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. Author manuscript; available in PMC: 2012 Aug 10.
Published in final edited form as: J Am Chem Soc. 2011 Jul 15;133(31):11912–11915. doi: 10.1021/ja204758c

Table 1.

Photophysical properties of the taxoid-pyrazolines and fluorescence turn-on efficiencya

Com-
pound
λmax
b
(nm)
εc
(M−1cm−1)
ε405d
(M−1cm−1)
λem
(nm)
ΦFe Fluorescence
turn-onf
1 310 6,400 460 ND ND -
1a 330 5,100 2,000 617 0.0024 21-fold
1ag 340 4,400 1,600 580 0.036 34-fold
2 311 12,000 540 ND ND -
2a 332 8,700 3,000 614 0.0041 30-fold
2ag 344 11,600 4,700 587 0.022 101-fold
3 262h 24,400 ND ND ND -
3a 358 12,900 6,900 584 0.034 111-fold
4 276h 30,300 ND ND ND -
4a 336 16,400 3,100 528 0.056 112-fold
a

Compounds were dissolved in ACN/PBS (1:1) to derive concentrations of 25 µM unless noted otherwise.

b

λmax in the 300 ~ 500 nm region.

c

Extinction coefficient at λmax.

d

Extinction coefficient at 405 nm.

e

Quantum yields were measured using DAPI as a standard (see ref. 20), and integrated over 415–790 nm.

f

Obtained by comparing the emission intensities at λem; λex = 405 nm.

g

Dissolved in DCM.

h

λmax in the 250 ~ 500 nm region.

ND = not detected.