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Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines

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Institut UTINAM UMR CNRS 6213, Université de Franche-Comté, Faculté des Sciences et des Techniques, 16 Route de Gray, 25030 Besançon, France; Tel.: +33-3-81676291, Fax: +33-3-81676738
  1. Corresponding author email
Associate Editor: P. J. Skabara
Beilstein J. Org. Chem. 2012, 8, 379–389. https://doi.org/10.3762/bjoc.8.41
Received 18 Nov 2011, Accepted 27 Feb 2012, Published 12 Mar 2012
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Abstract

Different synthetic routes leading to terpyridines functionalised with furan heterocycles are reviewed. The methodologies used to prepare such compounds include the ring closure of 1,5-diketones and cross-coupling reactions. These versatile terpyridines and their derived metal complexes find applications in various fields including coordination chemistry, medicinal chemistry and material sciences.

Keywords: chelate complexes; furan; heterocycles; oligopyridines; terpyridine

Introduction

Since their discovery [1,2] in the 1930s, 2,2’:6’,2’’-terpyridines (tpy) (Figure 1) have attracted widespread attention because of their excellent complexing properties as N-donor ligands toward numerous main-group, transition-metal and lanthanide cations [3].

[1860-5397-8-41-1]

Figure 1: Structure and atomic numbering of 2,2’:6’,2’’-terpyridines.

Coordination compounds LnM(tpy)m (n = 0–4; m = 1,2) ligated with terpyridine derivatives form stable assemblies due to the thermodynamic chelate effect. In the case of transition metal complexes, the σ-donor/π-acceptor character of the dative M–Npyridine bond contributes additionally to the stability of the resulting complexes. As a consequence, an impressive number of complexes have been prepared by varying the nature of the metal and by introducing various substituents onto the tpy part. A survey of the Cambridge Structural Database reveals that more than 600 complexes have been structurally characterised, with the number rapidly growing. Because of all these interesting features and properties, these compounds find widespread applications in biomedical sciences [4,5], for photovoltaic applications [6,7], as catalysts [8], etc.

On the other hand, five-membered heterocycles such as furan, pyrrole, selenophene, tellurophene or thiophene possess interesting features such as the capability to undergo chemical and electrochemical oxidation to afford polymers. These polymeric materials generally exhibit photophysical properties, making them interesting in materials science [9-12]. Finally, the rich chemistry associated with five-membered heterocycles easily allows various chemical modifications. In this respect, the attachment of such heterocycles, directly or through a linker, to a tpy system appears very interesting, since combining the intrinsic properties of the two heteroaromatics should allow both the preparation of original molecular compounds and the conception of advanced (polymeric) materials featuring novel properties. We have recently reviewed this concept for thienyl-functionalised terpyridines [13]. In contrast to the huge number of compounds of the latter type, furan-functionalised tpys have been studied to a lesser extend. Nevertheless, we feel that the interesting chemistry and potential of their furanyl-functionalised counterparts deserves to be highlighted. This minireview describes the state of the art concerning preparation and applications of such terpyridines bearing a furanyl ring.

Review

Synthesis by ring closure of 1,5-diketones

In 1976, Kröhnke introduced a synthetic methodology to prepare pyridine derivatives that relies on the ring closure of 1,5-diketo-derivatives [14]. This strategy was also successfully applied to the preparation of some furanyl-substituted terpyridines. The synthetic sequence starts from furanyl aldehydes 1–3 and 2-acetylpyridine (4). The first step is a base-mediated aldol-condensation that yields the α,β unsaturated ketones 5–7. Reacting these with pyridinium salt 8 afforded 1,5-diketo-derivatives 9–11 through Michael addition. These derivatives are generally not isolated, but undergo in situ ring closure performed in the presence of an ammonia source, such as ammonium acetate, leading to terpyridines 12–14 (Scheme 1) [4,15].

[1860-5397-8-41-i1]

Scheme 1: Synthesis of furanyl-substituted terpyridines 12–14 by using Kröhnke’s method.

In the context of a more environmentally friendly and “greener” chemistry, an adaptation of this well-established method was proposed with the aim of reducing the solvent use [16-18]. Namely, two equivalents of neat 2-acetylpyridine (4) were reacted with one equivalent of an aldehyde in the presence of sodium hydroxide without solvent, thus yielding 1,5-diketo-derivatives. Ring closure was then carried out in methanol in the presence of ammonium acetate, according to Scheme 2. In addition to reducing the amount of solvent , this one-pot two-steps procedure avoids preparation of pyridinium salt 8. Unfortunately, when applied to the synthesis of furanyl-substituted tpy 12, this method leads to irreproducible results [19]. Even turning to barium hydroxide as a base (which is known to favour Michael additions [20]) did not improve the course of the reaction in a substantial manner. Therefore, basic alumina [19,21] was tested, since it is known to be an efficient promoter of aldol condensations and Michael additions under solvent-free conditions [22,23]. Nevertheless, the treatment of furanyl-substituted aldehydes 1, 3 and 15 did not yield the targeted diketo-intermediates, but instead the chalcones 5, 7 and 16. The subsequent reaction of these with 8 afforded tpys 12, 14, and 17 in 51%, 4% and 7% yield, respectively (Scheme 2).

