메뉴 건너뛰기




Volumn 402, Issue , 2012, Pages 117-126

Influence of nanoscopic micellar confinements on spectroscopic probing and rotational dynamics of an antioxidative naphthalimide derivative

Author keywords

Microenvironment; Naphthalimides; Polarity; Rotational relaxation

Indexed keywords

AGGLOMERATION; ANIONIC SURFACTANTS; ANISOTROPY; BROMINE COMPOUNDS; CATIONIC SURFACTANTS; CHARGE TRANSFER; FLUORESCENCE; FLUOROPHORES; METAL IONS; NONIONIC SURFACTANTS;

EID: 84860915645     PISSN: 09277757     EISSN: 18734359     Source Type: Journal    
DOI: 10.1016/j.colsurfa.2012.03.035     Document Type: Article
Times cited : (13)

References (45)
  • 1
    • 11544314893 scopus 로고    scopus 로고
    • Oxidative strand scission of nucleic acids: routes initiated by hydrogen abstraction from the sugar moiety
    • Pogozelski W.K., Tullius T.D. Oxidative strand scission of nucleic acids: routes initiated by hydrogen abstraction from the sugar moiety. Chem. Rev. 1998, 98:1089-1108.
    • (1998) Chem. Rev. , vol.98 , pp. 1089-1108
    • Pogozelski, W.K.1    Tullius, T.D.2
  • 2
    • 0033611943 scopus 로고    scopus 로고
    • Nucleic acid oxidation mediated by naphthalene and benzophenone imide and diimide derivatives: consequences for DNA redox chemistry
    • Rogers J.E., Kelly L.A. Nucleic acid oxidation mediated by naphthalene and benzophenone imide and diimide derivatives: consequences for DNA redox chemistry. J. Am. Chem. Soc. 1999, 121:3854-3861.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3854-3861
    • Rogers, J.E.1    Kelly, L.A.2
  • 3
    • 0029056686 scopus 로고
    • Photoactivatable, DNA-cleaving amino acids: highly sequence-selective DNA photocleavage by novel l-lysine derivatives
    • Saito I., Takayama M., Kawanishi S. Photoactivatable, DNA-cleaving amino acids: highly sequence-selective DNA photocleavage by novel l-lysine derivatives. J. Am. Chem. Soc. 1995, 117:5590-5591.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5590-5591
    • Saito, I.1    Takayama, M.2    Kawanishi, S.3
  • 5
    • 0037151616 scopus 로고    scopus 로고
    • 1,8-Naphthalimides in phosphorescent organic LEDs: the interplay between dopant, exciplex, and host emission
    • Kolosov D., Adamovich V., Djurovich P., Thompson M.E., Adachi C. 1,8-Naphthalimides in phosphorescent organic LEDs: the interplay between dopant, exciplex, and host emission. J. Am. Chem. Soc. 2002, 124(33):9945-9954.
    • (2002) J. Am. Chem. Soc. , vol.124 , Issue.33 , pp. 9945-9954
    • Kolosov, D.1    Adamovich, V.2    Djurovich, P.3    Thompson, M.E.4    Adachi, C.5
  • 6
    • 77955094387 scopus 로고    scopus 로고
    • Density functional studies of the substituent effect on absorption and emission properties of 1,8-naphthalimide derivatives
    • Qi Q., Ha Y., Sun Y. Density functional studies of the substituent effect on absorption and emission properties of 1,8-naphthalimide derivatives. J. Mol. Model. 2010, 16:1179-1186.
    • (2010) J. Mol. Model. , vol.16 , pp. 1179-1186
    • Qi, Q.1    Ha, Y.2    Sun, Y.3
  • 8
    • 0034801770 scopus 로고    scopus 로고
    • Ultrafast molecular logic gate based on optical switching between two long-lived radical ion pair states
    • Lukas A.S., Bushard P.J., Wasielewski M.R. Ultrafast molecular logic gate based on optical switching between two long-lived radical ion pair states. J. Am. Chem. Soc. 2001, 123(10):2440-2441.
    • (2001) J. Am. Chem. Soc. , vol.123 , Issue.10 , pp. 2440-2441
    • Lukas, A.S.1    Bushard, P.J.2    Wasielewski, M.R.3
  • 10
    • 0034224241 scopus 로고    scopus 로고
    • Photoinduced electron transfer in covalently linked 1,8-naphthalimide/viologen systems
    • Le T.P., Rogers J.E., Kelly L.A. Photoinduced electron transfer in covalently linked 1,8-naphthalimide/viologen systems. J. Phys. Chem. A 2000, 104(29):6778-6785.
