메뉴 건너뛰기




Volumn 277, Issue , 2014, Pages 62-74

Selective ratiometric pH-sensing PAMAM light-harvesting dendrimer based on Rhodamine 6G and 1,8-naphthalimide

Author keywords

1,8 Naphthalimide Rhodamine 6G conjugate; Internal charge transfer (ICT); Light harvesting FRET based system; Photoinduced electron transfer (PET); Polyamidoamine (PAMAM) dendrimer; Selective ratiometric fluorescence pH probe

Indexed keywords


EID: 84891790936     PISSN: 10106030     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jphotochem.2013.12.005     Document Type: Article
Times cited : (46)

References (69)
  • 1
    • 0344722565 scopus 로고    scopus 로고
    • Photochemical molecular devices
    • V. Balzani Photochemical molecular devices Photochem. Photobiol. Sci. 2 2003 459 476
    • (2003) Photochem. Photobiol. Sci. , vol.2 , pp. 459-476
    • Balzani, V.1
  • 2
    • 23644444124 scopus 로고    scopus 로고
    • Luminescent sensors and switches in the early 21st century
    • J. Callan, A.P. de Silva, and D. Magri Luminescent sensors and switches in the early 21st century Tetrahedron 61 2005 8551 8588
    • (2005) Tetrahedron , vol.61 , pp. 8551-8588
    • Callan, J.1    De Silva, A.P.2    Magri, D.3
  • 3
    • 70449120080 scopus 로고    scopus 로고
    • "off-on-off" fluorescent proton switch synthesized by RAFT polymerization
    • J. Jiang, B. Leng, X. Xiao, P. Zhao, and H. Tian "Off-on-off" fluorescent proton switch synthesized by RAFT polymerization Polymer 50 2009 5681 5684
    • (2009) Polymer , vol.50 , pp. 5681-5684
    • Jiang, J.1    Leng, B.2    Xiao, X.3    Zhao, P.4    Tian, H.5
  • 4
    • 80051781024 scopus 로고    scopus 로고
    • Design, synthesis and pH sensing properties of novel 1,8-naphtalimide- based bichromophoric system
    • N. Marinova, V. Bojinov, and N. Georgiev Design, synthesis and pH sensing properties of novel 1,8-naphtalimide-based bichromophoric system J. Photochem. Photobiol. A: Chem. 222 2011 132 140
    • (2011) J. Photochem. Photobiol. A: Chem. , vol.222 , pp. 132-140
    • Marinova, N.1    Bojinov, V.2    Georgiev, N.3
  • 5
    • 79959790583 scopus 로고    scopus 로고
    • Turn-on fluorescent sensing with "reactive" probes
    • M. Jun, B. Roy, and K. Ahn Turn-on fluorescent sensing with "reactive" probes Chem. Commun. 47 2011 7583 7601
    • (2011) Chem. Commun. , vol.47 , pp. 7583-7601
    • Jun, M.1    Roy, B.2    Ahn, K.3
  • 6
    • 80051949467 scopus 로고    scopus 로고
    • A water-soluble 1,8-naphthalimide-based "turn on" fluorescent chemosensor for selective and sensitive recognition of mercury ion in water
    • H. Dai, and H. Xu A water-soluble 1,8-naphthalimide-based "turn on" fluorescent chemosensor for selective and sensitive recognition of mercury ion in water Bioorg. Med. Chem. Lett. 21 2011 5141 5144
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 5141-5144
    • Dai, H.1    Xu, H.2
  • 7
    • 78650355746 scopus 로고    scopus 로고
    • Recent progress on polymer-based fluorescent and colorimetric chemosensors
    • H. Kim, Z. Guo, W. Zhu, J. Yoon, and H. Tian Recent progress on polymer-based fluorescent and colorimetric chemosensors Chem. Soc. Rev. 40 2011 79 93
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 79-93
    • Kim, H.1    Guo, Z.2    Zhu, W.3    Yoon, J.4    Tian, H.5
  • 8
    • 35148888136 scopus 로고    scopus 로고
    • -) using naphthalimide-thiourea and -urea conjugates
    • -) using naphthalimide-thiourea and -urea conjugates Tetrahedron Lett. 48 2007 8043 8047
    • (2007) Tetrahedron Lett. , vol.48 , pp. 8043-8047
    • Duke, R.1    Gunnlaugsson, T.2
  • 9
    • 33745450416 scopus 로고    scopus 로고
    • Sensitive and selective photoinduced-electron-transfer-based sensing of alkylating agents