[1860-5397-8-41-i2]

Scheme 2: Synthesis of terpyridines under solvent-free conditions.

This “alumina” pathway not only offers better reproducibility but also allows access to tpys 14 and 17 (albeit in low yield) that could not be obtained by using sodium hydroxide or barium hydroxide. More recently, another one-pot two-steps procedure using the environmentally benign solvent ethanol was described [24]. The reaction is based on the same mechanism as the solvent-free synthesis described above, but provides better yields. This protocol was recently used to prepare the 4,4′,4′′-trisubstituted terpyridine 19 (Scheme 3), which bears two carboxylate groups at positions 4 and 4′′ and a furanyl ring on position 4′ [25]. The synthesis involves the use of ester-functionalised 2-acetylpyridine derivative 18 and furfuraldehyde (1). Since the reaction is performed in a basic medium, terpyridine formation is accompanied by ester hydrolysis.

[1860-5397-8-41-i3]

Scheme 3: Preparation of 4,4′,4′′-trisubstituted terpyridine containing carboxylate moieties.

It is interesting to note that Kröhnke’s methodology was also applied to the synthesis of a furanyl-substituted quinquepyridine, which can be considered as a terpyridine bearing two additional pyridine rings [26]. The synthesis starts with 6-carboxy-2-acetylpyridine (20), which is reacted with furfural (1), thus providing chalcone 21. This is then reacted with di-pyridinium salt 22 in the presence of ammonium acetate to afford quinquepyridine 23 (Scheme 4).

[1860-5397-8-41-i4]

Scheme 4: Synthetic pathway for the preparation of a furanyl-functionalised quinquepyridine.

Another possibility to access the key intermediate “1,5-diketone” is through the use of iminium salts as aldehyde equivalents [27]. For example, terpyridine 27 was obtained from the condensation of keto-pyridine 24 with salt 25. The reaction proceeds via diketo-intermediate 26, which is transformed to 27 in the presence of ammonium acetate (Scheme 5) [28].

[1860-5397-8-41-i5]

Scheme 5: Utilization of an iminium salt in the preparation of a furanyl-substituted tpy.

It is interesting to note that this cyclisation can lead to the formation of two different isomers [29,30], namely U- and S-shaped terpyridines 27, 28 (Figure 2). The ratio between both isomers is solvent dependent (Table 1).

[1860-5397-8-41-2]

Figure 2: Chemical structure of U- and S-shaped isomers.

Table 1: Influence of solvent on U/S ratio.

Solvent Ratio (U/S)
CH3CN 79/21
DMSO 100/0

In all of the above-mentioned examples, symmetric terpyridines were prepared. Nevertheless, it was demonstrated that also asymmetric tpys are accessible via the 1,5-diketone pathway [31]. Michael addition of ethyl picolinoylacetate 29 to chalcone 30 affords diketone 31 in 60% yield. Reaction with ammonium acetate to effect ring closure did not yield a terpyridine, but instead dihydropyridine 32. The latter undergoes aromatization upon reaction with benzoquinone to afford 33 (Scheme 6).

[1860-5397-8-41-i6]

Scheme 6: Preparation of an asymmetric furanyl-substituted terpyridine.

Synthesis by cross-coupling reaction

Cross-coupling reactions are widely used in organic chemistry [32] to create new C–C bonds. The importance of this technique was recently highlighted by the award of the 2010 Nobel Prize in Chemistry to Heck, Negishi and Suzuki for their contributions to the development of these reactions. Despite their widespread utilization in organic chemistry, cross-coupling reactions have been used rarely for the preparation of furanyl-substituted tpy. The only known literature example for this purpose uses the Stille reaction [33]. This C–C coupling, which involves the reaction between a halogenated or equivalent starting material and an organotin compound, was used to prepare 12 from 4′-(trifluoromethanesulfonyl)-2,2′′:6′,2′′-terpyridine (34) [34] and 2-tributylstannylfuran (35) in the presence of Pd(PPh3)4 as catalyst, according to Scheme 7 [15].

[1860-5397-8-41-i7]

Scheme 7: Synthesis of tpy by Stille cross-coupling reaction.

