Research Article

Linear and Angular Distyrylpyrazines with Terminal Donor Groups: Synthesis, Solvatochromism, and Acidochromism of the Electronic Spectra

Table 2

Solvatochromism of distyrylpyrazines 1–10, 𝜆 𝑚 𝑎 𝑥 /nm, ε /L mol−1 cm−1; 𝐸 𝑁 𝐼 [35].

Comp.CyclohexaneTolueneDichloromethaneAcetonitrileEthanol 𝜀 m a x (DCM)

E N I 0.0060.0990.3090.4600.654
1 𝜆 m a x 38238638337938143537
𝜆 F m a x 424428432429443
2 𝜆 m a x 37637937737337446865
𝜆 F m a x 415422423419428
3 𝜆 m a x 399405402397400
𝜆 F m a x 439453465463482
4 𝜆 m a x 407413409407407
𝜆 F m a x 448463476478501
5 𝜆 m a x 402406402399400
𝜆 F m a x 449463489499514
6 𝜆 m a x 40440840539840361976
𝜆 F m a x 451463495504520
7 𝜆 m a x 42342742742042358692
𝜆 F m a x 464478501501517
8 𝜆 m a x 400404400397400
𝜆 F m a x 440453463462482
9 𝜆 m a x 391397395395397
𝜆 F m a x 427443461471498
10 𝜆 m a x 376380381383382
𝜆 F m a x 424446474495513