메뉴 건너뛰기




Volumn 2009, Issue , 2009, Pages

Functional dyes, and some hi-tech applications

Author keywords

[No Author keywords available]

Indexed keywords

DYE-SENSITIZED SOLAR CELLS; MEDICAL APPLICATIONS;

EID: 73449101085     PISSN: 1110662X     EISSN: 1110662X     Source Type: Journal    
DOI: 10.1155/2009/434897     Document Type: Review
Times cited : (63)

References (147)
  • 2
    • 0028767567 scopus 로고
    • Revealing the blueprint of photosynthesis
    • Barber J., Andersson B., Revealing the blueprint of photosynthesis Nature 1994 370 6484 31 34
    • (1994) Nature , vol.370 , Issue.6484 , pp. 31-34
    • Barber, J.1    Andersson, B.2
  • 5
    • 0000253223 scopus 로고    scopus 로고
    • Photosynthetic light-harvesting pigment-protein complexes. Toward understanding how and why
    • Pullerits T., Sundstrm V., Photosynthetic light-harvesting pigment-protein complexes. Toward understanding how and why Accounts of Chemical Research 1996 29 8 381 389
    • (1996) Accounts of Chemical Research , vol.29 , Issue.8 , pp. 381-389
    • Pullerits, T.1    Sundstrm, V.2
  • 6
    • 0037066256 scopus 로고    scopus 로고
    • The quantum physics of photosynthesis
    • Ritz T., Damjanovi A., Schulten K., The quantum physics of photosynthesis ChemPhysChem 2002 3 3 243 248
    • (2002) ChemPhysChem , vol.3 , Issue.3 , pp. 243-248
    • Ritz, T.1    Damjanovi, A.2    Schulten, K.3
  • 7
    • 0035276506 scopus 로고    scopus 로고
    • Third generation photovoltaics: Ultra-high conversion efficiency at low cost
    • Green M. A., Third generation photovoltaics: ultra-high conversion efficiency at low cost Progress in Photovoltaics 2001 9 2 123 135
    • (2001) Progress in Photovoltaics , vol.9 , Issue.2 , pp. 123-135
    • Green, M.A.1
  • 8
    • 0006483573 scopus 로고
    • A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films
    • ORegan B., Grtzel M., A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films Nature 1991 353 6346 737 740
    • (1991) Nature , vol.353 , Issue.6346 , pp. 737-740
    • Oregan, B.1    Grtzel, M.2
  • 9
    • 0038010936 scopus 로고    scopus 로고
    • Perspectives for dye-sensitized nanocrystalline solar cells
    • Grtzel M., Perspectives for dye-sensitized nanocrystalline solar cells Progress in Photovoltaics 2000 8 1 171 185
    • (2000) Progress in Photovoltaics , vol.8 , Issue.1 , pp. 171-185
    • Grtzel, M.1
  • 10
    • 0035891138 scopus 로고    scopus 로고
    • Photoelectrochemical cells
    • Grtzel M., Photoelectrochemical cells Nature 2001 414 6861 338 344
    • (2001) Nature , vol.414 , Issue.6861 , pp. 338-344
    • Grtzel, M.1
  • 12
    • 33744543607 scopus 로고    scopus 로고
    • A review on mass transport in dye-sensitized nanocrystalline solar cells
    • Kalaignan G. P., Kang Y. S., A review on mass transport in dye-sensitized nanocrystalline solar cells Journal of Photochemistry and Photobiology C 2006 7 1 17 22
    • (2006) Journal of Photochemistry and Photobiology C , vol.7 , Issue.1 , pp. 17-22
    • Kalaignan, G.P.1    Kang, Y.S.2
  • 14
    • 28844470918 scopus 로고    scopus 로고
    • Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers
    • Nazeeruddin M. K., De Angelis F., Fantacci S., Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers Journal of the American Chemical Society 2005 127 48 16835 16847
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.48 , pp. 16835-16847
    • Nazeeruddin, M.K.1    De Angelis, F.2    Fantacci, S.3
  • 15
    • 0035961489 scopus 로고    scopus 로고
    • Engineering of efficient panchromatic sensitizers for nanocrystalline TiO2 -based solar cells
    • Nazeeruddin M. K., Pchy P., Renouard T., Engineering of efficient panchromatic sensitizers for nanocrystalline TiO2 -based solar cells Journal of the American Chemical Society 2001 123 8 1613 1624
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.8 , pp. 1613-1624
    • Nazeeruddin, M.K.1    Pchy, P.2    Renouard, T.3
  • 17
    • 0037448507 scopus 로고    scopus 로고
    • Molecular design of coumarin dyes for efficient dye-sensitized solar cells
    • Hara K., Sato T., Katoh R., Molecular design of coumarin dyes for efficient dye-sensitized solar cells Journal of Physical Chemistry B 2003 107 2 597 606
    • (2003) Journal of Physical Chemistry B , vol.107 , Issue.2 , pp. 597-606
    • Hara, K.1    Sato, T.2    Katoh, R.3
  • 18
    • 0034617039 scopus 로고    scopus 로고
    • Photosensitization of a porous TiO2 electrode with merocyanine dyes containing a carboxyl group and a long alkyl chain
    • Sayama K., Hara K., Mori N., Photosensitization of a porous TiO2 electrode with merocyanine dyes containing a carboxyl group and a long alkyl chain Chemical Communications 2000 13 1173 1174
    • (2000) Chemical Communications , Issue.13 , pp. 1173-1174
    • Sayama, K.1    Hara, K.2    Mori, N.3
  • 19
    • 0035909729 scopus 로고    scopus 로고
    • Spectral sensitization of TiO2 nanocrystalline electrodes with aggregated cyanine dyes
    • Ehret A., Stuhl L., Spitler M. T., Spectral sensitization of TiO2 nanocrystalline electrodes with aggregated cyanine dyes Journal of Physical Chemistry B 2001 105 41 9960 9965
    • (2001) Journal of Physical Chemistry B , vol.105 , Issue.41 , pp. 9960-9965
    • Ehret, A.1    Stuhl, L.2    Spitler, M.T.3
  • 20
    • 4644298314 scopus 로고    scopus 로고
    • High efficiency of dye-sensitized solar cells based on metal-free indoline dyes
    • Horiuchi T., Miura H., Sumioka K., Uchida S., High efficiency of dye-sensitized solar cells based on metal-free indoline dyes Journal of the American Chemical Society 2004 126 39 12218 12219
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.39 , pp. 12218-12219
    • Horiuchi, T.1    Miura, H.2    Sumioka, K.3    Uchida, S.4
  • 21
    • 0034699940 scopus 로고    scopus 로고
    • Highly efficient sensitization of nanocrystalline TiO2 films with styryl benzothiazolium propylsalfonate
    • Wang Z.-S., Li F.-U., Huang C.-H., Highly efficient sensitization of nanocrystalline TiO2 films with styryl benzothiazolium propylsalfonate Chemical Communications 2000 20 2063 2064
    • (2000) Chemical Communications , Issue.20 , pp. 2063-2064
