Journal of Chemistry

Volume 2013 (2013), Article ID 794810, 7 pages

http://dx.doi.org/10.1155/2013/794810

Research Article

Synthesis of 2-(1-Benzofuran-2-yl)-4-(1,3-benzoxazol-2-yl/ 1,3-benzothiazol-2-yl) Quinolines as Blue Green Fluorescent Probes

Yadav D. Bodke,¹ Sheelavanth Shankerrao,¹ and Hosanagara N. Harishkumar²

¹Department of P. G. Studies and Research in Industrial Chemistry, School of Chemical Sciences, Kuvempu University, Shivamogga, Karnataka, Shankaraghatta 577 451, India

²Department of P. G. Studies and Research in Chemistry, School of Chemical Sciences, Kuvempu University, Shivamogga, Karnataka, Shankaraghatta 577 451, India

Received 8 June 2012; Revised 29 August 2012; Accepted 7 September 2012

Academic Editor: José M. G. Martinho

Copyright © 2013 Yadav D. Bodke et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

A series of novel 2-(1-benzofuran-2-yl)-4-(1,3 benzoxazol-2-yl/1,3-benzothiazol-2-yl) quinoline derivatives 4(a–d) were synthesized in one step by the reaction of 2-(1-benzofuran-2-yl) quinoline-4-carboxylic acids 3(a-b) with o-aminophenol and o-amino thiophenol, respectively, using polyphosphoric acid (PPA) as a cyclizing agent. The fluorescent properties of newly synthesized compounds were investigated in three different organic solvents like chloroform (CHCl₃), tetrahydrofuran (THF), and dimethyl sulfoxide (DMSO). The photophysical constants such as quantum yield and stokes shift were determined. From the results of fluorescence study, it is evident that all synthesized compounds are fluorescent in solution. Compound 4a emitted green light (490.4 nm, 518.2 nm, and 522.4 nm) with high quantum yield in all the three solvents, while compounds 4b, 4c, and 4d emitted green light (512 nm, 499 nm, 510 nm) only in polar solvent DMSO. All fluorescent probes exhibited a bathochromic shift on increase in polarity of the solvent.

1. Introduction

There is an ever-increasing interest in the development of efficient photoluminescent materials especially those which emit light in the blue region of the visible spectrum. These materials play a vital role in optoelectronic devices such as tunable lasers and amplifiers, optical fibers, switches, or modulators with diverse applications in optical communications, photonics, medicines, optical spectroscopy, and organic electroluminescent diode (OLED) [1].

Among the various nitrogen-containing heterocyclic compounds, quinolines occur predominately in nature appreciable to their stability and ease of generation. They exhibit pronounced biological activities [2], and many derivatives have been reported to possess fluorescent property, having wide application as organic electroluminescent devices[3, 4], biosensors [5, 6], detection of metal ions [7–9], and so forth. On the other hand, benzofuran chromophore with high photoluminescence (PL) and quantum efficiencies [10] found wide application as organic electroluminescent devices [11–13] and chemosensors [14, 15].

The present work describes the synthesis and characterization of six new dyes. Initially the two derivatives of 2-(1-benzofuran-2-yl) quinoline-4-carboxylic acid 3(a-b) were synthesized, and it was found that they emit light in the blue region of the spectrum. Further it was planned to modify the carboxylic acid functionality by electron donor benzoxazole and benzothiazole ring system. Therefore, the present investigation involves the synthesis and fluorescent studies of new 2-(1-benzofuran-2-yl)-4-(1,3-benzoxazol-2-yl/1,3-benzothiazol-2-yl) quinoline derivatives 4(a–d) with a motive of getting possible application as blue OLE materials. Here we selected an unique combination of three different fused heterocyclic ring systems, where quinoline ring acts as core moiety, benzofuran nucleus substituted at second position acts as chromophore, and 3-benzoxazol-2-yl /benzothiazol-2-yl rings substituted on the fourth position of quinoline nucleus act as an electron acceptor system.

