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Table 1 Fluorescence absorption and emission maxima of compound 7a-7f in various solvents.

From: Synthesis and photo-physical properties of fluorescent 1,3,5-triazine styryl derivatives

Solvents

7a

7b

7c

 

λmax

λem

Δλ

λmax

λem

Δλ

λmax

λem

Δλ

DCM

329(1.030)

389(1.048)

408(079)

79

341(0.549)

404(0.589)

403(149)

62

359(1.361)

408(482)

49

EtOAc

323(0.898)

377(0.852)

403(490)

80

320(0.488)

371(0.531)

392(201)

87

356(0.956)

403(490)

47

Acetone

329(0.793)

377(0.927)

406(688)

77

323(0.375)

380(0.550)

410(108)

72

354(1.157)

403(216)

49

EtOH

326(0.585)

380(0.727)

428(288)

102

332(0.420)

389(0.503)

424(131)

92

353(1.061)

410(166)

57

DMF

329(0.458)

377(0.628)

401(487)

72

332(0.475)

380(0.461)

392(183)

60

350(0.994)

411(132)

61

DMSO

326(0.908)

383(0.982)

428(087)

102

323(0.455)

377(0.539)

418(229)

95

353(0.979)

418(164)

65

Solvents

7d

7e

7f

 

λmax

λem

Δλ

λmax

λem

Δλ

λmax

λem

Δλ

DCM

410(1.864)

458(1000)

48

356(2.322)

400(1000)

44

356(1.305)

416(1000)

60

EtOAc

353(1.319)

410(1000)

57

350(1.992)

410(1000)

60

353(1.424)

416(1000)

63

Acetone

350(1.621)

410(1000)

60

374(2.099)

400(1000)

26

353(1.571)

408(684)

55

EtOH

362(1.209)

418(600)

56

389(1.521)

408(1000)

19

353(1.213)

413(937)

57

DMF

356(1.380)

413(561)

57

353(1.616)

403(681)

50

353(1.229)

413(363)

60

DMSO

356(1.507)

420(400)

64

353(2.252)

408(476)

55

359(1.166)

416(359)

57

  1. DCM: Dichloromethane; EtOAc: Ethyl acetate; EtOH: Ethyl alcohol; DMF: Dimethyforamide; DMSO: Dimethylsulphoxide.