메뉴 건너뛰기




Volumn 83, Issue 2, 2009, Pages 230-236

Spectroscopic investigations of vinyl-substituted 10H-phenothiazine

Author keywords

Charge transfer; Contact ion pair; Fluorophores; Near infrared sensors; Phenothiazine; Spectral diversities

Indexed keywords

CONTACT ION PAIRS; CONTACT ION-PAIR; DONOR-ACCEPTOR; ELECTRON-DEFICIENT; INTRA-MOLECULAR CHARGE TRANSFER; NEAR INFRARED; NEAR INFRARED SENSORS; NITROGEN ATOM; PHENOTHIAZINE; PHENOTHIAZINE DERIVATIVES; PULL SYSTEMS; PYRIDINIUM; SPECTRAL DIVERSITIES; SPECTRAL VARIATION; SPECTROSCOPIC INVESTIGATIONS;

EID: 67649381639     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2009.05.004     Document Type: Article
Times cited : (20)

References (41)
  • 1
    • 0000315942 scopus 로고
    • Near-infrared absorbing dyes
    • Fabian J., Nakazumi H., and Matsuoka M. Near-infrared absorbing dyes. Chem Rev 92 (1992) 1197-1226
    • (1992) Chem Rev , vol.92 , pp. 1197-1226
    • Fabian, J.1    Nakazumi, H.2    Matsuoka, M.3
  • 2
    • 0346814452 scopus 로고
    • Organic photoconductive materials: recent trends and developments
    • Law K.Y. Organic photoconductive materials: recent trends and developments. Chem Rev 93 (1993) 449-486
    • (1993) Chem Rev , vol.93 , pp. 449-486
    • Law, K.Y.1
  • 3
    • 0344438130 scopus 로고    scopus 로고
    • Near-infrared optical imaging of proteases in cancer
    • Mahmood U., and Weissleder R. Near-infrared optical imaging of proteases in cancer. Mol Cancer Ther 2 (2003) 489-496
    • (2003) Mol Cancer Ther , vol.2 , pp. 489-496
    • Mahmood, U.1    Weissleder, R.2
  • 4
    • 33646937992 scopus 로고    scopus 로고
    • Near-infrared fluorescent deoxyglucose analogue for tumor optical imaging in cell culture and living mice
    • Cheng Z., Levi J., Xiong Z., Gheysens O., Keren S., Chen X., et al. Near-infrared fluorescent deoxyglucose analogue for tumor optical imaging in cell culture and living mice. Bioconjug Chem 17 (2006) 662-669
    • (2006) Bioconjug Chem , vol.17 , pp. 662-669
    • Cheng, Z.1    Levi, J.2    Xiong, Z.3    Gheysens, O.4    Keren, S.5    Chen, X.6
  • 5
    • 15744383910 scopus 로고    scopus 로고
    • Highly sensitive near-infrared fluorescent probes for nitric oxide and their application to isolated organs
    • Sasaki E., Kojima H., Nishimatsu H., Urano Y., Kikuchi K., Hirata Y., et al. Highly sensitive near-infrared fluorescent probes for nitric oxide and their application to isolated organs. J Am Chem Soc 127 (2005) 3684-3685
    • (2005) J Am Chem Soc , vol.127 , pp. 3684-3685
    • Sasaki, E.1    Kojima, H.2    Nishimatsu, H.3    Urano, Y.4    Kikuchi, K.5    Hirata, Y.6
  • 6
    • 0036434012 scopus 로고    scopus 로고
    • Bis(rylenedicarboximide)-a,d-1,5-cgdiaminoanthraquinones as unique infrared absorbing dyes
    • Kohl C., Becker S., and Müllen K. Bis(rylenedicarboximide)-a,d-1,5-cgdiaminoanthraquinones as unique infrared absorbing dyes. Chem Commun (2002) 2778-2779
    • (2002) Chem Commun , pp. 2778-2779
    • Kohl, C.1    Becker, S.2    Müllen, K.3
  • 7
    • 0141869055 scopus 로고    scopus 로고
    • An unexpectedly simple NIR dye for 1.1μm with a central mesoionic structure
    • Langhals H. An unexpectedly simple NIR dye for 1.1μm with a central mesoionic structure. Angew Chem Int Ed 42 (2003) 4286-4288