Chemical reactivity of furanyl-functionalised tpys: preparation of carboxylate derivatives

The principal application of furanyl-substituted terpyridines is their use as precursors for carboxylic acid-functionalised tpys. In fact, the furan ring can readily undergo oxidative cleavage under various conditions, thus providing an interesting route to carboxylates [35]. In the case of tpys, oxidation of the furanyl ring was performed by using potassium permanganate in a basic reaction medium, followed by acidification to recover the acids. This methodology allowed the preparation of compounds 36–38 (Scheme 8) [25,31,36-42].

[1860-5397-8-41-i8]

Scheme 8: Oxidation of the furan ring of furanyl-substituted terpyridines.

It is interesting to note that this procedure can be applied to the free ligand, but also directly on bis(terpyridine) Ru(II) complexes without degradation of the chelate cycles [43-47] (Scheme 9, Table 2). A series of carboxylic acid-functionalised complexes 44–48 was thus obtained from furanyl-functionalised complexes 39–43 using this methodology.

[1860-5397-8-41-i9]

Scheme 9: Direct oxidation of a furan ring attached on Ru(II) tpy complexes.

Table 2: Complexes obtained by direct oxidation of furanyl-functionalised tpys.

Starting materials Final products Yield
Compound R1 = Compound R2 =  
39 H 44 H 20%
40 OCH3 45 OCH3 68%
41 2-thienyl 46 2-thienyl 51%
42 3-thienyl 47 3-thienyl 64%
43 2-furanyl 48 COOH 48%

This “furan” route to carboxylic acid functionalised terpyridines, and their corresponding complexes, presents several advantages for the preparation of tpy-COOH compared to other methods [48-50]. In particular, the starting materials are easily available, the experimental protocol is very simple, yields are improved and purification is better facilitated compared to other methods.

The importance of the “furyl” route to carboxylic acid-functionalised tpys and tpys-complexes is highlighted by the fact that such compounds have found applications in various domains. For instance, tpy-based materials whose synthesis includes oxidation of a furan ring during their preparation, have been used as light-harvesting materials [36,42,45-47,51,52], as chemosensors [37], in supramolecular assemblies [38,39,44], as a photocatalyst for H2 generation [40,53] or for the preparation of hybrid materials, such as functionalised polyoxometalates as depicted in Figure 3 [41].

[1860-5397-8-41-3]

Figure 3: Example of polyoxometalate frameworks functionalised with tpy ligands and tpy-complex (reprinted with permission from [41], copyright (2011) American Chemical Society).

Utilization of furanyl-substituted terpyridines in biomedical sciences

Furanyl-terpyridines were probed in biomedical sciences as cytotoxic molecules. Compounds 12 and 13 were tested as anticancer agents against seven different cell lines [4]. Their activities were compared to that of doxorubicin, which is a currently used anticancer agent. Additionally, their cytotoxicity against normal cells was evaluated (Table 3).

Table 3: GI50 (μg/ml) for terpyridines 12 and 13 compared to doxorubicin. Cytotoxicities higher than the reference are highlighted in bold font.

Cell line Doxorubicin 12 13
A-498 (Human kidney carcinoma) 6.4 × 10−3 6.4 × 10−5 3.2 × 10−5
PC-3 (Human prostate adenocarcinoma) 2.9 × 10−2 2.5 × 10−3 4.4 × 10−3
HT-29 (Human colon adenocarcinoma) 4.6 × 10−3 2.4 × 10−3 2.6 × 10−3
A-549 (Human lung carcinoma) 9.2 × 10−2 2.2 × 10−1 8.0 × 10−2
HCT-15 (Human colon adenocarcinoma) 7.1 × 10−2 1.0 × 10−1 6.0 × 10−2
SK-OV-3 (Human ovary adenocarcinoma) 7.3 × 10−2 1.3 × 10−1 6.0 × 10−1
SK-MEL-2 (Human malignant melanoma) 5.9 × 10−2 9.9 3.3 × 10−1
RPTEC (Renal proximal tubule epithelial cells) 7.2 × 10−2 4.1 × 10−3 5.8 × 10−3

As can be seen from Table 3, these furanyl-functionalised terpyridines display, in many cases, better cytotoxicity than doxorubicin. Unfortunately, they are also more toxic toward normal cells (RPTEC). Note that, to date, the exact molecular mechanism of physiological action for these compounds has not yet been clearly elucidated.