    • Wang, Z.-S.1    Li, F.-U.2    Huang, C.-H.3
  • 22
    • 34047244966 scopus 로고    scopus 로고
    • New triphenylamine-based organic dyes for efficient dye-sensitized solar cells
    • Liang M., Xu W., Cai F., New triphenylamine-based organic dyes for efficient dye-sensitized solar cells Journal of Physical Chemistry C 2007 111 11 4465 4472
    • (2007) Journal of Physical Chemistry C , vol.111 , Issue.11 , pp. 4465-4472
    • Liang, M.1    Xu, W.2    Cai, F.3
  • 23
    • 19544383985 scopus 로고    scopus 로고
    • Organic dyes incorporating low-band-gap chromophores for dye-sensitized solar cells
    • Velusamy M., Thomas K. R. J., Lin J. T., Hsu Y.-C., Ho K.-C., Organic dyes incorporating low-band-gap chromophores for dye-sensitized solar cells Organic Letters 2005 7 10 1899 1902
    • (2005) Organic Letters , vol.7 , Issue.10 , pp. 1899-1902
    • Velusamy, M.1    Thomas, K.R.J.2    Lin, J.T.3    Hsu, Y.-C.4    Ho, K.-C.5
  • 24
    • 38149073109 scopus 로고    scopus 로고
    • Organic dyes containing 1 H -phenanthro[9,10- d ]imidazole conjugation for solar cells
    • Tsai M.-S., Hsu Y.-C., Lin J. T., Chen H.-C., Hsu C.-P., Organic dyes containing 1 H -phenanthro[9,10- d ]imidazole conjugation for solar cells Journal of Physical Chemistry C 2007 111 50 18785 18793
    • (2007) Journal of Physical Chemistry C , vol.111 , Issue.50 , pp. 18785-18793
    • Tsai, M.-S.1    Hsu, Y.-C.2    Lin, J.T.3    Chen, H.-C.4    Hsu, C.-P.5
  • 25
    • 42449147149 scopus 로고    scopus 로고
    • 2,3-disubstituted thiophene-based organic dyes for solar cells
    • Thomas K. R. J., Hsu Y.-C., Lin J. T., 2,3-disubstituted thiophene-based organic dyes for solar cells Chemistry of Materials 2008 20 5 1830 1840
    • (2008) Chemistry of Materials , vol.20 , Issue.5 , pp. 1830-1840
    • Thomas, K.R.J.1    Hsu, Y.-C.2    Lin, J.T.3
  • 27
    • 33845932597 scopus 로고    scopus 로고
    • Molecular engineering of organic sensitizers for solar cell applications
    • Kim S., Lee J. K., Kang S. O., Molecular engineering of organic sensitizers for solar cell applications Journal of the American Chemical Society 2006 128 51 16701 16707
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.51 , pp. 16701-16707
    • Kim, S.1    Lee, J.K.2    Kang, S.O.3
  • 28
    • 33847792872 scopus 로고    scopus 로고
    • Novel organic dyes containing bis-dimethylfluorenyl amino benzo[b]thiophene for highly efficient dye-sensitized solar cell
    • DOI 10.1016/j.tet.2007.02.018, PII S0040402007002177
    • Choi H., Lee J. K., Song K., Kang S. O., Ko J., Novel organic dyes containing bis-dimethylfluorenyl amino benzo[b]thiophene for highly efficient dye-sensitized solar cell Tetrahedron 2007 63 15 3115 3121 (Pubitemid 46389385)
    • (2007) Tetrahedron , vol.63 , Issue.15 , pp. 3115-3121
    • Choi, H.1    Lee, J.K.2    Song, K.3    Kang, S.O.4    Ko, J.5
  • 29
  • 30
    • 34249029361 scopus 로고    scopus 로고
    • Tetrahydroquinoline dyes with different spacers for organic dye-sensitized solar cells
    • Chen R., Yang X., Tian H., Sun L., Tetrahydroquinoline dyes with different spacers for organic dye-sensitized solar cells Journal of Photochemistry and Photobiology A 2007 189 2-3 295 300
    • (2007) Journal of Photochemistry and Photobiology A , vol.189 , Issue.23 , pp. 295-300
    • Chen, R.1    Yang, X.2    Tian, H.3    Sun, L.4
  • 33
    • 25144444335 scopus 로고    scopus 로고
    • Metal-assembling dendrimers with a triarylamine core and their application to a dye-sensitized solar cell
    • Satoh N., Nakashima T., Yamamoto K., Metal-assembling dendrimers with a triarylamine core and their application to a dye-sensitized solar cell Journal of the American Chemical Society 2005 127 37 13030 13038
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.37 , pp. 13030-13038
    • Satoh, N.1    Nakashima, T.2    Yamamoto, K.3
  • 34
    • 0037438661 scopus 로고    scopus 로고
    • Control of charge recombination dynamics in dye sensitized solar cells by the use of conformally deposited metal oxide blocking layers
    • Palomares E., Clifford J. N., Haque S. A., Lutz T., Durrant J. R., Control of charge recombination dynamics in dye sensitized solar cells by the use of conformally deposited metal oxide blocking layers Journal of the American Chemical Society 2003 125 2 475 482
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.2 , pp. 475-482
    • Palomares, E.1    Clifford, J.N.2    Haque, S.A.3    Lutz, T.4    Durrant, J.R.5
  • 35
    • 0038518668 scopus 로고    scopus 로고
    • Long-lived photoinduced charge separation and redox-type photochromism on mesoporous oxide films sensitized by molecular dyads
    • Bonhte P., Moser J.-E., Humphry-Baker R., Long-lived photoinduced charge separation and redox-type photochromism on mesoporous oxide films sensitized by molecular dyads Journal of the American Chemical Society 1999 121 6 1324 1336
    • (1999) Journal of the American Chemical Society , vol.121 , Issue.6 , pp. 1324-1336
    • Bonhte, P.1    Moser, J.-E.2    Humphry-Baker, R.3
  • 36
    • 0036263709 scopus 로고    scopus 로고
    • Molecular control of recombination dynamics in dye sensitised nanocrystalline TiO2 films
    • Clifford J. N., Yahioglu G., Milgrom L. R., Durrant J. R., Molecular control of recombination dynamics in dye sensitised nanocrystalline TiO2 films Chemical Communications 2002 126 12 1260 1261
    • (2002) Chemical Communications , vol.126 , Issue.12 , pp. 1260-1261
    • Clifford, J.N.1    Yahioglu, G.2    Milgrom, L.R.3    Durrant, J.R.4
  • 37
    • 24944514649 scopus 로고    scopus 로고
    • Supermolecular control of charge transfer in dye-sensitized nanocrystalline TiO2 films: Towards a quantitative structure-function relationship
    • Haque S. A., Handa S., Peter K., Palomares E., Thelakkat M., Durrant J. R., Supermolecular control of charge transfer in dye-sensitized nanocrystalline TiO2 films: towards a quantitative structure-function relationship Angewandte Chemie International Edition 2005 44 35 5740 5744
    • (2005) Angewandte Chemie International Edition , vol.44 , Issue.35 , pp. 5740-5744
    • Haque, S.A.1    Handa, S.2    Peter, K.3    Palomares, E.4    Thelakkat, M.5    Durrant, J.R.6
