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Table 1 The λ max and molar absorptivities of different classes of compounds

From: Benzimidazole, coumrindione and flavone derivatives as alternate UV laser desorption ionization (LDI) matrices for peptides analysis

S.N

Matrix classes

Structure

λmax (nm)

єa

Log Ñ”

 

Class (I) Benzimidazole derivatives

   

1.

4-(1H-Benzimidazol-2-yl)phenol

299

19041

4.3

2.

5-(1H-Benzimidazol-2-yl)-2-ethoxyphenol hydrate

229

16437

4.2

3.

2-(3-Chlorophenyl)-1H-benzimidazole

298

10987

4.0

4.

2-(1-Naphthyl)-1H-benzimidazole

230

13705

4.1

5.

2-(3,4-Dimethoxyphenyl)-1-phenyl-1H- benzimidazole

223

24942

4.4

6.

2-(1H-Benzimidazol-2-yl)-5-hydroperoxyphenol

315

20238

4.3

7.

2-(4-Isopropylphenyl)-1H-benzimidazole

298

19812

4.3

8.

3-(1H-Benzimidazol-2-yl) phenol

213

7143

3.8

9.

2-(1H-Benzimidazol-2-yl)-4-chlorophenol

214

9313

4.0

10.

2-(4-Ethoxyphenyl)-1H-benzimidazole

298

14002

4.1

11.

N, N-Dimethyl-4-(1-phenyl-1H-benzimidazol-2-yl) aniline

325

28295

4.4

12.

2-(3,4-Dimethoxyphenyl)-1H-benzimidazole

298

15107

4.2

13.

2-(3,4-Dichlorophenyl)-1H-benzimidazole

309

17452

4.2

14.

2-(1H-Benzimidazol-2-yl)-1,4-benzenediol

213

13545

4.1

 

Class-11 (Coumarin derivative)

   

15.

3-[(5-Methyl-2-furyl)methylidene]-2H-chromene-2,4-dione

213

16009

4.2

16.

3-[(2-Bromophenyl)methyl idene]-2H-chromene-2,4-dione

213

10209

4.0

17.

3-[(2-Nitrophenyl)methyl idene]-2H-chromene-2,4-dione

214

16985

4.2

18.

3-[(2,4-Dihydroxy phenyl)methylidene]-2H-chromene-2,4-dione

212

15120

4.2

19.

3-[2-Furylmethylidene]-2H-chromene-2,4-dione

214

16067

4.2

20.

3-[(2,3,4-Trihydroxyphenyl) methyl idene]-2H-chromene-2,4-dione

213

16720

4.2

21.

3-[(2-Ethoxyphenyl)methyl idene]-2H-chromene-2,4-dione

213

23618

4.4

22.

3-[(2-Hydroxy-3-methoxy phenyl)methylidene]-2H-chromene-2,4-dione

214

11682

4.1

23.

3-[(2-Fluorophenyl) methylidene]-2H-chromene-2,4-dione

213

13596

4.1

24.

3-[(3-Fluorophenyl) methylidene]-2H-chromene-2,4-dione

279

21981

4.3

25.

3-[(4-Hydroxyphenyl)methyl idene]-2H-chromene-2,4-dione

298

16720

4.2

26.

4-Methyl-2H-chromen-2-one

324

5779

3.8

 

Class-III (Flavones)

   

27.

7-Hydroxy-2-phenyl-4H-chromen-4-one

306

17642

4.2

28.

5-Methyl-2-phenyl-4H-chromen-4-one

261

15211

4.2

29.

5,7-Dihydroxy-2-phenyl-4H-chromen-4-one

268

22629

4.4

30.

2-(3,4-Dimethoxyphenyl)-4H-chromen-4-one

334

17175

4.2

31.

2-(3,4-Dimethoxyphenyl)-7-methyl-4H-chromen-4-one

334

14432

4.1