    • S. Tal, H. Salman, Y. Abraham, M. Botoshansky, and Y. Eichen Sensitive and selective photoinduced-electron-transfer-based sensing of alkylating agents Chem. Eur. J. 12 2006 4858 4864
    • (2006) Chem. Eur. J. , vol.12 , pp. 4858-4864
    • Tal, S.1    Salman, H.2    Abraham, Y.3    Botoshansky, M.4    Eichen, Y.5
  • 10
    • 33646055514 scopus 로고    scopus 로고
    • Fluorescent sensors for organophosphorus nerve agent mimics
    • J. Dale, and J. Rebek Fluorescent sensors for organophosphorus nerve agent mimics J. Am. Chem. Soc. 128 2006 4500 4501
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 4500-4501
    • Dale, J.1    Rebek, J.2
  • 11
    • 0037467426 scopus 로고    scopus 로고
    • Fluorescent detection of chemical warfare agents: Functional group specific ratiometric chemosensors
    • S. Zhang, and T. Swager Fluorescent detection of chemical warfare agents: functional group specific ratiometric chemosensors J. Am. Chem. Soc. 125 2003 3420 3421
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 3420-3421
    • Zhang, S.1    Swager, T.2
  • 12
    • 79955611347 scopus 로고    scopus 로고
    • Molecular logic gates and luminescent sensors based on photoinduced electron transfer
    • A.P. de Silva, and S. Uchiyama Molecular logic gates and luminescent sensors based on photoinduced electron transfer Top. Curr. Chem. 300 2011 1 28
    • (2011) Top. Curr. Chem. , vol.300 , pp. 1-28
    • De Silva, A.P.1    Uchiyama, S.2
  • 13
    • 79954418008 scopus 로고    scopus 로고
    • A fluoride selective dipyrromethane-TCNQ colorimetric sensor based on charge-transfer
    • P. Kaur, S. Kaur, and K. Singh A fluoride selective dipyrromethane-TCNQ colorimetric sensor based on charge-transfer Talanta 84 2011 947 951
    • (2011) Talanta , vol.84 , pp. 947-951
    • Kaur, P.1    Kaur, S.2    Singh, K.3
  • 14
    • 0009773493 scopus 로고    scopus 로고
    • Fluorescent sensors for transition metals based on electron-transfer and energy-transfer mechanisms
    • L. Fabbrizzi, M. Licchelli, P. Pallavicini, A. Perotti, A. Taglietti, and D. Sacchi Fluorescent sensors for transition metals based on electron-transfer and energy-transfer mechanisms Chem. Eur. J. 2 1996 75 82
    • (1996) Chem. Eur. J. , vol.2 , pp. 75-82
    • Fabbrizzi, L.1    Licchelli, M.2    Pallavicini, P.3    Perotti, A.4    Taglietti, A.5    Sacchi, D.6
  • 15
    • 84863338318 scopus 로고    scopus 로고
    • Fluorescent chemosensors based on spiroring-opening of xanthenes and related derivatives
    • X. Chen, T. Pradhan, F. Wang, J. Kim, and J. Yoon Fluorescent chemosensors based on spiroring-opening of xanthenes and related derivatives Chem. Rev. 112 2012 1910 1956
    • (2012) Chem. Rev. , vol.112 , pp. 1910-1956
    • Chen, X.1    Pradhan, T.2    Wang, F.3    Kim, J.4    Yoon, J.5
  • 16
    • 39449086422 scopus 로고    scopus 로고
    • Synthesis and energy-transfer properties of poly(amidoamine) dendrons modified with naphthyl and dansyl groups
    • W.-S. Li, M.-J. Teng, X.-R. Jia, B.-B. Wang, J.-M. Yeh, and Y. Wei Synthesis and energy-transfer properties of poly(amidoamine) dendrons modified with naphthyl and dansyl groups Tetrahedron Lett. 49 2008 1988 1992
    • (2008) Tetrahedron Lett. , vol.49 , pp. 1988-1992
    • Li, W.-S.1    Teng, M.-J.2    Jia, X.-R.3    Wang, B.-B.4    Yeh, J.-M.5    Wei, Y.6
  • 17
    • 84878237038 scopus 로고    scopus 로고
    • Design, synthesis and pH sensing properties of novel PAMAM light-harvesting dendrons based on rhodamine 6G and 1,8-naphthalimide
    • N. Georgiev, V. Bojinov, and A. Venkova Design, synthesis and pH sensing properties of novel PAMAM light-harvesting dendrons based on rhodamine 6G and 1,8-naphthalimide J. Fluoresc. 23 2013 459 471