    • (2003) Angew Chem Int Ed , vol.42 , pp. 4286-4288
    • Langhals, H.1
  • 8
    • 0001949810 scopus 로고    scopus 로고
    • Fully conjugated porphyrin tapes with electronic absorption bands that reach into infrared
    • Tsuda A., and Osuka A. Fully conjugated porphyrin tapes with electronic absorption bands that reach into infrared. Science 293 (2001) 79-82
    • (2001) Science , vol.293 , pp. 79-82
    • Tsuda, A.1    Osuka, A.2
  • 9
    • 33750274564 scopus 로고    scopus 로고
    • Dibenzopentarylenebis(dicarboximide)s: novel near-infrared absorbing dyes
    • Avlasevich Y., and Müllen K. Dibenzopentarylenebis(dicarboximide)s: novel near-infrared absorbing dyes. Chem Commun 42 (2006) 4440-4442
    • (2006) Chem Commun , vol.42 , pp. 4440-4442
    • Avlasevich, Y.1    Müllen, K.2
  • 12
    • 9644268987 scopus 로고    scopus 로고
    • In vitro evaluation of the effectiveness of the macrolide rokitamycin and chlorpromazine against Acanthamoeba castellanii
    • Mattana A., Biancu G., Alberty L., Accardo A., Delogu G., Fiori P.L., et al. In vitro evaluation of the effectiveness of the macrolide rokitamycin and chlorpromazine against Acanthamoeba castellanii. Antimicrob Agents Chemother 48 (2004) 4520-4527
    • (2004) Antimicrob Agents Chemother , vol.48 , pp. 4520-4527
    • Mattana, A.1    Biancu, G.2    Alberty, L.3    Accardo, A.4    Delogu, G.5    Fiori, P.L.6
  • 13
    • 37149022882 scopus 로고    scopus 로고
    • Phenothiazine as a redox-active DNA base substitute: comparison with phenothiazine-modified uridine
    • Wagner C., and Wagenknecht H.A. Phenothiazine as a redox-active DNA base substitute: comparison with phenothiazine-modified uridine. Org Biomol Chem 6 (2008) 48-50
    • (2008) Org Biomol Chem , vol.6 , pp. 48-50
    • Wagner, C.1    Wagenknecht, H.A.2
  • 14
    • 37349095714 scopus 로고    scopus 로고
    • Electrical measurements and thermal kinetics study of phenothiazine and a few of its derivatives
    • Achar B.N., and Ashok M.A. Electrical measurements and thermal kinetics study of phenothiazine and a few of its derivatives. Mat Chem Phys 108 (2008) 8-15
    • (2008) Mat Chem Phys , vol.108 , pp. 8-15
    • Achar, B.N.1    Ashok, M.A.2
  • 15
    • 33745685115 scopus 로고    scopus 로고
    • Photoinduced electron transfer processes in 1,8-naphthalimide linker phenothiazine dyads
    • Cho D.W., Fujitsuka M., Sugimoto A., Yoon U.C., Mariano P.S., and Majima T. Photoinduced electron transfer processes in 1,8-naphthalimide linker phenothiazine dyads. J Phys Chem B 110 (2006) 11062-11068
    • (2006) J Phys Chem B , vol.110 , pp. 11062-11068
    • Cho, D.W.1    Fujitsuka, M.2    Sugimoto, A.3    Yoon, U.C.4    Mariano, P.S.5    Majima, T.6
  • 16
    • 0037194918 scopus 로고    scopus 로고
    • Conformational control of photoinduced charge separation within phenothiazine-pyrene dyads
    • Stockmann A., Kurzawa J., Fritz N., Acar N., Schneider S., Daub J., et al. Conformational control of photoinduced charge separation within phenothiazine-pyrene dyads. J Phys Chem A 106 (2002) 7958-7970
    • (2002) J Phys Chem A , vol.106 , pp. 7958-7970
    • Stockmann, A.1    Kurzawa, J.2    Fritz, N.3    Acar, N.4    Schneider, S.5    Daub, J.6
  • 17
    • 0035803029 scopus 로고    scopus 로고
    • First synthesis and electronic properties of (hetero) aryl bridged and directly linked redox active phenothiazinyl dyads and triads
