Table 2 Photophysical properties of selected compounds

From: Organocatalytic iminium-assisted asymmetric B(sp²)-to-B(sp³) transformation

3

solvent

\({\lambda }_{{{{\rm{abs}}}}}^{\max }\)(nm)a

εabs (M1 cm−1)

Ф (%)b

\({\lambda }_{{{{\rm{em}}}}}^{\max }\)(nm)

Stokes shiftc (cm−1)

3a

CH2Cl2

434, 309

10600, 22600

2

540

4520

THF

430, 308

9800, 19600

1

541

4770

CH3CN

425, 308

10800, 22000

1

538

4940

Solid

  

4

548

 

3h

CH2Cl2

438, 304

24500, 4000

3

511

3260

THF

435, 305

26500, 5300

2

517

3650

CH3CN

431, 304

26700,5000

2

509

3560

Solid

  

49

548

 

3l

CH2Cl2

455

26700

4

517

2640

THF

451

25100

2

519

2910

CH3CN

450

29100

2

513

2730

Solid

  

56

599

 

3n

CH2Cl2

425

16000

1

563

5770

3o

CH2Cl2

425

18000

<1

536

4870

4j

CH2Cl2

425

14400

<1

672

8650

4q

CH2Cl2

447

16100

3

506

2610

  1. aCorresponding to the strongest absorption maximum. bAbsolute fluorescence quantum yield. cThe stokes shifts values of are rounded on the nearest 10 cm−1.