    • (2013) J. Fluoresc. , vol.23 , pp. 459-471
    • Georgiev, N.1    Bojinov, V.2    Venkova, A.3
  • 18
    • 0031659654 scopus 로고    scopus 로고
    • Arenedicarboximide building blocks for fluorescent photoinduced electron transfer pH sensors applicable with different media and communication wavelengths
    • L. Daffy, A.P. de Silva, H. Gunaratne, C. Huber, P. Lynch, T. Werner, and O. Wolfbeis Arenedicarboximide building blocks for fluorescent photoinduced electron transfer pH sensors applicable with different media and communication wavelengths Chem. Eur. J. 4 1998 1810 1815
    • (1998) Chem. Eur. J. , vol.4 , pp. 1810-1815
    • Daffy, L.1    De Silva, A.P.2    Gunaratne, H.3    Huber, C.4    Lynch, P.5    Werner, T.6    Wolfbeis, O.7
  • 20
    • 44349093391 scopus 로고    scopus 로고
    • Photochemical conversion of solar energy
    • V. Balzani, A. Credi, and M. Venturi Photochemical conversion of solar energy ChemSusChem 1 2008 26 58
    • (2008) ChemSusChem , vol.1 , pp. 26-58
    • Balzani, V.1    Credi, A.2    Venturi, M.3
  • 21
    • 0036432939 scopus 로고    scopus 로고
    • Cascade energy transfer in a conformationally mobile multichromophoric dendrimer
    • J. Serin, D. Brousmiche, and J. Frèchet Cascade energy transfer in a conformationally mobile multichromophoric dendrimer Chem. Commun. 2002 2605 2607
    • (2002) Chem. Commun. , pp. 2605-2607
    • Serin, J.1    Brousmiche, D.2    Frèchet, J.3
  • 22
    • 26444574728 scopus 로고    scopus 로고
    • Functionally layered dendrimers: A new building block and its application to the synthesis of multichromophoric light-harvesting systems
    • W.R. Dichtel, S. Hecht, and J. Frèchet Functionally layered dendrimers: a new building block and its application to the synthesis of multichromophoric light-harvesting systems Org. Lett. 7 2005 4451 4454
    • (2005) Org. Lett. , vol.7 , pp. 4451-4454
    • Dichtel, W.R.1    Hecht, S.2    Frèchet, J.3
  • 23
    • 3042564027 scopus 로고    scopus 로고
    • Dendron-functionalized macromolecules: Enhancing core luminescence and tuning carrier injection
    • P. Du, W.-H. Zhu, Y.-Q. Xie, F. Zhao, C.-F. Ku, Y. Cao, C.-P. Chang, and H. Tian Dendron-functionalized macromolecules: enhancing core luminescence and tuning carrier injection Macromolecules 37 2004 4387 4398
    • (2004) Macromolecules , vol.37 , pp. 4387-4398
    • Du, P.1    Zhu, W.-H.2    Xie, Y.-Q.3    Zhao, F.4    Ku, C.-F.5    Cao, Y.6    Chang, C.-P.7    Tian, H.8
  • 24
    • 7744220690 scopus 로고    scopus 로고
    • Energy transfer rates and pathways of single donor chromophores in a multichromophoric dendrimer built around a central acceptor core
    • R. Mètivier, F. Kulzer, T. Weil, K. Müllen, and T. Basch Energy transfer rates and pathways of single donor chromophores in a multichromophoric dendrimer built around a central acceptor core J. Am. Chem. Soc. 126 2004 14364 14365
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 14364-14365
    • Mètivier, R.1    Kulzer, F.2    Weil, T.3    Müllen, K.4    Basch, T.5
  • 25
    • 33748657609 scopus 로고    scopus 로고
    • Antenna-functionalized dendritic β-diketonates and europium complexes: Synthetic approaches to generation growth
    • S. Li, W. Zhu, Z. Xu, J. Pan, and H. Tian Antenna-functionalized dendritic β-diketonates and europium complexes: synthetic approaches to generation growth Tetrahedron 62 2006 5035 5048
    • (2006) Tetrahedron , vol.62 , pp. 5035-5048
    • Li, S.1    Zhu, W.2    Xu, Z.3    Pan, J.4    Tian, H.5
  • 26
    • 0346425992 scopus 로고    scopus 로고
    • Dendrimers as light harvesting antennae
    • A. Bar-Haim, and J. Klafter Dendrimers as light harvesting antennae J. Lumin. 76-77 1998 197 200
