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. 2020 Sep 23;59(48):21663–21670. doi: 10.1002/anie.202008700

Table 1.

Properties of compounds 110 (in DMSO) relevant for their photochromism.[a]

R

σ p [54]

S 0‐S 1 λ max (ϵ)

PSD

426 nm

PSD

526 nm

PSD 625 nm

φ t→c

φ c→t

φ c→t

×

ϵ c,426

φ t→c × ϵ t,526

φ t→c × ϵ t,625

half‐life at 25 °C

thermal cis to trans isomerization

trans

cis

[% cis]

[% cis]

[% cis]

[%]

[%]

[days]

ΔG calc [kJ mol−1]

ΔG exp [kJ mol−1]

ΔH exp [kJ mol−1]

ΔS exp [J mol−1]

1

NMe2

−0.83

483 (6301)

66

22

46

34

nd[b]

nd[b]

683

10

0.70

69.1

101.6

119.5

60.0

2

OMe

−0.27

463 (1100)

452 (1352)

15

58

88

63

51

506

264

8

14.3

72.4

108.7

107.6

−3.9

3

Me

−0.17

461 (814)

443 (1572)

15

56

90

30

72

963

87

<1

12.5

72.0

108.4

96.0

−41.7

4

H

0.0

457 (847)

441 (1569)

15

62

90

51

48

660

113

3

38.1

71.4

111.1

110.3

−2.9

5

SMe

0.0

465 (1616)

452 (2595)

18

52

87

21

37

663

155

4

7.4

70.0

107.1

103.6

−11.6

6

Cl

0.23

456 (866)

441 (1546)

12

54

89

43

nd[c]

nd[c]

104

6

32.4

72.2

110.7

113.5

9.2

7

OAc

0.31

444 (1324)

442 (1583)

12

55

85

57

73

1010

212

5

14.6

72.5

108.8

99.5

−31.0

8

OCF3

0.35

461 (618)

441 (1216)

12

52

87

41

nd[c]

nd[c]

87

2

28.6

72.4

110.4

111.0

1.9

9

CF3

0.54

459 (652)

444 (1290)

10

46

83

20

47

511

47

<1

4.4

73.1

105.8

118.1

41.5

10

NO2

0.78

467 (873)

448 (1673)

5

18

45

18

30

384

89

6

0.046

67.9

94.5

100.0

18.5

[a] Position of absorption maxima (λ max), molar attenuation coefficients (ϵ), photostationary state distributions (PSD) determined under blue (λ exc=426 nm), green (λ exc=526 nm), and red (λ exc=625 nm) light irradiation, quantum yields for forward switching determined at λ=532 nm irradiation (φ t→c), and for reverse switching (φ c→t) determined at λ=445 nm irradiation, photoswitching cross‐sections (φ×ϵ) at blue (λ exc=426 nm), green (λ exc=526 nm) and red (λ exc=625 nm) light, experimentally determined half‐life of the metastable cis isomer at 25 °C, and the calculated and measured activation barrier parameters for the thermal cis‐to‐trans isomerization. [b] Quantum yield for the reverse switching was not determined for compound 1 owing to the presence of the overlapping, bathochromically shifted π–π* band at the λ=445 nm part of the spectrum. [c] Quantum yield values could not be determined for compounds 6 and 8 owing to lack of clear convergence of obtained data to a convincing fit.