2. Result and Discussion

2.1. Chemistry

The photoluminescence properties of 2-(1-benzofuran-2-yl) quinoline-4-carboxylic acids (3a-b) have prompted us to replace the carboxyl group with fused heterocyclic ring system like benzoxazole 4(a-b) and benzothiazole 4(c–d), and to study the effect of alteration on the photoluminescence properties. The intermediate compounds 3(a-b) were prepared by reported method [16], and structures were confirmed by spectral data. The title compounds 2-(1-benzofuran-2-yl)-4-(1, 3-benzoxazol-2-yl/ 1,3-benzothiazol-2-yl) quinolines (4a–d) were synthesized by reacting 2-(1-benzofuran-2-yl) quinoline-4-carboxylic acids (3a-b)with o-aminophenol and o-amino thiophenol, respectively, using polyphosphoric acid as cyclizing agent. The structures of newly synthesized compounds were confirmed by IR, ¹HNMR, ¹³CNMR, mass spectral data, and elemental analyses. The schematic representation of reaction has been shown in Scheme 1.

Scheme 1

2.2. Fluorimetric Properties

In order to perform the spectral characterization of the new dyes, absorption and emission spectra of compounds 3(a-b) were recorded in two different solvents, namely, THF and DMSO (as these two compounds are insoluble in chloroform), and absorption and emission spectra of compounds 4(a–d) were recorded in CHCl₃, THF, and DMSO. The absorption spectra have been shown in Figures 1(a)–1(c), and fluorescence spectra in Figures 2(a)–2(f) and the relevant data is tabulated in Table 1. All fluorescent probes exhibited a bathochromic shift of the emission peak with decreased intensity of emitted light on raising the polarity of solvents, and a related increase of the Stokes shift and decrease in quantum yield are observed. Fluorescent probes 3a and 3b emitted light in the blue region of the spectrum, and 2-(1-benzofuran-2-yl)-6-chloroquinoline-4-carboxylic acid (3b) showed bathochromic shift by 11.5 nm when compared to 2-(1-benzofuran-2-yl) quinoline-4-carboxylic acid 3a. This may be due to the presence of electron releasing chloro substitution on the 6th position of quinoline ring system in compound 3b, which acts as a chromophore. On replacing carboxylic group of 2-(1-benzofuran-2-yl) quinoline-4-carboxylic acid with benzoxazole 4(a-b) and benzothiazole 4(c-d), we found bathochromic shift in emission peaks and this may be attributed to the electron accepting tendency of benzoxazole and benzothiazole ring system, which decreases the energy gap between LUMO () and HOMO () leading to shift towards longer wavelength than compared to carboxylic acid. On increasing the solvent polarity, all compounds exhibited shift towards longer wavelength. The emission peaks are at lower energy or longer wavelength than compared to absorption peak; this loss of energy is due to a variety of dynamic processes, which occur following light absorption. The fluorophore is typically excited to the first singlet state (), usually to an excited vibrational level within . The excess vibrational energy is rapidly lost to the solvent. If the fluorophore is excited to the second singlet state (), it rapidly decays to the state in s due to internal conversion. Solvent effects shift the emission to still lower energy owing to stabilization of the excited state by the polar solvent molecules. Typically, the fluorophore has a larger dipole moment in the excited state than in the ground state. Following excitation, the solvent dipoles can reorient or relax at that state, which lowers the energy of the excited state. As the solvent polarity is increased, this effect becomes larger, resulting in emission at lower energies or longer wavelengths [16].

Table 1: Photoluminescence properties of compound (3a-b) and (4a–d).

Compound
Solvent
Absorption nm
Emission nm
Molar absorpivity Mol⁻¹ cm⁻¹
Stokes shift nm
Quantum yield