  • 38
    • 58249110382 scopus 로고    scopus 로고
    • Triphenylamine-based dyes for dye-sensitized solar cells
    • Zhang F., Luo Y., Song J., Triphenylamine-based dyes for dye-sensitized solar cells Dyes and Pigments 2009 81 3 224 230
    • (2009) Dyes and Pigments , vol.81 , Issue.3 , pp. 224-230
    • Zhang, F.1    Luo, Y.2    Song, J.3
  • 41
    • 58049202097 scopus 로고    scopus 로고
    • Organic dyes with a novel anchoring group for dye-sensitized solar cell applications
    • Baik C., Kim D., Kang M.-S., Organic dyes with a novel anchoring group for dye-sensitized solar cell applications Journal of Photochemistry and Photobiology A 2009 201 2-3 168 174
    • (2009) Journal of Photochemistry and Photobiology A , vol.201 , Issue.23 , pp. 168-174
    • Baik, C.1    Kim, D.2    Kang, M.-S.3
  • 42
    • 43449137882 scopus 로고    scopus 로고
    • Starburst triarylamine based dyes for efficient dye-sensitized solar cells
    • Ning Z., Zhang Q., Wu W., Pei H., Liu B., Tian H., Starburst triarylamine based dyes for efficient dye-sensitized solar cells Journal of Organic Chemistry 2008 73 10 3791 3797
    • (2008) Journal of Organic Chemistry , vol.73 , Issue.10 , pp. 3791-3797
    • Ning, Z.1    Zhang, Q.2    Wu, W.3    Pei, H.4    Liu, B.5    Tian, H.6
  • 43
    • 33845932597 scopus 로고    scopus 로고
    • Molecular engineering of organic sensitizers for solar cell applications
    • Kim S., Lee J. K., Kang S. O., Molecular engineering of organic sensitizers for solar cell applications Journal of the American Chemical Society 2006 128 51 16701 16707
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.51 , pp. 16701-16707
    • Kim, S.1    Lee, J.K.2    Kang, S.O.3
  • 45
    • 59649086022 scopus 로고    scopus 로고
    • Organic dyes containing furan moiety for high-performance dye-sensitized solar cells
    • Lin J. T., Chen P.-C., Yen Y.-S., Hsu Y.-C., Chou H.-H., Yeh M.-C. P., Organic dyes containing furan moiety for high-performance dye-sensitized solar cells Organic Letters 2009 11 1 97 100
    • (2009) Organic Letters , vol.11 , Issue.1 , pp. 97-100
    • Lin, J.T.1    Chen, P.-C.2    Yen, Y.-S.3    Hsu, Y.-C.4    Chou, H.-H.5    Yeh, M.-C.P.6
  • 46
    • 60849133342 scopus 로고    scopus 로고
    • Novel zinc porphyrin sensitizers for dye-sensitized solar cells: Synthesis and spectral, electrochemical, and photovoltaic properties
    • Lee C.-W., Lu H.-P., Lan C.-M., Novel zinc porphyrin sensitizers for dye-sensitized solar cells: synthesis and spectral, electrochemical, and photovoltaic properties ChemistryA European Journal 2009 15 6 1403 1412
    • (2009) ChemistryA European Journal , vol.15 , Issue.6 , pp. 1403-1412
    • Lee, C.-W.1    Lu, H.-P.2    Lan, C.-M.3
  • 47
    • 50249132449 scopus 로고    scopus 로고
    • Red Sicilian orange and purple eggplant fruits as natural sensitizers for dye-sensitized solar cells
    • Calogero G., Di Marco G., Red Sicilian orange and purple eggplant fruits as natural sensitizers for dye-sensitized solar cells Solar Energy Materials and Solar Cells 2008 92 11 1341 1346
    • (2008) Solar Energy Materials and Solar Cells , vol.92 , Issue.11 , pp. 1341-1346
    • Calogero, G.1    Di Marco, G.2
  • 48
    • 0031556680 scopus 로고    scopus 로고
    • Ultrafast electron injection: Implications for a photoelectrochemical cell utilizing an anthocyanin dye-sensitized TiO2 nanocrystalline electrode
    • Cherepy N. J., Smestad G. P., Grtzel M., Zhang J. Z., Ultrafast electron injection: implications for a photoelectrochemical cell utilizing an anthocyanin dye-sensitized TiO2 nanocrystalline electrode Journal of Physical Chemistry B 1997 101 45 9342 9351
    • (1997) Journal of Physical Chemistry B , vol.101 , Issue.45 , pp. 9342-9351
    • Cherepy, N.J.1    Smestad, G.P.2    Grtzel, M.3    Zhang, J.Z.4
  • 50
    • 42149130273 scopus 로고    scopus 로고
    • Photochromic soft materials: Flavylium compounds incorporated into pluronic F-127 hydrogel matrixes
    • Pina F., Hatton T. A., Photochromic soft materials: flavylium compounds incorporated into pluronic F-127 hydrogel matrixes Langmuir 2008 24 6 2356 2364
    • (2008) Langmuir , vol.24 , Issue.6 , pp. 2356-2364
    • Pina, F.1    Hatton, T.A.2
  • 52
    • 0037028943 scopus 로고    scopus 로고
    • Multichannel digital transmission in an optical network of communicating molecules
    • Raymo F. M., Giordani S., Multichannel digital transmission in an optical network of communicating molecules Journal of the American Chemical Society 2002 124 9 2004 2007
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.9 , pp. 2004-2007
    • Raymo, F.M.1    Giordani, S.2
  • 53
    • 1642393147 scopus 로고    scopus 로고
    • Recent progresses on diarylethene based photochromic switches
    • Tian H., Yang S., Recent progresses on diarylethene based photochromic switches Chemical Society Reviews 2004 33 2 85 97
    • (2004) Chemical Society Reviews , vol.33 , Issue.2 , pp. 85-97
    • Tian, H.1    Yang, S.2
  • 54
    • 33847028286 scopus 로고    scopus 로고
    • Photochromic bisthienylethene as multi-function switches
    • Tian H., Wang S., Photochromic bisthienylethene as multi-function switches Chemical Communications 2007 8 781 792
    • (2007) Chemical Communications , Issue.8 , pp. 781-792
    • Tian, H.1    Wang, S.2
  • 55
    • 0348080703 scopus 로고    scopus 로고
    • Diarylethenes for memories and switches
    • Irie M., Diarylethenes for memories and switches Chemical Reviews 2000 100 5 1685 1716
    • (2000) Chemical Reviews , vol.100 , Issue.5 , pp. 1685-1716
    • Irie, M.1
  • 58
    • 0038813768 scopus 로고    scopus 로고
    • A multi-addressable photochromic 1,2-dithienylcyclopentene- phenoxynaphthacene-quinone hybrid
    • Myles A. J., Wigglesworth T. J., Branda N. R., A multi-addressable photochromic 1,2-dithienylcyclopentene-phenoxynaphthacene-quinone hybrid Advanced Materials 2003 15 9 745 748
    • (2003) Advanced Materials , vol.15 , Issue.9 , pp. 745-748
    • Myles, A.J.1    Wigglesworth, T.J.2    Branda, N.R.3
  • 59
    • 33751051989 scopus 로고    scopus 로고