    • (2000) J. Phys. Chem. A , vol.104 , Issue.29 , pp. 6778-6785
    • Le, T.P.1    Rogers, J.E.2    Kelly, L.A.3
  • 11
    • 53849106505 scopus 로고    scopus 로고
    • A versatile amino acid analogue of the solvatochromic fluorophore 4-N,N-dimethylamino-1,8-naphthalimide: a powerful tool for the study of dynamic protein interactions
    • Loving G., Imperiali B. A versatile amino acid analogue of the solvatochromic fluorophore 4-N,N-dimethylamino-1,8-naphthalimide: a powerful tool for the study of dynamic protein interactions. J. Am. Chem. Soc. 2008, 130(41):13630-13638.
    • (2008) J. Am. Chem. Soc. , vol.130 , Issue.41 , pp. 13630-13638
    • Loving, G.1    Imperiali, B.2
  • 12
    • 0031466854 scopus 로고    scopus 로고
    • Photochemical mechanisms responsible for the versatile application of naphthalimides and naphthaldiimides in biological systems
    • Aveline B.M., Matsugo S., Redmond R.W. Photochemical mechanisms responsible for the versatile application of naphthalimides and naphthaldiimides in biological systems. J. Am. Chem. Soc. 1997, 119:11785-11795.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11785-11795
    • Aveline, B.M.1    Matsugo, S.2    Redmond, R.W.3
  • 14
    • 0037170795 scopus 로고    scopus 로고
    • Synthesis and photochemical protein crosslinking studies of hydrophilic naphthalimides
    • Zhang J.X., Woods R.J., Brown P.B., Lee K.D., Kane R.R. Synthesis and photochemical protein crosslinking studies of hydrophilic naphthalimides. Bioorg. Med. Chem. Lett. 2002, 12:853-856.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 853-856
    • Zhang, J.X.1    Woods, R.J.2    Brown, P.B.3    Lee, K.D.4    Kane, R.R.5
  • 16
    • 0001116731 scopus 로고    scopus 로고
    • Naphthalimides as anti-cancer agents: synthesis and biological activity
    • Braña M.F., Ramos A. Naphthalimides as anti-cancer agents: synthesis and biological activity. Curr. Med. Chem. Anti-Cancer Agents 2001, 1:237-255.
    • (2001) Curr. Med. Chem. Anti-Cancer Agents , vol.1 , pp. 237-255
    • Braña, M.F.1    Ramos, A.2
  • 19
    • 0037046764 scopus 로고    scopus 로고
    • Influence of the structure of the amino group and polarity of the medium on the photophysical behavior of 4-amino-1,8-naphthalimide derivatives
    • Saha S., Samanta A. Influence of the structure of the amino group and polarity of the medium on the photophysical behavior of 4-amino-1,8-naphthalimide derivatives. J. Phys. Chem. A 2002, 106:4763-4771.
    • (2002) J. Phys. Chem. A , vol.106 , pp. 4763-4771
    • Saha, S.1    Samanta, A.2
  • 20
    • 79952758402 scopus 로고    scopus 로고
    • Tunable solvatochromic response of newly synthesized antioxidative naphthalimide derivatives: intramolecular charge transfer associated with hydrogen bonding effect
    • Dhar S., Singha Roy S., Rana D.K., Bhattacharya S., Bhattacharya S., Bhattacharya S.C. Tunable solvatochromic response of newly synthesized antioxidative naphthalimide derivatives: intramolecular charge transfer associated with hydrogen bonding effect. J. Phys. Chem. A 2011, 115:2216-2224.
    • (2011) J. Phys. Chem. A , vol.115 , pp. 2216-2224
    • Dhar, S.1    Singha Roy, S.2    Rana, D.K.3    Bhattacharya, S.4    Bhattacharya, S.5    Bhattacharya, S.C.6
  • 21
    • 49649088030 scopus 로고    scopus 로고
    • Modulated photophysics of 3-pyrazolyl-2-pyrazoline derivative entrapped in micellar assembly
    • Banerjee P., Pramanik S., Sarkar A., Bhattacharya S.C. Modulated photophysics of 3-pyrazolyl-2-pyrazoline derivative entrapped in micellar assembly. J. Phys. Chem. B 2008, 112:7211-7219.
    • (2008) J. Phys. Chem. B , vol.112 , pp. 7211-7219
    • Banerjee, P.1    Pramanik, S.2    Sarkar, A.3    Bhattacharya, S.C.4
  • 22
    • 80051573410 scopus 로고    scopus 로고
    • Aqueous block copolymer-surfactant mixtures-surface tension, DLS and viscosity measurements and their utility in solubilization of hydrophobic drug and its controlled release
