Synthesis and spectroscopic properties of β-meso directly linked porphyrin–corrole hybrid compounds

  1. Baris Temelli and
  2. Hilal Kalkan

Hacettepe University, Department of Chemistry, Beytepe Campus, 06800, Ankara, Turkey

  1. Corresponding author email

Associate Editor: J. Aubé
Beilstein J. Org. Chem. 2018, 14, 187–193. doi:10.3762/bjoc.14.13
Received 09 Oct 2017, Accepted 05 Jan 2018, Published 22 Jan 2018

Abstract

The preparation of β-meso directly linked porphyrin–corrole hybrids was realized for the first time via an InCl3-catalyzed condensation reaction of 2-formyl-5,10,15,20-tetraphenylporphyrins with meso-substituted dipyrromethanes. Hybrid compounds have been characterized by 1H NMR, 13C NMR, 2D NMR, UV–vis absorption and fluorescence spectroscopy.

Keywords: corrole; hybrid compounds; indium(III) chloride; porphyrin; porphyrinoids

Introduction

Porphyrins and metalloporphyrins play an important role in chemistry, biology, medical and materials sciences because of their presence in biological compounds such as chlorophyll and heme molecules that have very important functions in the metabolism of living organisms [1,2]. In recent years, efforts in porphyrin chemistry have been focused on the synthesis of multichromophore containing compounds and their potential applications in molecular wires, sensors, nonlinear optical devices, photosensitizers and organic conducting materials [3-6]. The first studies on the synthesis of multichromophores were based on obtaining multiporphyrin arrays [7-9] that could stabilize only metal ions in a bivalent state. To overcome this limitation, porphyrin conjugates with different chromophore groups such as fullerene [10-12], BODIPY [13-15], corrole [16-23], phthalocyanine [24-26], subporphyrin [27] and expanded porphyrins [28-30] were prepared and their photophysical and electrochemical properties were characterized. Among these compounds, corroles, contracted porphyrin analogues [31-33], assumed an important place in porphyrin chemistry due to their small cavities, trianionic characters, high fluorescence quantum yields and favorable electronic properties. Porphyrin–corrole conjugates have been successfully used as donor–acceptor systems in photoinduced charge separation processes. It was shown that derivatives of these conjugates could be potentially used in photovoltaic applications [21-23]. In order to achieve rapid energy and electron transfer between macrocycles, the short distance between subunits keeps an important place. Therefore, two important factors affect the physical and electronic properties of porphyrin–corrole conjugates: (i) type of linkers and (ii) position of substitution (meso or β). So far, corrole macrocyles have been integrated into porphyrin conjugates via anthracene, biphenylene, xanthene, dibenzofuran [16-20], amide [21] and triazole [22,23] linkers. Despite the large number of studies on the synthesis of porphyrin–corrole conjugates, systematic studies on directly linked porphyrin–corrole hybrid structures are limited and there is no report on β-porphyrin, meso-corrole linked hybrids of these conjugates. Zheng et al. synthesized mesomeso directly linked porphyrin–corrole dyads by the condensation reaction of meso-formylated porphyrin with meso-substituted dipyrromethanes (Scheme 1A) [34]. Later, Sankar et al. used the same type of condensation reaction to obtain mesomeso linked corrole–porphyrin–corrole (Scheme 1B) [35] and porphyrin–corrrole–porphyrin triads (Scheme 1C) [36]. The only report on the synthesis of meso-porphyrin, β-corrole-linked hybrid structure described a Suzuki–Miyaura cross-coupling reaction between a β-borylated corrole and meso-bromoporphyrins (Scheme 1D) [37].

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Scheme 1: Overview of the synthesis of directly linked porphyrin–corrole hybrid compounds.

Recently, we have successfully synthesized mesomeso and β-meso-linked imine-bridged porphyrin–corrole conjugates and investigated intramolecular energy transfer between macrocycles [38]. As a part of our ongoing research on porphyrin–corrole conjugates, herein we describe a convenient synthesis of a series of novel directly linked porphyrin–corrole hybrid compounds. For this purpose, acid-catalyzed reactions of dipyrromethanes and aldehydes, which have been used frequently for the synthesis of meso-substituted corroles, were carried out [31,39,40]. The key bilane-substituted porphyrin intermediates 3 were obtained by the addition of an excess amount of meso-substituted dipyrromethanes 2 to β-formylated porphyrins 1 and these intermediates were oxidized in the reaction medium to form the desired hybrid structures 4 (Scheme 2).