    • Two-photon 3D optical data storage via fluorescence modulation of an efficient fluorene dye by a photochromic diarylethene
    • Corredor C. C., Huang Z.-L., Belfield K. D., Two-photon 3D optical data storage via fluorescence modulation of an efficient fluorene dye by a photochromic diarylethene Advanced Materials 2006 18 21 2910 2914
    • (2006) Advanced Materials , vol.18 , Issue.21 , pp. 2910-2914
    • Corredor, C.C.1    Huang, Z.-L.2    Belfield, K.D.3
  • 60
    • 33751001768 scopus 로고    scopus 로고
    • Photochromic switching of excited-state intramolecular proton-transfer (ESIPT) fluorescence: A unique route to high-contrast memory switching and nondestructive readout
    • Lim S.-J., Seo J., Park S. Y., Photochromic switching of excited-state intramolecular proton-transfer (ESIPT) fluorescence: a unique route to high-contrast memory switching and nondestructive readout Journal of the American Chemical Society 2006 128 45 14542 14547
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.45 , pp. 14542-14547
    • Lim, S.-J.1    Seo, J.2    Park, S.Y.3
  • 61
    • 23744492737 scopus 로고    scopus 로고
    • Bistable photoswitching in the film of fluorescent photochromic polymer: Enhanced fluorescence emission and its high contrast switching
    • Lim S.-J., An B.-K., Park S. Y., Bistable photoswitching in the film of fluorescent photochromic polymer: enhanced fluorescence emission and its high contrast switching Macromolecules 2005 38 15 6236 6239
    • (2005) Macromolecules , vol.38 , Issue.15 , pp. 6236-6239
    • Lim, S.-J.1    An, B.-K.2    Park, S.Y.3
  • 62
    • 33644499464 scopus 로고    scopus 로고
    • Highly fluorescent contrast for rewritable optical storage based on photochromic bisthienylethene-bridged naphthalimide dimer
    • Jiang G., Wang S., Yuan W., Highly fluorescent contrast for rewritable optical storage based on photochromic bisthienylethene-bridged naphthalimide dimer Chemistry of Materials 2006 18 2 235 237
    • (2006) Chemistry of Materials , vol.18 , Issue.2 , pp. 235-237
    • Jiang, G.1    Wang, S.2    Yuan, W.3
  • 63
    • 0000872184 scopus 로고    scopus 로고
    • Spiropyrans and spirooxazines for memories and switches
    • Berkovic G., Krongauz V., Weiss V., Spiropyrans and spirooxazines for memories and switches Chemical Reviews 2000 100 5 1741 1753
    • (2000) Chemical Reviews , vol.100 , Issue.5 , pp. 1741-1753
    • Berkovic, G.1    Krongauz, V.2    Weiss, V.3
  • 64
    • 0035047107 scopus 로고    scopus 로고
    • Photoswitchable tetraethynylethene-dihydroazulene chromophores
    • Gobbi L., Seiler P., Diederich F., Photoswitchable tetraethynylethene- dihydroazulene chromophores Helvetica Chimica Acta 2001 84 4 743 777
    • (2001) Helvetica Chimica Acta , vol.84 , Issue.4 , pp. 743-777
    • Gobbi, L.1    Seiler, P.2    Diederich, F.3
  • 65
    • 0037139514 scopus 로고    scopus 로고
    • Ultrafast bidirectional dihydroazulene/vinylheptafulvene (DHA/VHF) molecular switches: Photochemical ring closure of vinylheptafulvene proven by a two-pulse experiment
    • De Waele V., Schmidhammer U., Mrozek T., Daub J., Riedle E., Ultrafast bidirectional dihydroazulene/vinylheptafulvene (DHA/VHF) molecular switches: photochemical ring closure of vinylheptafulvene proven by a two-pulse experiment Journal of the American Chemical Society 2002 124 11 2438 2439
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.11 , pp. 2438-2439
    • De Waele, V.1    Schmidhammer, U.2    Mrozek, T.3    Daub, J.4    Riedle, E.5
  • 68
    • 18244374178 scopus 로고    scopus 로고
    • A fast and stable photochromic switch based on the opening and closing of an oxazine ring
    • Tomasulo M., Sortino S., Raymo F. M., A fast and stable photochromic switch based on the opening and closing of an oxazine ring Organic Letters 2005 7 6 1109 1112
    • (2005) Organic Letters , vol.7 , Issue.6 , pp. 1109-1112
    • Tomasulo, M.1    Sortino, S.2    Raymo, F.M.3
  • 69
    • 0037058120 scopus 로고    scopus 로고
    • Photochromism of 2 H -naphtho[1,2- b ]pyrans: A spectroscopic investigation
    • Jockusch S., Turro N. J., Blackburn F. R., Photochromism of 2 H -naphtho[1,2- b ]pyrans: a spectroscopic investigation Journal of Physical Chemistry A 2002 106 40 9236 9241
    • (2002) Journal of Physical Chemistry A , vol.106 , Issue.40 , pp. 9236-9241
    • Jockusch, S.1    Turro, N.J.2    Blackburn, F.R.3
  • 70
    • 0036569584 scopus 로고    scopus 로고
    • Mechanistic insights into the photochromism of trans-10b, 10c-dimethyl-10b, 10c-dihydropyrene derivatives
    • Sheepwash M. A. L., Mitchell R. H., Bohne C., Mechanistic insights into the photochromism of trans-10b, 10c-dimethyl-10b, 10c-dihydropyrene derivatives Journal of the American Chemical Society 2002 124 17 4693 4700
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.17 , pp. 4693-4700
    • Sheepwash, M.A.L.1    Mitchell, R.H.2    Bohne, C.3
  • 71
    • 0001765706 scopus 로고    scopus 로고
    • Fulgides for memories and switches
    • Yokoyama Y., Fulgides for memories and switches Chemical Reviews 2000 100 5 1717 1739
    • (2000) Chemical Reviews , vol.100 , Issue.5 , pp. 1717-1739
    • Yokoyama, Y.1
  • 72
    • 53549115049 scopus 로고    scopus 로고
    • Digital information processing in molecular systems
    • Szaciowski K., Digital information processing in molecular systems Chemical Reviews 2008 108 9 3481 3548
    • (2008) Chemical Reviews , vol.108 , Issue.9 , pp. 3481-3548
    • Szaciowski, K.1
  • 73
    • 34250624466 scopus 로고    scopus 로고
    • Efficient synthesis and properties of isomeric photochromic diarylethenes having a pyrrole unit
    • Pu S., Liu G., Shen L., Xu J., Efficient synthesis and properties of isomeric photochromic diarylethenes having a pyrrole unit Organic Letters 2007 9 11 2139 2142
    • (2007) Organic Letters , vol.9 , Issue.11 , pp. 2139-2142
    • Pu, S.1    Liu, G.2    Shen, L.3    Xu, J.4
  • 74
    • 37249034580 scopus 로고    scopus 로고
    • Novel oxazabicycles as a new class of photochromic colorants
    • Yang D.-Y., Chen Y.-S., Kuo P.-Y., Novel oxazabicycles as a new class of photochromic colorants Organic Letters 2007 9 25 5287 5290
    • (2007) Organic Letters , vol.9 , Issue.25 , pp. 5287-5290