    • (1998) J. Lumin. , vol.76-77 , pp. 197-200
    • Bar-Haim, A.1    Klafter, J.2
  • 27
    • 36348953113 scopus 로고    scopus 로고
    • Synthesis and photophysical properties of fluorescence sensing ester- and amidoamine-functionalized 1,8-naphthalimides
    • V. Bojinov, N. Georgiev, and P. Nikolov Synthesis and photophysical properties of fluorescence sensing ester- and amidoamine-functionalized 1,8-naphthalimides J. Photochem. Photobiol. A: Chem. 193 2008 129 138
    • (2008) J. Photochem. Photobiol. A: Chem. , vol.193 , pp. 129-138
    • Bojinov, V.1    Georgiev, N.2    Nikolov, P.3
  • 28
    • 77958473948 scopus 로고    scopus 로고
    • Novel PAMAM light-harvesting antennae based on 1,8-naphthalimide: Synthesis, energy transfer, photophysical and pH sensing properties
    • N. Georgiev, V. Bojinov, and N. Marinova Novel PAMAM light-harvesting antennae based on 1,8-naphthalimide: synthesis, energy transfer, photophysical and pH sensing properties Sens. Actuators B: Chem. 150 2010 655 666
    • (2010) Sens. Actuators B: Chem. , vol.150 , pp. 655-666
    • Georgiev, N.1    Bojinov, V.2    Marinova, N.3
  • 29
    • 80052963826 scopus 로고    scopus 로고
    • Fluorescence properties and antiproliferative effects of mono-, bis-, and tris thiophenylnaphthalimides: Results of a comparative pilot study
    • I. Ott, Y. Xu, and X. Qian Fluorescence properties and antiproliferative effects of mono-, bis-, and tris thiophenylnaphthalimides: results of a comparative pilot study J. Photochem. Photobiol. B: Biol. 105 2011 75 80
    • (2011) J. Photochem. Photobiol. B: Biol. , vol.105 , pp. 75-80
    • Ott, I.1    Xu, Y.2    Qian, X.3
  • 30
    • 84867223934 scopus 로고    scopus 로고
    • Novel bisthienylethene containing ferrocenyl-substituted naphthalimide: A photo- and redox multi-addressable molecular switch
    • W. Zhu, L. Song, Y. Yang, and H. Tian Novel bisthienylethene containing ferrocenyl-substituted naphthalimide: a photo- and redox multi-addressable molecular switch Chem. Eur. J. 18 2012 13388 13394
    • (2012) Chem. Eur. J. , vol.18 , pp. 13388-13394
    • Zhu, W.1    Song, L.2    Yang, Y.3    Tian, H.4
  • 31
    • 34447114638 scopus 로고    scopus 로고
    • A novel blue fluorescent 4-(1,2,2,6,6-pentamethylpiperidin-4-yloxy)-1,8- naphthalimide pH chemosensor based on photoinduced electron transfer
    • V. Bojinov, D. Simeonov, and N. Georgiev A novel blue fluorescent 4-(1,2,2,6,6-pentamethylpiperidin-4-yloxy)-1,8-naphthalimide pH chemosensor based on photoinduced electron transfer Dyes Pigments 76 2008 41 46
    • (2008) Dyes Pigments , vol.76 , pp. 41-46
    • Bojinov, V.1    Simeonov, D.2    Georgiev, N.3
  • 32
    • 84857040922 scopus 로고    scopus 로고
    • A colorimetric probe for copper(II) ion based on 4-amino-1,8- naphthalimide
    • H. Wang, L. Yang, W. Zhang, Y. Zhou, B. Zhao, and X. Li A colorimetric probe for copper(II) ion based on 4-amino-1,8-naphthalimide Inorg. Chim. Acta 381 2012 111 116
    • (2012) Inorg. Chim. Acta , vol.381 , pp. 111-116
    • Wang, H.1    Yang, L.2    Zhang, W.3    Zhou, Y.4    Zhao, B.5    Li, X.6
  • 33
    • 34247567024 scopus 로고    scopus 로고
    • Fluorescent 4-(2,2,6,6-tetramethylpiperidin-4-ylamino)-1,8-naphthalimide pH chemosensor based on photoinduced electron transfer
    • V. Bojinov, and T. Konstantinova Fluorescent 4-(2,2,6,6- tetramethylpiperidin-4-ylamino)-1,8-naphthalimide pH chemosensor based on photoinduced electron transfer Sens. Actuators B: Chem. 123 2007 869 876
    • (2007) Sens. Actuators B: Chem. , vol.123 , pp. 869-876
    • Bojinov, V.1    Konstantinova, T.2
  • 34
    • 56049099723 scopus 로고    scopus 로고
