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R 1
R 1
Ph
Ph
N
R
meso
R
N
N
B
Ph
Ph
O
O
N
N
N
R 2
R 2
B
N
N
MeO
OMe
N
N
F
F
B
aza-BDP-VIII
B
F
F
BDP
generic structure
F
F
l abs = 765 nm
l em = 782 nm
F f = 0.18
e
= not available
MeO
OMe
aza-BDP-VI
R 1
R 1
l abs = 688 nm
l em = 715 nm
F f = 0.36
R 1
R = -OC 12 H 25
R 1
Solvent: CHCl 3
Ref. 130
= 85,000 cm - 1 M - 1
e
OMe, R 2 = H
l abs = 689 nm
l em = 710 nm
F f = 0.23
BDP-I R 1 =
-
R 1
N
N
B
R 2
R 2
= 173,900 cm - 1 M - 1
Solvent: CHCl 3
Ref. 128
F
F
e
O
O
N
N
BDP-IV R 1 = H, R 2 = Ph
R 2
R 2
B
l abs = 641 nm
l em = 663 nm
F f = 0.65
F
F
Solvent: CHCl 3
Ref. 126
Ph
Ph
= 103,700 cm - 1 M - 1
e
N
BDP-IX R 1 = H, R 2 = Ph
N
N
BDP-II R 1 = -OMe, R 2 =
l abs = 652 nm
l em = 661 nm
F f = 0.90
t
-Bu
Solvent: CH 2 Cl 2
Ref. 127
B
= 314,000 cm - 1 M - 1
e
F
F
l abs = 732 nm
= 127,900 cm - 1 M - 1
e
l em = 756 nm
F f = 0.34
R 1 = -OMe, R 2 =
MeO
OMe
Solvent: CHCl 3
Ref. 104
BDP-X R 1 = CF 3 , R 2 =
BDP-V
S
aza-BDP-VII
l abs = 732 nm
l em = 780 nm
F f = 0.16
Solvent: CHCl 3
Ref. 126
l abs = 740 nm
l em = 752 nm
F f = 0.28
= 77,800 cm - 1 M - 1
p
-MeO-C 6 H 4
e
= 159,000 cm - 1 M - 1
e
l abs = 723 nm
l em = 738 nm
F f = 0.56
R 1 = -N(CH 3 ) 2 , R 2 =
BDP-III
t
-Bu
= 253,000 cm - 1 M - 1
e
l abs = 797 nm
Solvent: CH 2 Cl 2
Ref. 127
Solvent: CHCl 3
Ref. 129
= 1,447,000 cm - 1 M - 1
e
l em = 835 nm
F f = 0.05
Solvent: CHCl 3
Ref. 131
Solvent: CHCl 3
Ref. 126
Chart 3.3 Structures and optical properties of representative red and near-IR BDP fluorophores.
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