    • Thummar A.D., Sastry N.V., Verma G., Hassan P.A. Aqueous block copolymer-surfactant mixtures-surface tension, DLS and viscosity measurements and their utility in solubilization of hydrophobic drug and its controlled release. Colloids Surf. A: Physicochem. Eng. Aspects 2011, 386:54-64.
    • (2011) Colloids Surf. A: Physicochem. Eng. Aspects , vol.386 , pp. 54-64
    • Thummar, A.D.1    Sastry, N.V.2    Verma, G.3    Hassan, P.A.4
  • 24
    • 39149087662 scopus 로고    scopus 로고
    • Interaction of 1-anthracene sulphonate with cationic micelles of alkyl trimethyl ammonium bromides (CnTAB): a spectroscopic study
    • Sarkar A., Pramanik S., Banerjee P., Bhattacharya S.C. Interaction of 1-anthracene sulphonate with cationic micelles of alkyl trimethyl ammonium bromides (CnTAB): a spectroscopic study. Colloids Surf. A: Physicochem. Eng. Aspects 2008, 317:585-591.
    • (2008) Colloids Surf. A: Physicochem. Eng. Aspects , vol.317 , pp. 585-591
    • Sarkar, A.1    Pramanik, S.2    Banerjee, P.3    Bhattacharya, S.C.4
  • 26
    • 35148890859 scopus 로고    scopus 로고
    • Photophysics of a cationic biological photosensitizer in anionic micellar environments: combined effect of polarity and rigidity
    • Das P., Chakrabarty A., Mallick A., Chattopadhyay N. Photophysics of a cationic biological photosensitizer in anionic micellar environments: combined effect of polarity and rigidity. J. Phys. Chem. B 2007, 111:11169-11176.
    • (2007) J. Phys. Chem. B , vol.111 , pp. 11169-11176
    • Das, P.1    Chakrabarty, A.2    Mallick, A.3    Chattopadhyay, N.4
  • 27
    • 0035816204 scopus 로고    scopus 로고
    • Mechanism of tumor-targeted delivery of macromolecular drugs, including the EPR effect in solid tumor and clinical overview of the prototype polymeric drug SMANCS
    • Maeda H., Sawa T., Konno T. Mechanism of tumor-targeted delivery of macromolecular drugs, including the EPR effect in solid tumor and clinical overview of the prototype polymeric drug SMANCS. J. Controlled Release 2001, 74:47-61.
    • (2001) J. Controlled Release , vol.74 , pp. 47-61
    • Maeda, H.1    Sawa, T.2    Konno, T.3
  • 29
    • 0346569869 scopus 로고
    • Fluorescence quantum yield determinations. 9,10-Diphenylanthracene as a reference standard in different solvents
    • Morris J.V., Mahaney M.A., Huber J.R. Fluorescence quantum yield determinations. 9,10-Diphenylanthracene as a reference standard in different solvents. J. Phys. Chem. 1976, 80:969-974.
    • (1976) J. Phys. Chem. , vol.80 , pp. 969-974
    • Morris, J.V.1    Mahaney, M.A.2    Huber, J.R.3
  • 31
    • 22744435291 scopus 로고    scopus 로고
    • Near-infrared fluorescent probes: synthesis and spectroscopic investigations of a few amphiphilic squaraine dyes
    • Arun K.T., Ramaiah D. Near-infrared fluorescent probes: synthesis and spectroscopic investigations of a few amphiphilic squaraine dyes. J. Phys. Chem. A 2005, 109:5571-5578.
    • (2005) J. Phys. Chem. A , vol.109 , pp. 5571-5578
    • Arun, K.T.1    Ramaiah, D.2
  • 32
    • 0032119838 scopus 로고    scopus 로고
    • Energetics of micellization: reassessment by a high-sensitivity titration microcalorimeter
    • Majhi P.R., Moulik S.P. Energetics of micellization: reassessment by a high-sensitivity titration microcalorimeter. Langmuir 1998, 14:3986-3990.
    • (1998) Langmuir , vol.14 , pp. 3986-3990
    • Majhi, P.R.1    Moulik, S.P.2
  • 33
    • 33845560552 scopus 로고
    • Dynamic and static aspects of solubilization of neutral arenes in ionic micellar solutions
    • Almgren M., Grieser F., Thomas J.K. Dynamic and static aspects of solubilization of neutral arenes in ionic micellar solutions. J. Am. Chem. Soc. 1979, 101:279-291.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 279-291