[1860-5397-14-13-i2]

Scheme 2: Synthesis of β-meso directly linked porphyrin–corrole hybrid compounds.

Results and Discussion

Initially, the reaction of 2-formyl-5,10,15,20-tetraphenylporphyrin (1) with 4 equivalents of phenyldipyrromethane (2a) was tested using p-toluenesulfonic acid (TsOH) as catalyst at room temperature but no product was observed in the reaction (Table 1, entry 1). Increasing the reaction temperature affected the production of 4a and the target compound could be obtained with 6% yield (Table 1, entries 2–4). A screen of solvents revealed that chloroform provided the best yield and was superior to 1,2-dichloroethane, toluene and methanol (Table 1, entries 3–6). The ratio of 1a/2a played a little role in improving the yield of product (Table 1, entries 7–9). The yield of 4a increased slightly to 7% when the reaction was carried out with 6 equiv of 2a (Table 1, entry 8). Further increasing the amount of 2a led to the formation of unidentified byproducts in the reaction medium and a reduction of the yield of 4a (Table 1, entry 9). Then, the activities of different catalysts, varying from clay catalysts to Lewis acids, were tested in the model reaction (Table 1, entries 10–19). AgOTf, AlCl3, ZnBr2 and InCl3-catalyzed the reaction in higher yields with an unexpected byproduct, meso–β-substituted directly linked porphyrin–porphyrin dyad 5a (Table 1, entries 16–19). The structure of 5a was confirmed by comparison with literature data [41]. The highest yield of 4a was obtained with InCl3 (19%, Table 1, entry 19). Other catalysts gave no (Table 1, entries 10 and 11) or lower yields of products (Table 1, entries 12–15). When the reaction temperature increased to 80 °C by using 1,2-dichloroethane as solvent in the presence of InCl3 as catalyst, the product yield decreased to 14% (Table 1, entry 20).

Table 1: Optimization of the reaction conditions.

[Graphic 1]
Entry 1a/2a Solvent Catalyst Temp (°C) 4a (%)a 5a (%)a
1 1:4 CHCl3 TsOHb rt
2 1:4 CHCl3 TsOHb 40
3 1:4 CHCl3 TsOHb 60 6
4 1:4 ClCH2CH2Cl TsOHb 60 5
5 1:4 MeOH TsOHb 60 2
6 1:4 toluene TsOHb 60 4
7 1:2 CHCl3 TsOHb 60 1
8 1:6 CHCl3 TsOHb 60 7
9 1:10 CHCl3 TsOHb 60 4
10 1:6 CHCl3 Mont. K-10c 60
11 1:6 CHCl3 BF3·OEt2d 60
12 1:6 CHCl3 Mont. KSFc 60 2
13 1:6 CHCl3 Cu(OTf)2b 60 4
14 1:6 CHCl3 Amberlyst-15c 60 3
15 1:6 CHCl3 TFAb 60 8
16 1:6 CHCl3 AgOTfb 60 17 3
17 1:6 CHCl3 AlCl3d 60 14 3
18 1:6 CHCl3 ZnBr2b 60 15 2
19 1:6 CHCl3 InCl3b 60 19 4
20 1:6 ClCH2CH2Cl InCl3b 80 14 3

aIsolated yield after column chromatography. Catalyst amount: b10 mol %, c1 mmol aldehyde/1 g of catalyst, d100 mol %.

With the optimized reaction conditions in hand, different meso-substituted dipyrromethanes 2 were subjected to the condensation reactions (Scheme 3). Electronic properties of the substituents on the dipyrromethane generally did not show significant effects on the reactions except for the electron-donating methoxy substituent (Scheme 3, 4d), which resulted in a mixture of unidentified compounds after the reaction. This might be due to an acid-catalyzed rearrangement of the substituents, called scrambling, which is a common problem in porphyrin synthesis in the reaction of dipyrromethanes with aldehydes [42]. When electron-withdrawing 4-nitrophenyl and pentafluorophenyl substituents were used on the dipyrromethane, hybrid compounds 4c and 4e were isolated in 16% and 20% yields, respectively. The synthesis of 4e with InCl3 afforded a very low yield, thus an equimolar amount of AlCl3 was used to obtain this product. In order to expand the scope of the reaction, metal complexes of formylated porphyrins were subjected to the reaction. While Zn-porphyrin containing hybrid compound 4f was isolated in 21%, the Cu(II) complex of β-formylated porphyrin underwent the reaction to produce the hybrid compound 4g in 17% yield (Scheme 3).

