.1039/b302356g
Sud, D.; Norsten, T. B.; Branda, N. R., Angew. Chem. Int. Ed. 2005, 44, 2019―2021

doi: 10.1002/anie.200462538
Kawata, S.; Kawata, Y., Chem. Rev. 2000, 100, 1777―1788

doi: 10.1021/cr980073p
Belfield, K. D.; Liu, Y.; Negres, R. A.; Fan, M.; Pan, G.; Hagan, D. J.; Hernandez, F. E., Chem. Mater. 2002, 14, 3663―3667

doi: 10.1021/cm0107981
Corredor, C. C.; Huang, Z. L.; Belfield, K. D., Adv. Mater. 2006, 18, 2910―2914

doi: 10.1002/adma.200600826
Tian, H.; Feng, Y., J. Mater. Chem. 2008, 18, 1617―1622

doi: 10.1039/b713216f
Feng, Y.; Yan, Y.; Wang, S.; Zhu, W.; Qian, S.; Tian, H., J. Mater. Chem. 2006, 16, 3685―3692

doi: 10.1039/b608545h
Chen, Y.; Zeng, D. X.; Fan, M. G., Org. Lett. 2003, 5, 1435―1437

doi: 10.1021/ol034166r
Irie, M.; Sayo, K., J. Phys. Chem. 1992, 96, 7671―7674

doi: 10.1021/j100198a035
Lucas, L. N.; van Esch, J.; Kellogg, R. M.; Feringa, B. L., Chem. Commun. 1998, 2313―2314

doi: 10.1039/a806998k
Chen, Y.; Xie, N., J. Mater. Chem. 2005, 15, 3229―3232

doi: 10.1039/b506381g
Xie, N.; Zeng, D. X.; Chen, Y., Synlett2006, 5, 737―740
Liu, H. H.; Chen, Y., J. Mater. Chem. 2009, 19, 706―709

doi: 10.1039/b812843j
[1] Hui LI, Shouzhi PU, Gang LIU, Weijun LIU, Baoli YAO, . Polarization holographic optical recording based on a new photochromic diarylethene compound[J]. Front. Chem. China, 2010, 5(2): 234-240.
[2] YIN Jinghua, LIAN Huiqin, ZHAO Jiyang, WU Xue, ZHOU Ziyan. Photochromic reactions of 6-hydroxy-5,12-naphthacenequinone and its derivatives bearing methyl or phenyl groups[J]. Front. Chem. China, 2008, 3(4): 400-405.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed