Rational design and synthesis of a novel class of highly fluorescent rhodamine dyes that have strong absorption at long wavelengths

Tetrahedron Letters

Volumn 44, Issue 23, 2003, Pages 4355-4359

  Liu, Jixiang ^a   Diwu, Zhenjun ^b   Leung, Wai Yee ^a   Lu, Yixin ^a   Patch, Brian ^a   Haugland, Richard P ^a  

^a MOLECULAR PROBES INC   (United States)

^b MOLECULAR DEVICES CORPORATION   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCENT DYE; RHODAMINE;

ARTICLE; CHROMATOPHORE; CONJUGATION; LIGHT ABSORPTION; QUANTUM YIELD; SPECTRAL SENSITIVITY; SYNTHESIS;

EID: 0038369773     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)00938-9     Document Type: Article

References (10)

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2. For a sourcebook and comprehensive references, see: Haugland R.P. Handbook of Fluorescent Probes and Research Products. 9th ed. 2002;Molecular Probes, Inc. Eugene, OR, USA.
3. Sauer M., Han K.-T., Muller R., Nord S., Schulz A., Seeger S., Wolfrum J., Arden-Jacob J., Deltau G., Marx N.J., Zander C., Drexhage K.H. J. Fluoresc. 5:1995;247-261.
4. Herrmann, R.; Josel, H. P.; Drexhage, K. H.; Arden-Jacob, J. US Patent 5,750,409, 1998.
5. Benson, S. C.; Lam, J. Y. L.; Menchen, S. M. US Patent 5,936,087, 1999.
6. Forster T. Fluoreszenz Organischer Verbindungen. 1951;Vandenhoeck and Ruprecht, Gottingen.
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8. +].
9. Arden, J.; Deltau, G.; Huth, V.; Kringel, U.; Peros, D.; Drexhage, K. H. J. Luminesc. 1991, 48 and 49, 352-358.
10. For bioconjugates and applications, see: Diwu, Z.; Liu, J.; Haugland, R. P.; Gee, K. R. PCT Int. Appl. WO 02 12,195, 2002.