    • Novel blue emitting tetra- and pentamethylpiperidin-4-yloxy-1,8- naphthalimides as photoinduced electron transfer based sensors for transition metal ions and protons
    • V. Bojinov, I. Panova, and J.-M. Chovelon Novel blue emitting tetra- and pentamethylpiperidin-4-yloxy-1,8-naphthalimides as photoinduced electron transfer based sensors for transition metal ions and protons Sens. Actuators B: Chem. 135 2008 172 180
    • (2008) Sens. Actuators B: Chem. , vol.135 , pp. 172-180
    • Bojinov, V.1    Panova, I.2    Chovelon, J.-M.3
  • 35
    • 77649261735 scopus 로고    scopus 로고
    • Synthesis and sensor activity of photostable blue emitting 1,8-naphthalimides containing s-triazine UV absorber and HALS fragments
    • V. Bojinov, I. Panova, D. Simeonov, and N. Georgiev Synthesis and sensor activity of photostable blue emitting 1,8-naphthalimides containing s-triazine UV absorber and HALS fragments J. Photochem. Photobiol. A: Chem. 210 2010 89 99
    • (2010) J. Photochem. Photobiol. A: Chem. , vol.210 , pp. 89-99
    • Bojinov, V.1    Panova, I.2    Simeonov, D.3    Georgiev, N.4
  • 36
    • 51249117555 scopus 로고    scopus 로고
    • Novel 4-(2,2,6,6-tetramethylpiperidin-4-ylamino)-1,8-naphthalimide based yellow-green emitting fluorescence sensors for transition metal ions and protons
    • V. Bojinov, and I. Panova Novel 4-(2,2,6,6-tetramethylpiperidin-4- ylamino)-1,8-naphthalimide based yellow-green emitting fluorescence sensors for transition metal ions and protons Dyes Pigments 80 2009 61 66
    • (2009) Dyes Pigments , vol.80 , pp. 61-66
    • Bojinov, V.1    Panova, I.2
  • 37
    • 84877765824 scopus 로고    scopus 로고
    • Synthesis, sensor activity and logic behavior of a highly water-soluble naphthalimide derivative
    • N. Georgiev, I. Yaneva, A. Surleva, A. Asiri, and V. Bojinov Synthesis, sensor activity and logic behavior of a highly water-soluble naphthalimide derivative Sens. Actuators B: Chem. 184 2013 54 63
    • (2013) Sens. Actuators B: Chem. , vol.184 , pp. 54-63
    • Georgiev, N.1    Yaneva, I.2    Surleva, A.3    Asiri, A.4    Bojinov, V.5
  • 38
    • 84860507094 scopus 로고    scopus 로고
    • Design, synthesis and sensor activity of a highly photostable blue emitting 1,8-naphthalimide
    • N. Georgiev, and V. Bojinov Design, synthesis and sensor activity of a highly photostable blue emitting 1,8-naphthalimide J. Lumin. 132 2012 2235 2241
    • (2012) J. Lumin. , vol.132 , pp. 2235-2241
    • Georgiev, N.1    Bojinov, V.2
  • 39
    • 77957836543 scopus 로고    scopus 로고
    • Design, synthesis and photophysical properties of two novel 1,8-naphthalimide fluorescent pH sensors based on PET and ICT
    • N. Georgiev, V. Bojinov, and P. Nikolov Design, synthesis and photophysical properties of two novel 1,8-naphthalimide fluorescent pH sensors based on PET and ICT Dyes Pigments 88 2011 350 357
    • (2011) Dyes Pigments , vol.88 , pp. 350-357
    • Georgiev, N.1    Bojinov, V.2    Nikolov, P.3
  • 40
    • 84865299278 scopus 로고    scopus 로고
    • Sensor activity and logic behavior of PET based dihydroimidazonaphthalimide diester
    • N. Georgiev, M. Lyulev, and V. Bojinov Sensor activity and logic behavior of PET based dihydroimidazonaphthalimide diester Spectrochim. Acta Part A 97 2012 512 520
    • (2012) Spectrochim. Acta Part A , vol.97 , pp. 512-520
    • Georgiev, N.1    Lyulev, M.2    Bojinov, V.3
  • 42
    • 84874704317 scopus 로고    scopus 로고
    • Facile synthesis, sensor activity and logic behaviour of 4-aryloxy substituted 1,8-naphthalimide
    • N. Marinova, N. Georgiev, and V. Bojinov Facile synthesis, sensor activity and logic behaviour of 4-aryloxy substituted 1,8-naphthalimide J. Photochem. Photobiol. A: Chem. 254 2013 54 61
    • (2013) J. Photochem. Photobiol. A: Chem. , vol.254 , pp. 54-61