    • Krämer C.S., Zeitler K., and Müller T.J.J. First synthesis and electronic properties of (hetero) aryl bridged and directly linked redox active phenothiazinyl dyads and triads. Tetrahedron Lett 42 (2001) 8619-8624
    • (2001) Tetrahedron Lett , vol.42 , pp. 8619-8624
    • Krämer, C.S.1    Zeitler, K.2    Müller, T.J.J.3
  • 18
    • 0141839149 scopus 로고    scopus 로고
    • Synthesis and electronic properties of alkynylated phenothiazines
    • Krämer C.S., Zeitler K., and Müller T.J.J. Synthesis and electronic properties of alkynylated phenothiazines. Eur J Org Chem (2003) 3534-3548
    • (2003) Eur J Org Chem , pp. 3534-3548
    • Krämer, C.S.1    Zeitler, K.2    Müller, T.J.J.3
  • 19
    • 31144477553 scopus 로고    scopus 로고
    • Synthesis and electronic properties of 3-acceptor-substituted and 3, 7-bisacceptor-substituted phenothiazines
    • Sailer M., Nonnenmacher M., Oeser T., and Müller T.J.J. Synthesis and electronic properties of 3-acceptor-substituted and 3, 7-bisacceptor-substituted phenothiazines. Eur J Org Chem 2 (2006) 423-435
    • (2006) Eur J Org Chem , vol.2 , pp. 423-435
    • Sailer, M.1    Nonnenmacher, M.2    Oeser, T.3    Müller, T.J.J.4
  • 20
    • 41949107046 scopus 로고    scopus 로고
    • Synthesis and electronic properties of monodisperse oligophenothiazines
    • Sailer M., Franz A.W., and Müller T.J.J. Synthesis and electronic properties of monodisperse oligophenothiazines. Chem Eur J 14 (2008) 2602-2614
    • (2008) Chem Eur J , vol.14 , pp. 2602-2614
    • Sailer, M.1    Franz, A.W.2    Müller, T.J.J.3
  • 21
    • 33846423171 scopus 로고    scopus 로고
    • Red emitting phenothiazine dendrimers encapsulated 2-{2-[2-(4-dimethylaminophenyl) vinyl]-6-methylpyran-4-ylidene} malononitrile derivatives
    • Kim G.W., Cho M.J., Yu Y.J., Kim Z.H., Jin J.I., Kim D.Y., et al. Red emitting phenothiazine dendrimers encapsulated 2-{2-[2-(4-dimethylaminophenyl) vinyl]-6-methylpyran-4-ylidene} malononitrile derivatives. Chem Mater 19 (2007) 42-50
    • (2007) Chem Mater , vol.19 , pp. 42-50
    • Kim, G.W.1    Cho, M.J.2    Yu, Y.J.3    Kim, Z.H.4    Jin, J.I.5    Kim, D.Y.6
  • 22
    • 30944458678 scopus 로고    scopus 로고
    • Saturated and efficient red light-emitting fluorene-based alternating polymers containing phenothiazine derivatives
    • Cho N.S., Park J.H., Lee S.K., Lee J., Shim H.K., Park M.J., et al. Saturated and efficient red light-emitting fluorene-based alternating polymers containing phenothiazine derivatives. Macromolecules 39 (2006) 177-183
    • (2006) Macromolecules , vol.39 , pp. 177-183
    • Cho, N.S.1    Park, J.H.2    Lee, S.K.3    Lee, J.4    Shim, H.K.5    Park, M.J.6
  • 23
    • 0022581711 scopus 로고
    • The chemistry and application of a angular phenothiazine derivatives
    • Okafor C.O. The chemistry and application of a angular phenothiazine derivatives. Dyes Pigments 7 (1986) 249
    • (1986) Dyes Pigments , vol.7 , pp. 249
    • Okafor, C.O.1
  • 25
    • 33846645732 scopus 로고
    • Electrical properties of phenothiazine
    • Aftergut S., and Brown G.P. Electrical properties of phenothiazine. Nature 193 (1962) 361-362
    • (1962) Nature , vol.193 , pp. 361-362
    • Aftergut, S.1    Brown, G.P.2
  • 26
