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. Author manuscript; available in PMC: 2017 Feb 1.
Published in final edited form as: J Photochem Photobiol A Chem. 2016 Feb 1;316:104–116. doi: 10.1016/j.jphotochem.2015.05.033

Table 1.

Styryl and bis-styryl fluorophores in solution

Namea Chemical Structure λAbsb, nm λEm c, nm
(Intensity)d
d1
(BMB)a 		graphic file with name nihms-698578-t0001.jpg 408 495
(106,800)
d2 graphic file with name nihms-698578-t0002.jpg 362 414
(246,900)
d3 graphic file with name nihms-698578-t0003.jpg 383 448
(84,300)
d4 graphic file with name nihms-698578-t0004.jpg 400 575
(200)
d5 graphic file with name nihms-698578-t0005.jpg 415 511
(93,300)
d6 graphic file with name nihms-698578-t0006.jpg 385 522
(2,800)
d7
(GE3082)a 		graphic file with name nihms-698578-t0007.jpg 417 491, 621*
(1,700; 2,520*)
d8 graphic file with name nihms-698578-t0008.jpg 412 518 (264)
d9
(GE3111)a 		graphic file with name nihms-698578-t0009.jpg 412 480, 624*
(2,250; 4,700*)
d10
(GE3126)a 		graphic file with name nihms-698578-t0010.jpg 414 510, 618*
(2,100; 3,970*)
d11 graphic file with name nihms-698578-t0011.jpg 396 532
(12,640)
d12 graphic file with name nihms-698578-t0012.jpg 467 582
(180)
d13 graphic file with name nihms-698578-t0013.jpg 419 533
(2,900)
d14 graphic file with name nihms-698578-t0014.jpg 482 649
(150)
a

The d-numbering scheme for each dye is used for simplicity. For previously published fluorophores, the original designations are shown in parenthesis.

b

Absorbance maximum wavelength measured in DMSO

c

Emission maximum wavelength measured in DMSO, the relative fluorescence intensity at the maximum wavelength shown in parenthesis

d

Relative emission intensity values at λEm RFU. For dual emissions, the emission intensities in parentheses correspond to the λEm shown, respectively.

*

Dual emission (TICT) in polar solvents.