[1860-5397-14-13-i3]

Scheme 3: Synthesis of porphyrin–corrole hybrid derivatives. *100 mol % of AlCl3 was used as a catalyst.

The structures of the hybrid compounds were identified by using 1H NMR, 13C NMR, 1H,1H-COSY NMR and HRMS techniques (see Supporting Information File 1). The 1H NMR spectrum of 4a is shown in Figure 1. As reported for similar dimeric porphyrin systems, one of the meso-linked phenyl substituents on the porphyrin core was located above the corrole macrocycle and was affected by the ring current. These phenyl protons appear strongly shifted toward higher field. The positions of the protons were assigned by comparing previously reported β–meso-substituted porphyrin arrays [41]. The para-proton (2), the meta-protons (3) and the ortho-protons (4) of the phenyl substituent appeared at 4.05 ppm, 4.64 ppm and 6.62 ppm, respectively. The β-protons of the porphyrin and the corrole macrocycles gave multiplets and doublets between 8.00 and 10.00 ppm as expected. Inner N–H protons of the corrole macrocycle gave a very broad signal and could not be determined due to its high unsymmetrical property and an excess amount of tautomeric structures. The N–H protons of the porphyrin macrocycle resonated at −2.46 ppm (Supporting Information File 1, Figure S1).

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Figure 1: 1H NMR spectrum of 4a in CDCl3.

The absorption spectra of hybrid compounds have been recorded and λmax values are listed with molar extinction coeffients (ε) in Table 2. Split Soret bands were observed for 4b, 4e and metalloporphyrin 4g. These results indicate a strong exciton coupling between the neighbor macrocycles in hybrid structures. The same effect was also observed in the emission spectra. Fluorescence spectra of the compounds gave split emission bands except for 4c. Fluorescence life times and quantum yields were further determined for the hybrid compounds (Table 2). Measured fluorescence life times (4–9 ns), and fluorescence quantum yields are in agreement with the literature data [35,36]. Strong electron-withdrawing pentafluorophenyl-substituted 4e and Zn–porphyrin complex 4f gave higher quantum yields compared to reported literature values for mesomeso-linked porphyrin–corrole dyads [34] and traids [35]. High fluorescence quantum yield properties of the new hybrid compounds are promising for many applications such as organic optoelectronics or biological imaging.

Table 2: Photophysical properties of hybrid compounds.

Compound λabs/nm (ε/10−5 M−1·cm−1)a λem/nmb Φc τ/nsd
4a 421 (5.35), 520 (4.34), 552 (4.08), 595 (4.03), 652 (3.92) 664, 723 0.10 7.4
4b 421 (5.32), 441 (4.96), 523 (4.18), 559 (4.08), 597 (4.04), 659 (3.53) 664, 725 0.22 7.1
4c 421 (4.94), 518 (4.08), 596 (3.90), 662 (3.81) 692 0.04 8.5
4e 420 (5.21), 443 (5.07), 521 (4.32), 554 (4.10), 591 (4.06), 646 (3.86) 663, 717 0.27 5.4
4f 421 (4.57), 442 (4.46), 524 (3.49), 553 (3.64), 657 (2.98) 663, 728 0.41 7.8
4g 418 (4.65), 438 (4.47), 542 (3.68), 656 (2.94) 651, 720 0,01 4.4

aAbsorption spectra were recorded in CHCl3. bFluorescence spectra were recorded in CHCl3ex: 420 nm). cBased on TPP in toluene (Φ = 0.11). dExcited at 390 nm.

Conclusion

In summary, we have synthesized the first examples of β-porphyrin, meso-corrole substituted directly linked porphyrin–corrole hybrid compounds via a condensation reaction of meso-substituted dipyrromethanes with β-formylated meso-tetraphenylporphyrins. Spectroscopic and photophysical properties of the new hybrid structures have been determined. Higher quantum yields of some of the synthesized hybrid compounds indicate that these compounds can be considered as good candidates for many important applications ranging from photovoltaics to medicine.

Supporting Information

Supporting Information File 1: General experimental information, experimental details on the synthesis of products 4 and 5a, and full characterization data of all products.
Format: PDF Size: 2.3 MB Download

Acknowledgements

The authors thank The Scientific and Technological Research Council of Turkey (project number: 115Z886) and Hacettepe University (BAP project 014 09 601 002-723) for financial support.

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