    • Yang, D.-Y.1    Chen, Y.-S.2    Kuo, P.-Y.3
  • 75
    • 58149168745 scopus 로고    scopus 로고
    • Synthesis and characterization of coumarin-based spiropyran photochromic colorants
    • Chen J.-R., Wong J.-B., Kuo P.-Y., Yang D.-Y., Synthesis and characterization of coumarin-based spiropyran photochromic colorants Organic Letters 2008 10 21 4823 4826
    • (2008) Organic Letters , vol.10 , Issue.21 , pp. 4823-4826
    • Chen, J.-R.1    Wong, J.-B.2    Kuo, P.-Y.3    Yang, D.-Y.4
  • 76
    • 0347318597 scopus 로고    scopus 로고
    • Three-dimensional optical data storage using photochromic materials
    • Kawata S., Kawata Y., Three-dimensional optical data storage using photochromic materials Chemical Reviews 2000 100 5 1777 1788
    • (2000) Chemical Reviews , vol.100 , Issue.5 , pp. 1777-1788
    • Kawata, S.1    Kawata, Y.2
  • 77
    • 14344282909 scopus 로고
    • Thermally irreversible photochromic systems. Reversible photocyclization of diarylethene derivatives
    • Irie M., Mohri M., Thermally irreversible photochromic systems. Reversible photocyclization of diarylethene derivatives Journal of Organic Chemistry 1988 53 4 803 808
    • (1988) Journal of Organic Chemistry , vol.53 , Issue.4 , pp. 803-808
    • Irie, M.1    Mohri, M.2
  • 78
    • 59649090897 scopus 로고    scopus 로고
    • Easy and efficient tuning of the photochromic properties of 1,2-bis[ 5′ -methyl- 2′ -(2 -pyridyl)thiazolyl]perfluorocyclopentene
    • Giraud M., Laustic A., Guillot R., Yu P., Maurel F., Nakatani K., Easy and efficient tuning of the photochromic properties of 1,2-bis[ 5′ -methyl- 2′ -(2 -pyridyl)thiazolyl]perfluorocyclopentene Tetrahedron Letters 2009 50 13 1485 1489
    • (2009) Tetrahedron Letters , vol.50 , Issue.13 , pp. 1485-1489
    • Giraud, M.1    Laustic, A.2    Guillot, R.3    Yu, P.4    Maurel, F.5    Nakatani, K.6
  • 79
    • 56949089713 scopus 로고    scopus 로고
    • The synthesis and photochromic properties of two bis(phosphine) ligands based on dithienylethene backbone and their oxides, sulfurets and selenides
    • Yin J., Lin Y., Cao X., Yu G.-A., Tu H., Liu S. H., The synthesis and photochromic properties of two bis(phosphine) ligands based on dithienylethene backbone and their oxides, sulfurets and selenides Dyes and Pigments 2009 81 2 152 155
    • (2009) Dyes and Pigments , vol.81 , Issue.2 , pp. 152-155
    • Yin, J.1    Lin, Y.2    Cao, X.3    Yu, G.-A.4    Tu, H.5    Liu, S.H.6
  • 80
    • 40549140828 scopus 로고    scopus 로고
    • Superior photochromic performance of naphthopyrans in a rigid host matrix using polymer conjugation: Fast, dark, and tunable
    • Malic N., Campbell J. A., Evans R. A., Superior photochromic performance of naphthopyrans in a rigid host matrix using polymer conjugation: fast, dark, and tunable Macromolecules 2008 41 4 1206 1214
    • (2008) Macromolecules , vol.41 , Issue.4 , pp. 1206-1214
    • Malic, N.1    Campbell, J.A.2    Evans, R.A.3
  • 81
    • 44649115346 scopus 로고    scopus 로고
    • Bistable photoswitching in poly(N-isopropylacrylamide) with spironaphthoxazine hydrogel for optical data storage
    • Wang S., Choi M.-S., Kim S.-H., Bistable photoswitching in poly(N-isopropylacrylamide) with spironaphthoxazine hydrogel for optical data storage Journal of Photochemistry and Photobiology A 2008 198 2-3 150 155
    • (2008) Journal of Photochemistry and Photobiology A , vol.198 , Issue.23 , pp. 150-155
    • Wang, S.1    Choi, M.-S.2    Kim, S.-H.3
  • 82
    • 57249088708 scopus 로고    scopus 로고
    • Direct coloration of textiles with photochromic dyespart 1: Application of spiroindolinonaphthoxazines as disperse dyes to polyester, nylon and acrylic fabrics
    • Billah S. M. R., Christie R. M., Shamey R., Direct coloration of textiles with photochromic dyespart 1: application of spiroindolinonaphthoxazines as disperse dyes to polyester, nylon and acrylic fabrics Coloration Technology 2008 124 4 223 228
    • (2008) Coloration Technology , vol.124 , Issue.4 , pp. 223-228
    • Billah, S.M.R.1    Christie, R.M.2    Shamey, R.3
  • 83
    • 57249097923 scopus 로고    scopus 로고
    • Direct coloration of textiles with photochromic dyespart 2: The effect of solvents on the colour change of photochromic textiles
    • Billah S. M. R., Christie R. M., Morgan K. M., Direct coloration of textiles with photochromic dyespart 2: the effect of solvents on the colour change of photochromic textiles Coloration Technology 2008 124 4 229 233
    • (2008) Coloration Technology , vol.124 , Issue.4 , pp. 229-233
    • Billah, S.M.R.1    Christie, R.M.2    Morgan, K.M.3
  • 84
    • 22544478743 scopus 로고    scopus 로고
    • Preliminary exhaustion studies of spiroxazine dyes on polyamide fibers and their photochromic properties
    • Lee S.-J., Son Y.-A., Suh H.-J., Lee D.-N., Kim S.-H., Preliminary exhaustion studies of spiroxazine dyes on polyamide fibers and their photochromic properties Dyes and Pigments 2006 69 1-2 18 21
    • (2006) Dyes and Pigments , vol.69 , Issue.12 , pp. 18-21
    • Lee, S.-J.1    Son, Y.-A.2    Suh, H.-J.3    Lee, D.-N.4    Kim, S.-H.5
  • 85
    • 33745488354 scopus 로고    scopus 로고
    • Exhaustion studies of spiroxazine dye having reactive anchor on polyamide fibers and its photochromic properties
    • Son Y.-A., Park Y.-M., Park S.-Y., Shin C.-J., Kim S.-H., Exhaustion studies of spiroxazine dye having reactive anchor on polyamide fibers and its photochromic properties Dyes and Pigments 2007 73 1 76 80
    • (2007) Dyes and Pigments , vol.73 , Issue.1 , pp. 76-80
    • Son, Y.-A.1    Park, Y.-M.2    Park, S.-Y.3    Shin, C.-J.4    Kim, S.-H.5
  • 86
    • 73449144527 scopus 로고    scopus 로고
    • Photochromic fabrics with improved durability and photochromic performance
    • Cheng T., Lin T., Brady R., Wang X., Photochromic fabrics with improved durability and photochromic performance Fibers and Polymers 2008 9 5 521 526
    • (2008) Fibers and Polymers , vol.9 , Issue.5 , pp. 521-526
    • Cheng, T.1    Lin, T.2    Brady, R.3    Wang, X.4
  • 90
    • 3042779537 scopus 로고    scopus 로고
    • Photodynamic therapy: A new antimicrobial approach to infectious disease?