    • Almgren, M.1    Grieser, F.2    Thomas, J.K.3
  • 34
    • 0000512832 scopus 로고    scopus 로고
    • The fluorescence response of a structurally modified 4-aminophthalimide derivative covalently attached to a fatty acid in homogeneous and micellar environments
    • Saroja G., Ramachandram B., Saha S., Samanta A. The fluorescence response of a structurally modified 4-aminophthalimide derivative covalently attached to a fatty acid in homogeneous and micellar environments. J. Phys. Chem. B 1999, 103:2906-2911.
    • (1999) J. Phys. Chem. B , vol.103 , pp. 2906-2911
    • Saroja, G.1    Ramachandram, B.2    Saha, S.3    Samanta, A.4
  • 35
    • 10944271894 scopus 로고    scopus 로고
    • Role of micellar size and hydration on solvation dynamics: a temperature dependent study in triton-X-100 and brij-35 micelles
    • Kumbhakar M., Goel T., Mukherjee T., Pal H. Role of micellar size and hydration on solvation dynamics: a temperature dependent study in triton-X-100 and brij-35 micelles. J. Phys. Chem. B 2004, 108:19246-19254.
    • (2004) J. Phys. Chem. B , vol.108 , pp. 19246-19254
    • Kumbhakar, M.1    Goel, T.2    Mukherjee, T.3    Pal, H.4
  • 37
    • 33745033613 scopus 로고    scopus 로고
    • Why are proteins charged? Networks of charge-charge interactions in proteins measured by charge ladders and capillary electrophoresis
    • Gitlin I., Carbeck J.D., Whitesides G.M. Why are proteins charged? Networks of charge-charge interactions in proteins measured by charge ladders and capillary electrophoresis. Angew. Chem. Int. Ed. 2006, 45:3022-3060.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3022-3060
    • Gitlin, I.1    Carbeck, J.D.2    Whitesides, G.M.3
  • 38
    • 77955044557 scopus 로고    scopus 로고
    • Macromolecular crowding remodels the energy landscape of a protein by favoring a more compact unfolded state
    • Hong J., Gierasch L.M. Macromolecular crowding remodels the energy landscape of a protein by favoring a more compact unfolded state. J. Am. Chem. Soc. 2010, 132:10445-10452.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 10445-10452
    • Hong, J.1    Gierasch, L.M.2
  • 40
    • 2142760512 scopus 로고
    • Environmental effects on vibronic band intensities in pyrene monomer fluorescence and their application in studies of micellar systems
    • Kalyanasundaram K., Thomas J.K. Environmental effects on vibronic band intensities in pyrene monomer fluorescence and their application in studies of micellar systems. J. Am. Chem. Soc. 1977, 99:2039-2044.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 2039-2044
    • Kalyanasundaram, K.1    Thomas, J.K.2
  • 42
    • 0346497602 scopus 로고    scopus 로고
    • Effect of the nature of the spacer on the aggregation properties of gemini surfactants in an aqueous solution
    • Wang X., Wang J., Wang Y., Yan H. Effect of the nature of the spacer on the aggregation properties of gemini surfactants in an aqueous solution. Langmuir 2004, 20:53-56.
    • (2004) Langmuir , vol.20 , pp. 53-56
    • Wang, X.1    Wang, J.2    Wang, Y.3    Yan, H.4
  • 43
    • 23844544802 scopus 로고    scopus 로고
    • Spectroscopic investigation on the interaction of ICT probe 3-acetyl-4-oxo-6,7-dihydro-12H indolo-[2,3-a] quinolizine with serum albumins
    • Mallick A., Haldar B., Chattopadhyay N. Spectroscopic investigation on the interaction of ICT probe 3-acetyl-4-oxo-6,7-dihydro-12H indolo-[2,3-a] quinolizine with serum albumins. J. Phys. Chem. B 2005, 109:14683-14690.
    • (2005) J. Phys. Chem. B , vol.109 , pp. 14683-14690
    • Mallick, A.1    Haldar, B.2    Chattopadhyay, N.3
  • 44
    • 0037195604 scopus 로고    scopus 로고
    • Water in confinement
    • Levinger N.E. Water in confinement. Science 2002, 298:1722-1723.
    • (2002) Science , vol.298 , pp. 1722-1723
    • Levinger, N.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.