    • 33751151638 scopus 로고
    • Luminescence stimulated by electron transfer: fluorescent donor/acceptor-substituted stilbenes containing pyrenoid and heteroaromatic subunits
    • Knorr A., and Daub J. Luminescence stimulated by electron transfer: fluorescent donor/acceptor-substituted stilbenes containing pyrenoid and heteroaromatic subunits. Angew Chem Int Ed Engl 34 (1995) 2664-2666
    • (1995) Angew Chem Int Ed Engl , vol.34 , pp. 2664-2666
    • Knorr, A.1    Daub, J.2
  • 28
    • 14544306480 scopus 로고    scopus 로고
    • Heterocyclic nonlinear optical chromophores composed of phenothiazine or carbazole donor and 2-cyanomethylene-3-cyano-4, 5, 5-trimethyl-2,5-dihydrofuran acceptor
    • Cho M.J., Kim J.Y., Kim J.H., Lee S.H., Dalton L.R., and Choi D.H. Heterocyclic nonlinear optical chromophores composed of phenothiazine or carbazole donor and 2-cyanomethylene-3-cyano-4, 5, 5-trimethyl-2,5-dihydrofuran acceptor. Bull Korean Chem Soc 26 (2005) 77-84
    • (2005) Bull Korean Chem Soc , vol.26 , pp. 77-84
    • Cho, M.J.1    Kim, J.Y.2    Kim, J.H.3    Lee, S.H.4    Dalton, L.R.5    Choi, D.H.6
  • 29
    • 0039844016 scopus 로고
    • Derivatives of 14H-Naphtho [2, 3-alPhenothiazine-8, 13-dione. Part 2: syntheses from 1, 4-dihydroxy-5-(6-, 7-, 8-) substituted anthraquinones
    • Peters A.T., and Wang N.J. Derivatives of 14H-Naphtho [2, 3-alPhenothiazine-8, 13-dione. Part 2: syntheses from 1, 4-dihydroxy-5-(6-, 7-, 8-) substituted anthraquinones. Dyes Pigments 28 (1995) 281-290
    • (1995) Dyes Pigments , vol.28 , pp. 281-290
    • Peters, A.T.1    Wang, N.J.2
  • 30
    • 0000886127 scopus 로고    scopus 로고
    • Multi-mode switching based on dihydroazulene/vinylheptafulvene photochromism: synergism of photochromism and redox switching in heteroaryl-functionalized systems
    • Spreitzer H., and Daub J. Multi-mode switching based on dihydroazulene/vinylheptafulvene photochromism: synergism of photochromism and redox switching in heteroaryl-functionalized systems. Chem Eur J 2 (1996) 1150-1158
    • (1996) Chem Eur J , vol.2 , pp. 1150-1158
    • Spreitzer, H.1    Daub, J.2
  • 32
    • 3042814814 scopus 로고    scopus 로고
    • Corrected emission spectra and quantum yields for a series of fluorescent compounds in the visible spectral region
    • Velapoldi R.A., and Tønnesen H.H. Corrected emission spectra and quantum yields for a series of fluorescent compounds in the visible spectral region. J Fluorescence 14 (2004) 465-472
    • (2004) J Fluorescence , vol.14 , pp. 465-472
    • Velapoldi, R.A.1    Tønnesen, H.H.2
  • 33
    • 33645141685 scopus 로고    scopus 로고
    • Solvent effect on photophysical properties of a fluorescence probe: bMVC
    • Chang C.C., Kuo S.H., Kang C.C., and Chang T.C. Solvent effect on photophysical properties of a fluorescence probe: bMVC. J Luminescence 119-120 (2006) 84-90
    • (2006) J Luminescence , vol.119-120 , pp. 84-90
    • Chang, C.C.1    Kuo, S.H.2    Kang, C.C.3    Chang, T.C.4
  • 34
    • 0033597837 scopus 로고    scopus 로고
    • Highly conjugated molecules from dibromonaphthyl derivatives and 4-vinylpyridine or 4-acetoxystyrene by the Heck reaction
    • Chang C.C., Chen K.J., and Yu L.J. Highly conjugated molecules from dibromonaphthyl derivatives and 4-vinylpyridine or 4-acetoxystyrene by the Heck reaction. J Org Chem 64 (1999) 5603-5610