    • Marinova, N.1    Georgiev, N.2    Bojinov, V.3
  • 43
    • 84884680644 scopus 로고    scopus 로고
    • Design and synthesis of pH-selective fluorescence sensing PAMAM light-harvesting dendrons based on 1,8-naphthalimides
    • N. Georgiev, A. Asiri, A. Qusti, K. Alamry, and V. Bojinov Design and synthesis of pH-selective fluorescence sensing PAMAM light-harvesting dendrons based on 1,8-naphthalimides Sens. Actuators B: Chem. 190 2014 185 198
    • (2014) Sens. Actuators B: Chem. , vol.190 , pp. 185-198
    • Georgiev, N.1    Asiri, A.2    Qusti, A.3    Alamry, K.4    Bojinov, V.5
  • 44
    • 79960212080 scopus 로고    scopus 로고
    • Photophysical property of rhodamine-cored poly(amidoamine) dendrimers: Simultaneous effect of spirolactam ring-opening and PET process on sensing trivalent chromium ion
    • Y. Lei, Y. Su, and J. Huo Photophysical property of rhodamine-cored poly(amidoamine) dendrimers: simultaneous effect of spirolactam ring-opening and PET process on sensing trivalent chromium ion J. Lumin. 131 2011 2521 2527
    • (2011) J. Lumin. , vol.131 , pp. 2521-2527
    • Lei, Y.1    Su, Y.2    Huo, J.3
  • 45
    • 84880042902 scopus 로고    scopus 로고
    • A new rhodamine B-based lysosomal pH fluorescent indicator
    • H.-S. Lv, S.-Y. Huang, B.-X. Zhao, and J.-Y. Miao A new rhodamine B-based lysosomal pH fluorescent indicator Anal. Chim. Acta 788 2013 177 182
    • (2013) Anal. Chim. Acta , vol.788 , pp. 177-182
    • Lv, H.-S.1    Huang, S.-Y.2    Zhao, B.-X.3    Miao, J.-Y.4
  • 46
    • 84880148749 scopus 로고    scopus 로고
    • 2 composites functionalized with spirolactam-based molecular switch
    • 2 composites functionalized with spirolactam-based molecular switch J. Colloid Interface Sci. 406 2013 178 185
    • (2013) J. Colloid Interface Sci. , vol.406 , pp. 178-185
    • Lei, Y.1    Zhang, C.2    Lei, H.3    Huo, J.4
  • 47
    • 80054047137 scopus 로고    scopus 로고
    • 3+ based on rhodamine-cored poly(amidoamine) dendrimer
    • 3+ based on rhodamine-cored poly(amidoamine) dendrimer Spectrochim. Acta Part A 81 2011 149 154
    • (2011) Spectrochim. Acta Part A , vol.81 , pp. 149-154
    • Lei, Y.1    Su, Y.2    Huo, J.3
  • 49
    • 71749121982 scopus 로고    scopus 로고
    • Synthesis and energy-transfer properties of fluorescence sensing bichromophoric system based on Rhodamine 6G and 1,8-naphthalimide
    • V. Bojinov, A. Venkova, and N. Georgiev Synthesis and energy-transfer properties of fluorescence sensing bichromophoric system based on Rhodamine 6G and 1,8-naphthalimide Sens. Actuators B: Chem. 143 2009 42 49
    • (2009) Sens. Actuators B: Chem. , vol.143 , pp. 42-49
    • Bojinov, V.1    Venkova, A.2    Georgiev, N.3
  • 50
    • 84887630991 scopus 로고    scopus 로고
    • A pH sensitive and selective ratiometric PAMAM wavelength-shifting bichromophoric system based on PET, FRET and ICT
    • N. Georgiev, A. Asiri, A. Qusti, K. Alamry, and V. Bojinov A pH sensitive and selective ratiometric PAMAM wavelength-shifting bichromophoric system based on PET, FRET and ICT Dyes Pigments 102 2014 35 45
    • (2014) Dyes Pigments , vol.102 , pp. 35-45
    • Georgiev, N.1    Asiri, A.2    Qusti, A.3    Alamry, K.4    Bojinov, V.5
  • 51
    • 0020954536 scopus 로고
    • Fluorescence quantum yields of some rhodamine dyes
    • R. Kubin, and A. Fletcher Fluorescence quantum yields of some rhodamine dyes J. Lumin. 27 1982 455 462
    • (1982) J. Lumin. , vol.27 , pp. 455-462
    • Kubin, R.1    Fletcher, A.2
  • 52
    • 0016484758 scopus 로고
    • New coumarin dyes with rigidized structure for flashlamp-pumped dye lasers
    • G. Reynolds, and K. Drexhage New coumarin dyes with rigidized structure for flashlamp-pumped dye lasers Opt. Commun. 13 1975 222 225
