Skip to main content
. Author manuscript; available in PMC: 2018 Feb 12.
Published in final edited form as: Chemistry. 2016 Mar 23;22(18):6361–6367. doi: 10.1002/chem.201600547

Table 1.

Optical properties of o-nitrophenylenthanols with various substituted groups and their corresponding oxindoles.[a]

graphic file with name nihms935909u1.jpg
Compds R1 R2 λmax[c] [nm] λmax[d] [nm] λem[e] [nm] φ[f] F/F0[g]
11a COOCH3 H 254 334 520 0.36 800
22a H COOCH3 230 290 401 0.15 200
33a COOCH3 OCH3 334 321 502 0.17 230
44a CN H 254 290 514 0.047 32
55a CHO H 258 317 585 0.13 161
66a COOH H 262 282 485 0.027 21
77a H H 260 281 450 0.001 3
88a CH2OH H 273 321 420 0.001 5
99a OCH3 H 312 325 458 0.001 5
10 H OCH3 345 275 457 0.002 6
[a]

All the spectra were recorded in MeOH/PBS (3:1, v/v) solution with a concentration of 10 μM.

[b]

Fluorescence emission was not detected.

[c]

Absorption maxima in the 225–450 nm region for compound 110.

[d]

Absorption maxima in the 250–450 nm region for compound 1a–10 a.

[e]

Fluorescence emission in the 400–650 nm region.

[f]

Fluorescence quantum yields were measured using fluorescein (1a, 3a, 4a, and 5a) and DAPI (2a and 6a10a) as standards.

[g]

Obtained by comparing the integrated area of emission.