    • Hamblin M. R., Hasan T., Photodynamic therapy: a new antimicrobial approach to infectious disease? Photochemical and Photobiological Sciences 2004 3 5 436 450
    • (2004) Photochemical and Photobiological Sciences , vol.3 , Issue.5 , pp. 436-450
    • Hamblin, M.R.1    Hasan, T.2
  • 91
    • 11244320460 scopus 로고    scopus 로고
    • Photodynamic therapy-from dyestuffs to high-tech clinical practice
    • Wainwright M., Photodynamic therapy-from dyestuffs to high-tech clinical practice Reverend Program Coloration 2004 34 95 109
    • (2004) Reverend Program Coloration , vol.34 , pp. 95-109
    • Wainwright, M.1
  • 92
  • 94
    • 0030823911 scopus 로고    scopus 로고
    • Implicit and explicit dosimetry in photodynamic therapy: A new paradigm
    • Wilson B. C., Patterson M. S., Lilge L., Implicit and explicit dosimetry in photodynamic therapy: a new paradigm Lasers in Medical Science 1997 12 3 182 199
    • (1997) Lasers in Medical Science , vol.12 , Issue.3 , pp. 182-199
    • Wilson, B.C.1    Patterson, M.S.2    Lilge, L.3
  • 95
    • 0035318612 scopus 로고    scopus 로고
    • A clearer vision for in vivo imaging
    • Weissleder R., A clearer vision for in vivo imaging Nature Biotechnology 2001 19 4 316 317
    • (2001) Nature Biotechnology , vol.19 , Issue.4 , pp. 316-317
    • Weissleder, R.1
  • 96
    • 0029912487 scopus 로고    scopus 로고
    • Light scattering of human skin: A comparison between zinc(II)- phthalocyanine and photofrin II
    • Ochsner M., Light scattering of human skin: a comparison between zinc(II)-phthalocyanine and photofrin II Journal of Photochemistry and Photobiology B 1996 32 1-2 3 9
    • (1996) Journal of Photochemistry and Photobiology B , vol.32 , Issue.12 , pp. 3-9
    • Ochsner, M.1
  • 97
    • 0017655857 scopus 로고
    • Measurements on the depth of penetration of light (0.35-1.0 m) in tissue
    • Eichler J., Knof J., Lenz H., Measurements on the depth of penetration of light (0.35-1.0 m) in tissue Radiation and Environmental Biophysics 1977 14 3 239 242
    • (1977) Radiation and Environmental Biophysics , vol.14 , Issue.3 , pp. 239-242
    • Eichler, J.1    Knof, J.2    Lenz, H.3
  • 98
    • 34249035446 scopus 로고    scopus 로고
    • Anterior eye tissue transmission for the radiation with the wavelength from eye safe region
    • Jelnkov H., Pata J., ulc J., Nmec M., Koranda P., Anterior eye tissue transmission for the radiation with the wavelength from eye safe region Laser Physics Letters 2005 2 12 603 607
    • (2005) Laser Physics Letters , vol.2 , Issue.12 , pp. 603-607
    • Jelnkov, H.1    Pata, J.2    Ulc, J.3    Nmec, M.4    Koranda, P.5
  • 100
    • 0033694993 scopus 로고    scopus 로고
    • Mechanisms of action of photodynamic therapy with verteporfin for the treatment of age-related macular degeneration
    • Schmidt-Erfurth U., Hasan T., Mechanisms of action of photodynamic therapy with verteporfin for the treatment of age-related macular degeneration Survey of Ophthalmology 2000 45 3 195 214
    • (2000) Survey of Ophthalmology , vol.45 , Issue.3 , pp. 195-214
    • Schmidt-Erfurth, U.1    Hasan, T.2
  • 101
    • 0028409859 scopus 로고
    • Photodynamic therapy with photofrin II induces programmed cell death in carcinoma cell lines
    • He X.-Y., Sikes R. A., Thomsen S., Chung L. W. K., Jacques S. L., Photodynamic therapy with photofrin II induces programmed cell death in carcinoma cell lines Photochemistry and Photobiology 1994 59 4 468 473
    • (1994) Photochemistry and Photobiology , vol.59 , Issue.4 , pp. 468-473
    • He, X.-Y.1    Sikes, R.A.2    Thomsen, S.3    Chung, L.W.K.4    Jacques, S.L.5
  • 103
    • 0030783698 scopus 로고    scopus 로고
    • Photodynamic therapy: The clinical perspective. Review on applications for control of diverse tumorous and non-tumorous diseases
    • Ochsner M., Photodynamic therapy: the clinical perspective. Review on applications for control of diverse tumorous and non-tumorous diseases Drug Research 1997 47 11 1185 1194
    • (1997) Drug Research , vol.47 , Issue.11 , pp. 1185-1194
    • Ochsner, M.1
  • 104
    • 60749125990 scopus 로고    scopus 로고
    • Synthesis of hydrophilic conjugated porphyrin dimers for one-photon and two-photon photodynamic therapy at NIR wavelengths
    • Balaz M., Collins H. A., Dahlstedt E., Anderson H. L., Synthesis of hydrophilic conjugated porphyrin dimers for one-photon and two-photon photodynamic therapy at NIR wavelengths Organic and Biomolecular Chemistry 2009 7 5 874 888
    • (2009) Organic and Biomolecular Chemistry , vol.7 , Issue.5 , pp. 874-888
    • Balaz, M.1    Collins, H.A.2    Dahlstedt, E.3    Anderson, H.L.4
  • 105
    • 0026268098 scopus 로고
    • Preclinical examination of first and second generation photosensitizers used in photodynamic therapy
    • Gomer C. J., Preclinical examination of first and second generation photosensitizers used in photodynamic therapy Photochemistry and Photobiology 1991 54 6 1093 1107
    • (1991) Photochemistry and Photobiology , vol.54 , Issue.6 , pp. 1093-1107
    • Gomer, C.J.1
  • 106
    • 0027563286 scopus 로고
    • Photophysical properties of 3, 3′ -dialkylthiacarbocyanine dyes in homogeneous solution
    • Krieg M., Redmond R. W., Photophysical properties of 3, 3′ -dialkylthiacarbocyanine dyes in homogeneous solution Photochemistry and Photobiology 1993 57 3 472 479
    • (1993) Photochemistry and Photobiology , vol.57 , Issue.3 , pp. 472-479
    • Krieg, M.1    Redmond, R.W.2
  • 107
    • 0028528701 scopus 로고
    • Merocyanine dyes: Effect of structural modifications on photophysical properties and biological activity
    • Redmond R. W., Srichai M. B., Bilitz J. M., Schlomer D. D., Krieg M., Merocyanine dyes: effect of structural modifications on photophysical properties and biological activity Photochemistry and Photobiology 1994 60 4 348 355
    • (1994) Photochemistry and Photobiology , vol.60 , Issue.4 , pp. 348-355
    • Redmond, R.W.1    Srichai, M.B.2    Bilitz, J.M.3    Schlomer, D.D.4    Krieg, M.5
  • 108
    • 0042080123 scopus 로고
    • Radiation chemistry of cyanine dyes: Oxidation and reduction of merocyanine 540
    • Harriman A., Shoute L. C. T., Neta P., Radiation chemistry of cyanine dyes: oxidation and reduction of merocyanine 540 Journal of Physical Chemistry 1991 95 6 2415 2420
    • (1991) Journal of Physical Chemistry , vol.95 , Issue.6 , pp. 2415-2420
    • Harriman, A.1    Shoute, L.C.T.2    Neta, P.3
  • 109
    • 0028208521 scopus 로고