3a
THF
418.0
451.6
223.6 × 10⁴
33.6
0.183

DMSO
423.2
483.8
153.9 × 10⁴
60.6
0.165

3b
THF
430.4
462.8
305.8 × 10⁴
32.4
0.186

DMSO
430.4
491.8
197.3 × 10⁴
61.4
0.181

4a
Chloroform
441.6
490.4
164.7 × 10⁴
48.8
0.247

THF
446.0
518.2
201.0 × 10⁴
72
0.243

DMSO
446.4
522.4
127.9 × 10⁴
76
0.228

4b
Chloroform
432.0
485.8
228.4 × 10⁴
53.8
0.184

THF
432.2
470.2
216.4 × 10⁴
38
0.167

DMSO
442.0
512.0
713.2 × 10⁴
70
0.132

4c
Chloroform
427.0
465.4
79.4 × 10⁴
38.4
0.206

THF
426.8
468.2
62.5 × 10⁴
41.4
0.205

DMSO
430.0
499.2
181.4 × 10⁴
69.2
0.198

4d
Chloroform
427.0
468.2
76.1 × 10⁴
41.2
0.143

THF
426.8
478.0
97.1 × 10⁴
51.2
0.136

DMSO
423.6
510.6
69.2 × 10⁴
87
0.134

(a)

(b)

(c)

Figure 1: Absorption spectra of compounds 3(a-b) and 4(a–d) in different solvents; 1(a) chloroform, 1(b) THF, and 1(c) DMSO.

(a)   Emission spectra of 3a

(b) Emission spectra of 3b

(c) Emission spectra of 4a

(d) Emission spectra of 4b

(e) Emission spectra of 4c

(f) Emission spectra of 4d

Figure 2: Emission spectra of compounds 3(a-b) and 4(a–d) in different solvents.

From the absorption data (Table 1), it is evident that the absorption wavelengths are slightly varied or no variations are observed on increasing polarity of the solvents. This may be because absorption of light occurs in about  s, a time that is too short for motion of the fluorophore or solvent. Absorption spectra are not affected by the decrease in the excited-state energy, which occurs after absorption has occurred [16].

Among the tested compounds, compound 4a emitted light in the green region in all three solvents CHCl₃, THF, and DMSO at wavelength of 490.4 nm, 518.2 nm, and 522.4 nm, respectively. Compound 4b, 4c, and 4d emitted light in the green region only in polar solvent DMSO.

3. Experimental

All the chemicals used were of analytical grade. Melting points were determined in open capillary tubes and are uncorrected. Purity of the compounds was checked by TLC on silica gel. The IR spectra were recorded on Nicolet-Impact-410 FT-IR spectrometer, using KBr pellets. ¹H NMR spectra were recorded on a Bruker Supercon FT NMR (400 MHz) spectrometer in CDCl₃ or DMSO- using TMS as an internal standard. The chemical shifts are expressed in units. Mass spectra were recorded on a JEOL SX 102/DA-6000 (10 kV) FAB mass spectrometer.

3.1. Synthesis of 2-(1-Benzofuran-2-yl) Quinoline-4-carboxylic Acid 3(a-b)

3.1.1. General Procedure

The compounds 3a-b were synthesized by the Pfitzinger method [17], with the slight modification in procedure. After completion of the reaction, the reaction mixture was cooled to room temperature, diluted with cold water and extracted using ethyl acetate to suspend the impurities in organic layer. The aqueous layer was acidified with dilute hydrochloric acid and the resulting yellow solid mass was filtered and dried to get pure compound.

3.1.2. 2-(1-Benzofuran-2-yl) Quinoline-4-carboxylic Acid (3a)

Yield, 88%, m.p. 245–248°C, (literature 248–50°C) [17], IR (KBr) (, cm⁻¹), 3426.9 (OH), 1702.1 (C=O), 1599, 1510, 1246: ¹H NMR (DMSO-, 400 MHz): 14.15 (s, 1H, COOH), 8.70–8.72 (, , 1H Ar–H), 8.48 (s, 1H quinoline 3C–H), 8.18–8.20 (, , 1H Ar–H), 8.014–8.018 (, , 1H, Ar–H), 7.78–7.82 (q, 2H, Ar–H), 7.72–7.77 (t, 1H, Ar–H), 7.45–7.49 (t, 1H,Ar–H), 7.34–7.38 (t, 1H, Ar–H). MS: (), 291.1 ().