    • (1975) Opt. Commun. , vol.13 , pp. 222-225
    • Reynolds, G.1    Drexhage, K.2
  • 53
    • 1642481092 scopus 로고    scopus 로고
    • Proton "off-on" behaviour of methylpiperazinyl derivative of naphthalimide: A pH sensor based on fluorescence enhancement
    • C. Niu, G. Zeng, L. Chen, G. Shena, and R. Yu Proton "off-on" behaviour of methylpiperazinyl derivative of naphthalimide: a pH sensor based on fluorescence enhancement Analyst 129 2004 20 24
    • (2004) Analyst , vol.129 , pp. 20-24
    • Niu, C.1    Zeng, G.2    Chen, L.3    Shena, G.4    Yu, R.5
  • 54
    • 77952242413 scopus 로고    scopus 로고
    • A series of highly sensitive and selective fluorescent and colorimetric "off-on" chemosensors for Cu(II) based on rhodamine derivatives
    • M. Dong, T.-H. Ma, A.-J. Zhang, Y.-M. Dong, Y.-W. Wang, and Y. Peng A series of highly sensitive and selective fluorescent and colorimetric "off-on" chemosensors for Cu(II) based on rhodamine derivatives Dyes Pigments 87 2010 164 172
    • (2010) Dyes Pigments , vol.87 , pp. 164-172
    • Dong, M.1    Ma, T.-H.2    Zhang, A.-J.3    Dong, Y.-M.4    Wang, Y.-W.5    Peng, Y.6
  • 56
    • 79957463323 scopus 로고    scopus 로고
    • An integrated system of pyrene and Rhodamine-6G for selective colorimetric and fluorometric sensing of mercury(II)
    • B. Ahamed, and P. Ghosh An integrated system of pyrene and Rhodamine-6G for selective colorimetric and fluorometric sensing of mercury(II) Inorg. Chim. Acta 372 2011 100 107
    • (2011) Inorg. Chim. Acta , vol.372 , pp. 100-107
    • Ahamed, B.1    Ghosh, P.2
  • 57
    • 55949084508 scopus 로고    scopus 로고
    • Design and synthesis of a novel pH sensitive core and peripherally 1,8-naphthalimide-labeled PAMAM dendron as light harvesting antenna
    • N. Georgiev, V. Bojinov, and P. Nikolov Design and synthesis of a novel pH sensitive core and peripherally 1,8-naphthalimide-labeled PAMAM dendron as light harvesting antenna Dyes Pigments 81 2009 18 26
    • (2009) Dyes Pigments , vol.81 , pp. 18-26
    • Georgiev, N.1    Bojinov, V.2    Nikolov, P.3
  • 58
    • 79951510561 scopus 로고    scopus 로고
    • Design, synthesis and photostability of novel 1,8-naphthalimide PAMAM light-harvesting dendrons
    • N. Georgiev, and V. Bojinov Design, synthesis and photostability of novel 1,8-naphthalimide PAMAM light-harvesting dendrons J. Fluoresc. 21 2011 51 63
    • (2011) J. Fluoresc. , vol.21 , pp. 51-63
    • Georgiev, N.1    Bojinov, V.2
  • 59
    • 0037380168 scopus 로고    scopus 로고
    • Luminescent properties and photo-induced electron transfer of naphthalimides with piperazine substituent
    • J. Gan, K. Chen, C. Chang, and H. Tian Luminescent properties and photo-induced electron transfer of naphthalimides with piperazine substituent Dyes Pigments 57 2003 21 28
    • (2003) Dyes Pigments , vol.57 , pp. 21-28
    • Gan, J.1    Chen, K.2    Chang, C.3    Tian, H.4
  • 60
    • 33847320174 scopus 로고    scopus 로고
    • Synthesis and absorption properties of new yellow-green emitting benzo[de]isoquinoline-1,3-diones containing hindered amine and 2-hydroxyphenylbenzotriazole fragments
    • V. Bojinov, and I. Panova Synthesis and absorption properties of new yellow-green emitting benzo[de]isoquinoline-1,3-diones containing hindered amine and 2-hydroxyphenylbenzotriazole fragments Dyes Pigments 74 2007 551 560
    • (2007) Dyes Pigments , vol.74 , pp. 551-560
    • Bojinov, V.1    Panova, I.2
  • 61
    • 80052918398 scopus 로고    scopus 로고
    • A study of the interaction between rhodamine 6G and hydroxy propyl β-cyclodextrin by steady state fluorescence