    • Effects of structural modifications on the photosensitizing properties of dialkylcarbocyanine dyes in homogeneous and heterogeneous solutions
    • Krieg M., Bilitz J. M., Srichai M. B., Redmond R. W., Effects of structural modifications on the photosensitizing properties of dialkylcarbocyanine dyes in homogeneous and heterogeneous solutions Biochimica et Biophysica Acta 1994 1199 2 149 156
    • (1994) Biochimica et Biophysica Acta , vol.1199 , Issue.2 , pp. 149-156
    • Krieg, M.1    Bilitz, J.M.2    Srichai, M.B.3    Redmond, R.W.4
  • 110
    • 0026515028 scopus 로고
    • Structure-activity relationships in the antiviral and antileukemic photoproperties of merocyanine dyes
    • Gunther W. H. H., Searle R., Sieber F., Structure-activity relationships in the antiviral and antileukemic photoproperties of merocyanine dyes Seminars in Hematology 1992 29 2 88 94
    • (1992) Seminars in Hematology , vol.29 , Issue.2 , pp. 88-94
    • Gunther, W.H.H.1    Searle, R.2    Sieber, F.3
  • 111
    • 36448953479 scopus 로고    scopus 로고
    • Delocalized cationic azo dyes containing a thiazole moiety
    • Salvador M. A., Reis L. V., Almeida P., Santos P. F., Delocalized cationic azo dyes containing a thiazole moiety Tetrahedron 2008 64 2 299 303
    • (2008) Tetrahedron , vol.64 , Issue.2 , pp. 299-303
    • Salvador, M.A.1    Reis, L.V.2    Almeida, P.3    Santos, P.F.4
  • 113
    • 58249095964 scopus 로고    scopus 로고
    • The synthesis and characterization of novel, aza-substituted squarylium cyanine dyes
    • Reis L. V., Serrano J. P., Almeida P., Santos P. F., The synthesis and characterization of novel, aza-substituted squarylium cyanine dyes Dyes and Pigments 2009 81 3 197 202
    • (2009) Dyes and Pigments , vol.81 , Issue.3 , pp. 197-202
    • Reis, L.V.1    Serrano, J.P.2    Almeida, P.3    Santos, P.F.4
  • 114
    • 33947500247 scopus 로고    scopus 로고
    • Chemical tools for biomolecular imaging
    • Johnsson N., Johnsson K., Chemical tools for biomolecular imaging ACS Chemical Biology 2007 2 1 31 38
    • (2007) ACS Chemical Biology , vol.2 , Issue.1 , pp. 31-38
    • Johnsson, N.1    Johnsson, K.2
  • 115
    • 33744487875 scopus 로고    scopus 로고
    • Molecular imaging in cancer
    • Weissleder R., Molecular imaging in cancer Science 2006 312 5777 1168 1171
    • (2006) Science , vol.312 , Issue.5777 , pp. 1168-1171
    • Weissleder, R.1
  • 117
    • 23644444124 scopus 로고    scopus 로고
    • Luminescent sensors and switches in the early 21st century
    • Callan J. F., de Silva A. P., Magri D. C., Luminescent sensors and switches in the early 21st century Tetrahedron 2005 61 36 8551 8588
    • (2005) Tetrahedron , vol.61 , Issue.36 , pp. 8551-8588
    • Callan, J.F.1    De Silva, A.P.2    Magri, D.C.3
  • 119
    • 0031191655 scopus 로고    scopus 로고
    • Signaling recognition events with fluorescent sensors and switches
    • de Silva A. P., Gunaratne H. Q. N., Gunnlaugsson T., Signaling recognition events with fluorescent sensors and switches Chemical Reviews 1997 97 5 1515 1566
    • (1997) Chemical Reviews , vol.97 , Issue.5 , pp. 1515-1566
    • De Silva, A.P.1    Gunaratne, H.Q.N.2    Gunnlaugsson, T.3
  • 120
    • 0035498894 scopus 로고    scopus 로고
    • Radiative decay engineering: Biophysical and biomedical applications
    • Lakowicz J. R., Radiative decay engineering: biophysical and biomedical applications Analytical Biochemistry 2001 298 1 1 24
    • (2001) Analytical Biochemistry , vol.298 , Issue.1 , pp. 1-24
    • Lakowicz, J.R.1
  • 122
    • 0037458343 scopus 로고    scopus 로고
    • Complexation of alkali metal and alkaline earth ions by anthracene based fluorophores with one and two appended monoaza coronand receptors
    • Geue J. P., Head N. J., Ward A. D., Lincoln S. F., Complexation of alkali metal and alkaline earth ions by anthracene based fluorophores with one and two appended monoaza coronand receptors Journal of the Chemical Society. Dalton Transactions 2003 4 521 526
    • (2003) Journal of the Chemical Society. Dalton Transactions , Issue.4 , pp. 521-526
    • Geue, J.P.1    Head, N.J.2    Ward, A.D.3    Lincoln, S.F.4
  • 123
    • 0037054117 scopus 로고    scopus 로고
    • The synthesis of azacrown ethers with quinoline-based sidearms as potential zinc(II) fluorophores
    • Xue G., Bradshaw J. S., Dalley N. K., The synthesis of azacrown ethers with quinoline-based sidearms as potential zinc(II) fluorophores Tetrahedron 2002 58 24 4809 4815
    • (2002) Tetrahedron , vol.58 , Issue.24 , pp. 4809-4815
    • Xue, G.1    Bradshaw, J.S.2    Dalley, N.K.3
  • 124
    • 0344444370 scopus 로고    scopus 로고
    • Fluorescent PET chemosensor for cadmium Ions in 100 aqueous solution
    • Kim S. K., Lee J. H., Yoon J., Fluorescent PET chemosensor for cadmium Ions in 100 aqueous solution Bulletin of the Korean Chemical Society 2003 24 7 1032 1034
    • (2003) Bulletin of the Korean Chemical Society , vol.24 , Issue.7 , pp. 1032-1034
    • Kim, S.K.1    Lee, J.H.2    Yoon, J.3
  • 127
    • 0037877975 scopus 로고    scopus 로고
    • Single-molecule-sensitive fluorescent sensors based on photoinduced intramolecular charge transfer
    • Sauer M., Single-molecule-sensitive fluorescent sensors based on photoinduced intramolecular charge transfer Angewandte Chemie International Edition 2003 42 16 1790 1793
    • (2003) Angewandte Chemie International Edition , vol.42 , Issue.16 , pp. 1790-1793
    • Sauer, M.1
  • 129
    • 4043169759 scopus 로고    scopus 로고
    • Highly selective chromogenic signaling of Hg2+ in aqueous media at nanomolar levels employing a squaraine-based reporter
    • Ros-Lis J. V., Martnez-Mnez R., Rurack K., Salcenn F., Soto J., Spieles M., Highly selective chromogenic signaling of Hg2+ in aqueous media at nanomolar levels employing a squaraine-based reporter Inorganic Chemistry 2004 43 17 5183 5185
    • (2004) Inorganic Chemistry , vol.43 , Issue.17 , pp. 5183-5185
    • Ros-Lis, J.V.1    Martnez-Mnez, R.2    Rurack, K.3    Salcenn, F.4    Soto, J.5    Spieles, M.6
  • 130
    • 22244438508 scopus 로고    scopus 로고
    • Two-stage sensing property via a conjugated donor-acceptor-donor constitution: Application to the visual detection of mercuric ion
    • Huang J.-H., Wen W.-H., Sun Y.-Y., Chou P.-T., Fang J.-M., Two-stage sensing property via a conjugated donor-acceptor-donor constitution: application to the visual detection of mercuric ion Journal of Organic Chemistry 2005 70 15 5827 5832
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.15 , pp. 5827-5832
    • Huang, J.-H.1    Wen, W.-H.2    Sun, Y.-Y.3    Chou, P.-T.4    Fang, J.-M.5
