메뉴 건너뛰기




Volumn 113, Issue , 2015, Pages 27-37

A microwave-assisted and environmentally benign approach to the synthesis of near-infrared fluorescent pentamethine cyanine dyes

Author keywords

Aqueous reaction methodology; Density functional theory; Dioxolane; Fluorescence; Microwave assisted organic synthesis (MAOS); Pentamethine cyanine dye

Indexed keywords

DENSITY FUNCTIONAL THEORY; FLUORESCENCE; SULFUR COMPOUNDS;

EID: 84906691672     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2014.07.035     Document Type: Article
Times cited : (29)

References (16)
  • 1
    • 84862988695 scopus 로고    scopus 로고
    • Two-wavelength near-infrared fluorescence for the quantitation of drug antiplatelet effects in large animal model systems
    • Y. Ashitate, S.H. Kim, E. Tanaka, M. Henary, H.S. Choi, and J.V. Frangioni et al. Two-wavelength near-infrared fluorescence for the quantitation of drug antiplatelet effects in large animal model systems J Vasc Surg 56 2012 171 180
    • (2012) J Vasc Surg , vol.56 , pp. 171-180
    • Ashitate, Y.1    Kim, S.H.2    Tanaka, E.3    Henary, M.4    Choi, H.S.5    Frangioni, J.V.6
  • 2
    • 80055036100 scopus 로고    scopus 로고
    • The effect of varying short-chain alkyl substitution on the molar absorptivity and quantum yield of cyanine dyes
    • G. Chapman, M. Henary, and G. Patonay The effect of varying short-chain alkyl substitution on the molar absorptivity and quantum yield of cyanine dyes Anal Chem Insights 6 2011 29 36
    • (2011) Anal Chem Insights , vol.6 , pp. 29-36
    • Chapman, G.1    Henary, M.2    Patonay, G.3
  • 3
    • 78149419820 scopus 로고    scopus 로고
    • Synthesis and characterization of new γ-substituted pentamethine cyanine dyes
    • A.M. Mehranpour, S. Hashemnia, and R. Maghamifar Synthesis and characterization of new γ-substituted pentamethine cyanine dyes Synth Commun 40 2010 3594 3602
    • (2010) Synth Commun , vol.40 , pp. 3594-3602
    • Mehranpour, A.M.1    Hashemnia, S.2    Maghamifar, R.3
  • 4
    • 3242789350 scopus 로고    scopus 로고
    • Noncovalent labeling of biomolecules with red and near-infrared dyes
    • G. Patonay, J. Salon, J. Sowell, and L. Strekowski Noncovalent labeling of biomolecules with red and near infrared dyes Molecules 9 2004 40 49 (Pubitemid 38982439)
    • (2004) Molecules , vol.9 , Issue.3 , pp. 40-49
    • Patonay, G.1    Salon, J.2    Sowell, J.3    Strekowski, L.4
  • 5
    • 79960835810 scopus 로고    scopus 로고
    • A review of NIR dyes in cancer targeting and imaging
    • S. Luo, E. Zhang, Y. Su, T. Cheng, and C. Shi A review of NIR dyes in cancer targeting and imaging Biomaterials 32 2011 7127 7138
    • (2011) Biomaterials , vol.32 , pp. 7127-7138
    • Luo, S.1    Zhang, E.2    Su, Y.3    Cheng, T.4    Shi, C.5
  • 7
    • 77649331093 scopus 로고    scopus 로고
    • Development and application of a near-infrared fluorescence probe for oxidative stress based on differential reactivity of linked cyanine dyes
    • D. Oushiki, H. Kojima, T. Terai, M. Arita, K. Hanaoka, and Y. Urano et al. Development and application of a near-infrared fluorescence probe for oxidative stress based on differential reactivity of linked cyanine dyes J Am Chem Soc 132 2010 2795 2801
    • (2010) J Am Chem Soc , vol.132 , pp. 2795-2801
    • Oushiki, D.1    Kojima, H.2    Terai, T.3    Arita, M.4    Hanaoka, K.5    Urano, Y.6
  • 9
    • 79951670919 scopus 로고    scopus 로고
    • Cyanine dyes in biophysical research: The photophysics of polymethine fluorescent dyes in biomolecular environments
    • M. Levitus, and S. Ranjit Cyanine dyes in biophysical research: the photophysics of polymethine fluorescent dyes in biomolecular environments Q Rev BIOPHYS 44 2011 123 151
    • (2011) Q Rev BIOPHYS , vol.44 , pp. 123-151
    • Levitus, M.1    Ranjit, S.2
  • 11
  • 12
    • 77952363968 scopus 로고    scopus 로고
    • Near IR heptamethine cyanine dye-mediated Cancer imaging
    • X. Yang, C. Shi, R. Tong, W. Qian, H.E. Zhau, and R. Wang et al. Near IR heptamethine cyanine dye-mediated Cancer imaging Clin Cancer Res 16 2010 2833 2844
    • (2010) Clin Cancer Res , vol.16 , pp. 2833-2844
    • Yang, X.1    Shi, C.2    Tong, R.3    Qian, W.4    Zhau, H.E.5    Wang, R.6
  • 13
    • 80455176526 scopus 로고    scopus 로고
    • Cyanine dyes as contrast agents for near-infrared imaging in vivo: Acute tolerance, pharmacokinetics, and fluorescence imaging
    • 066003-1-9
    • B. Ebert, B. Riefke, U. Sukowski, and K. Licha Cyanine dyes as contrast agents for near-infrared imaging in vivo: acute tolerance, pharmacokinetics, and fluorescence imaging J Biomed Opt 16 2011 066003-1-9
    • (2011) J Biomed Opt , vol.16
    • Ebert, B.1    Riefke, B.2    Sukowski, U.3    Licha, K.4
  • 14
    • 77957660114 scopus 로고    scopus 로고
    • Development of photostable near-infrared cyanine dyes
    • A. Samanta, M. Vendrell, R. Das, and Y.-T. Chang Development of photostable near-infrared cyanine dyes Chem Commun 46 2010 7406 7408
    • (2010) Chem Commun , vol.46 , pp. 7406-7408
    • Samanta, A.1    Vendrell, M.2    Das, R.3    Chang, Y.-T.4
  • 16
    • 0031988673 scopus 로고    scopus 로고
    • Synthesis and characterization of indodicarbocyanines
    • D. Zhifei, and P. Bixian Synthesis and characterization of indodicarbocyanines Dyes Pigments 36 1998 169 175
    • (1998) Dyes Pigments , vol.36 , pp. 169-175
    • Zhifei, D.1    Bixian, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.