    • (1999) J Org Chem , vol.64 , pp. 5603-5610
    • Chang, C.C.1    Chen, K.J.2    Yu, L.J.3
  • 35
    • 33947452896 scopus 로고
    • Color and constitution. XI. Anhydronium bases of p-hydroxystyryl dyes as solvent polarity indicators
    • Brooker L.G.S., Keyes G.H., and Heseltine D.W. Color and constitution. XI. Anhydronium bases of p-hydroxystyryl dyes as solvent polarity indicators. J Am Chem Soc 73 (1951) 5350-5356
    • (1951) J Am Chem Soc , vol.73 , pp. 5350-5356
    • Brooker, L.G.S.1    Keyes, G.H.2    Heseltine, D.W.3
  • 36
    • 0001166428 scopus 로고
    • Fluorescence and photoisomerisation of an amphiphilic aminostibazolium dye as controlled by the sensitivity of radiationless deactivation to polarity and viscosity
    • Ephardt H., and Fromherz P. Fluorescence and photoisomerisation of an amphiphilic aminostibazolium dye as controlled by the sensitivity of radiationless deactivation to polarity and viscosity. J Phys Chem 93 (1989) 7717-7725
    • (1989) J Phys Chem , vol.93 , pp. 7717-7725
    • Ephardt, H.1    Fromherz, P.2
  • 38
    • 41149155416 scopus 로고    scopus 로고
    • Synthesis and electronic properties of sterically demanding n-arylphenothiazines and unexpected Buchwald-Hartwig aminations
    • Franz A.W., Rominger F., and Muller T.J.J. Synthesis and electronic properties of sterically demanding n-arylphenothiazines and unexpected Buchwald-Hartwig aminations. J Org Chem 73 (2008) 1795-1802
    • (2008) J Org Chem , vol.73 , pp. 1795-1802
    • Franz, A.W.1    Rominger, F.2    Muller, T.J.J.3
  • 39
    • 4243562899 scopus 로고
    • The photophysics of alkali naphtholates: lifetimes of contact and solvent-separated ion pairs present simultaneously in weakly polar solvents
    • Vandereecken P., Soumillion J.P., Auweraer M.V.D., and Schryver F.C.D. The photophysics of alkali naphtholates: lifetimes of contact and solvent-separated ion pairs present simultaneously in weakly polar solvents. Chem Phys Lett 136 (1987) 441-446
    • (1987) Chem Phys Lett , vol.136 , pp. 441-446
    • Vandereecken, P.1    Soumillion, J.P.2    Auweraer, M.V.D.3    Schryver, F.C.D.4
  • 40
    • 0000078320 scopus 로고
    • Photophysical analysis of ion pairing of beta-naphtholate in medium polarity solvents: mixtures of contact and solvent-separated ion pairs
    • Soumillion J.P., Vandereecken P., Auweraer M.V.D., Schryver F.C.D., and Schanck A. Photophysical analysis of ion pairing of beta-naphtholate in medium polarity solvents: mixtures of contact and solvent-separated ion pairs. J Am Chem Soc 111 (1989) 2217-2225
    • (1989) J Am Chem Soc , vol.111 , pp. 2217-2225
    • Soumillion, J.P.1    Vandereecken, P.2    Auweraer, M.V.D.3    Schryver, F.C.D.4    Schanck, A.5
  • 41
    • 33750477306 scopus 로고    scopus 로고
    • Development of the charge-transfer-to-solvent process with increasing solvent fluid density: the effect of ion pairing
    • Sciaini G., Marceca E., and Ferna'ndez-Prini R. Development of the charge-transfer-to-solvent process with increasing solvent fluid density: the effect of ion pairing. Phys Chem Chem Phys 8 (2006) 4839-4848
    • (2006) Phys Chem Chem Phys , vol.8 , pp. 4839-4848
    • Sciaini, G.1    Marceca, E.2    Ferna'ndez-Prini, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.