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Table 1 Optical properities of polyamides 12-25, polyhydrazides 31, 32 and poly(1,3,4-oxadiazoles) 33, 34

From: Synthesis and characterization of thermally stable aromatic polyamides and poly(1,3,4-oxadiazole-amide)s nanoparticles containing pendant substituted bezamides

Polymer No

aλabs(nm)

εb(M-1 cm-1)

cλem(nm) (dλexat 300 nm)

12

292

2400

345, 647

13

288

4300

361, 696

14

286

20000

343, 642

15

278

7100

341, 650

16

284

12000

345, 650

17

276

4600

338, 646

18

297

17200

364, 407

325

18100

420, 744

19

285

6900

362, 644

323

9000

 

20

295

23500

347, 642

21

291

8500

340, 652

23

282

8700

341, 646

24

309

25000

346, 658

25

286

5200

336, 376

305

5700

400, 684

31

280

7700

357, 502

32

274

8400

363 (w), 427

33

283

10000

360 (w), 431

34

277

6800

363 (w), 428, 529 (w), 637(sh)

  1. aλabs: maximum wavelengths of absorption.
  2. bε: the molar absorption coefficient calculated from Beer-Lambert equation
  3. (A = ε x c x l); where A is absorbance, c is concentration, l = 1 cm).
  4. cλem: maximum wavelengths of emission.
  5. dλex: maximum wavelengths of excitation.