3.1.3. 2-(1-Benzofuran-2-yl)-6-chloroquinoline-4-carboxylic Acid (3b)

Yield, 76%, m.p. 283–285°C, IR (KBr) (, cm⁻¹) 3436 (OH), 1712 (C=O), 1570, 1514, 720, 640. ¹H NMR (DMSO-, 400 MHz): 13.85 (s, 1H, COOH) 8.80–8.82 (, , 1H Ar–H) 8.55 (s, 1H quinoline 3C–H), 8.17–8.20 (, , 1H Ar–H), 7.94 (s, 1H, furan–H), 7.89–7.91 (, , 1H, Ar–H), 7.77–7.81 (q, 2H, Ar–H), 7.44–7.49 (t, 1H, Ar–H), 7.34–7.37 (t, 1H, Ar–H). MS: (). Anal. Calc. (in %) for C₁₈H₁₀NO₃: C, 67.05; H, 2.48; N, 4.32. Found: C, 67.25; H, 2.68; N, 4.43.

3.2. Synthesis of 2-(1-Benzofuran-2-yl)-4-(1,3-benzoxazol- 2-yl/1,3-benzothiazol-2-yl) Quinoline Derivatives 4(a–d)

3.2.1. General Procedure

A mixture of 2-(1-benzofuran-2-yl) quinoline-4-carboxylic acid (3a-b) (0.5 mmol) and o-amino phenol/o-amino thiophenol was dissolved in 15 gm of polyphosphoric acid. The reaction mixture was heated with stirring at about 120–130°C for 8 hrs. After completion of the reaction, the reaction mixture was cooled, poured on to crushed ice, and neutralized using aqueous NaOH solution. The resulting solid was dried and purified by extracting using petroleum ether.

3.2.2. 2-(1-Benzofuran-2-yl)-4-(1, 3-benzoxazol-2-yl) Quinoline (4a)

Yield, 66%, m.p. 162–164°C, ¹H NMR (DMSO-, 400 MHz): 9.45–9.49 (, , 1H), 8.89 (s, 1H), 8.21–8.29 (t, , 1H), 7.958–8.009 (m, 4H), 7.831–7.899 (m, 3H), 7.602–7.644 (m, 2H), 7.469–7.581 (m, 1H), 7.361–7.402 (q, 1H), ¹³CNMR (CDCl₃, 100.5 MHz): 102.4 (1C), 103.2 (1C), 110.6 (1C), 111.5(1C), 119.1 (1C), 120.0 (1C), 120.9 (1C), 122.9 (1C), 123.8 (2C), 124.9 (1C), 125.1 (1C), 126.9 (1C), 128.3 (1C), 128.9(1C), 130.1 (1C), 142.2 (1C), 144.9(1C), 147.5 (1C), 149.9 (1C), 150.0 (1C), 155.3 (1C), 158.1 (1C), 162.7 (1C), MS: (), 364.2 (). Anal.Calc. (in %) for C₂₄H₁₄N₂O₂: C, 79.86; H, 3.86; N, 7.72. Found: C, 79.40; H, 3.95; N, 7.62.

3.2.3. 2-(1-Benzofuran-2-yl)-4-(1, 3-benzoxazol-2-yl)-6-chloroquinoline (4b)

Yield, 58%, m.p. 145–148°C, ¹H NMR (DMSO-, 400 MHz): 9.599 (s, 1H), 8.898 (s, 1H), 8.201–8.223 (, , 1H), 7.993–7.995 (, , 1H), 7.684–7.977 (m, 5H), 7.401–7.484 (m, 2H), 7.324–7.343 (t, 1H), 7.25–7.268 (m, 1H), ¹³CNMR (CDCl₃, 100.5 MHz): 102.4 (1C), 103.2 (1C), 110.6 (1C), 111.5 (1C), 119.1 (1C), 120.0 (1C), 120.9 (1C), 122.9 (1C), 123.8 (2C), 124.9 (1C), 125.1 (1C), 125.8 (1C), 130.1 (1C), 131.2 (1C), 132.6 (1C), 142.2 (1C), 144.9 (1C), 147.5 (1C), 149.9 (1C), 150.0 (1C), 155.3 (1C), 158.1 (1C), 162.7 (1C). MS: (), 399.8 (). Anal.Calc. (in %) for C₂₄H₁₃ClN₂O₂: C, 72.57; H, 3.25; N, 7.02. Found: C, 72.23; H, 3.85; N, 6.60.