    • S. Bakkialakshmi, and T. Menaka A study of the interaction between rhodamine 6G and hydroxy propyl β-cyclodextrin by steady state fluorescence Spectrochim. Acta Part A 81 2011 8 13
    • (2011) Spectrochim. Acta Part A , vol.81 , pp. 8-13
    • Bakkialakshmi, S.1    Menaka, T.2
  • 62
    • 84055223967 scopus 로고    scopus 로고
    • Anisotropic and isotropic solvent effects on the dipole moment and photophysical properties of rhodamine dyes
    • M. Zakerhamidi, M. Moghadam, A. Ghanadzadeh, and S. Hosseini Anisotropic and isotropic solvent effects on the dipole moment and photophysical properties of rhodamine dyes J. Lumin. 132 2012 931 937
    • (2012) J. Lumin. , vol.132 , pp. 931-937
    • Zakerhamidi, M.1    Moghadam, M.2    Ghanadzadeh, A.3    Hosseini, S.4
  • 64
    • 43049114247 scopus 로고    scopus 로고
    • Design and synthesis of core and peripherally functionalized with 1,8-naphthalimide units fluorescent PAMAM dendron as light harvesting antenna
    • V. Bojinov, N. Georgiev, and P. Nikolov Design and synthesis of core and peripherally functionalized with 1,8-naphthalimide units fluorescent PAMAM dendron as light harvesting antenna J. Photochem. Photobiol. A: Chem. 197 2008 281 289
    • (2008) J. Photochem. Photobiol. A: Chem. , vol.197 , pp. 281-289
    • Bojinov, V.1    Georgiev, N.2    Nikolov, P.3
  • 65
    • 79959241345 scopus 로고    scopus 로고
    • Design and synthesis of novel fluorescence sensing perylene diimides based on photoinduced electron transfer
    • N. Georgiev, A. Sakr, and V. Bojinov Design and synthesis of novel fluorescence sensing perylene diimides based on photoinduced electron transfer Dyes Pigments 91 2011 332 339
    • (2011) Dyes Pigments , vol.91 , pp. 332-339
    • Georgiev, N.1    Sakr, A.2    Bojinov, V.3
  • 66
    • 84857051828 scopus 로고    scopus 로고
    • Path-selective photoinduced electron transfer (PET) in a membrane-associated system studied by pH-dependent fluorescence
    • J. Liu, and A.P. de Silva Path-selective photoinduced electron transfer (PET) in a membrane-associated system studied by pH-dependent fluorescence Inorg. Chim. Acta 381 2012 243 246
    • (2012) Inorg. Chim. Acta , vol.381 , pp. 243-246
    • Liu, J.1    De Silva, A.P.2
  • 67
    • 70350210467 scopus 로고    scopus 로고
    • The design and synthesis of a novel 1,8-naphthalimide PAMAM light-harvesting dendron with fluorescence "off-on" switching core
    • N. Georgiev, and V. Bojinov The design and synthesis of a novel 1,8-naphthalimide PAMAM light-harvesting dendron with fluorescence "off-on" switching core Dyes Pigments 84 2010 249 256
    • (2010) Dyes Pigments , vol.84 , pp. 249-256
    • Georgiev, N.1    Bojinov, V.2
  • 68
    • 77953914714 scopus 로고    scopus 로고
    • Design and synthesis of highly photostable fluorescence sensing 1,8-naphthalimide-based dyes containing s-triazine UV absorber and HALS units
    • V. Bojinov, N. Georgiev, and N. Marinova Design and synthesis of highly photostable fluorescence sensing 1,8-naphthalimide-based dyes containing s-triazine UV absorber and HALS units Sens. Actuators B: Chem. 148 2010 6 16
    • (2010) Sens. Actuators B: Chem. , vol.148 , pp. 6-16
    • Bojinov, V.1    Georgiev, N.2    Marinova, N.3
  • 69
    • 59849119820 scopus 로고    scopus 로고
    • Design and synthesis of highly photostable yellow-green emitting 1,8-naphthalimides as fluorescent sensors for metal cations and protons
    • V. Bojinov, N. Georgiev, and P. Bosch Design and synthesis of highly photostable yellow-green emitting 1,8-naphthalimides as fluorescent sensors for metal cations and protons J. Fluoresc. 19 2009 127 139
    • (2009) J. Fluoresc. , vol.19 , pp. 127-139
    • Bojinov, V.1    Georgiev, N.2    Bosch, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.