  • 131
    • 60949099737 scopus 로고    scopus 로고
    • Progress in modifications and applications of fluorescent dye probe
    • Fei X., Gu Y., Progress in modifications and applications of fluorescent dye probe Progress in Natural Science 2009 19 1 1 7
    • (2009) Progress in Natural Science , vol.19 , Issue.1 , pp. 1-7
    • Fei, X.1    Gu, Y.2
  • 134
    • 1542721574 scopus 로고    scopus 로고
    • Fluorescence enhancement method for the determination of nucleic acids using cationic cyanine as a fluorescence probe
    • Zhu C.-Q., Zhuo S.-J., Zheng H., Fluorescence enhancement method for the determination of nucleic acids using cationic cyanine as a fluorescence probe Analyst 2004 129 3 254 258
    • (2004) Analyst , vol.129 , Issue.3 , pp. 254-258
    • Zhu, C.-Q.1    Zhuo, S.-J.2    Zheng, H.3
  • 135
    • 33846627852 scopus 로고    scopus 로고
    • Synthesis of novel cyanine dyes containing carbamoylethyl component - Noncovalent labels for nucleic acids detection
    • DOI 10.1016/j.dyepig.2006.02.010, PII S0143720806000854
    • Deligeorgiev T., Vasilev A., Drexhage K.-H., Synthesis of novel cyanine dyes containing carbamoylethyl componentnoncovalent labels for nucleic acids detection Dyes and Pigments 2007 74 2 320 328 (Pubitemid 46173041)
    • (2007) Dyes and Pigments , vol.74 , Issue.2 , pp. 320-328
    • Deligeorgiev, T.1    Vasilev, A.2    Drexhage, K.-H.3
  • 137
    • 33646591884 scopus 로고    scopus 로고
    • Synthesis of novel monomeric and homodimeric cyanine dyes with thioacetyl substituents for nucleic acid detection
    • Deligeorgiev T., Gadjev N., Vasilev A., Drexhage K.-H., Yarmoluk S. M., Synthesis of novel monomeric and homodimeric cyanine dyes with thioacetyl substituents for nucleic acid detection Dyes and Pigments 2007 72 1 28 32
    • (2007) Dyes and Pigments , vol.72 , Issue.1 , pp. 28-32
    • Deligeorgiev, T.1    Gadjev, N.2    Vasilev, A.3    Drexhage, K.-H.4    Yarmoluk, S.M.5
  • 138
    • 70349228721 scopus 로고    scopus 로고
    • Cyanine dye-nucleic acid interactions
    • Berlin, Germany Springer Topics in Heterocyclic Chemistry
    • Armitage B. A., Cyanine dye-nucleic acid interactions Heterocyclic Polymethine Dyes 2008 Berlin, Germany Springer 11 29 Topics in Heterocyclic Chemistry
    • (2008) Heterocyclic Polymethine Dyes , pp. 11-29
    • Armitage, B.A.1
  • 139
    • 0006460722 scopus 로고    scopus 로고
    • New asymmetric monomethine cyanine dyes for nucleic-acid labelling: Absorption and fluorescence spectral characteristics
    • Timtcheva I., Maximova V., Deligeorgiev T., Zaneva D., Ivanov I., New asymmetric monomethine cyanine dyes for nucleic-acid labelling: absorption and fluorescence spectral characteristics Journal of Photochemistry and Photobiology A 2000 130 1 7 11
    • (2000) Journal of Photochemistry and Photobiology A , vol.130 , Issue.1 , pp. 7-11
    • Timtcheva, I.1    Maximova, V.2    Deligeorgiev, T.3    Zaneva, D.4    Ivanov, I.5
  • 140
    • 0030960638 scopus 로고    scopus 로고
    • Fluorescence spectral characteristics of novel asymmetric monomethine cyanine dyes in nucleic acid solutions
    • Timcheva I. I., Maximova V. A., Deligeorgiev T. G., Gadjev N. I., Sabnis R. W., Ivanov I. G., Fluorescence spectral characteristics of novel asymmetric monomethine cyanine dyes in nucleic acid solutions FEBS Letters 1997 405 2 141 144
    • (1997) FEBS Letters , vol.405 , Issue.2 , pp. 141-144
    • Timcheva, I.I.1    Maximova, V.A.2    Deligeorgiev, T.G.3    Gadjev, N.I.4    Sabnis, R.W.5    Ivanov, I.G.6
  • 141
    • 0026696234 scopus 로고
    • Stable fluorescent complexes of double-stranded DNA with bis-intercalating asymmetric cyanine dyes: Properties and applications
    • Rye H. S., Yue S., Wemmer D. E., Stable fluorescent complexes of double-stranded DNA with bis-intercalating asymmetric cyanine dyes: properties and applications Nucleic Acids Research 1992 20 11 2803 2812
    • (1992) Nucleic Acids Research , vol.20 , Issue.11 , pp. 2803-2812
    • Rye, H.S.1    Yue, S.2    Wemmer, D.E.3
  • 142
  • 143
    • 54249153678 scopus 로고    scopus 로고
    • PH dependent spectral properties and electronic structure of benzothiazol containing cyanine dyes
    • Mazires M. R., Duprat C., Wolf J. G., Roshal A. D., pH dependent spectral properties and electronic structure of benzothiazol containing cyanine dyes Dyes and Pigments 2009 80 3 355 360
    • (2009) Dyes and Pigments , vol.80 , Issue.3 , pp. 355-360
    • Mazires, M.R.1    Duprat, C.2    Wolf, J.G.3    Roshal, A.D.4
  • 144
    • 29544437142 scopus 로고    scopus 로고
    • Synthesis and spectroscopic characterisation of heptamethincyanine NIR dyes for their use in optochemical sensors
    • Encinas C., Miltsov S., Otazo E., Rivera L., Puyol M., Alonso J., Synthesis and spectroscopic characterisation of heptamethincyanine NIR dyes for their use in optochemical sensors Dyes and Pigments 2006 71 1 28 36
    • (2006) Dyes and Pigments , vol.71 , Issue.1 , pp. 28-36
    • Encinas, C.1    Miltsov, S.2    Otazo, E.3    Rivera, L.4    Puyol, M.5    Alonso, J.6
  • 145
    • 33646200142 scopus 로고    scopus 로고
    • Synthesis of new ketocyanine dyes for the development of optical sensors. Optical characterisation and solvatochromic behaviour
    • Puyol M., Encinas C., Rivera L., Miltsov S., Alonso J., Synthesis of new ketocyanine dyes for the development of optical sensors. Optical characterisation and solvatochromic behaviour Sensors and Actuators B 2006 115 1 287 296
    • (2006) Sensors and Actuators B , vol.115 , Issue.1 , pp. 287-296
    • Puyol, M.1    Encinas, C.2    Rivera, L.3    Miltsov, S.4    Alonso, J.5
  • 146
    • 34249796365 scopus 로고    scopus 로고
    • Novel cyanine dyes as fluorescent pH sensors: PET, ICT mechanism or resonance effect?
    • Xu Y., Liu Y., Qian X., Novel cyanine dyes as fluorescent pH sensors: PET, ICT mechanism or resonance effect? Journal of Photochemistry and Photobiology A 2007 190 1 1 8
    • (2007) Journal of Photochemistry and Photobiology A , vol.190 , Issue.1 , pp. 1-8
    • Xu, Y.1    Liu, Y.2    Qian, X.3
  • 147
    • 33745621026 scopus 로고    scopus 로고
    • A new Vilsmeier-type reaction for one-pot synthesis of pH sensitive fluorescent cyanine dyes
    • El-Shishtawy R. M., Almeida P., A new Vilsmeier-type reaction for one-pot synthesis of pH sensitive fluorescent cyanine dyes Tetrahedron 2006 62 33 7793 7798
    • (2006) Tetrahedron , vol.62 , Issue.33 , pp. 7793-7798
    • El-Shishtawy, R.M.1    Almeida, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.