3.2.4. 2-(1-Benzofuran-2-yl)-4-(1, 3-benzothiazol-2-yl) Quinoline (4c)

Yield, 63%, m.p. 178–180°C, ¹H NMR (DMSO-, 400 MHz): 8.90–8.98 (, , 1H), 8.56(s, 1H), 8.21–8.42 (m, , 3H), 8.02 (s, 1H), 7.939–7.963 (q, 1H), 7.787–7.844 (m, 3H), 7.626–7.728 (m, 2H), 7.465–7.504 (q, 1H), 7.361–7.463 (q, 1H), ¹³CNMR (CDCl₃, 100.5 MHz): 102.4 (1C), 103.2 (1C), 111.5 (1C), 119.1 (1C), 120.0 (1C), 120.9 (1C), 121.8 (1C), 122.9 (1C), 123.8 (1C), 125.1 (1C), 125.6 (1C), 126.0 (1C), 126.9 (1C), 128.3 (1C), 128.9 (1C), 130.1 (1C), 135.5 (1C), 144.9 (1C), 147.5 (1C), 149.9 (1C), 153.5 (1C), 155.3 (1C), 158.1 (1C), 162.7 (1C), MS: (). Anal. Calc. (in %) for C₂₄H₁₄N₂OS: C, 76.16; H, 3.69; N, 7.39. Found: C, 76.03; H, 3.55; N, 7.30.

3.2.5. 2-(1-Benzofuran-2-yl)-4-(1, 3-benzothiazol-2-yl)-6-chloroquinoline (4d)

Yield, 70%, m.p. 165–168°C, ¹H NMR (DMSO-, 400 MHz): 9.16 (s, 1H), 8.78 (s, 1H), 8.201–8.223 (, , 1H), 7.993–7.995 (, , 1H), 7.686–7.979 (m, 5H), 7.401–7.484 (m, 2H), 7.324–7.343 (t, 1H), 7.25–7.268 (m, 1H), ¹³CNMR (CDCl₃, 100.5 MHz): 102.4 (1C), 103.2 (1C), 111.5 (1C), 119.1 (1C), 120.0 (1C), 120.7 (1C), 121.8, 122.9 (1C), 123.8 (1C), 125.1 (1C), 125.6 (1C), 125.9 (1C), 126.0, 130.5 (1C), 131.5 (1C), 132.6 (1C), 135.5, 144.9 (1C), 146.1 (1C), 149.9 (1C), 153.5, 155.3 (1C), 158. 1 (1C), 162.7 (1C). MS: (), 414.9 (). Anal. Calc. (in %) for C₂₄H₁₃ClN₂OS: C, 69.8; H, 3.14; N, 6.78. Found: C, 69.4; H, 3.22; N, 6.67.

3.3. Fluorescent Studies

The fluorescence spectra were recorded on F-7000 spectrofluorometer (Hitachi) with Xenon flash lamp. The spectra were recorded by preparing the solutions of test compounds at the concentration of  mole/mL in three different solvents CHCl₃, THF, and DMSO. The solutions of each sample were scanned after keeping it at room temperature for about 1 h. The emission and excitation wavelength data are recorded using glass cuvettes. The emission quantum yields were determined at corresponding to the maximum of the absorption band () of quinine sulphate in 0.1 M H₂SO₄, which was used as a fluorimetric standard ().

4. Conclusion

In conclusion, we have demonstrated a convenient and efficient method for the synthesis of an important class of 2-(1-benzofuran-2-yl)-4-(1,3-benzoxazol-2-yl/ benzothiazol-2-yl) quinolines (4a–d) by reacting 2-(1-benzofuran-2-yl) quinoline-4-carboxylic acids (3a-b) with o-aminophenol and o-aminothiophenol respectively using PPA as cyclizing agent. All synthesized compounds displayed good fluorescent properties.

Acknowledgments

The authors are thankful to USIC, Karnataka University Dharwad for providing fluorescence spectra. One of the authors (S. Shankerro) is thankful to DST-Government of India, for awarding Inspire fellowship.

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