Terpyridines 12 and 14 were also used as starting materials for the preparation of chelating agents and complexes with the aim of making fluorescent labels for biomolecules [15]. The synthetic pathway begins with the preparation of N,N′-dioxides 49 and 50 upon reaction with MCPBA. Treatment with trimethylsilyl cyanide allowed the introduction of a cyano group at the α-position with respect to the N-atoms, thus yielding the bis(nitrile) compounds 51 and 52. The cyano group was then converted to an amine function by reduction with BH3. Subsequent treatment with tert-butyl bromoacetate afforded amino esters 53 and 54. Ester groups of compound 53 were then hydrolyzed to the free acids to afford 55. The latter was then reacted with europium(III) or samarium(III) chlorides to provide lanthanide complexes 56 and 57 (Scheme 10).

[1860-5397-8-41-i10]

Scheme 10: Synthetic pathway to europium(III) and samarium(III) chelates 56 and 57.

The bromo-derivative 54 was further functionalised by cross-coupling reactions. Namely, the treatment of 54 with aminophenylacetylene in a Sonogashira reaction afforded terpyridine 58. The triple bond was then reduced by hydrogenation providing tpy 59, which features an alkyl spacer between the furanyl and phenyl ring. Cleavage of the pending ester moieties yielded polycarboxylic acid compound 60, which was reacted with EuCl3 leading to chelate complex 61. Finally, nucleophilic addition of the –NH2 groups of 61 to thiophosgene yielded terpyridine complex 62, which bears a thiocyanato group at the para-position (Scheme 11).

[1860-5397-8-41-i11]

Scheme 11: Synthetic pathway to prepare thiocyanato-functionalised tpys as potential biomolecule-labelling agents.

Because of the presence of a thiocyanato moiety in its structural motif and due to its fluorescence properties, compound 62 could be used potentially as a labelling agent for biomolecules. In fact, reaction between the reactive electrophilic thiocyanato group and a nucleophilic residue present on the biomolecule (amine, thiol, for example) should allow anchorage of 62. Another approach that was envisioned for the linking of fluorescent europium–terpyridine complexes to biomolecules is the use of click chemistry [54]. Again, 54 was used as a starting material and reacted with trimethylsilyl acetylene in a Sonogashira reaction. After deprotection of the trimethylsilyl moiety with tetrabutylammonium fluoride, terpyridine 63 was obtained. Reaction of the latter with 3-azidopropanol afforded the triazinyl-containing compound 64. Finally, the hydrolysis of the ester moieties followed by complexation to Eu(III) yielded the lanthanide complex 65 (Scheme 12).

[1860-5397-8-41-i12]

Scheme 12: Synthetic sequence envisioned for biomolecules labelling by click-chemistry.

This synthetic sequence was used to demonstrate the possibility to prepare labelled oligonucleotides starting from azido-functionalised ones and alkynyl-containing terpyridines. In all the examples cited above, furanyl-functionalised terpyridines were selected because of their capability to absorb light and to transfer the excitation energy to the chelated lanthanide metal ion. This gives rise to a strong fluorescence, a feature which is required for labelling studies.

Miscellaneous utilization of furanyl-functionalised tpys

Terpyridines functionalised with five-membered heterocycles, especially thiophene [13], and their derived complexes have proved to be interesting materials in the field of dye-sensitized solar cells (DSSC) [55]. Understanding in depth both the electrochemical and photophysical properties of such compounds is therefore of crucial importance. In this context, the octahedral Ru(II) complex 43 was studied and compared with analogous pyrrolyl, thienyl and bithienyl-substituted compounds 66–68 (Figure 4) in order to obtain information about the influence of the pendant heterocycle on the physicochemical properties [56].

[1860-5397-8-41-4]

Figure 4: Structure of pyrrolyl (66), thienyl (67) and bithienyl (68)-substituted complexes analogous to compound 43. PF6− counter-anions are omitted.

It appeared from this study that the bithienyl substituent has the most pronounced effect on the photophysical properties of this series of Ru complexes. Especially, 68 absorbs at a longer wavelength (Table 4), which constitutes an important requirement for sensitizers to be used in DSSC [6].

Table 4: UV–vis and emission data for complexes 43 and 66–68.

Complex λmax,abs (nm) λmax,em (nm)
43 500 660
66 507 665
67 499 670
68 514 710

Conclusion

This short review demonstrates that the combination of the furan heterocycle and the terpyridine ligand leads to a series of quite versatile functional molecules. The attached furan ring serves mainly as a precursor to carboxylic acid moieties with the final aim of preparing functionalised materials for application in devices, especially solar cells. Recent results obtained in this field with furan-containing molecules [57-59] demonstrate that the introduction of this heterocycle onto terpyridine is an interesting strategy. Additionally, furan-functionalised terpyridines revealed a potential utility in biomedical sciences. Owing to the rich chemistry associated with furan and pyridine rings, it is realistic to imagine the use of furanyl-functionalised terpyridines as a platform for further functionalisation to elaborate even more sophisticated compounds that may be useful in diverse domains.

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